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Sample records for sub-3 nm particle

  1. Nucleation and growth of sub-3 nm particles in the polluted urban atmosphere of a megacity in China

    Directory of Open Access Journals (Sweden)

    H. Yu

    2016-03-01

    Full Text Available Particle size distribution down to 1.4 nm was measured in the urban atmosphere of Nanjing, China, in spring, summer, and winter during 2014–2015. Sub-3 nm particle event, which is equivalent to nucleation event, occurred on 42 out of total 90 observation days, but new particles could grow to cloud condensation nuclei (CCN-active sizes on only 9 days. In summer, infrequent nucleation was limited by both unfavorable meteorological conditions (high temperature and relative humidity – RH and reduced anthropogenic precursor availability due to strict emission control measures during the 2014 Youth Olympic Games in Nanjing. The limiting factors for nucleation in winter and spring were meteorological conditions (radiation, temperature, and RH and condensation sink, but for the further growth of sub-3 nm particles to CCN-active sizes, anthropogenic precursors again became limiting factors. Nucleation events were strong in the polluted urban atmosphere. Initial J1.4 at the onset and peak J1.4 at the noontime could be up to 2.1 × 102 and 2.5 × 103 cm−3 s−1, respectively, during the eight nucleation events selected from different seasons. Time-dependent J1.4 usually showed good linear correlations with a sulfuric acid proxy for every single event (R2 = 0.56–0.86, excluding a day with significant nocturnal nucleation, but the correlation among all eight events deteriorated (R2 =  0.17 due to temperature or season change. We observed that new particle growth rate (GR did not increase monotonically with particle size, but had a local maximum up to 25 nm h−1 between 1 and 3 nm. The existence of local maxima GR in sub-3 nm size range, though sensitive to measurement uncertainties, gives new insight into cluster dynamics in polluted environments. In this study such growth rate behavior was interpreted as the solvation effect of organic activating vapor in newly formed inorganic nuclei.

  2. Size-resolved fluxes of sub-100-nm particles over forests

    DEFF Research Database (Denmark)

    Pryor, Sara; Barthelmie, Rebecca Jane; Spaulding, A.M.

    2009-01-01

    Dry deposition of atmospheric particles is critically dependent on particle size and plays a key role in dictating the mass and number distributions of atmospheric particles. However, modeling dry deposition is constrained by a lack of understanding of controlling dependencies and accurate size......-resolved observations. We present size-resolved particle number fluxes for sub-100-nm particle diameters (Dp) over a deciduous forest derived using eddy covariance applied to data from a fast mobility particle sizer. The size-resolved particle number fluxes in 18 diameters between 8 and 100 nm were collected during...... leaf-on and are statistically robust. Particle deposition velocities normalized by friction velocity (v d +) are approximately four times smaller than comparable values for coniferous forests reported elsewhere. Comparison of the data with output from a new one-dimensional mechanistic particle...

  3. Influence of defects on sub-Å optical linewidths in Eu{sup 3+}: Y{sub 2}O{sub 3} particles

    Energy Technology Data Exchange (ETDEWEB)

    Oliveira Lima, Karmel de [PSL Research University, Chimie ParisTech – CNRS, Institut de Recherche de Chimie Paris, 75005 Paris (France); Rocha Gonçalves, Rogéria [Departamento de Química, Faculdade de Filosofia Ciências e Letras de Ribeirão Preto, Universidade de São Paulo, Avenida Bandeirantes, 3900, CEP 14040-901 Ribeirão Preto, São Paulo, Brasil (Brazil); Giaume, Domitille [PSL Research University, Chimie ParisTech – CNRS, Institut de Recherche de Chimie Paris, 75005 Paris (France); Ferrier, Alban, E-mail: alban.ferrier@chimie-paristech.fr [PSL Research University, Chimie ParisTech – CNRS, Institut de Recherche de Chimie Paris, 75005 Paris (France); Sorbonne Universités, UPMC Univ Paris 06, 75005 Paris (France); Goldner, Philippe, E-mail: philippe.goldner@chimie-paristech.fr [PSL Research University, Chimie ParisTech – CNRS, Institut de Recherche de Chimie Paris, 75005 Paris (France)

    2015-12-15

    Rare earth doped nanocrystals have been recently suggested as useful materials for applications in quantum information processing. To reach optical properties closer to bulk crystals ones, it is still necessary to reduce the defects that can arise in nanoscale structures. Here, we probe the defects level by monitoring the inhomogeneous broadening of the {sup 7}F{sub 0}→{sup 5}D{sub 0} transition in particles of 0.3% at% Eu{sup 3+}:Y{sub 2}O{sub 3}. We find that lines as narrow as 14 GHz (0.015 nm), a value comparable to single crystals, can be obtained in 150 nm particles calcinated at 1200 °C. The additional broadening observed for particles calcinated at lower temperature is attributed to defects inside crystallites and not to surface effects. A linear correlation is also observed between optical and Raman linewidths, suggesting that both processes are sensitive to the same defects. {sup 5}D{sub 0} excited state lifetimes are well described by a model based on an effective refractive index and we conclude that the defects causing the inhomogeneous broadening have no effect on the excited state population.

  4. Structural, morphological and luminescence properties of nanocrystalline up-converting Y{sub 1.89}Yb{sub 0.1}Er{sub 0.01}O{sub 3} phosphor particles synthesized through aerosol route

    Energy Technology Data Exchange (ETDEWEB)

    Lojpur, V.; Mancic, L. [Institute of Technical Sciences of the Serbian Academy of Sciences and Arts, K. Mihailova 35/IV, 11000 Belgrade (Serbia); Rabanal, M.E. [University Carlos III of Madrid, Avd. Universidad 30, 28911 Leganes, Madrid (Spain); Dramicanin, M.D. [Vinca Institute of Nuclear Science, University of Belgrade, P.O. Box 522, Belgrade (Serbia); Tan, Z.; Hashishin, T.; Ohara, S. [JWRI, Osaka University, 11-1 Mihogaoka, Ibaraki, Osaka 567-0047 (Japan); Milosevic, O., E-mail: olivera.milosevic@itn.sanu.ac.rs [Institute of Technical Sciences of the Serbian Academy of Sciences and Arts, K. Mihailova 35/IV, 11000 Belgrade (Serbia)

    2013-12-15

    Highlights: •The Y{sub 1.89}Yb{sub 0.1}Er{sub 0.01}O{sub 3} phosphor particles are synthesized via aerosol route. •We report influence of process parameters on the particle structure and morphology. •Spherical, submicronic size and nano-crystalline particle morphology are confirmed. •The particles show improved luminescence properties and decay time. •Synthesized powders exhibit the temperature dependant up-conversion emission. -- Abstract: Nanocrystalline up-converting Y{sub 2}O{sub 3}:Yb{sup 3+}, Er{sup 3+} phosphor particles were processed in a dispersed system-aerosol, generated ultrasonically at 1.3 MHz from common nitrate precursor solution having fixed ytterbium-to-erbium concentration ratio. The appropriate process parameters: residence time 21 s, carrier gas (air) flow rate 1.6 dm{sup 3}/min, synthesis temperature 900 °C, led to the formation of un-agglomerated spherical nanostructured secondary particles, having mean particle size of approx 450 nm, composed of primary nanoscaled (20 nm) subunits. In order to reach targeting phase crystallinity, the as-prepared particles were additionally annealed at 1100 °C in air for 12, 24 and 48 h, respectively. Particle structure, morphology and purity were analyzed by X-ray powder diffraction (XRPD), scanning electron microscopy (FESEM/SEM), analytical and high resolution transmission electron microscopy (TEM/HRTEM) in combination with energy dispersive X-ray analysis and Fourier Transform Infrared Spectroscopy (FTIR). All samples crystallized in a cubic bixbyte-structure, space group Ia-3. The crystallite size changed with annealing time from 30 nm in as-prepared sample to 135 nm in sample annealed for 48 h, respectively. Emission spectra were assigned to the following trivalent erbium f–f electronic transitions: {sup 2}H{sub 9/2} → {sup 4}I{sub 15/2} (blue: 407–420 nm), ({sup 2}H{sub 11/2}, {sup 4}S{sub 3/2}) → {sup 4}I{sub 15/2} (green: 510–590 nm), and {sup 4}F{sub 9/2} → {sup 4}I{sub 15

  5. Particles on surfaces of laser ablated Y{sub 1}Ba{sub 2}Cu{sub 3}O{sub 7-{delta}} films

    Energy Technology Data Exchange (ETDEWEB)

    Zheng, X.Y.; Zhu, S. [Tennessee Univ., Knoxville, TN (United States); Lowndes, D.H.; Warmack, R.J. [Oak Ridge National Lab., TN (United States)

    1993-09-01

    Pulsed laser deposition of Y{sub 1}Ba{sub 2}Cu{sub 3}O{sub 7-{delta}} films grown at heater temperature of 720 and 800 C on SrTiO{sub 3} and MgO substrates with thickness ranging from a nominal 5 unit cells to 200 nm were studied by STM and SEM. Size and density of particles present in the films were found to depend on film thickness, growth temperature and substrate. STM images indicate a correlation between film growth mode and particle density: the onset of big particles comes after the growth mode changes from layer-like to island growth.

  6. Laboratory observations of temperature and humidity dependencies of nucleation and growth rates of sub-3 nm particles

    Science.gov (United States)

    Yu, Huan; Dai, Liang; Zhao, Yi; Kanawade, Vijay P.; Tripathi, Sachchida N.; Ge, Xinlei; Chen, Mindong; Lee, Shan-Hu

    2017-02-01

    Temperature and relative humidity (RH) are the most important thermodynamic parameters in aerosol formation, yet laboratory studies of nucleation and growth dependencies on temperature and RH are lacking. Here we report the experimentally observed temperature and RH dependences of sulfuric acid aerosol nucleation and growth. Experiments were performed in a flow tube in the temperature range from 248 to 313 K, RH from 0.8% to 79%, and relative acidity (RA) of sulfuric acid from 6 × 10-5 to 0.38 (2 × 107-109 cm-3). The impurity levels of base compounds were determined to be NH3 nucleation at fixed sulfuric acid concentration but impede nucleation when RA is fixed. It is also shown that binary nucleation of sulfuric acid and water is negligible in planetary boundary layer temperature and sulfuric acid ranges. An empirical algorithm was derived to correlate the nucleation rate with RA, RH, and temperature together. Collision-limited condensation of free-sulfuric acid molecules fails to predict the observed growth rate in the sub-3 nm size range, as well as its dependence on temperature and RH. This suggests that evaporation, sulfuric acid hydration, and possible involvement of other ternary molecules should be considered for the sub-3 nm particle growth.

  7. The effect of diameter ratio between transducers and reactor in sonication-assisted synthesis of Ba{sub 0.7}Sr{sub 0.3}TiO{sub 3} and Ba{sub 0.3}Sr{sub 0.7}TiO{sub 3} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Manaf, A., E-mail: azwar@ui.ac.id; Fahmi, Agam Aidil [Department of Physics, FMIPA, Universitas Indonesia, Kampus UI Depok (Indonesia); Yustanti, Erlina [Department of Physics, FMIPA, Universitas Indonesia, Kampus UI Depok (Indonesia); Department of Metallurgy, Faculty of Engineering, University of Sultan AgengTirtayasa Jl. Jenderal Sudirman KM 03 Cilegon-Banten 65134 (Indonesia)

    2016-04-19

    This paper describes the particle size characterization of mechanically alloyed Ba{sub 0.7}Sr{sub 0.3}TiO{sub 3} and Ba{sub 0.3}Sr{sub 0.7}TiO{sub 3} prepared with the aid of a high-power ultrasonic destruction. Analytical-grade BaCO{sub 3}, TiO{sub 2} and SrCO{sub 3} with a purity greater than 99 wt.% were used as precursors for Ba{sub 0.7}Sr{sub 0.3}TiO{sub 3} and Ba{sub 0.3}Sr{sub 0.7}TiO{sub 3}. The mechanically powders were respectively sintered at 1200 °C for 3 hours to form crystalline powders. This work is aimed at studying the effect of diameter ratio between reactor and transducer of a high power sonicator on the Ba{sub 0.7}Sr{sub 0.3}TiO{sub 3} and Ba{sub 0.3}Sr{sub 0.7}TiO{sub 3} nanoparticles formation. The presence of a single phase of the two materials was confirmed by X-Ray Diffraction (XRD). The concentration of the particles in demineralized water was 3.0 g / 100 mL which become the object of 3 hours ultrasonic destruction subjected to the application of transducer in which the ratio between the diameter of the reactor and the transducer (D/d) was fixed at 1.4, 1.6 and 1.8 respectively. It was found that the mean particle size before the ultrasonic destruction was 538 nm for Ba{sub 0.7}Sr{sub 0.3}TiO{sub 3} and 480 nm for Ba{sub 0.3}Sr{sub 0.7}TiO{sub 3}. With D/d of 1.8, the mean particle size of the two materials was found to decrease drastically to 38 nm and 24 nm, respectively. These mean particle sizes were respectively comparable with that of the crystallite size of the particles derived using the Whole Powder Pattern Modelling (WPPM) from which the mean crystallite size of 22 nm for Ba{sub 0.7}Sr{sub 0.3}TiO{sub 3} and 14 nm for Ba{sub 0.3}Sr{sub 0.7}TiO{sub 3} were obtained. It is then confirmed single nanocrystallite Ba{sub 0.7}Sr{sub 0.3}TiO{sub 3} and Ba{sub 0.3}Sr{sub 0.7}TiO{sub 3} particles were already achieved. We can conclude that the ultrasonic destruction to mechanically milled crystalline particles would be one

  8. Investigations of mussel-inspired polydopamine deposition on WC and Al{sub 2}O{sub 3} particles: The influence of particle size and material

    Energy Technology Data Exchange (ETDEWEB)

    Mondin, Giovanni, E-mail: giovanni.mondin@chemie.tu-dresden.de [Department of Inorganic Chemistry, Dresden University of Technology, Bergstrasse 66, 01069 Dresden (Germany); Haft, Marcel, E-mail: m.haft@ifw-dresden.de [Leibniz Institute for Solid State and Materials Research (IFW) Dresden, Institute for Solid State Research, Helmholtzstr. 20, 01069 Dresden (Germany); Wisser, Florian M., E-mail: florian.wisser@chemie.tu-dresden.de [Department of Inorganic Chemistry, Dresden University of Technology, Bergstrasse 66, 01069 Dresden (Germany); Leifert, Annika, E-mail: annika.leifert@chemie.tu-dresden.de [Department of Inorganic Chemistry, Dresden University of Technology, Bergstrasse 66, 01069 Dresden (Germany); Mohamed-Noriega, Nasser, E-mail: nasser.mohamed-noriega@chemie.tu-dresden.de [Department of Inorganic Chemistry, Dresden University of Technology, Bergstrasse 66, 01069 Dresden (Germany); Dörfler, Susanne, E-mail: susanne.doerfler@chemie.tu-dresden.de [Department of Inorganic Chemistry, Dresden University of Technology, Bergstrasse 66, 01069 Dresden (Germany); Hampel, Silke, E-mail: s.hampel@ifw-dresden.de [Leibniz Institute for Solid State and Materials Research (IFW) Dresden, Institute for Solid State Research, Helmholtzstr. 20, 01069 Dresden (Germany); Grothe, Julia, E-mail: stefan.kaskel@chemie.tu-dresden.de [Department of Inorganic Chemistry, Dresden University of Technology, Bergstrasse 66, 01069 Dresden (Germany); Kaskel, Stefan, E-mail: julia.grothe@chemie.tu-dresden.de [Department of Inorganic Chemistry, Dresden University of Technology, Bergstrasse 66, 01069 Dresden (Germany)

    2014-12-15

    Polydopamine, formed by oxidation of dopamine, is a bioinspired polymer developed for multifunctional coatings by Lee et al. in 2007 by drawing inspiration from the adhesive proteins found in mussels. Due to their high versatility and substrate-independence, polydopamine coatings are gaining considerable attention in a plethora of research fields, particularly in the coating of particles, but systematic investigations of the polydopamine coating process are lacking in the literature. In this study, we explore by TEM and thermogravimetric analysis the polydopamine coating process on alumina microparticles, tungsten carbide microparticles and tungsten carbide nanoparticles. By choosing two substrates with similar size but different material (Al{sub 2}O{sub 3} and WC), as well as two substrates of the same material but different size (WC micro- and nanoparticles) we investigate the effects of both substrate material and substrate size, in order to gain some insights into the polydopamine particle coating process. As opposed to what is generally assumed in the literature, we found that the polydopamine coating thicknesses on particles, as well as the thickness growing trend, depend on the particles size and material. In particular, after 24 h of polymerization time the polydopamine coatings reached a thickness of 65 ± 10 nm in the case of Al{sub 2}O{sub 3} microparticles, 18 ± 4 nm in the case of WC microparticles and 33 ± 6 nm in the case of WC nanoparticles. - Highlights: • The coating of different particles with polydopamine was systematically investigated. • Al{sub 2}O{sub 3} microparticles and WC microparticles and nanoparticles were investigated. • The thickness of the polydopamine coating depends on the particle size. • The thickness of the polydopamine coating depends on the particle material.

  9. Fabrication of BaTiO{sub 3}/Ni composite particles and their electro-magneto responsive properties

    Energy Technology Data Exchange (ETDEWEB)

    Lu, Yaping [Key Laboratory of Applied Surface and Colloid Chemistry (Shaanxi Normal University), Ministry of Education, Xi’an 710119 (China); School of Chemistry & Chemical Engineering, Shaanxi Normal University, Xi’an 710119 (China); Gao, Lingxiang, E-mail: gaolx@snnu.edu.cn [Key Laboratory of Applied Surface and Colloid Chemistry (Shaanxi Normal University), Ministry of Education, Xi’an 710119 (China); School of Chemistry & Chemical Engineering, Shaanxi Normal University, Xi’an 710119 (China); Wang, Lijuan [Key Laboratory of Applied Surface and Colloid Chemistry (Shaanxi Normal University), Ministry of Education, Xi’an 710119 (China); School of Chemistry & Chemical Engineering, Shaanxi Normal University, Xi’an 710119 (China); Xie, Zunyuan, E-mail: zyxie123@snnu.edu.cn [Key Laboratory of Applied Surface and Colloid Chemistry (Shaanxi Normal University), Ministry of Education, Xi’an 710119 (China); School of Chemistry & Chemical Engineering, Shaanxi Normal University, Xi’an 710119 (China); Gao, Meixiang [Yulin Vocational and Technical College, Yulin 719000 (China); Zhang, Weiqiang [Key Laboratory of Applied Surface and Colloid Chemistry (Shaanxi Normal University), Ministry of Education, Xi’an 710119 (China); School of Chemistry & Chemical Engineering, Shaanxi Normal University, Xi’an 710119 (China)

    2017-07-15

    Graphical abstract: The spherical BaTiO{sub 3}/Ni particles with excellent structure were made by one-step method through fixing the metal Ni(0) reduced by a specific reducing agent (N{sub 2}H{sub 4}·H{sub 2}O) on the surface of the BaTiO{sub 3} particles with grain diameter of ∼500 nm. BaTiO{sub 3}/Ni particle has double responses of electric and magnetic field simultaneously. Consequentially, coating magnetic metal on BT particle is proposed an effective method to prepare novel electro-magneto responsive particles and one basis of electro-magneto responsive elastomers. - Highlights: • The BaTiO{sub 3}/Ni composite particles were fabricated. • The content of Ni(0) in nickel sheath is 70.2%. • The BaTiO{sub 3}/Ni particles have double responses of electric and magnetic field. - Abstract: BaTiO{sub 3} (BT)/Ni composite particles were made by one-step method through agglomerating the metal Ni(0) nanoparticles reduced by a specific reducing agent (N{sub 2}H{sub 4}·H{sub 2}O) on the surface of BT sphere with diameter of ∼500 nm. The BT/Ni composite particles were characterized by the means of scanning electron microscope (SEM), transmission electron microscopy (TEM), X-ray diffractometer (XRD) and X-ray photoelectron spectroscopy (XPS). In BT/Ni particles, pure BT spherical particle was coated with Ni nanoparticles agglomerated on its surface. The average thickness of the Ni sheath was ∼30 nm and the content of Ni(0) and Ni (II) in the sheath were 70.2% and 29.8%, respectively. The responsive effects of BT/Ni particles filled in hydrogel elastomer were investigated by the viscoelastic properties. The results indicate that the BT/Ni particles exhibit electro and magneto coordinated responsive properties (E = 1 kV/mm, H = 0.1 T/mm), which is superior to BT particles with individual electro response.

  10. Particle size effect on magnetic and transport properties of La/sub 0.7/Ca/sub 0.3/MnO/sub 3/ nanoparticles

    International Nuclear Information System (INIS)

    Qaseem, S.; Mumtaz, A.; Hasanain, S.K.; Maaz, K.

    2010-01-01

    La/sub 0.7/Ca/sub 0.3/MnO/sub 3/ nanoparticles have been synthesized by modified citrate route with particle sizes of 20, 26 and 32 +- 3 nm respectively. The structural characterization has been performed by XRD and TEM analyses while magnetic characterization has been performed by vibrating sample magnetometer (VSM). This work presents the study of size effects on magnetic and electrical properties of Ca-doped CMR nanoparticles (La/sub 0.7/Ca/sub 0.3.MnO/sub 3/). Different particle sizes have been prepared by a wet chemical route. Magnetic characterization reveals that magnetization increases with the increase in the particle size and the magnetic transition temperature for larger particles is the same as in the bulk (258K). The ferromagnetic and resistive transitions are however broad compared to the case of bulk presumably due to the role of the surface. The metal-insulator transition temperature is found to be at 158K while the resistivity shows anomalous low temperature behavior with an upturn at low temperatures presu due to coulomb blockade effects. Furthermore, the field dependence of the resistivity displays nonmonotonic behavior and is explained in terms of the field assisted tunneling between grains. (author)

  11. Y{sub 2}O{sub 3}: Eu{sup 3+}, Tb{sup 3+} spherical particles based anti-reflection and wavelength conversion bi-functional films: Synthesis and application to solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Miao, Hui [School of Physics, Northwest University, Xi’an 710069 (China); National Photoelectric Technology and Functional Materials & Application of Science and Technology International Cooperation Base, Northwest University, Xi’an 710069 (China); Ji, Ruonan [School of Physics, Northwest University, Xi’an 710069 (China); Hu, Xiaoyun, E-mail: hxy3275@nwu.edu.cn [School of Physics, Northwest University, Xi’an 710069 (China); National Photoelectric Technology and Functional Materials & Application of Science and Technology International Cooperation Base, Northwest University, Xi’an 710069 (China); Han, Linzi; Hao, Yuanyuan; Sun, Qian [School of Physics, Northwest University, Xi’an 710069 (China); Zhang, Dekai [School of Physics, Northwest University, Xi’an 710069 (China); National Photoelectric Technology and Functional Materials & Application of Science and Technology International Cooperation Base, Northwest University, Xi’an 710069 (China); Fan, Jun [School of Chemical Engineering, Northwest University, Xi’an 710069 (China); Bai, Jintao [School of Physics, Northwest University, Xi’an 710069 (China); National Photoelectric Technology and Functional Materials & Application of Science and Technology International Cooperation Base, Northwest University, Xi’an 710069 (China); and others

    2015-04-25

    Highlights: • Eu{sup 3+} and Tb{sup 3+} co-doped Y{sub 2}O{sub 3} particles were successfully prepared. The as prepared particles can convert UV region photos to visible photons between 460 nm and 640 nm, which just matched the spectral response of most solar cells. • Y{sub 2}O{sub 3} is not only a good photoluminescence host material, but also it has high corrosion resistivity, thermal stability, and transparency from violet to infrared light. Cooperated with SiO{sub 2} sols, it could realize a better anti-reflection property. • As a proof-of-concept application, the as prepared bi-functional films could effectively improve the photoelectric conversion efficiency by 0.23% compared to pure SiO{sub 2} AR coating film and 0.55% compared to glass. - Abstract: In this study, Eu{sup 3+} and Tb{sup 3+} co-doped Y{sub 2}O{sub 3} particles were prepared via the simple, cost-effective urea homogeneous precipitation method without additives. The chosen particles were added in the SiO{sub 2} sols to get anti-reflection (AR) and wavelength conversion bi-functional films. Careful investigations were carried out to find the optimum preparation conditions and proper morphology. SEM images showed that the particle sizes reduced as metal ion/urea ratio decreased. Additionally, the extracted particles turned from sphere to lamellar type when the deionized water, which was used as solvent, reduced to a certain extent. The mechanisms of the morphology formation and diversification were proposed as well. The as prepared materials can convert UV region photos to visible photons between 460 nm and 640 nm, which just matched the spectral response of most solar cells. The spherical sample showed better luminescence performance than the one with lamellar morphology. In addition, the optical transmittance spectra indicated that the films adding spherical particles had better anti-reflective performance, and the best adding amount was 0.08 g. Finally, As a proof-of-concept application

  12. Performance of diethylene glycol-based particle counters in the sub-3 nm size range

    CERN Document Server

    Wimmer, D; Franchin, A; Kangasluoma, J; Kreissl, F; Kürten, A; Kupc, A; Metzger, A; Mikkilä, J; Petäjä, J; Riccobono, F; Vanhanen, J; Kulmala, M; Curtius, J

    2013-01-01

    When studying new particle formation, the uncertainty in determining the "true" nucleation rate is considerably reduced when using condensation particle counters (CPCs) capable of measuring concentrations of aerosol particles at sizes close to or even at the critical cluster size (1–2 nm). Recently, CPCs able to reliably detect particles below 2 nm in size and even close to 1 nm became available. Using these instruments, the corrections needed for calculating nucleation rates are substantially reduced compared to scaling the observed formation rate to the nucleation rate at the critical cluster size. However, this improved instrumentation requires a careful characterization of their cut-off size and the shape of the detection efficiency curve because relatively small shifts in the cut-off size can translate into larger relative errors when measuring particles close to the cut-off size. Here we describe the development of two continuous-flow CPCs using diethylene glycol (DEG) as the working fluid. The desig...

  13. Bactericidal effect of blue LED light irradiated TiO{sub 2}/Fe{sub 3}O{sub 4} particles on fish pathogen in seawater

    Energy Technology Data Exchange (ETDEWEB)

    Cheng, T.C. [Department of Tropical Agriculture and International Cooperation, National Pingtung University of Science and Technology, Taiwan (China); Yao, K.S. [Department of Horticulture, National Taitung Junior College, Taiwan (China); Yeh, N. [Mingdao University, Taiwan (China); Chang, C.I. [Aquaculture Division, Fisheries Research Institute, Council of Agriculture, Taiwan (China); Hsu, H.C. [Department of Life Science, Mingdao University, Taiwan (China); Gonzalez, F. [Department of Tropical Agriculture and International Cooperation, National Pingtung University of Science and Technology, Taiwan (China); Chang, C.Y., E-mail: cyc1136@yahoo.com.tw [Center of General Education, National Taitung Junior College, Taiwan (China)

    2011-05-31

    This study uses blue LED light ({lambda}{sub max} = 475 nm) activated TiO{sub 2}/Fe{sub 3}O{sub 4} particles to evaluate the particles' photocatalytic activity efficiency and bactericidal effects in seawater of variable salinities. Different TiO{sub 2} to Fe{sub 3}O{sub 4} mole ratios have been synthesized using sol-gel method. The synthesized particles contain mainly anatase TiO{sub 2}, Fe{sub 3}O{sub 4} and FeTiO{sub 3}. The study has identified TiO{sub 2}/Fe{sub 3}O{sub 4}'s bactericidal effect to marine fish pathogen (Photobacterium damselae subsp. piscicida BCRC17065) in seawater. The SEM photo reveals the surface destruction in bacteria incubated with blue LED irradiated TiO{sub 2}/Fe{sub 3}O{sub 4}. The result of this study indicates that 1) TiO{sub 2}/Fe{sub 3}O{sub 4} acquires photocatalytic activities in both the freshwater and the seawater via blue LED irradiation, 2) higher photocatalytic activities appear in solutions of higher TiO{sub 2}/Fe{sub 3}O{sub 4} mole ratio, and 3) photocatalytic activity decreases as salinity increases. These results suggest that the energy saving blue LED light is a feasible light source to activate TiO{sub 2}/Fe{sub 3}O{sub 4} photocatalytic activities in both freshwater and seawater.

  14. Microstructure and tensile properties of oxide dispersion strengthened Fe–14Cr–0.3Y{sub 2}O{sub 3} and Fe–14Cr–2W–0.3Ti–0.3Y{sub 2}O{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Auger, M.A., E-mail: mauger@fis.uc3m.es [Departamento de Física, Universidad Carlos III de Madrid, 28911 Leganés (Spain); Castro, V. de; Leguey, T.; Monge, M.A.; Muñoz, A.; Pareja, R. [Departamento de Física, Universidad Carlos III de Madrid, 28911 Leganés (Spain)

    2013-11-15

    Two ODS ferritic steels with nominal compositions (wt.%): Fe–14Cr–0.3Y{sub 2}O{sub 3} and Fe–14Cr–2W–0.3Ti–0.3Y{sub 2}O{sub 3} have been produced by mechanical alloying and consolidation by hot isostatic pressing. The microstructure and tensile properties of these materials after being forged and heat-treated at 1123 K have been investigated to clarify the interrelation between composition, microstructure and mechanical properties. The second-phase precipitates in these alloys have been analyzed by high-angle annular dark-field imaging in scanning TEM mode and electron diffraction. Fe–14Cr–2W–0.3Ti–0.3Y{sub 2}O{sub 3} exhibits a duplex microstructure consisting of large recrystallized grains, as large as 1.5 μm, and unrecovered regions containing submicron equiaxed grains. In addition, three types of secondary phase particles have been found: large M{sub 23}C{sub 6} particles containing W and Cr, (Cr + Ti) rich spherical particles with diameters between 50 and 500 nm, and fine (Y + Ti) oxide particles with sizes below 30 nm. In contrast, Fe14CrY shows a uniform structure of equiaxed grains, with sizes in the range 0.5–3 μm, containing a fine dispersion of Y oxide particles (<30 nm) homogeneously distributed inside the grains, as well as large carbide and oxide particles. Tensile tests performed over the temperature range 273–973 K have revealed that the alloy containing W and Ti has lower yield and tensile strengths than Fe–14Cr–0.3Y{sub 2}O{sub 3} at temperatures up to 773 K, but the opposite appears to occur beyond this temperature.

  15. Synthesis of magnetic Fe sub 3 O sub 4 particles covered with a modifiable phospholipid coat

    CERN Document Server

    Cuyper, M D; Lueken, H; Hodenius, M

    2003-01-01

    This work reports the synthesis of iron oxide cores by coprecipitation of Fe sup 2 sup + and Fe sup 3 sup + ions with NaHCO sub 3 or NH sub 3. Depending on the experimental conditions, particles of two different sizes (13 or 130 nm diameter) were produced. X-ray diffractometry revealed Fe sub 3 O sub 4 (magnetite) to be the main constituent. The smaller particles, which, in contrast to the larger ones, are superparamagnetic, were stabilized with a phospholipid bilayer consisting of a 9:1 molar ratio of dimyristoylphosphatidylcholine and dimyristoylphosphatidylglycerol, thereby creating so-called magnetoliposomes. In a subsequent step, poly(ethylene glycol)-(PEG-) derivatized dipalmitoylphosphatidylethanolamine was introduced into the lipid envelope by incubating the magnetoliposomes with pre-formed sonicated vesicles containing the PEGylated lipid. The mechanism by which lipid transfer occurred was determined from the kinetic profiles. The relevance of these observations to a wide range of biomedical applicat...

  16. Production and characterization of submicron hematite (α−Fe{sub 2}O{sub 3}) particles by ultrasonic spray pyrolysis method

    Energy Technology Data Exchange (ETDEWEB)

    Kırcı, Burak; Ebin, Burçak; Gürmen, Sebahattin [Department of Metallurgical and Materials Engineering, Istanbul Technical University Istanbul (Turkey)

    2013-12-16

    The ultrasonic spray pyrolysis (USP) method has been used to prepare submicron hematite (α−Fe{sub 2}O{sub 3}) particles using two different industrial pickling solutions of iron chloride (41 g/L FeCl{sub 2} and 54 g/L FeCl{sub 3}) Particles were obtained by thermal decomposition of generated aerosols from precursor solutions using 1.7 MHz ultrasonic atomizer. Reaction temperature was set up at 800 °C and aerosol droplets were carried into the heated zone by 0.7 L/min air flow rate. X-Ray Diffraction (XRD) studies were used to determine the crystal structure and crystallite size of the particles. Results indicate that patterns correspond to hematite phase with rhombohedral crystal structure (space group: R3c). The crystallite sizes of particles prepared from FeCl{sub 2} and FeCl{sub 3} solutions that were calculated from Scherrer equation are 59 and 33 nm, respectively. Scanning electron microscope (SEM) and energy dispersive spectroscopy (EDS) investigations give detailed information about particle size, morphology and composition. SEM micrographs show that hematite nanoparticles aggregate and formed spherical secondary particles in submicron range.

  17. Y{sub 2}O{sub 3}: Dy{sup 3+}/Li{sup +} phosphors synthesized by spray

    Energy Technology Data Exchange (ETDEWEB)

    Balderas X, R.; Carmona T, S.; Falcony, C., E-mail: scarmonat81@gmail.com [IPN, Centro de Investigacion y de Estudios Avanzados, Apdo. Postal 14-740, 07000 Ciudad de Mexico (Mexico)

    2017-11-01

    Dysprosium and lithium-activated yttrium oxide phosphor was synthesized at 1100 degrees Celsius by ultrasonic spray pyrolysis (Usp) using Di water as solvent and metal chlorides as precursors. The characteristic emission peak of Dy{sup 3+} due to the transitions {sup 4}F{sub 9/2} to {sup 6}H{sub 15/2} at 483 nm, {sup 4}F{sub 9/2} to {sup 6}H{sub 13/2} at 573 nm, {sup 4}F{sub 9/2} to {sup 6}H{sub 11/2} at 667 nm and {sup 4}F{sub 9/2} to {sup 6}H{sub 9/2} at 766 nm were observed. Scanning electron microscopy and transmission electron microscopy measurements were carried out to understand surface morphological features and the particle size of the phosphor. The uniformity of phase of Dy{sup 3+} - Li{sup +} doped Y{sub 2}O{sub 3} phosphors was checked by X-ray diffraction technique. The phosphors form clusters that were found to be ∼ 1 μm in size, however, particles that form these clusters have sizes between 40 and 120 nm. (Author)

  18. Magnetic relaxation phenomena and inter-particle interactions in nanosized gamma-Fe sub 2 O sub 3 systems

    CERN Document Server

    Predoi, D; Tronc, E; Nogues, M; Russo, U; Principi, G; Filoti, G

    2003-01-01

    Samples of gamma-Fe sub 2 O sub 3 nano-particles with a mean size of 4.0(3) nm and with different hydration and surfactant degrees were prepared by sol-gel methods. Morphology and structural data were obtained by transmission electron microscopy and x-ray diffraction, whereas the surface effects and hyperfine interactions were analysed mainly by Moessbauer spectroscopy. The relative number of surface iron positions was found to be proportional to the amount of OH sup - and SO sub 4 sup 2 sup - groups on the particle surface, which in turn is strictly dependent on the preparation conditions. Strong relaxation processes versus temperature were evidenced in the analysed systems. New criteria for the evaluation of the blocking temperature via Moessbauer measurements are proposed. The results are in good agreement with blocking temperatures obtained by magnetic measurements. Moreover, it was shown that the inter-particle magnetic interactions decrease with the number of iron surface states.

  19. Low field magnetoresistance effects in fine particles of La sub 0 sub . sub 6 sub 7 Ca sub 0 sub . sub 3 sub 3 MnO sub 3 perovskites

    CERN Document Server

    Rivas, J; Fondado, A; Rivadulla, F; López-Quintela, M A

    2000-01-01

    In this work magnetic and magnetotransport experimental data in well-characterized small particles of La sub 0 sub . sub 6 sub 7 Ca sub 0 sub . sub 3 sub 3 MnO sub 3 are presented. Grain size reduction leads to a larger resistivity and a decrease in metal-insulator transition temperature. Intrinsic colossal magnetoresistance (CMR) is destroyed while intergranular one is promoted to larger values. This low field MR can be explained taking into account magnetization data through spin-polarized tunneling model, which ensures an acceptable first-order fit between both magnitudes. Finally, low-temperature resistivity upturn present in small particle size samples can be understood in terms of an electrostatic barrier between grains.

  20. Synthesis, microstructure and magnetic properties of Fe{sub 3}Si{sub 0.7}Al{sub 0.3}@SiO{sub 2} core–shell particles and Fe{sub 3}Si/Al{sub 2}O{sub 3} soft magnetic composite core

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Jian, E-mail: snove418562@163.com [The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Key Laboratory for Ferrous Metallurgy and Resources Utilization of Ministry of Education, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Fan, Xi’an, E-mail: groupfxa@163.com [The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Key Laboratory for Ferrous Metallurgy and Resources Utilization of Ministry of Education, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Wu, Zhaoyang, E-mail: wustwuzhaoyang@163.com [The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Key Laboratory for Ferrous Metallurgy and Resources Utilization of Ministry of Education, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Li, Guangqiang [The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Key Laboratory for Ferrous Metallurgy and Resources Utilization of Ministry of Education, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China)

    2015-11-15

    Fe{sub 3}Si{sub 0.7}Al{sub 0.3}@SiO{sub 2} core–shell particles and Fe{sub 3}Si/Al{sub 2}O{sub 3} soft magnetic composite core have been synthesized via a modified stöber method combined with following high temperature sintering process. Most of conductive Fe{sub 3}Si{sub 0.7}Al{sub 0.3} particles could be uniformly coated by insulating SiO{sub 2} using the modified stöber method. The Fe{sub 3}Si{sub 0.7}Al{sub 0.3}@SiO{sub 2} core–shell particles exhibited good soft magnetic properties with low coercivity and high saturation magnetization. The reaction 4Al+3SiO{sub 2}=2α-Al{sub 2}O{sub 3}+3Si took place during the sintering process. As a result the new Fe{sub 3}Si/Al{sub 2}O{sub 3} composite was formed. The Fe{sub 3}Si/Al{sub 2}O{sub 3} composite core displayed more excellent soft magnetic properties, better frequency stability at high frequencies, much higher electrical resistivity and lower core loss than the pure Fe{sub 3}Si{sub 0.7}Al{sub 0.3} core. The method of introducing insulating layers surrounding magnetic particles provides a promising route to develop new and high compact soft magnetic materials with good magnetic and electric properties. - Graphical abstract: In Fe{sub 3}Si/Al{sub 2}O{sub 3} composite, Fe{sub 3}Si phases are separated by Al{sub 2}O{sub 3} layers and the eddy currents are confined in Fe{sub 3}Si phases, thus increasing resistivity and reducing core loss. - Highlights: • Fe{sub 3}Si{sub 0.7}Al{sub 0.3}@SiO{sub 2} core–shell particles and Fe{sub 3}Si/Al{sub 2}O{sub 3} cores were prepared. • Fe{sub 3}Si{sub 0.7}Al{sub 0.3} particles could be uniformly coated by nano-sized SiO{sub 2} clusters. • Fe{sub 3}Si{sub 0.7}Al{sub 0.3}@SiO{sub 2} particles and Fe{sub 3}Si/Al{sub 2}O{sub 3} cores showed good soft magnetic properties. • Fe{sub 3}Si/Al{sub 2}O{sub 3} had lower core loss and better frequency stability than Fe{sub 3}Si{sub 0.7}Al{sub 0.3} cores.

  1. Advanced Characterization: 3D chemistry and structure at sub-nm resolution

    Energy Technology Data Exchange (ETDEWEB)

    Kotula, Paul Gabriel [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Rye, Michael J. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States)

    2014-10-01

    This work has started the process of extending nanometer-scale comprehensive microanalysis to the 3rd dimension by combining full x-ray spectral imaging with previously developed computed tomography techniques whereby we acquire a series of spectral images for a large number of projections of the same specimen in the transmission electron microscope and then analyze the composite computed tomographic spectral image data prior to application of existing tomographic reconstruction software. We have demonstrated a needle-shaped specimen geometry (shape/size and preparation method) by focused ion beam preparation and acquisition and analysis of a complete tomographic spectral image on a test material consisting of fine-grained Ni with sub-10 nm alumina particles.

  2. Synthesis of MSnO{sub 3} (M = Ba, Sr) nanoparticles by reverse micelle method and particle size distribution analysis by whole powder pattern modeling

    Energy Technology Data Exchange (ETDEWEB)

    Ahmed, Jahangeer; Blakely, Colin K.; Bruno, Shaun R. [Department of Chemistry, Michigan State University, East Lansing, MI 48824 (United States); Poltavets, Viktor V., E-mail: poltavets@chemistry.msu.edu [Department of Chemistry, Michigan State University, East Lansing, MI 48824 (United States)

    2012-09-15

    Highlights: ► BaSnO{sub 3} and SrSnO{sub 3} nanoparticles synthesized using the reverse micelle method. ► Particle size and size distribution studied by whole powder pattern modeling. ► Nanoparticles are of optimal size for investigation in dye-sensitized solar cells. -- Abstract: Light-to-electricity conversion efficiency in dye-sensitized solar cells critically depends not only on the dye molecule, semiconducting material and redox shuttle selection but also on the particle size and particle size distribution of the semiconducting photoanode. In this study, nanocrystalline BaSnO{sub 3} and SrSnO{sub 3} particles have been synthesized using the microemulsion method. Particle size distribution was studied by whole powder pattern modeling which confirmed narrow particle size distribution with an average size of 18.4 ± 8.3 nm for SrSnO{sub 3} and 15.8 ± 4.2 nm for BaSnO{sub 3}. These values are in close agreement with results of transmission electron microscopy. The prepared materials have optimal microstructure for successive investigation in dye-sensitized solar cells.

  3. Effect of ZrB{sub 2} particles on the microstructure and mechanical properties of hybrid (ZrB{sub 2} + Al{sub 3}Zr)/AA5052 insitu composites

    Energy Technology Data Exchange (ETDEWEB)

    Gautam, Gaurav, E-mail: gauravgautamm1988@gmail.com; Mohan, Anita, E-mail: amohan.app@iitbhu.ac.in

    2015-11-15

    Present study outlines the effect of ZrB{sub 2} particles variation on the morphology and mechanical properties of (ZrB{sub 2}+Al{sub 3}Zr)/AA5052Al alloy composites. Composites with varying amount of ZrB{sub 2} particles have been produced by direct melt reaction (DMR) technique. These composites have been characterized by X-ray diffractometer (XRD) and energy-dispersive spectroscopy (EDS) to confirm the presence of ZrB{sub 2} and Al{sub 3}Zr particles. Optical microscopy (OM) and scanning-electron microscopy (SEM) have been used to understand the morphology. To see the effect of ZrB{sub 2} variation on mechanical properties, hardness and tensile properties have been evaluated. The XRD and EDS results confirm the successful formation of ZrB{sub 2} particles in matrix of AA5052Al alloy. SEM and TEM studies exhibit that ZrB{sub 2} particles are mostly in hexagonal and some rectangular shape while Al{sub 3}Zr particles are in polyhedron and rectangular shapes. Most of ZrB{sub 2} particles are within a size range of 10–190 nm. Interface region is free of any impurity. OM studies show grain refinement of AA5052Al alloy matrix with formation of second phase ZrB{sub 2} particles. Tensile results indicate that the UTS and YS improve up to 3 vol.% of ZrB{sub 2} but beyond this composition a decreasing trend is observed. The strength coefficient increases with increase in ZrB{sub 2} particles up to 3 vol.% in the Al{sub 3}Zr/Al alloy composites, whereas strain hardening decreases. While beyond 3 vol.% ZrB{sub 2} particles in the Al{sub 3}Zr/Al alloy composite, opposite trend is observed in strength coefficient and strain hardening. Percentage elongation also improves with 1vol.% ZrB{sub 2}, but further addition of ZrB{sub 2} shows an adverse effect. However, a continuous increasing trend has been observed in bulk hardness. Fracture studies show facets of Al{sub 3}Zr particles and dimples of matrix, but with inclusion of ZrB{sub 2} dimple size decreases. Increase in ZrB{sub

  4. Highly dispersed spherical Bi{sub 3.25}La{sub 0.75}Ti{sub 3}O{sub 12} nanocrystals via topotactic crystallization of aggregation-free gel particles from an effective inverse miniemulsion sol–gel approach

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Aijun; Zeng, Yanwei, E-mail: zengyw-njut@126.com, E-mail: stephen-zeng@njtech.edu.cn, E-mail: stephen-zeng@163.com; Han, Longxiang; Ding, Chuan; Cao, Liangliang; Li, Rongjie [Nanjing Tech University, State Key Laboratory of Materials-Oriented Chemical Engineering, College of Materials Science and Engineering (China)

    2015-09-15

    Aggregation-free spherical lanthanum-doped bismuth titanate (Bi{sub 3.25}La{sub 0.75}Ti{sub 3}O{sub 12}, BLT) gel particles with an average size of about 150 nm were successfully obtained from an inverse miniemulsion sol–gel process, with Span-80 acting as surfactant, n-butanol as co-surfactant, cyclohexane as continuous phase, and submicro-droplets of aqueous solution containing Bi{sup 3+}, La{sup 3+} and Ti{sup 4+} ions as dispersed phase, and then topotactically transformed into highly dispersed spherical BLT nanocrystals after an in situ crystallization at 600 °C for 8 h. It has been found that the BLT gel particles can be obtained via a moderate sol–gel reaction inside the miniemulsion droplets at 65 °C, but their morphology and aggregation degree are strongly affected by the relative amounts of Span-80 and n-butanol. The perfect spherical BLT gel particles with no aggregation can be achieved only under the condition of 3 wt% n-butanol relative to the mass of cyclohexane, with excessive amount of n-butanol leading to the formation of ill-gelled particles with irregular shapes, while insufficient addition of n-butanol resulting in terrible aggregation of gel particles. To understand the formation of aggregation-free spherical BLT gel particles, a tentative mechanism is proposed and discussed, which reveals that a well-coordinated oil–water interfacial film made up of Span-80 and n-butanol molecules and the appropriately enhanced evaporation of water from such interfaces should be responsible for the formation of aggregation-free spherical BLT gel particles. Graphical Abstract: Aggregation-free spherical BLT (Bi{sub 3.25}La{sub 0.75}Ti{sub 3}O{sub 12}) gel particles can be prepared from an effective inverse miniemulsion sol–gel process, and subsequently topotactically transformed into spherical BLT nanocrystals through an in situ crystallization.

  5. Preparation of sub 3 nm copper nanoparticles by microwave irradiation in the presence of triethylene tetramin

    Science.gov (United States)

    Tseng, Po-Hao; Wang, Yen-Zen; Hsieh, Tar-Hwa; Ho, Ko-Shan; Tsai, Cheng-Hsien; Chen, Kuan-Ting

    2018-02-01

    The preparation of sub 3 nm copper nanoparticles (CuNPs) in ethylene glycol (EG) using triethylene tetramine (TETA) as chelating and reducing agents via a rapid microwave (MW) irradiation is reported. The sub 3 nm CuNPs after MW irradiation are clearly seen from the electronic micrographs. The firm chelation of Cu2+ by TETA is illustrated by the dark blue color of Cu2+/TETA/EG solution and the redox reaction is confirmed by the appearance of red color of the mixtures. The optimal mole ratio of TETA/Cu 2+ is found to be 2.5/1 for preparing sub 3 nm CuNPs under the MW irradiation, operated at 800 W for 1 min. The plasmonic absorption λ max demonstrated in UV-vis spectra are found to close to 200 nm for sub 3 nm CuNPs, comparing to 500 ˜ 600 nm for regular, larger CuNPs. The extremely low Tm around 30 °C and the fusion/recrystallization sequence of sub 3 nm CuNPs can be directly measured by their differential scanning calorimetry thermograms.

  6. Thermoluminescence of LaAlO{sub 3}; Termoluminescencia de LaAlO{sub 3}:Dy

    Energy Technology Data Exchange (ETDEWEB)

    Morales H, A.; Zarate M, J. [Universidad Michoacana de San Nicolas de Hidalgo, Instituto de Investigacion en Metalurgia y Materiales, Ciudad Universitaria, Edif. U, 58060 Morelia, Michoacan (Mexico); Rivera M, T. [IPN, Centro de Investigacion en Ciencia Aplicada y Tecnologia Avanzada, Av. Legaria 694, 11500 Mexico D. F. (Mexico); Azorin N, J., E-mail: feyo_yo@hotmail.com [Universidad Autonoma Metropolitana, Unidad Iztapalapa, Av. San Rafael Atlixco 186, Col. Vicentina, 09340 Mexico D. F. (Mexico)

    2015-10-15

    In this paper the thermoluminescent properties of doped lanthanum aluminate (LaAlO{sub 3}) with dysprosium ion (Dy) were studied. The thermoluminescence characteristics in the samples were obtained using an ultraviolet radiation of 220 nm. The LaAlO{sub 3}:Dy samples were prepared by the modified Pechini method (Spray Dryer). The structural and morphological characterization was obtained by X-ray diffraction (XRD) and scanning electron microscopy (Sem) techniques respectively. The size particle composing the agglomerate was determined by Sem, agglomerated particles composed size of 2μm were observed. The thermoluminescence response of LaAlO{sub 3}:Dy was compared with that obtained with the undoped sample. Thermoluminescence brightness curves of LaAlO{sub 3}:Dy showed a peak centered at 185 grades C. Sensitivity of doped sample was greater, about 100 times compared with the undoped sample. Thermoluminescence response in function of the wavelength showed a maximum at 220 nm. Also the fading in thermoluminescence response was studied. (Author)

  7. Hierarchically structured carbon-coated SnO{sub 2}-Fe{sub 3}O{sub 4} microparticles with enhanced lithium storage performance

    Energy Technology Data Exchange (ETDEWEB)

    Chai, Xiaohan; Shi, Chunsheng [School of Materials Science and Engineering and Tianjin Key Laboratory of Composites and Functional Materials, Tianjin University, Tianjin, 300072 (China); Liu, Enzuo [School of Materials Science and Engineering and Tianjin Key Laboratory of Composites and Functional Materials, Tianjin University, Tianjin, 300072 (China); Collaborative Innovation Center of Chemical Science and Engineering, Tianjin 300072 (China); Li, Jiajun [School of Materials Science and Engineering and Tianjin Key Laboratory of Composites and Functional Materials, Tianjin University, Tianjin, 300072 (China); Zhao, Naiqin [School of Materials Science and Engineering and Tianjin Key Laboratory of Composites and Functional Materials, Tianjin University, Tianjin, 300072 (China); Collaborative Innovation Center of Chemical Science and Engineering, Tianjin 300072 (China); Key Laboratory of Advanced Ceramics and Machining Technology, Ministry of Education, Tianjin University, Tianjin, 300072 (China); He, Chunnian, E-mail: cnhe08@tju.edu.cn [School of Materials Science and Engineering and Tianjin Key Laboratory of Composites and Functional Materials, Tianjin University, Tianjin, 300072 (China); Collaborative Innovation Center of Chemical Science and Engineering, Tianjin 300072 (China); Key Laboratory of Advanced Ceramics and Machining Technology, Ministry of Education, Tianjin University, Tianjin, 300072 (China)

    2016-01-15

    Graphical abstract: Hierarchically structured SnO{sub 2}-Fe{sub 3}O{sub 4}@C microparticles for lithium-ion battery anode are developed by a facile and scalable strategy. - Highlights: • Hierarchically structured SnO{sub 2}-Fe{sub 3}O{sub 4}@C micrometer-sized particles were synthesized. • The SnO{sub 2}-Fe{sub 3}O{sub 4}@C micrometer-sized particles deliver high reversible lithium storage capacity. • The wrapped carbon layer can buffer the volume expansion of SnO{sub 2}-Fe{sub 3}O{sub 4}. - Abstract: A facile and scalable strategy was developed to fabricate SnO{sub 2}-Fe{sub 3}O{sub 4}@C micrometer-sized particles as a good lithium-ion battery anode. The obtained materials were constructed by aggregated nanoclusters (100–200 nm) consisting of SnO{sub 2}-Fe{sub 3}O{sub 4}@C nanospheres (20 ∼ 30 nm), in which SnO{sub 2} and Fe{sub 3}O{sub 4} nanoparticles (5 ∼ 8 nm) were homogeneously embedded in a percolating carbonaceous network with an average thickness of about 3 nm. SnO{sub 2}-Fe{sub 3}O{sub 4}@C microparticles were synthesized by a one-pot hydrothermal process followed by annealing under Ar and subsequent chemical vapor transformation (CVT) under vacuum. The peculiar strategy allows to obtain hierarchical structure of micrometer-sized particles including nanospheres, nanoclusters and micro-scale particles, and the combination of SnO{sub 2} and Fe{sub 3}O{sub 4} could promote the synergistic effects to enhance the reversible capacity as well as the structural stability. Meanwhile, the carbon layer, homogeneously covering the nanoparticles does not only accommodate the volume change of active materials to maintain the structural integrity but also forms a conductive network throughout the whole micro-sized structure during charge/discharge processes. As a result, the electrode of SnO{sub 2}-Fe{sub 3}O{sub 4}@C microparticles exhibits good rate performance (1056 mAh g{sup −1} at 0.1 C, 734 mAh g{sup −1} at 0.2 C, 449 mAh g{sup −1} at 0.5 C, 212

  8. Photocatalytic performance of nano-photocatalyst from TiO{sub 2} and Fe{sub 2}O{sub 3} by mechanochemical synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Ghorai, Tanmay K., E-mail: tanmay_ghorai@yahoo.co.in [Department of Chemistry, West Bengal State University, Barasat, North 24 Pgs, Kolkata 700126 (India); Department of Chemistry, Indian Institute of Technology Kharagpur, Kharagpur 721302 (India); Chakraborty, Mukut [Department of Chemistry, West Bengal State University, Barasat, North 24 Pgs, Kolkata 700126 (India); Pramanik, Panchanan [Department of Chemistry, Indian Institute of Technology Kharagpur, Kharagpur 721302 (India)

    2011-08-11

    Graphical abstract: Nano-particles of homogeneous solution between TiO{sub 2} and Fe{sub 2}O{sub 3} (up to 5 mol%) have been prepared by mechanochemical milling. The results show that the alloy of TiO{sub 2} with 5 mol% of Fe{sub 2}O{sub 3} (YFT1) exhibit photocatalytic activity 3-5 times higher than that of P25 TiO{sub 2} for oxidation of various dyes (RB, MO, TB and BG) under visible light irradiation. The average particle size and crystallite size of YFT1 were found to be 30 {+-} 5 nm and 12 nm measured from TEM and XRD. Optical adsorption edge is found to be 2.26 eV. Tentative schematic diagram of reaction mechanism of YFT/RFT photocatalysts under visible light irradiation. Highlights: > Synthesis of nano-sized homogeneous solid solution between Fe{sub 2}O{sub 3} and TiO{sub 2} with high photocatalytic activity for oxidative degradation of different dyes was successfully obtained through mechanochemical synthesis. XRD data shows the formation of solid solution having anatase structure with no free Fe{sub 2}O{sub 3} up to 5 mol% of Fe{sub 2}O{sub 3}. Fe{sub 2}O{sub 3}/TiO{sub 2} catalyst have crystallite size about 12-13 nm measured from XRD and particle size about 30 {+-} 5 nm measured from TEM. FT-IR of all Fe{sub 2}O{sub 3}/TiO{sub 2} prepared catalysts is similar to pure TiO{sub 2}. The maximum solubility of Fe{sub 2}O{sub 3} in TiO{sub 2} is 5 mol% of Fe{sub 2}O{sub 3} irrespective of source and this composition has highest photocatalytic activity that is 3-5 times higher than P25 TiO{sub 2} for the oxidation of different dyes. We also observed that the rate of degradation of Rhodamine B is faster among all the four dyes under prepared catalyst and visible light. - Abstract: Nano-particles of homogeneous solid solution between TiO{sub 2} and Fe{sub 2}O{sub 3} (up to 10 mol%) have been prepared by mechanochemical milling of TiO{sub 2} and yellow Fe{sub 2}O{sub 3}/red Fe{sub 2}O{sub 3}/precipitated Fe (OH){sub 3} using a planetary ball mill. Such novel solid

  9. Magnetic fluid with high dispersion and heating performance using nano-sized Fe{sub 3}O{sub 4} platelets

    Energy Technology Data Exchange (ETDEWEB)

    Kishimoto, Mikio, E-mail: kishimoto.mikio.gb@u.tsukuba.ac.jp [Institute of Applied Physics, University of Tsukuba, Tsukuba, Ibaraki 305-8573 (Japan); Miyamoto, Ryoichi; Oda, Tatsuya [Department of Surgery, Division of Medicine, University of Tsukuba, Tsukuba, Ibaraki 305-8573 (Japan); Yanagihara, Hideto [Institute of Applied Physics, University of Tsukuba, Tsukuba, Ibaraki 305-8573 (Japan); Ohkohchi, Nobuhiro [Department of Surgery, Division of Medicine, University of Tsukuba, Tsukuba, Ibaraki 305-8573 (Japan); Kita, Eiji [Institute of Applied Physics, University of Tsukuba, Tsukuba, Ibaraki 305-8573 (Japan)

    2016-01-15

    Magnetic fluid with high dispersion and heating performance was developed using 30 to 50 nm platelet Fe{sub 3}O{sub 4} particles. This fluid was prepared by mechanical dispersion in ethyl alcohol with a silane coupling agent, bonding with polyethylene glycol (PEG), and removal of aggregates formed by precipitation. The peak diameter of the resulting Fe{sub 3}O{sub 4} particles, measured by dynamic light scattering, was approximately 150 nm. The fluid exhibited a 300 W/g specific loss power (measured at 114 kHz by a 50.9 kA/m magnetic field). Distribution of the Fe{sub 3}O{sub 4} particles in tissues was observed by intravenously administrating the fluid in mice. The Fe{sub 3}O{sub 4} particles passed through the lungs, and were uniformly distributed throughout the liver and spleen. High dispersion and high heating performance were simultaneously achieved in the magnetic fluid using platelet Fe{sub 3}O{sub 4} particles surface modified with PEG. - Highlights: • Magnetic fluid with high dispersion and heating performance using Fe{sub 3}O{sub 4} particles. • Fluid prepared by mechanical dispersion, bonding with polyethylene glycol. • TEM observation and measurements of particle size distribution and specific loss power of fluid. • Observation of distribution of particles in mice tissues intravenously administrated fluid.

  10. Size-dependent properties of YBa sub 2 Cu sub 3 O sub 6 sub + sub x nanopowder

    CERN Document Server

    Paturi, P; Huhtinen, H; Huhtala, V P; Laiho, R

    2003-01-01

    YBa sub 2 Cu sub 3 O sub 6 sub + sub x nanopowder, prepared by the citrate sol-gel method, is segregated by sedimentation in ethanol into three size groups with average particle heights of 0.7, 1.6 and 2.3 nm. The structural properties and composition of the powders, investigated by x-ray diffraction, atomic force microscopy, Auger electron spectroscopy and EPR-spectroscopy, show no clear differences, except the size. According to investigations by magnetometry and by non-resonant microwave absorption the as-prepared powder contains weak links which, however, disappear during the segregation. The magnetic susceptibility of the samples decreases with the decreasing particle size, in agreement with the susceptibility values calculated from the London equations for cylindrical particles smaller than the London penetration depth. In all three size groups the critical temperature of superconductivity is 92 K.

  11. Generation of MoS{sub 2} quantum dots by laser ablation of MoS{sub 2} particles in suspension and their photocatalytic activity for H{sub 2} generation

    Energy Technology Data Exchange (ETDEWEB)

    Baldoví, Herme G.; Latorre-Sánchez, Marcos; Esteve-Adell, Iván [Universitat Politècnica de València, Instituto Universitario de Tecnología Química CSIC-UPV and Departamento de Química (Spain); Khan, Anish; Asiri, Abdullah M. [King Abdulaziz University, Center of Excellence for Advanced Materials Research (Saudi Arabia); Kosa, Samia A. [King Abdulaziz University, Chemistry Department, Faculty of Science (Saudi Arabia); Garcia, Hermenegildo, E-mail: hgarcia@qim.upv.es [Universitat Politècnica de València, Instituto Universitario de Tecnología Química CSIC-UPV and Departamento de Química (Spain)

    2016-08-15

    MoS{sub 2} quantum dots (QDs) have been obtained in colloidal suspensions by 532 nm laser ablation (7 ns fwhp/pulse, 50 mJ/pulse) of commercial MoS{sub 2} particles in acetonitrile. High-resolution transmission electron microscopy images show a lateral size distribution from 5 to 20 nm, but a more homogeneous particle size of 20 nm can be obtained by silica gel chromatography purification in acetonitrile. MoS{sub 2} QDs obtained by laser ablation are constituted by 3–6 MoS{sub 2} layers (1.8–4 nm thickness) and exhibit photoluminescence whose λ{sub PL} varies from 430 to 530 nm depending on the excitation wavelength. As predicted by theory, the confinement effect and the larger periphery in MoS{sub 2} QDs increasing the bandgap and having catalytically active edges are reflected in an enhancement of the photocatalytic activity for H{sub 2} generation upon UV–Vis irradiation using CH{sub 3}OH as sacrificial electron donor due to the increase in the reduction potential of conduction band electrons and the electron transfer kinetics.

  12. Magnetic properties of nanocrystalline KNbO{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Golovina, I. S., E-mail: golovina@isp.kiev.ua; Shanina, B. D.; Kolesnik, S. P. [Institute of Semiconductor Physics of NAS of Ukraine, Pr. Nauky 41, 03028 Kyiv (Ukraine); Geifman, I. N. [Quality Engineering Education, Inc., Buffalo Grove, Illinois 60089 (United States); Andriiko, A. A. [National Technical University of Ukraine “KPI”, pr. Peremogy 37, 03056 Kyiv (Ukraine)

    2013-11-07

    Newly synthesized undoped and iron-doped nanoscale powders of KNbO{sub 3} are investigated using magnetic resonance and static magnetization methods in order to determine how the crystal size and doping affect the structure of magnetic defects and material properties. Although the bulk crystals of KNbO{sub 3} are nonmagnetic, the undoped KNbO{sub 3} powder with average particle size of 80 nm exhibits magnetic properties. The ferromagnetic resonance signal and the magnetization curve registered on the powder are thoroughly analyzed. It is concluded that the appearance of the defect driven ferromagnetism in the undoped powder is due to the nano-size of the particles. This effect disappears in the iron-doped KNbO{sub 3} powder with particle sizes above 300 nm. In case of low doping (<1 mol. % Fe), a new electron paramagnetic resonance signal with g{sub eff} = 4.21 is found out in the KNbO{sub 3}:Fe powder. Such a signal has not been observed in the bulk crystals of KNbO{sub 3}:Fe. We suppose that this signal corresponds to individual paramagnetic Fe{sup 3+} ions having rhombic symmetry.

  13. Photodissociation of C{sub 3}H{sub 5}Br and C{sub 4}H{sub 7}Br at 234 nm

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Hyun Kook; Paul, Dababrata; Hong, Ki Ryong; Cho, Ha Na; Kim, Tae Kyu [Pusan National University, Busan (Korea, Republic of); Lee, Kyoung Seok [Korea Research Institute of Standards and Science, Daejeon (Korea, Republic of)

    2012-01-15

    The photodissociation dynamics of cyclopropyl bromide (C-3H{sub 5}Br) and cyclobutyl bromide (C{sub 4}H{sub 7}Br) at 234 nm was investigated. A two-dimensional photofragment ion-imaging technique coupled with a [2+1] resonance enhanced multiphoton ionization scheme was utilized to obtain speed and angular distributions of the nascent Br({sup 2}P{sub 3/2}) and Br*({sup 2}P{sub 1/2}) atoms. The recoil anisotropies for the Br and Br* channels were measured to be βBr = 0.92 ± 0.03 and βBr* = 1.52 ± 0.04 for C{sub 3}H{sub 5}Br and βBr = 1.10 ± 0.03 and βBr* = 1.49 ± 0.05 for C{sub 4}H{sub 7}Br. The relative quantum yield for Br was found to be ΦBr = 0.13 ± 0.03 and for C{sub 3}H{sub 5}Br and C{sub 4}H{sub 7}Br, respectively. The soft radical limit of the impulsive model adequately modeled the related energy partitioning. The nonadiabatic transition probability from the 3A' and 4A' potential energy surfaces was estimated and discussed.

  14. Magnetic rotational hysteresis study on spherical 85-160 nm Fe3O4 particles

    Science.gov (United States)

    Schmidbauer, E.

    1988-05-01

    Rotational hysteresis losses Wr were determined as a function of magnetic field H for dispensed spherical Fe3O4 particles of mean grain sizes 85 nm, 127 nm and 162 nm between 78 K and 294 K. The observed Wr-H curves are compared with theoretical curves for single domain particles. The analysed particles reveal centers of high magnetic anisotropy. Such centers can be of importance during the generation of a thermoremanent magnetization, as they may be the origin of enhanced magnetic stability.

  15. Surface passivation of Fe{sub 3}O{sub 4} nanoparticles with Al{sub 2}O{sub 3} via atomic layer deposition in a rotating fluidized bed reactor

    Energy Technology Data Exchange (ETDEWEB)

    Duan, Chen-Long; Deng, Zhang; Cao, Kun [State Key Laboratory of Digital Manufacturing Equipment and Technology, School of Mechanical Science and Engineering, Huazhong University of Science and Technology, 1037 Luoyu Road, Wuhan, Hubei 430074 (China); Yin, Hong-Feng [Ningbo Institute of Material Technology and Engineering, Chinese Academy of Sciences, Ningbo, Zhejiang 315201 (China); Shan, Bin [State Key Laboratory of Material Processing and Die and Mould Technology, School of Materials Science and Engineering, Huazhong University of Science and Technology, 1037 Luoyu Road, Wuhan, Hubei 430074 (China); Chen, Rong, E-mail: rongchen@mail.hust.edu.cn [State Key Laboratory of Digital Manufacturing Equipment and Technology, School of Mechanical Science and Engineering, School of Optical and Electronic Information, Huazhong University of Science and Technology, 1037 Luoyu Road, Wuhan, Hubei 430074 (China)

    2016-07-15

    Iron(II,III) oxide (Fe{sub 3}O{sub 4}) nanoparticles have shown great promise in many magnetic-related applications such as magnetic resonance imaging, hyperthermia treatment, and targeted drug delivery. Nevertheless, these nanoparticles are vulnerable to oxidation and magnetization loss under ambient conditions, and passivation is usually required for practical applications. In this work, a home-built rotating fluidized bed (RFB) atomic layer deposition (ALD) reactor was employed to form dense and uniform nanoscale Al{sub 2}O{sub 3} passivation layers on Fe{sub 3}O{sub 4} nanoparticles. The RFB reactor facilitated the precursor diffusion in the particle bed and intensified the dynamic dismantling of soft agglomerates, exposing every surface reactive site to precursor gases. With the aid of in situ mass spectroscopy, it was found that a thicker fluidization bed formed by larger amount of particles increased the residence time of precursors. The prolonged residence time allowed more thorough interactions between the particle surfaces and the precursor gas, resulting in an improvement of the precursor utilization from 78% to nearly 100%, even under a high precursor feeding rate. Uniform passivation layers around the magnetic cores were demonstrated by both transmission electron microscopy and the statistical analysis of Al mass concentrations. Individual particles were coated instead of the soft agglomerates, as was validated by the specific surface area analysis and particle size distribution. The results of thermogravimetric analysis suggested that 5 nm-thick ultrathin Al{sub 2}O{sub 3} coatings could effectively protect the Fe{sub 3}O{sub 4} nanoparticles from oxidation. The x-ray diffraction patterns also showed that the magnetic core crystallinity of such passivated nanoparticles could be well preserved under accelerated oxidation conditions. The precise thickness control via ALD maintained the saturation magnetization at 66.7 emu/g with a 5 nm-thick Al{sub

  16. Role of grain size on the magnetic properties of La{sub 0.7}Sr{sub 0.3}MnO{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Yadav, P.A. [Center for Advanced Studies in Materials Science and Condensed Matter Physics, Department of Physics, University of Pune, Pune 411007 (India); Deshmukh, A.V. [Department of Physics, Fergusson College, Pune 411004 (India); Adhi, K.P. [Center for Advanced Studies in Materials Science and Condensed Matter Physics, Department of Physics, University of Pune, Pune 411007 (India); Kale, B.B. [Centre for Materials for Electronics Technology, Pune 411008 (India); Basavaih, N. [Indian Institute of Geomagnetism, New Mumbai 410218 (India); Patil, S.I., E-mail: patil@physics.unipune.ac.in [Center for Advanced Studies in Materials Science and Condensed Matter Physics, Department of Physics, University of Pune, Pune 411007 (India)

    2013-02-15

    Nanophasic La{sub 0.7}Sr{sub 0.3}MnO{sub 3} samples were synthesized using the citrate-gel method. The samples were annealed at different temperatures ranging from 600 to 1200 Degree-Sign C. Grain size was observed to increase with the increase in annealing temperature. Furthermore, the magnetization data of these samples show well defined hysteresis. Saturation magnetization was observed to increase with increase in particle size. This gives evidence of formation of a magnetically dead layer at the surface. The thickness of the dead layer has also been calculated. The coercivity of nanoparticles follows the same trend as predicted theoretically and particles below 22 nm are found to be single domain. The ferromagnetic to paramagnetic transition temperature also increases with increase in particle size. - Highlights: Black-Right-Pointing-Pointer Synthesis of nanocrystalline La{sub 0.7}Sr{sub 0.3}MnO{sub 3} by the citrate-gel method. Black-Right-Pointing-Pointer Saturation magnetization increases with increase in particle size. Black-Right-Pointing-Pointer Formation of dead magnetic layer.

  17. Synthesis and characterization of rod-like ZnO decorated with γ-Fe{sub 2}O{sub 3} nanoparticles monolayer

    Energy Technology Data Exchange (ETDEWEB)

    Balti, Imen, E-mail: imenbalti12@yahoo.fr [Unité de Recherche 99/UR12-30, Faculté des Sciences de Bizerte, Université de Carthage, 7021 Jarzouna (Tunisia); Laboratoire des Sciences des Procédés et Matériaux, LSPM, CNRS, UPR 3407, Université Paris XIII, 99 Avenue J.B. Clément, 93430 Villetaneuse (France); Smiri, Laila Samia [Unité de Recherche 99/UR12-30, Faculté des Sciences de Bizerte, Université de Carthage, 7021 Jarzouna (Tunisia); Rabu, Pierre [Département de Chimie des Matériaux Inorganiques, IPCMS, UMR 7504, CNRS–UDS, 23, rue du Loess, BP 43, Strasbourg Cedex 2 (France); Gautron, Eric [Institut des Matériaux Jean Rouxel (IMN)-UMR 6502, Université de Nantes, CNRS, 2 rue de la Houssinière, BP 32229, 44322 Nantes Cedex 3 (France); Viana, Bruno [LCMCP, Chimie-Paristech, UPMC, Collège de France, UMR CNRS 7574, 11 rue Pierre et Marie Curie, 75005 Paris (France); Jouini, Noureddine [Laboratoire des Sciences des Procédés et Matériaux, LSPM, CNRS, UPR 3407, Université Paris XIII, 99 Avenue J.B. Clément, 93430 Villetaneuse (France)

    2014-02-15

    Highlights: ► Rod-like ZnO decorated with γ-Fe{sub 2}O{sub 3} nanoparticles have been prepared using forced hydrolysis in polyol medium. ► The system presents excellent UV photoluminescence properties along with superparamagnetic behavior. -- Abstract: Decorated rod-like ZnO particles with γ-Fe{sub 2}O{sub 3} nanoparticles monolayer (ZnO@γ-Fe{sub 2}O{sub 3}) were prepared via a simple route using forced hydrolysis of metal acetates in a polyol medium. The phases and purity of the as-prepared particles were established by powder X-ray diffraction (PXRD) and X-ray photo-electron spectroscopy (XPS) analyses. Transmission electron microscopy (TEM) showed that the ZnO particles present a typical rod-like morphology with ∼80 nm diameter and ∼200–400 nm length. These nanorods are decorated with well-organized γ-Fe{sub 2}O{sub 3} spherical nanoparticles showing a narrow size distribution around 5 nm. The photoluminescence (PL) spectra of the bare ZnO particles show predominant UV-excitonic and weak visible emission. The latter vanishes after covering the surface with the γ-Fe{sub 2}O{sub 3} nanoparticles suggesting an effect on the oxygen stoichiometry at the surface of the ZnO nanorods. The decorated nanoparticles exhibit magnetic response to an external magnetic field at room temperature and a superparamagnetic character with very low blocking temperature likely related to the organisation of γ-Fe{sub 2}O{sub 3} nanoparticles as monolayer.

  18. Core–shell structured FeSiAl/SiO{sub 2} particles and Fe{sub 3}Si/Al{sub 2}O{sub 3} soft magnetic composite cores with tunable insulating layer thicknesses

    Energy Technology Data Exchange (ETDEWEB)

    Fan, Xi’an, E-mail: groupfxa@163.com [The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Key Laboratory for Ferrous Metallurgy and Resources Utilization of Ministry of Education, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Wang, Jian, E-mail: snove418562@163.com [The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Key Laboratory for Ferrous Metallurgy and Resources Utilization of Ministry of Education, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Wu, Zhaoyang, E-mail: wustwuzhaoyang@163.com [The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Key Laboratory for Ferrous Metallurgy and Resources Utilization of Ministry of Education, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Li, Guangqiang, E-mail: ligq-wust@mail.wust.edu.cn [The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Key Laboratory for Ferrous Metallurgy and Resources Utilization of Ministry of Education, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China)

    2015-11-15

    Graphical abstract: - Highlights: • FeSiAl/SiO{sub 2} core–shell particles and Fe{sub 3}Si/Al{sub 2}O{sub 3} composite cores were prepared. • SiO{sub 2} surrounding FeSiAl were replaced by Al{sub 2}O{sub 3} during sintering process. • Fe{sub 3}Si particles were separated by Al{sub 2}O{sub 3} with tunable thickness in composite cores. • Fe{sub 3}Si/Al{sub 2}O{sub 3} had lower core loss and better frequency stability than FeSiAl core. • The insulating layer between ferromagnetic particles can reduce core loss. - Abstract: FeSiAl/SiO{sub 2} core–shell particles and Fe{sub 3}Si/Al{sub 2}O{sub 3} composite cores with tunable insulating layer thicknesses have been synthesized via a modified Stöber method combined with following high temperature sintering process. Most of the conductive FeSiAl particles could be coated by insulating SiO{sub 2} using the modified Stöber method. During the sintering process, the reaction 4Al + 3SiO{sub 2} ≣ 2α-Al{sub 2}O{sub 3} + 3Si took place and the new Fe{sub 3}Si/Al{sub 2}O{sub 3} composite was formed. The Fe{sub 3}Si/Al{sub 2}O{sub 3} composite cores displayed more excellent soft magnetic properties, better frequency stability at high frequencies, much higher resistivity and lower core loss than the raw FeSiAl core. Based on this, several types of FeSiAl/SiO{sub 2} particles and Fe{sub 3}Si/Al{sub 2}O{sub 3} composite cores with tunable insulating layer thicknesses were selectively prepared by simply varying TEOS contents. The thickness of Al{sub 2}O{sub 3} insulating layer and resistivity of Fe{sub 3}Si/Al{sub 2}O{sub 3} composite cores increased with increasing the TEOS contents, while the permeability and core loss changed in the opposite direction.

  19. Reduction under hydrogen of ferrite MFe{sub 2}O{sub 4} (M: Fe, Co, Ni) nanoparticles obtained by hydrolysis in polyol medium: A novel route to elaborate CoFe{sub 2}, Fe and Ni{sub 3}Fe nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Ballot, N.; Schoenstein, F.; Mercone, S.; Chauveau, T.; Brinza, O. [Laboratoire des Sciences des Procedes et des Materiaux, CNRS, LSPM - UPR 3407, Universite Paris 13, PRES Sorbonne-Paris-Cite, 99 Avenue J.-B. Clement, 93430 Villetaneuse (France); Jouini, N., E-mail: jouini@univ-paris13.fr [Laboratoire des Sciences des Procedes et des Materiaux, CNRS, LSPM - UPR 3407, Universite Paris 13, PRES Sorbonne-Paris-Cite, 99 Avenue J.-B. Clement, 93430 Villetaneuse (France)

    2012-09-25

    Highlights: Black-Right-Pointing-Pointer Spinels nano-particles MFe{sub 2}O{sub 4} (M: Co, Fe or Ni) are obtained by hydrolysis in polyol medium. Black-Right-Pointing-Pointer Gentle reduction under hydrogen flow of spinel nano-particles yields metal and alloy nanoparticles. Black-Right-Pointing-Pointer TEM and X-ray analysis show that CoFe{sub 2}, Fe and Ni{sub 3}Fe nano-particles are monocrystalline particles with size less than 160 nm. Black-Right-Pointing-Pointer Iron with size of 150 nm presents ferromagnetic behavior. Black-Right-Pointing-Pointer CoFe{sub 2} alloy with size of 55 nm could be considered as a superparamagnetic material. - Abstract: A novel method to process metal and various alloy particles of nanometric size is described. The first step consists in the elaboration of MFe{sub 2}O{sub 4} (M: Fe, Ni or Co) spinel nanoparticles in polyol medium via hydrolysis and the second one in gently reducing these latter under hydrogen at 300 Degree-Sign C. X-ray diffraction analysis shows that pure Fe and CoFe{sub 2} alloy are well obtained by reducing Fe{sub 3}O{sub 4} and CoFe{sub 2}O{sub 4}, respectively. This is not the case when we try to reduce NiFe{sub 2}O{sub 4}. A mixture of Fe and Ni{sub 3}Fe is observed. TEM analysis reveals that the size of metal particles stays within the range of a few tenths of nm up to 150 nm, while the precursors (MFe{sub 2}O{sub 4}) never exceed 5 nm. Our results show that the formation of metal particles occurs via two main steps: (i) reduction of the spinel oxide nanoparticles into metal ones and (ii) aggregation of the latter, leading to larger metal nanoparticles. Magnetic measurements indicate that the as-obtained metallic materials have good magnetic properties mainly affected by the sizes of the nanoparticles and the purity of the reduced phases.

  20. Synthesis and study of bifunctional core–shell nanostructures based on ZnO@Gd{sub 2}O{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Babayevska, Nataliya, E-mail: natbab@amu.edu.pl; Nowaczyk, Grzegorz; Jarek, Marcin; Załęski, Karol; Jurga, Stefan

    2016-07-05

    Bifunctional nanostructures based on ZnO nanoparticles (NPs) with controlled Gd{sub 2}O{sub 3} shell thicknesses were obtained by simple low-temperature methods (sol–gel technique and seed deposition method). The morphology, nanostructure, phase and chemical composition as well as luminescent and magnetic properties of the obtained core–shell nanostructures were investigated by transmission electron microscopy (HRTEM), energy dispersive x-ray spectroscopy (EDS), x-ray diffraction (XRD) techniques, optical spectroscopy, and SQUID magnetometer. As-obtained ZnO NPs are highly monodispersed and crystalline with mean particles size distribution of about 7 nm. Modification of the ZnO NPs surface by Gd{sub 2}O{sub 3} shell leads to an increase of the ZnO particles size up to 80–160 nm and the formation the Gd{sub 2}O{sub 3} shell with size of 2–4 nm. The dependence of the phase composition, luminescent and magnetic properties on Gd{sub 2}O{sub 3} content are also discussed. - Highlights: • The bifunctional ZnO@Gd{sub 2}O{sub 3} nanostructures were obtained by sol–gel technique. • ZnO@Gd{sub 2}O{sub 3} have intensive luminescence in the visible range under 325 nm excitation. • Gd{sup 3+} content allows to control paramagnetic properties of the ZnO@Gd{sub 2}O{sub 3}. • ZnO@Gd{sub 2}O{sub 3} nanostructures are potential objects for application in medicine.

  1. Synthesis of KMgCl{sub 3} nanomaterial and luminescence of Ce{sup 3+}/Dy{sup 3+}/Eu{sup 3+} by different routes

    Energy Technology Data Exchange (ETDEWEB)

    Poddar, Anuradha [Department of Physics, Sindhu Mahavidyalaya, Nagpur 440017 (India); Gedam, S.C., E-mail: gedam_sc@rediffmail.com [Department of Physics, K.Z.S. Science College, Kalmeshwar, Nagpur 441501 (India); Dhoble, S.J. [Department of Physics, RTM Nagpur University, Nagpur 440033 (India)

    2015-02-15

    The present KMgCl{sub 3} phosphor has been synthesized through wet chemical synthesis (WCS), solid state diffusion (SSD) and Hispersed centrifuge (HC) routes in the same atmospheric conditions and characterized for luminescence properties. XRDs of the sample prepared by all three methods have been placed at the same position, phase and matched well with standard data. The particle size of 20 nm of KMgCl{sub 3} by a Hispersed centrifuged method was detected using a transmission electron microscope (TEM). The PL emission spectra have been observed for Ce{sup 3+} at 353 nm and 375 nm due to 5d→4f transition, whereas luminescence of Dy{sup 3+} efficiently observed at 484 nm and 579 nm for an excitation of 384 nm due to {sup 4}F{sub 9/2}→ {sup 6}H{sub 15/2} and {sup 6}H{sub 13/2} (blue–yellow region) transition and Eu{sup 3+} is peaking at 596 nm and 616 nm (λ{sub ex}=394 nm) due to level {sup 5}D{sub 0} to {sup 7}F{sub j} (j=0, 1, 2, and 3) radiative transitions. The presented phosphors are excited in the range of 300–400 nm which is mercury free excited range. Synthesis and photoluminescence spectra of trivalent Ce, Dy or Eu rare-earths in KMgCl{sub 3} are described for all three routes, for the first time in the present work. The CIE chromaticity coordinates were also calculated for KMgCl{sub 3}:X (Ce{sup 3+}, Dy{sup 3+} and Eu{sup 3+}) phosphors, which are close to the NTSC standard values. KMgCl{sub 3} matrix is not only suitable for different and easy synthesis but efficient luminescence also. The paper discuses the XRD, crystallinity (morphology) and luminescence of Ce, Dy or Eu rare-earths in KMgCl{sub 3} synthesized by three (WCS, SSD and HC) different routes. - Highlights: • The particle size 20 nm of KMgCl{sub 3} was detected by Hispersed centrifuged method using TEM. • The phosphors are prepared by very simple WCM, SSD and HS technique. • An efficient luminescence is observed in KMgCl{sub 3}:X (X=Ce{sup 3+}, Dy{sup 3+} and Eu{sup 3

  2. Synthesis of sub-10 nm VO{sub 2} nanoparticles films with plasma-treated glass slides by aqueous sol–gel method

    Energy Technology Data Exchange (ETDEWEB)

    Lan, Shi-Di [Department of Materials Science and Engineering, National Taiwan University of Science and Technology, 43, Sec. 4, Keelung Rd, Taipei 106, Taiwan, ROC (China); Cheng, Chih-Chia [Graduate Institute of Applied Science and Technology, National Taiwan University of Science and Technology, Taipei, Taiwan (China); Huang, Chi-Hsien [Department of Materials Engineering, Ming Chi University of Technology, 84 Gungjuan Road, Taishan Dist., New Taipei City 24301, Taiwan (China); Chen, Jem-Kun, E-mail: jkchen@mail.ntust.edu.tw [Department of Materials Science and Engineering, National Taiwan University of Science and Technology, 43, Sec. 4, Keelung Rd, Taipei 106, Taiwan, ROC (China)

    2015-12-01

    Highlights: • Sub-10 nm VO{sub 2} nanoparticles (VNPs) are synthesized on a plasma-treated glass. • Glass slides generate negative charges sites after plasma treatment to attract VO{sub 2}{sup +}. • Doping tungsten with 1 wt% in VNPs did not change particle size significantly. • The particle size of VNP can be tuned by the density of negative charge sites. • Sub-10 nm structured VO{sub 2} particle films exhibited high visible transmittance. - Abstract: This paper describes an aqueous sol–gel synthesis of thermochromic thin films consisted of vanadium dioxide nanoparticles (VNPs) on glass slides. The glass slides were treated by argon/oxygen plasma to generate dispersedly negative charge sites on the surface to attract VO{sub 2}{sup +} from a sol–gel solution. After heat treatment in a low-pressure carbon monoxide/carbon dioxide (CO/CO{sub 2}) atmosphere, the VNPs could be generated in sub-10 nm of particle size on the surface. Various levels of doping were achieved by adding small quantities of a water-soluble tungsten compound to the sol; however, the particle size increased slightly with the tungsten doping levels. The change in electrical conductivity with temperature for VNP films were measured and compared to VO{sub 2} crystalline films. VNP films exhibited the lower transition temperature of the semiconductor to metal phase change; at a doping level of 4 wt% the transition temperature was measured at 32.2 ± 1.2 and 24.1 ± 1.2 °C for the VO{sub 2} and VNP films, respectively. The VNP films showed excellent visible transparency and a large change in transmittance at near-infrared (NIR) wavelengths before and after the metal–insulator phase transition (MIT). The current method is a landmark in the development of nanostructured material toward applications in energy-saving smart windows.

  3. Bacteria-assisted preparation of nano α-Fe{sub 2}O{sub 3} red pigment powders from waste ferrous sulfate

    Energy Technology Data Exchange (ETDEWEB)

    Li, Xiang; Wang, Chuankai; Zeng, Yu; Li, Panyu; Xie, Tonghui; Zhang, Yongkui, E-mail: zhangyongkui@scu.edu.cn

    2016-11-05

    Highlights: • A route to prepare nano α-Fe{sub 2}O{sub 3} red pigment from waste ferrous sulfate is proposed. • Acidithiobacillus ferrooxidans is introduced for accelerating iron oxidation. • The particle size of synthetic α-Fe{sub 2}O{sub 3} is ranged from 22 nm to 86 nm. • The prepared nano α-Fe{sub 2}O{sub 3} red pigment fulfills ISO 1248-2006. - Abstract: Massive ferrous sulfate with excess sulfuric acid is produced in titanium dioxide industry each year, ending up stockpiled or in landfills as solid waste, which is hazardous to environment and in urgent demand to be recycled. In this study, waste ferrous sulfate was used as a second raw material to synthesize nano α-Fe{sub 2}O{sub 3} red pigment powders with a bacteria-assisted oxidation process by Acidithiobacillus ferrooxidans. The synthesis route, mainly consisting of bio-oxidation, precipitation and calcination, was investigated by means of titration, thermogravimetric analysis (TGA), X-ray diffraction (XRD), scanning electron microscope (SEM) and X-ray fluorescence (XRF) to obtain optimum conditions. Under the optimum conditions, nano α-Fe{sub 2}O{sub 3} red pigment powders contained 98.24 wt.% of Fe{sub 2}O{sub 3} were successfully prepared, with a morphology of spheroidal and particle size ranged from 22 nm to 86 nm and averaged at 45 nm. Moreover, the resulting product fulfilled ISO 1248-2006, the standards of iron oxide pigments.

  4. Influence of particle sizes on the electronic behavior of Zn{sub x}Co{sub 1−x}Fe{sub 2}O{sub 4} spinels (x = 0.2, 0.3)

    Energy Technology Data Exchange (ETDEWEB)

    Viñas, R. [Departamento de Química Inorgánica, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Avda. Complutense s/n, 28040 Madrid (Spain); Álvarez-Serrano, I., E-mail: ias@quim.ucm.es [Departamento de Química Inorgánica, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Avda. Complutense s/n, 28040 Madrid (Spain); López, M.L.; Pico, C.; Veiga, M.L. [Departamento de Química Inorgánica, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Avda. Complutense s/n, 28040 Madrid (Spain); Mompeán, F.; García-Hernández, M. [Instituto de Ciencia de Materiales, CSIC, Sor Juana Inés de la Cruz, 3, 28049 Madrid (Spain)

    2014-07-15

    Graphical abstract: Relaxor ferroelectric behavior and superparamagnetism in nanoparticles of Zn{sub x}Co{sub 1−x}Fe{sub 2}O{sub 4} obtained in supercritical water. - Highlights: • Title ferrites were prepared by hydrothermal techniques (sub and supercritical). • In supercritical (SCW) conditions highly monodispersive samples were obtained. • All samples are semiconductors; n-type or p-type response depends on the composition. • Superparamagnetic and relaxor ferroelectric response coexist in SCW samples. - Abstract: The effect of composition and particle size on the electrical and magnetic behavior of Zn{sub x}Co{sub 1−x}Fe{sub 2}O{sub 4} spinels (x = 0.2 and 0.3) has been studied. Powdered samples of these ferrites have been synthetized by the liquid mix technique and hydrothermal method (in sub and supercritical conditions), leading to average particle sizes of ca. 50 and 10 nm, respectively. They have been characterized by means of X-ray diffraction, Thermogravimetric analysis, Energy-Dispersive X-ray Spectroscopy and impedance and magnetic measurements. Permittivity values up to ca. 500 were registered at 375 K, which remained almost constant at moderate frequencies, between 10{sup 3} and 10{sup 6} Hz. Stabilization of polarization phenomena is very sensitive to grain size and composition. Dielectric behavior evolves to a relaxor ferroelectric response when grain size becomes nanometric and, particularly, when the sample shows high monodispersion. The conduction mechanism and type of majority charge carriers have been established from Seebeck measurements. The x = 0.3 sample, prepared in supercritical water for the first time, exhibits homogeneous particle size distribution, superparamagnetic behavior and Curie temperature lower than those corresponding to similar microsized samples. The electronic response of the ferrites obtained in supercritical conditions is interpreted considering the possible short scale polarization of nanodomains.

  5. Structural and Mössbauer studies of nanocrystalline Mn{sup 4+}-doped Li{sub 0.5}Fe{sub 2.5}O{sub 4} particles prepared by mechanical milling

    Energy Technology Data Exchange (ETDEWEB)

    Widatallah, H. M., E-mail: hishammw@squ.edu.om; Al-Mabsali, F. N.; Al-Hajri, F. S. [Sultan Qaboos University, Physics Department, College of Science (Oman); Khalifa, N. O. [University of Khartoum, Physics Department, Faculty of Science (Sudan); Gismelseed, A. M.; Al-Rawas, A. D.; Elzain, M.; Yousif, A. [Sultan Qaboos University, Physics Department, College of Science (Oman)

    2016-12-15

    The structure and magnetic properties of spinel-related Mn{sup 4+}-doped Li{sub 0.5}Fe{sub 2.5}O{sub 4} nanocrystalline particles of the composition Li{sub 0.5}Fe{sub 2.25}Mn{sub 0.1875}O{sub 4}, prepared by milling a pristine sample for different times, were investigated. The average crystallite and particle size, respectively, decreased form ∼40 nm to ∼10 nm and ∼2.5 μm to ∼10 nm with increasing milling time from 0 h to 70 h. Rietveld refinement of the XRD data of the non-milled sample show the Mn{sup 4+} dopant ions to substitute for Fe{sup 3+} at the octahedral B-sites of the spinel-related structure. The Mössbauer spectra of the milled ferrites indicate that more particles turn superparamagnetic with increasing milling time. The Mössbauer data collected at 78 K suggest that while in the non-milled sample the Mn{sup 4+} ions substitute for Fe{sup 3+} at the octahedral B-sites, this is reversed as milling proceeds with doped Mn{sup 4+} ions, balancing Fe{sup 3+} vacancies and possibly Li{sup +} ions progressively migrate to the tetrahedral A-sites. This is supported by the slight increase observed in the magnetization of the milled samples relative to that of the non-milled one. The magnetic data suggest that in addition to the increasing superparamagentic component of the milled particles, thermal spin reversal and/or spin canting effects are possible at the surface layers of the nanoparticles.

  6. Optical and magnetic properties of La{sub 1−x}Ga{sub x}FeO{sub 3} nanoparticles synthesized by polymerization complex method

    Energy Technology Data Exchange (ETDEWEB)

    Hunpratub, Sitchai [Department of Physics, Faculty of Science, Udon Thani Rajabhat University, Udon Thani 41000 (Thailand); Karaphun, Attaphol [Nanotec-KKU Center of Excellence on Advanced Nanomaterials for Energy Production and Storage, Khon Kaen 40002 (Thailand); Phokha, Sumalin [Department of Physics, Faculty of Science, Udon Thani Rajabhat University, Udon Thani 41000 (Thailand); Swatsitang, Ekaphan, E-mail: ekaphan@kku.ac.th [Integrated Nanotechnology Research Center, Department of Physics, Faculty of Science, Khon Kaen University, Khon Kaen 40002 (Thailand); Nanotec-KKU Center of Excellence on Advanced Nanomaterials for Energy Production and Storage, Khon Kaen 40002 (Thailand)

    2016-09-01

    Graphical abstract: This figure shows the hysteresis loops of LaFeO{sub 3} and La{sub 0.6}Ga{sub 0.4}FeO{sub 3} nanoparticles with corresponding TEM images. Undoped sample exhibits antiferromagnetic behavior, whereas doped sample becomes ferromagnetic material. Particle sizes estimated by TEM are decreased from 70.2 ± 4.5 to 21.4 ± 8.5 nm with increasing Ga content. The decrease of particle size causes the disordering spins at the surface of particle which can induce a net magnetic moment and significantly enhance the magnetization (M), coercive field (H{sub c}) and remanent magnetization (M{sub r}). - Highlights: • Ga-doped LaFeO{sub 3} nanoparticles prepared by polymerization complex were studied. • Lattice, crystallite and particle size of sample decrease with increasing Ga content. • Decreasing of the lattice can distort the structure and enhance magnetic properties. • Optical band gaps of LaGaFeO{sub 3} nanoparticles are also decreased. • RT-FM of LaGaFeO{sub 3} nanoparticle is due to the disordering spins at surface particle. - Abstract: La{sub 1−x}Ga{sub x}FeO{sub 3} (x = 0.0, 0.1, 0.2, 0.3 and 0.4) nanoparticles were synthesized by polymerization complex method. X-ray diffraction (XRD) results reveal a pure orthorhombic phase structure. Increasing of Ga content, resulting in the decrease of average crystallite sizes calculated by XRD from 58.4 ± 5.9 to 13.4 ± 4.3 nm and the average particle sizes estimated by transmission electron microscope (TEM) images from 70.2 ± 4.5 to 21.4 ± 8.5 nm. The optical band gaps determined by UV–vis spectra showed a redshift from 2.145 to 1.954 eV that originates from surface effect caused by Ga substitution. The magnetic properties were investigated using a vibrating sample magnetometer (VSM). The room temperature hysteresis loops of La{sub 1–x}Ga{sub x}FeO{sub 3} nanopowders indicate the antiferromagnetic behavior of pure sample and all doped samples of ferromagnetic behavior with the enhancement of

  7. Luminescence properties of phosphate phosphor Ba{sub 3}Y(PO{sub 4}){sub 3}:Sm{sup 3+}

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Fu [College of Science, Hebei North University, Zhangjiakou 075000 (China); Liu, Yufeng, E-mail: liuyufeng4@126.com [State Key Lab of Power Systems, Department of Thermal Engineering, Tsinghua University, Beijing 100084 (China); Tian, Xiaodong; Dong, Guoyi [College of Physics Science and Technology, Hebei University, Baoding 071002 (China); Yu, Quanmao [Institute of Functional Materials, Jiangxi University of Finance & Economics, Nanchang 330013 (China)

    2015-05-15

    A series of reddish orange-emitting phosphate phosphors Ba{sub 3}Y{sub 1−x}(PO{sub 4}){sub 3}:xSm{sup 3+}(0.01≤x≤0.20) were synthesized by solid-state reaction. X-ray diffraction and photoluminescence spectra were utilized to characterize the structure and luminescence properties of as-synthesized phosphors. The optimized phosphors Ba{sub 3}Y{sub 0.95}(PO{sub 4}){sub 3}:0.05Sm{sup 3+} present several excitation bands from 300 to 500 nm, and exhibit intense reddish orange-emitting properties. The energy transfer type between Sm{sup 3+} ions was confirmed as d–d interaction by using Van Uitert model. The chromatic properties of the typical sample Ba{sub 3}Y(PO{sub 4}){sub 3}:0.05Sm{sup 3+} phosphor have been found to have chromaticity coordinates of (0.583, 0.405), which are located in reddish orange region under the excitation of 401 nm. These results indicated that Ba{sub 3}Y(PO{sub 4}){sub 3}:Sm{sup 3+} phosphors have potential applications in the field of lighting and display due to their effective excitation in the near-ultraviolet range. - Graphical abstract: The color coordinates for 5 mol% Sm{sup 3+} doped Ba{sub 3}Y(PO{sub 4}){sub 3} phosphor were calculated to be (0.583, 0.405), which are located in reddish orange region under the excitation of 401 nm. The peaks of Ba{sub 3}Y{sub 0.95}(PO{sub 4}){sub 3}:0.05Sm{sup 3+} phosphor with the highest emission intensity at 600 nm are broader than those of Y{sub 2}O{sub 3}:Eu{sup 3+} and Y{sub 2}O{sub 2}S:Eu{sup 3+} phosphors. All these characteristics suggest that Ba{sub 3}Y(PO{sub 4}){sub 3}:Sm{sup 3+} phosphors are suitable for near-UV (370–410 nm) excitation and can be applicable to near UV-based WLEDs. ▪ - Highlights: • Different concentration Sm{sup 3+}-doped Ba{sub 3}Y(PO{sub 4}){sub 3} phosphors were fabricated by solid state method. • The optimized phosphors present the several excitation bands from 300 to 500 nm. • The Ba{sub 3}Y(PO{sub 4}){sub 3}:Sm{sup 3+} shows bright reddish orange

  8. Crossover from disordered to core-shell structures of nano-oxide Y{sub 2}O{sub 3} dispersed particles in Fe

    Energy Technology Data Exchange (ETDEWEB)

    Higgins, M. P.; Wang, L. M.; Gao, F., E-mail: gaofeium@umich.edu [Department of Nuclear Engineering and Radiological Sciences, University of Michigan, Ann Arbor, Michigan 48109 (United States); Lu, C. Y. [Department of Nuclear Engineering and Radiological Sciences, University of Michigan, Ann Arbor, Michigan 48109 (United States); Key Laboratory for Anisotropy and Texture of Materials (Ministry of Education), Northeastern University, Shenyang, Liaoning 110819 (China); Lu, Z. [Key Laboratory for Anisotropy and Texture of Materials (Ministry of Education), Northeastern University, Shenyang, Liaoning 110819 (China); Shao, L. [Department of Nuclear Engineering, Texas A& M University, College Station, Texas 77843 (United States)

    2016-07-18

    Molecular dynamic simulations of Y{sub 2}O{sub 3} in bcc Fe and transmission electron microscopy (TEM) observations were used to understand the structure of Y{sub 2}O{sub 3} nano-clusters in an oxide dispersion strengthened steel matrix. The study showed that Y{sub 2}O{sub 3} nano-clusters below 2 nm were completely disordered. Y{sub 2}O{sub 3} nano-clusters above 2 nm, however, form a core-shell structure, with a shell thickness of 0.5–0.7 nm that is independent of nano-cluster size. Y{sub 2}O{sub 3} nano-clusters were surrounded by off-lattice Fe atoms, further increasing the stability of these nano-clusters. TEM was used to corroborate our simulation results and showed a crossover from a disordered nano-cluster to a core-shell structure.

  9. Production, characterization and application of Gd{sub 2}O{sub 3} and Er{sub 2}O{sub 3} nanoparticles as radiosensitizers in radiotherapy beams; Produção, caracterização e aplicação de nanopartículas de Gd{sub 2}O{sub 3} e Er{sub 2}O{sub 3} como radiossensibilizadores em feixes de radioterapia

    Energy Technology Data Exchange (ETDEWEB)

    Corrêa, Eduardo de Lima

    2017-07-01

    In this study Gd{sub 2}O{sub 3} and Er{sub 2}O{sub 3} nanoparticles were produced for application as radiosensitizers in radiotherapy beams. They were synthesized at the Hyperfine Interactions Laboratory, IPEN, using thermal decomposition method and characterized by X-ray diffraction, to verify crystalline structure, transmission electron microscopy, to obtain information about shape, size and size distribution, neutron activation analysis, whereby it was possible to determine samples purity and gadolinium and erbium concentration. Magnetization and perturbed γ-γ angular correlation (PAC) measurements were performed in order to study particles magnetic behavior and quadrupole interactions, respectively. Characterization results showed a bixbyite structure, 5 nm diameter post-synthesis particles with narrow size distribution. Rare-earth mass determination in each sample was important to perform normalization in magnetic susceptibility measurements, making possible the view of a high magnetization under 30 K for post-synthesis samples, what was not observed in larger particles, together with an effective magnetic moment enhancement for nanoparticles, not seen in bulk samples, and a change in the antiferromagnetic ordering temperature for Er{sub 2}O{sub 3}. PAC spectroscopy results show possible surface effects. The absence of a well-defined frequency in 5 nm samples indicates the amount of {sup 111}In({sup 111}Cd) at particle surface is bigger than in the core, resulting in a non-evident hyperfine interaction between the probe nuclei and the host. The X-ray diffraction and PAC spectroscopy joint was vital to understand the particles structural damage caused by {sup 60}Co irradiation. About radiosensitizer measurements a dose enhancement factor (DEF) of up to 1,67 and 1,09 for Gd{sub 2}O{sub 3} nanoparticles under {sup 60}Co and 6MV irradiation, respectively, were observed. Under same conditions DEF values of up to 1,37 and 1,06 were found for Er{sub 2}O{sub 3

  10. Influence of clay particles on Al{sub 2}O{sub 3} and TiO{sub 2} nanoparticles transport and retention through limestone porous media: measurements and mechanisms

    Energy Technology Data Exchange (ETDEWEB)

    Bayat, Ali Esfandyari, E-mail: ali.esfandiari.bayat@gmail.com; Junin, Radzuan [Universiti Teknologi Malaysia, Department of Petroleum Engineering, Faculty of Petroleum and Renewable Energy Engineering (Malaysia); Mohsin, Rahmat [Universiti Teknologi Malaysia, UTM-MPRC Institute for Oil and Gas, N29A, Lengkuk Suria (Malaysia); Hokmabadi, Mehrdad [Universiti Teknologi Malaysia, Department of Petroleum Engineering, Faculty of Petroleum and Renewable Energy Engineering (Malaysia); Shamshirband, Shahaboddin [University of Malaya, Department of Computer System and Information Technology, Faculty of Computer System and Information Technology (Malaysia)

    2015-05-15

    Utilization of nanoparticles (NPs) for a broad range of applications has caused considerable quantities of these materials to be released into the environment. Issues of how and where the NPs are distributed into the subsurface aquatic environments are questions for those in environmental engineering. This study investigated the influence of three abundant clay minerals namely kaolinite, montmorillonite, and illite in the subsurface natural aquatic systems on the transport and retention of aluminum oxide (Al{sub 2}O{sub 3}, 40 nm) and titanium dioxide (TiO{sub 2}, 10–30 nm) NPs through saturated limestone porous media. The clay concentrations in porous media were set at 2 and 4 vol% of the holder capacity. Breakthrough curves in the columns outlets were measured using a UV–Vis spectrophotometer. It was found that the maximum NPs recoveries were obtained when there was no clay particle in the porous medium. On the other hand, increase in concentration of clay particles has resulted in the NPs recoveries being significantly declined. Due to fibrous structure of illite, it was found to be more effective for NPs retention in comparison to montmorillonite and kaolinite. Overall, the position of clay particles in the porous media pores and their morphologies were found to be two main reasons for increase of NPs retention in porous media.

  11. Microwave synthesis of α-Fe{sub 2}O{sub 3} nanoparticles and their lithium storage properties: A comparative study

    Energy Technology Data Exchange (ETDEWEB)

    Mondal, Anjon Kumar, E-mail: anjonmondal@yahoo.com; Chen, Shuangqiang; Su, Dawei; Kretschmer, Katja; Liu, Hao; Wang, Guoxiu, E-mail: Guoxiu.Wang@uts.edu.au

    2015-11-05

    This work introduces a simple microwave method for the preparation of α-Fe{sub 2}O{sub 3} nanoparticles with two different sizes. Both the materials were characterized by X-ray powder diffraction, scanning electron microscopy, transmission electron microscopy and Brunauer–Emmett–Teller methods. The lithium storage properties were evaluated and compared in terms of their reversible capacity, rate capability and cycling performance. Interestingly, the electrode made of large particles (200–300 nm) show the reversible capacity of 1012 mA h g{sup −1}, better rate capability and excellent cycling stability than those of the small particles (20–30 nm). The poor electrochemical performances of small particles can be ascribed to their agglomeration during repeated charging and discharge process. The agglomeration of small particles may substantially decrease the surface area, which results in the lack of sufficient electro active sites for electrochemical reaction. - Highlights: • A microwave method was employed to prepare α-Fe{sub 2}O{sub 3} nanoparticles with two different sizes. • Larger particles of α-Fe{sub 2}O{sub 3} showed the reversible capacity of 1012 mA h g{sup −1}. • Compared to small particles larger particles presented excellent cycling stability. • Larger particles exhibited high rate capability.

  12. Fabrication and luminescence properties of Al{sub 2}O{sub 3}:Tb{sup 3+} microspheres via a microwave solvothermal route

    Energy Technology Data Exchange (ETDEWEB)

    Zhu Zhenfeng, E-mail: zhuzf@sust.edu.cn [School of Materials Science and Engineering, Shaanxi University of Science and Technology, Xi' an 710021 (China); Liu Dianguang; Liu Hui; Li Guangjun; Du Juan; He Zuoli [School of Materials Science and Engineering, Shaanxi University of Science and Technology, Xi' an 710021 (China)

    2012-02-15

    Al{sub 2}O{sub 3}:Tb{sup 3+} green phosphors were synthesized via a microwave solvothermal and thermal decomposition route, and characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), photoluminescence (PL) spectra, and decay curves. XRD results indicate that Tb{sup 3+} doped samples are {gamma}-Al{sub 2}O{sub 3} after being calcined at 773 K. SEM results show that the particles of Al{sub 2}O{sub 3}:Tb{sup 3+} are hierarchically nanostructured microspheres assembled from nanosheets. The PL spectra indicate that the {sup 5}D{sub 4}{yields}{sup 7}F{sub 5} (545 nm) electric dipole transition is the most intensive when excited at 235 nm. It is shown that 0.7 mol% of doping concentration of Tb{sup 3+} ions in {gamma}-Al{sub 2}O{sub 3}:Tb{sup 3+} is optimum. According to Dexter's theory, the critical distance between Tb{sup 3+} ions for energy transfer was determined to be 18.4 A. It is found that the curve followed the single-exponential decay. The excellent chromaticity coordinates of Al{sub 2}O{sub 3}:Tb{sup 3+} phosphors, as defined by the International Commission on Illumination (CIE), indicate that it is a good candidate for use in light display systems and optoelectronic devices. - Highlights: Black-Right-Pointing-Pointer Al{sub 2}O{sub 3}:Tb{sup 3+} phosphors prepared via a microwave solvothermal route. Black-Right-Pointing-Pointer The particles were hierarchically nanostructured microspheres packaged by nanosheets. Black-Right-Pointing-Pointer {sup 5}D{sub 4}{yields}{sup 7}F{sub 5} electric dipole transition is the most intensive when excited at 235 nm. Black-Right-Pointing-Pointer 0.7 mol% of doping concentration of Tb{sup 3+} ions in {gamma}-Al{sub 2}O{sub 3}:Tb{sup 3+} is optimum. Black-Right-Pointing-Pointer Critical distance between Tb{sup 3+} ions for energy transfer is 18.4 A.

  13. Interactions between sub-10-nm iron and cerium oxide nanoparticles and 3T3 fibroblasts: the role of the coating and aggregation state

    Energy Technology Data Exchange (ETDEWEB)

    Safi, M; Sarrouj, H; Berret, J-F [Matiere et Systemes Complexes, UMR 7057 CNRS, Universite Denis Diderot Paris VII, Batiment Condorcet, 10 rue Alice Domon et Leonie Duquet, F-75205 Paris (France); Sandre, O [UPMC Universite Paris VI-Laboratoire de Physico-chimie des Electrolytes, Colloides et Sciences Analytiques, UMR 7195 UPMC Universite Paris 6/CNRS/ESPCI Paristech, 4 place Jussieu, F-75252 Paris Cedex 05 (France); Mignet, N, E-mail: jean-francois.berret@univ-paris-diderot.fr [CNRS UMR 8151, Faculte de Pharmacie, 4 avenue de l' Observatoire, F-75270 Paris (France)

    2010-04-09

    Recent nanotoxicity studies revealed that the physico-chemical characteristics of engineered nanomaterials play an important role in the interactions with living cells. Here, we report on the toxicity and uptake of cerium and iron oxide sub-10-nm nanoparticles by NIH/3T3 mouse fibroblasts. Coating strategies include low-molecular weight ligands (citric acid) and polymers (poly(acrylic acid), M{sub W} = 2000 g mol{sup -1}). Electrostatically adsorbed on the surfaces, the organic moieties provide a negatively charged coating in physiological conditions. We find that most particles were biocompatible, as exposed cells remained 100% viable relative to controls. Only the bare and the citrate-coated nanoceria exhibit a slight decrease in mitochondrial activity at very high cerium concentrations (>1 g l{sup -1}). We also observe that the citrate-coated particles are internalized/adsorbed by the cells in large amounts, typically 250 pg/cell after 24 h incubation for iron oxide. In contrast, the polymer-coated particles are taken up at much lower rates (<30 pg/cell). The strong uptake shown by the citrated particles is related to the destabilization of the dispersions in the cell culture medium and their sedimentation down to the cell membranes. In conclusion, we show that the uptake of nanomaterials by living cells depends on the coating of the particles and on its ability to preserve the colloidal nature of the dispersions.

  14. Synthesis of green emission upconversion phosphor nanosheets (LaNb{sub 2}O{sub 7}) doped with Er{sup 3+} and Yb{sup 3+}

    Energy Technology Data Exchange (ETDEWEB)

    Takasugi, Soichi [Course of Science and Technology, Graduate School of Science and Technology, Tokai University, 4-1-1 Kitakaname, Hiratsuka, Kanagawa 259-1292 (Japan); Iida, Riku [Department of Chemistry, School of Science, Tokai University, 4-1-1 Kitakaname, Hiratsuka, Kanagawa 259-1292 (Japan); Tomita, Koji, E-mail: tomita@keyaki.cc.u-tokai.ac.jp [Department of Chemistry, School of Science, Tokai University, 4-1-1 Kitakaname, Hiratsuka, Kanagawa 259-1292 (Japan); Iwaoka, Michio [Course of Science and Technology, Graduate School of Science and Technology, Tokai University, 4-1-1 Kitakaname, Hiratsuka, Kanagawa 259-1292 (Japan); Department of Chemistry, School of Science, Tokai University, 4-1-1 Kitakaname, Hiratsuka, Kanagawa 259-1292 (Japan); Katagiri, Kiyofumi [Department of Applied Chemistry, Graduate School of Engineering, Hiroshima University, 1-4-1 Kagamiyama, Higashi-Hiroshima 739-8527 (Japan); Osada, Minoru [International Center for Materials Nano architectonics (MANA), National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki 305-0044 (Japan); Kakihana, Masato [Institute of Multidisciplinary Research for Advanced Materials (IMRAM), Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai 980-8577 (Japan)

    2016-05-15

    LaNb{sub 2}O{sub 7}:Er{sup 3+},Yb{sup 3+} upconversion (UPC) phosphor nanosheets were prepared by exfoliating a KLaNb{sub 2}O{sub 7}:Er{sup 3+},Yb{sup 3+} layered compound. Highly crystalline nanosheets with a thickness and lateral size of 3.91 nm and approximately 300 nm, respectively, were obtained. The UPC emission intensity of the nanosheets was 7.6 times greater than that of mechanically milled particles (100–500 nm) of bulk KLaNb{sub 2}O{sub 7}:Er{sup 3+},Yb{sup 3+}. The UPC emission intensities of the nanosheets dispersed in different solvents (H{sub 2}O, D{sub 2}O, CH{sub 3}OH, CH{sub 2}Cl{sub 2}, and CCl{sub 4}) were measured, and the intensities were observed to decrease in the order CCl{sub 4}>CH{sub 2}Cl{sub 2}>D{sub 2}O>CH{sub 3}OH>H{sub 2}O. Because of the large surface area of the nanosheets, their emission intensity was decreased depending on the solvent's vibrational energy. - Highlights: • La{sub 0.45}Er{sub 0.05}Yb{sub 0.5}Nb{sub 2}O{sub 7} nanosheets were synthesized by a soft breakdown method (exfoliation). • The lateral size and thickness of the nanosheets were approximately 300 nm and approximately 3.91 nm, respectively. • The exfoliated nanosheets exhibited bright upconversion emission 7.6 times more intense than that of the milled sample (100–500 nm). • The nanosheets dispersed in solvents exhibited greatly different upconversion emission intensities depending on the solvent's vibrational energy.

  15. Methanesulfonates of high-valent metals. Syntheses and structural features of MoO{sub 2}(CH{sub 3}SO{sub 3}){sub 2}, UO{sub 2}(CH{sub 3}SO{sub 3}){sub 2}, ReO{sub 3}(CH{sub 3}SO{sub 3}), VO(CH{sub 3}SO{sub 3}){sub 2}, and V{sub 2}O{sub 3}(CH{sub 3}SO{sub 3}){sub 4} and their thermal decomposition under N{sub 2} and O{sub 2} atmosphere

    Energy Technology Data Exchange (ETDEWEB)

    Betke, Ulf; Neuschulz, Kai; Wickleder, Mathias S. [Carl von Ossietzky University of Oldenburg, Institute of Pure and Applied Chemistry (Germany)

    2011-11-04

    Oxide methanesulfonates of Mo, U, Re, and V have been prepared by reaction of MoO{sub 3}, UO{sub 2}(CH{sub 3}COO){sub 2}.2 H{sub 2}O, Re{sub 2}O{sub 7}(H{sub 2}O){sub 2}, and V{sub 2}O{sub 5} with CH{sub 3}SO{sub 3}H or mixtures thereof with its anhydride. These compounds are the first examples of solvent-free oxide methanesulfonates of these elements. MoO{sub 2}(CH{sub 3}SO{sub 3}){sub 2} (Pbca, a=1487.05(4), b=752.55(2), c=1549.61(5) pm, V=1.73414(9) nm{sup 3}, Z=8) contains [MoO{sub 2}] moieties connected by [CH{sub 3}SO{sub 3}] ions to form layers parallel to (100). UO{sub 2}(CH{sub 3}SO{sub 3}){sub 2} (P2{sub 1}/c, a=1320.4(1), b=1014.41(6), c=1533.7(1) pm, β=112.80(1) {sup circle}, V=1.8937(3) nm{sup 3}, Z=8) consists of linear UO{sub 2}{sup 2+} ions coordinated by five [CH{sub 3}SO{sub 3}] ions, forming a layer structure. VO(CH{sub 3}SO{sub 3}){sub 2} (P2{sub 1}/c, a=1136.5(1), b=869.87(7), c=915.5(1) pm, β=113.66(1) {sup circle}, V=0.8290(2) nm{sup 3}, Z=4) contains [VO] units connected by methanesulfonate anions to form corrugated layers parallel to (100). In ReO{sub 3}(CH{sub 3}SO{sub 3}) (P anti 1, a=574.0(1), b=1279.6(3), c=1641.9(3) pm, α=102.08(2), β=96.11(2), γ=99.04(2) {sup circle}, V=1.1523(4) nm{sup 3}, Z=8) a chain structure exhibiting infinite O-[ReO{sub 2}]-O-[ReO{sub 2}]-O chains is formed. Each [ReO{sub 2}]-O-[ReO{sub 2}] unit is coordinated by two bidentate [CH{sub 3}SO{sub 3}] ions. V{sub 2}O{sub 3}(CH{sub 3}SO{sub 3}){sub 4} (I2/a, a=1645.2(3), b=583.1(1), c=1670.2(3) pm, β=102.58(3), V=1.5637(5) pm{sup 3}, Z=4) adopts a chain structure, too, but contains discrete [VO]-O-[VO] moieties, each coordinated by two bidentate [CH{sub 3}SO{sub 3}] ligands. Additional methanesulfonate ions connect the [V{sub 2}O{sub 3}] groups along [001]. Thermal decomposition of the compounds was monitored under N{sub 2} and O{sub 2} atmosphere by thermogravimetric/differential thermal analysis and XRD measurements. Under N{sub 2} the decomposition proceeds

  16. Improving pure red upconversion emission of Co-doped Y{sub 2}O{sub 3}:Yb{sup 3+}–Er{sup 3+} nanocrystals with a combination of sodium sulfide and surfactant Pluronic-F127

    Energy Technology Data Exchange (ETDEWEB)

    López-Luke, T., E-mail: tzarara@cio.mx [Centro de Investigaciones en Óptica, A.P. 1-948, León, Gto. 37160, México (Mexico); De la Rosa, E., E-mail: elder@cio.mx [Centro de Investigaciones en Óptica, A.P. 1-948, León, Gto. 37160, México (Mexico); Campos Villalobos, I. [Centro de Investigaciones en Óptica, A.P. 1-948, León, Gto. 37160, México (Mexico); Rodriguez, R.A. [Universidad de Guadalajara, Unidad Lagos, Lagos de Moreno, Jal. 47460, México (Mexico); Ángles-Chávez, C. [Instituto Mexicano del Petróleo, Cd. México, D.F. 07730, México (Mexico); Salas, P. [Centro de Física Aplicada y Tecnología Avanzada, Universidad Nacional Autónoma de México, A.P. 1-1010, Querétaro, Qro. 76000, México (Mexico); Wheeler, Damon A.; Zhang, J.Z. [Department of Chemistry and Biochemistry, University of California, Santa Cruz, CA 95064 (United States)

    2014-01-15

    Nanocrystals of Y{sub 2}O{sub 3}:Yb{sup 3+}–Er{sup 3+} (2:1 mol% Yb{sup 3+}:Er{sup 3+}) were prepared by a novel precipitation technique using Na{sub 2}S and Pluronic-F127 (PF127) surfactant. Crystal structure, particle size, red emission intensity and fluorescence decay lifetimes were determined using microscopy and spectroscopy techniques. TEM analysis indicates that the average particle size ranged from 40 to 70 nm. The nanocrystals showed a strong red emission band centered at 663 nm after excitation at 970 nm. The upconverted signal intensity was improved 250% with an optimum concentration of Na{sub 2}S (0.48 M) and PF127 (0.1 mM). The improvement was explained in terms of the reduction of surface contaminants as well as the cubic crystalline phase of the parent Y{sub 2}O{sub 3} material. Interestingly, the formation of sulfates (SO{sub 4}{sup 2−}) is faster than that of O–H, which is responsible for quenching the red and green emissions. The results suggest that Na{sub 2}S and PF127 are good candidates for surface passivation, especially when used in conjunction. The preparation of Y{sub 2}O{sub 3}:Yb{sup 3+}–Er{sup 3+} using Na{sub 2}S with strong red emission band was produced at a lower cost than that of other sulfuration processes. -- Highlights: • . • Strong red emission band centered at 663 nm was obtained after excitation at 970 nm. • Yb-Er codoped Y2O3 nanocrystals with average size ranging from 40 to 70 nm. • Improvement of the red emission in Y2O3:Yb-Er nanocrystals by the introduction of sodium sulfide and pluronic. • Passivation of nanocrystal surface with sodium sulfide and pluoronic.

  17. YVO{sub 4}:Eu{sup 3+}, Dy{sup 3+}-Fe{sub 3}O{sub 4} co-doped nanocomposites: preparation, luminescent, and magnetic properties

    Energy Technology Data Exchange (ETDEWEB)

    Liu Deming; Shi Jianhui; Tong Lizhu; Ren Xiaozhen; Li Quanhong; Yang Hua, E-mail: huayang86@sina.com [Jilin University, College of Chemistry (China)

    2012-11-15

    A series of different concentrations of Eu{sup 3+} and Dy{sup 3+} ions co-doping yttrium vanadate phosphors coated with Fe{sub 3}O{sub 4} (YVO{sub 4}:Eu{sup 3+}, Dy{sup 3+}-Fe{sub 3}O{sub 4}) was successful prepared by using two steps route including sol-gel method and hydrothermal method. The resulting phase formation, particle morphology, structure, luminescent, and magnetic properties were examined by X-ray diffraction, transmission electron microscopy, photoluminescence spectra, and vibrating sample magnetometer. The results indicate that the diameter of the YVO{sub 4}:Eu{sup 3+}, Dy{sup 3+}-Fe{sub 3}O{sub 4} nanocomposites is 100-300 nm. The special saturation magnetization Ms of the nanocomposites is 53 emu/g. Additionally, the emission intensities of YVO{sub 4}:Eu{sup 3+} or Dy{sup 3+} ions are regularly changed with the emission doping concentrations. After coating with Fe{sub 3}O{sub 4}, the variation of the luminescent intensity of YVO{sub 4}:Eu{sup 3+}, Dy{sup 3+}-Fe{sub 3}O{sub 4} magnetic phosphors is different.

  18. Interparticle interactions of FePt core and Fe{sub 3}O{sub 4} shell in FePt/Fe{sub 3}O{sub 4} magnetic nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Akbari, Hossein, E-mail: Akbari.ph@iauardabil.ac.ir [Department of Physics, Ardabil Branch, Islamic Azad University, Ardabil (Iran, Islamic Republic of); Zeynali, Hossein [Department of Physics, Kashan Branch, Islamic Azad University, Kashan (Iran, Islamic Republic of); Bakhshayeshi, Ali [Department of Physics, Mashhad Branch, Islamic Azad University, Mashhad (Iran, Islamic Republic of)

    2016-02-22

    Monodisperse FePt nanoparticles were successfully synthesized using simple wet chemical method. Fe{sub 3}O{sub 4} was used as a magnetic shell around each FePt nanoparticles. In FePt/Fe{sub 3}O{sub 4} core/shell system, core thickness is 2 nm and shell thickness varies from zero to 2.5 nm. A theoretical model presented to calculate the shell thickness dependence of Coercivity. Presented model is compared with the results from Stoner–Wohlfarth model to interpret the shell thickness dependence of Coercivity in FePt/Fe{sub 3}O{sub 4} core/shell nanoparticles. There is a difference between the results from Stoner–Wohlfarth model and experimental data when the shell thickness increases. In the presented model, the effects of interparticle exchange and random magneto crystalline anisotropy are added to the previous models of magnetization reversal for core/shell nanostructures in order to achieve a better agreement with experimental data. For magnetic shells in FePt/Fe{sub 3}O{sub 4} core/shell, effective coupling between particles increases with increasing shell thickness which leads to Coercivity destruction for stronger couplings. According to the boundary conditions, in the harder regions with higher exchange stiffness, there is small variation in magnetization and so the magnetization modes become more localized. We discussed both localized and non-localized magnetization modes. For non-zero shell thickness, non-localized modes propagate in the soft phase which effects the quality of particle exchange interactions. - Highlights: • Monodisperse FePt nanoparticles were successfully synthesized using simple wet chemical method. • Fe{sub 3}O{sub 4} was used as a magnetic shell around each FePt nanoparticles. • A theoretical model presented to calculate the shell thickness dependence of Coercivity. • Magnetic shells increase effective coupling between particles with increasing shell thickness. • Magnetization modes are more localized in the regions with

  19. Effects of Tb{sup 3+} concentration on the La{sub 2}Sr{sub 3}(BO{sub 3}){sub 4}: X% Tb{sup 3+} polycrystalline nanophosphor

    Energy Technology Data Exchange (ETDEWEB)

    Mlotswa, D.V. [Physics Department, University of the Free State, Private Bag x13, Phuthaditjhaba 9866 (South Africa); Madihlaba, R.M. [Chemistry Department, University of the Western Cape, Private Bag x17, Bellville 7535 (South Africa); Koao, L.F. [Physics Department, University of the Free State, Private Bag x13, Phuthaditjhaba 9866 (South Africa); Onani, M.O., E-mail: monani@uwc.ac.za [Chemistry Department, University of the Western Cape, Private Bag x17, Bellville 7535 (South Africa); Dejene, F.B. [Physics Department, University of the Free State, Private Bag x13, Phuthaditjhaba 9866 (South Africa)

    2016-01-01

    A new green phosphor, La{sub 2}Sr{sub 3}(BO{sub 3}){sub 4}): x% Tb{sup 3+} was fabricated by solution-combustion method using urea as a fuel and ammonium nitrate as an oxidizer. The phosphor was characterised using Fourier transform infrared spectroscopy (FTIR), Thermogravimetric analysis (TGA), Differential scanning calorimetry (DSC), Energy dispersive spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM) and photoluminescence spectroscopy (PL. The results exhibit that La{sub 2}Sr{sub 3}(BO{sub 3}){sub 4}): x% Tb{sup 3+} phosphor has the strongest excitation at 209 nm with a full-width at half-maximum (FWHM) of 20 nm, and can emit bright green light at 545 nm under 209 nm excitation. The optimum concentration for Tb{sup 3+} in La{sub 2}Sr{sub 3}(BO{sub 3}){sub 4}): x% Tb{sup 3+} is 0.033 mol%. The prominent green luminescence was due to the {sup 5}D{sub 4}–{sup 7}F{sub 5} transition of Tb{sup 3+} ion. Herein, the green phosphors are promising good candidates employed in tri-color lamps.

  20. Synthesis and luminescence properties of novel Sr{sub 3}Gd(PO{sub 4}){sub 3}:Dy{sup 3+} phosphor

    Energy Technology Data Exchange (ETDEWEB)

    Xu, Qiguang; Sun, Jiayue, E-mail: Jiayue_sun@126.com; Cui, Dianpeng; Di, Qiumei; Zeng, Junhui

    2015-02-15

    Sr{sub 3}(Gd{sub 1−x}Dy{sub x})(PO{sub 4}){sub 3} phosphors for white light-emitting diodes (w-LEDs) were prepared by the conventional solid-state reaction. X-ray diffraction (XRD) and photoluminescence spectra were utilized to characterize the structure and luminescence properties of the as-synthesized phosphors. Luminescence properties shows that the phosphor can be efficiently excited by the ultraviolet visible light in the region from 300 to 450 nm, and it exhibits blue (483 nm) and yellow (575 nm) emission corresponding to {sup 4}F{sub 9/2}→{sup 6}H{sub 15/2} transition and {sup 4}F{sub 9/2}→{sup 6}H{sub 13/2} transition, respectively. It has been found that concentration quenching occurs via dipole–dipole interaction according to Dexter's theory. The temperature dependence of photoluminescence properties is investigated from 25 to 250 °C and the prepared Sr{sub 3}Gd(PO{sub 4}){sub 3}:Dy{sup 3+} phosphors show good thermal quenching properties. - Highlights: • Sr{sub 3}Gd(PO{sub 4}){sub 3}:Dy{sup 3+} phosphors were synthesized by a solid-state reaction method. • The phosphor could be efficiently excited by the UV–vis light region from 300 to 450 nm. • Sr{sub 3}Gd(PO{sub 4}){sub 3}:Dy{sup 3+} phosphors exhibited blue (483 nm) and yellow (575 nm) emission. • The Sr{sub 3}Gd(PO{sub 4}){sub 3}:Dy{sup 3+} phosphors concentration quenching occurred as a result of dipole–dipole interaction. • Sr{sub 3}Gd(PO{sub 4}){sub 3}:Dy{sup 3+} phosphors showed good thermal quenching properties.

  1. Ultralow-Power Electronic Trapping of Nanoparticles with Sub-10 nm Gold Nanogap Electrodes.

    Science.gov (United States)

    Barik, Avijit; Chen, Xiaoshu; Oh, Sang-Hyun

    2016-10-12

    We demonstrate nanogap electrodes for rapid, parallel, and ultralow-power trapping of nanoparticles. Our device pushes the limit of dielectrophoresis by shrinking the separation between gold electrodes to sub-10 nm, thereby creating strong trapping forces at biases as low as the 100 mV ranges. Using high-throughput atomic layer lithography, we manufacture sub-10 nm gaps between 0.8 mm long gold electrodes and pattern them into individually addressable parallel electronic traps. Unlike pointlike junctions made by electron-beam lithography or larger micron-gap electrodes that are used for conventional dielectrophoresis, our sub-10 nm gold nanogap electrodes provide strong trapping forces over a mm-scale trapping zone. Importantly, our technology solves the key challenges associated with traditional dielectrophoresis experiments, such as high voltages that cause heat generation, bubble formation, and unwanted electrochemical reactions. The strongly enhanced fields around the nanogap induce particle-transport speed exceeding 10 μm/s and enable the trapping of 30 nm polystyrene nanoparticles using an ultralow bias of 200 mV. We also demonstrate rapid electronic trapping of quantum dots and nanodiamond particles on arrays of parallel traps. Our sub-10 nm gold nanogap electrodes can be combined with plasmonic sensors or nanophotonic circuitry, and their low-power electronic operation can potentially enable high-density integration on a chip as well as portable biosensing.

  2. Kinetics of gas to particle conversion in the NH/sub 3/-Chl system

    Energy Technology Data Exchange (ETDEWEB)

    Luria, M; Cohen, B

    1980-01-01

    Particle formation in the reaction of NH/sub 3/ and Chl under 1 atm of N/sub 2/ and at 25/sup 0/C was studied in a flow reactor. The critical concentration below which NO particle can be formed was found to be 3.5 x 10/sup +14/ molecule/CM/sup 3/ for (NH/sub 3/)=(HCl). Above this concentration, gas-particle conversion percentage increases rapidly to approach 100%.

  3. Synthesis and characterization of Fe{sub 2}O{sub 3} nanoparticles by simple precipitation method

    Energy Technology Data Exchange (ETDEWEB)

    Sankadiya, Siyaram, E-mail: siyaramsankdiya@gmail.com; Oswal, Nidhi, E-mail: oswal03nidhi@gmail.com [Dept. of Applied Physics, Shri Govindram Sakseria Inst. of Tech. and Sci., 23 Park Road, Indore(MP) 452003 (India); Jain, Pranat, E-mail: pranatjain@gmail.com [Dept. of Material Sc. & Metallurgical Eng., Maulana Azad National Inst. of Tech., Bhopal (MP) 4620003 (India); Gupta, Nitish, E-mail: nitish.nidhi75@gmail.com [Dept. of Applied Chemistry, Shri Govindram Sakseria Inst. of Tech. and Sci., 23 Park Road, Indore (MP) 452003 (India)

    2016-04-13

    A simple and efficient synthesis of Iron-oxide nanoparticles was carried out by precipitation method using ferric chloride as precursor and ammonium hydroxide as a stabilizing agent at different calcination temperatures. The synthesized powder was characterized by powder X-Ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR), Field Emission Scanning Electron Microscope (FE-SEM) and Transmission Electron Microscopy (TEM). X-ray diffraction indicated the formation hematite Fe{sub 2}O{sub 3} structure. FTIR showed various functional groups of particles and absorption bands related to metal oxygen vibration modes. The heating temperatures were varied at 100 °C, 200°C, and 300°C. The Fe{sub 2}O{sub 3} nanostructures with the average particle size of about 36.22 nm were prepared at 300°C for 4h. TEM study is also confirming the nanosize of Fe{sub 2}O{sub 3} particle. This aqueous precipitation method gives a large scale production of Fe{sub 2}O{sub 3} nanoparticles easily.

  4. Synthesis, surface modification/decoration of luminescent–magnetic core/shell nanomaterials, based on the lanthanide doped fluorides (Fe{sub 3}O{sub 4}/SiO{sub 2}/NH{sub 2}/PAA/LnF{sub 3})

    Energy Technology Data Exchange (ETDEWEB)

    Runowski, Marcin; Lis, Stefan, E-mail: blis@amu.edu.pl

    2016-02-15

    The synthesized magnetite nanoparticles (10–15 nm) were successfully coated with amine modified silica nanoshell, which led to the formation of core/shell type nanostructures (30–50 nm). The as-prepared nanoparticles were surface modified with polyacrylic acid (PAA) via electrostatic interactions of –NH{sub 2} and –COOH groups. Afterwards, the surface PAA molecules acted as complexing agents of the introduced lanthanide (Ln{sup 3+}) ions. Subsequently, the as-prepared nanostructures were surface decorated with luminescent LnF{sub 3} nanoparticles, forming Eu{sup 3+} or Tb{sup 3+} doped Fe{sub 3}O{sub 4}/SiO{sub 2}/NH{sub 2}/PAA/LnF{sub 3} nanomaterials (50–100 nm). The obtained luminescent–magnetic products exhibited simultaneously bright red or green emission under UV lamp irradiation (λ{sub ex}=254 nm), and a response for the applied magnetic field (strong magnet attracts the colloidal particles, dispersed in aqueous medium). After the synthesis, properties of the nanomaterials were investigated by powder X-ray diffraction (XRD) technique, transmission electron microscopy (TEM), infrared spectroscopy (IR) and spectrofluorometry (analysis of excitation/emission spectra and luminescence decay curves). Such advanced nanomaterials can be potentially used in multimodal imaging, targeted therapies and as multifunctional contrast agents, novel luminescent–magnetic tracers, protection of documents, etc. - Highlights: • Luminescent–magnetic nanomaterials Fe{sub 3}O{sub 4}/SiO{sub 2}/NH{sub 2}/PAA/LnF{sub 3} were synthesized. • Core/shell nanostructures were obtained by surface modification of nanoparticles. • Luminescent lanthanide fluoride nanoparticles doped with Eu{sup 3+} and Tb{sup 3+} ions. • Multifunctional core/shell nanostructures exhibited red or green emission. • Nanomaterials formed stable aqueous colloids.

  5. Effect of 6 MeV electrons on luminescence properties of Y{sub 2}O{sub 3}:Tb{sup 3+} nanophosphors

    Energy Technology Data Exchange (ETDEWEB)

    Sunitha, D.V., E-mail: sunithaprasad8@gmail.com [School of Physics, Reva University, Yelahanka, Bangalore 560064 (India); Nagabhushana, H. [Prof. C.N.R. Rao Centre for Advanced Materials Research, Tumkur University, Tumkur 572103 (India); Hareesh, K., E-mail: appi.2907@gmail.com [Department of Physics, Savitribai Phule Pune University, Pune 411007 (India); Bhoraskar, V.N. [Department of Physics, Savitribai Phule Pune University, Pune 411007 (India); Dhole, S.D., E-mail: sanjay@physics.unipune.ac.in [Department of Physics, Savitribai Phule Pune University, Pune 411007 (India)

    2016-09-15

    Y{sub 2}O{sub 3}:Tb{sup 3+} nanophosphors were synthesized by solution combustion technique and irradiated with 6 MeV energetic electrons in the fluence range 2–10×10{sup 13} e{sup −}cm{sup −2}. Powder X-ray diffraction (PXRD) patterns confirm cubic phase of Y{sub 2}O{sub 3}. The crystallite size was estimated using Scherrer method and was found to be in the order of ~39 nm. SEM micrographs revealed the formation of non-uniform spherical shaped particles for higher electron fluence. Photoluminescence spectra (PL) of pristine and Tb{sup 3+} doped Y{sub 2}O{sub 3} were recorded in the fluence range 2–10×10{sup 13} e{sup −}cm{sup −2}. PL intensity was found to increase up to 4×10{sup 13} e{sup −}cm{sup −2} and thereafter it decreases with further increase in electron fluence. This may be attributed to lattice disorder produced by dense electronic excitation under electron irradiation. The characteristic emission peaks of Tb{sup 3+} were observed at ~ 484–490 nm ({sup 5}D{sub 4}→{sup 7}F{sub 6}), 548 nm ({sup 5}D{sub 4}→{sup 7}F{sub 5}) and 587 nm ({sup 5}D{sub 4}→{sup 7}F{sub 4}) at excited wavelength 397 nm. Two TL glow peaks were recorded in both pristine and electron irradiated samples indicate that two types of traps were created. The color co-ordinate values (x, y) were located in the green region of the CIE diagram suggests that electron irradiated Y{sub 2}O{sub 3}:Tb{sup 3+} phosphor could be used in white LEDs.

  6. Dielectric properties of Zr doped CaCu{sub 3}Ti{sub 4}O{sub 12} synthesized by sol-gel route

    Energy Technology Data Exchange (ETDEWEB)

    Jesurani, S. [Department of Physics, Jeyaraj Annapackium College for Women, Periyakulam 625 601, Tamil Nadu (India); Center for Material Science and Nano Devices, Department of Physics, SRM University, Kattankulathur 603 203, Tamil Nadu (India); Kanagesan, S., E-mail: kanagu1980@gmail.com [Materials Synthesis and Characterization Laboratory (MSCL), Institute of Advanced Technology (ITMA), Universiti Putra Malaysia, 43400 Serdang, Selangor (Malaysia); Hashim, M. [Materials Synthesis and Characterization Laboratory (MSCL), Institute of Advanced Technology (ITMA), Universiti Putra Malaysia, 43400 Serdang, Selangor (Malaysia); Physics Department, Faculty of Science, Universiti Putra Malaysia, 43400 Serdang, Selangor (Malaysia); Ismail, I. [Materials Synthesis and Characterization Laboratory (MSCL), Institute of Advanced Technology (ITMA), Universiti Putra Malaysia, 43400 Serdang, Selangor (Malaysia)

    2013-02-25

    Highlights: Black-Right-Pointing-Pointer Zr doped CaCu{sub 3}Ti{sub 4}O{sub 12} samples have been synthesized using sol-gel process. Black-Right-Pointing-Pointer The particle size of the powder ranges from 47 to 85 nm. Black-Right-Pointing-Pointer Less sintering at 1040 Degree-Sign C results in high density and high dielectric constant. - Abstract: Zr substituted CaCu{sub 3}Ti{sub 4-x}Zr{sub x}O{sub 12} (CCTZO) with x = 0.00, 0.02, 0.10, 0.20 and 0.50 mol% were prepared by sol-gel route from the metal nitrate solutions, Titanium isoproxide, and zirconium oxy chloride. XRD analysis confirmed the formation of a single phase material in the samples calcinated at 800 Degree-Sign C for 3 h. The crystal structure did not change on doping with zirconium and it remained cubic in all the four studied compositions. The permittivity and dielectric loss of 0.1 mol% Zr doped CaCu{sub 3}Ti{sub 4}O{sub 12} were improved for K Almost-Equal-To 6020 and tan {delta} Almost-Equal-To 0.52 at 1 kHz after the sample had been sintered at 1040 Degree-Sign C for 4 h. AFM studies showed that the particle size of the CCTZO powder ranged from 47 to 85 nm. FE-SEM micrographs of the CaCu{sub 3}Ti{sub 4-x}Zr{sub x}O{sub 12} samples showed that the grain size was in the range of 250 nm to 5 {mu}m for these samples. EDX studies showed the presence of calcium, copper, titanium, oxygen and zirconium. Remarkably, the dielectric constant increased and dielectric loss had lower values compared to the undoped CCTO.

  7. Electron microscopy characterization of mechanically alloyed and hot consolidates Cu-Cr<sub>3sub>C>2sub> particles

    Directory of Open Access Journals (Sweden)

    López, M.

    2005-08-01

    Full Text Available Mechanically alloyed copper-ceramic composites have been obtained with the purpose of studying their use as copper-based material for electrical equipment. For high-temperature applications, dispersion-strengthened copper alloys are attractive due to their excellent combination of thermal and electrical conductivity, mechanical strength retention and microstructural stability. In this work, powder mixtures of pure copper with 2 vol % Cr<sub>3sub>C>2sub>, milled during 4, 6, 10, 12 and 15 h in a high-energy planetary balls mill under argon atmosphere, were consolidated by hot isostatic pressing, applying a pressure of 100 MPa at 1073 K for two hours, to obtain materials with a fine microstructure. The Cu-Cr<sub>3sub>C>2sub> alloys were studied by scanning electron microscopy (SEM, electron microprobe (EPMA and transmission electron microscopy (TEM. Mechanical properties and electrical conductivity were also studied. The average tensile strength and electrical conductivity were found to be 500 MPa and 50 % IACS, respectively. The Cr<sub>3sub>C>2sub> ceramics show good stability during hot consolidation. Contributing to a further strengthening of the alloy during the hot consolidation, uniformly-distributed Fe-carbide particles of nanometric size precipitated in the copper matrix. Fe-Cr oxycarbides formed in the interphase between Cr<sub>3sub>C>2sub> particles and the copper matrix cause the low ductility of Cu-Cr<sub>3sub>C>2sub> alloys. Said particles are attributed to impurities/contamination generated from the milling process.

    Se obtuvieron aleaciones compuestas de Cu-Cr<sub>3sub>C>2sub>, aleadas mecánicamente, para estudiar futuras aplicaciones en componentes eléctricos. A altas temperaturas, las aleaciones de base cobre reforzadas por dispersión, son atractivas por su excelente conductividad térmica y eléctrica, propiedades mecánicas y estabilidad microstructural. En este estudio

  8. Laser ablation of ceramic Al{sub 2}O{sub 3} at 193 nm and 248 nm: The importance of single-photon ionization processes

    Energy Technology Data Exchange (ETDEWEB)

    Pelaez, R. J.; Afonso, C. N. [Laser Processing Group, Instituto de Optica, CSIC, Serrano 121, Madrid 28006 (Spain); Bator, M.; Lippert, T. [General Energy Research Department, Paul Scherrer Institut, CH-5232 Villigen PSI (Switzerland)

    2013-06-14

    The aim of this work is to demonstrate that single-photon photoionization processes make a significant difference in the expansion and temperature of the plasma produced by laser ablation of ceramic Al{sub 2}O{sub 3} in vacuum as well as to show their consequences in the kinetic energy distribution of the species that eventually will impact on the film properties produced by pulsed laser deposition. This work compares results obtained by mass spectrometry and optical spectroscopy on the composition and features of the plasma produced by laser ablation at 193 nm and 248 nm, i.e., photon energies that are, respectively, above and below the ionization potential of Al, and for fluences between threshold for visible plasma and up to Almost-Equal-To 2 times higher. The results show that the ionic composition and excitation of the plasma as well as the ion kinetic energies are much higher at 193 nm than at 248 nm and, in the latter case, the population of excited ions is even negligible. The comparison of Maxwell-Boltzmann temperature, electron temperatures, and densities of the plasmas produced with the two laser wavelengths suggests that the expansion of the plasma produced at 248 nm is dominated by a single population. Instead, the one produced at 193 nm is consistent with the existence of two populations of cold and hot species, the latter associated to Al{sup +} ions that travel at the forefront and produced by single photon ionization as well as Al neutrals and double ionized ions produced by electron-ion impact. The results also show that the most energetic Al neutrals in the plasma produced at the two studied wavelengths are in the ground state.

  9. Effect of Fe{sub 2}O{sub 3} in Fe{sub 2}O{sub 3}/AP composite particles on thermal decomposition of AP and on burning rate of the composite propellant

    Energy Technology Data Exchange (ETDEWEB)

    Ma, Zhenye [National Special Superfine Powder Engineering Research Center, Nanjing University of Science and Technology, Nanjing, 210094 (China); Nanjing University of Technology, Nanjing (China); Li, Fengsheng; Bai, Huaping [National Special Superfine Powder Engineering Research Center, Nanjing University of Science and Technology, Nanjing, 210094 (China)

    2006-12-15

    A technique of composite processing of Fe{sub 2}O{sub 3} and ammonium perchlorate (AP) was employed in making the propellant. The effects of composite processing of Fe{sub 2}O{sub 3} on catalytic activity, on the thermal decomposition of AP, and on the burning rate of the composite propellant were investigated in this paper. Fe{sub 2}O{sub 3}/AP composite particles were prepared by a novel solvent-nonsolvent method. The results show that AP is successfully coated on the surface of Fe{sub 2}O{sub 3}. Composite processing of Fe{sub 2}O{sub 3} and AP can improve the catalytic activity of Fe{sub 2}O{sub 3}. Fe{sub 2}O{sub 3} exhibits better catalytic effect with increasing Fe{sub 2}O{sub 3} content. The larger interface between Fe{sub 2}O{sub 3} and AP and lower density of composite propellant (with the added Fe{sub 2}O{sub 3}/AP composite particles) are responsible for the enhancement of the catalytic activity of Fe{sub 2}O{sub 3}. (Abstract Copyright [2006], Wiley Periodicals, Inc.)

  10. Preparation and characterization of sub-20 nm Cu{sub X}@Ag{sub 1} core-shell nanoparticles by changing concentration of silver precursor

    Energy Technology Data Exchange (ETDEWEB)

    Chee, Sang-Soo; Lee, Jong-Hyun, E-mail: pljh@snut.ac.kr

    2017-01-01

    Ultrafine Ag-coated Cu (Cu@Ag) nanoparticles (NPs) less than 20 nm in diameter were prepared. After synthesizing ultrafine Cu NPs using a solvothermal method to serve as the core particles, Cu@Ag NPs were fabricated with different initial Ag precursor concentrations, resulting in different thicknesses, densities, and uniformities of Ag shells. The average thickness and density of the Ag shell increased with increasing initial Ag precursor concentration in a Cu:Ag atomic ratio from 6:1 to 1:1. However, excessive Ag precursor concentrations induced homogeneous nucleation and growth of surplus fine pure NPs. Ag dewetting behavior and Cu oxidation in the Cu{sub 4}@Ag{sub 1} NPs were observed, they occurred during heating at 200 and 250 °C, respectively. The electrical resistivities of sintered Cu{sub 4}@Ag{sub 1} films decreased with increasing temperature from 200 to 240 °C. The resistivity after washing the OA and sintering for 60 min at 240 °C in air was measured to be 4.96 × 10{sup −3} Ω cm. The film was sintered in nitrogen using the ink containing non-washed Cu{sub 4}@Ag{sub 1} NPs indicated the lower resistivity of 2.70 × 10{sup −3} Ω cm owing to the non-oxidation atmosphere, although the chemically capped oleylamine in the core-shell NPs hindered the sintering behavior. - Highlights: • Ultrafine Ag-coated Cu nanoparticles less than 20 nm in diameter were fabricated. • Different Ag precursor concentrations influenced thickness and density of Ag shell. • Excessive Ag precursor concentrations induced formation of surplus fine pure NPs. • Ag dewetting behavior and Cu oxidation in Cu{sub 4}@Ag{sub 1} nanoparticles were observed. • Electrical resistivities of sintered Cu{sub 4}@Ag{sub 1} films were 2.70–4.96 × 10{sup −3} Ω cm.

  11. Controllable synthesis of magnetic Fe{sub 3}O{sub 4} particles with different morphology by one-step hydrothermal route

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Zhongtao; Du, Yi, E-mail: duyi1964@126.com; Li, Zhongfu; Yang, Kai; Lv, Xingjie

    2017-03-15

    Well-defined Fe{sub 3}O{sub 4} particles were successfully fabricated by a facile triethanolamine (TEA)-assisted method under mild hydrothermal conditions. Hydrated ferric salt was employed as the single iron precursor. TEA was used as the complexing agent and/or alkaline source. The crystalline phases of the as-obtained samples were characterized by X-ray diffraction (XRD). Furthermore, the morphology as well as the compositions of the samples were investigated by scanning electron microscopy (SEM) equipped with an energy dispersion spectroscopy (EDS). The results indicated that the products were Fe{sub 3}O{sub 4} crystal phase, and the morphology and powder size of the particles were varied with adding different amount of NaOAc and keeping the content of TEA unchanged. On the basis of these results, the possible formation mechanism of Fe{sub 3}O{sub 4} was discussed. It was observed that TEA and NaOAc affected the growth rate of crystal planes and nucleation. Besides, the magnetic property tested by a vibrating sample magnetometer (VSM) showed that the products exhibited a ferromagnetic behavior and possessed the excellent saturation magnetization (Ms) at room temperature. - Highlights: • Fe{sub 3}O{sub 4} particles were obtained by employing TEA as single alkali source. • Morphology and size of Fe{sub 3}O{sub 4} particles varied by adjusting the TEA/NaOAc ratio. • Magnetic properties of products were influenced by particle size and morphology.

  12. Luminescence investigation of Yb{sup 3+}/Er{sup 3+} codoped single LiYF{sub 4} microparticle

    Energy Technology Data Exchange (ETDEWEB)

    Gao, Wei; Zheng, Hairong, E-mail: hrzheng@snnu.edu.cn; He, Enjie; Lu, Ying; Gao, Fangqi

    2014-08-01

    Tetragonal phase LiYF{sub 4}:Yb{sup 3+}/Er{sup 3+} microparticles are synthesized via facile hydrothermal method. Single LiYF{sub 4} microparticle is excited with IR laser at 980 nm in a confocal setup, and strong green and weak red emissions are observed. It is found that single LiYF{sub 4}:Yb{sup 3+}/Er{sup 3+} microparticle with sub-structure presents stronger upconversion luminescence emission and smaller intensity ratio of red to green emission than that from LiYF{sub 4}:Yb{sup 3+}/Er{sup 3+} microparticle with no sub-structure. The possible mechanism, the influence of particle size and the existence of EDTA on the upconversion luminescence emission are investigated. The current study suggests that the luminescence observation with single micropaticle can effectively avoid the influence of environment and neighbor particles, which is important for investigating the luminescence properties of micro- or nano-crystals and for extending their application. - Highlights: • Single LiYF{sub 4} microparticle is excited with IR laser at 980 nm in a confocal setup, and strong green and weak red emissions are observed. • Single LiYF{sub 4} microparticle with different morphology exhibits different fluorescence emission intensity and intensity ratio of red to green emission. • The possible mechanism, the influence of particle size and the existence of EDTA on the upconversion emission are investigated.

  13. Nanostructure investigation of magnetic nanomaterial Ni{sub 0.5}Zn{sub 0.3}Cu{sub 0.2}Fe{sub 2}O{sub 4} synthesized by sol-gel method

    Energy Technology Data Exchange (ETDEWEB)

    Pransisco, Prengki, E-mail: prengkipransisco@gmail.com [Department of Fundamental and Applied Sciences, Universiti Teknologi PETRONAS, Bandar Seri Iskandar, 31750 Tronoh, Perak (Malaysia); Badan Lingkungan Hidup Derah Kabupaten Empat Lawang South of Sumatera (Indonesia); Shafie, Afza, E-mail: afza@petronas.com.my; Guan, Beh Hoe, E-mail: beh.hoeguan@petronas.com.my [Department of Fundamental and Applied Sciences, Universiti Teknologi PETRONAS, Bandar Seri Iskandar, 31750 Tronoh, Perak (Malaysia)

    2015-07-22

    Magnetic nanomaterial Ni{sub 0.5}Zn{sub 0.3}Cu{sub 0.2}Fe{sub 2}O{sub 4} was successfully prepared by using sol-gel method. Heat treatment on material is always giving defect on properties of material. This paper investigates the effect of heat treatment on nanostructure of magnetic nanomaterial Ni{sub 0.5}Zn{sub 0.3}Cu{sub 0.2}Fe{sub 2}O{sub 4}. According to thermo gravimetric analysis (TGA) that after 600°C there is no more weight loss detected and it was decided as minimum calcination temperature. Intensity, crystallite size, structure, lattice parameter and d-spacing of the material were investigated by using X-ray diffraction (XRD). High resolution transmission electron microscope (HRTEM) was used to examine nanostructure, nanosize, shape and distribution particle of magnetic material Ni{sub 0.5}Zn{sub 0.3}Cu{sub 0.2}Fe{sub 2}O{sub 4} and variable pressure field emission scanning electron microscope (VP-FESEM) was used to investigate the surface morphology and topography of the material. The XRD result shows single-phase cubic spinel structure with average crystallite size in the range of 25.6-95.9 nm, the value of the intensity of the material was increased with increasing temperature, and followed by lattice parameter was increased with increasing calcination temperature, value of d-spacing was relatively decreased with accompanied increasing temperature. From HRTEM result the distribution of particles was tend to be agglomerates with particle size of 7.8-17.68 nm. VP-FESEM result shows that grain size of the material increases with increasing calcination temperature and the surface morphology shows that the material is in hexagonal shape and it was also proved by mapping result which showing the presence each of constituents inside the compound.

  14. Photoluminescence characteristics of Sm{sup 3+} doped Ba{sub 3}La(PO{sub 4}){sub 3} as new orange-red emitting phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Ruijin [College of Science, Northwest A and F University, Yangling, Shaanxi 712100 (China); Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of); Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Mi Noh, Hyeon; Kee Moon, Byung; Chun Choi, Byung [Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of); Hyun Jeong, Jung, E-mail: jhjeong@pknu.ac.kr [Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of); Sueb Lee, Ho [Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Jang, Kiwan, E-mail: kwjang@changwon.ac.kr [Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Soo Yi, Soung [Department of Electronic Material Engineering, Silla University, Busan 617-736 (Korea, Republic of)

    2014-01-15

    A series of orange-red emitting Ba{sub 3}La(PO{sub 4}){sub 3}:xSm{sup 3+} (0.01≤x≤0.30) phosphors was synthesized by the convenient solid-state reaction. X-ray diffraction and photoluminescence spectra were utilized to characterize the structure and luminescence properties of the as-synthesized phosphors. The emission spectra of the Ba{sub 3}La(PO{sub 4}){sub 3}:Sm{sup 3+} phosphors consisted of some sharp emission peaks of Sm{sup 3+} ions centered at 563 nm, 600 nm, 647 nm, 710 nm. The strongest one is located at 600 nm due to {sup 4}G{sub 5/2}–{sup 6}H{sub 7/2} transition of Sm{sup 3+}, generating bright orange-red light. The optimum dopant concentration of Sm{sup 3+} ions in Ba{sub 3}La(PO{sub 4}):xSm{sup 3+} is around 5 mol% and the critical transfer distance of Sm{sup 3+} is calculated as 22 Å. The CIE chromaticity coordinates of the Ba{sub 3}La(PO{sub 4}){sub 3}:0.05Sm{sup 3+} phosphors was is located in the orange reddish region. The Ba{sub 3}La(PO{sub 4}){sub 3}:Sm{sup 3+} phosphors may be potentially used as red phosphors for white light-emitting diodes. -- Highlights: • A new Sm{sup 3+}-doped Ba{sub 3}La(PO{sub 4}){sub 3} phosphor was firstly synthesized. • Its structure, luminescent properties are well studied and characterized. • The Ba{sub 3}La(PO{sub 4}){sub 3}:Sm{sup 3+} shows bright orange reddish emissions under UV excitation.

  15. Effect of calcination temperature on the H{sub 2}O{sub 2} decomposition activity of nano-crystalline Co{sub 3}O{sub 4} prepared by combustion method

    Energy Technology Data Exchange (ETDEWEB)

    Makhlouf, M.Th. [Chemistry Department, Faculty of Science, Assiut University, 71516 Assiut (Egypt); Abu-Zied, B.M., E-mail: babuzied@aun.edu.eg [Chemistry Department, Faculty of Science, Assiut University, 71516 Assiut (Egypt); Mansoure, T.H. [Chemistry Department, Faculty of Science, Assiut University, 71516 Assiut (Egypt)

    2013-06-01

    Cobalt oxide nano-particles were prepared by combustion method using urea as a combustion fuel. The effects of calcination temperature, 350–1000 °C, on the physicochemical, surface and catalytic properties of the prepared Co{sub 3}O{sub 4} nano-particles were studied. The products were characterized by thermal analyses (TGA and DTA), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and transmission electron microscopy (TEM) techniques. Textural features of the obtained catalysts were investigated using nitrogen adsorption at −196 °C. X-ray diffraction confirmed that the resulting oxide was pure single-crystalline Co{sub 3}O{sub 4} nano-particles. Transmission electron microscopy indicating that, the crystallite size of Co{sub 3}O{sub 4} nano-crystals was in the range of 8–34 nm. The catalytic activities of prepared nano-crystalline Co{sub 3}O{sub 4} catalysts were tested for H{sub 2}O{sub 2} decomposition at 35–50 °C temperature range. Experimental results revealed that, the catalytic decomposition of H{sub 2}O{sub 2} decreases with increasing the calcination temperature. This was correlated with the observed particle size increase accompanying the calcination temperature rise.

  16. Interaction of Ce{sub 1−x}Er{sub x}O{sub 2−y} nanoparticles with Al{sub 2}O{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Krajczyk, L.; Kraszkiewicz, P.; Kepinski, L., E-mail: L.Kepinski@int.pan.wroc.pl

    2015-02-01

    The interaction of nanocrystalline Ce{sub 0.5}Er{sub 0.5}O{sub 1.75} mixed oxide with an amorphous Al{sub 2}O{sub 3} in oxidizing and reducing atmosphere up to 1100 °C was studied by XRD, TEM, SEM-EDS and BET. Uniform, chemically homogeneous Ce{sub 0.5}Er{sub 0.5}O{sub 1.75} nanoparticles (2 nm in size) were prepared by microemulsion method and deposited on a high surface γ-alumina support. The nanoparticles were structurally and chemically stable in the oxidizing atmosphere up to 1100 °C, exhibiting only an increase of the mean crystallite size to 9 nm after 3 h treatment. Prolonged heating (24 h) at 1100 °C caused partial decomposition of the mixed oxide and reaction of the extracted erbium with the support with formation of hexagonal (P6{sub 3}/mmc) ErAlO{sub 3} aluminate. The same hexagonal ErAlO{sub 3} occurred also in Er/Al{sub 2}O{sub 3} sample prepared by impregnation of Al{sub 2}O{sub 3} support with an aqueous solution of Er nitrate and subjected to heating in air or hydrogen at 1100 °C. In the reducing atmosphere the Ce{sub 0.5}Er{sub 0.5}O{sub 1.75} reacted with Al{sub 2}O{sub 3} already at 800 °C, to form an amorphous surface phase. At 900 °C monoclinic (P2{sub 1}/c) (Er,Ce){sub 4}Al{sub 2}O{sub 9} mixed aluminate was formed with the unit cell volume 4.5% bigger than that of pure Er{sub 4}Al{sub 2}O{sub 9} phase. After 3 h treatment at 1000 °C more than half of the (Er,Ce){sub 4}Al{sub 2}O{sub 9} aluminate decomposed into two nanocrystalline mixed monoaluminates: tetragonal (I4/mcm) (Ce,Er)AlO{sub 3} and hexagonal (P6{sub 3}/mmc) (Er,Ce)AlO{sub 3}. Nanocrystalline mixed aluminate particles with Er{sup 3+} ions placed in well-defined lattice sites and supported at the surface of Al{sub 2}O{sub 3} support, may be interesting as highly efficient active components of optical waveguides amplifiers. - Graphical abstract: Structure evolution of Ce{sub 0.5}Er{sub 0.5}O{sub 1.75} on Al{sub 2}O{sub 3} in air and in H{sub 2}. - Highlights:

  17. Microwave properties of La{sub 0.8}Ag{sub 0.2}MnO{sub 3} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Rostamnejadi, Ali [Malek Ashtar University of Technology, Electroceram Research Center, Shahin Shahr, Isfahan (Iran, Islamic Republic of)

    2016-11-15

    In this research, single-phase nanoparticles of La{sub 0.8}Ag{sub 0.2}MnO{sub 3} with mean particle size of 15 nm have been synthesized by sol-gel method. The microwave properties of La{sub 0.8}Ag{sub 0.2}MnO{sub 3}/paraffin nanocomposite are studied by measuring the complex permittivity and permeability in the frequency range of 1-18 GHz. The composite shows both reflection and absorption electromagnetic shielding effectiveness with maximum total value of 36 dB, which is suitable for defense and microwave radiation shielding applications at high temperatures. The electromagnetic absorption properties are described in terms of dielectric relaxation processes. (orig.)

  18. Photoluminescence properties of the Eu-doped alpha-Al{sub 2}O{sub 3} microspheres

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Dianguang, E-mail: dianguang12@gmail.com [State Key Laboratory of Solidification Processing, Northwestern Polytechnical University, West Youyi Rd., No. 127, Xi’an, Shaanxi 710072 (China); Science and Technology on Thermostructure Composite Materials Laboratory, Northwestern Polytechnical University, West Youyi Rd., No. 127, Xi’an, Shaanxi 710072 (China); Zhu, Zhenfeng [School of Materials Science and Engineering, Shaanxi University of Science and Technology, Xi’an 710021 (China)

    2014-01-15

    Highlights: • Al{sub 2}O{sub 3}:Eu{sup 3+} phosphors were prepared via a microwave solvothermal route. • The particles were hierarchically nanostructured microspheres packaged by nanosheets. • The powders presented excellent orange–red emission when excited at 393 nm. • Critical concentration and distance of Eu{sup 3+} in Al{sub 2}O{sub 3} is 0.007, 18 Å, respectively. -- Abstract: Al{sub 2}O{sub 3}:Eu{sup 3+} samples were synthesized via microwave solvothermal method and thermal decomposition of Eu{sup 3+} doped precursors. The sample characterizations were carried out by means of X-ray diffraction (XRD), scanning electron microscope (SEM) and photoluminescence (PL) spectra. XRD results indicated that Eu{sup 3+} doped samples were most of α-Al{sub 2}O{sub 3} phase after being calcined at 1473 K. SEM results showed that the obtained α-Al{sub 2}O{sub 3} based powders via microwave solvothermal method were microspheres with an average diameter about 1.6 μm. PL spectra showed that upon excitation at 393 nm, the orange–red emission bands at the wavelength longer than 560 nm were from {sup 5}D{sub 0} → {sup 7}F{sub J} (J = 1, 2) transitions. The asymmetry ratio of ({sup 5}D{sub 0} → {sup 7}F{sub 2})/({sup 5}D{sub 0} → {sup 7}F{sub 1}) intensity is about 1 and this value suggests that Eu{sup 3+} ions occupy the same ratio of symmetry and asymmetry sites. It is shown that the 0.7 mol% of doping concentration of Eu{sup 3+} ions in α-Al{sub 2}O{sub 3}:Eu{sup 3+} is optimum. According to Dexter’s theory, the critical distance between Eu{sup 3+} ions for energy transfer was determined to be 18 Å.

  19. Oleate-based hydrothermal preparation of CoFe{sub 2}O{sub 4} nanoparticles, and their magnetic properties with respect to particle size and surface coating

    Energy Technology Data Exchange (ETDEWEB)

    Repko, Anton, E-mail: anton@a-repko.sk [Department of Inorganic Chemistry, Faculty of Science, Charles University in Prague, Hlavova 2030/8, 128 43 Prague 2 (Czech Republic); Vejpravová, Jana, E-mail: vejpravo@fzu.cz [Department of Magnetic Nanosystems, Institute of Physics AS CR, v.v.i., Na Slovance 2, 182 21 Prague 8 (Czech Republic); Vacková, Taťana [Institute of Macromolecular Chemistry, Academy of Sciences of the Czech Republic, Heyrovsky Sq. 2, 162 06 Prague 6 (Czech Republic); Zákutná, Dominika [Department of Inorganic Chemistry, Faculty of Science, Charles University in Prague, Hlavova 2030/8, 128 43 Prague 2 (Czech Republic); Nižňanský, Daniel, E-mail: daniel.niznansky@natur.cuni.cz [Department of Inorganic Chemistry, Faculty of Science, Charles University in Prague, Hlavova 2030/8, 128 43 Prague 2 (Czech Republic)

    2015-09-15

    We present a facile and high-yield synthesis of cobalt ferrite nanoparticles by hydrothermal hydrolysis of Co–Fe oleate in the presence of pentanol/octanol/toluene and water at 180 or 220 °C. The particle size (6–10 nm) was controlled by the composition of the organic solvent and temperature. Magnetic properties were then investigated with respect to the particle size and surface modification with citric acid or titanium dioxide (leading to hydrophilic particles). The as-prepared hydrophobic nanoparticles (coated by oleic acid) had a minimum inter-particle distance of 2.5 nm. Their apparent blocking temperature (estimated as a maximum of the zero-field-cooled magnetization) was 180 K, 280 K and 330 K for the particles with size of 6, 9 and 10.5 nm, respectively. Replacement of oleic acid on the surface by citric acid decreased inter-particle distance to less than 1 nm, and increased blocking temperature by ca. 10 K. On the other hand, coating with titanium dioxide, supported by nitrilotri(methylphosphonic acid), caused increase of the particle spacing, and lowering of the blocking temperature by ca. 20 K. The CoFe{sub 2}O{sub 4}@TiO{sub 2} nanoparticles were sufficiently stable in water, methanol and ethanol. The particles were also investigated by Mössbauer spectroscopy and alternating-current (AC) susceptibility measurements, and their analysis with Vögel–Fulcher and power law. Effect of different particle coating and dipolar interactions on the magnetic properties is discussed. - Highlights: • CoFe{sub 2}O{sub 4} nanoparticles were prepared by facile hydrothermal method from Co–Fe oleate. • Blocking temperature (T{sub B}) is 180–330 K for 6–10.5 nm oleate-coated particles. • The apparent T{sub B} changes with oleic acid, citrate or TiO{sub 2} coating.

  20. Mössbauer studies of stoichiometry of Fe{sub 3}O{sub 4}: characterization of nanoparticles for biomedical applications

    Energy Technology Data Exchange (ETDEWEB)

    Johnson, C. E., E-mail: cjohnson@utsi.edu; Johnson, J. A.; Hah, H. Y.; Cole, M.; Gray, S. [University of Tennessee Space Institute, Center for Laser Applications (United States); Kolesnichenko, V. [Xavier University, Department of Chemistry (United States); Kucheryavy, P. [Rutgers University, Department of Chemistry (United States); Goloverda, G. [Xavier University, Department of Chemistry (United States)

    2016-12-15

    The iron oxide Fe{sub 3}O{sub 4}, the mineral magnetite sometimes called ferrosoferric oxide, is notoriousy non-stoichiometric even in bulk form so its formula may be written Fe{sub 3−δ}O{sub 4}. In nanoparticle form, where it has applications in medicine and information technology, it is even more susceptible to oxidation. In this paper we report synthesis and studies of superparamagnetic Fe{sub 3}O{sub 4} nanoparticles with controlled diameters of 5.3, 10.6 and 11.9 nm. In room temperature spectra, departures from stoichiometry δ of up to 0.02 were estimated from the relative amounts of Fe {sup 3+}/ Fe {sup 2+} and from their isomer shifts. This cannot be used for very small particles of diameter 10.6 nm and less as they are superparamagnetic at room temperature and do not show hyperfine splitting owing to fast relaxation. Such particles have promise for use in enhancing MRI signals. The magnetic spectrum is restored by the application of a relatively small magnetic field (10 kG). As the temperature is lowered the relaxation slows down and 6-line magnetic hyperfine patterns appear below a blocking temperature T{sub B}. The values of T{sub B} obtained are lower than those of many other researchers reported in the literature, suggesting that our particles are less affected by magnetic interactions between them. At low temperatures all the spectra are similar and closely resemble that of bulk Fe{sub 3}O{sub 4} confirming that departures from stoichiometry are small.

  1. Monodisperse and core-shell structured SiO{sub 2}-Lu{sub 2}O{sub 3}:Ln{sup 3+} (Ln=Eu, Tb, Dy, Sm, Er, Ho, and Tm) spherical particles: A facile synthesis and luminescent properties

    Energy Technology Data Exchange (ETDEWEB)

    Xu, Zhenhe, E-mail: xuzh056@163.com [College of Applied Chemistry, Shenyang University of Chemical Technology, Shenyang 100142 (China); Feng, Bin [China National Aviation Fuel Group Corporation, Planning and Development Department, Beijing 100088 (China); Bian, Shasha; Liu, Tao; Wang, Mingli; Gao, Yu; Sun, Di; Gao, Xin [College of Applied Chemistry, Shenyang University of Chemical Technology, Shenyang 100142 (China); Sun, Yaguang, E-mail: yaguangsun@yahoo.com.cn [College of Applied Chemistry, Shenyang University of Chemical Technology, Shenyang 100142 (China)

    2012-12-15

    The core-shell structured SiO{sub 2}-Lu{sub 2}O{sub 3}:Ln{sup 3+} particles were realized by coating the Lu{sub 2}O{sub 3}:Ln{sup 3+} phosphors onto the surface of non-aggregated, monodisperse and spherical SiO{sub 2} particles by the Pechini sol-gel method. The as-synthesized products were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), energy-dispersive X-ray (EDX) spectra, scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), photolumiminescence (PL), and low-voltage cathodoluminescence (CL). The results indicate that the 800 Degree-Sign C annealed sample consists of crystalline Lu{sub 2}O{sub 3} shells and amorphous SiO{sub 2} cores, in spherical shape with a narrow size distribution. The as-obtained particles show strong light emission with different colors corresponding to different Ln{sup 3+} ions under ultraviolet-visible light excitation and low-voltage electron beams excitation, which have potential applications in fluorescent lamps and field emission displays. - Graphical Abstract: Representative SEM and TEM images of the core-shell structured SiO{sub 2}-Lu{sub 2}O{sub 3}:Eu{sup 3+} particles; CIE chromaticity diagram showing the emission colors for SiO{sub 2}-Lu{sub 2}O{sub 3}:Ln{sup 3+}; Multicolor emissions of SiO{sub 2}-Lu{sub 2}O{sub 3}:Ln{sup 3+} particles. Highlights: Black-Right-Pointing-Pointer The core-shell particles were realized by coating the phosphors onto the surface of SiO{sub 2} particles. Black-Right-Pointing-Pointer The sample consists of crystalline Lu{sub 2}O{sub 3} shells and amorphous SiO{sub 2} cores. Black-Right-Pointing-Pointer The particles show different light emission colors corresponding to Ln{sup 3+} ions. Black-Right-Pointing-Pointer They have potential applications in fluorescent lamps and field emission displays.

  2. Optimization of production and properties of the nanoscaled ferritic ODS-alloy 13Cr-1W-0,3Y{sub 2}O{sub 3}-0,3TiH{sub 2} and characterization of structure and property correlations; Eigenschaftsoptimierung der nanoskaligen ferritischen ODS-Legierung 13Cr-1W-0,3Y{sub 2}O{sub 3}-0,3TiH{sub 2}, metallkundliche Charakterisierung und Bestimmung von Struktur-Eigenschaftskorrelationen

    Energy Technology Data Exchange (ETDEWEB)

    Eiselt, Charles Christopher

    2010-01-15

    Fusion power reactors next to renewable energy sources shall form an important basis for a future energy scenario avoiding damaging emissions due to the lack of fossil primary energy carriers. An efficient operation of such reactors necessitate temperatures >700 C, which require new kinds of structural materials. Today only reduced activated oxide dispersion-strengthened (ODS-) materials based on iron, which have high strengths at elevated temperatures, offer the possibility to meet those criterias, which are developed in internationally coordinated programs. Therefore a nearly industrial production process based on the powdermetallurgical route is iteratively and systematically optimized to produce the ferritic ODS-alloy 13Cr-1W-0,3Y{sub 2}O{sub 3}-0,3TiH{sub 2}. Through TEM elemental analyses of mechanically alloyed steel powder it is confirmed, that the additives Y{sub 2}O{sub 3} and TiH{sub 2} dissolve completely in the powder and form the ODS-particles during the HIP-cycle. Detailed studies of powder contamination during mechanical alloying reveal correlations between the contamination behaviour of certain elements and the milling parameters. A specially designed procedure of powder encapsulation and sealing leads to a successful powder compaction to the ODS-material 13Cr-1W-0,3Y{sub 2}O{sub 3}-0,3TiH{sub 2}. Detailed TEM studies show a bimodal grain size distribution within the material at first. The alloy's recrystallization behaviour is the main reason for this phenomenon and is therefore discussed in detail. A high dispersion of ODS-particles as the decisive material's component with particle sizes von 3-5nm within grains and 12-36nm at the grain boundaries is successfully reached and verified by numerous TEM-Elemental Mappings. By applying hot rolling as an additional step during production a more even grain structure by equally maintaining the fine nanoskaled particle dispersion is set up. The microstructure is highly stable, since no grain- or

  3. Thermoluminescence studies of γ-irradiated Al{sub 2}O{sub 3}:Ce{sup 3+} phosphor

    Energy Technology Data Exchange (ETDEWEB)

    Reddy, S. Satyanarayana [Physics R & D Center, PES Institute of Technology, BSK 3rd Stage, Bangalore 560085 (India); Nagabhushana, K.R., E-mail: bhushankr@gmail.com [Physics R & D Center, PES Institute of Technology, BSK 3rd Stage, Bangalore 560085 (India); Department of Physics, PES University, BSK 3rd Stage, Bangalore 560085 (India); Singh, Fouran [Inter University Accelerator Centre, Aruna Asaf Ali Marg, New Delhi 110 067 (India)

    2016-07-15

    Pure and Ce{sup 3+} doped Al{sub 2}O{sub 3} phosphors were synthesized by solution combustion method. The synthesized samples were characterized by X-ray diffraction (XRD) and its shows α-phase of Al{sub 2}O{sub 3}. Crystallite size was estimated by Williamson–Hall (W–H) method and found to be 49, 59 and 84 nm for pure, 0.1 mol% and 1 mol% Ce{sup 3+} doped Al{sub 2}O{sub 3} respectively. Trace elemental analysis of undoped Al{sub 2}O{sub 3} shows impurities viz. Fe, Cr, Mn, Mg, Ti, etc. Photoluminescence (PL) spectra of Al{sub 2}O{sub 3}:Ce{sup 3+} shows emission at 367 nm and excitation peak at 273 nm, which are corresponding to {sup 5}D → {sup 4}F and {sup 4}F → {sup 5}D transitions respectively. PL intensity decreases with concentration up to 0.4 mol%, beyond this mol% PL intensity increases with doping concentration up to 2 mol%. Thermoluminescence (TL) studies of γ-rayed pure and Ce{sup 3+} doped Al{sub 2}O{sub 3} have been studied. Two well resolved TL glow peaks at 457.5 K and 622 K were observed in pure Al{sub 2}O{sub 3}. Additional glow peak at 566 K was observed in Al{sub 2}O{sub 3}:Ce{sup 3+}. Maximum TL intensity was observed for Al{sub 2}O{sub 3}:Ce{sup 3+} (0.1 mol%) beyond this TL intensity decreases with increasing Ce{sup 3+} concentration. Computerized glow curve deconvolution (CGCD) method was used to resolve the multiple peaks and to calculate TL kinetic parameters. Thermoluminescence emission (TLE) spectra of pure Al{sub 2}O{sub 3} glow peaks (457.5 K and 622 K) shows sharp emission at 694 nm and two small humps at 672 nm and 709 nm. The sharp peak at 696 nm corresponds to Cr{sup 3+} impurity of {sup 2}E{sub g} → {sup 4}A{sub 2g} transition of R lines and 713 nm hump is undoubtedly belongs to Cr{sup 3+} emission of near neighbor pairs. The emission at 672 nm is characteristic of Mn{sup 4+} impurity ions of {sup 2}E → {sup 4}A{sub 2} transition. TLE of Al{sub 2}O{sub 3}:Ce{sup 3+} (0.1 mol%) shows additional broad emission at 412 nm

  4. Surface modification of submicronic TiO{sub 2} particles prepared by ultrasonic spray pyrolysis for visible light absorption

    Energy Technology Data Exchange (ETDEWEB)

    Dugandzic, Ivan M. [Institute of Technical Sciences of SASA (Serbia); Jovanovic, Dragana J. [University of Belgrade, Vinca Institute of Nuclear Sciences (Serbia); Mancic, Lidija T. [Institute of Technical Sciences of SASA (Serbia); Zheng, Nan; Ahrenkiel, Scott P. [South Dakota School of Mines and Technology (United States); Milosevic, Olivera B. [Institute of Technical Sciences of SASA (Serbia); Saponjic, Zoran V.; Nedeljkovic, Jovan M., E-mail: jovned@vinca.rs [University of Belgrade, Vinca Institute of Nuclear Sciences (Serbia)

    2012-10-15

    Spherical, submicronic TiO{sub 2} assemblage with high specific surface area and controllable phase composition was prepared in the process of ultrasonic spray drying/pyrolysis in a wide temperature range (150-800 Degree-Sign C) by using as a precursor aqueous colloidal solution consisting of TiO{sub 2} nanoparticles (4.5 nm). Submicronic, soft and grained spherical TiO{sub 2} particles (d = 370-500 nm) comprising clustered nanocrystals (<10 nm) were obtained at low processing temperature, while particle densification, intensive growth of the clustered primary units and anatase-to-rutile transformation ({approx}30 wt%) were observed at the higher temperatures. Detailed structural and morphological characterisation were performed by X-ray powder diffraction, scanning and field emission electron microscopy, transmission electron microscopy, and laser particle size analysis. Moreover, the surface modification of TiO{sub 2} particles through the formation of charge-transfer (CT) complex was achieved with different ligands: ascorbic acid, dopamine, catechol, 2,3-dihydroxynaphthalene, and anthrarobin. Optical properties of the surface-modified TiO{sub 2} particles were studied by using diffuse reflection spectroscopy. The binding structure between the surface titanium atoms and different ligands was determined by using Fourier transform infrared spectroscopy. The formation of CT complexes induced significant red shift of optical absorption in comparison to unmodified TiO{sub 2} particles.

  5. Facile fabrication of flower like self-assembled mesoporous hierarchical microarchitectures of In(OH){sub 3} and In{sub 2}O{sub 3}: In(OH){sub 3} micro flowers with electron beam sensitive thin petals

    Energy Technology Data Exchange (ETDEWEB)

    Arul Prakasam, Balasubramaniam, E-mail: arul7777@yahoo.com [Laboratory of Green Chemistry, School of Engineering Science, Lappeenranta University of Technology, Sammonkatu 12, FI-50130, Mikkeli (Finland); Lahtinen, Manu; Peuronen, Anssi [Department of Chemistry, Laboratories of Inorganic and Analytical Chemistry, P.O. Box 35, FI-40014, University of Jyväskylä (Finland); Muruganandham, Manickavachagam [Department of Civil and Environmental Engineering, Temple University, Philadelphia, PA, 19122 (United States); Sillanpää, Mika [Laboratory of Green Chemistry, School of Engineering Science, Lappeenranta University of Technology, Sammonkatu 12, FI-50130, Mikkeli (Finland)

    2016-12-01

    A template and capping-reagent free facile fabrication method for mesoporous hierarchical microarchitectures of flower-like In(OH){sub 3} particles under benign hydrothermal conditions is reported. Calcination of In(OH){sub 3} to In{sub 2}O{sub 3} with the retention of morphology is also described. Both In(OH){sub 3} and In{sub 2}O{sub 3} microstructures were analyzed with SEM, EDX, TEM and powder X-ray diffraction. The crystal sizes for In(OH){sub 3} and In{sub 2}O{sub 3} were calculated using the Scherrer equation. In In(OH){sub 3} the thin flakes at the periphery of micro flowers were electron beam sensitive. The mechanism of self-assembly process was analyzed as well. - Highlights: • Hydrothermal fabrication In(OH){sub 3} self-assembled porous hierarchical architectures. • Induced dehydration in beam sensitive In(OH){sub 3} micro flowers. • Calcination of In(OH){sub 3} to In{sub 2}O{sub 3} with the retention of flower like morphology. • Phase pure synthesis of In{sub 2}O{sub 3} with the average crystal size of ∼37 nm.

  6. Size dependent magnetic and electrical properties of Ba-doped nanocrystalline BiFeO{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Hasan, Mehedi, E-mail: mhrizvi@gce.buet.ac.bd; Hakim, M. A.; Zubair, M. A.; Hussain, A.; Islam, Md. Fakhrul [Department of Glass and Ceramic Engineering, Bangladesh University of Engineering and Technology, Dhaka 1000 (Bangladesh); Basith, M. A., E-mail: mabasith@phy.buet.ac.bd [Department of Physics, Bangladesh University of Engineering and Technology, Dhaka-1000 (Bangladesh); Hossain, Md. Sarowar [S. N. Bose National Centre for Basic Sciences, Salt Lake City, Kolkata, West Bengal 700098 (India); Ahmmad, Bashir [Graduate School of Science and Engineering, Yamagata University, 4-3-16 Jonan, Yonezawa 992-8510 (Japan)

    2016-03-15

    Improvement in magnetic and electrical properties of multiferroic BiFeO{sub 3} in conjunction with their dependence on particle size is crucial due to its potential applications in multifunctional miniaturized devices. In this investigation, we report a study on particle size dependent structural, magnetic and electrical properties of sol-gel derived Bi{sub 0.9}Ba{sub 0.1}FeO{sub 3} nanoparticles of different sizes ranging from ∼ 12 to 49 nm. The substitution of Bi by Ba significantly suppresses oxygen vacancies, reduces leakage current density and Fe{sup 2+} state. An improvement in both magnetic and electrical properties is observed for 10 % Ba-doped BiFeO{sub 3} nanoparticles compared to its undoped counterpart. The saturation magnetization of Bi{sub 0.9}Ba{sub 0.1}FeO{sub 3} nanoparticles increase with reducing particle size in contrast with a decreasing trend of ferroelectric polarization. Moreover, a first order metamagnetic transition is noticed for ∼ 49 nm Bi{sub 0.9}Ba{sub 0.1}FeO{sub 3} nanoparticles which disappeared with decreasing particle size. The observed strong size dependent multiferroic properties are attributed to the complex interaction between vacancy induced crystallographic defects, multiple valence states of Fe, uncompensated surface spins, crystallographic distortion and suppression of spiral spin cycloid of BiFeO{sub 3}.

  7. Evaluation of luminescent properties and detection of Eu{sup 2}+ in nano structured particles of Gd{sub 2}-x Eu{sub x}O{sub 3} system (x= 0.05, 0.10 and 0.30); Evaluacion de las propiedades luminiscentes y deteccion de Eu{sup 2}+ en particulas nanoestructuradas del sistema Gd{sub 2}-xEu{sub x} O{sub 3} (x= 0.05, 0.10 y 0.30)

    Energy Technology Data Exchange (ETDEWEB)

    Barroso, J.; Mena, I.; Gomez, L. S.; Milosevic, O.; Rabanal, M. E.

    2012-11-01

    Spray Pyrolysis (SP) is performed at 700 degree centigrade in dry air atmosphere using common nitrate aqueous solutions (0,1M) as precursor in order to obtain nano structured particles with the composition Gd{sub 2}-xEu{sub x}O{sub 3} (x= 0.05, 0.10 and 0.30). In this work, three samples with different atomic europium concentration (1, 2 and 6%) were studied. After, the obtained particles were subjected to different thermal treatments with varying temperatures between 800 and 1000 degree centigrade/12 h in dry air atmosphere. The obtained particles were characterized by XRD, SEM techniques, laser dispersion and steady state fluorescence spectroscopy. The existence of two cubic phases with different symmetry cubic phases (Ia-3, Fm-3m) was identified within the as-prepared samples. Moreover, the presence of Gd{sub 2}O{sub 3} monoclinic phase (C{sub 2}/m) which disappears during the thermal treatments was proved. In all thermally treated samples, it was observed the stabilization of an only Ia-3 phase. Fluorescence emission measurements in all studied samples the presence of Eu{sup 2}+ ({lambda}= 430nm), whose intensity increases as long as the content of the monoclinic phase decreases of the Eu{sup 3}+ percentage. (Author) 35 refs.

  8. Fe{sub 2}O{sub 3}-Poly-pyrrole hybrid nano-composite materials for super-capacitors

    Energy Technology Data Exchange (ETDEWEB)

    Mallouki, M.; Tran-Van, F.; Sarrazin, C.; Chevrot, C. [Cergy-Pontoise Univ., Lab. de Physicochimie des Polymeres et des Interfaces (LPPI), EA 2528 95 (France); Fauvarque, J.F. [CNAM, Lab. d' Electrochimie Industrielle, 75 - Paris (France); Simon, P. [Universite Paul Sabatier, CIRIMAT-LCMIE, UMR 5085, 31 - Toulouse (France); De, A. [Saha Institute of Nuclear Physics, Calcutta (India)

    2004-07-01

    Fe{sub 2}O{sub 3}-Poly-pyrrole hybrid nano-composite materials chemically synthesized from colloid particles of iron oxide in aqueous solution have been processed to realize electrode materials for super-capacitor applications. The performances have been evaluated by cyclic voltammetry and galvano-static techniques in a three-electrode cell. The capacitance of Fe{sub 2}O{sub 3}-PPy hybrid nano-composite doped with para-toluene-sulfonate reaches 47 mAh/g in PC/NEt{sub 4}BF{sub 4} with a good stability during cycling (loss of 3% after 1000 cycles). Transmission Electronic Microscopy indicates a porous nano-structure with spherical particles in a range of 400-500 nm which ensures a good accessibility of the electrolyte in the bulk of the electro-active hybrid material. Preliminary studies with room temperature ionic liquid show promising results since the specific capacitance reaches 427 F/g in 1- ethyl-3-methyl-imidazolium bis((tri-fluoro-methyl)sulfonyl)amide (EMITFSI). (authors)

  9. Hydrothermally synthesised Fe{sub 2}O{sub 3} nanoparticles as catalyst precursors for the CVD production of graphitic nanofibres

    Energy Technology Data Exchange (ETDEWEB)

    Edwards, H K [School of Mechanical, Materials and Manufacturing Engineering, University of Nottingham, University Park, Nottingham, NG7 2RD (United Kingdom); Evans, E [School of Chemistry, University of Nottingham, University Park, Nottingham, NG7 2RD (United Kingdom); McCaldin, S [School of Mechanical, Materials and Manufacturing Engineering, University of Nottingham, University Park, Nottingham, NG7 2RD (United Kingdom); Blood, P [School of Chemistry, University of Nottingham, University Park, Nottingham, NG7 2RD (United Kingdom); Gregory, D H [School of Chemistry, University of Nottingham, University Park, Nottingham, NG7 2RD (United Kingdom); Poliakoff, M [School of Chemistry, University of Nottingham, University Park, Nottingham, NG7 2RD (United Kingdom); Lester, E [School of Chemical Engineering and Mining Engineering, University of Nottingham, University Park, Nottingham, NG7 2RD (United Kingdom); Walker, G S [School of Mechanical, Materials and Manufacturing Engineering, University of Nottingham, University Park, Nottingham, NG7 2RD (United Kingdom); Brown, P D [School of Mechanical, Materials and Manufacturing Engineering, University of Nottingham, University Park, Nottingham, NG7 2RD (United Kingdom)

    2006-02-22

    Graphitic nanofibres (GNFs) have been grown by chemical vapour deposition at 500 deg. C and 700 deg. C, using 6 nm and 20 nm particles of Fe{sub 2}O{sub 3} produced by supercritical water hydrothermal synthesis (scWHS). The morphologies of catalyst and GNFs have been examined using the combined techniques of conventional transmission electron microscopy, high resolution electron microscopy, selected area electron diffraction and powder X-ray diffraction. GNF production varied from well ordered nanofibres with an average diameter of 100 nm, to very large, disordered fibres with diameters ranging from 500 nm to {approx}2 {mu}m. Larger fibres were found to have a compound structure composed of discreet domains of graphite and multiwall nanotubes. 20 nm particles produced by scWHS were associated with significant increases in the yield of GNFs as compared with traditional catalyst precipitation routes.

  10. Magneto-optical and catalytic properties of Fe{sub 3}O{sub 4}@HA@Ag magnetic nanocomposite

    Energy Technology Data Exchange (ETDEWEB)

    Amir, Md., E-mail: mdamir01031001@gmail.com [Department of Chemistry, Fatih University, 34500 B.Çekmece-İstanbul, Turkey (Turkey); Bio & Nanotechnology Engineering, Faculty of Engineering, Istanbul University, 34452 Beyazıt/Fatih-İstanbul (Turkey); Güner, S. [Department of Physics, Fatih University, 34500 B.Çekmece-İstanbul, Turkey (Turkey); Yıldız, A. [Department of Textile Engineering, Namık Kemal University, 59860 Çorlu-Tekirdağ, Turkey (Turkey); Baykal, A. [Department of Chemistry, Fatih University, 34500 B.Çekmece-İstanbul, Turkey (Turkey)

    2017-01-01

    Fe{sub 3}O{sub 4}@HA@Ag magnetic nanocomposites (MNCs) were successfully synthesized by the simple reflux method for the removal of azo dyes from the industrial aqueous media. Fe{sub 3}O{sub 4}@HA@AgMNCs exhibited high catalytic activity to reduce MB within 20 min from the waste water. The obtained materials were characterized by the means of different techniques. Powder X-ray diffraction (XRD) analysis confirmed the single-phase of Fe{sub 3}O{sub 4} spinel structure. SEM and TEM analysis indicated that Fe{sub 3}O{sub 4}@HA@AgMNCs were nanoparticles like structure with small agglomeration. TG result showed that the products contained 9% of HA. The characteristic peaks of HA at 1601 cm{sup −1} and 1703 cm{sup −1} was observed by the means of FT-IR spectra of Fe{sub 3}O{sub 4}@HA@AgMNCs. The hysteresis (σ–H) curves revealed Fe{sub 3}O{sub 4}@HA@Ag MNCs exhibit a typical superparamagnetic characteristic with a saturation magnetization of 59.11 emu/g and measured magnetic moment is 2.45 µ{sub B}. The average magnetic particle dimension (D{sub mag}) is 13.25 nm. In accordance, the average crystallite and particle dimensions were obtained as 11.50 nm and 13.10 nm from XRD and TEM measurements, respectively. Magnetocrystalline anisotropy was offered as uniaxial and calculated effective anisotropy constant (K{sub eff}) is 2.96×10{sup 5} Erg/g. The blocking temperature was estimated as 522 K. The size-dependent saturation magnetization suggests the existence of a magnetically dead layer as 0.793 nm for Fe{sub 3}O{sub 4}@HA@Ag MNCs. The UV–vis diffuse reflectance spectroscopy (DRS) and Kubelka–Munk theory were applied to determine the optical properties of powder samples. The direct optical energy band gap (E{sub g}) values were estimated from Tauc plots between 1.62 eV and 2.12 eV. - Graphical abstract: An illustration for the fabrication of Fe{sub 3}O{sub 4}@HA@Ag MNCs. - Highlights: • The reduction of azo dye such Methylene Blue was instantly completed with

  11. Superior hydrogen storage kinetics of MgH{sub 2} nanoparticles doped with TiF{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Xie, L. [Beijing National Laboratory for Molecular Sciences (BNLMS), State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China); Liu, Y. [Beijing National Laboratory for Molecular Sciences (BNLMS), State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China); Wang, Y.T. [Beijing National Laboratory for Molecular Sciences (BNLMS), State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China); Zheng, J. [Beijing National Laboratory for Molecular Sciences (BNLMS), State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China); Li, X.G. [Beijing National Laboratory for Molecular Sciences (BNLMS), State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China) and College of Engineering, Peking University, Beijing 100871 (China)]. E-mail: xgli@pku.edu.cn

    2007-08-15

    MgH{sub 2} nanoparticles were obtained by hydriding ultrafine magnesium particles which were prepared by hydrogen plasma-metal reaction. The X-ray diffraction (XRD) and transmission electron microscopy (TEM) results show that the obtained sample is almost pure MgH{sub 2} phase, without residual magnesium and with an average particle size of {approx}300 nm. Milled with 5 wt.% TiF{sub 3} as a doping precursor in a hydrogen atmosphere, the sample desorbed 4.5 wt.% hydrogen in 6 min under an initial hydrogen pressure of {approx}0.001 bar at 573 K and absorbed 4.2 wt.% hydrogen in 1 min under {approx}20 bar hydrogen at room temperature. Compared with MgH{sub 2} micrometer particles doped with 5 wt.% TiF{sub 3} under the same conditions as the MgH{sub 2} nanoparticles, it is suggested that decrease of particle size is beneficial for enhancing absorption capacity at low temperatures, but has no effect on desorption. In addition, the catalyst was mainly responsible for improving the sorption kinetics and its catalytic mechanism is discussed.

  12. TEA controllable preparation of magnetite nanoparticles (Fe{sub 3}O{sub 4} NPs) with excellent magnetic properties

    Energy Technology Data Exchange (ETDEWEB)

    Han, Chengliang, E-mail: clhan@issp.ac.cn [Department of Chemical and Material Engineering, Hefei University, Hefei 230601 (China); Zhu, Dejie [State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002 (China); Wu, Hanzhao; Li, Yao; Cheng, Lu; Hu, Kunhong [Department of Chemical and Material Engineering, Hefei University, Hefei 230601 (China)

    2016-06-15

    A fast and controllable synthesis method for superparamagnetic magnetite nanoparticles (Fe{sub 3}O{sub 4} NPs) was developed in Fe(III)-triethanolamine (TEA) solution. The phase structure, morphology and particle size of the as-synthesized samples were characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). The results showed that the magnetic particles were pure Fe{sub 3}O{sub 4} with mean sizes of approximately 10 nm. The used TEA has key effects on the formation of well dispersing Fe{sub 3}O{sub 4} NPs. Vibrating sample magnetometer (VSM) result indicated that the as-obtained Fe{sub 3}O{sub 4} NPs exhibited superparamagnetic behavior and the saturation magnetization (M{sub s}) was about 70 emu/g, which had potential applications in magnetic science and technology. - Highlights: • The Fe{sub 3}O{sub 4} NPs are synthesized by a simple and low-cost hydrothermal approach. • The triethanolamine (TEA) played vital roles in the formation of Fe{sub 3}O{sub 4} NPs. • Our samples exhibited superparamagnetic and excellent dispersing properties in water.

  13. FMR study of carbon nanotubes filled with Fe{sub 3}O{sub 4} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Kopyl, S., E-mail: svitlanakopyl@ua.pt [NRD-TEMA, Department of Mechanical Engineering, Aveiro Institute of Nanotechnology (AIN), University of Aveiro, Aveiro 3810-193 (Portugal); Timopheev, A.A., E-mail: andreyt@ua.pt [Physics Department and I3N, University of Aveiro, Aveiro 3810-193 (Portugal); Bystrov, V.S. [Department of Materials and Ceramic Engineering and CICECO, University of Aveiro, Aveiro 3810-193 (Portugal); Institute of Mathematical Problems of Biology RAS, 142290 Pushchino (Russian Federation); Bdikin, I. [NRD-TEMA, Department of Mechanical Engineering, Aveiro Institute of Nanotechnology (AIN), University of Aveiro, Aveiro 3810-193 (Portugal); Teixeira, B.M.S. [Physics Department and I3N, University of Aveiro, Aveiro 3810-193 (Portugal); Maevskij, E. [Institute of Theoretical and Experimental Biophysics RAS, 142290 Puschino (Russian Federation); Sobolev, N.A. [Physics Department and I3N, University of Aveiro, Aveiro 3810-193 (Portugal); Sousa, A.C.M. [NRD-TEMA, Department of Mechanical Engineering, Aveiro Institute of Nanotechnology (AIN), University of Aveiro, Aveiro 3810-193 (Portugal)

    2014-05-01

    Ordered arrays of carbon nanotubes were produced using a non-catalytic chemical vapour deposition. The multiwall nanotubes with an inner diameter of 120 nm were grown inside porous alumina templates and then filled with a magnetic colloid of 7.5 nm Fe{sub 3}O{sub 4} particles. X-ray diffraction, electron microscopy and ferromagnetic resonance (FMR) were used to characterize structural and magnetic properties of the grown samples. To estimate the filling factor from the angular dependence of the FMR resonance field, we have derived an effective demagnetization factor for our system using the formalism proposed by Skomsky and Dubowik. Angular dependence of the FMR line width allows one to conclude about the non-uniform filling, while temperature dependent measurements reflect typical features of a superparamagnetic resonance. - Highlights: • Synthesis of CNTs inside of alumina membrane and filling it with Fe{sub 3}O{sub 4} particles. • X-ray diffraction and electron microscopy study of the samples. • Magnetic properties of the samples studied by FMR. • Filling factor has been determined from the angular dependences of FMR. • Resulted magnetic CNTs are attractive for production of magnetic nanofluids.

  14. Effect of temperature on structural, morphological and magnetic properties of Cd{sub 0.7}Co{sub 0.3}Fe{sub 2}O{sub 4} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Prabhakar Vattikuti, S.V., E-mail: vsvprabu@gmail.com [School of Mechanical Engineering, Yeungnam University, Gyeongsan, Gyeongsangbuk-do 712-749, Republic of Korea, (Korea, Republic of); Byon, Chan [School of Mechanical Engineering, Yeungnam University, Gyeongsan, Gyeongsangbuk-do 712-749, Republic of Korea, (Korea, Republic of); Shim, Jaesool, E-mail: jshim@ynu.ac.kr [School of Mechanical Engineering, Yeungnam University, Gyeongsan, Gyeongsangbuk-do 712-749, Republic of Korea, (Korea, Republic of); Reddy, Ch. Venkata, E-mail: cvrphy@gmail.com [School of Mechanical Engineering, Yeungnam University, Gyeongsan, Gyeongsangbuk-do 712-749, Republic of Korea, (Korea, Republic of)

    2015-11-01

    Cadmium-substituted cobalt ferrite (Cd{sub 0.7}Co{sub 0.3}Fe{sub 2}O{sub 4}) nanoparticles were synthesized using a chemical synthesis method and synthesized particles were calcinated at 300 °C and 600 °C respectively. The samples were characterized in order to understand the temperature effect on structural, morphological, thermal, and magnetic properties. X-ray diffraction data confirm the formation of single-phase cubic structure and the average grain sizes were evaluated. The microstructural features were examined by scanning electron microscopy (SEM) and transmission electron microscopy (TEM), and compositional analysis carried out by energy dispersive spectroscopy (EDS). A vibrating sample magnetometer (VSM) was used to investigate the magnetic properties. The hysteresis curves of Cd{sub 0.7}Co{sub 0.3}Fe{sub 2}O{sub 4} nanoparticles show enhancement of the coercivity with the increasing calcinated temperature. This enhancement is attributed to the transition from a multi-domain to a single-domain nature. The high and low frequency absorption bands of Cd{sub 0.7}Co{sub 0.3}Fe{sub 2}O{sub 4} were investigated using FT-IR analysis. - Highlights: • Cd{sub 0.7}Co{sub 0.3}Fe{sub 2}O{sub 4} nano particles are prepared by the chemical synthesis method. • X-ray diffraction data confirms the single phase cubic spinel structure. • The estimated particle sizes from the XRD are approximately 25 and 35 nm. • The coercivity and magnetization values increase with increasing the particle size. • FT-IR spectra indicate the fundamental vibrations of host lattices.

  15. Synthesis, morphology and microstructure of pomegranate-like hematite ({alpha}-Fe{sub 2}O{sub 3}) superstructure with high coercivity

    Energy Technology Data Exchange (ETDEWEB)

    Tadic, Marin, E-mail: marint@vinca.rs [Condensed Matter Physics Laboratory, Vinca Institute, University of Belgrade, P.O. Box 522, 11001 Belgrade (Serbia); Citakovic, Nada [Military Academy, Generala Pavla Jurisica Sturma 33, University of Belgrade, 11000 Belgrade (Serbia); Panjan, Matjaz [Jozef Stefan Institute, Jamova 39, 1000 Ljubljana (Slovenia); Stanojevic, Boban [Vinca Institute of Nuclear Sciences, P.O. Box 522, 11001 Belgrade, University of Belgrade (Serbia); Markovic, Dragana [Condensed Matter Physics Laboratory, Vinca Institute, University of Belgrade, P.O. Box 522, 11001 Belgrade (Serbia); Jovanovic, Dorde [Center for Solid State Physics and New Materials, Institute of Physics, University of Belgrade, Pregrevica 118, 11080 Belgrade (Serbia); Spasojevic, Vojislav [Condensed Matter Physics Laboratory, Vinca Institute, University of Belgrade, P.O. Box 522, 11001 Belgrade (Serbia)

    2012-12-05

    Highlights: Black-Right-Pointing-Pointer We found superior magnetic properties of the hematite ({alpha}-Fe{sub 2}O{sub 3}). Black-Right-Pointing-Pointer TEM and HRTEM images show a pomegranate-like superstructure. Black-Right-Pointing-Pointer Magnetic measurements display high coercivity H{sub C} = 4350 Oe at the room temperature. - Abstract: We found novel and superior magnetic properties of the hematite ({alpha}-Fe{sub 2}O{sub 3}) that originate from an internal microstructure of particles and strong inter-particle interactions between nanocrystal sub-units. The hematite particles were synthesized by thermal decomposition of iron (III) nitrate without any template or surfactant. The purity, size, crystallinity, morphology, microstructure and magnetic features of the as-prepared particles were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), energy-dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM), Raman spectroscopy (RS) and SQUID magnetometry. An XRD study reveals a pure phase of {alpha}-Fe{sub 2}O{sub 3} whereas TEM shows {alpha}-Fe{sub 2}O{sub 3} spheres with a diameter of about 150 nm. RS also shows high quality and purity of the sample. Moreover, TEM and HRTEM images show a pomegranate-like superstructure and evidence that the spherical particles are composed of individual well-crystallized nanoparticle sub-units (self-assembled nanoparticles) with a size of about 20 nm. Magnetic measurements display hysteretic behavior at the room temperature with remanent magnetization M{sub r} = 0.731 emu/g, saturation magnetization M{sub S} = 6.83 emu/g and coercivity H{sub C} = 4350 Oe, as well as the Morin transition at T{sub M} = 261 K. These results and comparison with those in the literature reveal that the sample has extremely high coercivity. The magnetic properties of the sample are discussed in relation to morphology, internal microstructure, surface

  16. Size dependences of crystal structure and magnetic properties of DyMnO{sub 3} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Tajiri, T., E-mail: tajiri@fukuoka-u.ac.jp [Faculty of Science, Fukuoka University, Fukuoka 814-0180 (Japan); Terashita, N.; Hamamoto, K.; Deguchi, H.; Mito, M. [Faculty of Engineering, Kyushu Institute of Technology, Kitakyushu 804-8550 (Japan); Morimoto, Y.; Konishi, K. [Graduate School of Science and Engineering, Ehime University, Matsuyama 790-8577 (Japan); Kohno, A. [Faculty of Science, Fukuoka University, Fukuoka 814-0180 (Japan)

    2013-11-15

    We synthesized DyMnO{sub 3} nanoparticles with particle sizes of about 7.5–15.3 nm in the pores of mesoporous silica and investigated their crystal structure and magnetic properties. As the particle size decreased, the lattice constants of the DyMnO{sub 3} nanoparticles deviated from those of the bulk crystal, and the Jahn–Teller distortion in the nanoparticle systems decreased. In addition, the estimated lattice strain increased with decreasing particle size. The DyMnO{sub 3} nanoparticles showed superparamagnetic behavior. The blocking temperature and the coercive field increased with decreasing particle size, and this behavior was contrary to the usual magnetic size effects. It is deduced that these unique size dependences of the magnetic properties for the DyMnO{sub 3} nanoparticles were derived from the changes in lattice constants and lattice strain. The anisotropic lattice deformation in the crystal structure of the nanoparticles induces an enhancement of the magnetic anisotropy, which results in the increase in blocking temperature and coercive field with decreasing particle size. - Highlights: • We successfully synthesized DyMnO{sub 3} nanoparticles with particle size of 7.5–15.3 nm. • Lattice strain increases with decreasing particle size. • Lattice constants exhibit anisotropic change with decreasing particle size. • Distortion of crystal structure leads to enhancement of magnetic anisotropy constant. • Blocking temperature and coercive field increases with decreasing particle size.

  17. Formation, cationic site exchange and surface structure of mechanosynthesized EuCrO{sub 3} nanocrystalline particles

    Energy Technology Data Exchange (ETDEWEB)

    Widatallah, H M; Al-Harthi, S H; Gismelseed, A M; Al-Rawas, A D [Department of Physics, Sultan Qaboos University, PO Box 36, 123, Muscat (Oman); Johnson, C; Moore, E A [School of Chemistry and Analytical Sciences, The Open University, Milton Keynes, MK7 6AA (United Kingdom); Klencsar, Z [Chemical Research Center, Hungarian Academy of Sciences, 1025 Budapest (Hungary); Wynter, C I [Nassau Community College, Garden City, NY 11530-6793 (United States); Brown, D E, E-mail: hishammw@squ.edu.om, E-mail: hisham@ictp.it [Department of Physics, Northern Illinois University, De Kalb, IL 60115 (United States)

    2011-07-06

    Nanocrystalline EuCrO{sub 3} particles ({approx}25 nm) have been prepared by pre-milling a 1 : 1 molar mixture of Eu{sub 2}O{sub 3} and Cr{sub 2}O{sub 3} for 60 h followed by sintering at 700 {sup 0}C (12 h). This temperature is {approx}500-600 {sup 0}C lower than those at which the material, in bulk form, is conventionally prepared. Rietveld analysis of the x-ray powder diffraction pattern of the EuCrO{sub 3} nanoparticles favours a structural model involving a slight degree of cationic exchange where {approx}11% of the Eu{sup 3+} and Cr{sup 3+} ions exchange their normal dodecahedral A- and octahedral B-sites, respectively, in the perovskite-related structure. This cationic site exchange, which is unusual in a perovskite structure, has been well supported by the corresponding room-temperature {sup 151}Eu Moessbauer spectrum of the nanoparticles that in addition to displaying a distribution in the principal component of the EFG tensor (V{sub zz}) at the usual A-sites of the {sup 151}Eu nuclei, also revealed the presence of a subcomponent with {approx}11% area fraction and a considerably increased |V{sub zz}| value that was associated with Eu{sup 3+} ions at octahedral B-sites. X-ray photoelectron and Auger electron spectroscopic techniques reveal a complex surface structure where extremely thin layers of un-reacted Eu{sub 2}O{sub 3} and Cr{sub 2}O{sub 3} cover most of the EuCrO{sub 3} nanoparticles' surfaces together with some traces of elemental Cr. The binding energies associated with Eu{sup 3+} 3d{sub 5/2}, Eu{sup 3+} 4d{sub 3/2}, Cr{sup 3+} 2p{sub 3/2} and O{sup 2-} 1s core-level electrons in EuCrO{sub 3} are estimated from the x-ray photoelectron data for the first time.

  18. Growth, thermal and spectral characteristics of Yb{sup 3+}:Sr{sub 6}YSc(BO{sub 3}){sub 6} crystal

    Energy Technology Data Exchange (ETDEWEB)

    Yuan, Feifei [Key Laboratory of Optoelectronic Materials Chemistry and Physics, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002 (China); University of Chinese Academy of Sciences, Beijing 100049 (China); Zhang, Lizhen; Huang, Yisheng; Sun, Shijia [Key Laboratory of Optoelectronic Materials Chemistry and Physics, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002 (China); Lin, Zhoubin, E-mail: lzb@fjirsm.ac.cn [Key Laboratory of Optoelectronic Materials Chemistry and Physics, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002 (China); Wang, Guofu [Key Laboratory of Optoelectronic Materials Chemistry and Physics, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002 (China)

    2014-09-15

    Highlights: • A new crystal of Yb{sup 3+}:Sr{sub 6}YSc(BO{sub 3}){sub 6} was grown successfully from a Li{sub 6}B{sub 4}O{sub 9} flux. • Yb{sup 3+}:Sr{sub 6}YSc(BO{sub 3}){sub 6} crystal has good thermal, mechanical and spectral properties. • Yb{sup 3+}:Sr{sub 6}YSc(BO{sub 3}){sub 6} has long fluorescence lifetime, broad absorption and emission bands. - Abstract: A crystal of Yb{sup 3+}:Sr{sub 6}YSc(BO{sub 3}){sub 6} was grown successfully from Li{sub 6}B{sub 4}O{sub 9} flux by the top-seeded solution growth method. The crystal's thermal, mechanical and spectral characteristics were investigated in detail. It possesses small thermal expansion coefficients, moderate thermal conductivities, and large hardness. The crystal has a strong absorption band at 967 nm with a full width at half-maximum of about 3.4 nm. The crystal has a broad emission band at 1016 nm with the full width at half-maximum of about 64 nm. The emission cross sections were calculated by reciprocity method and Füchtbauer-Ladenburg formula. The fluorescence lifetime is 5.98 ms. The results reveal that Yb{sup 3+}:Sr{sub 6}YSc(BO{sub 3}){sub 6} crystal is a new promising tunable and ultrashort pulse laser crystal.

  19. Synthesis and characterization of Gd{sub 2}O{sub 3} doped UO{sub 2} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Soldati, A.L., E-mail: asoldati@cab.cnea.gov.ar [Centro Atómico Bariloche (CAB) – Comisión Nacional de Energía Atómica (CNEA), Av. Bustillo 9500, CP: 8400 Bariloche (Argentina); Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Av. De los Pioneros 2300, CP: 8400 Bariloche (Argentina); Gana Watkins, I. [Centro Atómico Bariloche (CAB) – Comisión Nacional de Energía Atómica (CNEA), Av. Bustillo 9500, CP: 8400 Bariloche (Argentina); Fernández Zuvich, A. [Centro Atómico Bariloche (CAB) – Comisión Nacional de Energía Atómica (CNEA), Av. Bustillo 9500, CP: 8400 Bariloche (Argentina); Instituto Balseiro, Universidad Nacional de Cuyo, Av. Bustillo 9500, CP: 8400 Bariloche (Argentina); Napolitano, F.; Troiani, H. [Centro Atómico Bariloche (CAB) – Comisión Nacional de Energía Atómica (CNEA), Av. Bustillo 9500, CP: 8400 Bariloche (Argentina); Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Av. De los Pioneros 2300, CP: 8400 Bariloche (Argentina); and others

    2016-10-15

    UO{sub 2} nanoparticles doped with 4, 8, 10 and 15 wt% Gd{sub 2}O{sub 3}were synthesized by a reverse strike method. Crystal structure and chemical homogeneity were evaluated using a combination of X-ray diffraction and microscopy tools. An exhaustive study of the composition and its homogeneity at the micro and at the nanometer level was carried out in this nuclear fuel material. Field Emission Gun Scanning and Transmission Electron Microscopy images revealed the presence of micrometer scale agglomerates of nanoparticles, with rounded morphology and an average crystallite size of 100 nm. Rietveld refinements of high-statistic X-ray Diffraction data determined the crystal structure and composition. Furthermore, Energy Dispersive Spectroscopy using a 2 nm{sup 2} spot on the sample surface determined a Gd concentration variation around the average of ±5% in different spots of a single crystallite and of ±10% between different crystallites. However, when measuring large amounts of nanoparticles the concentration averages, producing a homogeneous composition distribution at the micrometer scale. - Highlights: • Synthesis of 4, 8, 10 and 15wt% Gd{sub 2}O{sub 3} doped UO{sub 2} nanoparticles. • Crystallite sizes around 100 nm and rounded morphology. • 90% Gd distribution homogeneity between particles for the less concentrated sample. • High Statistic X-ray Rietveld analysis determined an U{sub 1−x}Gd{sub x}O{sub 2−δ} fcc structure. • Phases with similar crystal structure and symmetry, but different lattice parameter.

  20. Effect of annealing on particle size, microstructure and gas sensing properties of Mn substituted CoFe{sub 2}O{sub 4} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Kumar, E. Ranjith, E-mail: ranjueaswar@gmail.com [Department of Physics, Dr. NGP Institute of Technology, Coimbatore 641048, Tamil Nadu (India); Kamzin, A.S. [Ioffe Physical-Technical Institute, Russian Academy of Sciences, St. Petersburg 194021 (Russian Federation); Janani, K. [Department of Physics, Kongunadu Arts and Science College, Coimbatore, Tamil Nadu (India)

    2016-11-01

    Microstructure, morphological and gas sensor studies of Mn substituted cobalt ferrite nanoparticles synthesized by a simple evaporation method and auto- combustion method. The influence of heat treatment on phase and particle size of spinel ferrite nanoparticles were determined by X-ray diffraction and Mossbauer spectroscopy. The XRD study reveals that the lattice constant and crystallite size of the samples increases with the increase of annealing temperature. Last one was confirmed by Mossbauer data. The lowest size of particles of MnCoFe{sub 2}O{sub 4} (~3 nm) is obtained by auto combustion method. The spherical shaped nanoparticles are recorded by TEM. Furthermore, conductance response of Mn–Co ferrite nanomaterial was measured by exposing the material to reducing gas like liquefied petroleum gas (LPG) which showed a sensor response of ~0.19 at an optimum operating temperature of 250 °C. - Highlights: • ~3 nm sized particles were prepared by auto combustion method. • Mossbauer study was analyzed for different annealed samples. • The size of the particles increased with increasing annealing temperature.

  1. Effect of ball milling and dynamic compaction on magnetic properties of Al{sub 2}O{sub 3}/Co(P) composite particles

    Energy Technology Data Exchange (ETDEWEB)

    Denisova, E. A. [Kirensky Institute of Physics SB RAS, Krasnoyarsk (Russian Federation); Krasnoyarsk Institute of Railways Transport, Krasnoyarsk (Russian Federation); Kuzovnikova, L. A. [Krasnoyarsk Institute of Railways Transport, Krasnoyarsk (Russian Federation); Iskhakov, R. S., E-mail: rauf@iph.krasn.ru; Eremin, E. V. [Kirensky Institute of Physics SB RAS, Krasnoyarsk (Russian Federation); Bukaemskiy, A. A. [Institut fur Sicherheitsforschung und Reaktortechnik, D-52425 Juelich (Germany); Nemtsev, I. V. [Krasnoyarsk Scientific Center SB RAS, Krasnoyarsk (Russian Federation)

    2014-05-07

    The evolution of the magnetic properties of composite Al{sub 2}O{sub 3}/Co(P) particles during ball milling and dynamic compaction is investigated. To prepare starting composite particles, the Al{sub 2}O{sub 3} granules were coated with a Co{sub 95}P{sub 5} shell by electroless plating. The magnetic and structural properties of the composite particles are characterized by scanning electron microscopy, X-ray diffraction, and the use of the Physical Property Measurement System. The use of composite core-shell particles as starting powder for mechanoactivation allows to decrease treatment duration to 1 h and to produce a more homogeneous bulk sample than in the case of the mixture of Co and Al{sub 2}O{sub 3} powders. The magnetic properties of the milled composite particles are correlated with changes in the microstructure. Reduction in grain size of Co during milling leads to an increase of the volume fraction of superparamagnetic particles and to a decrease of the saturation magnetization. The local magnetic anisotropy field depends on the amount of hcp-Co phase in sample. The anisotropy field value decreases from 8.4 kOe to 3.8 kOe with an increase in milling duration up to 75 min. The regimes of dynamic compaction were selected so that the magnetic characteristics—saturation magnetization and coercive field—remained unchanged.

  2. Hydrothermal synthesis of Gd{sub 2}O{sub 3}:Eu{sup 3+} nanophosphors: Effect of surfactant on structural and luminescence properties

    Energy Technology Data Exchange (ETDEWEB)

    Dhananjaya, N., E-mail: dhanu.siri@yahoo.co.in [B.S. Narayan Centre of Excellence for Advanced Materials, B.M.S. Institute of Technology, Bangalore 560 064 (India); Department of Physics, B.M.S. Institute of Technology, Bangalore 560 064 (India); Nagabhushana, H., E-mail: bhushanvlc@gmail.com [Prof. C.N.R. Rao Centre for Advanced Materials, Tumkur University, Tumkur 572 103 (India); Sharma, S.C. [B.S. Narayan Centre of Excellence for Advanced Materials, B.M.S. Institute of Technology, Bangalore 560 064 (India); Department of Mechanical Engineering, B.M.S. Institute of Technology, Bangalore 560 064 (India); Rudraswamy, B. [Department of Physics, J.B. Campus, Bangalore University, Bangalore 560 056 (India); Shivakumara, C. [Solid State and Structural Chemistry Unit, Indian Institute of Science, Bangalore 560 012 (India); Nagabhushana, B.M. [Department of Chemistry, M.S. Ramaiah Institute of Technology, Bangalore 560 054 (India)

    2014-02-25

    Highlights: • Gd(OH){sub 3}:Eu{sup 3+}, GdOOH:Eu{sup 3+} and Gd{sub 2}O{sub 3}:Eu{sup 3+} phases were prepared by hydrothermal method. • Phosphors were well characterized by XRD, SEM, TEM, Raman, UV–Vis, FT-IR. • Cubic Gd{sub 2}O{sub 3}:Eu{sup 3+} show intense red emission, which was highly useful for photonics application. • HDA surfactant plays an important role in conversion of cubic to hexagonal phases. -- Abstract: Various morphologies of Eu{sup 3+} activated gadolinium oxide have been prepared by hydrothermal method using hexadecylamine (HDA) as surfactant at different experimental conditions. The powder X-ray diffraction studies reveal as-formed product is hexagonal Gd(OH){sub 3}:Eu{sup 3+} phase and subsequent heat treatment at 350 and 600 °C transforms to monoclinic GdOOH:Eu{sup 3+} and cubic Gd{sub 2}O{sub 3}:Eu{sup 3+} phases respectively. SEM pictures of without surfactant show irregular shaped rods along with flakes. However, in the presence of HDA surfactant, the particles are converted into rods of various sizes. The temperature dependent morphological evolution of Gd{sub 2}O{sub 3}:Eu{sup 3+} without and with HDA surfactant is studied. TEM micrographs of Gd(OH){sub 3}:Eu{sup 3+} sample with HDA confirms smooth nanorods with various diameters in the range 20–100 nm. FTIR studies reveal that HDA surfactant plays an important role in conversion of cubic to hexagonal phases. Among these three phases, cubic phase Gd{sub 2}O{sub 3}:Eu{sup 3+} (λ{sub ex} = 254 nm) show red emission at 612 nm corresponding to {sup 5}D{sub 0} → {sup 7}F{sub 2} and is more efficient host than the monoclinic counterpart. The band gap for hexagonal Gd(OH){sub 3}:Eu{sup 3+} is more when compared to monoclinic GdOOH:Eu{sup 3+} and cubic Gd{sub 2}O{sub 3}:Eu{sup 3+}.

  3. Influence of Eu{sup 3+} doping content on antioxidant properties of Lu{sub 2}O{sub 3} sol-gel derived nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Olvera Salazar, Arturo [Universidad Del Valle de México Campus Lomas Verde, Paseo de las Aves No.1 Col. San Mateo Nopala. Naucalpan de Juárez, Edo. Méx. C.P. 53220 (Mexico); García Hernández, Margarita, E-mail: margarita.garcia@itcm.edu.mx [Tecnológico Nacional de México-Instituto Tecnológico de Ciudad Madero. Av. 1o. de Mayo esq. Sor Juana Inés de la Cruz s/n Col. Los Mangos Cd. Madero Tamaulipas C.P.89440 (Mexico); López Camacho, Perla Yolanda [Universidad Autónoma Metropolitana, Unidad Cuajimalpa. Av. Vasco de Quiroga 4871, Col. Santa Fé Cuajimalpa, Cuajimalpa D.F. C.P. 05348 (Mexico); López Marure, Arturo [Instituto Politécnico Nacional, CICATA Altamira. Carretera Tampico-Puerto Industrial Altamira, Altamira, Tamaulipas C.P. 89600 (Mexico); Reyes de la Torre, Adriana Isabel [Tecnológico Nacional de México-Instituto Tecnológico de Ciudad Madero. Av. 1o. de Mayo esq. Sor Juana Inés de la Cruz s/n Col. Los Mangos Cd. Madero Tamaulipas C.P.89440 (Mexico); Morales Ramírez, Ángel de Jesús [Instituto Politécnico Nacional, CIITEC Azcapotzalco. Cerrada de Cecati S/N, Col. Santa Catarina, Azcapotzalco, D.F. C.P. 02250 (Mexico); and others

    2016-12-01

    This paper presents the synthesis of pure and europium-doped lutetium oxide (Lu{sub 2}O{sub 3}) powders prepared by sol-gel method. The influence of europium ion concentration into Lu{sub 2}O{sub 3} nanocrystallites was investigated for first time in an in vitro system using a modified ABTS radical cation decolorization assay to determine the antioxidant activity. The crystalline structure of Lu{sub 2}O{sub 3} and Eu:Lu{sub 2}O{sub 3} powders was elucidated by XRD obtaining cubic phase in all system without secondary products in accordance with FT-IR results. By TEM and Scherrer equation, it was determined that Lu{sub 2}O{sub 3} and Eu:Lu{sub 2}O{sub 3} powders presented nearly spherical particle morphology with crystallites sizes in the range of 8 to 13 nm. The antioxidant assays results revealed that europium ion enhance Lu{sub 2}O{sub 3} powders antioxidant properties, showing that 12.5 mol% of europium is sufficient to reach its maximum capacity. - Highlights: • For first time the effect of the Eu content vs antioxidant properties was studied. • Sol-gel particles of Lu{sub 2}O{sub 3}:Eu{sup 3+} nanopowders showed relevant antioxidant properties. • The antioxidant behavior remains stable at higher Eu levels.

  4. Interactions between sub-10-nm iron and cerium oxide nanoparticles and 3T3 fibroblasts: the role of the coating and aggregation state

    International Nuclear Information System (INIS)

    Safi, M; Sarrouj, H; Berret, J-F; Sandre, O; Mignet, N

    2010-01-01

    Recent nanotoxicity studies revealed that the physico-chemical characteristics of engineered nanomaterials play an important role in the interactions with living cells. Here, we report on the toxicity and uptake of cerium and iron oxide sub-10-nm nanoparticles by NIH/3T3 mouse fibroblasts. Coating strategies include low-molecular weight ligands (citric acid) and polymers (poly(acrylic acid), M W = 2000 g mol -1 ). Electrostatically adsorbed on the surfaces, the organic moieties provide a negatively charged coating in physiological conditions. We find that most particles were biocompatible, as exposed cells remained 100% viable relative to controls. Only the bare and the citrate-coated nanoceria exhibit a slight decrease in mitochondrial activity at very high cerium concentrations (>1 g l -1 ). We also observe that the citrate-coated particles are internalized/adsorbed by the cells in large amounts, typically 250 pg/cell after 24 h incubation for iron oxide. In contrast, the polymer-coated particles are taken up at much lower rates (<30 pg/cell). The strong uptake shown by the citrated particles is related to the destabilization of the dispersions in the cell culture medium and their sedimentation down to the cell membranes. In conclusion, we show that the uptake of nanomaterials by living cells depends on the coating of the particles and on its ability to preserve the colloidal nature of the dispersions.

  5. Interactions between sub-10-nm iron and cerium oxide nanoparticles and 3T3 fibroblasts: the role of the coating and aggregation state

    Science.gov (United States)

    Safi, M.; Sarrouj, H.; Sandre, O.; Mignet, N.; Berret, J.-F.

    2010-04-01

    Recent nanotoxicity studies revealed that the physico-chemical characteristics of engineered nanomaterials play an important role in the interactions with living cells. Here, we report on the toxicity and uptake of cerium and iron oxide sub-10-nm nanoparticles by NIH/3T3 mouse fibroblasts. Coating strategies include low-molecular weight ligands (citric acid) and polymers (poly(acrylic acid), MW = 2000 g mol - 1). Electrostatically adsorbed on the surfaces, the organic moieties provide a negatively charged coating in physiological conditions. We find that most particles were biocompatible, as exposed cells remained 100% viable relative to controls. Only the bare and the citrate-coated nanoceria exhibit a slight decrease in mitochondrial activity at very high cerium concentrations (>1 g l - 1). We also observe that the citrate-coated particles are internalized/adsorbed by the cells in large amounts, typically 250 pg/cell after 24 h incubation for iron oxide. In contrast, the polymer-coated particles are taken up at much lower rates (<30 pg/cell). The strong uptake shown by the citrated particles is related to the destabilization of the dispersions in the cell culture medium and their sedimentation down to the cell membranes. In conclusion, we show that the uptake of nanomaterials by living cells depends on the coating of the particles and on its ability to preserve the colloidal nature of the dispersions.

  6. Microstrucural characterization of gas atomized Fe{sub 73.5}Si{sub 13.5}B{sub 9}Nb{sub 3}Cu{sub 1} and Fe{sub 97}Si{sub 3} alloys

    Energy Technology Data Exchange (ETDEWEB)

    Garcia-Escorial, A., E-mail: age@cenim.csic.es [CENIM-CSIC, Avda. Gregorio del Amo, 8, 28040 Madrid (Spain); Lieblich, M. [CENIM-CSIC, Avda. Gregorio del Amo, 8, 28040 Madrid (Spain); Lopez, M.; Marin, P. [Instituto de Magnetismo Aplicado, P.O. Box 155, 28230 Madrid (Spain)

    2011-06-15

    Research highlights: > Two FeSi-base alloys as precursors for small dimension soft magnets. > Small particles rapidly solidified by gas atomisation. > Increase effective magnetic anisotropy constant by alloying segregation. > Magnetic hardenning due to volume decrease. - Abstract: Powder particles of Fe{sub 73.5}Si{sub 13.5}B{sub 9}Nb{sub 3}Cu{sub 1} and Fe{sub 97}Si{sub 3} soft magnetic alloys have been prepared by gas atomization. The gas atomized powder was microstructurally characterized and the dependence of coercivity with the composition and powder particle size investigated. As-atomized powder particles of both compositions were constituted by a bcc {alpha}-Fe (Si) solid solution. The Fe{sub 73.5}Si{sub 13.5}B{sub 9}Nb{sub 3}Cu{sub 1} powder particles presented a grain microstructure with dendrite structure, which dendrite arms were enriched in Nb. The coercivity increased as the particle size decreased, with a minimum coercivity, of 5 Oe, measured in the Fe{sub 97}Si{sub 3} alloy in the range of 50-100 {mu}m powder particle size. The coercive fields were quite higher in the Fe{sub 73.5}Si{sub 13.5}B{sub 9}Nb{sub 3}Cu{sub 1} than in the Fe{sub 97}Si{sub 3} powder, due to the Nb addition, which produced a phase segregation that leads to a noticeable magnetic hardening.

  7. Observation of the strain-driven charge-ordered state in La sub 0 sub . sub 7 sub C a sub 0 sub . sub 3 MnO sub 3 sub - sub d elta thin film with oxygen deficiency

    CERN Document Server

    Prokhorov, V G; Kaminsky, G G; Svetchnikov, V L; Zandbergen, H W; Lee, Y P; Park, J S; Kim, K W

    2003-01-01

    The magnetic and transport properties of La sub 0 sub . sub 7 Ca sub 0 sub . sub 3 MnO sub 3 sub - sub d elta films with an oxygen deficiency (delta approx 0.1) and a La sub 0 sub . sub 9 Ca sub 0 sub . sub 1 MnO sub 3 film with the stoichiometric oxygen content are investigated in a wide temperature range. It is shown that the charge-ordered insulating (COI) state is observed for a La sub 0 sub . sub 7 Ca sub 0 sub . sub 3 MnO sub 2 sub . sub 9 film with thickness d <= 30 nm, which manifests mainly a cubic crystal structure with an anomalously small lattice parameter for this composition. An increase in the film thickness (d approx 60 nm) leads to a structural transition from the lattice-strained cubic to the relaxed rhombohedral phase, is accompanied by a shift of the Curie point (T sub C) to lower temperature and a frustration of the COI state. The magnetic and transport properties of the La sub 0 sub . sub 7 Ca sub 0 sub . sub 3 MnO sub 2 sub . sub 9 film with d approx 60 nm are similar to those exhibi...

  8. In(OH){sub 3} and In{sub 2}O{sub 3} nanorice and microflowers: morphology transformation and optical properties

    Energy Technology Data Exchange (ETDEWEB)

    Ren Weian; Liu Ying; Mei Zongwei; Wen Xiaogang, E-mail: wenxg2001@163.com [Sichuan University, School of Materials Science and Engineering (China); Wang Suhua [Chinese Academy of Sciences, Institute of Intelligent Machines (China)

    2013-02-15

    In this work, In(OH){sub 3} and In{sub 2}O{sub 3} nanostructures with controllable complex morphologies were successfully synthesized through a simple hydrothermal process followed by annealing. The In(OH){sub 3} nanostructures were synthesized using urea as the alkaline source at a relatively low temperature without any templates or surfactants. The morphology transformation of In(OH){sub 3} from nanorice to microflowers was observed. The In(OH){sub 3} nanorice are 180 nm in diameter and 550 nm in length, the microflowers are about 3 {mu}m in diameter and composed of thin nanoflakes with 4-nm thickness. In{sub 2}O{sub 3} with similar morphology was formed by annealing In(OH){sub 3} precursors. The nanostructures were characterized using X-ray diffraction, scanning electron microscopy, and transmission electron microscopy. Our results suggest that a new nucleation-growth-etching-regrowth mechanism can explain the morphology transformation from nanorice to flower-like frameworks. Raman spectrum and photoluminescence (PL) properties of In{sub 2}O{sub 3} were also measured, and a 3-nm blue-shift of PL spectrum was observed due to the thinness of the nanostructures.

  9. In vitro cytotoxicity tests of ZnO‐Bi{sub 2}O{sub 3}‐Mn{sub 2}O{sub 3}-based varistor fabricated from ZnO micro and nanoparticle powders on L929 mouse cells

    Energy Technology Data Exchange (ETDEWEB)

    Sendi, Rabab Khalid, E-mail: last-name3@hotmail.com, E-mail: shahromx@hotmail.com, E-mail: ameerah7@hotmail.com; Mahmud, Shahrom, E-mail: last-name3@hotmail.com, E-mail: shahromx@hotmail.com, E-mail: ameerah7@hotmail.com; Munshi, Ayman, E-mail: last-name3@hotmail.com, E-mail: shahromx@hotmail.com, E-mail: ameerah7@hotmail.com [Nano-optoelectronics Research and Technology Laboratory (N.O.R.), School of Physics, Universiti Sains Malaysia, 11800, Penang (Malaysia); Seeni, Azman, E-mail: azanseeni@gmail.com [Advanced Medical and Dental Institute (AMDI), Universiti Sains Malaysia, 13200, Bertam, Pulau Pinang (Malaysia)

    2014-10-24

    The present study investigated the cytotoxicity of ZnO‐Bi{sub 2}O{sub 3}‐Mn{sub 2}O{sub 3}-varistors. To this effect, ZnO‐Bi{sub 2}O{sub 3}‐Mn{sub 2}O{sub 3} varistors fabricated from ZnO micro-and nanoparticle powders are prepared via conventional ceramic processing method. The effects of ZnO particle size on the properties of ZnO varistors are also investigated. The strong solid-state reaction during sintering may be attributed to the high surface area of the 20 nm ZnO nanoparticles that promote strong surface reaction. The intensity of XRD peaks reflected the high degree of crystallinity of the ZnO nanoparticles. However, the width of the peaks in case of ZnO nanoparticles has increased due to the quantum size effect. The cytotoxicity evaluation of ZnO varistor was conducted on mouse connective tissue fibroblast cells (L929) using Trypan Blue Exclusion Assay analysis. The results show that the four types of varistor samples lead to cellular mitochondrial dysfunction, morphological modifications and apoptosis at the various concentration range and the toxic effects are obviously displayed in high concentration samples. 20nm-VDR is the most toxic materials followed by 40nm-VDR, P8-VDR, and W4-VDR in a descending order.

  10. Blue and red emission in wide band gap BaZrO{sub 3}:Yb{sup 3+},Tm{sup 3+}

    Energy Technology Data Exchange (ETDEWEB)

    Borja-Urby, R. [Centro de Investigaciones en Optica, A. C., C. P. 37150 Leon, Gto. (Mexico); Diaz-Torres, L.A., E-mail: ditlacio@cio.mx [Centro de Investigaciones en Optica, A. C., C. P. 37150 Leon, Gto. (Mexico); Salas, P. [Centro de Fisica Aplicada y Tecnologia Avanzada, Universidad Nacional Autonoma de Mexico, A. P. 1-1010, Queretaro 76000 (Mexico); Vega-Gonzalez, M. [Centro de Geociencias-Universidad Nacional Autonoma de Mexico, A. P. 1-1010, Queretaro 76000 (Mexico); Angeles-Chavez, C. [Instituto Mexicano del Petroleo, Programa de Ingenieria Molecular, Cd. Mexico D.F. 07730 (Mexico)

    2010-10-25

    Under NIR excitation at 967 intense blue and red photoluminescence (PL) emissions are observed at room temperature in codoped Tm{sup 3+}-Yb{sup 3+} barium zirconate (BaZrO{sub 3}:Yb,Tm) powders. Powders were prepared by a simple hydrothermal method, and present a wide band gap that depends on the total rare earth content due to the degree of disorder induced in the BaZrO{sub 3} lattice by the substitution of the rare earth ions. Rietveld refinements of the XRD patterns indicated the presence of primary nanocrystallites with sizes between 50 and 70 nm depending on the Tm{sup 3+} content. Scanning transmission electron microscopy (STEM) shows that these primary particles self-aggregated in larger secondary particles which present a regular morphology with sizes around 1 {mu}m. The intense blue and red PL emissions in BaZrO{sub 3} powders under 967 nm excitation are governed by energy transfer processes from Yb{sup 3+} ions to Tm{sup 3+} ions and crossrelaxation among Tm{sup 3+} ions.

  11. The film thickness dependent thermal stability of Al{sub 2}O{sub 3}:Ag thin films as high-temperature solar selective absorbers

    Energy Technology Data Exchange (ETDEWEB)

    Xiao Xiudi; Xu Gang, E-mail: xiudixiao@163.com; Xiong Bin; Chen Deming; Miao Lei [Chinese Academy of Sciences, Key Laboratory of Renewable Energy and Gas Hydrates, Guangzhou Institute of Energy Conversion (China)

    2012-03-15

    The monolayer Al{sub 2}O{sub 3}:Ag thin films were prepared by magnetron sputtering. The microstructure and optical properties of thin film after annealing at 700 Degree-Sign C in air were characterized by transmission electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and spectrophotometer. It revealed that the particle shape, size, and distribution across the film were greatly changed before and after annealing. The surface plasmon resonance absorption and thermal stability of the film were found to be strongly dependent on the film thickness, which was believed to be associated with the evolution process of particle diffusion, agglomeration, and evaporation during annealing at high temperature. When the film thickness was smaller than 90 nm, the film SPR absorption can be attenuated until extinct with increasing annealing time due to the evaporation of Ag particles. While the film thickness was larger than 120 nm, the absorption can keep constant even after annealing for 64 h due to the agglomeration of Ag particles. On the base of film thickness results, the multilayer Al{sub 2}O{sub 3}:Ag solar selective thin films were prepared and the thermal stability test illustrated that the solar selectivity of multilayer films with absorbing layer thickness larger than 120 nm did not degrade after annealing at 500 Degree-Sign C for 70 h in air. It can be concluded that film thickness is an important factor to control the thermal stability of Al{sub 2}O{sub 3}:Ag thin films as high-temperature solar selective absorbers.

  12. On the thermal stability of ultrafine-grained Al stabilized by in-situ amorphous Al{sub 2}O{sub 3} network

    Energy Technology Data Exchange (ETDEWEB)

    Balog, Martin, E-mail: martin.balog@savba.sk [Institute of Materials and Machine Mechanics, Slovak Academy of Sciences, Racianska 75, 83102 Bratislava (Slovakia); Department of Chemical Engineering and Materials Science, University of California, Davis, CA 95616 (United States); Hu, Tao [Department of Chemical Engineering and Materials Science, University of California, Davis, CA 95616 (United States); Krizik, Peter [Institute of Materials and Machine Mechanics, Slovak Academy of Sciences, Racianska 75, 83102 Bratislava (Slovakia); Castro Riglos, Maria Victoria [Centro Atómico Bariloche, Av. Bustillo 9.500 (8400) Bariloche, Río Negro (Argentina); Saller, Brandon D.; Yang, Hanry; Schoenung, Julie M.; Lavernia, Enrique J. [Department of Chemical Engineering and Materials Science, University of California, Davis, CA 95616 (United States)

    2015-11-11

    Bulk Al materials with average grain sizes of 0.47 and 2.4 µm, were fabricated by quasi-isostatic forging consolidation of two types of Al powders with average particle sizes of 1.3 and 8.9 μm, respectively. By utilizing the native amorphous Al{sub 2}O{sub 3} (am-Al{sub 2}O{sub 3}) film on the Al powders surfaces, a continuous, ∼7 nm thick, am-Al{sub 2}O{sub 3} network was formed in situ in the Al specimens. Systematic investigation of the changes to the am-Al{sub 2}O{sub 3} network embedded in the Al matrix upon heating and annealing up to 600 °C was performed by transmission electron microscopy (TEM). At the same time, the stability of the Al grain structure was studied by transmission Kikuchi diffraction (TKD), electron back-scatter diffraction (EBSD), and TEM. The am-Al{sub 2}O{sub 3} network remained stable after annealing at 400 °C for 24 h. In-situ TEM studies revealed that at temperatures ≥450 °C, phase transformation of the am-Al{sub 2}O{sub 3} network to crystalline γ-Al{sub 2}O{sub 3} particles occurred. After annealing at 600 °C for 24 h the transformation was completed, whereby only nanometric γ-Al{sub 2}O{sub 3} particles with an average size of 28 nm resided on the high angle grain boundaries of Al. Due to the pinning effect of γ-Al{sub 2}O{sub 3}, the Al grain and subgrain structures remained unchanged during annealing up to 600 °C for 24 h. The effect of the am-Al{sub 2}O{sub 3}→γ-Al{sub 2}O{sub 3} transformation on the mechanical properties of ultrafine- and fine-grained Al is discussed from the standpoint of the underlying mechanisms.

  13. Study of Pd-Sn/Al{sub 2}O{sub 3} catalysts prepared by an oxide colloidal route; Etude de catalyseurs Pd-Sn/Al{sub 2}O{sub 3} prepares par voie colloidale oxyde

    Energy Technology Data Exchange (ETDEWEB)

    Verdier, St.

    2001-09-01

    The oxide colloidal route, developed in the laboratory for mono-metallic catalysts, consists in preparing a metallic oxide hydro-sol which leads to the supported catalyst after deposition onto a support and an activation stage. In this work, this method has been adapted to the preparation of alumina supported bimetallic Pd-Sn catalysts to determine its interest for the control of the properties of the bimetallic phase (size, composition and structure). In the preliminary study concerning tin oxide sols, SnO{sub 2} (size=2,3 nm) and Sn{sub 6}O{sub 4}(OH){sub 4} (size = 25 nm) nano-particles were synthesized by neutralization respectively for tin(IV) and tin(H). The control through the pH of the aggregation of the PdO and SnO{sub 2} particles revealed that increasing oxide solubility promotes integral re-dispersion of the oxide particles. To synthesize oxide bimetallic sols, three strategies were defined. Copolymerization (formation of a mixed oxide nano-sol by cross condensation of both metals) does not lead to a mixed oxide Pd-Sn phase. Surface precipitation (neutralization of the second metal in the presence of the first oxide sol) yields nano-particles of both oxides in close interaction. Adsorption (adsorption of the second metal onto the first oxide sol) significantly occurs when contacting tin with a basic PdO sol (hydrolytic adsorption). The characterization and the assessment of the catalytic properties (selective hydrogenation of buta-1,3-diene) of the catalysts prepared by deposition of oxide bimetallic sols showed that the oxide colloidal route allows the control of the properties of the supported bimetallic phase. Moreover, our results display that both Pd-Sn alloy formation and,aggregation of the metallic particles contribute to increase the selectivity for this reaction. (author)

  14. Synthesis and electrochemical study of Mg{sub 1.5}MnO{sub 3}: A defect spinel cathode for rechargeable magnesium battery

    Energy Technology Data Exchange (ETDEWEB)

    Saha, Partha [Department of Bioengineering, Swanson School of Engineering, University of Pittsburgh, PA 15261 (United States); US Department of Energy, National Energy Technology Laboratory, Morgantown, WV 26507 (United States); Jampani, Prashanth H., E-mail: pjampani@pitt.edu [Department of Bioengineering, Swanson School of Engineering, University of Pittsburgh, PA 15261 (United States); Hong, DaeHo [Department of Bioengineering, Swanson School of Engineering, University of Pittsburgh, PA 15261 (United States); Gattu, Bharat [Mechanical Engineering and Materials Science, Swanson School of Engineering, University of Pittsburgh, PA 15261 (United States); Poston, James A.; Manivannan, Ayyakkannu [US Department of Energy, National Energy Technology Laboratory, Morgantown, WV 26507 (United States); Datta, Moni Kanchan [Department of Bioengineering, Swanson School of Engineering, University of Pittsburgh, PA 15261 (United States); US Department of Energy, National Energy Technology Laboratory, Morgantown, WV 26507 (United States); Kumta, Prashant N., E-mail: pkumta@pitt.edu [Department of Bioengineering, Swanson School of Engineering, University of Pittsburgh, PA 15261 (United States); US Department of Energy, National Energy Technology Laboratory, Morgantown, WV 26507 (United States); Mechanical Engineering and Materials Science, Swanson School of Engineering, University of Pittsburgh, PA 15261 (United States); Chemical and Petroleum Engineering, Swanson School of Engineering, University of Pittsburgh, PA 15261 (United States); School of Dental Medicine, University of Pittsburgh, PA 15261 (United States); Center for Complex Engineered Multifunctional Materials, University of Pittsburgh, Pittsburgh, PA 15261 (United States)

    2015-12-15

    Graphical abstract: Mg{sub 1.5}MnO{sub 3}, a defect oxide spinel derived by the Pechini route, was tested as cathode for rechargeable magnesium battery. TEM and XRD analyses of Mg{sub 1.5}MnO{sub 3} shows the formation of ∼100 nm sized nano particles in the cubic defect spinel structure (space group: Fd3m; unit cell: 0.833294 nm). Cyclic voltammetry illustrates a reversible reaction occurring between 0.3 and 1.5 V versus magnesium. Galvanostatic cycling of the Mg{sub 1.5}MnO{sub 3} cathode exhibits a low capacity of ∼12.4 mAh/g up to 20 cycle with ∼99.9% Coulombic efficiency when cycled at a current rate of ∼C/27. XPS (X-ray photoelectron spectroscopy) surface probe of magnesiated/de-magnesiated electrodes confirm a change in the redox center of Mn-ions during intercalation/de-intercalation of Mg-ion from the Mg{sub 1.5}MnO{sub 3} electrode. The low capacity of Mg{sub 1.5}MnO{sub 3} electrode mainly stem from the kinetic limitation of Mg-ion removal from the defect oxide spinel as the electrochemical impedance spectroscopy results of electrodes after 1st and 2nd cycle show that charge transfer resistance, R{sub e}, increases post charge state whereas interfacial resistance, R{sub i}, increases after discharge state, respectively. - Highlights: • Pechini process yields 100 nm sized particles of the defect cubic spinel Mg{sub 1.5}MnO{sub 3}. • Stable capacity of ∼12.4 mAh/g obtained at C/27 rate and 99.9% Coulombic efficiency. • XPS shows change in valence state of Mn{sup 3+}/Mn{sup 4+} center with cycling. • Low capacity stems from increase in charge-transfer and interfacial resistances with cycling. - Abstract: Mg{sub 1.5}MnO{sub 3}, a defect oxide spinel (space group: Fd3m; unit cell: 0.833294 nm) of particle size ∼100 nm derived by the Pechini route was tested as a cathode for rechargeable magnesium battery. Cyclic voltammetry illustrates a reversible reaction occurring in the 0.3–2.0 V potential window versus magnesium. The spinel however

  15. Luminescent characteristics of UV excited Sr{sub 0.5}Ca{sub 0.5}TiO{sub 3}: Pr{sup 3+} reddish-orange phosphor

    Energy Technology Data Exchange (ETDEWEB)

    Vidyadharan, Viji; Mohan P, Remya; Joseph, Cyriac; Unnikrishnan, N.V.; Biju, P.R., E-mail: prb.mgu@gmail.com

    2016-02-15

    Pr{sup 3+} doped Sr{sub 0.5}Ca{sub 0.5}TiO{sub 3} phosphors were synthesised by solid state reaction process. The structure, surface morphology and photoluminescence of the prepared phosphors were analysed using XRD, SEM and photoluminescence spectroscopy respectively. The XRD pattern confirmed orthorhombic perovskite structure of the Sr{sub 0.5}Ca{sub 0.5}TiO{sub 3}: x Pr{sup 3+} phosphor. Agglomeration of particles with irregular shapes is observed from the SEM images. The emission spectra of Sr{sub 0.5}Ca{sub 0.5}TiO{sub 3}: x Pr{sup 3+} phosphor shows the samples can be effectively excited with UV light at 336 nm and exhibit a strong reddish-orange emission at 611 nm. Concentration dependence of emission intensity shows concentration quenching effect on increasing Pr{sup 3+} concentration after x = 0.1 because of dipole–dipole interaction. Using Blasse's formula, critical distance for energy transfer was calculated. The CIE co-ordinates, CCT, colour purity and luminescence decay of the prepared phosphors were also calculated. These results offer the prepared phosphor as a suitable candidate for various photonic applications. - Highlights: • Sr{sub 0.5}Ca{sub 0.5}TiO{sub 3}: x Pr{sup 3+} perovskite structured phosphors were synthesized. • Under UV excitation, the PL spectra show strong reddish-orange emission. • The emission from {sup 3}P{sub J} levels of Pr{sup 3+} were absent due to the presence of IVCT band. • Concentration quenching due to dipole–dipole interaction was observed. • For x = 0.1, sample shows a maximum emission intensity with 91.7% colour purity.

  16. Optimizing magnetic anisotropy of La{sub 1−x}Sr{sub x}MnO{sub 3} nanoparticles for hyperthermia applications

    Energy Technology Data Exchange (ETDEWEB)

    Rashid, Amin ur [Magnetism Laboratory, Department of Physics, COMSATS Institute of Information Technology, Islamabad (Pakistan); Department of Applied Physical and Material Sciences, University of Swat, Khyber Pakhtunkhwa (Pakistan); Manzoor, Sadia, E-mail: sadia_manzoor@comsats.edu.pk [Magnetism Laboratory, Department of Physics, COMSATS Institute of Information Technology, Islamabad (Pakistan)

    2016-12-15

    Maximizing the magnetothermal response of magnetic nanoparticles (MNP's) for hyperthermia applications is a complex problem, because it depends sensitively upon interrelated magnetic and structural parameters. The task is somewhat simpler for systems with fixed composition, e.g. Fe{sub 3}O{sub 4} or CoFe{sub 2}O{sub 4}, in which the particle size is the only means of modifying the magnetic anisotropy, and hence the magnetothermal response. In the La{sub 1−x}Sr{sub x}MnO{sub 3} system however, the magnetic interactions as well as the particle size both change with the Sr concentration x, which makes it a much more complex system for which to optimize the hyperthermia response. We have investigated the effect of magnetic anisotropy on the magnetothermal response of La{sub 1−x}Sr{sub x}MnO{sub 3} nanoparticles as a function of the particle size as well as the Sr concentration x where 0.20≤x≤0.45. The optimum particle size range is 25–30 nm for all concentrations, where the specific absorption rate (SAR) has a maximum. The linear response theory (LRT) has been applied to this system and good agreement has been found between the experimental and theoretically determined values of the SAR for samples lying in the single domain regime and having large enough anisotropy energies. The agreement is much better for the intermediate concentrations of 0.27 and 0.33, because of their large anisotropy as compared to other concentrations. It is concluded that the LRT can be successfully used to predict the SAR of these nanoparticles, provided they possess large enough effective anisotropies. Values of the ILP have been obtained for these samples and found to be comparable to those of magnetite and some commercial ferrofluids. - Highlights: • For La{sub 1-x}Sr{sub x}MnO{sub 3} system, the magnetic anisotropy is determined not only by the particle size, but also by the strontium content x, we made a systematic study of both these parameters on its magnetothermal

  17. Formation of nanoparticles and defects in YBa{sub 2}Cu{sub 3}O{sub 7-{delta}} prepared by the metal organic deposition process

    Energy Technology Data Exchange (ETDEWEB)

    Goswami, R. [Naval Research Laboratory, Washington, DC 20375 (United States); SAIC, Washington, DC 20003 (United States)], E-mail: goswami@anvil.nrl.navy.mil; Holtz, R.L. [Naval Research Laboratory, Washington, DC 20375 (United States); Rupich, M.W. [American Superconductors Inc., Westborough, MA 01581 (United States); Spanos, G. [Naval Research Laboratory, Washington, DC 20375 (United States)

    2007-11-15

    Nanoparticles and defects have been investigated using transmission electron microscopy in fully reacted YBa{sub 2}Cu{sub 3}O{sub 7-{delta}} (YBCO), prepared by the metal-organic deposition (MOD) process. Two types of particles, Y{sub 2}O{sub 3} and CuY{sub 2}O{sub 5}, ranging from 10 to 100 nm, have been observed in the YBCO matrix. The YBCO contains a large number of planar defects and a considerable number of (1 1 0) rotational twins. Details of the nanoparticles and defects in the MOD-processed YBCO films are presented in this paper.

  18. Rapid preparation of ultrafine BaSO{sub 3} by SO{sub 2} storage material

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Fei; Sha, Feng; Qiao, Xian Shu; Zhao, Tian Xiang; Guo, Bo; Zhang, Jian Bin [College of Chemical Engineering, Inner Mongolia University of Technology, Huhhot (Korea, Republic of)

    2017-01-15

    In this work, a green and efficient process was developed for the preparation of ultrafine BaSO{sub 3} with layered nanostructure surface via the reaction of BaCl{sub 2} with a SO{sub 2} storage material (SO{sub 2}SM) at room temperature. The absorption of SO{sub 2} with equimolar ethylenediamine (EDA) and ethylene glycol (EG) afforded SO{sub 2}SM, which not only offered alkyl sulfite but also released EDA and EG that served as efficient surfactants to promote the formation of BaSO{sub 3} with spherical morphology and porous structure in the process of synthesis of ultrafine BaSO{sub 3}. The factors affecting the morphology and size of BaSO{sub 3} particle were assessed by investigating the effects of SO{sub 2}SM concentration, BaCl{sub 2} concentration, stirring time and speed. It was found that a higher SO{sub 2}SM concentration led to a higher degree of supersaturation, and the particle size of BaSO{sub 3} could be reduced by increasing SO{sub 2}SM concentration. Moreover, under the identified optimal reaction conditions, ultrafine BaSO{sub 3} was obtained with an average diameter of 450 nm. In addition, a plausible formation process of BaSO{sub 3} was proposed to explain the observed reaction results. Overall, the developed process in this work provides an efficient method for the capture, utilization, and conversion of SO{sub 2} into a valuable chemical.

  19. Particle morphology and magnetic properties of Ba{sub 0.5}Sr{sub 0.5}Fe{sub 12}O{sub 19} powder calcined conventionally and by microwave heating

    Energy Technology Data Exchange (ETDEWEB)

    Kanagesan, S., E-mail: kanagu1980@gmail.com [Materials Synthesis and Characterization Laboratory (MSCL), Institute of Advanced Technology (ITMA), Universiti Putra Malaysia, Serdang 43400, Selangor (Malaysia); Hashim, M. [Materials Synthesis and Characterization Laboratory (MSCL), Institute of Advanced Technology (ITMA), Universiti Putra Malaysia, Serdang 43400, Selangor (Malaysia); Physics Department, Faculty of Science, Universiti Putra Malaysia, Serdang 43400, Selangor (Malaysia); Jesurani, S. [Department of Physics, Jeyaraj Annapackium College for Women, Periyakulam 625601, Tamil Nadu (India); Kalaivani, T. [Center for material science and Nano Devices, Department of Physics, SRM University, Kattankulathur 603203, Tamil Nadu (India); Ismail, I.; Shafie, M.S.E. [Materials Synthesis and Characterization Laboratory (MSCL), Institute of Advanced Technology (ITMA), Universiti Putra Malaysia, Serdang 43400, Selangor (Malaysia)

    2012-12-05

    Highlights: Black-Right-Pointing-Pointer Synthesis of Ba{sub 0.5}Sr{sub 0.5}Fe{sub 12}O{sub 19} by sol-gel technique. Black-Right-Pointing-Pointer Crystallization temperature is reduced to 900 Degree-Sign C due to the addition of D-Fructose. Black-Right-Pointing-Pointer Results of conventional and microwave calcined samples are reported. - Abstract: Barium strontium hexaferrite (Ba{sub 0.5}Sr{sub 0.5}Fe{sub 12}O{sub 19}-BSF) has been prepared by sol-gel process involving use of D-Fructose as a fuel. The prepared precursor was calcined in two different calcinations techniques conventional and microwave furnace. X-ray powder diffraction studies confirmed the formation of single phase Ba{sub 0.5}Sr{sub 0.5}Fe{sub 12}O{sub 19}. HR-SEM results show the morphology of the particles is hexagonal structures in platelet form. The average particle size of conventionally calcined BSF powder is 100-250 nm and that of microwave calcined powder is 30-100 nm. The broad hysteresis loop reveals that powder is well crystallized and exhibits hard magnetic properties.

  20. Characterization of γ- Al{sub 2}O{sub 3} nanopowders synthesized by Co-precipitation method

    Energy Technology Data Exchange (ETDEWEB)

    Jbara, Ahmed S., E-mail: ahmedsbhe@yahoo.com [Center for Sustainable Nanomaterials, Universiti Teknologi Malaysia, Skudai - 81310, Johor Bahru (Malaysia); Physics Department, Science College, Al-Muthanna University, Samawah - 66001 (Iraq); Department of Physics, Faculty of Science, Universiti Teknologi Malaysia, Skudai - 81310, Johor Bahru (Malaysia); Othaman, Zulkafli [Center for Sustainable Nanomaterials, Universiti Teknologi Malaysia, Skudai - 81310, Johor Bahru (Malaysia); Department of Physics, Faculty of Science, Universiti Teknologi Malaysia, Skudai - 81310, Johor Bahru (Malaysia); Ati, Ali A. [Department of Physics, Faculty of Science, Universiti Teknologi Malaysia, Skudai - 81310, Johor Bahru (Malaysia); Saeed, M.A., E-mail: moalsd@gmail.com [Department of Physics, Faculty of Science, Universiti Teknologi Malaysia, Skudai - 81310, Johor Bahru (Malaysia); Division of Science and Technology, University of Education, Township, Lahore - 54770 (Pakistan)

    2017-02-15

    Co-precipitation technique has been used to synthesize gamma-Al{sub 2}O{sub 3} (γ-Al{sub 2}O{sub 3}) nanopowders under annealing temperature effect. The crystalline phase and purity for the prepared powder were characterized by different spectroscopy techniques. XRD analysis confirms the gamma phase of alumina nanopowders with particle diameter ranging from 6 to 24 nm, which confirms the quantum dots formation, which is also supported by the BET measurement. The surface area of the prepared nanopowders is in the range of 109–367 m{sup 2}/g. Morphology analysis indicates that γ-Al{sub 2}O{sub 3} nanopowders are consisted of grains almost spherical in shape. Some agglomeration of nanoparticles occurs, which become more regular hexagonal shaped with the increasing annealing temperature. The small nanoparticles size and the high surface area from a simple procedure for preparing γ-Al{sub 2}O{sub 3} may make it more suitable for use as an adsorbent for malachite green. - Highlights: • Co-precipitation technique is used to synthesize gamma- Al{sub 2}O{sub 3} nanopowders. • Pure gamma- Al{sub 2}O{sub 3} phase was obtained having maximum nanoparticle size is 24 nm. • The quantum dots were formed inside powder. • High surface area of nanopowders at the low annealing temperature. • Increasing annealing temperature causes the hexagonal agglomeration shape.

  1. Preparation of nano-sized {alpha}-Al{sub 2}O{sub 3} from oil shale ash

    Energy Technology Data Exchange (ETDEWEB)

    An, Baichao; Wang, Wenying; Ji, Guijuan; Gan, Shucai; Gao, Guimei; Xu, Jijing; Li, Guanghuan [College of Chemistry, Jilin University, Changchun 130026 (China)

    2010-01-15

    Oil shale ash (OSA), the residue of oil shale semi-coke roasting, was used as a raw material to synthesize nano-sized {alpha}-Al{sub 2}O{sub 3}. Ultrasonic oscillation pretreatment followed by azeotropic distillation was employed for reducing the particle size of {alpha}-Al{sub 2}O{sub 3}. The structural characterization at molecular and nanometer scales was performed using X-ray diffraction (XRD), transmission electron microscopy (TEM), respectively. The interaction between alumina and n-butanol was characterized by Fourier transform infrared spectroscopy (FT-IR). The results revealed that the crystalline phase of alumina nanoparticles was regular and the well dispersed alumina nanoparticles had a diameter of 50-80 nm. In addition, the significant factors including injection rate of carbon oxide (CO{sub 2}), ultrasonic oscillations, azeotropic distillation and surfactant were investigated with respect to their effects on the size of the alumina particles. (author)

  2. Dust Explosion Characteristics of Agglomerated 35 nm and 100 nm Aluminum Particles

    Directory of Open Access Journals (Sweden)

    Hong-Chun Wu

    2010-01-01

    Full Text Available In the experiment, nanoparticles of 35 nm Al and 100 nm Al powders, respectively, formed particles with average sizes of 161 nm and 167 nm in agglomeration. The characteristics of dust cloud explosions with the two powder sizes, 35 nm and 100 nm, revealed considerable differences, as shown here: (dp/dtmax-35 nm = 1254 bar/s, (dp/dtmax-100 nm = 1105 bar/s; Pmax-35 nm = 7.5 bar, Pmax-100 nm = 12.3 bar, and MEC-35 nm = 40 g/m3, MEC-100 nm = 50 g/m3. The reason of Pmax-35 nm value is smaller than Pmax-100 nm may be due to agglomeration. From an analysis of the explosive residue, the study found that nanoparticles of 35 nm Al powder became filamentous strands after an explosion, where most of 100 nm Al nanoparticles maintained a spherical structure, This may be because the initial melting temperature of 35 nm Al is 435.71°C, while that for 100 nm Al is 523.58°C, higher by 87.87°C. This study discovered that explosive property between the 35 nm Al and 100 nm Al powders after agglomeration were different.

  3. Magnetic BaFe{sub 12}O{sub 19} nanofiber filter for effective separation of Fe{sub 3}O{sub 4} nanoparticles and removal of arsenic

    Energy Technology Data Exchange (ETDEWEB)

    Byun, Jeehye; Patel, Hasmukh A.; Yavuz, Cafer T., E-mail: yavuz@kaist.ac.kr [Korea Advanced Institute of Science and Technology (KAIST), Graduate School of EEWS (Korea, Republic of)

    2014-12-15

    Magnetic nanoparticles are promising in applications where magnetic separation is intended, although material losses via leaching mechanisms are often inevitable. Magnetic separations with widely available permanent magnets can effectively trap particles, leading to a complete removal of used or waste particles. In this report, we first demonstrate the synthesis of the thinnest (112.7 ± 16.4 nm) and most magnetic (71.96 emu g{sup −1}) barium hexaferrite (BaFe{sub 12}O{sub 19}, BHF—fridge magnet) via an organic solvent-free electrospinning procedure. When the fibers are then packed into a column, they clearly remove 12 nm magnetite (Fe{sub 3}O{sub 4}) nanoparticles quantitatively. The same BHF cartridge also removes more than 99.9 % As-treated magnetite nanoparticles at capacities up to 70 times of its weight. As a result, one liter of 150 μg L{sup −1} As-contaminated water can be purified rapidly at a material cost of less than 2 US cents.

  4. Development of Tb{sup 3+} activated gadolinium aluminate garnet (Gd{sub 3}Al{sub 5}O{sub 12}) as highly efficient green-emitting phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Teng, Xin; Li, Jinkai, E-mail: mse_lijk@ujn.edu.cn; Duan, Guangbin; Liu, Zongming, E-mail: ost_liuzm@ujn.edu.cn

    2016-11-15

    The powder processing of (Gd{sub 1-x}Tb{sub x}){sub 3}Al{sub 5}O{sub 12} (GdAG:Tb{sup 3+}) solid solutions was achieved through precursor synthesized via carbonate precipitation, followed by calcination at 1500 °C. The performance of the GdAG:Tb{sup 3+} phosphors were characterized by the combined techniques of XRD, FE-SEM, HR-TEM, PLE/PL, and fluorescence decay analyses. Lower Tb{sup 3+} doping can stabilize the crystal structure of GdAG garnet against its thermal decomposition. The GdAG:Tb{sup 3+} phosphors with good dispersion and fairly uniform particle morphology exhibit a series of {sup 5}D{sub 4}–{sup 7}F{sub J} transitions of Tb{sup 3+} with strongest green emission at ~544 nm ({sup 5}D{sub 4}–{sup 7}F{sub 5} transitions of Tb{sup 3+}) under UV excitation at ~277 nm (4f{sup 8}−4f{sup 7}5d{sup 1} transition of Tb{sup 3+}). The later is overlapping with {sup 8}S{sub 7/2}–{sup 6}I{sub J} intra f–f transition of Gd{sup 3+} indirectly suggesting the existence of energy transfer from Gd{sup 3+} to Tb{sup 3+}. With the Gd{sup 3+}–Tb{sup 3+} energy transfer, higher Tb{sup 3+} emission and quantum efficiency than the well-known YAG:Tb{sup 3+} and LuAG:Tb{sup 3+} were obtained in the present work. The effects of Tb{sup 3+} content on luminescent property of the phosphor, especially PLE/PL properties, fluorescence lifetime and quantum efficient, were thoroughly investigated, which were also compared to those of Tb{sup 3+}-activated YAG and LuAG compounds. The CIE chromaticity coordinates and quenching concentration of GdAG:Tb{sup 3+} were determined to be (~0.37, ~0.56) and ~10 at%, respectively. Keeping the optimum Tb{sup 3+} content at ~10 at%, the (Gd{sub 0.9}Tb{sub 0.1})AG phosphor possesses high internal and external quantum efficiencies of ~88.7% and ~73.6% under ~277 nm excitation, respectively. Owing to its improved luminescent property and high theoretical density, the phosphors of (Gd{sub 1-x}Tb{sub x})AG garnet developed in the present work are

  5. Role of Gd{sup 3+} ion on downshifting and upconversion emission properties of Pr{sup 3+}, Yb{sup 3+} co-doped YNbO{sub 4} phosphor and sensitization effect of Bi{sup 3+} ion

    Energy Technology Data Exchange (ETDEWEB)

    Dwivedi, A.; Rai, S. B., E-mail: sbrai49@yahoo.co.in [Department of Physics, Banaras Hindu University, Varanasi 221005 (India); Mishra, Kavita [Department of Physics, University of Lucknow, Lucknow 226007 (India)

    2016-07-28

    Dual-mode luminescence (downshifting-DS and upconversion-UC) properties of Pr{sup 3+}/Yb{sup 3+} co-doped Y{sub 1−x}Gd{sub x}NbO{sub 4} (x = 0.0, 0.5, and 1.0) phosphors synthesized by solid state reaction technique have been explored with and without Gd{sup 3+} ion. The structural characterizations (XRD, SEM, and FTIR) confirm the pure phase of YNbO{sub 4} phosphor. Further, with the Gd{sup 3+} ion co-doping, the YNbO{sub 4} phosphors having a random shape and the large particle size are found to be transformed into nearly spherical shape particles with the reduced particle size. The optical band gaps (E{sub g}) of Y{sub 1−x}Gd{sub x}NbO{sub 4} (x = 0.00, 0.25, 0.50, and 1.00) calculated from UV-Vis-NIR measurements are ∼3.69, 4.00, 4.38, and 4.44 eV, respectively. Moreover, YNbO{sub 4} phosphor is a promising blue emitting material, whereas Y{sub 1−x−y−z}Pr{sub y}Yb{sub z}Gd{sub x}NbO{sub 4} phosphor gives intense green, blue, and red emissions via dual-mode optical processes. The broad blue emission arises due to (NbO{sub 4}){sup 3−} group of the host with λ{sub ex} = 264 nm, whereas Pr{sup 3+} doped YNbO{sub 4} phosphor gives dominant red and blue emissions along with comparatively weak green emission on excitation with λ{sub ex} = 300 nm and 491 nm. The concentration dependent variation in emission intensity at 491 nm ({sup 3}P{sub 0}→{sup 3}H{sub 4} transition) and 612 nm ({sup 1}D{sub 2}→{sup 3}H{sub 4} transition); at 612 nm ({sup 1}D{sub 2}→{sup 3}H{sub 4} transition) and 658 nm ({sup 3}P{sub 0}→{sup 3}F{sub 2} transition) of Pr{sup 3+} ion in YNbO{sub 4} phosphor with λ{sub ex} = 300 nm and 491 nm excitations, respectively, has been thoroughly explored and explained by the cross-relaxation process through different channels. The sensitization effect of Bi{sup 3+} ion co-doping on DS properties of the phosphor has also been studied. The observed DS results have been optimized by varying the

  6. Biofunctionalized ferromagnetic CoPt{sub 3}/polymer nanocomposites

    Energy Technology Data Exchange (ETDEWEB)

    Martins, M A [Department of Chemistry, CICECO, University of Aveiro, 3810-193 Aveiro (Portugal); Neves, M C [Department of Chemistry, CICECO, University of Aveiro, 3810-193 Aveiro (Portugal); Esteves, A C C [Department of Chemistry, CICECO, University of Aveiro, 3810-193 Aveiro (Portugal); Girginova, P I [Department of Chemistry, CICECO, University of Aveiro, 3810-193 Aveiro (Portugal); Guiomar, A J [Department of Biochemistry and CNC, University of Coimbra, 3001-401 Coimbra (Portugal); Amaral, V S [Department of Physics, CICECO, University of Aveiro, 3810-193 Aveiro (Portugal); Trindade, T [Department of Chemistry, CICECO, University of Aveiro, 3810-193 Aveiro (Portugal)

    2007-05-30

    Magnetic latexes were prepared by the encapsulation of organically capped CoPt{sub 3} nanoparticles via miniemulsion in situ radical polymerization of tert-butyl acrylate (tBA). This is the first example of a CoPt{sub 3} based polymer nanocomposite showing ferromagnetic behaviour at room temperature. Each nanocomposite particle contains a magnetic core composed of CoPt{sub 3} nanoparticles (d{approx}7 nm, a{sub 0} = 3.848 A) encapsulated by poly(t-butyl acrylate). The CoPt{sub 3}/PtBA latexes contain polyester groups that can be readily hydrolysed, rendering the surface with carboxylic functionalities and hence allowing bioconjugation. Complementary to such surface modification experiments, we report that bovine IgG antibodies can bind to the magnetic latexes, and the potential of the nanocomposites for in vitro specific bioapplications is discussed.

  7. Synthesis and anomalous magnetic properties of LaFeO{sub 3} nanoparticles by hot soap method

    Energy Technology Data Exchange (ETDEWEB)

    Fujii, Tatsuo, E-mail: tfujii@cc.okayama-u.ac.jp [Department of Applied Chemistry, Okayama University, Tsushima-naka 3-1-1, Okayama 700-8530 (Japan); Matsusue, Ikkoh; Nakatsuka, Daisuke; Nakanishi, Makoto; Takada, Jun [Department of Applied Chemistry, Okayama University, Tsushima-naka 3-1-1, Okayama 700-8530 (Japan)

    2011-10-03

    Highlights: {yields} Nanocrystalline LaFeO{sub 3} particles were synthesized by using hot soap technique. {yields} Average diameter of the obtained LaFeO{sub 3} nanoparticles was about 15 nm. {yields} They exhibited superparamagnetic behavior with a blocking temperature of 30 K. {yields} Large magnetization due to the presence of uncompensated surface spins was induced. - Abstract: Nanocrystalline LaFeO{sub 3} particles were synthesized at low temperatures by using hot soap technique. The synthesis was based on the thermal decomposition of organometallic compounds precipitated in a hot coordinating solvent. Moderate heat treatment at low temperature far below the combustion point of organic compounds produced spherical LaFeO{sub 3} nanoparticles with average diameter of about 15 nm. The crystalline phase, structure and particle size of obtained products were characterized by X-ray diffraction, infrared spectroscopy and transmission electron microscopy observations. In spite of the antiferromagnetic nature of bulk LaFeO{sub 3}, the obtained nanoparticles exhibited anomalous large magnetization. Superparamagnetic behavior with a blocking temperature of about 30 K was observed in both magnetization and Moessbauer spectroscopic analyses.

  8. Luminescence properties of Ce{sup 3+} and Tb{sup 3+} co-activated ZnAl{sub 2}O{sub 4} phosphor

    Energy Technology Data Exchange (ETDEWEB)

    Tshabalala, K.G. [Department of Physics, University of the Free State, Bloemfontein, ZA 9300 (South Africa); Cho, S.-H.; Park, J.-K. [Nano-Materials Center, Korea Institute of Science and Technology, Cheongryang, Seoul 130-650 (Korea, Republic of); Pitale, Shreyas S.; Nagpure, I.M.; Kroon, R.E.; Swart, H.C. [Department of Physics, University of the Free State, Bloemfontein, ZA 9300 (South Africa); Ntwaeaborwa, O.M., E-mail: ntwaeab@ufs.ac.za [Department of Physics, University of the Free State, Bloemfontein, ZA 9300 (South Africa)

    2012-05-15

    In this study, a solution combustion method was used to prepare green emitting Ce{sup 3+}-Tb{sup 3+} co-activated ZnAl{sub 2}O{sub 4} phosphor. The samples were annealed at 700 Degree-Sign C in air or hydrogen atmosphere to improve their crystallinity and optical properties. X-ray diffraction study confirmed that both as-prepared and post-preparation annealed samples crystallized in the well known cubic spinel structure of ZnAl{sub 2}O{sub 4}. An agglomeration of irregular platelet-like particles whose surfaces were encrusted with smaller spheroidal particles was confirmed by scanning electron microscopy (SEM). The fluorescence data collected from the annealed samples with different concentrations of Ce{sup 3+} and Tb{sup 3+} show the enhanced green emission at 543 nm associated with {sup 5}D{sub 4}{yields}{sup 7}F{sub 5} transitions of Tb{sup 3+}. The enhancement was attributed to energy transfer from Ce{sup 3+} to Tb{sup 3+}. Possible mechanism of energy transfer via a down conversion process is discussed. Furthermore, cathodoluminescence (CL) intensity degradation of this phosphor was also investigated and the degradation data suggest that the material was chemically stable and the CL intensity was also stable after 10 h of irradiation by a beam of high energy electrons.

  9. One-step synthesis Fe{sub 3}N surface-modified Fe{sub 3}O{sub 4} nanoparticles with excellent lithium storage ability

    Energy Technology Data Exchange (ETDEWEB)

    Li, Yabin [College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123 (China); Institute of Chemical Power Sources, Soochow University, Suzhou 215006 (China); Yan, Yuerong [Department of Science and Technology, Jiaozuo Teachers College, Jiaozuo 454000 (China); Ming, Hai, E-mail: lunaticmh@163.com [College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123 (China); Institute of Chemical Power Sources, Soochow University, Suzhou 215006 (China); Zheng, Junwei, E-mail: jwzheng@suda.edu.cn [College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123 (China); Institute of Chemical Power Sources, Soochow University, Suzhou 215006 (China)

    2014-06-01

    The Fe{sub 3}N modified Fe{sub 3}O{sub 4} nanoparticles with an excellent performance in lithium-ion batteries were prepared via a one-step and an efficient method. The layer of Fe{sub 3}N could significantly decrease the variation of volume and enhance the conductivity of Fe{sub 3}O{sub 4} simultaneously during the reaction of lithium ions in the charge-discharge process. There are two main advantages of this material: (1) their size distribution, ranging from 100 to 500 nm and (2) the fact that these particles are connected with each other by the Fe{sub 3}N layer. These two features allow such material to exhibit a high reversible capacity of 739 and 620 mA h g{sup −1} after each 60 cycles at the current density of 50 and 200 mA g{sup −1}, respectively. More importantly, since its introduction, this new concept of coating metal oxides with a layer of metal nitride to form core-shell structured metal oxide@metal nitride can be widely applied in the fields of catalysis, electrochemistry, energy, environmental and materials science with improved performance.

  10. Nanocasting synthesis of co-doped In{sub 2}O{sub 3}: a 3D diluted magnetic semiconductor composed of nanospheres

    Energy Technology Data Exchange (ETDEWEB)

    Deng, Ni; Li, Jing; Hong, Bo; Jin, Dingfeng; Peng, Xiaoling; Wang, Xinqing; Ge, Hongliang; Jin, Hongxiao, E-mail: hxjin@cjlu.edu.cn, E-mail: hxjin5704@qq.com [China Jiliang University, Zhejiang Province Key Laboratory of Magnetism, College of Materials Science and Engineering (China)

    2015-04-15

    Mesoporous 3D nanosphere arrays of In{sub 2−x}Co{sub x}O{sub 3} (x = 0, 0.01, 0.03, 0.05, and 0.07) were synthesized via nanocasting using the mesoporous silica LP-FDU-12 as a hard template. The mesostructure, morphology, optical properties, and magnetic properties of the materials were determined. The diameter of the nanospheres was about 15–22 nm, and the nanospheres stacked into 0.5–5 μm arrays (particles). The data revealed that the Co ions entered the lattice of the In{sub 2}O{sub 3} bixbyite phase leading to a reduction of the cell parameter. The result also demonstrated that the size of the mesostructured ordering was approximately the same as the particle diameter. Moreover, the optical band gap of Co-doped In{sub 2}O{sub 3} decreased monotonically with the increase of Co concentration and the room-temperature photoluminescence was also observed. The un-doped In{sub 2}O{sub 3} exhibited a ferromagnetic behavior superimposed on a diamagnetic background, while the doped In{sub 2}O{sub 3} displayed a room-temperature ferromagnetic behavior superimposed on a paramagnetic background, which may be correlated with the surface texture of the mesostructure. The mesoporous diluted magnetic semiconductors may find their applications in spintronic nanodevices because of their 3D uniform arrangement of nanospheres and their room-temperature ferromagnetic behavior.

  11. The effect of sintering time on synthesis of in situ submicron {alpha}-Al{sub 2}O{sub 3} particles by the exothermic reactions of CuO particles in molten pure Al

    Energy Technology Data Exchange (ETDEWEB)

    Dikici, Burak, E-mail: burakdikici@yyu.edu.tr [Yuzuncu Yil University, Department of Mechanical Engineering, 65080 Van (Turkey); Gavgali, Mehmet [Ataturk University, Department of Mechanical Engineering, 25240 Erzurum (Turkey)

    2013-02-25

    Highlights: Black-Right-Pointing-Pointer Al-Cu/Al{sub 2}O{sub 3} composites were prepared successfully by means of hot pressing method. Black-Right-Pointing-Pointer Sintering time of the Al-CuO system effect the reaction rate and formation of Al{sub 2}O{sub 3}. Black-Right-Pointing-Pointer Increase in sintering time accelerates formation of submicron in situ {alpha}-Al{sub 2}O{sub 3} phase. Black-Right-Pointing-Pointer Hardness of the sintered composite for 30 min at 1000 Degree-Sign C increased from 60 to 174 HV. - Abstract: In this study, in situ {alpha}-Al{sub 2}O{sub 3} reinforcing particles have been successfully synthesised in an Al-Cu matrix alloy by means of the conventional Hot Pressing (HP) method. The effect of sintering time on the forming of the {alpha}-Al{sub 2}O{sub 3} phase at 1000 Degree-Sign C was investigated using Differential Thermal Analysis (DTA), X-ray Diffraction (XRD) and a Scanning Electron Microscope (SEM). The sintered composites contained thermodynamically stable {alpha}-Al{sub 2}O{sub 3} particles and {theta}-Al{sub 2}Cu eutectic phases, which were embedded in the Al-Cu matrix. The in situ {alpha}-Al{sub 2}O{sub 3} particles were generally spherical and their mean size was observed to be less than 0.5 {mu}m. The results showed that sintering time influences not only the reaction rate of copper and the formation of Al{sub 2}O{sub 3}. Also, an increase in the sintering time accelerates the formation of submicron in situ {alpha}-Al{sub 2}O{sub 3} particles and decreases the quantity of {theta}-Al{sub 2}Cu intermetallic phase in the liquid aluminium. Additionally, sintering of composite for 30 min at 1000 Degree-Sign C increased the hardness from 60 to 174 HV.

  12. Static and dynamic magnetic properties of CoPt{sub 3}. Nanoparticles in comparison with bulk matter; Statische und dynamische magnetische Eigenschaften von CoPt{sub 3}. Nanopartikel im Vergleich zum Volumenmaterial

    Energy Technology Data Exchange (ETDEWEB)

    Raeder, C.

    2006-09-22

    In this work the structural and magnetic characteristics of CoPt{sub 3}-particles are examined. In particular the determination of the g-factor is of interest as well as the damping behavior of the magnetization vector under influence of a microwave radiation. Moreover the magnetic anisotropy energy density of individual particles is covered by the presented thesis. The particles exist in the chemically disordered phase. They are monocrystalline and monodisperse with a mean diameter of d=4.04 nm and a width of the size distribution of {sigma}=0.15, as determined by transmission electron microscopy. Moreover the particles are embedded into a polymer with high dilution (0.08 vol%). To compare the results for the particles CoPt{sub 3} films and bulk-material are prepared and examined with the same procedure. X-ray diffraction (XRD) shows that all three sample systems are an alloy and do not appear as cobalt clusters embedded in platinum. The lattice constant of the particles is increased by 0.5% in comparison to the bulk material (a{sub NP}=0.388{+-}0.003 nm). The evaluation of the peak widths of the XRD experiments exhibit a crystalline size of 95.5{+-}6.5 nm of the films and 48.5{+-}6.5 nm of the bulk material. The evaluation of the relative intensities of (111)- and (200)-peaks points the fact that both the film and the particles preferentially grow in the (111)-direction. The films are polycrystalline in the film-plane. From magnetic resonance measurements the g-factor and the damping constant {alpha} is extracted. The measurement shows that both the g-factor (about 2%) and the damping-constant {alpha} (about 125%) is increased in comparison to the film, and/or bulk material. For the films M{sub eff} is determined from angle-dependent resonance-field measurements. From the temperature dependence of the resonance field the magnetic anisotropy is determined. Because of the fact that the measurements could be done only to a minimum of 50 K the value of the anisotropy

  13. Yb{sup 3+}:Sr{sub 5}(VO{sub 4}){sub 3}F: Crystal growth, spectroscopic characterization and laser development; Yb{sup 3+}:Sr{sub 5}(VO{sub 4}){sub 3}F: Crescimento, caracterizacao espectroscopica e desenvolvimento do laser

    Energy Technology Data Exchange (ETDEWEB)

    Bustamante, Andrea Nora Pino

    1999-07-01

    Crystal growth, spectroscopic characterization and laser development of Yb{sup 3+}:SVAP [Sr{sub 5}(VO{sub 4}){sub 3}F] was performed to demonstrate for the first time, operation of tunable laser emission centered at 1120 nm. Initially, SVAP crystals were grown with high dopant concentrations, up to 6.0 mol % of Yb{sub 2} O{sub 3} in the melt, in order to investigate the material for potential laser operation at a new laser wavelength. Additional research was performed to alleviate highly doped SVAP crystals of defects previously observed. Basic spectroscopic characterization including absorption and luminescent properties were measured to better understand the behavior of Yb{sup 3+} ions in SVAP. Based upon these studies, discussion of the 1120 nm laser transition is presented as it arises from a ground state vibrational level. Investigations of the charge compensation process and the optical parameters as a function of dopant concentration are also presented. The laser development of Yb{sup 3+}:SVAP included continuous and pulsed modes of operation of the 1044 nm and 1120 nm transitions. Initial laser action of the 1044 nm transition was achieved using a Yi: Saphire laser pump source in order to compare with previously results. Further development of a diode-pumped Yb{sup 3+}:SVAP laser system demonstrated continuously tunable laser operation from 1103 nm for the first time. The laser investigations also proved that this high gain media does provide continuous wave laser action at 1044 nm and 1120 simultaneously without significant gain depletion. (author)

  14. Synthesis and characterization of metastable, 20 nm-sized Pna2{sub 1}-LiCoPO{sub 4} nanospheres

    Energy Technology Data Exchange (ETDEWEB)

    Ludwig, Jennifer [Technical University of Munich, Department of Chemistry, Synthesis and Characterization of Innovative Materials, Lichtenbergstr. 4, 85747 Garching (Germany); Nordlund, Dennis [Stanford Synchrotron Radiation Lightsource, SLAC National Accelerator Laboratory, 2575 Sand Hill Rd, Menlo Park, CA 94025 (United States); Doeff, Marca M. [Lawrence Berkeley National Laboratory, Environmental Energy Technologies Division, 1 Cyclotron Rd, Berkeley, CA 94720 (United States); Nilges, Tom, E-mail: tom.nilges@lrz.tum.de [Technical University of Munich, Department of Chemistry, Synthesis and Characterization of Innovative Materials, Lichtenbergstr. 4, 85747 Garching (Germany)

    2017-04-15

    The majority of research activities on LiCoPO{sub 4} are focused on the phospho-olivine (space group Pnma), which is a promising high-voltage cathode material for Li-ion batteries. In contrast, comparably little is known about its metastable Pna2{sub 1} modification. Herein, we present a comprehensive study on the structure–property relationships of 15–20 nm Pna2{sub 1}-LiCoPO{sub 4} nanospheres prepared by a simple microwave-assisted solvothermal process. Unlike previous reports, the results indicate that the compound is non-stoichiometric and shows cation-mixing with Co ions on the Li sites, which provides an explanation for the poor electrochemical performance. Co L{sub 2,3}-edge X-ray absorption spectroscopic data confirm the local tetrahedral symmetry of Co{sup 2+}. Comprehensive studies on the thermal stability using thermogravimetric analysis, differential scanning calorimetry, and in situ powder X-ray diffraction show an exothermic phase transition to olivine Pnma-LiCoPO{sub 4} at 527 °C. The influence of the atmosphere and the particle size on the thermal stability is also investigated. - Graphical abstract: Blue nano-sized Pna2{sub 1}-LiCoPO{sub 4,} featuring tetrahedrally-coordinated Co{sup 2+}, was synthesized in a rapid one-step microwave-assisted solvothermal process. The phase relation between this metastable and the stable polymorph was analyzed and electrochemical properties are discussed. - Highlights: • Preparation of uniform 15–20 nm nanospheres of metastable Pna2{sub 1}-LiCoPO{sub 4} polymorph. • Structure redetermination shows cation-mixing (Co blocking Li sites). • In situ investigation of phase transformation to olivine Pnma-LiCoPO{sub 4} at 527 °C. • Pna2{sub 1}-LiCoPO{sub 4} reemerges as a stable high-temperature phase above 800 °C. • X-ray absorption spectroscopy confirms local tetrahedral symmetry (T{sub d} Co{sup 2+}).

  15. Sub-10-nm Graphene Nanoribbons with Tunable Surface Functionalities for Lithium-ion Batteries

    International Nuclear Information System (INIS)

    Li, Yan-Sheng; Ao, Xiang; Liao, Jia-Liang; Jiang, Jianjun; Wang, Chundong; Chiang, Wei-Hung

    2017-01-01

    Highlights: •A green and scalable method to produce sub-10-nm GNR is present. •The surface functionality of sub-10-nm GNR is critical for the LIB properties. •The sub-10-nm GNR showed superior LIB capacity of 490.4 mAh g −1 after 100 cycles. -- Abstract: A systematic study to reveal the relationship between the surface oxygen-containing functionalities of sub-10-nm GNRs and their electrochemical properties for lithium-ion batteries has been presented. Sub-10-nm GNRs with controlled oxygen-containing groups were synthesized by a green and scalable intercalation-assisted unzipping SWCNTs. Detailed materials characterizations including TEM, XRD, Raman and XPS indicate that KNO 3 could be an effective intercalation agent to facilitate the SWCNT unzipping by reducing the strong Van der Waals force attraction of bundled SWCNT. The levels of surface functionalities of sub-10-nm GNR were tuned by carefully controlling the KMnO 4 concentration during the unzipping process. The electrochemical analysis suggests that the as-produced sub-10-nm GNR with 31.4 atomic percent (atom %) oxygen-containing functional groups showed the highest capacity of 490.4 mAh g −1 after 100 cycles. This work proposed that sub-10-nm GNRs with appropriate oxygen-functional groups can be a promising electrode material for high performance lithium-ion batteries.

  16. Al{sub 2}O{sub 3}:Cr{sup 3+} microfibers by hydrothermal route: Luminescence properties

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Dianguang [School of Materials Science and Engineering, Shaanxi University of Science and Technology, Xi’an 710021 (China); Zhu, Zhenfeng, E-mail: zhuzf@sust.edu.cn [School of Materials Science and Engineering, Shaanxi University of Science and Technology, Xi’an 710021 (China); Liu, Hui; Zhang, Zhengyang; Zhang, Yanbin; Li, Gege [School of Materials Science and Engineering, Shaanxi University of Science and Technology, Xi’an 710021 (China)

    2012-09-15

    Highlights: ► Uniform Al{sub 2}O{sub 3}:Cr{sup 3+} microfibers were synthesized via a hydrothermal route and thermal decomposition. ► The length and diameter of Al{sub 2}O{sub 3}:Cr{sup 3+} microfibers were about 3–9 μm and 300 nm, respectively. ► Al{sub 2}O{sub 3}:Cr{sup 3+} microfibers presented a broad R band at 696 nm when excited at 400 nm. ► It is shown that the 0.07 mol% of doping concentration of Cr{sup 3+} ions in α-Al{sub 2}O{sub 3}:Cr{sup 3+} is optimum. ► Critical distance between Cr{sup 3+} ions for energy transfer was determined to be 38 Å. -- Abstract: Uniform Al{sub 2}O{sub 3}:Cr{sup 3+} microfibers were synthesized by using a hydrothermal route and thermal decomposition of a precursor of Cr{sup 3+} doped ammonium aluminum hydroxide carbonate (denoted as AAHC), and characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), photoluminescence (PL) spectra and decay curves. XRD indicated that Cr{sup 3+} doped samples calcined at 1473 K were the most of α-Al{sub 2}O{sub 3} phase. SEM showed that the length and diameter of these Cr{sup 3+} doped alumina microfibers were about 3–9 μm and 300 nm, respectively. PL spectra showed that the Al{sub 2}O{sub 3}:Cr{sup 3+} microfibers presented a broad R band at 696 nm. It is shown that the 0.07 mol% of doping concentration of Cr{sup 3+} ions in α-Al{sub 2}O{sub 3}:Cr{sup 3+} was optimum. According to Dexter's theory, the critical distance between Cr{sup 3+} ions for energy transfer was determined to be 38 Å. It is found that the curve followed the single-exponential decay.

  17. A soft chemical route to the synthesis of BiFeO{sub 3} nanoparticles with enhanced magnetization

    Energy Technology Data Exchange (ETDEWEB)

    Hasan, Mehedi, E-mail: mhrizvi@gce.buet.ac.bd [Department of Glass and Ceramic Engineering, Bangladesh University of Engineering and Technology, Dhaka 1000, Bangladesh (India); Islam, Md. Fakhrul, E-mail: fislam@gce.buet.ac.bd [Department of Glass and Ceramic Engineering, Bangladesh University of Engineering and Technology, Dhaka 1000, Bangladesh (India); Mahbub, Rubayyat, E-mail: rubayyatm@gce.buet.ac.bd [Department of Glass and Ceramic Engineering, Bangladesh University of Engineering and Technology, Dhaka 1000, Bangladesh (India); Hossain, Md. Sarowar, E-mail: sakil_phy@yahoo.com [S.N. Bose National Centre for Basic Sciences, Salt Lake City, Kolkata, West Bengal 700098 (India); Hakim, M.A., E-mail: hakim.akm@gmail.com [Department of Glass and Ceramic Engineering, Bangladesh University of Engineering and Technology, Dhaka 1000, Bangladesh (India)

    2016-01-15

    Highlights: • Pure BiFeO{sub 3} nanoparticles have been synthesized at relatively low temperature. • Decomposition behavior of BiFeO{sub 3} precursor gel is investigated. • Particle size dependent magnetic properties have been confirmed. • Greatly improved magnetization is observed for BiFeO{sub 3} nanostructure. - Abstract: Utilization of BiFeO{sub 3} (BFO) into modern device applications is restricted by its very low magnetic moments and high leakage current. Enhancement in magnetization is a real challenge for multiferroic BFO in the context of device miniaturization and high density information storage system. In this study a significant improvement in magnetization has been recorded for BFO nanoparticles, exploiting the beneficial effect of size confinement. BFO nanoparticles with different size in the range of 21–68 nm are synthesized via modified Pechini sol–gel approach followed by leaching with acetic acid. X-ray diffraction result confirms pure and well crystallized BFO annealed at temperature lower than 600 °C, compared to more than 800 °C for the traditional solid-state sintering process. A strong size-dependent magnetization which increases with decreasing particle size is confirmed with a value of 1.4 emu/g for 40 nm particles in contrast to 7.5 emu/g for 21 nm particles.

  18. Luminescence properties and energy transfer investigations of Sr{sub 3}Lu(PO{sub 4}){sub 3}:Ce{sup 3+}, Tb{sup 3+} phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Zaifa; Xu, Denghui, E-mail: xudh@btbu.edu.cn; Sun, Jiayue; Du, Jiangnan; Gao, Xuedong

    2016-09-15

    Highlights: • A phosphor Sr{sub 3}Lu(PO{sub 4}){sub 3}:Ce{sup 3+}, Tb{sup 3+} for UV-based white LEDs was firstly synthesized successfully. • The phase structure and photoluminescence properties of samples were studied in detail. • The energy transfer process from Ce{sup 3+} to Tb{sup 3+} ions was illustrated in detail. • Sr{sub 3}Lu(PO{sub 4}){sub 3}:Ce{sup 3+}, Tb{sup 3+} phosphor has potential applications as an UV-convertible phosphor for white light emitting diodes. - Abstract: A series of Ce{sup 3+} or Tb{sup 3+} doped and Ce{sup 3+}/Tb{sup 3+} co-doped Sr{sub 3}Lu(PO{sub 4}){sub 3} phosphors were prepared via the conventional high temperature solid-state reaction. The phase structure, photoluminescence and energy transfer properties of samples were studied in detail. The optimal proportion of Ce{sup 3+} single doping is 4 mol% with maximal fluorescence intensity. The Sr{sub 3}Lu(PO{sub 4}){sub 3}:Ce{sup 3+}, Tb{sup 3+} phosphor shows both a blue emission (428 nm) from Ce{sup 3+} and a yellowish-green emission (545 nm) from Tb{sup 3+} with considerable intensity under ultraviolet (UV) excitation (268 nm). The energy transfer from Ce{sup 3+} to Tb{sup 3+} ions takes place in the Sr{sub 3}Lu(PO{sub 4}){sub 3}:Ce{sup 3+}, Tb{sup 3+} phosphor on the basis of the analysis of the luminescence spectra. The energy transfer mechanism from Ce{sup 3+} to Tb{sup 3+} ions was proved to be dipole–dipole interaction. The energy transfer behaviors in Sr{sub 3}Lu(PO{sub 4}){sub 3}:Ce{sup 3+}, Tb{sup 3+} phosphor is also investigated by the lifetime measurement. The results show that this phosphor has potential applications for UV white-light LEDs.

  19. Surface morphology analysis of nanostructured (Ba sub x , Sr sub 1 sub - sub x)TiO sub 3 thin films using fractal method

    CERN Document Server

    Hong, K J; Choi, W K; Cho, J C

    2003-01-01

    Based on the fractal theory, this paper uses scanning electron microscopy images to investigate the roughness characteristics of nanostructured (Ba Sr)TiO sub 3 thin films by sol-gel methods. The percentage grain area, surface fractal dimensions and 3D image are evaluated using image analysis methods. The thickness of the (Ba Sr)TiO sub 3 thin films was 260-280 nm. The surface fractal dimensions were increased with strontium doping, and grain area, were decreased with it. The fractal dimension and the grain areas of the (Ba sub 0 sub . sub 7 Sr sub 0 sub . sub 3)TiO sub 3 thin films were 1.81 and 81%. Based on the image analysis, the roughness height of 3D images as 256 levels was about 3 nm and its distribution was about 35-40% for the (Ba sub 0 sub . sub 8 Sr sub 0 sub . sub 2)TiO sub 3 and (Ba sub 0 sub . sub 7 Sr sub 0 sub . sub 3)TiO sub 3 thin films. The roughness height of the BST thin films was distributed from 35% to 40% ranging from 3 nm to 4 nm. By increasing the strontium doping, the roughness hei...

  20. Li{sub 3}Gd{sub 3}Te{sub 2}O{sub 12}:Eu{sup 3+}- an intense red phosphor for solid state lighting applications

    Energy Technology Data Exchange (ETDEWEB)

    Tiwari, Hansnath [Department of Chemistry, Indian Institute of Technology Madras, Chennai 600036 (India); Asiri Naidu, S. [Department of Chemistry, Rajiv Gandhi University of Knowledge Technologies, Nuzvid, Andhra Pradesh 521202 (India); Varadaraju, U.V., E-mail: varada@iitm.ac.in [Department of Chemistry, Indian Institute of Technology Madras, Chennai 600036 (India)

    2017-02-15

    Li{sub 3}Gd{sub 33x}Eu{sub 3x}Te{sub 2}O{sub 12} (x=0.05−1.0) phases with garnet structure were synthesized by high temperature solid state reaction and the photoluminescence properties were investigated. The appearance of bands due to intra 4 f transitions of Gd{sup 3+} in the excitation spectra recorded by monitoring the 612 nm emission line of the activator indicates Gd{sup 3+}→Eu{sup 3+} energy transfer in this host lattice. Under 395 nm excitation, the electric dipole transition is predominant in the emission spectrum of Eu{sup 3+} and is in agreement with the C{sub 2} point group (noncentrosymmetric) of the EuO{sub 8} polyhedron. The critical concentration of the Eu{sup 3+} activator in this series was found to be 0.6 (x=0.2) above which, concentration quenching occurs. The emission intensity of the phosphor composition, Li{sub 3}Gd{sub 2.4}Eu{sub 0.6}Te{sub 2}O{sub 12} is ~4 times that of the commercial sample of Y{sub 2}O{sub 3}:Eu{sup 3+} phosphor. - Highlights: • New Eu{sup 3+} doped garnet. • Intense electric dipole emission. • Gd{sup 3+}→Eu{sup 3+} energy transfer.

  1. XPS, TEM and SAD investigations of nanosized Co{sub x}B{sub y}H{sub z} particles obtained by two different borohydride methods

    Energy Technology Data Exchange (ETDEWEB)

    Krastev, V. [Bulgarian Acad. of Sci., Sofia (Bulgaria). Inst. of General and Inorg. Chem.; Stoycheva, M. [Central Laboratory of Electrochemical Power Sources, Bulgarian Academy of Sciences, Sofia 1113 (Bulgaria); Lefterova, E. [Central Laboratory of Electrochemical Power Sources, Bulgarian Academy of Sciences, Sofia 1113 (Bulgaria); Dragieva, I. [Central Laboratory of Electrochemical Power Sources, Bulgarian Academy of Sciences, Sofia 1113 (Bulgaria); Stoynov, Z. [Central Laboratory of Electrochemical Power Sources, Bulgarian Academy of Sciences, Sofia 1113 (Bulgaria)

    1996-07-01

    The nanosized Co{sub x}B{sub y}H{sub z} particles synthesised by the ``tea`` and ``antigravity`` methods using a borohydride reduction process have been subjected to structure and composition studies by X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM) and selected area diffraction (SAD). The amounts of the elements Co, B, O{sub 2}, H{sub 2} and C as mean volume values, and surface values for the as-prepared particles, as well as after Ar{sup +} etching to a depth of about 15 nm and 30 nm from the initial particle surface, are determined. About 1.5 atoms of cobalt per atom of boron correspond to samples obtained by the ``antigravity`` method. The binding energy (BE) of 1s electrons of boron atoms has only one value. These particles are angular and are in the typical nanocrystalline state. In the case of samples prepared by the ``tea`` method, two atoms of cobalt per atom of boron are found. The presence of two kinds of BE (B{sup I} and B{sup II}) of 1s electrons of boron atoms in the particles obtained by the ``tea`` method is observed and almost equal amounts of these two states are established in the spectrum. The particles` shape and structure are typical of the amorphous state. The fact that there is one peak when the ``antigravity`` method is applied, in contrast to the two peaks with the ``tea`` method indicates the presence of a metal amorphous state in the latter case. (orig.)

  2. Solid-state thermal decomposition of the [Co(NH{sub 3}){sub 5}CO{sub 3}]NO{sub 3}{center_dot}0.5H{sub 2}O complex: A simple, rapid and low-temperature synthetic route to Co{sub 3}O{sub 4} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Farhadi, Saeid, E-mail: sfarhad2001@yahoo.com [Department of Chemistry, Lorestan University, Khorramabad 68135-465 (Iran, Islamic Republic of); Safabakhsh, Jalil [Department of Chemistry, Lorestan University, Khorramabad 68135-465 (Iran, Islamic Republic of)

    2012-02-25

    Highlights: Black-Right-Pointing-Pointer [Co(NH{sub 3}){sub 5}CO{sub 3}]NO{sub 3}{center_dot}0.5H{sub 2}O complex was used for preparing pure Co{sub 3}O{sub 4} nanoparticles. Black-Right-Pointing-Pointer Co{sub 3}O{sub 4} nanoparticles were prepared at low temperature of 175 Degree-Sign C. Black-Right-Pointing-Pointer Co{sub 3}O{sub 4} nanoparticles show a weak ferromagnetic behaviour at room temperature. Black-Right-Pointing-Pointer The method is simple, low-cost and suitable for the production of Co{sub 3}O{sub 4}. - Abstract: Co{sub 3}O{sub 4} nanoparticles were easily prepared via the decomposition of the pentammine(carbonato)cobalt(III) nitrate precursor complex [Co(NH{sub 3}){sub 5}CO{sub 3}]NO{sub 3}{center_dot}0.5H{sub 2}O at low temperature (175 Degree-Sign C). The product was characterized by thermal analysis, X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), UV-visible spectroscopy, transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDX), Raman spectroscopy, Brunauer-Emmett-Teller (BET) specific surface area measurements and magnetic measurements. The FT-IR, XRD, Raman and EDX results indicated that the synthesized Co{sub 3}O{sub 4} nanoparticles are highly pure and have a single phase. The TEM analysis revealed nearly uniform and quasi-spherical Co{sub 3}O{sub 4} nanoparticles with an average particle size of approximately 10 nm. The optical absorption spectrum of the Co{sub 3}O{sub 4} nanoparticles showed two direct band gaps of 2.18 and 3.52 eV with a red shift in comparison with previous reported values. The prepared Co{sub 3}O{sub 4} nanoparticles showed a weak ferromagnetic behaviour that could be attributed to uncompensated surface spins and/or finite-size effects. Using the present method, Co{sub 3}O{sub 4} nanoparticles can be produced without expensive organic solvents and complicated equipment. This simple, rapid, safe and low-cost synthetic route can be extended to the synthesis of other

  3. Electrodeposition of Fe{sub 3}O{sub 4} layer from solution of Fe{sub 2}(SO{sub 4}){sub 3} with addition ethylene glycol

    Energy Technology Data Exchange (ETDEWEB)

    Dahlan, Dahyunir, E-mail: dahyunir@yahoo.com; Asrar, Allan [Department of Physics, Andalas University, Limau Manih Padang 25163, West Sumatera (Indonesia)

    2016-03-11

    The electrodeposition of Fe{sub 3}O{sub 4} layer from the solution Fe{sub 2}(SO{sub 4}){sub 3} with the addition of ethylene glycol on Indium Tin Oxide (ITO) substrate has been performed. The electrodeposition was carried out using a voltage of 5 volts for 120 seconds, with and without the addition of 2% wt ethylene glycol. Significant effects of temperature on the resulting the samples is observed when they are heated at 400 °C. Structural characterization using X-ray diffraction (XRD) shows that all samples produce a layer of Fe{sub 3}O{sub 4} with particle size less than 50 nanometers. The addition of ethylene glycol and the heating of the sample causes a shrinkage in particle size. The scanning electron microscopy (SEM) characterization shows that Fe{sub 3}O{sub 4} layer resulting from the process of electrodeposition of Fe{sub 2}(SO{sub 4}){sub 3} without ethylene glycol, independent of whether the sample is heated or not, is uneven and buildup. Layer produced by the addition of ethylene glycol without heating produces spherical particles. On contrary, when the layer is heated the spherical particles transform to irregularly-shaped particles with smaller size.

  4. Modeling and optimization of effective parameters on the size of synthesized Fe{sub 3}O{sub 4} superparamagnetic nanoparticles by coprecipitation technique using response surface methodology

    Energy Technology Data Exchange (ETDEWEB)

    Ghazanfari, Mohammad Reza, E-mail: Ghazanfari.mr@gmail.com [Department of Materials Science and Engineering, Ferdowsi University of Mashhad, 9177948974 Mashhad (Iran, Islamic Republic of); Kashefi, Mehrdad, E-mail: m-kashefi@um.ac.ir [Department of Materials Science and Engineering, Ferdowsi University of Mashhad, 9177948974 Mashhad (Iran, Islamic Republic of); Jaafari, Mahmoud Reza [Biotechnology Research Center, Nanotechnology Research Center, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad (Iran, Islamic Republic of)

    2016-05-01

    Generally, the statistical methods are defined as appropriate techniques to study the processes trends. In current research, the Fe{sub 3}O{sub 4} superparamagnetic nanoparticles were synthesized by coprecipitation method. In order to investigate the size properties of synthesized particles, the experimental design was done using central composite method (CCD) of response surface methodology (RSM) while the temperature, pH, and cation ratio of reaction were selected as influential factors. After particles synthesis based on designed runs, the different responses such as hydrodynamic size of particles (both freeze dried and air dried), size distribution, crystallite size, magnetic size, and zeta potential were evaluated by different techniques i.e. dynamic light scattering (DLS), X-ray diffraction (XRD), and vibrating sample magnetometer (VSM). Based on these results, the quadratic polynomial model was fitted for each response that could predict the response amounts. In following, the study of factors effects was carried out that showed the temperature, pH, and their interactions had higher effectiveness. Finally, by optimizing, it was clear that the minimum amounts of particle size (10.15 nm) and size distribution (13.01 nm) were reached in the minimum temperature (70 °C) and cation ratio (0.5) amounts and maximum pH amount (10.5). Moreover, the characterizations showed the particles size was about 10 nm while the amounts of M{sub s}, H{sub c}, and M{sub r} were equal to 60 (emu/g), 0.2 (Oe) and 0.22 (emu/g), respectively. - Highlights: • The Fe{sub 3}O{sub 4} nanoparticles were successfully synthesized by coprecipitation method. • By RSM technique, some predicted models were presented for particles size. • Temperature, pH and their interactions had most effectiveness on the particles size. • The drying techniques can effect on the size properties.

  5. Magnetic resonance and antiresonance in microwave transmission through nanocomposites with Fe{sub 3}Ni{sub 2} and FeNi{sub 3} particles

    Energy Technology Data Exchange (ETDEWEB)

    Rinkevich, A.B. [M.N. Miheev Institute of Metal Physics Ural Branch of RAS, 18 S.Kovalevskaya St, Ekaterinburg 620990 (Russian Federation); Samoylovich, M.I. [OAO TsNITI “TEKHNOMASH”, 4 Ivana Franko St, Moscow 121108 (Russian Federation); Nemytova, O.V., E-mail: mif-83@mail.ru [M.N. Miheev Institute of Metal Physics Ural Branch of RAS, 18 S.Kovalevskaya St, Ekaterinburg 620990 (Russian Federation); Kuznetsov, E.A. [Nizhny Tagil branch of the Ekaterinburg state social-pedagogical university, 57 Krasnogvardeyskaya St, Nizhny Tagil 622031 (Russian Federation)

    2017-06-15

    Investigation of magnetic properties and microwave resonance phenomena in nanocomposites based on opal matrices containing the particles of intermetallide of Fe{sub 3}Ni{sub 2} and FeNi{sub 3} is carried out. The interactions which lead to the resonance changes of transmission and reflection coefficients are determined. Electromagnetic properties are measured in the millimeter frequency range. Special attention is paid to comparison between static and dynamic magnetic properties of nanocomposites. Frequency dependences of magnitude of lines of resonance features are obtained. Spectra of resonance and antiresonance are studied. The conditions when the magnetic antiresonance is observed are clarified. The X-ray phase analysis of the nanocomposites is performed and their structure is studied.

  6. Scintillation characteristics of nonstoichiometric phases formed in MF sub 2 -GdF sub 3 -CeF sub 3 systems Part III. Dense Gd sub 1 sub - sub x sub - sub y M sub x Ce sub y F sub 3 sub - sub x tysonite-related crystals (M=Ca, Sr)

    CERN Document Server

    Kobayashi, M; Sobolev, B P; Zhmurova, Z I; Krivandina, E A; Nikl, M

    1999-01-01

    We evaluated the scintillation characteristics and the radiation hardness of Gd sub 1 sub - sub x Ca sub x F sub 3 sub - sub x and Gd sub 1 sub - sub x Sr sub x F sub 3 sub - sub x tysonite-type solid solutions (close to 6.6 g/cm sup 3 in density) doped with Ce which were grown from the congruent melt. As the Ce concentration increased, the Ce sup 3 sup + emission at 345 nm increased to a level comparable with the Gd sup 3 sup + emission at 310 nm. Both emissions, however, were slow with the decay constant in the order of ms. The radiation hardness, which was roughly 10 sup 4 rad, tends to degrade as the wavelength decreases and/or the Ce concentration increases. Both spontaneous recovery and UV annealing of the radiation damages were significant. The intensity of the gamma-ray excited luminescence, integrated over time, was as large as 50% of that in BaF sub 2 (12% of that in CdWO sub 4). When the Ce concentration is nil or only small, the yellow-green luminescence for UV excitation was as intense as in CdWO...

  7. Luminescence and luminescence quenching of Sr{sub 3}Lu{sub 2}(Si{sub 3}O{sub 9}){sub 2}:Ce{sup 3+} phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Mikalauskaite, I.; Raudonyte-Svirbutaviciene, E. [Institute of Chemistry, Faculty of Chemistry and Geosciences, Vilnius University, Naugarduko 24, LT-03225 Vilnius (Lithuania); Linkeviciute, A. [State Research Institute, Centre for Physical Sciences and Technology, Sauletekio Avenue 3, LT-10257 Vilnius (Lithuania); Urbonas, M. [Institute of Chemistry, Faculty of Chemistry and Geosciences, Vilnius University, Naugarduko 24, LT-03225 Vilnius (Lithuania); Katelnikovas, A., E-mail: arturas.katelnikovas@chf.vu.lt [Institute of Chemistry, Faculty of Chemistry and Geosciences, Vilnius University, Naugarduko 24, LT-03225 Vilnius (Lithuania)

    2017-04-15

    A series of near-UV to blue emitting Sr{sub 3}Lu{sub 2}(Si{sub 3}O{sub 9}){sub 2}:Ce{sup 3+} phosphors were prepared by a solid state reaction. The optical properties of synthesized phosphors were investigated as a function of Ce{sup 3+} concentration and temperature. These luminescent materials strongly absorb UV radiation shorter than 360 nm. The optimal Ce{sup 3+} concentration was 0.1% (external quantum efficiency ca. 45%). Temperature dependent measurements showed that Sr{sub 3}Lu{sub 2}(Si{sub 3}O{sub 9}){sub 2}:Ce{sup 3+} phosphors possess good thermal stability and loses only about 40% to 50% of initial intensity in the temperature range of 77–500 K depending on activator concentration.

  8. Growth and spectroscopic properties of Er{sup 3+}-doped Li{sub 3}Ba{sub 2}Y{sub 3}(MoO{sub 4}){sub 8} crystal

    Energy Technology Data Exchange (ETDEWEB)

    Song Mingjun, E-mail: smj521@hotmail.com [College of Chemistry and Chemical Engineering, Weifang University, Weifang, Shandong 261061 (China); Wang Lintong [College of Chemistry and Chemical Engineering, Weifang University, Weifang, Shandong 261061 (China); Zhao Wang [Department of Physics, Huainan Normal University, Huainan, Anhui 232001 (China); Wang Guofu [Fujian Institute of Research on the Structure of Matter, The Chinese Academy of Sciences, Fuzhou, Fujian 350002 (China); Zhao Meili; Meng Qingguo [College of Chemistry and Chemical Engineering, Weifang University, Weifang, Shandong 261061 (China)

    2011-06-15

    Highlights: > Er{sup 3+}:Li{sub 3}Ba{sub 2}Y{sub 3}(MoO{sub 4}){sub 8} crystal was grown by the top seeded solution growth method and the appearance and composition of the crystal were analyzed. > The spectroscopic parameters were calculated based on the Judd-Ofelt theory. > The lifetime of the crystal and powder sample was measured and the radiation trapping effect was discussed. > The up-conversion fluorescence spectra were measured and the possible up-conversion mechanisms were proposed. - Abstract: Er{sup 3+}:Li{sub 3}Ba{sub 2}Y{sub 3}(MoO{sub 4}){sub 8} crystal has been grown by the top seeded solution growth method (TSSG) from a flux of Li{sub 2}MoO{sub 4} and its morphology was analyzed. The polarized absorption spectra, fluorescence spectra and fluorescence decay curves of the crystal were measured. Based on the Judd-Ofelt (J-O) theory, spectroscopic parameters of Er{sup 3+}:Li{sub 3}Ba{sub 2}Y{sub 3}(MoO{sub 4}){sub 8} crystal, including the oscillator intensity parameters {Omega}{sub t} (t = 2, 4, 6), spontaneous emission probabilities, fluorescence branching ratios, and radiative lifetimes were calculated and analyzed. Stimulated emission cross-sections of the {sup 4}I{sub 13/2} {yields} {sup 4}I{sub 15/2} transition were estimated by the reciprocity method (RM) and the Fuchtbauer-Ladenburg (F-L) formula. Five up-conversion fluorescence bands around 490, 530, 550, 660 and 800 nm were observed with 977 nm excitation, and the possible up-conversion mechanisms were proposed.

  9. Luminescence properties of ZnMoO{sub 4}:Eu{sup 3+}:Y{sup 3+} materials synthesized by solution combustion synthesis method

    Energy Technology Data Exchange (ETDEWEB)

    Verma, Naveen, E-mail: vermanaveen17@gmail.com; Singh, Krishan Chander; Jindal, Jitender; Yadav, Suprabha [Department of chemistry, Maharshi Dayanand University, Rohtak-124001 – India (India); Mari, Bernabe; Mollar, Miguel [Institut de Disseny per la Fabricació Automatitzada - Departament de Física Aplicada, Universitat Politècnica de València, Camí de Vera s/n, 46022 València (Spain)

    2016-04-13

    The Zn{sub (1-x-y)}MoO{sub 4}:Eu{sup 3+}{sub (x)}: Y{sup 3+}{sub (y)} (x = 1 mol% and y = 1 or 2 mol%) compounds were prepared by combustion synthesis method. The crystal structure of the samples was identified by X-ray diffraction (XRD). The photoluminescence properties were investigated and it is observed that the co-doping of Y{sup 3+} enhances the luminescence emission intensity of ZnMoO{sub 4}:Eu{sup 3+} material. The Y{sup 3+} acts as a sensitizer in the ZnMoO{sub 4}:Eu{sup 3+} lattice. The particle size is calculated from XRD data by using Scherer Equation. The particles has been found in the range of 30-40 nm.

  10. Synthesis, crystal and electronic structures and optical properties of (HIm)<sub>2sub> Hg<sub>3sub>Cl>8sub> and (HIm)HgI<sub>3sub> (HIm = imidazolium)

    Energy Technology Data Exchange (ETDEWEB)

    Nhalil, Hariharan [Univ. of Oklahoma, Norman, OK (United States). Dept. of Chemistry and Biochemistry; Whiteside, Vincent R. [Univ. of Oklahoma, Norman, OK (United States). Homer L. Dodge Dept. of Physics & Astronomy; Sellers, Ian R. [Univ. of Oklahoma, Norman, OK (United States). Homer L. Dodge Dept. of Physics & Astronomy; Ming, Wenmei [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Materials Science & Technology Division; Du, Mao-Hua [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Materials Science & Technology Division; Saparov, Bayrammurad [Univ. of Oklahoma, Norman, OK (United States). Dept. of Chemistry and Biochemistry

    2017-11-22

    Here, we report synthesis, crystal and electronic structures, and optical properties of two new Hg-based zero-dimensional hybrid organic-inorganic halides (HIm)2Hg3Cl8 and (HIm)HgI3 (HIm = imidazolium). (HIm)<sub>2sub>Hg>3sub>Cl>8sub> crystallizes in the triclinic P-1 space group with a pseudo-layered structure made of organic imidazolium cation layers and anionic inorganic layers containing [Hg<sub>2sub>Cl>6sub>]2- units and linear [HgCl<sub>2sub>]0 molecules. (HIm)HgI<sub>3sub> crystallizes in the monoclinic P2<sub>1sub>/c space group featuring anionic [HgI<sub>3sub>]- units that are surrounded by imidazolium cations. Based on density functional theory calculations, (HIm)<sub>2sub>Hg>3sub>Cl>8sub> has an indirect band gap, whereas (HIm)HgI<sub>3sub> has a direct band gap with the measured onsets of optical absorption at 3.43 and 2.63 eV, respectively. (HIm)<sub>2sub>Hg>3sub>Cl>8sub> and (HIm)HgI<sub>3sub> are broadband light emitters with broad photoluminescence peaks centered at 548 nm (2.26 eV) and 582 nm (2.13 eV), respectively. In conclusion, following the crystal and electronic structure considerations, the PL peaks are assigned to self-trapped excitons.

  11. Optical investigation of Tb{sup 3+}-doped Y{sub 2}O{sub 3} nanocrystals prepared by Pechini-type sol-gel process

    Energy Technology Data Exchange (ETDEWEB)

    Back, M., E-mail: m.back@hotmail.it; Massari, A.; Boffelli, M.; Gonella, F.; Riello, P.; Cristofori, D. [Universita Ca' Foscari di Venezia and INSTM, Dipartimento di Scienze Molecolari e Nanosistemi (Italy); Ricco, R.; Enrichi, F., E-mail: enrichi@civen.org [CIVEN (Coordinamento Interuniversitario Veneto per le Nanotecnologie) (Italy)

    2012-03-15

    We report an optical study of Tb{sup 3+}-doped Y{sub 2}O{sub 3} nanocrystals synthesized by Pechini-type sol-gel method. The particles are investigated in terms of size and morphology by means of X-ray diffraction and transmission electron microscopy analysis. It is shown how the simple Pechini method allows for the growth of monocrystalline nanoparticles with a volume-weighted average size of about 30 nm. The optical properties of Tb{sup 3+} in the host lattice are studied in terms of PL, PLE, and lifetimes. Moreover, a correlation between the type of decay curves, the emission and excitation bands' shapes, and the site location of the emitting Tb{sup 3+} in the host material Y{sub 2}O{sub 3} is proposed.

  12. Nano ZrO{sub 2} particles in nanocrystalline Fe–14Cr–1.5Zr alloy powders

    Energy Technology Data Exchange (ETDEWEB)

    Xu, W.Z.; Li, L.L.; Saber, M.; Koch, C.C.; Zhu, Y.T., E-mail: ytzhu@ncsu.edu; Scattergood, R.O.

    2014-09-15

    Here we report on the formation of nano ZrO{sub 2} particles in Fe–14Cr–1.5Zr alloy powders synthesized by mechanical alloying. The nano ZrO{sub 2} particles were found uniformly dispersed in the ferritic matrix powders with an average size of about 3.7 nm, which rendered the alloy powders so stable that it retained nanocrystalline structure after annealing at 900 °C for 1 h. The ZrO{sub 2} nanoparticles have a tetragonal crystal structure and the following orientation relationship with the matrix: (0 0 2){sub ZrO2}//(0 0 2){sub Matrix} and [0 1 0]{sub ZrO2}//[1 2 0]{sub Matrix}. The size and dispersion of the ZrO{sub 2} particles are comparable to those of Y–Ti–O enriched oxides reported in irradiation-resistant ODS alloys. This suggests a potential application of the new alloy powders for nuclear energy applications.

  13. A novel UV-emitting phosphor: NaSr{sub 4}(BO{sub 3}){sub 3}: Pb{sup 2+}

    Energy Technology Data Exchange (ETDEWEB)

    Pekgözlü, İlhan, E-mail: pekgozluilhan@yahoo.com

    2016-01-15

    Pb{sup 2+} doped NaSr{sub 4}(BO{sub 3}){sub 3} materials were prepared by a solution combustion synthesis method. The phase analysis of all synthesized materials was carried out using the powder XRD. The synthesized materials were investigated using spectrofluorometer at room temperature. The excitation and emission bands of NaSr{sub 4}(BO{sub 3}){sub 3}: Pb{sup 2+} were observed at 291 and 368 nm, respectively. The dependence of the emission intensity on the Pb{sup 2+} concentration for the NaSr{sub 4}(BO{sub 3}){sub 3} was studied in detail. It was observed that the concentration quenching of Pb{sup 2+} in NaSr{sub 4}(BO{sub 3}){sub 3} is 0.01 mol. The Stokes shifts of NaSr{sub 4}(BO{sub 3}){sub 3}: Pb{sup 2+} phosphor were calculated to be 7190 cm{sup −1}. - Highlights: • A novel UV-emitting phosphor, NaSr{sub 4}(BO{sub 3}){sub 3}: Pb{sup 2+}, was prepared by combustion method. • The excitation and emission bands of NaSr{sub 4}(BO{sub 3}){sub 3}: Pb{sup 2+} were observed at 291 and 368 nm, respectively. • It was observed that the concentration quenching of Pb{sup 2+} in NaSr{sub 4}(BO{sub 3}){sub 3} is 0.01 mol.

  14. Sub-micron particle number size distribution characteristics at two urban locations in Leicester

    Science.gov (United States)

    Hama, Sarkawt M. L.; Cordell, Rebecca L.; Kos, Gerard P. A.; Weijers, E. P.; Monks, Paul S.

    2017-09-01

    The particle number size distribution (PNSD) of atmospheric particles not only provides information about sources and atmospheric processing of particles, but also plays an important role in determining regional lung dose. Owing to the importance of PNSD in understanding particulate pollution two short-term campaigns (March-June 2014) measurements of sub-micron PNSD were conducted at two urban background locations in Leicester, UK. At the first site, Leicester Automatic Urban Rural Network (AURN), the mean number concentrations of nucleation, Aitken, accumulation modes, the total particles, equivalent black carbon (eBC) mass concentrations were 2002, 3258, 1576, 6837 # cm-3, 1.7 μg m-3, respectively, and at the second site, Brookfield (BF), were 1455, 2407, 874, 4737 # cm-3, 0.77 μg m-3, respectively. The total particle number was dominated by the nucleation and Aitken modes, with both consisting of 77%, and 81% of total number concentrations at AURN and BF sites, respectively. This behaviour could be attributed to primary emissions (traffic) of ultrafine particles and the temporal evolution of mixing layer. The size distribution at the AURN site shows bimodal distribution at 22 nm with a minor peak at 70 nm. The size distribution at BF site, however, exhibits unimodal distribution at 35 nm. This study has for the first time investigated the effect of Easter holiday on PNSD in UK. The temporal variation of PNSD demonstrated a good degree of correlation with traffic-related pollutants (NOX, and eBC at both sites). The meteorological conditions, also had an impact on the PNSD and eBC at both sites. During the measurement period, the frequency of NPF events was calculated to be 13.3%, and 22.2% at AURN and BF sites, respectively. The average value of formation and growth rates of nucleation mode particles were 1.3, and 1.17 cm-3 s-1 and 7.42, and 5.3 nm h-1 at AURN, and BF sites, respectively. It can suggested that aerosol particles in Leicester originate mainly

  15. Structural, magnetic and Moessbauer spectral studies of aluminum substituted Mg-Mn-Ni ferrites (Mg{sub 0.2}Mn{sub 0.5}Ni{sub 0.3}Al{sub y}Fe{sub 2-y}O{sub 4})

    Energy Technology Data Exchange (ETDEWEB)

    Verma, Satish, E-mail: satishapurva@gmail.com [Department of Physics, Govt. P.G. College, Solan-173212 (India); Chand, Jagdish [Department of Physics, Govt. P.G. College, Solan-173212 (India); Batoo, Khalid Mujasam [King Abdullah Institute of Nanotechnology, King Saud University, Riyadh 11451 (Saudi Arabia); Singh, M. [Department of Physics, Himachal Pradesh University, Summer-Hill, Shimla-171005 (India)

    2013-02-25

    Highlights: Black-Right-Pointing-Pointer Single phase nanocrystalline Al{sup 3+} ions doped Mg-Mn-Ni ferrite have been synthesized by citrate precursor method. Black-Right-Pointing-Pointer Particle size decreases as non-magnetic Al content increases. Black-Right-Pointing-Pointer The presence of doublets in the Moessbauer spectra can be attributed to superparamagnetic relaxation. - Abstract: Nanocrystalline Al{sup 3+} ions doped Mg{sub 0.2}Mn{sub 0.5}Ni{sub 0.3}Al{sub y}Fe{sub 2-y}O{sub 4} compositions, where y = 0.0, 0.05 and 0.10 have been synthesized by citrate precursor method. Crystal structure and magnetic properties have been investigated at 300 K by means of X-ray diffraction, transmission electron microscope (TEM), vibrating sample magnetometer (VSM) and Moessbauer spectra measurements. XRD study reveals that particle size decreases from 102.25 nm to 41.65 nm. A decrease in lattice constant and saturation magnetization was attributed to smaller ionic radius of Al{sup 3+} ions and weakening of super exchange interaction. Experimental and X-ray density decrease with increasing aluminum concentration. Though Moessbauer spectra of y = 0.0 exhibit normal Zeeman split sextets, spectra of samples for y = 0.05 and 0.10 are characterized by simultaneous presence of a central paramagnetic doublet. Dependence of Moessbauer parameters such as isomer shift, quadrupole splitting, linewidth and hyperfine magnetic field on Al{sup 3+} ions concentration have been discussed. Initial permeability '{mu}{sub i}', saturation magnetization (4 {pi}M{sub S}), retentivity (M{sub R}), Bohr magneton number (n{sub B}{sup N}), magneto crystalline anisotropy constant (K{sub 1}) and magnetic loss decreases while coercivity (H{sub C}) increases with increasing substitution of Al{sup 3+} ions. Magnetic loss has very low value in the range of 10{sup -3} which is two orders of magnitude less than samples prepared by conventional method.

  16. Photoluminescence properties of a novel red phosphor Sr{sub 3}Ga{sub 2}O{sub 5}Cl{sub 2}:Eu{sup 3+}

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Zhonghua; Hu, Yihua; Zhang, Shaoan; Lin, Jun [Guangdong University of Technology, School of Physics and Optoelectronic Engineering, Guangzhou (China)

    2016-02-15

    Eu{sup 3+}-doped Sr{sub 3}Ga{sub 2}O{sub 5}Cl{sub 2} phosphors were synthesized successfully via a two-step solid-state reaction method. Phase purity and morphology of the phosphor were confirmed by XRD and SEM techniques. In the excitation spectra of Sr{sub 3}Ga{sub 2}O{sub 5}Cl{sub 2}:Eu{sup 3+} phosphor, the broad excitation band centering at 310 nm is due to the combination of charge transfer from Eu{sup 3+}→O{sup 2-} and host absorption. And it matches well the emission wavelength from UV LEDs. Sr{sub 3}Ga{sub 2}O{sub 5}Cl{sub 2}:Eu{sup 3+} phosphors show a bright orange-red luminescence under excitation with 301 nm. However, concentration quenching of Eu{sup 3+} in Sr{sub 3}Ga{sub 2}O{sub 5}Cl{sub 2}:Eu{sup 3+} occurs at a low content of 0.07 in this work. The quenching mechanism of Sr{sub 3}Ga{sub 2}O{sub 5}Cl{sub 2}:Eu{sup 3+} was discussed in detail on the basis of the experimental results. (orig.)

  17. Growth mechanism and magnetism in carbothermal synthesized Fe{sub 3}O{sub 4} nanoparticles from solution combustion precursors

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Xuanli [School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing, 100083 China (China); Qin, Mingli, E-mail: qinml@mater.ustb.edu.cn [School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing, 100083 China (China); Cao, Zhiqin [School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing, 100083 China (China); School of Materials Science and Engineering, Pan Zhihua University, Pan Zhihua, 617000 China (China); Jia, Baorui; Gu, Yueru; Qu, Xuanhui [School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing, 100083 China (China); Volinsky, Alex A. [Department of Mechanical Engineering, University of South Florida, Tampa, 33620 (United States)

    2016-12-15

    Magnetic Fe{sub 3}O{sub 4} nanoparticles were prepared by carbothermal reduction using solution combustion synthesis precursors derived from ferric nitrate (oxidizer), glycine (fuel) and glucose (carbon source) mixed solution. In this paper, the growth mechanism and magnetism in Fe{sub 3}O{sub 4} nanoparticles were investigated by adjusting the glucose content in precursor and the heat temperature in carbothermal process. The products were analyzed by X-ray diffraction, Field emission scanning electron microscopy, Infrared adsorption method and Vibrating sample magnetometry. The results revealed that the more amount of glucose, the earlier Fe{sub 3}O{sub 4} phase generated as temperature increasing. Depending on glucose content and thermal temperature, the average grain size of Fe{sub 3}O{sub 4} nanoparticles varied from 19.9 nm to 48 nm and saturation magnetization changed from 21.2 emu/g to 71.77 emu/g, which indicated that the saturation magnetization of Fe{sub 3}O{sub 4} nanoparticles fell off as the average grain size decreasing. These results were crucial not only from the application stand-point, but more importantly leaded to a new platform for further studies of high quality magnetic Fe{sub 3}O{sub 4} particles at nanoscale. - Highlights: • Solution combustion. • Carbothermal. • Fe{sub 3}O{sub 4} nanoparticles. • Magnetic properties.

  18. Reversible Exsolution of Nanometric Fe<sub>2sub>O>3 sub> Particles in BaFe<sub>2-xsub>(PO>4sub>)>2sub> (0 ≤ x ≤ 2/3):The Logic of Vacancy Ordering in Novel Metal-Depleted Two-Dimensional Lattices

    Energy Technology Data Exchange (ETDEWEB)

    Alcover, Ignacio Blazquez; David, Rénald; Daviero-Minaud, Sylvie; Filimonov, Dmitry; Huvé, Marielle; Roussel, Pascal; Kabbour, Houria; Mentré, Olivier [CNRS-UMR

    2015-08-12

    We show here that the exsolution of Fe2+ ions out of two-dimensional (2D) honeycomb layers of BaFe<sub>2sub>(PO>4sub>)>2 sub>into iron-deficient BaFe<sub>2–xsub>(PO>4sub>)>2sub> phases and nanometric α-Fe<sub>2sub>O>3sub> (typically 50 nm diameter at the grain surface) is efficient and reversible until x = 2/3 in mild oxidizing/reducing conditions. It corresponds to the renewable conversion of 12 wt % of the initial mass into iron oxide. After analyzing single crystal X-ray diffraction data of intermediate members x = 2/7, x = 1/3, x = 1/2 and the ultimate Fe-depleted x = 2/3 term, we then observed a systematic full ordering between Fe ions and vacancies (V<sub>Fe>) that denote unprecedented easy in-plane metal diffusion driven by the Fe2+/Fe3+ redox. Besides the discovery of a diversity of original depleted triangular <sub>∞>{Fe2/3+<sub>2–xsub>O>6sub>} topologies, we propose a unified model correlating the x Fe-removal and the experimental Fe/V<sub>Fe> ordering into periodic one-dimensional motifs paving the layers, gaining insights into predictive crystahemistry of complex low dimensional oxides. When we increased the x values it led to a progressive change of the materials from 2D ferromagnets (Fe2+) to 2D ferrimagnets (Fe2/3+) to antiferromagnets for x = 2/3 (Fe3+).

  19. Magnetically tunable photocurrent in La{sub 0.7}Sr{sub 0.3}MnO{sub 3}/BaSnO{sub 3} heterojunctions

    Energy Technology Data Exchange (ETDEWEB)

    Luo, Bingcheng; Hu, Junbiao [Department of Applied Physics, Northwestern Polytechnical University, Xi' an (China); Wang, Jing [Department of Applied Physics, Northwestern Polytechnical University, Xi' an (China); Department of Physics, Pennsylvania State University, University Park, PA (United States)

    2017-12-15

    Artificially constructed oxide heterointerfaces have attracted much attention. Herein, the novel all-perovskite p-n heterojunction composed of a colossal magnetoresistive manganite La{sub 0.7}Sr{sub 0.3} MnO{sub 3} (LSMO) and an n-type transparent semiconducting BaSnO{sub 3} (BSO) is designed via optimizing the growth condition. This LSMO/BSO p-n junction exhibits good rectification with a forward-to-reverse ratio of 275 at 1 V, high photo detection capability with a photo-to-dark current of 581.9 at -0.5 V, high ultraviolet light sensitivity with a UV (360 nm)-to-visible (532 nm) ratio of ∝2.4 x 10{sup 3}, and a significantly magneto-tunable photocurrent with a variation ratio of ∝1.25 % under 532 nm illumination and 0.5 T magnetic field. As a result, combining synergistically the functionality of diode and magnetically tunable photo detector, the LSMO/BSO p-n junction is a promising candidate for advanced magneto-optoelectronic devices. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  20. Y{sub 3}Fe{sub 5}O{sub 12} nanoparticulate garnet ferrites: Comprehensive study on the synthesis and characterization fabricated by various routes

    Energy Technology Data Exchange (ETDEWEB)

    Niaz Akhtar, Majid, E-mail: majidniazakhtar@ciitlahore.edu.pk [Department of Physics, COMSATS Institute of Information Technology, Lahore 54000 (Pakistan); Department of Mechanical and Materials Engineering, Faculty of Engineering and Built Environment, Universiti Kebangsaan Malaysia, 43600 Bangi,Selangor (Malaysia); Azhar Khan, Muhammad [Department of Physics, The Islamia University of Bahawalpur, 63100 (Pakistan); Ahmad, Mukhtar [Department of Physics, COMSATS Institute of Information Technology, Islamabad (Pakistan); Murtaza, G. [Centre for Advanced Studies in Physics, G.C. University, Lahore (Pakistan); Raza, Rizwan; Shaukat, S.F.; Asif, M.H. [Department of Physics, COMSATS Institute of Information Technology, Lahore 54000 (Pakistan); Nasir, Nadeem [Fundamental and Applied Sciences Department, National Textile University, Faisalabad (Pakistan); Abbas, Ghazanfar [Department of Physics, COMSATS Institute of Information Technology, Islamabad (Pakistan); Nazir, M.S. [Department of Chemical Engineering, COMSATS Institute of Information Technology, Lahore 54000 (Pakistan); Raza, M.R. [Department of Mechanical and Materials Engineering, Faculty of Engineering and Built Environment, Universiti Kebangsaan Malaysia, 43600 Bangi,Selangor (Malaysia)

    2014-11-15

    The effects of synthesis methods such as sol–gel (SG), self combustion (SC) and modified conventional mixed oxide (MCMO) on the structure, morphology and magnetic properties of the (Y{sub 3}Fe{sub 5}O{sub 12}) garnet ferrites have been studied in the present work. The samples of Y{sub 3}Fe{sub 5}O{sub 12} were sintered at 950 °C and 1150 °C (by SG and SC methods). For MCMO route the sintering was done at 1350 °C for 6 h. Synthesized samples prepared by various routes were investigated using X-ray diffraction (XRD) analysis, Field emission scanning electron microscopy (FESEM), Impedance network analyzer and transmission electron microscopy (TEM). The structural analysis reveals that the samples are of single phase structure and shows variations in the particle sizes and cells volumes, prepared by various routes. FESEM and TEM images depict that grain size increases with the increase of sintering temperature from 40 nm to 100 nm.Magnetic measurements reveal that garnet ferrite synthesized by sol gel method has high initial permeability (60.22) and low magnetic loss (0.0004) as compared to other garnet ferrite samples, which were synthesized by self combustion and MCMO methods. The M–H loops exhibit very low coercivity which enables the use of these materials in relays and switching devices fabrications. Thus, the garnet nanoferrites with low magnetic loss prepared by different methods may open new horizon for electronic industry for their use in high frequency applications. - Highlights: • Y{sub 3}Fe{sub 5}O{sub 12} garnet ferrites nanoparticles were synthesized by three different routes. • Impact of sintering temperature on the particle size of Y{sub 3}Fe{sub 5}O{sub 12} was evaluated. • The magnetic studies suggest the applications in relays and switching devices.

  1. Structural and magnetic properties of γ-Fe{sub 2}O{sub 3} nanostructured compacts processed by spark plasma sintering

    Energy Technology Data Exchange (ETDEWEB)

    Saravanan, P., E-mail: psdrdo@gmail.com [Department of Physics, National Taiwan University, Taipei 106, Taiwan (China); Defence Metallurgical Research Laboratory, Hyderabad 500058 (India); Hsu, Jen-Hwa, E-mail: jhhsu@phys.ntu.edu.tw [Department of Physics, National Taiwan University, Taipei 106, Taiwan (China); Sivaprahasam, D. [International Advanced Research Centre for Powder Metallurgy and New Materials, Chennai 600113 (India); Kamat, S.V. [Defence Metallurgical Research Laboratory, Hyderabad 500058 (India)

    2013-11-15

    Gram quantities of γ-Fe{sub 2}O{sub 3} nanopowders having mean particle size of 20±4 nm were synthesized using a hydrothermal method and then consolidated into dense nanostructured compacts by spark plasma sintering (SPS) at relatively low temperatures: 300–350 °C. The cubic spinel structure of the as-synthesized γ-Fe{sub 2}O{sub 3} nanoparticles (NPs) did not get altered by the SPS process; nevertheless, a moderate increase in their grain sizes was evident in the SPSed compacts (80–125 nm). The physical properties such as density (ρ), coercivity (H{sub c}) and magnetization (M{sub s}) values of γ-Fe{sub 2}O{sub 3} NPs were affected by the SPS temperature. Significantly, higher values of ρ (4.45 g/cm{sup 3}), H{sub c} (274 Oe) and M{sub s} (67.2 emu/g) were achieved for the bulk compact SPSed at 350 °C. This work highlights the merits of sintering γ-Fe{sub 2}O{sub 3} NPs by SPS –as a new method of compaction with useful magnetic properties; which cannot be realized with the conventional sintering techniques. Highlights: • γ-Fe{sub 2}O{sub 3} nanoparticles with mean size of 20±4 nm were hydrothermally synthesized. • Spark plasma sintering of γ-Fe{sub 2}O{sub 3} was performed below phase transition temperature. • Sintered compacts were investigated with respect to SPS temperature: 300–350 °C. • Cubic spinel structure of γ-Fe{sub 2}O{sub 3} nanoparticles was retained in sintered compacts. • Maximum values: ρ (4.45 g/cm{sup 3}), H{sub c} (274 Oe) and M{sub s} (67.2 emu/g) obtained at 350 °C.

  2. Solar photocatalytic activity of TiO{sub 2} modified with WO{sub 3} on the degradation of an organophosphorus pesticide

    Energy Technology Data Exchange (ETDEWEB)

    Ramos-Delgado, N.A. [Universidad Autónoma de Nuevo León, Facultad de Ciencias Químicas, San Nicolás de los Garza, N.L. (Mexico); Gracia-Pinilla, M.A. [Universidad Autónoma de Nuevo León, Facultad de Ciencias Físico-Matemáticas, Av. Universidad, Cd. Universitaria, San Nicolás de los Garza, N.L. (Mexico); Universidad Autónoma de Nuevo León, Centro de Investigación e Innovación en Desarrollo de Ingeniería y Tecnología, PIIT Km 6, Carretera al Aeropuerto, Apodaca, N.L. (Mexico); Maya-Treviño, L.; Hinojosa-Reyes, L.; Guzman-Mar, J.L. [Universidad Autónoma de Nuevo León, Facultad de Ciencias Químicas, San Nicolás de los Garza, N.L. (Mexico); Hernández-Ramírez, A., E-mail: aracely.hernandezrm@uanl.edu.mx [Universidad Autónoma de Nuevo León, Facultad de Ciencias Químicas, San Nicolás de los Garza, N.L. (Mexico)

    2013-12-15

    Highlights: • TiO{sub 2} and WO{sub 3}/TiO{sub 2} (2 and 5%) were tested in the photocatalytic malathion degradation. • The use of solar radiation in the photocatalytic degradation process was evaluated. • Modified catalyst showed greater photocatalytic activity than pure TiO{sub 2}. • The mineralization rate was improved when WO{sub 3} content on TiO{sub 2} was 2%. -- Abstract: In this study, the solar photocatalytic activity (SPA) of WO{sub 3}/TiO{sub 2} photocatalysts synthesized by the sol–gel method with two different percentages of WO{sub 3} (2 and 5%wt) was evaluated using malathion as a model contaminant. For comparative purpose bare TiO{sub 2} was also prepared by sol–gel process. The powders were characterized by X-ray diffraction (XRD), Raman spectroscopy, diffuse reflectance UV–vis spectroscopy (DRUV–vis), specific surface area by the BET method (SSA{sub BET}), scanning electron microscopy (SEM), high resolution transmission electron microscopy (HRTEM) and scanning transmission electron microscopy with a high annular angle dark field detector (STEM-HAADF). The XRD, Raman, HRTEM and STEM-HAADF analyses indicated that WO{sub 3} was present as a monoclinic crystalline phase with nanometric cluster sizes (1.1 ± 0.1 nm for 2% WO{sub 3}/TiO{sub 2} and 1.35 ± 0.3 nm for 5% WO{sub 3}/TiO{sub 2}) and uniformly dispersed on the surface of TiO{sub 2}. The particle size of the materials was 19.4 ± 3.3 nm and 25.6 ± 3 nm for 2% and 5% WO{sub 3}/TiO{sub 2}, respectively. The SPA was evaluated on the degradation of commercial malathion pesticide using natural solar light. The 2% WO{sub 3}/TiO{sub 2} photocatalyst exhibited the best photocatalytic activity achieving 76% of total organic carbon (TOC) abatement after 300 min compared to the 5% WO{sub 3}/TiO{sub 2} and bare TiO{sub 2} photocatalysts, which achieved 28 and 47% mineralization, respectively. Finally, experiments were performed to assess 2% WO{sub 3}/TiO{sub 2} catalyst activity on

  3. Fluoride adsorption from aqueous solution by magnetic core-shell Fe{sub 3}O{sub 4}@alginate-La particles fabricated via electro-coextrusion

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Yahui [School of Materials Science and Engineering, Southwest University of Science and Technology, Mianyang 621010, Sichuan (China); Engineering Research Center of Biomass Materials, Ministry of Education, Mianyang 621010, Sichuan (China); Lin, Xiaoyan, E-mail: lxy20100205@163.com [School of Materials Science and Engineering, Southwest University of Science and Technology, Mianyang 621010, Sichuan (China); Engineering Research Center of Biomass Materials, Ministry of Education, Mianyang 621010, Sichuan (China); Zhou, Quisheng [A State Key Laboratory of Pulp & Paper Engineering, South China University of Technology, Guangzhou 510640 (China); Luo, Xuegang [Engineering Research Center of Biomass Materials, Ministry of Education, Mianyang 621010, Sichuan (China)

    2016-12-15

    Graphical abstract: The magnetic core-shell Fe{sub 3}O{sub 4}@Alg-La particles were fabricated successfully by a simple method of electro-coextrusion, and employed as an adsorbent for separation of fluoride from aqueous solution. - Highlights: • Magnetic core-shell Fe{sub 3}O{sub 4}@Alg-La particles were prepared by electro-coextrusion. • The maximum adsorption capacity for fluoride at 298.15 K was 45.230 mg/g. • The adsorbent has a good saturation magnetization value. • The adsorbent has a great potential in removing the fluoride. - Abstract: The magnetic core-shell Fe{sub 3}O{sub 4}@Alg-La particles were fabricated successfully by a simple method of electro-coextrusion, and employed as an adsorbent for separation of fluoride from aqueous solution. Main factors affecting the removal of fluoride, including pH, adsorbent dosage, initial concentration, temperature and contact time were investigated. The adsorption isotherm and adsorption kinetics were studied to understand the adsorption process in detail. The experimental data were fitted well by the non-linear Freundlich isotherm and linear pseudo-second-order model, the maximum fluoride adsorption capacity was 45.230 mg/g at pH 4, 298.15 K. Thermodynamic parameters indicated that the fluoride adsorption process was feasible and spontaneous. The presence of other anions like Cl{sup −}, SO{sub 4}{sup 2−}, HCO{sub 3}{sup −} and PO{sub 4}{sup 3−} had almost no effect on the fluoride adsorption. The adsorbent can be easily separated from the solution by a magnet. The magnetic core-shell Fe{sub 3}O{sub 4}@Alg-La particles before and after fluoride adsorption were studied by SEM, FTIR, EDX and XPS, which indicated that the adsorption mechanism may be related to electrostatic attraction and Lewis acid-base interaction.

  4. Superparamagnetism and spin-glass like state for the MnFe{sub 2}O{sub 4} nano-particles synthesized by the thermal decomposition method

    Energy Technology Data Exchange (ETDEWEB)

    Gao Ruorui [Key Laboratory of Artificial Micro- and Nano-structures of Ministry of Education, School of Physics and Technology, Wuhan University, Wuhan 430072 (China); Zhang Yue, E-mail: yue-zhang@mail.hust.edu.cn [Key Laboratory of Artificial Micro- and Nano-structures of Ministry of Education, School of Physics and Technology, Wuhan University, Wuhan 430072 (China); Department of Electric Science and Technology, Huazhong University of Science and Technology, Wuhan 430074 (China); Yu Wei [Key Laboratory of Artificial Micro- and Nano-structures of Ministry of Education, School of Physics and Technology, Wuhan University, Wuhan 430072 (China); Xiong Rui [Key Laboratory of Artificial Micro- and Nano-structures of Ministry of Education, School of Physics and Technology, Wuhan University, Wuhan 430072 (China); Key Laboratory for the Green Preparation and Application of Functional Materials of Ministry of Education, Hubei University, Wuhan 430062 (China); Shi Jing [Key Laboratory of Artificial Micro- and Nano-structures of Ministry of Education, School of Physics and Technology, Wuhan University, Wuhan 430072 (China); Key Laboratory for the Green Preparation and Application of Functional Materials of Ministry of Education, Hubei University, Wuhan 430062 (China); International Center for Material Physics, Shen Yang 110015 (China)

    2012-08-15

    MnFe{sub 2}O{sub 4} nano-particles with an average size of about 7 nm were synthesized by the thermal decomposition method. Based on the magnetic hysteresis loops measured at different temperatures the temperature-dependent saturation magnetization (M{sub S}) and coercivity (H{sub C}) are determined. It is shown that above 20 K the temperature-dependence of the M{sub S} and H{sub C} indicates the magnetic behaviors in the single-domain nano-particles, while below 20 K, the change of the M{sub S} and H{sub C} indicates the freezing of the spin-glass like state on the surfaces. By measuring the magnetization-temperature (M-T) curves under the zero-field-cooling (ZFC) and field-cooling procedures at different applied fields, superparamagnetism behavior is also studied. Even though in the ZFC M-T curves peaks can be observed below 160 K, superparamagnetism does not appear until the temperature goes above 300 K, which is related with the strong inter-particle interaction. - Highlights: Black-Right-Pointing-Pointer MnFe{sub 2}O{sub 4} nano-particles with size of 7 nm were prepared. Black-Right-Pointing-Pointer The surface spin-glass like state is frozen below 20 K. Black-Right-Pointing-Pointer The peaks in ZFC magnetization-temperature curves are observed below 160 K. Black-Right-Pointing-Pointer The inter-particle interaction inhibits the superparamagnetism at room temperature.

  5. Phase Transformation Behavior of Oxide Particles Formed in Mechanically Alloyed Fe-5Y{sub 2}O{sub 3} Powder

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Ga Eon; Choi, Jung-Sun; Noh, Sanghoon; Kang, Suk Hoon; Choi, Byoung Kwon; Kim, Tae Kyu [Korea Atomic Energy Research Institute, Deajeon (Korea, Republic of); Kim, Young Do [Hanyang University, Seoul (Korea, Republic of)

    2017-05-15

    The phase transformation behavior of the oxides formed in mechanically alloyed Fe-5Y{sub 2}O{sub 3} powder is investigated. Non-stoichiometric Y-rich and Fe-rich oxides with sizes of less than 300 nm are observed in the mechanically alloyed powder. The diffusion and redistribution reactions of the elements in these oxides during heating of the powder above 800 ℃ were observed, and these reactions result in the formation of a Y{sub 3}Fe{sub 5}O{sub 12} phase after heating at 1050 ℃. Thus, it is considered that the Y{sub 2}O{sub 3} powder and some Fe powder are formed from the non-stoichiometric Y-rich and Fe-rich oxides after the mechanical alloying process, and a considerable energy accumulated during the mechanical alloying process leads to a phase transformation of the Y-rich and Fe-rich oxides to Y{sub α}Fe{sub β}O{sub γ}-type phase during heating.

  6. Synthesis and upconversion luminescence properties of YF{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers derived from Y{sub 2}O{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers

    Energy Technology Data Exchange (ETDEWEB)

    Li Dan; Dong Xiangting, E-mail: dongxiangting888@163.com; Yu Wensheng; Wang Jinxian; Liu Guixia [Changchun University of Science and Technology, Key Laboratory of Applied Chemistry and Nanotechnology at Universities of Jilin Province (China)

    2013-06-15

    YF{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers were successfully fabricated via fluorination of the relevant Y{sub 2}O{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers which were obtained by calcining the electrospun PVP/[Y(NO{sub 3}){sub 3} + Yb(NO{sub 3}){sub 3} + Er(NO{sub 3}){sub 3}] composite nanofibers. The morphology and properties of the products were investigated in detail by X-ray diffraction, scanning electron microscope, transmission electron microscope, and fluorescence spectrometer. YF{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers were pure orthorhombic phase with space group Pnma and were hollow-centered structure with mean diameter of 174 {+-} 22 nm, and YF{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers are composed of nanoparticles with size in the range of 30-60 nm. Upconversion emission spectrum analysis manifested that YF{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers emitted strong green and weak red upconversion emissions centering at 523, 545, and 654 nm, respectively. The green and red emissions were, respectively, originated from {sup 2}H{sub 11/2}/{sup 4}S{sub 3/2} {yields} {sup 4}I{sub 15/2} and {sup 4}F{sub 9/2} {yields} {sup 4}I{sub l5/2} energy levels transitions of the Er{sup 3+} ions. Moreover, the emitting colors of YF{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers were located in the green region in CIE chromaticity coordinates diagram. This preparation technique could be applied to prepare other rare earth fluoride upconversion luminescence hollow nanofibers.Graphical AbstractYF{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers with orthorhombic structure were synthesized by fluorination of the electrospun Y{sub 2}O{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers via a double-crucible method using NH{sub 4}HF{sub 2} as fluorinating agent. The mean diameter of YF{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers was 174 {+-} 22 nm. The fluorination method we proposed here has been proved to be an important method, as it can not only

  7. Mesoporous silica-coated NaYF{sub 4}:Yb{sup 3+}, Er{sup 3+} particles for drug release

    Energy Technology Data Exchange (ETDEWEB)

    Kong Deyan; Fan Yong; Zhang Cuimiao; Lin Jun, E-mail: jlin@ciac.jl.c [Chinese Academy of Sciences, State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry (China)

    2010-02-15

    NaYF{sub 4}:Yb{sup 3+}, Er{sup 3+} nanoparticles were successfully prepared by a polyol process using diethyleneglycol (DEG) as solvent. These NaYF{sub 4}:Yb{sup 3+}, Er{sup 3+} nanoparticles can be coated with mesoporous silica using nonionic triblock copolymer EO{sub 20}PO{sub 70}EO{sub 20} (P 123) as structure-directing agent and other materials. The composites can load ibuprofen and release the drug in the phosphate buffer solution (PBS). The composites were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), nitrogen absorption/desorption isotherms, fluorescence spectra, and UV/Vis absorption spectra, respectively. The composites have the mesoporous structure. In addition, the composites emit red fluorescence (from Er{sup 3+}) under 980 nm near infrared laser excitation, which can be used as fluorescent probes in the drug-delivery system.

  8. Femosecond dynamics of quasi-particles in YBa sub 2 Cu sub 3 O sub 7 minus. delta. superconductor films

    Energy Technology Data Exchange (ETDEWEB)

    Han, S.G.; Vardeny, Z.V.; Symko, O.G. (Utah Univ., Salt Lake City, UT (United States). Dept. of Physics); Koren, G. (Technion-Israel Inst. of Tech., Haifa (Israel). Dept. of Physics)

    1991-03-01

    This paper reports on the transient electronic response of YBa{sub 2}Cu{sub 3}O{sub 7{minus}{delta}} epitaxially grown HT{sub c} superconductor thin films in the femtosecond time domain, using transient photoinduced reflectivity ({Delta}R) with 60 fsec time resolution. For temperatures T {gt} T{sub c} only a bolometric signal was observed with {Delta}R {gt} O. For T {lt} T{sub c} {Delta}R {lt} O with a temperature dependent rise time of order 300 fsec followed by a relaxation (of order 3 psec) into a state with {Delta} are explained in terms of quasi-particle (QP) electronic response giving {Delta}R {lt} O. Thus the femtosecond rise time is interpreted as avalanche multiplication of QP across the gap 2{Delta} and the subsequent picosecond relaxation as QP recombination. The QP optical response is explained within the two fluid model.

  9. Luminescence and thermoluminescence properties of Sr{sub 3}WO{sub 6}:Eu{sup 3+} phosphor

    Energy Technology Data Exchange (ETDEWEB)

    Emen, F.M., E-mail: femen106@gmail.com [Department of Chemistry, Faculty of Arts and Science, Mehmet Akif Ersoy University, TR 15030, Burdur (Turkey); Altinkaya, R. [Department of Chemistry, Faculty of Arts and Science, Mersin University, TR 33343, Mersin (Turkey)

    2013-02-15

    Sr{sub 3-x}WO{sub 6}:xEu{sup 3+} (x varies from 0.01 to 0.06) phosphors have been prepared at high temperature by the solid-state method. The crystal structure of Sr{sub 2.95}WO{sub 6}:0.05Eu{sup 3+} phosphor has been determined as a triclinic P-1 space group with a=8.3608 (19) A, b=8.2903 (24) A, c=8.2145 (23) A, {alpha}=89.79 (3){sup Degree-Sign }, {beta}=89.82 (3){sup Degree-Sign }, and {gamma}=89.753 (22){sup Degree-Sign }. The excitation spectrum of Sr{sub 2.95}WO{sub 6}:0.05Eu{sup 3+} phosphor reveals five excitation bands: one is assigned to the charge-transfer (CTLM) band of Sr{sub 3}WO{sub 6} host at 307 nm, and another is assigned to intra-4f transitions between 393 nm and 600 nm. The emission spectrum of Sr{sub 2.95}WO{sub 6}:0.05Eu{sup 3+} phosphor exhibits a series of emission bands, which are attributed to the {sup 5}D{sub 0}{yields}{sup 7}F{sub j} (j=0-4) transitions of Eu{sup 3+} ions. The luminescence studies revealed that the Eu{sup 3+} ions show high luminescent efficiency in emitting red light at 616 nm. The thermoluminescence glow curve shows one dominant glow peak observed at 56 Degree-Sign C which is related to the defects at shallow trap depth. The trap parameters mainly activation energy (E{sub a}) and the order of the kinetics (b) were evaluated by using Rasheedy's three points method (TPM). - Highlights: Black-Right-Pointing-Pointer The Sr{sub 3}WO{sub 6}:Eu{sup 3+} phosphor was prepared by using conventional ceramic method. Black-Right-Pointing-Pointer The diffraction peaks of phosphor have been indexed to triclinic system. Black-Right-Pointing-Pointer The emission peak at 616 nm belongs to {sup 5}D{sub 0}{yields}{sup 7}F{sub 2} electric dipole transitions of Eu{sup 3+}. Black-Right-Pointing-Pointer The emission band of WO{sub 6} and excitation bands of Eu{sup 3+} are overlapping each other. Black-Right-Pointing-Pointer The energy transfer from WO{sub 6} groups to the Eu{sup 3+} ions occurs under the UV excitation.

  10. FORMATION OF N{sub 3}, CH{sub 3}, HCN, AND HNC FROM THE FAR-UV PHOTOLYSIS OF CH{sub 4} IN NITROGEN ICE

    Energy Technology Data Exchange (ETDEWEB)

    Lo, Jen-Iu; Chou, Sheng-Lung; Peng, Yu-Chain; Lin, Meng-Yeh; Lu, Hsiao-Chi; Cheng, Bing-Ming, E-mail: bmcheng@nsrrc.org.tw [National Synchrotron Radiation Research Center, No. 101, Hsin-Ann Road, Hsinchu Science Park, Hsinchu 30076, Taiwan (China)

    2015-11-15

    The irradiation of pure solid N{sub 2} at 3 K with far-ultraviolet light from a synchrotron produced infrared absorption lines at 1657.7, 1655.6, and 1652.4 cm{sup −1} and an ultraviolet absorption line at 272.0 nm, which are characteristic of the product N{sub 3}. The threshold wavelength at which N{sub 3} was generated was 145.6 ± 2.9 nm, corresponding to an energy of 8.52 ± 0.17 eV. The photolysis of isotopically labeled {sup 15}N{sub 2} at 3 K consistently led to the formation of {sup 15}N{sub 3} with the same threshold wavelength of 145.6 ± 2.9 nm for its formation. The photolysis of CH{sub 4} in nitrogen ice in low concentrations also led to the formation of N{sub 3}, together with CH{sub 3}, HCN, and HNC, with the same threshold wavelength of 145.6 ± 2.9 nm. These results indicate that N{sub 3} radicals may play an important role in the photochemistry of nitrogen ices in astronomical environments.

  11. Structure and phase transition of BiFeO{sub 3} cubic micro-particles prepared by hydrothermal method

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Jian-Ping, E-mail: zhoujp@snnu.edu.cn [College of Physics and Information Technology, Shaanxi Normal University, Xi’an 710062 (China); Yang, Ruo-Lin; Xiao, Rui-Juan; Chen, Xiao-Ming [College of Physics and Information Technology, Shaanxi Normal University, Xi’an 710062 (China); Deng, Chao-Yong [Department of Electronic Science, Guizhou University, Guizhou Guiyang 550025 (China)

    2012-11-15

    Graphical abstract: Bismuth ferrite (BiFeO{sub 3}) cubic micro-particles with smooth surfaces were synthesized. BiFeO{sub 3} has a hexagonal perovskite structure with a space group R3c below 370 °C and rhombohedral perovskite structure with a space group R3m below 755 °C, undergoes a phase transition in the temperature range of 755–817 °C to a cubic structure, then decompose to liquid and Fe{sub 2}O{sub 3} above 939 °C. Highlights: ► BiFeO{sub 3} micro-particles with smooth surface were synthesized by hydrothermal method. ► BiFeO{sub 3} enjoys hexagonal structure with well element ratio and chemical valence. ► BiFeO{sub 3} transition from rhombohedral phase to cubic phase lasts 60 °C. -- Abstract: Single-phase bismuth ferrite (BiFeO{sub 3}) powders were synthesized with a hydrothermal method by controlling the experimental conditions carefully. The powder structure, morphology and composition were characterized by using X-ray diffraction (XRD), scanning electron microscopy, transmission electron microscope, Raman measurement and X-ray photoelectron spectroscopy. The particles change from irregular agglomerations to regular cubes with increasing KOH concentration. The large BiFeO{sub 3} cubic particles enjoy much smooth surfaces with well-matched element ratio (Bi:Fe:O = 1:1:3) and chemical valence (Bi{sup 3+}, Fe{sup 3+} and O{sup 2−}). The high temperature XRD and differential scanning calorimetry show that BiFeO{sub 3} powders have a hexagonal perovskite structure with a space group R3c below 370 °C and a rhombohedral structure with a space group R3m below 755 °C. BiFeO{sub 3} undergoes a phase transition in the temperature range of 755–817 °C from rhombohedral structure to a cubic phase, then decomposes to liquid and Fe{sub 2}O{sub 3} above 939 °C.

  12. Influence of crystallite size on the magnetic properties of Fe{sub 3}O{sub 4} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Upadhyay, Sneha [Dept of Applied Science, Symbiosis Institute of Technology, SIU, Lavale, Mulshi, Pune 412 115 (India); Parekh, Kinnari [K C Patel R & D Center, Charotar University of Science & Technology, Changa 388421 (India); Pandey, Brajesh, E-mail: bpandey@gmail.com [Dept of Applied Science, Symbiosis Institute of Technology, SIU, Lavale, Mulshi, Pune 412 115 (India)

    2016-09-05

    Structural and magnetic properties of chemically synthesized magnetite nanoparticles have been studied using X-ray diffraction, Transmission Electron Microscopy and Vibrating Sample Magnetometer. Magnetically the synthesized nanoparticles are ranging from superparamagnetic to multi domain state. Average crystallite size of the synthesized magnetite nanoparticles were determined using X-ray line broadening and are found to be in the range of 9–53 nm. On the other hand, the TEM images show that the size is ranging between 7.9 and 200 nm with the transition from spherical superparamagnetic particles to faceted cubic multi domain particles. Magnetic parameters of the samples show a strong dependence on average crystallite size. The ratio of coercive field at 20 K to that at 300 K (H{sub c} (20 K)/H{sub c} (300 K)) increased sharply with decrease in crystallite size. A critical crystallite diameter of order 36 nm may be inferred as boundary between single domain to multi domain transition. Zero-field-cooled (ZFC) and field-cooled (FC) measurements at 10 Oe field validate the same for smallest and largest size samples, confirming that the anisotropy energy is greater than thermal energy upto 300 K temperature. For 9 nm sample broad ZFC curve with overlapping of FC curve is observed just at 300 K, indicating the effect of strong dipolar field in superparamagnetic system. - Graphical abstract: We present our study on magnetite nanoparticles. We observed that the synthesized nanoparticles behave like single domain particles in the range of 14 nm–36 nm. They show superparamagnetic properties if particles are smaller than 14 nm and multi-domain properties when the particles are bigger than 36 nm. - Highlights: • Magnetite nanoparticles have been synthesized using chemical precipitation method. • Smaller magnetite particles below 14 nm in size are in super-paramagnetic state. • Bigger particles show multi-domain character. • Magnetite in the size range 14–36 is

  13. Quasi-homoepitaxial growth of a-axis oriented PrBa sub 2 Cu sub 3 O sub 7 sub - subdelta thick film on (100) YBa sub 2 Cu sub 3 O sub 7 sub - subdelta single crystal

    CERN Document Server

    Sato, M; Morishita, T

    2003-01-01

    The structural characterizations of the quasi-homoepitaxial growth of a-axis oriented PrBa sub 2 Cu sub 3 O sub 7 sub - subdelta thick film grown on (100) YBa sub 2 Cu sub 3 O sub 7 sub - subdelta single crystal were investigated in comparison with those of the film grown on (001) YBa sub 2 Cu sub 3 O sub 7 sub - subdelta single crystal. The a-axis oriented PrBa sub 2 Cu sub 3 O sub 7 sub - subdelta films, expected to be a barrier layer, were prepared using a dc-95 MHz hybrid plasma sputtering on (100) and (001) YBa sub 2 Cu sub 3 O sub 7 sub - subdelta single crystals that are superconducting ground planes. The atomic force microscopy image revealed that the surfaces of 700-nm-thick a-axis PrBa sub 2 Cu sub 3 O sub 7 sub - subdelta films on (100) YBa sub 2 Cu sub 3 O sub 7 sub - subdelta single crystals were smooth with a mean roughness of 2.8 nm. X-ray diffraction scans showed that a-axis PrBa sub 2 Cu sub 3 O sub 7 sub - subdelta films deposited on (100) YBa sub 2 Cu sub 3 O sub 7 sub - subdelta single cry...

  14. Ion generation and CPC detection efficiency studies in sub 3-nm size range

    Energy Technology Data Exchange (ETDEWEB)

    Kangasluoma, J.; Junninen, H.; Sipilae, M.; Kulmala, M.; Petaejae, T. [Department of Physics, P.O. Box 64, 00014, University of Helsinki, Helsinki (Finland); Lehtipalo, K. [Department of Physics, P.O. Box 64, 00014, University of Helsinki, Helsinki (Finland); Airmodus Ltd., Finland, Gustaf Haellstroemin katu 2 A, 00560 Helsinki (Finland); Mikkilae, J.; Vanhanen, J. [Airmodus Ltd., Finland, Gustaf Haellstroemin katu 2 A, 00560 Helsinki (Finland); Attoui, M. [University Paris Est Creteil, University Paris-Diderot, LISA, UMR CNRS 7583 (France); Worsnop, D. [Department of Physics, P.O. Box 64, 00014, University of Helsinki, Helsinki (Finland) and Aerodyne Research Inc., Billerica, MA (United States)

    2013-05-24

    We studied the chemical composition of commonly used condensation particle counter calibration ions with a mass spectrometer and found that in our calibration setup the negatively charged ammonium sulphate, sodium chloride and tungsten oxide are the least contaminated whereas silver on both positive and negative and the three mentioned earlier in positive mode are contaminated with organics. We report cut-off diameters for Airmodus Particle Size Magnifier (PSM) 1.1, 1.3, 1.4, 1.6 and 1.6-1.8 nm for negative sodium chloride, ammonium sulphate, tungsten oxide, silver and positive organics, respectively. To study the effect of sample relative humidity on detection efficiency of the PSM we used different humidities in the differential mobility analyzer sheath flow and found that with increasing relative humidity also the detection efficiency of the PSM increases.

  15. Ion generation and CPC detection efficiency studies in sub 3-nm size range

    International Nuclear Information System (INIS)

    Kangasluoma, J.; Junninen, H.; Sipilä, M.; Kulmala, M.; Petäjä, T.; Lehtipalo, K.; Mikkilä, J.; Vanhanen, J.; Attoui, M.; Worsnop, D.

    2013-01-01

    We studied the chemical composition of commonly used condensation particle counter calibration ions with a mass spectrometer and found that in our calibration setup the negatively charged ammonium sulphate, sodium chloride and tungsten oxide are the least contaminated whereas silver on both positive and negative and the three mentioned earlier in positive mode are contaminated with organics. We report cut-off diameters for Airmodus Particle Size Magnifier (PSM) 1.1, 1.3, 1.4, 1.6 and 1.6-1.8 nm for negative sodium chloride, ammonium sulphate, tungsten oxide, silver and positive organics, respectively. To study the effect of sample relative humidity on detection efficiency of the PSM we used different humidities in the differential mobility analyzer sheath flow and found that with increasing relative humidity also the detection efficiency of the PSM increases.

  16. Preparation, microstructure and magnetic properties of Sm(Co,Hf){sub 7}/Co nanocomposite particles by polyol method

    Energy Technology Data Exchange (ETDEWEB)

    Bu, Shao-Jing; Duan, Xiu-Li; Han, Xu-Hao; Sun, Ji-Bing, E-mail: hbgdsjb@126.com; Chi, Xiang; Cui, Chun-Xiang

    2017-02-01

    Hard/soft Sm-Co/Co nanocomposite particles were prepared by reducing CoCl{sub 2}·6H{sub 2}O in the solution containing ball-milled Sm(Co, Hf){sub 7} particles by a simple polyol method with ethylene glycol as the solvent. Phase composition, microstructure and magnetic properties of the particles were analyzed by XRD, TEM (HRTEM) and VSM, respectively. It has been found that Sm-Co/Co core/shell structure is formed in which the Co shell is 3–5 nm in thickness and mainly exists in hcp-Co phase. At the same time, fcc-Co tends to nucleate and grow independently between Sm-Co particles. The formation mechanism of Sm-Co/Co composite particles is discussed and corresponding model is established. Sm-Co/Co composite particles perform obvious remanence enhancement effects especially after being heated at 450 °C for 15 min.

  17. Strengthening analyses and mechanical assessment of Ti/Al{sub 2}O{sub 3} nano-composites produced by friction stir processing

    Energy Technology Data Exchange (ETDEWEB)

    Shafiei-Zarghani, Aziz, E-mail: ashafiei@ut.ac.ir [Center of Excellence for Surface Engineering and Corrosion Protection of Industries, School of Metallurgy and Materials Engineering, College of Engineering, University of Tehran, Tehran (Iran, Islamic Republic of); Kashani-Bozorg, Seyed Farshid, E-mail: fkashani@ut.ac.ir [Center of Excellence for Surface Engineering and Corrosion Protection of Industries, School of Metallurgy and Materials Engineering, College of Engineering, University of Tehran, Tehran (Iran, Islamic Republic of); Gerlich, Adrian P., E-mail: adrian.gerlich@uwaterloo.ca [Department of Mechanical and Mechatronics Engineering, University of Waterloo, Waterloo (Canada)

    2015-04-17

    The present work investigates strengthening mechanisms and mechanical assessment of Ti/Al{sub 2}O{sub 3} nano-composites produced by friction stir processing of commercially pure titanium using nano-sized Al{sub 2}O{sub 3} with different volume fractions and particle sizes. Microstructural analyses were conducted to characterize the grain size of matrix, size and dispersion of reinforcing particles. The mean grain size of the composites ranged from ~0.7 to 1.1 μm that is much lower than 28 μm of the as-received material. Reduction of grain size was found to be in agreement with Rios approach (based on energy dissipated during the motion of an interface through particle dispersion), and showed deviation from Zener pinning model. Scanning and transmission electron microscopies revealed a near uniform dispersion of Al{sub 2}O{sub 3} nano-particles, with only a small fraction of widely spaced clusters. The maximum compression yield strength of the fabricated nano-composite (Ti/3.9%vol of 20 nm-Al{sub 2}O{sub 3}) was found to be ~494 MPa that is ~1.5 times higher than that of the as-received material. Strengthening analyses based on grain refining (Hall–Petch approach), load transfer from matrix to reinforcements, Orowan looping, and enhanced dislocation density due to thermal mismatch effects were carried out considering Al{sub 2}O{sub 3} reinforcement with different volume fractions and sizes. However, Hall–Petch approach was found to be the dominant mechanism for the enhancement of yield strength.

  18. Orthorhombic MoO{sub 3} nanobelts based NO{sub 2} gas sensor

    Energy Technology Data Exchange (ETDEWEB)

    Mane, A.A. [Thin Film Nanomaterials Laboratory, Department of Physics, Shivaji University, Kolhapur 416 004 (India); General Science and Humanities Department, Sant Gajanan Maharaj College of Engineering, Mahagaon, 416 503 (India); Moholkar, A.V., E-mail: avmoholkar@gmail.com [Thin Film Nanomaterials Laboratory, Department of Physics, Shivaji University, Kolhapur 416 004 (India)

    2017-05-31

    Highlights: • The effect of thickness on physicochemical and NO{sub 2} gas sensing properties of sprayed MoO{sub 3} nanobelts has been reported. • The sprayed MoO{sub 3} nanobelts show the NO{sub 2} gas response of 68% for 100 ppm concentration at an operating temperature of 200 °C. • The lower detection limit of MoO{sub 3} nanobelts based NO{sub 2} sensor is found to be half of the IDLH value (20 ppm). - Abstract: Molybdenum trioxide (MoO{sub 3}) nanobelts have been deposited onto the glass substrates using chemical spray pyrolysis (CSP) deposition method. The XRD patterns reveal that films are polycrystalline having an orthorhombic crystal structure. Raman spectra confirm that the films are orthorhombic in phase. The XPS study shows the presence of two well resolved spectral lines of Mo-3d core levels appearing at the binding energy values of 232.82 eV and 235.95 eV corresponding to Mo-3d{sub 5/2} and Mo-3d{sub 3/2}, respectively. These binding energy values are assigned to Mo{sup 6+} oxidation state of fully oxidized MoO{sub 3}. The FE-SEM micrographs show the formation of nanobelts-like morphology. The AFM micrographs reveal that the RMS surface roughness increases from 16.5 nm to 17.5 nm with increase in film thickness from 470 nm to 612 nm and then decreases to 16 nm for 633 nm film thickness. The band gap energy is found to be decreased from 3.40 eV to 3.38 eV. To understand the electronic transport phenomenon in MoO{sub 3} thin films, dielectric properties are studied. For 612 nm film thickness, the highest NO{sub 2} gas response of 68% is obtained at an operating temperature of 200 °C for 100 ppm concentration with response and recovery times of 15 s and 150 s, respectively. The lower detection limit is found to be 10 ppm which is half of the immediately dangerous to life or health (IDLH) value of 20 ppm. Finally, NO{sub 2} gas sensing mechanism in an orthorhombic MoO{sub 3} crystal structure is discussed in detail.

  19. Positively charged TiO{sub 2} particles in non-polar system for electrophoretic display

    Energy Technology Data Exchange (ETDEWEB)

    Chang, Young Seon

    2005-02-15

    Electrophoretic display uses a technique called electrophoresis to represent images and letters electronically with electronic ink. Although it has good characteristics such as wide viewing angle, high contrast ratio and extremely low power consumption, there are still several issues to be resolved to improve its performances. Higher mobility and stability of the ink particles are the most important issues among them. In this study, TiO{sub 2} particles coated with acrylamide were found to be effective ink particles that satisfy higher mobility and stability. The TiO{sub 2} particles coated with 5∼40% acrylamide were prepared by dispersion polymerization using monomers of methyl methacrylate (MMA) and acrylamide. The TiO{sub 2} particles coated with acrylamide were dispersed in isopar-G with sorbitan esters such as span 20, span 80 and span 85. The size of the TiO{sub 2} particles were changed from 200±150 nm to 350∼500 nm by the coating process. The morphology of coated particles was observed using a transmission electron microscope (TEM) and thermogravimetric analysis (TGA). From the TGA results, the weight fraction of TiO{sub 2} and polymer in coated particle were calculated. From the zeta potential measurement, it was shown that as acrylamide concentration was increased from 5% to 30%, zeta potential of the coated TiO{sub 2} particles was increased from 50mV to about 230mV. The zeta potential of the coated TiO{sub 2} particles with 40% acrylamide was decreased to 50mV. As a stabilizer, span 85 was the most effective surfactant to improve stability of the TiO{sub 2} particles coated with acrylamide among used surfactants in this study. Span 85 showed best stability in the storage test with TiO{sub 2} particles coated with 10% acrylamide. The mobility of TiO{sub 2} particles coated with acrylamide with span 85 in dye solution (Oil Blue-N dissolved in isopar-G) were measured by ITO cell test. The mobility of TiO{sub 2} particles coated with 10∼30

  20. Sub-10-nm suspended nano-web formation by direct laser writing

    Science.gov (United States)

    Wang, Sihao; Yu, Ye; Liu, Hailong; Lim, Kevin T. P.; Madurai Srinivasan, Bharathi; Zhang, Yong Wei; Yang, Joel K. W.

    2018-06-01

    A diffraction-limited three-dimensional (3D) direct laser writing (DLW) system based on two-photon polymerization can routinely pattern structures at the 100 nm length scale. Several schemes have been developed to improve the patterning resolution of 3D DLW but often require customized resist formulations or multi-wavelength exposures. Here, we introduce a scheme to produce suspended nano-webs with feature sizes below 10 nm in IP-Dip resist using sub-threshold exposure conditions in a commercial DLW system. The narrowest suspended lines (nano-webs) measured 7 nm in width. Larger ∼20 nm nano-webs were patterned with ∼80% yield at increased laser powers. In addition, closely spaced nano-gaps with a center-to-center distance of 33 nm were produced by patterning vertically displaced suspended lines followed by metal deposition and liftoff. We provide hypotheses and present preliminary results for a mechanism involving the initiation of a percolative path and a strain-induced narrowing in the nano-web formation. Our approach allows selective features to be patterned with dimensions comparable to the sub-10 nm patterning capability of electron-beam lithography (EBL).

  1. The anomalous behaviour of Ag-Al sub 2 O sub 3 Cermet electroformed devices

    CERN Document Server

    Khan, M S R

    2003-01-01

    Cermet coating consisting of silver particles in an aluminium oxide matrix were prepared on glass substrates by vacuum deposition. Variation of the circulating current with potential difference was obtained in evaporated Al/Ag-Al sub 2 O sub 3 /Cu sandwich structures, 100 to 200 nm thick containing 10 wt % Ag. It was observed that the investigated sandwich structures exhibit anomalous behaviour such as electroforming with Voltage-Controlled-Negative Resistance (VCNR) in vacuo of approx 4 x 10 sup - sup 6 torr. The formed characteristics were explained on the basis of filamentary model.

  2. Structural and photoluminescence investigations of Sm{sup 3+} doped BaY{sub 2}ZnO{sub 5} nanophosphors

    Energy Technology Data Exchange (ETDEWEB)

    Chahar, Sangeeta; Taxak, V.B.; Dalal, Mandeep; Singh, Sonika; Khatkar, S.P., E-mail: s_khatkar@rediffmail.com

    2016-05-15

    Highlights: • BaY{sub 2(1−x)}Sm{sub 2x}ZnO{sub 5} nanophosphors have been synthesized via solution combustion. • The nanophosphors have been characterized by XRD, TEM and PL spectroscopy. • The crystal structure reveals influence of doping on lattice parameters. • This nanophosphor executes orange–red emission under near UV excitation. - Abstract: BaY{sub 2}ZnO{sub 5}:Sm{sup 3+} nanophosphor was successfully synthesized using solution combustion process. XRD and photoluminescence (PL) techniques were used to analyze the structural and photoluminescence properties. Morphological study of the thermally stable powder was carried out using transmission electron microscope (TEM). Rietveld refinement technique has been used to analyze the samples qualitatively as well as quantitatively. X-Ray diffraction analysis confirms that the highly crystalline single phased Sm{sup 3+} doped BaY{sub 2}ZnO{sub 5} nanophosphor crystallizes in orthorhombic lattice with Pbnm space group. The average particle size lies in the range 80–90 nm with spherical morphology. The photoluminescence excitation at 411 nm yields an intense orange–red emission centered at 610 nm due to {sup 4}G{sub 5/2}–{sup 6}H{sub 7/2} transition. The concentration dependent luminescent behavior of BaY{sub 2(1−x)}Sm{sub 2x}ZnO{sub 5} nanophosphor shows that the optimum concentration for best luminescence is 3 mol%. These results indicate that these nanophosphors find potential applications in the field of phosphor-converted white LED systems.

  3. Aerosol fluxes and particle growth above managed grassland

    Directory of Open Access Journals (Sweden)

    E. Nemitz

    2009-08-01

    Full Text Available Particle deposition velocities (11–3000 nm diameter measured above grassland by eddy covariance during the EU GRAMINAE experiment in June 2000 averaged 0.24 and 0.03 mm s−1 to long (0.75 m and short (0.07 m grass, respectively. After fertilisation with 108 kg N ha−1 as calcium ammonium nitrate, sustained apparent upward fluxes of particles were observed. Analysis of concentrations and fluxes of potential precursor gases, including NH<sub>3sub>, HNO<sub>3sub>, HCl and selected VOCs, shows that condensation of HNO<sub>3sub> and NH<sub>3sub> on the surface of existing particles is responsible for this effect. A novel approach is developed to derive particle growth rates at the field scale, from a combination of measurements of vertical fluxes and particle size-distributions. For the first 9 days after fertilization, growth rates of 11 nm particles of 7.04 nm hr−1 and 1.68 nm hr−1 were derived for day and night-time conditions, respectively. This implies total NH<sub>4sub>NO>3sub> production rates of 1.11 and 0.44 μg m3 h−1, respectively. The effect translates into a small error in measured ammonia fluxes (0.06% day, 0.56% night and a large error in NH<sub>4sub>+ and NO<sub>3sub> aerosol fluxes of 3.6% and 10%, respectively. By converting rapidly exchanged NH<sub>3sub> and HNO<sub>3sub> into slowly depositing NH<sub>4sub>NO>3sub>, the reaction modifies the total N budget, though this effect is small (<1% for the 10 days following fertilization, as NH<sub>3sub> emission dominates the net flux. It is estimated that 3.8% of the fertilizer N was volatilised as NH<sub>3sub>, of which 0.05% re-condensed to form NH<sub>4sub>NO>3sub> particles within the lowest 2 m of the surface layer. This surface induced process would at least scale up to a global NH<sub>4sub>NO>3sub> formation of ca. 0.21 kt N yr

  4. Synthesis and characterization of Ni{sub 0.7}Zn{sub 0.3}Fe{sub 2}O{sub 4} ferrospinel: performance evaluation for methyl and ethyl esterification; Sintese e caracterizacao do ferroespinelio Ni{sub 0,7}Zn{sub 0,3}Fe{sub 2}O{sub 4}: avaliacao de desempenho na esterificacao metilica e etilica

    Energy Technology Data Exchange (ETDEWEB)

    Mapossa, A.B., E-mail: mapossabenjox@gmail.com [Curso de Quimica, Dept. de Ciencias Naturais, Universidade Pedagogica de Mocambique, Delegacao de Manica, Chimoio (Mozambique); Dantas, J.; Diniz, V.C.S.; Costa, A.C.F.M. [Universidade Federal de Campina Grande (UFCG), PB (Brazil). Programa de Pos-Graduacao em Ciencia e Engenharia de Materiais; Silva, M.R. [Universidade Federal de Itajuba (UNIFEI), MG (Brazil). Dept. de Fisica; Kiminami, R.H.G.A. [Universidade Federal de Sao Carlos (UFSCar), SP (Brazil). Departamento de Engenharia de Materiais

    2017-04-15

    Ni{sub 0.7}Zn{sub 0.3}Fe{sub 2}O{sub 4} ferrospinel was synthesized by combustion and its catalytic performance in methyl and ethyl esterification of the soybean oil was investigated. The samples were characterized by X-ray diffraction, Rietveld refinement analysis, energy dispersive X-ray fluorescence spectroscopy, Fourier transform infrared spectroscopy, textural analysis, scanning electron microscopy, density by picnometry, particle size analysis, thermogravimetric analysis, magnetic measurements, and catalytic tests. The synthesis was efficient resulting in a ferrospinel with single phase Ni{sub 0.7}Zn{sub 0.3}Fe{sub 2}O{sub 4} with crystallite size of 20 nm, high surface area (86 m{sup 2}/g) and saturation magnetization of 18 emu/g. The ferrospinel had promising catalytic activity in both reaction conditions studied, being more active in the conversion of soybean oil to biodiesel in methyl esterification with an average conversion of 93.9±2.8%. (author)

  5. Analysis of (Ba,Ca,Sr){sub 3}MgSi{sub 2}O{sub 8}:Eu{sup 2+}, Mn{sup 2+} phosphors for application in solid state lighting

    Energy Technology Data Exchange (ETDEWEB)

    Han, J.K. [University of California, San Diego, Materials Science and Engineering Program, La Jolla, CA 92093 (United States); Piqutte, A.; Hannah, M.E. [OSRAM SYLVANIA Central Research, 71 Cherry Hill Drive Beverly, MA 01915 (United States); Hirata, G.A. [Centro de Nanociencias y Nanotecnolgía, Universidad Nacional Autónoma de México, Km. 107 Carretera Tijuana-Ensenada Apdo, Ensenada MX CP 22860 (Mexico); Talbot, J.B. [University of California, San Diego, Materials Science and Engineering Program, La Jolla, CA 92093 (United States); University of California, San Diego, Department of Nanoengineering, La Jolla, CA 92093 (United States); Mishra, K.C. [OSRAM SYLVANIA Central Research, 71 Cherry Hill Drive Beverly, MA 01915 (United States); McKittrick, J., E-mail: jmckittrick@ucsd.edu [University of California, San Diego, Materials Science and Engineering Program, La Jolla, CA 92093 (United States); University of California, San Diego, Department of Mechanical and Aerospace Engineering, La Jolla, CA 92093 (United States)

    2014-04-15

    The luminescence properties of Eu{sup 2+} and Mn{sup 2+} co-activated (Ba,Ca,Sr){sub 3}MgSi{sub 2}O{sub 8} phosphors prepared by combustion synthesis were studied. Eu{sup 2+}-activated (Ba,Ca,Sr){sub 3}MgSi{sub 2}O{sub 8} has a broad blue emission band centered at 450–485 nm and Eu{sup 2+}–Mn{sup 2+}-activated (Ba,Ca,Sr){sub 3}MgSi{sub 2}O{sub 8} exhibits a red emission around 620–703 nm, depending on the relative concentrations of Ba, Ca and Sr. The particle size of Eu{sup 2+} and Mn{sup 2+} co-activated (Ba,Ca){sub 3}MgSi{sub 2}O{sub 8} ranges from 300 nm to 1 μm depending on the metal ion and are agglomerated due to post-synthesis, high temperature annealing. The green emission of Ba{sub 3}MgSi{sub 2}O{sub 8} originates from secondary phases (Ba{sub 2}SiO{sub 4} and BaMgSiO{sub 4}) confirmed by emission spectra and X-ray diffraction patterns. The secondary phases of Ba{sub 3}MgSi{sub 2}O{sub 8} are removed by the addition of Sr. The quantum efficiencies range from 45% to 70% under 400 nm excitation and the lifetime of red emission of Ba{sub 3}MgSi{sub 2}O{sub 8} decreases significantly with increasing temperature, which is 54% at 400 K of that at 80 K compared to that of blue emission (90% at 400 K of that at 80 K). -- highlights: • (Ba,Ca,Sr){sub 3}MgSi{sub 2}O{sub 8}:Eu{sup 2+}, Mn{sup 2+} phosphors were prepared by a combustion synthesis method. • The emission spectra consist of broad blue-emission band and red-emission band. • The quantum efficiencies range between 45% and 70%, depending on the relative concentrations of Ba, Ca and Sr. • The secondary phases were eliminated by additions of Sr. • Lifetime of the red-emission decreases with increasing temperature, suggesting that these phosphors are not useful for solid state lighting applications.

  6. Formation and microstructure of Al{sub 2}O{sub 3}-YAG eutectic ceramics by phase transformation from metastable system to equilibrium system

    Energy Technology Data Exchange (ETDEWEB)

    Nagira, Tomoya; Yasuda, Hideyuki; Yoshiya, Masato [Department of Adaptive Machine Systems, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871 (Japan)], E-mail: nagira@ams.eng.osaka-u.ac.jp

    2009-05-01

    Unidirectionally solidified Al{sub 2}O{sub 3}-YAG(Y{sub 3}Al{sub 5}O{sub 12}: yttrium-aluminum-garnet) eutectic ceramic composites have been recognized as encouraging heat-resistance materials because of the superior mechanical properties at high temperatures. In addition to the excellent mechanical properties at high temperatures, some interesting solidification phenomena have been reported in the Al{sub 2}O{sub 3}-Y{sub 2}O{sub 3} system. The Al{sub 2}O{sub 3}-YAG equilibrium eutectic at 2099 K and the Al{sub 2}O{sub 3}-YAP metastable eutectic at 1975 K exist in the Al{sub 2}O{sub 3}-Y{sub 2}O{sub 3} system. The heating the metastable eutectic up to temperatures above the metastable eutectic temperature produced the undercooled melt. Solidification in the equilibrium path accompanied the melting of the metastable eutectic. The solidification process using undercooled melt resulted in the fine and uniform eutectic structure. In this study, the effect of the initial Al{sub 2}O{sub 3}-YAP particles size on the undercooled melt formation was examined. The Al{sub 2}O{sub 3}-YAP particles with diameters more than several {mu}m resulted in the transformation through the undercooled melt. EBSD analysis showed that the domains of Al{sub 2}O{sub 3} grains with same crystallographic orientation were observed and that their domain size depended on the Al{sub 2}O{sub 3}-YAP particles size. On the other hand, for the Al{sub 2}O{sub 3}-YAP particles with a diameter of 500 nm, the each Al{sub 2}O{sub 3} grain with diameter of about 1 {mu}m had the different crystallographic orientations, which suggested that the transformation from metastable eutectic to equilibrium eutectic occurred in the solid state. The increase in the Al{sub 2}O{sub 3}-YAP free surface area suppressed the undercooled melt formation.

  7. Synthesis, vibrational and optical properties of a new three-layered organic-inorganic perovskite (C{sub 4}H{sub 9}NH{sub 3}){sub 4}Pb{sub 3}I{sub 4}Br{sub 6}

    Energy Technology Data Exchange (ETDEWEB)

    Dammak, T., E-mail: thameurlpa@yahoo.f [Laboratoire de Physique appliquee (LPA), Faculte des Sciences de Sfax, 3018, BP 802 (Tunisia); Elleuch, S. [Laboratoire de Physique appliquee (LPA), Faculte des Sciences de Sfax, 3018, BP 802 (Tunisia); Bougzhala, H. [Laboratoire de cristallochimie et des materiaux, Faculte des Sciences de Tunis (Tunisia); Mlayah, A. [Centre d' Elaboration de Materiaux et d' Etudes Structurales, CNRS-Universite Paul Sabatier, 29 rue Jeanne Marvig, 31055 Toulouse, Cedex 4 (France); Chtourou, R. [Centre de Recherche et des Technologies de l' Energie CRTEn BP. 95, Hammam-Lif 2050, Laboratoire de Photovoltaique et de Semiconducteur (Tunisia); Abid, Y. [Laboratoire de Physique appliquee (LPA), Faculte des Sciences de Sfax, 3018, BP 802 (Tunisia)

    2009-09-15

    An organic-inorganic hybrid perovskite (C{sub 4}H{sub 9}NH{sub 3}){sub 4}Pb{sub 3}I{sub 4}Br{sub 6} was synthesized and studied by X-ray diffraction, Raman and infrared spectroscopies, optical transmission and photoluminescence. The title compound, abbreviated (C{sub 4}){sub 4}Pb{sub 3}I{sub 4}Br{sub 6}, crystallises in a periodic two-dimensional multilayer structure with P2{sub 1}/a space group. The structure is built up from alternating inorganic and organic layers. Each inorganic layer consists of three sheets of PbX{sub 6} (X=I, Br) octahedra. Raman and infrared spectra of the title compound were recorded in the 100-3500 and 400-4000 cm{sup -1} frequency ranges, respectively. An assignment of the observed vibration modes is reported. Optical transmission measurements, performed on thin films of (C{sub 4}){sub 4}Pb{sub 3}I{sub 4}Br{sub 6}, revealed two absorption bands at 474 and 508 nm. Photoluminescence measurements have shown a green emission peak at 519 nm.

  8. Chemical vapour deposition of freestanding sub-60 nm graphene gyroids

    Science.gov (United States)

    Cebo, Tomasz; Aria, Adrianus I.; Dolan, James A.; Weatherup, Robert S.; Nakanishi, Kenichi; Kidambi, Piran R.; Divitini, Giorgio; Ducati, Caterina; Steiner, Ullrich; Hofmann, Stephan

    2017-12-01

    The direct chemical vapour deposition of freestanding graphene gyroids with controlled sub-60 nm unit cell sizes is demonstrated. Three-dimensional (3D) nickel templates were fabricated through electrodeposition into a selectively voided triblock terpolymer. The high temperature instability of sub-micron unit cell structures was effectively addressed through the early introduction of the carbon precursor, which stabilizes the metallized gyroidal templates. The as-grown graphene gyroids are self-supporting and can be transferred onto a variety of substrates. Furthermore, they represent the smallest free standing periodic graphene 3D structures yet produced with a pore size of tens of nm, as analysed by electron microscopy and optical spectroscopy. We discuss generality of our methodology for the synthesis of other types of nanoscale, 3D graphene assemblies, and the transferability of this approach to other 2D materials.

  9. Photocatalytic hydrogen production using visible-light-responsive Ta{sub 3}N{sub 5} photocatalyst supported on monodisperse spherical SiO{sub 2} particulates

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Xiaoming [Division of Physical Sciences and Engineering, KAUST Catalysis Center (KCC), King Abdullah University of Science and Technology (KAUST), 4700 KAUST, Thuwal 23955-6900 (Saudi Arabia); School of Environment and Chemical Engineering, Nanchang Hangkong University, Nanchang 330063 (China); Zhao, Lan [Advanced Nanofabrication, Imaging and Characterization Core Lab, King Abdullah University of Science and Technology (KAUST), 4700 KAUST, Thuwal 23955-6900 (Saudi Arabia); Domen, Kazunari [Department of Chemical System Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656 (Japan); Takanabe, Kazuhiro, E-mail: kazuhiro.takanabe@kaust.edu.sa [Division of Physical Sciences and Engineering, KAUST Catalysis Center (KCC), King Abdullah University of Science and Technology (KAUST), 4700 KAUST, Thuwal 23955-6900 (Saudi Arabia)

    2014-01-01

    Graphical abstract: A simple and effective sol–gel process followed by nitridation in an NH{sub 3} flow has been developed to deposit Ta{sub 3}N{sub 5} semiconductor photocatalyst layers onto monodisperse spherical SiO{sub 2} particles. The obtained Ta{sub 3}N{sub 5}/SiO{sub 2} particles maintain an original spherical morphology of SiO{sub 2} and a sub-micrometer size with a narrow size distribution and without aggregation. The presence of SiO{sub 2} support shows at least no detrimental effects on photocatalytic activity, but tunes the secondary particle size to control dispersibility of the photocatalyst in the solution. - Highlights: • Fine nanoparticles of Ta{sub 3}N{sub 5} were immobilized on the surfaces of SiO{sub 2} giving SiO{sub 2}@Ta{sub 3}N{sub 5} core–shell spheres successfully produced H{sub 2} from methanol solution under visible light. • The presence of support (SiO{sub 2}) ensures the dispersion of the particulate in solution maintaining high photocatalytic activity of Ta{sub 3}N{sub 5}. • The obtained supported photocatalyst gives uniform size distribution and control the degree of dispersibility in the solution, which may control nature of light absorption and reflection of the photoreactor. - Abstract: Fine nanoparticles of Ta{sub 3}N{sub 5} (10–20 nm) were synthesized on the surfaces of SiO{sub 2} spheres with a diameter of ∼550 nm. A sol–gel method was used to modify the surface of SiO{sub 2} with Ta{sub 2}O{sub 5} from TaCl{sub 5} dissolved in ethanol in the presence of citric acid and polyethylene glycol. The resulting oxide composites were treated in an NH{sub 3} flow at 1123 K to form core–shell structured Ta{sub 3}N{sub 5}/SiO{sub 2} sub-microspheres. The obtained samples were characterized using powder X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectra (EDX), transmission electron microscopy (TEM), and

  10. Size-dependent photodegradation of CdS particles deposited onto TiO{sub 2} mesoporous films by SILAR method

    Energy Technology Data Exchange (ETDEWEB)

    Ahmed, Rasin; Will, Geoffrey; Bell, John; Wang Hongxia, E-mail: hx.wang@qut.edu.au [Queensland University of Technology, School of Chemistry, Physics and Mechanical Engineering (Australia)

    2012-09-15

    The particle size, size distribution and photostability of CdS nanoparticles incorporated onto mesoporous TiO{sub 2} films by a successive ionic layer adsorption and reaction (SILAR) method were investigated by Raman spectroscopy, UV-Visible spectroscopy, transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). High-resolution TEM indicated that the synthesized CdS particles were hexagonal phase and the particle sizes were less than 5 nm for up to nine SILAR deposition cycles. Quantum size effect was found with the CdS-sensitized TiO{sub 2} films prepared with up to nine SILAR cycles. The band gap of CdS nanoparticles decreased from 2.65 to 2.37 eV with the increase of the SILAR cycles from 1 to 11. The investigation of the stability of the CdS/TiO{sub 2} films in air under illumination (440.6 {mu}W/cm{sup 2}) showed that the photodegradation rate was up to 85 % per day for the sample prepared with three SILAR cycles. XPS analysis indicated that the photodegradation was due to the oxidation of CdS, leading to the transformation from sulphide to sulphate (CdSO{sub 4}). Furthermore, the degradation rate was strongly dependent upon the particle size of CdS. Smaller particles showed faster degradation rate. The size-dependent photo-induced oxidization was rationalized with the variation of size-dependent distribution of surface atoms of CdS particles. Molecular dynamics-based theoretical calculation has indicated that the surface sulphide anion of a large CdS particle such as CdS made with 11 cycles (CdS Multiplication-Sign 11, average particle size = 5.6 nm) accounts for 9.6 % of the material whereas this value is increased to 19.2 % for (CdS Multiplication-Sign 3)-based smaller particles (average particle size = 2.7 nm). The photostability of CdS nanoparticles was significantly enhanced when coated with ZnS particles deposited with four SILAR cycles. The growth mechanism of ZnS upon CdS nanoparticles was discussed.

  11. Improvement of slip property of magnetic tape by wet silica surface treatment on cobalt-coating type {gamma}-Fe{sub 2}O{sub 3} magnetic particles; Kobaruto hichakugata {gamma}-Fe{sub 2}O{sub 3} jiseibiryushi no shisshiki shirika hyomenshori niyoru jikitepu no suberi tokusei no kaizen

    Energy Technology Data Exchange (ETDEWEB)

    Hayashi, Kazuyuki; Iwasaki, Keisuke; Tanaka, Yasuyuki; Morii, Hiroko

    1999-02-05

    During the running of a magnetic taper coated with magnetic particles, sometimes troubles of the slip property between the magnetic tape and a magnetic head occur. In this research, silica coating onto the surfaces of magnetic iron oxide particles in water slurry was carried out, and a magnetic tape coated with these surface-modified particles was prepared so as to investigate the effect of the silica coating on the slip property of the magnetic tape. It was found that, for needle cobalt-coating type {gamma}- Fe{sub 2}O{sub 3}, the dynamic friction coefficient of the magnetic tape can be reduced from about 0.4 to abut 0.2 by coating silica at nm order. This was estimated that the adsorption amount of myristic acid as a lubricator component existing in the magnetic tape to the magnetic particles are reduced by the silica coating so that the amount of myristic acid effectively acting on the slip property of the magnetic tape surface is increased. Further, within the investigation scope of the present research, it has been clarified that the magnetic characteristics of the magnetic particles and coating dispersion property are not deteriorated by the surface treatment with silica, and a preferable magnetic recording medium retaining both magnetic characteristic and slip property can be obtained. (translated by NEDO)

  12. Three-dimensional vortex pinning by nano-precipitates in a Sm-doped YBa{sub 2}Cu{sub 3}O{sub 7-x} coated conductor

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Z [University of Wisconsin-Madison, Madison, WI 53706 (United States); Feldmann, D M [University of Wisconsin-Madison, Madison, WI 53706 (United States); Song, X [University of Wisconsin-Madison, Madison, WI 53706 (United States); Kim, S I [University of Wisconsin-Madison, Madison, WI 53706 (United States); Gurevich, A [University of Wisconsin-Madison, Madison, WI 53706 (United States); Reeves, J L [SuperPower Incorporated, 450 Duane Avenue, Schenectady, NY 12304 (United States); Xie, Y Y [SuperPower Incorporated, 450 Duane Avenue, Schenectady, NY 12304 (United States); Selvamanickam, V [SuperPower Incorporated, 450 Duane Avenue, Schenectady, NY 12304 (United States); Larbalestier, D C [University of Wisconsin-Madison, Madison, WI 53706 (United States)

    2007-09-15

    We report on the thickness and angular dependence of the critical current density J{sub c}(H,{theta}), the irreversibility field H{sup irr}, and the bulk pinning force F{sub p}(H) of a metal-organic chemical vapour deposition (MOCVD) grown YBa{sub 2}Cu{sub 3}O{sub 7-x} (YBCO) coated conductor, which contains {approx}17 vol% of {approx}10 nm sized (Y,Sm){sub 2}O{sub 3} precipitates with an average spacing of {approx}10-15 nm. Some surface porosity and amorphous second-phase particles on the scale of {approx}0.5-1 {mu}m appear to reduce the current-carrying cross-section, which controls the magnitude of J{sub c} but not the vortex pinning. We observed an enhanced H{sup irr}{approx}9 T at 77 K along the c-axis which, like the shape of J{sub c}(H) and F{sub p}(H), was independent of thickness as the sample was milled down to {approx}0.16 {mu}m. Angular-dependent measurements of J{sub c} showed the usual excess vortex pinning along the c-axis and along the ab-plane, but with a background that could only be fitted with an unusually small anisotropy parameter of 3, which, like the high H{sup irr} and the thickness-independent shape of F{sub p}(H), we ascribe to strong vortex pinning centre interactions. Together, these measurements show very different behaviour from most pulsed-laser-deposited films, which exhibit strong thickness-dependent properties. We ascribe the present different results to the dense array of small, insulating precipitates, which act as strong pinning centres and produce strong three-dimensional (3D) vortex pinning, because their separation of 10-15 nm is always much smaller than the film thickness.

  13. Investigation of magnetic properties of Fe{sub 3}O{sub 4} nanoparticles using temperature dependent magnetic hyperthermia in ferrofluids

    Energy Technology Data Exchange (ETDEWEB)

    Nemala, H.; Thakur, J. S.; Lawes, G.; Naik, R., E-mail: rnaik@wayne.edu [Department of Physics and Astronomy, Wayne State University, Detroit, Michigan 48202 (United States); Naik, V. M. [Department of Natural Sciences, University of Michigan-Dearborn, Dearborn, Michigan 48128 (United States); Vaishnava, P. P. [Department of Physics, Kettering University, Flint, Michigan 48504 (United States)

    2014-07-21

    Rate of heat generated by magnetic nanoparticles in a ferrofluid is affected by their magnetic properties, temperature, and viscosity of the carrier liquid. We have investigated temperature dependent magnetic hyperthermia in ferrofluids, consisting of dextran coated superparamagnetic Fe{sub 3}O{sub 4} nanoparticles, subjected to external magnetic fields of various frequencies (188–375 kHz) and amplitudes (140–235 Oe). Transmission electron microscopy measurements show that the nanoparticles are polydispersed with a mean diameter of 13.8 ± 3.1 nm. The fitting of experimental dc magnetization data to a standard Langevin function incorporating particle size distribution yields a mean diameter of 10.6 ± 1.2 nm, and a reduced saturation magnetization (∼65 emu/g) compared to the bulk value of Fe{sub 3}O{sub 4} (∼95 emu/g). This is due to the presence of a finite surface layer (∼1 nm thickness) of non-aligned spins surrounding the ferromagnetically aligned Fe{sub 3}O{sub 4} core. We found the specific absorption rate, measured as power absorbed per gram of iron oxide nanoparticles, decreases monotonically with increasing temperature for all values of magnetic field and frequency. Using the size distribution of magnetic nanoparticles estimated from the magnetization measurements, we have fitted the specific absorption rate versus temperature data using a linear response theory and relaxation dissipation mechanisms to determine the value of magnetic anisotropy constant (28 ± 2 kJ/m{sup 3}) of Fe{sub 3}O{sub 4} nanoparticles.

  14. Investigation of luminescence mechanism in La{sub 0.2}Y{sub 1.8}O{sub 3} scintillator

    Energy Technology Data Exchange (ETDEWEB)

    Sahi, Sunil [Department of Physics, The University of Texas at Arlington, Arlington, TX 76019-0059 (United States); Wang, Zhiqiang [Department of Chemistry, The University of Western Ontario, London, Ontario, Canada N6A 5B7 (Canada); Luo, Junming [School of Materials Science and Engineering, Nanchang Hangkong University, Nanchang 330063 (China); Groza, Michael [Department of Life and Physical Sciences, Fisk University, Nashville, TN 37208-3051 (United States); Li, Jiang [Key Laboratory of Transparent Opto-functional Inorganic Materials, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050 (China); Zhang, Junying [Department of Physics, Beihang University, Beijing 100191 (China); Chen, Wei, E-mail: weichen@uta.edu [Department of Physics, The University of Texas at Arlington, Arlington, TX 76019-0059 (United States); Pan, Yubai [Key Laboratory of Transparent Opto-functional Inorganic Materials, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050 (China); Burger, Arnold [Department of Life and Physical Sciences, Fisk University, Nashville, TN 37208-3051 (United States); Sham, Tsun-Kong [Department of Chemistry, The University of Western Ontario, London, Ontario, Canada N6A 5B7 (Canada)

    2016-05-15

    La{sub 0.2}Y{sub 1.8}O{sub 3} is a new and promising scintillator which is based on the host material without doping. Here the time gated X-ray excited optical luminescence is measured by using the excitation energy below, above and at the La L{sub 3}-edge. A relatively slow and broad emission with peak at 415 nm has been observed as the dominant emission. Also, a weak emission at 360 nm is observed at the fast window, associated with the recombination of trapped excitons in Y{sub 2}O{sub 3} host. The observations show that the broad emission at 415 nm is most likely due to the recombination of trapped excitons associated with the La{sup 3+} doping into Y{sub 2}O{sub 3} sites.

  15. γ-Fe{sub 2}O{sub 3} by sol–gel with large nanoparticles size for magnetic hyperthermia application

    Energy Technology Data Exchange (ETDEWEB)

    Lemine, O.M., E-mail: leminej@yahoo.com [Physics Department, College of Sciences, Al Imam Mohammad Ibn Saud Islamic University (IMSIU), Riyadh (Saudi Arabia); Omri, K. [Laboratory of Physics of Materials and Nanomaterials Applied at Environment (LaPhyMNE), Faculty of Sciences in Gabes, Gabes (Tunisia); Iglesias, M.; Velasco, V. [Instituto de Magnetismo Aplicado, UCM-ADIF-CSIC (Spain); Crespo, P.; Presa, P. de la [Instituto de Magnetismo Aplicado, UCM-ADIF-CSIC (Spain); Dpto. Física de Materiales, Universidad Complutense de Madrid (Spain); El Mir, L. [Physics Department, College of Sciences, Al Imam Mohammad Ibn Saud Islamic University (IMSIU), Riyadh (Saudi Arabia); Laboratory of Physics of Materials and Nanomaterials Applied at Environment (LaPhyMNE), Faculty of Sciences in Gabes, Gabes (Tunisia); Bouzid, Houcine [Promising Centre for Sensors and Electronic Devices (PCSED), Najran University, P.O. Box 1988, Najran 11001 (Saudi Arabia); Laboratoire des Matériaux Ferroélectriques, Faculté des Sciences de Sfax, Route Soukra Km 3 5, B.P. 802, F-3018 Sfax (Tunisia); Yousif, A. [Department of Physics, College of Science, Sultan Qaboos University, P.O. Box 36, Code 123, Al Khoud (Oman); Al-Hajry, Ali [Promising Centre for Sensors and Electronic Devices (PCSED), Najran University, P.O. Box 1988, Najran 11001 (Saudi Arabia)

    2014-09-01

    Highlights: • Iron oxides nanoparticles with different sizes are successfully synthesized using sol–gel method. • The obtained nanoparticles are mainly composed of maghemite phase (γ-Fe{sub 2}O{sub 3}). • A non-negligible coercive field suggests that the particles are ferromagnetic. • A mean heating efficiency of 30 W/g is obtained for the smallest particles at 110 kHz and 190 Oe. - Abstract: Iron oxides nanoparticles with different sizes are successfully synthesized using sol–gel method. X-ray diffraction (XRD) and Mössbauer spectroscopy show that the obtained nanoparticles are mainly composed of maghemite phase (γ-Fe{sub 2}O{sub 3}). XRD and transmission electron microscopy (TEM) results suggest that the nanoparticles have sizes ranging from 14 to 30 nm, which are indeed confirmed by large magnetic saturation and high blocking temperature. At room temperature, the observation of a non-negligible coercive field suggests that the particles are ferro/ferrimagnetic. The specific absorption rate (SAR) under an alternating magnetic field is investigated as a function of size, frequency and amplitude of the applied magnetic field. A mean heating efficiency of 30 W/g is obtained for the smallest particles at 110 kHz and 190 Oe, whereas further increase of particle size does not improve significantly the heating efficiency.

  16. Synthesis and photoluminescence properties of Pb{sup 2+} doped inorganic borate phosphor NaSr{sub 4}(BO{sub 3}){sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Chauhan, A. O., E-mail: abhi2718@gmail.com; Koparkar, K. A.; Omanwar, S. K. [Department of Physics, SantGadge Baba Amravati University, Amravati MH, 444602 (India); Bajaj, N. S. [Department of Physics, Toshniwal Art, Commerce and Science College, Sengoan, Hingoli MH (India)

    2016-05-06

    A series of Inorganic borate phosphors NaSr{sub 4}(BO{sub 3}){sub 3} doped with Pb{sup 2+} was successfully synthesized by modified solid state diffusion method. The crystal structure and the phase purity of sample were characterized by powder X-ray diffraction (XRD). The photoluminescence properties of synthesized materials were investigated using spectrofluorometer at room temperature. The phosphor show strong broad band emission spectra in UVA region maximum at 370 nm under the excitation of 289 nm. The dependence of the emission intensity on the Pb{sup 2+} concentration for the NaSr{sub 4}(BO{sub 3}){sub 3} were studied in details. The concentration quenching of Pb{sup 2+} doped NaSr{sub 4}(BO{sub 3}){sub 3} was observed at 0.02 mol. The Stokes shifts of NaSr{sub 4}(BO{sub 3}){sub 3}: Pb{sup 2+} phosphor was calculated to be 7574 cm{sup −1}.

  17. Preparation and studies of Eu{sup 3+} and Tb{sup 3+} co-doped Gd{sub 2}O{sub 3} and Y{sub 2}O{sub 3} sol-gel scintillating films

    Energy Technology Data Exchange (ETDEWEB)

    Morales Ramirez, A. de J, E-mail: amoralesra@ipn.m [Centro de Investigacion en Ciencia Aplicada y Tecnologia Avanzada (CICATA) Unidad Altamira Instituto Politecnico Nacional Km. 14.5 Carr. Tampico-Puerto Industrial, C.P. 89600, Altamira, Tamaulipas (Mexico); Depto. de Ingenieria Metalurgica, ESIQIE-Instituto Politecnico Nacional UPALM C.P. 07738, Mexico D.F. (Mexico); Garcia Murillo, A.; Carrillo Romo, F. de J [Depto. de Ingenieria Metalurgica, ESIQIE-Instituto Politecnico Nacional UPALM C.P. 07738, Mexico D.F. (Mexico); Ramirez Salgado, J. [Programa de Ingenieria Molecular, Instituto Mexicano del Petroleo, Eje Lazaro Cardenas No. 152, CP 07730, Mexico D.F. (Mexico); Le Luyer, C. [LPCML, CNRS-UMR 5620/Universite Claude Bernard Lyon 1/69622 Villeurbanne Cedex (France); Chadeyron, G.; Boyer, D. [Laboratoire des Materiaux Inorganiques, CNRS-UMR 6002, Universite Blaise Pascal, 24 Ave des Landais F 63177 Aubiere Cedex (France); Moreno Palmerin, J. [Depto. de Ingenieria Metalurgica, ESIQIE-Instituto Politecnico Nacional UPALM C.P. 07738, Mexico D.F. (Mexico)

    2009-10-30

    Eu{sup 3+} (2.5 at.%) and Tb{sup 3+} (0.005-0.01 at.%) co-doped gadolinium and yttrium oxide (Gd{sub 2}O{sub 3} and Y{sub 2}O{sub 3}) powders and films have been prepared using the sol-gel process. High density and optical quality thin films were prepared with the dip-coating technique. Gadolinium (III) 2,4-pentadionate and yttrium (III) 2,4-pentadionate were used as precursors, and europium and terbium in their nitrate forms were used as doping agents. Chemical and structural analyses (infrared spectroscopy, X-ray diffraction and high-resolution transmission electron microscopy) were conducted on both sol-gel precursor powders and dip-coated films. The morphology of thin films heat-treated at 700 {sup o}C was studied by means of atomic force microscopy. It was shown that the highly dense and very smooth films had a root mean roughness (RMS) of 2 nm {+-} 0.2 (A = 0.0075 Tb{sup 3+}) and 24 nm {+-} 3.0 (B = 0.01 Tb{sup 3+}). After treatment at 700 {sup o}C, the crystallized films were in the cubic phase and presented a polycrystalline structure made up of randomly oriented crystallites with grain sizes varying from 20 to 60 nm. The X-ray induced emission spectra of Eu{sup 3+}- and Tb{sup 3+}-doped Gd{sub 2}O{sub 3} and Y{sub 2}O{sub 3} powders showed that Tb{sup 3+} contents of 0.005, 0.0075 and 0.01 at.% affected their optical properties. Lower Tb{sup 3+} concentrations (down to 0.005 at.%) in both systems enhanced the light yield.

  18. Spin-Coating and Characterization of Multiferroic MFe{sub 2}O{sub 4} (M=Co, Ni) / BaTiO{sub 3} Bilayers

    Energy Technology Data Exchange (ETDEWEB)

    Quandt, Norman [Institute of Chemistry, Martin Luther University Halle-Wittenberg, Kurt-Mothes-Straße 2, 06120 Halle (Germany); Roth, Robert [Institute of Physics, Martin Luther University Halle-Wittenberg, Von-Danckelmann-Platz 3, 06120 Halle (Germany); Syrowatka, Frank [Interdisciplinary Center of Materials Science, Martin Luther University Halle-Wittenberg, Heinrich-Damerow-Straße 4, 06120 Halle (Germany); Steimecke, Matthias [Institute of Chemistry, Martin Luther University Halle-Wittenberg, Von-Danckelmann-Platz 4, 06120 Halle (Germany); Ebbinghaus, Stefan G., E-mail: stefan.ebbinghaus@chemie.uni-halle.de [Institute of Chemistry, Martin Luther University Halle-Wittenberg, Kurt-Mothes-Straße 2, 06120 Halle (Germany)

    2016-01-15

    Bilayer films of MFe{sub 2}O{sub 4} (M=Co, Ni) and BaTiO{sub 3} were prepared by spin coating of N,N-dimethylformamide/acetic acid solutions on platinum coated silicon wafers. Five coating steps were applied to get the desired thickness of 150 nm for both the ferrite and perovskite layer. XRD, IR and Raman spectroscopy revealed the formation of phase-pure ferrite spinels and BaTiO{sub 3}. Smooth surfaces with roughnesses in the order of 3 to 5 nm were found in AFM investigations. Saturation magnetization of 347 emu cm{sup −3} for the CoFe{sub 2}O{sub 4}/BaTiO{sub 3} and 188 emu cm{sup −3} for the NiFe{sub 2}O{sub 4}/BaTiO{sub 3} bilayer, respectively were found. For the CoFe{sub 2}O{sub 4}/BaTiO{sub 3} bilayer a strong magnetic anisotropy was observed with coercivity fields of 5.1 kOe and 3.3 kOe (applied magnetic field perpendicular and parallel to film surface), while for the NiFe{sub 2}O{sub 4}/BaTiO{sub 3} bilayer this effect is less pronounced. Saturated polarization hysteresis loops prove the presence of ferroelectricity in both systems. - Graphical abstract: The SEM image of the CoFe{sub 2}O{sub 4}/BaTiO{sub 3} bilayer on Pt–Si-substrate (left), magnetization as a function of the magnetic field perpendicular and parallel to the film plane (right top) and P–E and I–V hysteresis loops of the bilayer at room temperature. - Highlights: • Ferrite and perovskite oxides grown on platinum using spin coating technique. • Columnar growth of cobalt ferrite particle on the substrate. • Surface investigation showed a homogenous and smooth surface. • Perpendicular and parallel applied magnetic field revealed a magnetic anisotropy. • Switching peaks and saturated P–E hysteresis loops show ferroelectricity.

  19. NIR optimized dual mode photoluminescence in Nd doped Y{sub 2}O{sub 3} ceramic phosphor

    Energy Technology Data Exchange (ETDEWEB)

    Sukul, Prasenjit Prasad; Mahata, Manoj Kumar; Kumar, Kaushal, E-mail: kumar.bhu@gmail.com

    2017-05-15

    Authors here report the dual mode photo luminescence emission in neodymium doped yttrium oxide ceramic phosphor upon 808 nm diode laser excitation. Single cubic phase Nd{sup 3+} doped Y{sub 2}O{sub 3} phosphor was synthesized using urea assisted combustion route. Nd{sup 3+} doped Y{sub 2}O{sub 3} ceramic phosphor has given photoluminescence in a wide wavelength range covering near infrared window (850–1100 nm) to the visible region i.e. green (525 nm) and red (680 nm) upon 808 nm diode laser excitation. The two most intense bands on 808 nm excitation were observed at 750 nm and 1064 nm due to the upconversion and downconversion emission processes. The sample was also tested for emission using 980 nm and intense green emission due to the trace presence of Er{sup 3+} in the raw materials was seen in the sample. The excitation power dependent upconversion measurements have shown that transitions {sup 4}F{sub 9/2}→{sup 4}I{sub 9/2} and {sup 4}S{sub 3/2}→{sup 4}I{sub 9/2} are thermally coupled and can be used to estimate the sample temperature using Boltzmann relation.

  20. Spectroscopic and structural properties of polycrystalline Y{sub 2}Si{sub 2}O{sub 7} doped with Er{sup 3+}

    Energy Technology Data Exchange (ETDEWEB)

    Marciniak, L., E-mail: L.Marciniak@int.pan.wroc.pl [Institute for Low Temperature and Structure Research, Polish Academy of Sciences, Wroclaw (Poland); Hreniak, D.; Strek, W. [Institute for Low Temperature and Structure Research, Polish Academy of Sciences, Wroclaw (Poland); Piccinelli, F., E-mail: fabio.piccinelli@univr.it [Laboratorio di Chimica dello Stato Solido, DB, Università di Verona and INSTM, UdR Verona, Strada Le Grazie 15, 37134 Verona (Italy); Speghini, A.; Bettinelli, M. [Laboratorio di Chimica dello Stato Solido, DB, Università di Verona and INSTM, UdR Verona, Strada Le Grazie 15, 37134 Verona (Italy); Miritello, M., E-mail: maria.miritello@ct.infn.it [CNR-IMM MATIS and Dipartimento di Fisica e Astronomia, Università di Catania, Via S. Sofia 64, 95123 Catania (Italy); Lo Savio, R.; Cardile, P.; Priolo, F. [CNR-IMM MATIS and Dipartimento di Fisica e Astronomia, Università di Catania, Via S. Sofia 64, 95123 Catania (Italy)

    2016-02-15

    Powders of yttrium disilicate (Y{sub 2}Si{sub 2}O{sub 7}) doped with Er{sup 3+} have been prepared by the sol–gel method. The structure of the obtained powders has been determined. Room temperature emission spectra have been recorded and excited state decay profiles have been analyzed. Differences between the spectroscopic properties of Er{sup 3+} in monoclinic α-Y{sub 2}Si{sub 2}O{sub 7} (space group P-1) and β-Y{sub 2}Si{sub 2}O{sub 7} (space group C2/m) polymorphs have been investigated and shown. The significant broadening of the emission spectra recorded for the α phase compared to the one for the β phase was discussed in terms of higher number of Y{sup 3+} sites (4) present in the α phase with respect to only one Y{sup 3+} site in the case of β phase. The higher value of the luminescence decay time of β phase (11.2 ms) compared to the α phase (8.5 ms) is associated with the higher site symmetry of β-Y{sub 2}Si{sub 2}O{sub 7}. Moreover it was found that Er{sup 3+} concentration affects the shape of the {sup 4}I{sub 13/2}→{sup 4}I{sub 15/2} emission band. It results in changes of the relative emission intensities of peaks localized at 1527 nm and 1532 nm; this indicates changes of the Y{sup 3+} sites occupation on increasing the Er{sup 3+} concentration. The luminescence lifetime was observed to decrease with the increase of Er{sup 3+} concentration. The spectroscopic results have been compared with the ones relative to thin films of Y{sub 2}Si{sub 2}O{sub 7}:Er{sup 3+} with a similar composition. The lower value of the luminescence decay time observed for thin films compared to the powder of α phase was explained with the changes of the particles packing resulting in the change of the effective refractive index.

  1. The effect of urea:nitrate ratio on the structure and luminescence properties of YVO{sub 4}:Dy{sup 3+} phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Foka, K.E., E-mail: fokake@gmail.com [Department of Physics, University of the Free State (Qwaqwa), Private Bag x13, Phuthaditjhaba 9866 (South Africa); Dejene, B.F. [Department of Physics, University of the Free State (Qwaqwa), Private Bag x13, Phuthaditjhaba 9866 (South Africa); Swart, H.C. [Department of Physics, University of the Free State, P. O. Box 339, Bloemfontein 9300 (South Africa)

    2016-01-01

    YVO{sub 4}:Dy{sup 3+} phosphor has been successfully synthesised using combustion method. The dependence of the properties of YVO{sub 4}:Dy{sup 3+} phosphor upon urea:nitrate concentration was investigated. The single tetragonal phase was observed by x-ray diffraction spectra. A highly crystalline YVO{sub 4}:Dy{sup 3+} sample was obtained when increasing the ratio of the urea to 2. The estimated crystalline sizes from the Scherrer’s formula were found to be 20, 38, 33, 30, and 27 nm for the sample prepared with the ratio of 1, 2, 2.5, 3 and 4, respectively. The formation of agglomerated particles was observed by Scanning electron microscope images and it was observed that when increasing the concentration of urea further, flake-like particles formed. The diffuse reflectance spectra of YVO{sub 4}:Dy{sup 3+} with various ratios of urea indicated that the determined optical band gap was ranging from 3.3 to 2.3 eV. Luminescence properties of YVO{sub 4}:Dy{sup 3+} showed that the phosphor emit yellow colour at 573 nm and blue colour at 482 nm corresponding to {sup 4}F{sub 9/2}→{sup 6}H{sub 13/2} and {sup 4}F{sub 9/2}→{sup 6}H{sub 15/2} transitions, respectively. A very weak band at 663 nm which correspond to the {sup 4}F{sub 9/2}→{sup 6}H{sub 11/2} transition was also observed. It was found that the Photoluminescent emission intensity increased with an increase in the ratio of urea and reached a maximum at 2 then decreased when increasing the ratio of urea further.

  2. Growth and spectroscopic properties of Yb{sup 3+}-doped Li{sub 6}Y(BO{sub 3}){sub 3} single crystal

    Energy Technology Data Exchange (ETDEWEB)

    Brenier, A. [Laboratoire de Physico-Chimie des Materiaux Luminescents, UMR CNRS no 5620, Universite Claude Bernard-Lyon1, 10 rue Ampere, 69622 Villeurbanne (France)]. E-mail: brenier@pcml.univ-lyon1.fr; Yoshikawa, A. [Institute of Multidisciplinary for Advanced Materials, Tohoku University, Sendai 980 8577 (Japan); Lebbou, K. [Laboratoire de Physico-Chimie des Materiaux Luminescents, UMR CNRS no 5620, Universite Claude Bernard-Lyon1, 10 rue Ampere, 69622 Villeurbanne (France); Jouini, A. [Laboratoire de Physico-Chimie des Materiaux Luminescents, UMR CNRS no 5620, Universite Claude Bernard-Lyon1, 10 rue Ampere, 69622 Villeurbanne (France); Institute of Multidisciplinary for Advanced Materials, Tohoku University, Sendai 980 8577 (Japan); Aloui-Lebbou, O. [Laboratoire de Physico-Chimie des Materiaux Luminescents, UMR CNRS no 5620, Universite Claude Bernard-Lyon1, 10 rue Ampere, 69622 Villeurbanne (France); Boulon, G. [Laboratoire de Physico-Chimie des Materiaux Luminescents, UMR CNRS no 5620, Universite Claude Bernard-Lyon1, 10 rue Ampere, 69622 Villeurbanne (France); Institute of Multidisciplinary for Advanced Materials, Tohoku University, Sendai 980 8577 (Japan); Fukuda, T. [Institute of Multidisciplinary for Advanced Materials, Tohoku University, Sendai 980 8577 (Japan)

    2007-10-15

    The spectroscopic properties of high-quality Czochralski grown 20% Yb{sup 3+}-doped Li{sub 6}Y(BO{sub 3}){sub 3} single crystal as new promising laser material are presented. The crystal was seeded-grown in the <0 1 0> direction and its crystallinity was measured using X-ray rocking curve analysis. Low temperature transmission spectrum exhibits broad bands in a short range of wavelengths and two sharp lines at 972.5 and 978 nm, interpreted as two zero-lines of two nonequivalent Yb{sup 3+} centers inside the lattice. The fluorescence lifetimes associated to these two intense lines are different: 0.867 and 1.33 ms. An attempt of determination of the Stark sublevels energies of the {sup 4}F{sub 5/2} and {sup 4}F{sub 7/2} manifolds of the two Yb{sup 3+} nonequivalent ions is given. The polarized absorption and emission spectra were also recorded at room temperature and we conclude that the most favorable emission line for laser application could be around 1042 nm in n {sub g} polarization.

  3. Color-tunable up-conversion emission of luminescent-plasmonic, core/shell nanomaterials – KY{sub 3}F{sub 10}:Yb{sup 3+},Tm{sup 3+}/SiO{sub 2}-NH{sub 2}/Au

    Energy Technology Data Exchange (ETDEWEB)

    Runowski, Marcin, E-mail: runowski@amu.edu.pl

    2017-06-15

    Multifunctional luminescent-plasmonic KY{sub 3}F{sub 10}:Yb{sup 3+},Tm{sup 3+}/SiO{sub 2}-NH{sub 2}/Au nanomaterials were successfully obtained. The lanthanide-doped fluoride nanoparticles (NPs), synthesized under hydrothermal conditions exhibited bright blue up-conversion luminescence (λ{sub ex}=980 nm). Such lanthanide nanocrystals (20–40 nm) were coated with amine modified silica shell, forming core/shell nanostructures. Their surface was further uniformly covered with ultra-small gold NPs (4–7 nm). The as-prepared luminescent-plasmonic core/shell nanomaterials exhibited tunable up-conversion emission, due to the interactions between plasmonic and luminescent phases. The emission of Tm{sup 3+} ion was affected by the surface Au NPs, which exhibited strong plasmonic absorption in the visible range (450–650 nm). The increasing amount of the surface Au NPs, led to the significant alterations in a ratio of the Tm{sup 3+} emission bands. The NIR band ({sup 3}H{sub 4}→{sup 3}H{sub 6}) was unchanged, whereas the ratio and relative intensity of the bands in a visible range ({sup 1}G{sub 4}→{sup 3}H{sub 6} and {sup 1}G{sub 4}→{sup 3}F{sub 4}) was altered. This led to the significant change of the emission spectra shape and influenced color of emission, tuning it from bright blue to blue-violet. The products obtained were characterized by transmission electron microscopy (TEM), energy dispersive X-ray analysis (EDX), powder X-ray diffraction (XRD), UV–vis absorption spectroscopy and luminescence spectroscopy (excitation/emission spectra and luminescence decay curves).

  4. Temperature dependence of structural and luminescence properties of Eu{sup 3+}-doped Y{sub 2}O{sub 3} red-emitting phosphor thin films by pulsed laser deposition

    Energy Technology Data Exchange (ETDEWEB)

    Ali, A.G.; Dejene, B.F. [University of the Free State (Qwaqwa Campus), Department of Physics, Phuthaditjhaba (South Africa); Swart, H.C. [University of the Free State, Department of Physics, Bloemfontein (South Africa)

    2016-04-15

    Pulse laser deposition was used to obtain nanocrystalline red-emitting Y{sub 2}O{sub 3}:Eu{sup 3+} thin-film phosphors. X-ray diffraction measurements show that the un-annealed thin film was amorphous, while those annealed were crystalline. At lower annealing temperature of 600-700 C, cubic bixbyite Y{sub 2}O{sub 3}:Eu{sup 3+} was formed. As the annealing temperatures were increased to 800 C, hexagonal phase emerged. The average crystallite size of the film was 64 nm. Photoluminescence measurement indicates intense red emission around 612 nm due to the {sup 5}D{sub 0} → {sup 7}F{sub 2} transition. Scanning electron microscopy indicated that agglomerates of non-crystalline particles with spherical shapes were present for the un-annealed films. After annealing at high temperature, finer morphology was revealed. Atomic force microscopy further confirmed the formation of new morphology at the higher annealing temperatures. UV-Vis measurement indicated a band gap in the range of 4.6-4.8 eV. It was concluded that the annealing temperature played an important role in the luminescence intensity and crystallinity of these films. (orig.)

  5. Magnetic and transport properties of YBa{sub 2}Cu{sub 3}O{sub 7} - La{sub 0.7}Ca{sub 0.3}MnO{sub 3} heterostructures

    Energy Technology Data Exchange (ETDEWEB)

    Mustafa, Luqman

    2016-11-25

    The exploration of interface properties in complex oxide heterostructures and superlattices is one of the new exciting fields in condensed matter sciences. This is particularly originating from the technological advances in synthesizing heterostructures with atomic scale precision by advanced thin film deposition techniques. There is a plethora of novel achievements culminating in unexpected results, such as generating artificial multifunctional materials with the prominent example of the appearance of interface electrical conductivity and even superconductivity in between insulating films (SrTiO{sub 3} - LaAlO{sub 3}). In this thesis a special case of heterostructures is treated. Here, heterostructures composed of superconducting YBa{sub 2}Cu{sub 3}O{sub 7} and half-metallic ferromagnetic La{sub 2/3}Ca{sub 1/3}MnO{sub 3} are investigated and the interplay of the two long-range antagonistic ordering principles - superconductivity and ferromagnetism - is intended to be studied. Whereas the physics of such structures with the CuO{sub 2} planes of the superconducting YBa{sub 2}Cu{sub 3}O{sub 7} oriented parallel to the substrate plane (i.e. the short coherence length of the superconductor, ξ{sub c} ∝ 0.1 nm is facing the interface perpendicular) has been explored in great detail, little is known in the case of the CuO{sub 2} planes oriented perpendicular to the substrate plane and thus ξ{sub ab} ∝ 1.6 nm is pointing perpendicular to the interface. In the former case, the properties of the heterostructures and superlattices are determined by an interplay of charge transfer and orbital reconstruction, but the mechanisms occurring in the latter case are unknown so far. Prior to elaborated experiments to study the interface properties at an atomistic scale, the technology of fabricating such structures has to be accomplished and their macroscopic properties (structure, transport and magnetic properties) have to be investigated. It is the goal of this thesis to

  6. Effects of neutron irradiation of Ti{sub 3}SiC{sub 2} and Ti{sub 3}AlC{sub 2} in the 121–1085 °C temperature range

    Energy Technology Data Exchange (ETDEWEB)

    Tallman, Darin J. [Department of Materials Science and Engineering, Drexel University, Philadelphia, PA 19104 (United States); He, Lingfeng; Gan, Jian [Idaho National Laboratory, Idaho Falls, ID 83415 (United States); Caspi, El' ad N. [Department of Materials Science and Engineering, Drexel University, Philadelphia, PA 19104 (United States); Physics Department, Nuclear Research Centre – Negev, 84190 Israel (Israel); Hoffman, Elizabeth N. [Savannah River National Laboratory, Savannah River Site, Aiken, SC 29808 (United States); Barsoum, Michel W., E-mail: barsoumw@drexel.edu [Department of Materials Science and Engineering, Drexel University, Philadelphia, PA 19104 (United States)

    2017-02-15

    Herein we report on the formation of defects in response to neutron irradiation of polycrystalline Ti{sub 3}SiC{sub 2} and Ti{sub 3}AlC{sub 2} samples exposed to total fluences of ≈6 × 10{sup 20} n/m{sup 2}, 5 × 10{sup 21} n/m{sup 2} and 1.7 × 10{sup 22} n/m{sup 2} at irradiation temperatures of 121(12), 735(6) and 1085(68)°C. These fluences correspond to 0.14, 1.6 and 3.4 dpa, respectively. After irradiation to 0.14 dpa at 121 °C and 735 °C, black spots are observed via transmission electron microscopy in both Ti{sub 3}SiC{sub 2} and Ti{sub 3}AlC{sub 2}. After irradiation to 1.6 and 3.4 dpa at 735 °C, basal dislocation loops, with a Burgers vector of b = ½ [0001] are observed in Ti{sub 3}SiC{sub 2}, with loop diameters of 21(6) and 30(8) nm after 1.6 dpa and 3.4 dpa, respectively. In Ti{sub 3}AlC{sub 2}, larger dislocation loops, 75(34) nm in diameter are observed after 3.4 dpa at 735 °C, in addition to stacking faults. Impurity particles of TiC, as well as stacking fault TiC platelets in the MAX phases, are seen to form extensive dislocation loops under all conditions. Cavities were observed at grain boundaries and within stacking faults after 3.4 dpa irradiation, with extensive cavity formation in the TiC regions at 1085 °C. Remarkably, denuded zones on the order of 1 μm are observed in Ti{sub 3}SiC{sub 2} after irradiation to 3.4 dpa at 735 °C. Small grains, 3–5 μm in diameter, are damage free after irradiation at 1085 °C at this dose. The results shown herein confirm once again that the presence of the A-layers in the MAX phases considerably enhance their irradiation tolerance. Based on these results, and up to 3.4 dpa, Ti{sub 3}SiC{sub 2} remains a promising candidate for high temperature nuclear applications as long as the temperature remains >700 °C.

  7. A high performance hydrogen sulfide gas sensor based on porous α-Fe{sub 2}O{sub 3} operates at room-temperature

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Yanwu; Chen, Weimei; Zhang, Shouchao; Kuang, Zhong; Ao, Dongyi [School of Physical Electronics, University of Electronic Science and Technology of China, Chengdu, 610054 (China); Alkurd, Nooraldeen Rafat; Zhou, Weilie [Advanced Materials Research Institute, University of New Orleans, New Orleans, LA 70148 (United States); Liu, Wei [School of Physical Electronics, University of Electronic Science and Technology of China, Chengdu, 610054 (China); Shen, Wenzhong [Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan, 030001 (China); Li, Zhijie, E-mail: zhijieli@uestc.edu.cn [School of Physical Electronics, University of Electronic Science and Technology of China, Chengdu, 610054 (China)

    2015-10-01

    Highlights: • Novel porous α-Fe{sub 2}O{sub 3} nanoparticles were prepared by a facile hydrothermal method. • The sensor based on porous α-Fe{sub 2}O{sub 3} exhibits high sensitivity towards H{sub 2}S gas. • The detection limit towards H{sub 2}S gas was as low as 50 ppb at room temperature. • The sensor exhibits excellent selectivity against other toxic and noxious gases. - Abstract: Porous α-Fe{sub 2}O{sub 3} nanoparticles were synthesized by simple annealing of β-FeOOH precursor derived from a facile hydrothermal route, the structures and morphologies of the as-prepared product were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The results showed that the average crystallite size of the obtained porous α-Fe{sub 2}O{sub 3} was 34 nm and exits numerous irregularly distributed pores with a diameter varying from 2 nm to 10 nm on the particle surface. The gas-sensing properties of the sensor based on porous α-Fe{sub 2}O{sub 3} nanoparticles were investigated, and the result showed that the sensor exhibited a high performance in hydrogen sulfide (H{sub 2}S) detection at room temperature. The highest sensitivity reached 38.4 for 100 ppm H{sub 2}S, and the detection limit was as low as 50 ppb. In addition, the response of the sensor towards other gases including C{sub 2}H{sub 5}OH, CO, H{sub 2} and NH{sub 3} indicates the sensor has an excellent selectivity to detection H{sub 2}S gas. Finally, the sensing mechanism of the sensor towards H{sub 2}S was also discussed.

  8. Preparation mechanism of (Bi{sub 2}O{sub 3}){sub 0.75}(Dy{sub 2}O{sub 3}){sub 0.25} nano-crystalline solid electrolyte

    Energy Technology Data Exchange (ETDEWEB)

    Li Rong [Nano-science and Nano-technology Research Center, School of Materials Science and Engineering, Shanghai University, Shanghai 200444 (China); UCCS: Unite de Catalyse et de Chimie du Solide - UMR CNRS 8181, ENSCL, Batiment C7, BP 90108, 59652 Villeneuve d' Ascq Cedex (France); Zhen Qiang, E-mail: zhenqiang@263.ne [Nano-science and Nano-technology Research Center, School of Materials Science and Engineering, Shanghai University, Shanghai 200444 (China); Drache, Michel; Rubbens, Annick; Vannier, Rose-Noelle [UCCS: Unite de Catalyse et de Chimie du Solide - UMR CNRS 8181, ENSCL, Batiment C7, BP 90108, 59652 Villeneuve d' Ascq Cedex (France)

    2010-04-02

    (Bi{sub 2}O{sub 3}){sub 0.75}(Dy{sub 2}O{sub 3}){sub 0.25} nanopowder was prepared by reverse chemical titration co-precipitation method. The reaction mechanism during the precipitation process was discussed by thermodynamic analysis. Thermal decomposition behavior of the precursor was investigated using X-ray diffractometry and TG-MS analysis. The precursor was calcined at 500 {sup o}C for 3 h to obtain (Bi{sub 2}O{sub 3}){sub 0.75}(Dy{sub 2}O{sub 3}){sub 0.25} nanopowder. Using the nanopowder, pellets with relative density higher than 94% were obtained at 700 {sup o}C for 2 h by pressureless sintering, and the grains remained at the nano-scale with size of 72 nm.

  9. Luminescence, scintillation, and energy transfer in SiO{sub 2}-Al{sub 2}O{sub 3}-B{sub 2}O{sub 3}-Gd{sub 2}O{sub 3}:Ce{sup 3+},Pr{sup 3+} glasses

    Energy Technology Data Exchange (ETDEWEB)

    Lertloypanyachai, Prapon; Chewpraditkul, Weerapong; Pattanaboonmee, Nakarin [Department of Physics, King Mongkut' s University of Technology Thonburi, Bangkok (Thailand); Chen, Danping [Shanghai Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, Shanghai (China); Babin, Vladimir; Beitlerova, Alena; Nikl, Martin [Institute of Physics, AS CR, Prague (Czech Republic)

    2017-09-15

    Ce{sup 3+},Pr{sup 3+}-codoped SiO{sub 2}-Al{sub 2}O{sub 3}-B{sub 2}O{sub 3}-Gd{sub 2}O{sub 3} glasses (SABG:Ce,Pr) were prepared by melt quenching under a CO reducing atmosphere. Luminescence properties were investigated under UV and X-ray excitations. A dominant emission band at 430 nm belonging to the Ce{sup 3+}:5d{sub 1} → 4f transition was observed in the photo- and radio-luminescence spectra. The energy transfer occurs from this Ce{sup 3+} band toward the {sup 3}P{sub J} levels of Pr{sup 3+} with an efficiency of up to 24%, followed by the reduction of integrated luminescence intensity with an increasing Pr{sup 3+} concentration. This result is attributed to the increase in the reabsorption of Ce{sup 3+} luminescence and the non-radiative energy transfer toward the {sup 3}P{sub J} levels of Pr{sup 3+}. The cross-relaxation process within the Pr{sup 3+} pairs can further diminish the total luminescence yield at high Pr{sup 3+} concentrations. The integral scintillation efficiency and light yield measurements were carried out and compared to the reference Bi{sub 4}Ge{sub 3}O{sub 12} (BGO) crystal. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  10. Porous sulfated metal oxide SO{sub 4}{sup 2−}/Fe{sub 2}O{sub 3} as an anode material for Li-ion batteries with enhanced electrochemical performance

    Energy Technology Data Exchange (ETDEWEB)

    Li, Zhen; Lv, Qianqian; Huang, Xiaoxiong; Tan, Yueyue; Tang, Bohejin, E-mail: tangbohejin@sues.edu.cn [Shanghai University of Engineering Science, College of Chemistry and Chemical Engineering (China)

    2017-01-15

    Sulfated metal oxide SO{sub 4}{sup 2−}/Fe{sub 2}O{sub 3} was prepared by a novel facile sol–gel method combined with a subsequent heating treatment process. The as-synthesized products were analyzed by XRD, FTIR, and FE-SEM. Compared with the unsulfated Fe{sub 2}O{sub 3}, the agglomeration of particles has been alleviated after the incorporation of SO{sub 4}{sup 2−}. Interestingly, the primary particle size of the SO{sub 4}{sup 2−}/Fe{sub 2}O{sub 3} (about 5 nm) is similar to its normal counterparts even after the calcination treatment. More importantly, SO{sub 4}{sup 2−}/Fe{sub 2}O{sub 3} exhibits a porous architecture, which is an intriguing feature for electrode materials. When used as anode materials in Li-ion batteries, SO{sub 4}{sup 2−}/Fe{sub 2}O{sub 3} delivered a higher reversible discharge capacity (992 mAh g{sup −1}), with smaller charge transfer resistance, excellent rate performance, and better cycling stability than normal Fe{sub 2}O{sub 3}. We believed that the presence of SO{sub 4}{sup 2−} and porous architecture should be responsible for the enhanced electrochemical performance, which could provide more continuous and accessible conductive paths for Li{sup +} and electrons.

  11. Particle size, spin wave and surface effects on magnetic properties of MgFe{sub 2}O{sub 4} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Aslibeiki, B., E-mail: b.aslibeiki@tabrizu.ac.ir [Department of Physics, University of Tabriz, Tabriz 51666-16471 (Iran, Islamic Republic of); Varvaro, G.; Peddis, D. [Istituto di Struttura della Materia, National Research Council, Monterotondo Scalo, Roma 00015 (Italy); Kameli, P. [Department of Physics, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of)

    2017-01-15

    Magnesium ferrite, MgFe{sub 2}O{sub 4}, nanoparticles with a mean diameter varying from ∼6 to ∼17 nm were successfully synthesized using a simple thermal decomposition method at different annealing temperatures ranging in between 400 and 600 °C. Pure spinel ferrite nanoparticles were obtained at temperatures lower than 500 °C, while the presence of hematite (α-Fe{sub 2}O{sub 3}) impurities was observed at higher temperatures. Single-phase samples show a superparamagnetic behavior at 300 K, the saturation magnetization (M{sub s}) becoming larger with the increase of particles size. The temperature dependence of M{sub s} was explained in terms of surface spin-canting as well as spin wave excitations in the core. Using a modified Bloch law, [M{sub s}(T)=M{sub s}(0)(1−βT{sup α})], we observed a size dependent behavior of the Bloch constant β and the exponent α, whose values increase and decrease, respectively, as the particle size reduces. - Highlights: • MgFe{sub 2}O{sub 4} nanoparticles were synthesized using a thermal decomposition method. • Pure ferrite nanoparticles were obtained at temperatures lower than 500 °C. • Samples show a superparamagnetic behavior at room temperatures. • Spin wave excitations were studied using a modified Bloch law.

  12. Colossal anisotropic resistivity and oriented magnetic domains in strained La{sub 0.325}Pr{sub 0.3}Ca{sub 0.375}MnO{sub 3} films

    Energy Technology Data Exchange (ETDEWEB)

    Jiang, Tao; Yang, Shengwei; Liu, Yukuai; Zhao, Wenbo; Feng, Lei; Li, Xiaoguang, E-mail: lixg@ustc.edu.cn [Hefei National Laboratory for Physical Sciences at Microscale, Department of Physics, University of Science and Technology of China, Hefei 230026 (China); Zhou, Haibiao; Lu, Qingyou [Hefei National Laboratory for Physical Sciences at Microscale, Department of Physics, University of Science and Technology of China, Hefei 230026 (China); High Magnetic Field Laboratory, Chinese Academy of Sciences and University of Science and Technology of China, Hefei 230031 (China); Hou, Yubin [High Magnetic Field Laboratory, Chinese Academy of Sciences and University of Science and Technology of China, Hefei 230031 (China)

    2014-05-19

    Magnetic and resistive anisotropies have been studied for the La{sub 0.325}Pr{sub 0.3}Ca{sub 0.375}MnO{sub 3} films with different thicknesses grown on low symmetric (011)-oriented (LaAlO{sub 3}){sub 0.3}(SrAl{sub 0.5}Ta{sub 0.5}O{sub 3}){sub 0.7} substrates. In the magnetic and electronic phase separation region, a colossal anisotropic resistivity (AR) of ∼10{sup 5}% and an anomalous large anisotropic magnetoresistance can be observed for 30 nm film. However, for 120 nm film, the maximum AR decreases significantly (∼2 × 10{sup 3}%) due to strain relaxation. The colossal AR is strongly associated with the oriented formation of magnetic domains, and the features of the strain effects are believed to be useful for the design of artificial materials and devices.

  13. Y{sub 2}BaCuO{sub 5} particle distribution in YBa{sub 2}Cu{sub 3}O{sub 7-y} grains of melt growth processed YBCO oxides; Y{sub 2}BaCuO{sub 5}-Partikelverteilung in YBa{sub 2}Cu{sub 3}O{sub 7-y}-Koernern durch das Melt-Growth-Verfahren verarbeiteter YBCO-Oxide

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Chan-Joong; Park, Soon-Dong [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of). Neutron Science Div.; Park, Hai-Woong [Korea Univ. of Technology and Education, Chungnam (Korea, Republic of). College of Energy, Materials and Chemical Engineering

    2013-02-01

    Y{sub 2}BaCuO{sub 5} (Y211) particle distribution within YBa{sub 2}Cu{sub 3}O{sub 7-y} (Y123) grains of YBCO samples melt growth (MG) processed was examined. To understand the processing variables on the Y211 distribution, a cooling rate (R{sub C}=1 K/h to R{sub C}=20 K/h) through a peritectic temperature (T{sub p} = 1010 C), a precursor powder size and composition were changed. Two different Y211 distributions (a linear x-like track and planar butterfly-like pattern) were observed, depending on the processing variables. The linear x-like Y211 tracks were observed in the Y123 samples prepared using a stoichiometric Y123 precursor, whereas the planar butterfly-like Y211 patterns were observed in the Y{sub 1.8}Ba{sub 2.4}Cu{sub 3.4}O{sub 7-d} (Y1.8) samples prepared using an Y211-excess composition precursor. The track and planar Y211 patterns were clearer at lower R{sub C} (slower growth rate of Y123 grains) and for the smaller Y211 particles. In contrast, the random Y211 distribution was dominant at the higher R{sub C} and for the larger Y211 particles. The Y211 distribution patterns in the Y123 grains were explained in terms of the interfacial energy difference among growing Y123 fronts. (orig.)

  14. Improvement microstructural and damage characterization of ceramic composites Y{sub 2}O{sub 3} – V{sub 2}O{sub 5} with MgO nano particles

    Energy Technology Data Exchange (ETDEWEB)

    Issa, T. T., E-mail: alazbrh@yahoo.com; Hasan, J. M.; Abdullah, E. T. [University of Baghdad, College of Science, Physics Department, Jaderiha, Baghdad (Iraq); Shokr, F. S. [King Abdul Aziz Universit, Faculty of Science& Art, Physics Department, Rabigh, KSA (Saudi Arabia)

    2016-04-21

    Compacted samples of Y{sub 2}O{sub 3}-V{sub 2}O{sub 5} – MgO Nano – particles wt. % sintered at different sintering temperature (700, 900, 1100, 1300) ) C° for 2 hours under static air were investigated by x-ray diffraction and differential thermal analysis(DTA), to identify the phase present .Microstructure examination achieved by scanning electron microscopy .Sintered density and porosity were measured for all sintered samples .Compression was tested too and the Brake down voltage and dielectric strength were measure for all sintered samples .The clear improvement were noticed in both microstructure and damage characterization respectively after existing the MgO Nano-particles, by increasing in about 30% in sintered density and 25% for the compressive strength .The improvement also noticed on both brake down voltage and dielectric strength.

  15. Spectral characteristics and white emission of Dy{sup 3+}/Tm{sup 3+}-BaLaGa{sub 3}O{sub 7} phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Gao, Shufang, E-mail: shfgao@yangtzeu.edu.cn [School of Physics and Optoelectronic Engineering, Yangtze University, Jingzhou 434023 (China); Xu, Shan [School of Physics and Optoelectronic Engineering, Yangtze University, Jingzhou 434023 (China); Wang, Yeqing [Department of Applied Physics, East China Jiaotong University, Nanchang, Jiangxi 330013 (China); Tu, Chaoyang, E-mail: tcy@fjirsm.ac.cn [Key Laboratory of Optoelectronic Materials Chemistry and Physics of CAS, Fujian Institute of Research on the Structure of Matter, CAS, Fuzhou, Fujian 350002 (China)

    2016-10-15

    Tm{sup 3+}-, Dy{sup 3+}-BaLaGa{sub 3}O{sub 7} phosphors have been synthesized by solid-phase sintering. X-ray diffraction (XRD) and photoluminescence properties of the phosphors were investigated in detail. The sample Tm{sup 3+} and Dy{sup 3+} ions co-doped BaLaGa{sub 3}O{sub 7} obtain white light emission by integrating a blue emission band located at 455 nm ({sup 1}D{sub 2}→{sup 3}F{sub 4}) and an orange one located at 573 nm ({sup 4}F{sub 9/2}→{sup 6}H{sub 13/2}) attributed to Tm{sup 3+} and Dy{sup 3+} ions, respectively. The study on the luminescence mechanism showed that there is the energy transfer between Tm{sup 3+} and Dy{sup 3+} in Tm{sup 3+}/Dy{sup 3+}-BaLaGa{sub 3}O{sub 7} phosphors.

  16. Improvement of tribological properties of magnetic tape by silica coating onto the Co-{gamma}-Fe{sub 2}O{sub 3} fine particles; Kobaruto hichakugata {gamma}-Fe{sub 2}O{sub 3} jisei biryushi no shisshiki shirika hyomen shori ni yoru jikitepu no suberi tokusei no kaizen

    Energy Technology Data Exchange (ETDEWEB)

    Hayashi, Kazuyuki; Iwasaki, Keisuke; Tanaka, Yasuyuki; Morii, Hiroko [Toda Kogyo Corporation, Hiroshima (Japan). R and D Center

    1999-01-10

    In order to improve the tribological properties of magnetic tape with Co-{gamma}-Fe{sub 2}O{sub 3} fine particles against a magnetic head, the silica coating onto the surface of Co-{gamma}-Fe{sub 2}O{sub 3} particles in aqueous slurry is investigated experimentally, and the kinetic friction coefficient of magnetic tapes prepared using the coated particles is measured. By this silica coating, the amount of myristic acid absorbed on the Co-{gamma}-Fe{sub 2}O{sub 3} particles tends to decrease and the kinetic friction coefficient of the magnetic tapes can be reduced from 0.4 to 0.2 because of the increase of the effective amount of myristic acid working as the lubricant when the magnetic tape is moving. Since the magnetic properties and the dispersibility of Co-{gamma}-Fe{sub 2}O{sub 3} pigment in the magnetic lacquer are not degraded by the silica coating, this coating method is expected to result in magnetic recording media with both good magnetic and low friction properties. (author)

  17. Hygroscopicity and chemical composition of Antarctic sub-micrometre aerosol particles and observations of new particle formation

    Directory of Open Access Journals (Sweden)

    E. Asmi

    2010-05-01

    Full Text Available The Antarctic near-coastal sub-micrometre aerosol particle features in summer were characterised based on measured data on aerosol hygroscopicity, size distributions, volatility and chemical ion and organic carbon mass concentrations. Hysplit model was used to calculate the history of the air masses to predict the particle origin. Additional measurements of meteorological parameters were utilised. The hygroscopic properties of particles mostly resembled those of marine aerosols. The measurements took place at 130 km from the Southern Ocean, which was the most significant factor affecting the particle properties. This is explained by the lack of additional sources on the continent of Antarctica. The Southern Ocean was thus a likely source of the particles and nucleating and condensing vapours. The particles were very hygroscopic (HGF 1.75 at 90 nm and very volatile. Most of the sub-100 nm particle volume volatilised below 100 °C. Based on chemical data, particle hygroscopic and volatile properties were explained by a large fraction of non-neutralised sulphuric acid together with organic material. The hygroscopic growth factors assessed from chemical data were similar to measured. Hygroscopicity was higher in dry continental air masses compared with the moist marine air masses. This was explained by the aging of the marine organic species and lower methanesulphonic acid volume fraction together with the changes in the inorganic aerosol chemistry as the aerosol had travelled long time over the continental Antarctica. Special focus was directed in detailed examination of the observed new particle formation events. Indications of the preference of negative over positive ions in nucleation could be detected. However, in a detailed case study, the neutral particles dominated the particle formation process. Freshly nucleated particles had the smallest hygroscopic growth factors, which increased subsequent to particle aging.

  18. Effect of Ce{sup 3+} ion on Dy{sup 3+} or Mn{sup 2+} in KMgSO{sub 4}Cl synthesized by centrifuge method

    Energy Technology Data Exchange (ETDEWEB)

    Shinde, Nita [Department of Physics R.T.M. Nagpur University, Nagpur 440033 (India); Dhoble, N.S. [Department of Chemistry, Sevadal Mahila Mahavidyalaya, Nagpur 440018 (India); Gedam, S.C., E-mail: gedam_sc@rediffmail.com [K.Z.S. Science College, Kalmeshwar, Nagpur 441501 (India); Dhoble, S.J. [Department of Physics R.T.M. Nagpur University, Nagpur 440033 (India)

    2016-04-15

    In this paper effect of Ce{sup 3+} ion on Dy{sup 3+} and Mn{sup 2+} ions in microcrystalline KMgSO{sub 4}Cl host prepared by ethanol (centrifuge technique) method has been discussed. In KMgSO{sub 4}Cl sample X-ray diffraction (XRD), scanning electron microscopy (SEM) and photoluminescence (PL) characteristics have been studied. Powder X-ray diffraction analysis shows the crystalline nature of the phosphor prepared by this new route. The morphological structures of the samples were conducted using SEM technique. An average crystallite size was found to be 5 μm. Photoluminescence in KMgSO{sub 4}Cl:Ce{sup 3+} is observed at 324 nm and 344 nm along with red emission broad band at around 644 nm. In KMgSO{sub 4}Cl: Ce, Dy phosphor Ce{sup 3+} emission around 324 and 344 nm overlaps rather well with Dy{sup 3+} excitation. The addition of Ce{sup 3+} showed higher photoluminescence (PL) intensity for the Dy{sup 3+} emissions around 482 and 576 nm excited via Ce{sup 3+} ions at 284 nm due to {sup 4}F{sub 9/2} to {sup 6}H{sub 15/2} and {sup 6}H{sub 13/2} levels. Ce{sup 3+}→Mn{sup 2+} energy transfer process occurs in KMgSO{sub 4}Cl host. KMgSO{sub 4}Cl: Mn does not give PL at 284 nm excitation but for co-doped samples with cerium, Mn{sup 2+} ions exhibits efficient fluorescence at around 560 nm due to {sup 4}T{sub 1}–{sup 6}A{sub 1} transition. KMgSO{sub 4}Cl: Dy or KMgSO{sub 4}Cl: Mn directly exciting does not show any emission while addition of Mn{sup 2+}, enhances red emission of Ce{sup 3+} at 644 nm. The CIE co-ordinates of KMgSO{sub 4}Cl:Ce; KMgSO{sub 4}Cl:Ce, Dy and KMgSO{sub 4}Cl:Ce, Mn phosphors reveals that the emission colour varies from blue to deep-red. Hence this material may be a potential lamp phosphor. - Highlights: • KMgSO{sub 4}Cl: Ce3{sup +} along with Dy3{sup +} and Mn2{sup +} was prepared by centrifuge method. • Particle size was found to be 5 μm using SEM technique. • The emission varies from blue to deep-red.

  19. Hygroscopic growth of sub-micrometer and one-micrometer aerosol particles measured during ACE-Asia

    Directory of Open Access Journals (Sweden)

    A. Massling

    2007-06-01

    Full Text Available Hygroscopic properties of aerosol particles in the sub-micrometer and one-micrometer size ranges were measured during the ACE-Asia study (Aerosol Characterization Experiment-Asia in spring 2001. The measurements took place off the coasts of Japan, Korea, and China. All instruments contributing to this study were deployed in a container on the forward deck of the NOAA Research Vessel Ronald H. Brown. Air masses with primarily marine influence and air masses from the Asian continent affected by both anthropogenic sources and by the transport of desert dust aerosol were encountered during the cruise.

    Results showed very different hygroscopic behavior in the sub-micrometer size range compared to the one-micrometer size range. In general, for all continentally influenced air masses, the one-micrometer particle population was characterized by two different particle groups – a nearly hydrophobic fraction with growth factors around 1.0 representative of dust particles and a sea salt fraction with hygroscopic growth factors around 2.0. The number fraction of dust particles was generally about 60% independent of long-range air mass origin.

    For sub-micrometer particles, a dominant, more hygroscopic particle fraction with growth factors between 1.5 and 1.9 (depending on dry particle size consistent with ammonium sulfate or non-neutralized sulfates as major component was always found. In marine air masses and for larger sizes within the sub-micrometer range (Dp=250 and 350 nm, a sea salt fraction with growth factors between 2.0 and 2.1 was also observed. For all other air masses, the more hygroscopic particle fraction in the sub-micrometer size range was mostly accompanied by a less hygroscopic particle fraction with growth factors between 1.20 and 1.55 depending on both the continental sources and the dry particle size. Number fractions of this particle group varied between 4 and 39% depending on dry particle size and air mass

  20. Fe{sub 3}O{sub 4}/carbon nanocomposite: Investigation of capacitive & magnetic properties for supercapacitor applications

    Energy Technology Data Exchange (ETDEWEB)

    Sinan, Neriman, E-mail: sinanneriman@gmail.com [Department of Advanced Technologies, Materials Science and Engineering Program, Bursa Technical University, Yildirim 16310, Bursa (Turkey); Unur, Ece, E-mail: eceunur@yahoo.com [Department of Energy Systems Engineering, Bursa Technical University, Yildirim 16310, Bursa (Turkey)

    2016-11-01

    Fe{sub 3}O{sub 4} nanoparticles with ∼10 nm diameters were synthesized by an extremely low-cost, scalable and relatively biocompatible chemical co-precipitation method. Magnetic measurements revealed that Fe{sub 3}O{sub 4} nanoparticles have bifunctional superparamagnetic and ferromagnetic character with saturation magnetization (M{sub s}) values of 64 and 71 emu g{sup −1} at 298 K and 10 K, respectively. Pseudocapacitive Fe{sub 3}O{sub 4} nanoparticles were then integrated into hazelnut shells - an abundant agricultural biomass - by an energy efficient hydrothermal carbonization method. Presence of magnesium oxide (MgO) ceramic template or its precursor in the hydrothermal reactor allowed simultaneous introduction of pores into the composite structure. Hierarchically micro-mesoporous Fe{sub 3}O{sub 4}/C nanocomposite possesses a high specific surface area of 344 m{sup 2} g{sup −1}. Electrochemical properties of Fe{sub 3}O{sub 4}/C nanocomposite were investigated by cyclic voltammetry and galvanostatic charge-discharge measurements in a conventional three-electrode cell. The Fe{sub 3}O{sub 4}/C nanocomposite is able to operate in a large negative potential window in 1 M Na{sub 2}SO{sub 4} aqueous electrolyte (−1.2–0 V vs. Ag/AgCl). Synergistic effect of the Fe{sub 3}O{sub 4} and carbon leads to enhanced specific capacitance, rate capability and cyclability making Fe{sub 3}O{sub 4}/C nanocomposite a very promising negative electrode material for asymmetric supercapacitors. - Highlights: • Fe{sub 3}O{sub 4} (magnetite) particles with ∼10 nm dia. were prepared by a facile chemical co-precipitation. • Fe{sub 3}O{sub 4} nanospheres are superparamagnetic at 298K with high saturation magnetization of 64 emu g{sup −1}. • Porous Fe{sub 3}O{sub 4}/C nanocomposite was also prepared by a green HTC method combined with MgO templating. • Electrochemical properties of Fe{sub 3}O{sub 4}/C were studied in 1 M Na{sub 2}SO{sub 4} (between −1.2 and 0 V vs. Ag

  1. Synthesis of Ce(III)-doped Fe{sub 3}O{sub 4} magnetic particles for efficient removal of antimony from aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Qi, Zenglu; Joshi, Tista Prasai [Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China); University of Chinese Academy of Sciences, Beijing 100049 (China); Liu, Ruiping, E-mail: liuruiping@rcees.ac.cn [Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China); University of Chinese Academy of Sciences, Beijing 100049 (China); Liu, Huijuan [University of Chinese Academy of Sciences, Beijing 100049 (China); State Key Laboratory of Environmental Aquatic Chemistry, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, 100085 (China); Qu, Jiuhui [Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China); University of Chinese Academy of Sciences, Beijing 100049 (China)

    2017-05-05

    Highlights: • Doping of Ce into Fe{sub 3}O{sub 4} was achieved based on a facile solvothermal method. • After doping, the removal capacity was increased by 5 times for “Sb(V)” and 2 times for “Sb(III)”. • Decreasing pH improved adsorption of Sb(V) but decreased adsorption of Sb(III). • Antimony sorption mechanisms on Ce-doped Fe{sub 3}O{sub 4} were illustrated. - Abstract: Aqueous antimony (Sb) pollution from human activity is of great concern in drinking water due to its adverse health effect. Magnetic Fe{sub 3}O{sub 4} particles, with high separation ability from solution, have been considered as a low-cost Sb adsorbent for contaminants. However, the limited adsorption capacity has restricted its practical application. In this study, a solvothermal approach was developed for doping Ce(III) into Fe{sub 3}O{sub 4}, thereby increasing the adsorption efficacy for both Sb(III) and Sb(V). In contrast to un-doped Fe{sub 3}O{sub 4}, the adsorption capacity towards Sb(III) and Sb(V) in Ce-doped materials increased from 111.4 to 224.2 mg/g and from 37.2 to 188.1 mg/g at neutral pH, respectively. Based on the combined results of XPS, XRD, and FTIR, it confirmed that Ce atom successfully doped into the Fe{sub 3}O{sub 4} structure, resulting in the decreased particle size, increased the surface area, and isoelectric point. Furthermore, the vibrating sample magnetometer (VSM) results showed that the Ce doping process had some side effects on the primitive magnetic property, but remaining the high separation potential during water treatment. According to the high removal efficiency and magnetic property, the Ce-doped Fe{sub 3}O{sub 4} of great simplicity should be a promising adsorbent for aqueous Sb removal.

  2. Spin-glass like behaviour in the nanoporous Fe{sub 2}O{sub 3} with amorphous structure

    Energy Technology Data Exchange (ETDEWEB)

    Thakur, M; Majumdar, S; Giri, S [Department of Solid State Physics and Center for Advanced Materials, Indian Association for the Cultivation of Science, Jadavpur, Kolkata 700 032 (India); Bhaumik, A; Nandi, M [Department of Materials Science and Center for Advanced Materials, Indian Association for the Cultivation of Science, Jadavpur, Kolkata 700 032 (India); Nakamura, H; Kobayashi, H; Kohara, T [Graduate School of Material Science, University of Hyogo, Kamigori, Ako-gun, Hyogo 678-1297 (Japan)], E-mail: sspsg2@iacs.res.in

    2008-07-23

    The porous Fe{sub 2}O{sub 3} was synthesized chemically. The average size of the particle was {approx}85.0 nm, which was observed by scanning electron microscopy. The signature of porous structure was confirmed by a N{sub 2} adsorption/desorption isotherm and intense x-ray powder diffraction peak at low angle. The x-ray diffraction pattern at high angle indicates the amorphous structure. Moessbauer investigations show that the value of the hyperfine field is {approx}498.0 kOe at 4.2 K which is much smaller than that of the hyperfine field of crystalline {alpha}/{gamma}-Fe{sub 2}O{sub 3} and consistent with the values of amorphous Fe{sub 2}O{sub 3}. The temperature dependence of zero-field cooled magnetization exhibits a peak at 18.0 K (T{sub f}), where T{sub f} follows the Almeida-Thouless relation as T{sub f} {proportional_to} H{sup 2/3}. The ageing phenomenon of the magnetic relaxation below T{sub f} and the memory effect in the field-cooled magnetization indicate the typical features of the classical spin-glass compounds below the spin freezing temperature at T{sub f}.

  3. Growth mechanisms for spherical mixed hydroxide agglomerates prepared by co-precipitation method: A case of Ni{sub 1/3}Co{sub 1/3}Mn{sub 1/3}(OH){sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Yue [Institute of Nuclear and New Energy Technology, Tsinghua University, Beijing 100084 (China); Xu, Shengming, E-mail: smxu@stinghua.edu.cn [Institute of Nuclear and New Energy Technology, Tsinghua University, Beijing 100084 (China); Xie, Ming [The State Key Laboratory of Advanced Technologies for Comprehensive Utilization of Precious Metals, Kunming 650106 (China); He, Yinghe, E-mail: yinghe.he@jcu.edu.au [School of Engineering and Physical Sciences, James Cook University, Douglas, Queensland 4811 (Australia); Huang, Guoyong [Institute of Nuclear and New Energy Technology, Tsinghua University, Beijing 100084 (China); Yang, Youcai [The State Key Laboratory of Advanced Technologies for Comprehensive Utilization of Precious Metals, Kunming 650106 (China)

    2015-01-15

    Highlights: • Anisotropic growth of Ni{sub 1/3}Co{sub 1/3}Mn{sub 1/3}(OH){sub 2} along the [0 0 1] direction was revealed. • DFT calculation results show crystal surface energies of (0 0 1) plane is highest. • A new model was proposed to explain the formation of spherical agglomerates. - Abstract: Spherical Ni{sub 1/3}Co{sub 1/3}Mn{sub 1/3}(OH){sub 2} agglomerates were synthesized by the co-precipitation method in the presence of ammonia. The results show that the growth mechanism of spherical agglomerates follows three-stages, i.e. nucleation and anisotropic growth of single crystals; agglomeration of polycrystalline crystallites agglomerated by single crystal grains as primary particles to form embryonic agglomerates; formation, growth and consolidation of spherical agglomerates or particles by agglomeration of embryonic agglomerates, continued growth of individual crystals in the agglomerates and further attachment of primary particles. The first two stages are very fast while the last stage takes almost the entire process to complete. The main reason for the anisotropic growth of Ni{sub 1/3}Co{sub 1/3}Mn{sub 1/3}(OH){sub 2} crystal is that crystal surface energy of E{sub (001)}, E{sub (100)}, E{sub (101)} and E{sub (102)} is different with E{sub (001)} being the highest. The morphology of the final spherical agglomerates is explained by partial re-crystallization of contacting primary particles. The growth process of spherical agglomerates was examined by X-ray diffraction, scanning electron microscope, transmission electron microscope and calculation of crystal surface energy using density function theory.

  4. Scintillation and optical properties of Pb-doped YCa{sub 4}O(BO{sub 3}){sub 3} crystals

    Energy Technology Data Exchange (ETDEWEB)

    Fujimoto, Yutaka, E-mail: fuji-you@tagen.tohoku.ac.jp [IMRAM, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai 980-8577 (Japan); JSPS, 8 Ichibanmachi, Chiyoda-ku, Tokyo 102-8472 (Japan); Yanagida, Takayuki; Yokota, Yuui [IMRAM, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai 980-8577 (Japan); Kawaguchi, Noriaki [Tokuyama Corporation, 3 Shibuya Shibuya-ku, Tokyo 150-8383 (Japan); Fukuda, Kentaro [IMRAM, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai 980-8577 (Japan); Tokuyama Corporation, 3 Shibuya Shibuya-ku, Tokyo 150-8383 (Japan); Totsuka, Daisuke [Nihon Kessho Kogaku Co., Ltd., 810-5 Nobe-cho Tatebayashi Gunma (Japan); Watanabe, Kenichi; Yamazaki, Atsushi [Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8603 (Japan); Chani, Valery [IMRAM, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai 980-8577 (Japan); Yoshikawa, Akira [IMRAM, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai 980-8577 (Japan); NICHe, Tohoku University, 6-6-10 Aoba, Aramaki, Aoba-ku, Sendai 980-8579 (Japan)

    2011-10-01

    This communication reports optical properties and radiation responses of Pb{sup 2+} 0.5 and 1.0 mol%-doped YCa{sub 4}O(BO{sub 3}){sub 3} (YCOB) single crystals grown by the micro-pulling-down ({mu}-PD) method for neutron scintillator applications. The crystals had no impurity phases according to the results of X-ray powder diffraction. These Pb{sup 2+}-doped crystals demonstrated blue-light luminescence at 330 nm because of Pb{sup 2+1}S{sub 0}-{sup 3}P{sub 0,1} transition in the photoluminescence spectra. The main emission decay component was determined to be about 250-260 ns under 260 nm excitation wavelength. When irradiated by a {sup 252}Cf source, the relative light yield of 0.5% Pb{sup 2+}-doped crystal was about 300 ph/n that was determined using the light yield of a reference Li-glass scintillator.

  5. Fabrication, characterization, and photocatalytic property of {alpha}-Fe{sub 2}O{sub 3}/graphene oxide composite

    Energy Technology Data Exchange (ETDEWEB)

    Li Hong; Zhao Qidong; Li Xinyong, E-mail: xinyongli@hotmail.com [School of Environmental Science and Technology, Dalian University of Technology, State Key Laboratory of Fine Chemical, Key Laboratory of Industrial Ecology and Environmental Engineering (MOE) (China); Zhu Zhengru [Research Center of Hydrology and Engineering, Academy of City and Environment, Liaoning Normal University (China); Tade, Moses; Liu Shaomin, E-mail: shaomin.liu@curtin.edu.au [Curtin University, Department of Chemical Engineering (Australia)

    2013-06-15

    Spindle-shaped microstructure of {alpha}-Fe{sub 2}O{sub 3} was successfully synthesized by a simple hydrothermal method. The {alpha}-Fe{sub 2}O{sub 3}/graphene oxide (GO) composites was prepared using a modified Hummers' strategy. The properties of the samples were systematically investigated by X-ray powder diffraction (XRD), UV-Vis diffuse reflectance spectrophotometer, transmission electron microscope, atomic force microscope, X-ray photoelectron spectroscopy, and Raman spectroscopy (Raman) techniques. GO nanosheets act as supporting materials for anchoring the {alpha}-Fe{sub 2}O{sub 3} particles. The average crystallite sizes of the {alpha}-Fe{sub 2}O{sub 3} and {alpha}-Fe{sub 2}O{sub 3}/GO samples are ca. 27 and 24 nm, respectively. The possible growth of {alpha}-Fe{sub 2}O{sub 3} onto GO layers led to a higher absorbance capacity for visible light by {alpha}-Fe{sub 2}O{sub 3}/GO than {alpha}-Fe{sub 2}O{sub 3} composite. The photocatalytic degradation of toluene over the {alpha}-Fe{sub 2}O{sub 3} and {alpha}-Fe{sub 2}O{sub 3}/GO samples under xenon-lamp irradiation was comparatively studied by in situ FTIR technique. The results indicate that the {alpha}-Fe{sub 2}O{sub 3}/GO sample synthesized exhibited a higher capacity for the degradation of toluene. The composite of {alpha}-Fe{sub 2}O{sub 3}/GO could be promisingly applied in photo-driven air purification.

  6. Preparation of ultra-thin and high-quality WO{sub 3} compact layers and comparision of WO{sub 3} and TiO{sub 2} compact layer thickness in planar perovskite solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Jincheng; Shi, Chengwu, E-mail: shicw506@foxmail.com; Chen, Junjun; Wang, Yanqing; Li, Mingqian

    2016-06-15

    In this paper, the ultra-thin and high-quality WO{sub 3} compact layers were successfully prepared by spin-coating-pyrolysis method using the tungsten isopropoxide solution in isopropanol. The influence of WO{sub 3} and TiO{sub 2} compact layer thickness on the photovoltaic performance of planar perovskite solar cells was systematically compared, and the interface charge transfer and recombination in planar perovskite solar cells with TiO{sub 2} compact layer was analyzed by electrochemical impedance spectroscopy. The results revealed that the optimum thickness of WO{sub 3} and TiO{sub 2} compact layer was 15 nm and 60 nm. The planar perovskite solar cell with 15 nm WO{sub 3} compact layer gave a 9.69% average and 10.14% maximum photoelectric conversion efficiency, whereas the planar perovskite solar cell with 60 nm TiO{sub 2} compact layer achieved a 11.79% average and 12.64% maximum photoelectric conversion efficiency. - Graphical abstract: The planar perovskite solar cell with 15 nm WO{sub 3} compact layer gave a 9.69% average and 10.14% maximum photoelectric conversion efficiency, whereas the planar perovskite solar cell with 60 nm TiO{sub 2} compact layer achieved a 11.79% average and 12.64% maximum photoelectric conversion efficiency. Display Omitted - Highlights: • Preparation of ultra-thin and high-quality WO{sub 3} compact layers. • Perovskite solar cell with 15 nm-thick WO{sub 3} compact layer achieved PCE of 10.14%. • Perovskite solar cell with 60 nm-thick TiO{sub 2} compact layer achieved PCE of 12.64%.

  7. Synthesis and luminescence properties of Ce{sup 3+}-doped Y{sub 3}Al{sub 3.5}Ga{sub 1.5}O{sub 12} green phosphor for white LEDs

    Energy Technology Data Exchange (ETDEWEB)

    Qiang, Yaochun [Fujian Key Laboratory of Advanced Materials, Department of Materials Science and Engineering, College of Materials, Xiamen University, Xiamen 361005 (China); Yu, Yuxi, E-mail: yu_heart@xmu.edu.cn [Fujian Key Laboratory of Advanced Materials, Department of Materials Science and Engineering, College of Materials, Xiamen University, Xiamen 361005 (China); Chen, Guolong [Fujian Engineering Research Center for Solid-state Lighting, Department of Electronic Science, Xiamen University, Xiamen 361005 (China); Fang, Jiyu [Advanced Materials Processing and Analysis Center, Department of Materials Science and Engineering, University of Central Florida, Orlando, FL 32816 (United States)

    2016-04-15

    A series of Ce{sup 3+}-doped Y{sub 3}Al{sub 3.5}Ga{sub 1.5}O{sub 12} green phosphors were successfully synthesized by a solid-state reaction method. The microstructure, morphology, luminescence spectra, luminescence quantum yield (QY) and thermal stability of the phosphor were investigated. The critical concentration of Ce{sup 3+} ions in Y{sub 3−m}Al{sub 3.5}Ga{sub 1.5}O{sub 12}:mCe{sup 3+} is m=0.06. The QY of Y{sub 2.94}Al{sub 3.5}Ga{sub 1.5}O{sub 12}:0.06Ce{sup 3+} phosphor is as high as 94% under excitation at 450 nm and its luminescence intensity at 150 °C still maintains 90% of that measured at 25 °C, which are just a little worse than those of commercial Lu{sub 3}Al{sub 5}O{sub 12}:Ce{sup 3+} green phosphor but much better than those of commercial (Sr,Ba){sub 2}SiO{sub 4}:Eu{sup 2+} green phosphor. A white LED lamp was fabricated by employing Y{sub 2.94}Al{sub 3.5}Ga{sub 1.5}O{sub 12}:0.06Ce{sup 3+} as a green phosphor and commercial (Ca,Sr)AlSiN{sub 3}:Eu{sup 2+} as a red phosphor (628 nm), its Ra value, correlated color temperature (CCT), CIE1931 chromaticity coordinates and luminous efficiency is 84, 3081 K, (x=0.4369, y=0.4142) and 102 lm/W, respectively. The experimental results demonstrate that Y{sub 2.94}Al{sub 3.5}Ga{sub 1.5}O{sub 12}:0.06Ce{sup 3+} is a promising green phosphor not only can be used for high color rendering index white LEDs but also for high-power white LEDs.

  8. Au and Pd nanoparticles supported on CeO{sub 2}, TiO{sub 2}, and Mn{sub 2}O{sub 3} oxides

    Energy Technology Data Exchange (ETDEWEB)

    Nascente, P.A.P., E-mail: nascente@ufscar.br [Federal University of Sao Carlos, Department of Materials Engineering, Sao Carlos, SP (Brazil); Maluf, S.S.; Afonso, C.R.M. [Federal University of Sao Carlos, Department of Materials Engineering, Sao Carlos, SP (Brazil); Landers, R. [State University of Campinas, Institute of Physics, Department of Applied Physics, Campinas, SP (Brazil); Pinheiro, A.N.; Leite, E.R. [Federal University of Sao Carlos, Department of Chemistry, Sao Carlos, SP (Brazil)

    2014-10-01

    Highlights: • CeO{sub 2}, TiO{sub 2}, and Mn{sub 2}O{sub 3} supported Au and Pd nanoparticles. • Additions of 0.5 wt% of Au and Pd onto CeO{sub 2}, TiO{sub 2}, and Mn{sub 2}O{sub 3} supports. • Characterization by XRD, XPS, EDS, TEM, HRTEM, STEM, and EFTEM. - Abstract: Gold and palladium nanoparticles were incorporated on CeO{sub 2}, TiO{sub 2}, and Mn{sub 2}O{sub 3} supports prepared by a sol–gel method. The samples were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), energy dispersive spectroscopy (EDS), transmission electron microscopy (TEM), high resolution TEM (HRTEM), scanning TEM (STEM) in high angle annular dark field mode (HAADF), and energy filtered TEM (EFTEM) using electron energy loss spectroscopy (EELS). The XRD diffractograms presented sharp and intense peaks indicating that the samples are highly crystalline, but it did not detected any peak corresponding to Au or Pd phases. This indicates that the Au and Pd NPs were incorporated into the structures of the oxides. It was not possible to obtain an Au 4f spectrum for Au/Mn{sub 2}O{sub 3} due to an overlap with the Mn 3p spectrum. The XPS Au 4f spectra for Au/CeO{sub 2} and Au/TiO{sub 2} present negative chemical shifts that could be attributed to particle-size-related properties. The XPS Pd 3d spectra indicate that for both CeO{sub 2} and TiO{sub 2} substrates, the Pd NPs were in the metallic state, while for the Mn{sub 2}O{sub 3} substrate, the Pd NPs were oxidized. The HRTEM results show the formation of nanocrystalline oxides having particles sizes between 50 and 200 nm. TEM micrographs show that the addition of Au caused the formation of Au clusters in between the CeO{sub 2} NPS, formation of Au NPs for the TiO{sub 2} support, and homogeneous distribution of Au clusters for the Mn{sub 2}O{sub 3} support. The addition of Pd yielded a homogeneous dispersion throughout the CeO{sub 2} and TiO{sub 2}, but caused the formation of Pd clusters for the Mn{sub 2}O{sub

  9. Up-conversion emission of Er{sup 3+}/Yb{sup 3+}co-doped BaBi{sub 2}Nb{sub 2}O{sub 9} (BBN) phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Façanha, M.X., E-mail: marcello.facanha@uece.br [Departamento de Química, Centro de Ciências, Universidade Federal do Ceará (UFC), Fortaleza, Ceará (Brazil); Faculdade de Educação de Crateús (FAEC), Universidade Estadual do Ceará (UECE), Fortaleza, Ceará (Brazil); Laboratório de Telecomunicações e Ciências e Engenharia de Materiais (LOCEM), Universidade Federal do Ceará (UFC), Fortaleza, Ceará (Brazil); Nascimento, J.P.C. do [Departamento de Química, Centro de Ciências, Universidade Federal do Ceará (UFC), Fortaleza, Ceará (Brazil); Laboratório de Telecomunicações e Ciências e Engenharia de Materiais (LOCEM), Universidade Federal do Ceará (UFC), Fortaleza, Ceará (Brazil); Silva, M.A.S., E-mail: marceloassilva@yahoo.com.br [Laboratório de Telecomunicações e Ciências e Engenharia de Materiais (LOCEM), Universidade Federal do Ceará (UFC), Fortaleza, Ceará (Brazil); and others

    2017-03-15

    On this paper, polycrystalline samples of the tetragonal systems BaBi{sub 2}Nb{sub 2}O{sub 9} (BBN) and BBN co-doped with Er{sup 3+}/Yb{sup 3+} (BBN: 0.04Er{sup 3+}yYb{sup 3+}, where y=0.02, 0.04, 0.06 and 0.08 mol%) were synthesized by the solid state method. The crystalline structure and photoluminescent properties of the ceramic phosphors were investigated by powder X-ray diffraction (PXRD), Raman spectroscopy and spectral analysis of up-conversion (UC) emission. The results reveal that all compositions crystallize in the I4/mmm space group at room temperature, and show UC green emissions (centered at 525 nm and 550 nm) and red (around 660 nm) coming from ({sup 2}H{sub 11/2}, {sup 4}S{sub 3/2}→{sup 4}I{sub 15/2}) and ({sup 4}F{sub 9/2}→{sup 4}I{sub 15/2}) transitions, respectively, under excitation at 980 nm. Increasing variations of the Yb{sup 3+} sensitizer concentration in the host BBN, lead to a significant intensity increase in both UC emissions due to the efficiency of the energy-transfer process. The BBN: 0.04 mol%Er{sup 3+}0.08 mol%Yb{sup 3+} composition showed the higher intensity bands, thus establishing the BBN as an alternative host material for luminescent centers.

  10. Study of magnetic behavior in hexagonal-YMn{sub 1−x}Fe{sub x}O{sub 3} (x=0 and 0.2) nanoparticles using remanent magnetization curves

    Energy Technology Data Exchange (ETDEWEB)

    Chauhan, Samta; Singh, Amit Kumar; Srivastava, Saurabh Kumar; Chandra, Ramesh, E-mail: ramesfic@iitr.ac.in

    2016-09-15

    We have studied the magnetic behavior of YMn{sub 1−x}Fe{sub x}O{sub 3} (x=0 and 0.2) nanoparticles synthesized by conventional solid state reaction method. The as-synthesized nanoparticles were found to have hexagonal phase with P6{sub 3cm} space group confirmed by X-Ray diffraction. The particle size was found to be ~70 nm as confirmed by both X-Ray diffraction and Transmission Electron Microscopy. DC magnetization and memory effect measurements imply that the h-YMnO{sub 3} nanoparticles bear a resemblance to super spin-glass state following de Almeida–Thouless like behavior which is being suppressed by Fe-doping. The Fe-doping in YMnO{sub 3} enhances the antiferromagnetic (AFM) transition temperature T{sub N} to ~79 K and induces a new magnetic state due to the surface spins which is realized as diluted antiferromagnet in a field (DAFF) as explored by the thermoremanent and isothermoremanent magnetization measured with different applied magnetic field. - Highlights: • Magnetic behavior of h-YMn{sub 1−x}Fe{sub x}O{sub 3} (x=0 and 0.2) nanoparticles have been studied. • The nanoparticles (~70 nm) were synthesized by solid state reaction method. • Magnetic data reveal spin-glass behavior in YMnO{sub 3} which was suppressed in YMn{sub 0.8}Fe{sub 0.2}O{sub 3}. • The h-YMnO{sub 3} nanoparticles show memory effect and obey de-Almeida Thouless line. • TRM and IRM suggest spin glass nature for YMnO{sub 3}, while the YMn{sub 0.8}Fe{sub 0.2}O{sub 3} resembles DAFF.

  11. Characterization of the insulator barrier and the superconducting transition temperature in GdBa{sub 2}Cu{sub 3}O{sub 7−δ}/BaTiO{sub 3} bilayers for application in tunnel junctions

    Energy Technology Data Exchange (ETDEWEB)

    Navarro, H., E-mail: henrynavarro@cab.cnea.gov.ar; Sirena, M.; Haberkorn, N. [Instituto Balseiro, Universidad Nacional de Cuyo and CNEA, 8400 Bariloche (Argentina); Centro Atómico Bariloche, Comisión Nacional de Energía Atómica. Av. Bustillo 9500, 8400 San Carlos de Bariloche (Argentina); Yang, Ilkyu [Department of Physics, Pohang University of Science and Technology, Pohang (Korea, Republic of); Kim, Jeehoon [Department of Physics, Pohang University of Science and Technology, Pohang (Korea, Republic of); CALDES, Institute for Basic Science, Pohang (Korea, Republic of)

    2015-07-28

    The optimization of the superconducting properties in a bottom electrode and the quality of an insulator barrier are the first steps in the development of superconductor/insulator/superconductor tunnel junctions. Here, we study the quality of a BaTiO{sub 3} tunnel barrier deposited on a 16 nm thick GdBa{sub 2}Cu{sub 3}O{sub 7−δ} thin film by using conductive atomic force microscopy. We find that the tunnel current is systematically reduced (for equal applied voltage) by increasing the BaTiO{sub 3} barrier thickness between 1.6 and 4 nm. The BaTiO{sub 3} layers present an energy barrier of ≈1.2 eV and an attenuation length of 0.35–0.5 nm (depending on the applied voltage). The GdBa{sub 2}Cu{sub 3}O{sub 7−δ} electrode is totally covered by a BaTiO{sub 3} thickness above 3nm. The presence of ferroelectricity was verified by piezoresponse force microscopy for a 4 nm thick BaTiO{sub 3} top layer. The superconducting transition temperature of the bilayers is systematically suppressed by increasing the BaTiO{sub 3} thickness. This fact can be associated with stress at the interface and a reduction of the orthorhombicity of the GdBa{sub 2}Cu{sub 3}O{sub 7−δ}. The reduction in the orthorhombicity is expected by considering the interface mismatch and it can also be affected by reduced oxygen stoichiometry (poor oxygen diffusion across the BaTiO{sub 3} barrier)

  12. Structural and optical properties of Er{sup 3+} doped SiO{sub 2}–Al{sub 2}O{sub 3}–GeO{sub 2} compounds prepared by a simple route

    Energy Technology Data Exchange (ETDEWEB)

    Filho, Fausto M. Faria [Instituto de Física, Universidade Federal de Goiás-UFG, Campus II, Caixa Postal 131, CEP 74001-970 Goiânia, GO (Brazil); Gonçalves, Rogéria R. [Departamento de Química, Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo-USP, Av. Bandeirantes, 3900, CEP 14040-901 Ribeirão Preto, SP (Brazil); Ribeiro, Sidney J.L. [Institute of Chemistry, São Paulo State University-UNESP, Rua Professor Francisco Degni, 55, CEP 14801-970 Araraquara, SP (Brazil); Maia, Lauro J.Q., E-mail: lauro@ufg.br [Instituto de Física, Universidade Federal de Goiás-UFG, Campus II, Caixa Postal 131, CEP 74001-970 Goiânia, GO (Brazil)

    2015-04-15

    Highlights: • We developed a simple route to obtain gels and powders using GeO{sub 2}, TEOS and TMAH solution. • Al{sub 6}Ge{sub 2}O{sub 13} crystalline nanoparticles embedded in amorphous matrix were obtained. • The Al{sub 2}O{sub 3} enhance Er{sup 3+} dispersion in GeO{sub 2}–SiO{sub 2} increasing its emission and the full width at half maximum from 41 to 56 nm. • The {sup 4}I{sub 13/2} Er{sup 3+} level lifetime varies between 4.8 and 5.6 ms (1533 nm emission). - Abstract: Samples of (1 − x)[0.70SiO{sub 2} + 0.30Al{sub 2}O{sub 3}] + xGeO{sub 2} compositions, containing x = 0.05, 0.10, 0.20, 0.30, 0.40 and 0.50, and doped with 1 mol% of Er{sup 3+}, were prepared by a mixed route (sol–gel process and Pechini method). Transparent gels were synthesized and homogeneous powders were obtained by heat treatments from 800 °C to 1050 °C. The final powders were characterized by X-ray diffraction, Fourier transform infrared spectroscopy and high-resolution transmission electron microscopy. The optical properties were studied by photoluminescence measurements in the infrared region, and the average lifetime of the metastable state {sup 4}I{sub 13/2} of Er{sup 3+} ions and the full-width at half maximum (FWHM) were determined. A silica-rich amorphous phase and nanocrystallites with orthorhombic structure of Al{sub 6}Ge{sub 2}O{sub 13} phase were obtained. The samples present a broad emission centered at around 1532 nm under excitation at 977 nm, with a FWHM of 53 nm and a lifetime of 5.6 ms. The synthesized compounds by an easy chemical procedure are potentially applicable in integrated optical systems.

  13. Creation of Y{sub 2}Ti{sub 2}O{sub 7} nanoprecipitates to strengthen the Fe-14Cr-3Al-2W steels by adding Ti hydride and Y{sub 2}O{sub 3} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Linbo; Bai, Zhonglian; Shen, Hailong; Wang, Chenxi; Liu, Tong, E-mail: tongliu@buaa.edu.cn

    2017-05-15

    In order to prohibit the formation of large Y-Al-O precipitates, Ti hydride nanoparticles (NPs) were prepared and used to replace Ti as raw particles to fabricate the oxide dispersion strengthened (ODS) Fe-14Cr-3Al-2W-0.35Y{sub 2}O{sub 3} steels by mechanical alloying (MA) and hot isostatic pressing (HIP). As the content of Ti hydride increases from 0.1 to 0.5 and 1.0 wt%, the oxide nanoprecipitates in the ODS steels changes from Y{sub 3}Al{sub 5}O{sub 12} phase to Y{sub 2}Ti{sub 2}O{sub 7} phase (semicoherent with the matrix), and the particle size is successfully reduced. The tensile strength of the ODS steel increases remarkably with increasing Ti hydride content. The sample with 1.0 wt% Ti hydride exhibits a high strength of 1049 MPa at 25 °C and 278 MPa at 700 °C. The creation of Y{sub 2}Ti{sub 2}O{sub 7} nanoprecipitates by adding Ti hydride NPs opens a new way to control the structure and size of the oxide precipitates in the ODS steels. - Graphical abstract: The creation of Y{sub 2}Ti{sub 2}O{sub 7} nanoprecipitates by adding Ti hydride nanoparticles remarkably increases the mechanical properties of the Al-containing ODS steels. - Highlights: •TiH{sub 1.971} reacts with Y{sub 2}O{sub 3} to form Y{sub 2}Ti{sub 2}O{sub 7} in the Al-containing ODS steel. •Addition of TiH{sub 1.971} nanoparticles can prevent the formation of Y-Al-O phases. •Y{sub 2}Ti{sub 2}O{sub 7} nanoparticles share semicoherent interface with the ferrite matrix. •The mean size of oxide dispersion is reduced to 11.2 ± 7.1 nm with 1.0 wt% TiH{sub 1.971}. •The tensile strength of the ODS steel enlarges with increasing TiH{sub 1.971} content.

  14. Cr{sub 2}O{sub 3} thin films grown at room temperature by low pressure laser chemical vapour deposition

    Energy Technology Data Exchange (ETDEWEB)

    Sousa, P.M. [Universidade de Lisboa, Faculdade de Ciencias, Departamento de Fisica and ICEMS, Campo Grande, Ed. C8, 1749-016 Lisboa (Portugal); Silvestre, A.J., E-mail: asilvestre@deq.isel.ipl.p [Instituto Superior de Engenharia de Lisboa and ICEMS, R. Conselheiro Emidio Navarro 1, 1959-007 Lisboa (Portugal); Conde, O. [Universidade de Lisboa, Faculdade de Ciencias, Departamento de Fisica and ICEMS, Campo Grande, Ed. C8, 1749-016 Lisboa (Portugal)

    2011-03-31

    Chromia (Cr{sub 2}O{sub 3}) has been extensively explored for the purpose of developing widespread industrial applications, owing to the convergence of a variety of mechanical, physical and chemical properties in one single oxide material. Various methods have been used for large area synthesis of Cr{sub 2}O{sub 3} films. However, for selective area growth and growth on thermally sensitive materials, laser-assisted chemical vapour deposition (LCVD) can be applied advantageously. Here we report on the growth of single layers of pure Cr{sub 2}O{sub 3} onto sapphire substrates at room temperature by low pressure photolytic LCVD, using UV laser radiation and Cr(CO){sub 6} as chromium precursor. The feasibility of the LCVD technique to access selective area deposition of chromia thin films is demonstrated. Best results were obtained for a laser fluence of 120 mJ cm{sup -2} and a partial pressure ratio of O{sub 2} to Cr(CO){sub 6} of 1.0. Samples grown with these experimental parameters are polycrystalline and their microstructure is characterised by a high density of particles whose size follows a lognormal distribution. Deposition rates of 0.1 nm s{sup -1} and mean particle sizes of 1.85 {mu}m were measured for these films.

  15. Tuning from green to red the upconversion emission of Y{sub 2}O{sub 3}:Er{sup 3+}-Yb{sup 3+} nanophosphors

    Energy Technology Data Exchange (ETDEWEB)

    Diaz-Torres, L.A. [Centro de Investigaciones en Optica, Grupo de Espectroscopia de Materiales Avanzados y Nanoestructurados (GEMANA), A. P. 1-948, Leon, GTO (Mexico); Salas, P.; Resendiz-L, E.; Rodriguez-Gonzalez, C. [Universidad Nacional Autonoma de Mexico, Centro de Fisica Aplicada y Tecnologia Avanzada, Apartado Postal 1-1010, Queretaro, QRO (Mexico); Oliva, J. [Conacyt-Facultad Ciencias Quimicas Universidad Autonoma de Coahuila, Saltillo, Coahuila (Mexico); Meza, O. [Benemerita Universidad Autonoma de Puebla, Instituto de Fisica, A.P. J-48, Centro Historico, PUE (Mexico)

    2017-01-15

    In this work, the structural, morphological and luminescent properties of Y{sub 2}O{sub 3} nanophosphors doped with Er{sup 3+} (1 mol%) and different Yb{sup 3+} concentrations (2-12 mol%) have been studied. Those nanophosphors were synthesized using a simple hydrothermal method. XRD analysis indicates that all the samples presented a pure cubic phase even for Yb concentrations as high as 12 mol%. In addition, SEM images show nanoparticles with quasi-spherical shapes with average sizes in the range of 300-340 nm. Photoluminescence measurements obtained after excitation at 967 nm revealed that our samples have strong green (563 nm) and red emissions (660 nm) corresponding to {sup 2}H{sub 11/2} + {sup 4}S{sub 3/2} → {sup 4}I{sub 15/2} and {sup 4}F{sub 9/2} → {sup 4}I{sub 15/2} transitions of Er{sup 3+} ions, respectively. We also observed that the green band is quenched and the red emission enhanced as the Yb concentration increases. In consequence, the CIE coordinates changed from (0.35, 0.64) in the green region to (0.59, 0.39) in the red region. Thus, the tuning properties of Y{sub 2}O{sub 3} nanophosphors suggest that they are good candidates for applications in lighting. (orig.)

  16. Analysis of energy transfer based emission spectra of (Sm{sup 3+}, Dy{sup 3+}): Li{sub 2}O–LiF–B{sub 2}O{sub 3}–CdO glasses

    Energy Technology Data Exchange (ETDEWEB)

    Naresh, V., E-mail: varna.naresh@gmail.com; Buddhudu, S., E-mail: profsb_svuniv@hotmail.com

    2014-03-15

    The present paper brings out the results concerning the preparation and optical properties of Sm{sup 3+} and Dy{sup 3+} each ion separately in four different concentrations (0.1, 0.5, 1.0 and 1.5 mol%) and also together doped (1 mol% Dy{sup 3+}+x mol% Sm{sup 3+}): Li{sub 2}O–LiF–B{sub 2}O{sub 3}–CdO (where x=0.1, 0.5, 1.0 and 1.5 mol%) glasses by a melt quenching method. Sm{sup 3+} doped base glasses have displayed an intense orange emission at 602 nm ({sup 4}G{sub 5/2}→{sup 6}H{sub 7/2}) with an excitation at 403 nm and Dy{sup 3+} doped glasses have shown two emissions located at 486 nm ({sup 4}F{sub 9/2}→{sup 6}H{sub 15/2}; blue) and 577 nm ({sup 4}F{sub 9/2}→{sup 6}H{sub 13/2}; yellow) with λ{sub exci}=387 nm. The co-doped (Dy{sup 3+}+Sm{sup 3+}) lithium fluoro-boro cadmium glasses have been excited with an excitation at 387 nm of Dy{sup 3+} which has resulted in with a significant reduction in Dy{sup 3+} emission, at the same time there exists an increase in the reddish-orange emission of Sm{sup 3+} due to an energy transfer from Dy{sup 3+} to Sm{sup 3+}. The non-radiative energy transfer from Dy{sup 3+} to Sm{sup 3+} is governed by dipole–quadrupole interactions as is explained in terms of their emission spectra, donor lifetime, energy level diagram and energy transfer characteristic factors. -- Highlights: • In co-doped (Dy{sup 3+}+Sm{sup 3+}): LFBCd glass, reddish-orange emission due to Sm{sup 3+} ({sup 4}F{sub 9/2}→{sup 6}H{sub J}) has been enhanced due to an energy transfer from Dy{sup 3+} ions in the glass. • This has been evidenced from a lowering trend in the emission transition lifetimes of donor (Dy{sup 3+}) ions with increasing acceptor (Sm{sup 3+}) concentration. • Energy transfer mechanism involved in Dy{sup 3+}→Sm{sup 3+} has been explained in terms of I–H luminescence decay curve analysis.

  17. Downshifting by energy transfer in Eu{sup 3+}/Yb{sup 3+} codoped Ba{sub 4}La{sub 6}(SiO{sub 4}){sub 6}O glass ceramics

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, W.J., E-mail: wjzhang03@163.com [School of Material Science and Engineering and Shandong Provincial Key Lab of Preparation and Measurement of Building Materials, University of Jinan, Jinan 250022 (China); State Key Lab of Luminescent Materials and Devices and Institute of Optical Communication Materials, South China University of Technology, Guangzhou 510641 (China); Li, X.B.; Wu, L.J.; Yu, Y.Y.; Wang, X.Z.; Liu, S.Q.; Wang, Z. [School of Material Science and Engineering and Shandong Provincial Key Lab of Preparation and Measurement of Building Materials, University of Jinan, Jinan 250022 (China); Wang, W.C.; Liu, Y. [State Key Lab of Luminescent Materials and Devices and Institute of Optical Communication Materials, South China University of Technology, Guangzhou 510641 (China)

    2017-03-01

    We report on an efficient near-infrared downshifting in Eu{sup 3+}/Yb{sup 3+} codoped glass ceramics containing Ba{sub 4}La{sub 6}(SiO{sub 4}){sub 6}O crystals. The structural and luminescence properties were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), static and dynamic photoemission and excitation spectroscopy. After crystallization, the doping ions are found to be selectively incorporated into the precipitated oxyapatite crystals on La{sup 3+} sites, contributing to the remarkably enhanced visible emission of Eu{sup 3+} under 394 nm excitation. The Eu{sup 3+}/Yb{sup 3+} codoped glass ceramics additionally exhibits efficient near-infrared luminescence of Yb{sup 3+} around 1000 nm upon photon excitation of Eu{sup 3+} within the 300–550 nm range. The reduced visible emission and decay time of {sup 5}D{sub 0} state with Yb{sup 3+} codoping further confirm the energy transfer from Eu{sup 3+} to Yb{sup 3+}, which is promoted due to the shortened distance between Eu{sup 3+} and Yb{sup 3+} within crystals. The maximum energy transfer efficiency is evaluated to be 61%. It is revealed that energy transfer process occurs predominantly through the cross relaxation of Eu{sup 3+}({sup 5}D{sub 0}) + Yb{sup 3+}({sup 2}F{sub 7/2}) → Eu{sup 3+}({sup 7}F{sub 6}) + Yb{sup 3+}({sup 7}F{sub 5/2}).

  18. Structural and optical properties of glancing angle deposited In{sub 2}O{sub 3} columnar arrays and Si/In{sub 2}O{sub 3} photodetector

    Energy Technology Data Exchange (ETDEWEB)

    Mondal, A.; Shougaijam, B.; Goswami, T.; Dhar, J.C.; Singh, N.K. [National Institute of Technology, Department of Electronics and Communication Engineering, Agartala (India); Choudhury, S. [North Eastern Hill University, Department of Electronics and Communication Engineering, Shillong (India); Chattopadhay, K.K. [Jadavpur University, Department of Physics, Kolkata (India)

    2014-04-15

    Ordered and perpendicular columnar arrays of In{sub 2}O{sub 3} were synthesized on conducting ITO electrode by a simple glancing angle deposition (GLAD) technique. The as-deposited In{sub 2}O{sub 3} columns were investigated by field emission gun-scanning electron microscope (FEG-SEM). The average length and diameter of the columns were estimated ∝400 nm and ∝100 nm, respectively. The morphology of the structure was examined by transmission electron microscopy (TEM). X-ray diffraction (XRD) analysis shows the polycrystalline nature of the sample which was verified by selective area electron diffraction (SAED) analysis. The growth mechanism and optical properties of the columns were also discussed. Optical absorption shows that In{sub 2}O{sub 3} columns have a high band to band transition at ∝3.75 eV. The ultraviolet and green emissions were obtained from the In{sub 2}O{sub 3} columnar arrays. The P-N junction was formed between In{sub 2}O{sub 3} and P-type Si substrate. The GLAD synthesized In{sub 2}O{sub 3} film exhibits low current conduction compared to In{sub 2}O{sub 3} TF. However, the Si/GLAD-In{sub 2}O{sub 3} detector shows ∝1.5 times enhanced photoresponsivity than that of Si/In{sub 2}O{sub 3} TF. (orig.)

  19. α-Fe{sub 2}O{sub 3} lithium battery anodes by nanocasting strategy from ordered 2D and 3D templates

    Energy Technology Data Exchange (ETDEWEB)

    Di Lupo, F. [GAME Lab, Department of Applied Science and Technology – DISAT, Politecnico di Torino, C.so Duca degli Abruzzi 24, 10129 Turin (Italy); Gerbaldi, C., E-mail: claudio.gerbaldi@polito.it [GAME Lab, Department of Applied Science and Technology – DISAT, Politecnico di Torino, C.so Duca degli Abruzzi 24, 10129 Turin (Italy); Casino, S.; Francia, C.; Meligrana, G. [GAME Lab, Department of Applied Science and Technology – DISAT, Politecnico di Torino, C.so Duca degli Abruzzi 24, 10129 Turin (Italy); Tuel, A. [Institut de Recherches sur la Catalyse, IRC-CNRS (UPR 5401), 2 Avenue Albert Einstein, 69626 Villeurbanne Cedex (France); Penazzi, N. [GAME Lab, Department of Applied Science and Technology – DISAT, Politecnico di Torino, C.so Duca degli Abruzzi 24, 10129 Turin (Italy)

    2014-12-05

    Highlights: • Nanosized α-Fe{sub 2}O{sub 3} lithium battery conversion anodes with tunable morphology. • Nanocasting technique using MCM-41 and MCM-48 silica moulds is adopted. • Textural/morphological characteristics define the electrochemical behaviour. • α-Fe{sub 2}O{sub 3} replica of MCM-41 exhibits stable capacity (∼300 mA h g{sup −1}) after 100 cycles. • α-Fe{sub 2}O{sub 3} replica of MCM-41 shows promising prospects as high-capacity Li-ion battery anode. - Abstract: Nanocasting strategy is here proposed as effective approach to tune structure and size of α-Fe{sub 2}O{sub 3} active nanoparticles as a promising anode material for Li-ion cells. MCM-41 and MCM-48 silicas, presenting hexagonal 2D and cubic 3D symmetry, respectively, and regular pore diameter of about 4 nm are selected as moulds. The structural–morphological and electrochemical characteristics are assessed by X-ray diffraction, transmission electron microscopy, N{sub 2} physisorption at 77 K, cyclic voltammetry and galvanostatic discharge/charge cycling. It is here demonstrated that structural–morphological features change accordingly to the template used and careful control of the texture/particle characteristics is likely a fundamental variable noticeably affecting the cycling behaviour.

  20. Electronic structure and luminescence properties of self-activated and Eu{sup 2+}/Ce{sup 3+} doped Ca{sub 3}Li{sub 4-y}Si{sub 2}N{sub 6-y}O{sub y} red-emitting phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Wu, Quansheng; Ding, Jianyan; Li, Yanyan; Wang, Xicheng [Key Laboratory for Special Function Materials and Structural Design of the Ministry of the Education (China); Department of Material Science, School of Physical Science and Technology, Lanzhou University, Lanzhou 730000 (China); Wang, Yuhua, E-mail: wyh@lzu.edu.cn [Key Laboratory for Special Function Materials and Structural Design of the Ministry of the Education (China); Department of Material Science, School of Physical Science and Technology, Lanzhou University, Lanzhou 730000 (China)

    2017-06-15

    The undoped and Eu{sup 2+}/Ce{sup 3+} doped Ca{sub 3}Li{sub 4-y}Si{sub 2}N{sub 6-y}O{sub y} (0≤y≤1.5) (CLSN) were successfully prepared by solid-state reaction and their luminescence properties were studied. The undoped CLSN shows red defect-related luminescence with maximum emission intensity at 710 nm, Eu{sup 2+} and Ce{sup 3+} doped CLSN also show red emission centered at 702 nm and 673 nm, respectively. The electronic structure and the thermal stability of CLSN were investigated in this work. The results indicate that CLSN:Eu{sup 2+}/Ce{sup 3+} could be conducive to the development of phosphor-converted light-emitting diodes.

  1. Solid-state synthesis of Li{sub 4}Ti{sub 5}O{sub 12} for high power lithium ion battery applications

    Energy Technology Data Exchange (ETDEWEB)

    Han, Seung-Woo [School of Materials Science and Engineering, Yeungnam University, Gyeongsan 712-749 (Korea, Republic of); Ryu, Ji Heon [Graduate School of Knowledge-Based Technology and Energy, Korea Polytechnic University, Siheung 429-793 (Korea, Republic of); Jeong, Joayoung [Cell Precedence Development Group, Samsung SDI, Yongin 446-577 (Korea, Republic of); Yoon, Dang-Hyok, E-mail: dhyoon@ynu.ac.kr [School of Materials Science and Engineering, Yeungnam University, Gyeongsan 712-749 (Korea, Republic of)

    2013-09-05

    Highlights: •High energy milling using 0.30 and 0.45 mm beads for Li{sub 4}Ti{sub 5}O{sub 12} synthesis. •Synthesis of 162 nm-sized pure Li{sub 4}Ti{sub 5}O{sub 12} by solid-state reaction. •Spray drying using fine starting materials to confer paste tackiness. •High capacity of 174 mAh/g and adequate rate properties for high power LIBs applications. -- Abstract: Li{sub 4}Ti{sub 5}O{sub 12} was synthesized by a solid-state reaction between Li{sub 2}CO{sub 3} and anatase TiO{sub 2} for applications to high power lithium ion batteries. The starting materials underwent 6 h of high energy milling using ZrO{sub 2} beads with two different sizes, 0.30 and 0.45 mm. The smaller ZrO{sub 2} beads resulted in finer starting materials. Spray drying was also performed on the 0.30 mm beads-treated particles to enhance the screen printability of a paste containing this powder. The finer starting materials showed a pure 162 nm-sized Li{sub 4}Ti{sub 5}O{sub 12} due to the decreased diffusion length for a solid-state reaction, whereas the 0.45 mm beads-treated starting materials resulted in a 242 nm-sized Li{sub 4}Ti{sub 5}O{sub 12} phase containing 2 wt.% of rutile TiO{sub 2} that had transformed from the anatase phase during heat treatment at 800 °C for 3 h. The finer Li{sub 4}Ti{sub 5}O{sub 12} showed higher charge capacity and better charge/discharge rates than the coarser particles, which highlights the importance of the primary particle size on the electrochemical properties of Li{sub 4}Ti{sub 5}O{sub 12} for high power applications. The fine Li{sub 4}Ti{sub 5}O{sub 12} particles had a discharge capacity of 174 mAh/g at 0.1 C and capacity retention of 80% at 10.0 C.

  2. Solvothermal synthesis, crystal structure, and second-order nonlinear optical properties of a new noncentrosymmetric gallium-organic framework material, [N(C{sub 3}H{sub 7}){sub 4}]{sub 3}Ga{sub 3}[C{sub 6}H{sub 3}(CO{sub 2}){sub 3}]{sub 4}

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Dong Woo; Jo, Vinna [Department of Chemistry, Chung-Ang University, Seoul, 156-756 (Korea, Republic of); Ok, Kang Min, E-mail: kmok@cau.ac.kr [Department of Chemistry, Chung-Ang University, Seoul, 156-756 (Korea, Republic of)

    2012-10-15

    A novel noncentrosymmetric (NCS) gallium-organic framework material, [N(C{sub 3}H{sub 7}){sub 4}]{sub 3}Ga{sub 3}[C{sub 6}H{sub 3}(CO{sub 2}){sub 3}]{sub 4} (CAUMOF-11) has been synthesized by a solvothermal reaction using Ga(NO{sub 3}){sub 3}{center_dot}xH{sub 2}O, 1,3,5-C{sub 6}H{sub 3}(CO{sub 2}H){sub 3}, N(C{sub 3}H{sub 7}){sub 4}Cl, HNO{sub 3}, and HCON(CH{sub 3}){sub 2} at 180 Degree-Sign C. The structure of the reported material has been determined by single-crystal X-ray diffraction. CAUMOF-11 has an anionic three-dimensional framework with aligned four-coordinate GaO{sub 4} tetrahedra and 1,3,5-benzenetricarboxylate groups. Tetrapropylammonim cations reside within the channel and maintain the charge balance. Detailed structural analyses with full characterization including infrared spectroscopy, thermogravimetric analysis, elemental analysis, ion-exchange reactions, topotactic decomposition, and gas adsorption experiments are reported. Powder second-harmonic generating (SHG) measurements on CAUMOF-11, using 1064 nm radiation, exhibit SHG efficiency of 15 times that of {alpha}-SiO{sub 2} and the material is phase-matchable (type-1). - Graphical Abstract: Second-order nonlinear optical measurements on CAUMOF-11 reveal that the material is phase-matchable (type-1) with SHG efficiency of 15 times that of {alpha}-SiO{sub 2}. Highlights: Black-Right-Pointing-Pointer A new NCS Ga-organic framework was solvothermally synthesized. Black-Right-Pointing-Pointer CAUMOF-11 exhibits SHG efficiency of 15 times that of {alpha}-SiO{sub 2}. Black-Right-Pointing-Pointer Thermal decomposition of CAUMOF-11 crystal maintains the original morphology.

  3. Preparation and drug-loading properties of Fe{sub 3}O{sub 4}/Poly(styrene-co-acrylic acid) magnetic polymer nanocomposites

    Energy Technology Data Exchange (ETDEWEB)

    Lu, Wensheng [School of Chemistry and Chemical Engineering, Anhui University, Hefei 230039 (China); Coordination Chemistry Institute, School of Chemistry and Chemical Engineering and Life Science, Chaohu University, Chaohu 238000 (China); Shen, Yuhua, E-mail: s_yuhua@163.com [School of Chemistry and Chemical Engineering, Anhui University, Hefei 230039 (China); Xie, Anjian [School of Chemistry and Chemical Engineering, Anhui University, Hefei 230039 (China); Zhang, Weiqiang [School of Chemistry and Chemical Engineering, Anhui University, Hefei 230039 (China); Coordination Chemistry Institute, School of Chemistry and Chemical Engineering and Life Science, Chaohu University, Chaohu 238000 (China)

    2013-11-15

    Fe{sub 3}O{sub 4}/poly(styrene-co-acrylic acid) magnetic polymer nanocomposites were synthesized by the dispersion polymerization method using styrene as hard monomer, acrylic acid as functional monomer, Fe{sub 3}O{sub 4} nanoparticles modified with oleic acid as core, and poly(styrene-co-acrylic acid) as shell. Drug-loading properties of magnetic polymer nanocomposites with curcumin as a model drug were also studied. The results indicated that magnetic polymer nanocomposites with monodisperse were obtained, the particle size distribution was 50–120 nm, and the average size was about 100 nm. The contents of poly(styrene-co-acrylic acid) and Fe{sub 3}O{sub 4} nanoparticles in magnetic polymer nanocomposites were 74% and 24.7%, respectively. The drug-loading capacity and entrapment efficiency were 2.5% and 44.4%, respectively. The saturation magnetization of magnetic polymer nanocomposites at 300 K was 20.2 emu/g without coercivity and remanence. The as-prepared magnetic polymer nanocomposites have not only lots of functional carboxyl groups but also stronger magnetic response, which might have potential applications in drug carrier and targeted drug release.

  4. Enhanced thermoelectric properties in p-type Bi{sub 0.4}Sb{sub 1.6}Te{sub 3} alloy by combining incorporation and doping using multi-scale CuAlO{sub 2} particles

    Energy Technology Data Exchange (ETDEWEB)

    Song, Zijun; Liu, Yuan; Zhou, Zhenxing; Lu, Xiaofang; Wang, Lianjun [State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Donghua University, Shanghai (China); Institute of Functional Materials, Donghua University, Shanghai (China); Zhang, Qihao [State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai (China); University of Chinese Academy of Sciences, Beijing (China); Jiang, Wan [State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Donghua University, Shanghai (China); Institute of Functional Materials, Donghua University, Shanghai (China); School of Material Science and Engineering, Jingdezhen Ceramic Institute, Jingdezhen (China); Chen, Lidong [State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai (China)

    2017-01-15

    Multi-scale CuAlO{sub 2} particles are introduced into the Bi{sub 0.4}Sb{sub 1.6}Te{sub 3} matrix to synergistically optimize the electrical conductivity, Seebeck coefficient, and the lattice thermal conductivity. Cu element originating from fine CuAlO{sub 2} grains diffuses into the Bi{sub 0.4}Sb{sub 1.6}Te{sub 3} matrix and tunes the carrier concentration while the coarse CuAlO{sub 2} particles survive as the second phase within the matrix. The power factor is improved at the whole temperatures range due to the low-energy electron filtering effect on Seebeck coefficient and enhanced electrical transport property by mild Cu doping. Meanwhile, the remaining CuAlO{sub 2} inclusions give rise to more boundaries and newly built interfaces scattering of heat-carrying phonons, resulting in the reduced lattice thermal conductivity. Consequently, the maximum ZT is found to be enhanced by 150% arising from the multi-scale microstructure regulation when the CuAlO{sub 2} content reaches 0.6 vol.%. Not only that, but the ZT curves get flat in the whole temperature range after introducing the multi-scale CuAlO{sub 2} particles, which leads to a remarkable increase in the average ZT. (copyright 2016 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  5. Freeze drying synthesis of Li{sub 3}MnO{sub 4} cathode material for Li-ion batteries: A physico-electrochemical study

    Energy Technology Data Exchange (ETDEWEB)

    Surace, Yuri; Simões, Mário; Karvonen, Lassi; Yoon, Songhak; Pokrant, Simone [Laboratory Materials for Energy Conversion, EMPA – Swiss Federal Laboratories for Materials Science and Technology, Überlandstrasse 129, CH-8600 Dübendorf (Switzerland); Weidenkaff, Anke, E-mail: weidenkaff@imw.uni-stuttgart.de [Materials Chemistry, Institute for Materials Science, University of Stuttgart, Heisenbergstrasse 3, DE-70569 Stuttgart (Germany)

    2015-09-25

    Highlights: • Facilitated synthesis of Li{sub 3}MnO{sub 4} with a smaller thermal budget via freeze drying. • Electrochemical activity enhanced by micro- and nanostructure modifications. • Capacity increase of 30% at 1st discharge versus standard synthesis process. - Abstract: Li{sub 3}MnO{sub 4}, a lithium rich phase containing manganese (V), is a promising cathode material for Li-ion batteries due to its very high theoretical capacity (698 A h kg{sup −1}). Li{sub 3}MnO{sub 4} was synthesized from freeze dried precursors at 398 K. Combined structural, morphological and chemical characterization by XRD, TGA, SEM, TEM and XPS revealed improvements in the micro- and nanostructure in comparison to the material synthesized by a standard solid state chemistry route. The average particle size decreased from 10 μm to 3.5 μm and the average crystallite size from close to 100 nm to around 30 nm. These modifications enhanced the capacity (23% at 10 A kg{sup −1} and up to 31% at 50 A kg{sup −1} with a maximum discharge capacity of 290 A h kg{sup −1}) and the rate capability.

  6. Paclitaxel conjugated Fe{sub 3}O{sub 4}@LaF{sub 3}:Ce{sup 3+},Tb{sup 3+} nanoparticles as bifunctional targeting carriers for Cancer theranostics application

    Energy Technology Data Exchange (ETDEWEB)

    Mangaiyarkarasi, Rajendiran; Chinnathambi, Shanmugavel; Karthikeyan, Subramani; Aruna, Prakasarao; Ganesan, Singaravelu, E-mail: sganesan@annauniv.edu

    2016-02-01

    The bi-functional Chitosan functionalized magnetite doped luminescent rare earth nanoparticles (Fe{sub 3}O{sub 4}@LaF{sub 3}: Ce{sup 3+},Tb{sup 3+}/chi NPs) as a carrier of paclitaxel (PTX) drug was designed using a co-precipitation and facile direct precipitation method. The synthesized nanoparticles are spherical in shape with a typical diameter of 19–37 nm respectively. They are water soluble, super paramagnetic and biocompatible, in which the amino groups on the nanoparticles surface are used for the conjugation with an anticancer drug, paclitaxel. The nature of PTX binding with Fe{sub 3}O{sub 4}@LaF{sub 3}: Ce{sup 3+},Tb{sup 3+}/chi nanoparticles were studied using X-ray diffraction, vibrating sample magnetometer and scanning electron micrograph. The nature of interactions between PTX and Fe{sub 3}O{sub 4}@LaF{sub 3}: Ce{sup 3+},Tb{sup 3+}/chi NPs due to complex formation were conceded out by various spectroscopic methods viz., UV–visible, steady state and excited state fluorescence spectroscopy. The photo-physical characterization reveals that the adsorption and release of PTX from Fe{sub 3}O{sub 4}@LaF{sub 3}:Tb{sup 3+}/chi nanoparticles is quicker when compared with other nanoparticles and also confirms that this may be due to the hydrogen bond formation between the hydroxyl group of drug and amino group of nanoparticles respectively. The maximum loading capacity and entrapment efficiency of 83.69% and 80.51% were attained at a ratio of 5:8 of PTX and Fe{sub 3}O{sub 4}@LaF{sub 3}: Ce{sup 3+},Tb{sup 3+}/chi NPs respectively. In addition with that, antitumoral activity study of PTX conjugated Fe{sub 3}O{sub 4}@LaF{sub 3}:Tb{sup 3+}/chi nanoparticles exhibits increased cytotoxic effects on A549 lung cancer cell lines than that of unconjugated PTX. - Highlights: • Fe{sub 3}O{sub 4}@LaF{sub 3}: Ce{sup 3+},Tb{sup 3+}/chi nanoparticles as a carrier of paclitaxel. • These particles are water soluble, super paramagnetic and biocompatible. • The maximum

  7. Crystal structure and luminescence properties of Bi{sup 3+}activated Ca{sub 2}Y{sub 8}(SiO{sub 4}){sub 6}O{sub 2} phosphors under near UV excitation

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Zhihua [Electronic Materials Research Laboratory, Key Laboratory of the Ministry of Education, Xian Jiaotong University, Xian 710049, ShannXi (China); International Center for Dielectric Research, Xian Jiaotong University, Xian 710049, ShannXi (China); School of Materials Science and Engineer, Chang’an University, Xi’an 710061, ShannXi (China); Wang, Minqiang, E-mail: mqwang@mail.xjtu.edu.cn [Electronic Materials Research Laboratory, Key Laboratory of the Ministry of Education, Xian Jiaotong University, Xian 710049, ShannXi (China); International Center for Dielectric Research, Xian Jiaotong University, Xian 710049, ShannXi (China); Yang, Zhi [Electronic Materials Research Laboratory, Key Laboratory of the Ministry of Education, Xian Jiaotong University, Xian 710049, ShannXi (China); International Center for Dielectric Research, Xian Jiaotong University, Xian 710049, ShannXi (China); Liu, Kaiping; Zhu, Feiyan [School of Materials Science and Engineer, Chang’an University, Xi’an 710061, ShannXi (China)

    2016-07-15

    Oxyapatite Ca{sub 2}Y{sub 8−x}(SiO{sub 4}){sub 6}O{sub 2}:xBi{sup 3+}phosphor has been prepared via high temperature solid-state reaction. Its crystal structure and PL properties were investigated by X-ray diffraction, photoluminescence excitation and emission spectra. The results indicated that the Ca{sub 2}Y{sub 8}(SiO{sub 4}){sub 6}O{sub 2} crystallizes as a hexagonal structure with a space group of P6{sub 3}/m and lattice constants of a=b=9.3507 Å, c=6.7899 Å, α=β=90.00°, γ=120.00°, V=514.14 Å{sup 3}; The phosphor has two prominent emission bands: when excited under 320–360 nm, the phosphors emit a broad band centered at 495 nm due to the {sup 3}P{sub 1}–{sup 1}S{sub 0} transition of Bi{sup 3+} in 4f (C{sub 3}) sites; when excited under 380 nm, the phosphors emit a broad band centered at 411 nm due to the {sup 3}P{sub 1}–{sup 1}S{sub 0} transition of Bi{sup 3+} in 6h (C{sub s}) sites. The emission color varies from the greenish blue to blue as the excitation wavelength increases from 335 to 380 nm. The optimal intensity of emission band was observed when x=0.015 in the Ca{sub 2}Y{sub 8−x}(SiO{sub 4}){sub 6}O{sub 2}:xBi{sup 3+} series. The average critical distance Rc among Bi{sup 3+} ions is determined to be 20.15 Å.

  8. A novel binary Pt{sub 3}Te{sub x}/C nanocatalyst for ethanol electro-oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Meihua; Wang, Fei; Li, Lirong; Guo, Yonglang [College of Chemistry and Chemical Engineering, Fuzhou University, Fuzhou 350002 (China)

    2008-03-15

    The Pt{sub 3}Te{sub x}/C nanocatalyst was prepared and its catalytic performance for ethanol oxidation was investigated for the first time. The Pt{sub 3}Te/C nanoparticles were characterized by an X-ray diffractometer (XRD), transmission electron microscope (TEM) and energy dispersive X-ray spectroscopy equipped with TEM (TEM-EDX). The Pt{sub 3}Te/C catalyst has a typical fcc structure of platinum alloys with the presence of Te. Its particle size is about 2.8 nm. Among the synthesized catalysts with different atomic ratios, the Pt{sub 3}Te/C catalyst has the highest anodic peak current density. The cyclic voltammograms (CV) show that the anodic peak current density for the Pt{sub 3}Te/C, commercial PtRu/C and Pt/C catalysts reaches 1002, 832 and 533 A g{sup -1}, respectively. On the current-time curve, the anodic current on the Pt{sub 3}Te/C catalyst was higher than those for the catalysts reported. So, these findings show that the Pt{sub 3}Te/C catalyst has uniform nanoparticles and the best activity among the synthesized catalysts, and it is better than commercial PtRu/C and Pt/C catalysts for ethanol oxidation at room temperature. (author)

  9. Synthesis, magnetic and dielectric characterization of nanocrystalline solid solutions of In{sub 2−x}Ni{sub x}O{sub 3} (x = 0.05, 0.10 and 0.15)

    Energy Technology Data Exchange (ETDEWEB)

    Ahmad, Tokeer, E-mail: tahmad3@jmi.ac.in [Nanochemistry Laboratory, Department of Chemistry, Jamia Millia Islamia, New Delhi 110025 (India); Khatoon, Sarvari [Nanochemistry Laboratory, Department of Chemistry, Jamia Millia Islamia, New Delhi 110025 (India); Coolahan, Kelsey [Department of Physics and Astronomy, Rowan University, 201 Mullica Hill Road, Glassboro, NJ 08028 (United States)

    2013-09-01

    Graphical abstract: Monophasic and crystalline In{sub 2−x}Ni{sub x}O{sub 3} nanoparticles of size 8–15 nm have been synthesized solvothermally and showed red shift in energy band gap which decreases on increasing Ni{sup 2+} concentration in In{sub 2}O{sub 3} host lattice. - Highlights: • Monophasic Ni-doped In{sub 2}O{sub 3} nanoparticles by solvothermal method for first time. • Plausible reaction mechanism using thermogravimetric analysis. • High surface area with small particle size obtained. • Solid solutions exhibit paramagnetism with very weak antiferromagnetic interactions. - Abstract: In{sub 2−x}Ni{sub x}O{sub 3} (x = 0.05, 0.10 and 0.15) nanoparticles were successfully synthesized by solvothermal method by the thermal decomposition of oxalate precursor at 450 °C for the first time. X-ray diffraction studies showed the formation of highly crystalline and monophasic cubic structure of In{sub 2}O{sub 3} which is attributed to the formation of solid solution. These nanoparticles show good optical transmittance in the visible region. Optical measurements showed an energy band gap which decreases with increasing Ni concentration. The grain size decreases from 15 nm to 8 nm and surface area increases from 90 to 254 m{sup 2} g{sup −1} on increasing the Ni concentration. High dielectric constant and dielectric loss has been obtained which indicates the conducting nature of these solid solutions. Magnetic measurements showed that the samples are strong paramagnetic in nature with very weak antiferromagnetic interactions. No evidence of ferromagnetism is observed for these solid solutions at room temperature.

  10. Characterization and magnetic properties of Nd{sub x}Bi{sub 1−x}Fe{sub 0.95}Co{sub 0.05}O{sub 3} nanopowders synthesized by combustion-derived method at low temperature

    Energy Technology Data Exchange (ETDEWEB)

    Hernández, N., E-mail: netzahualpille.hernandeznv@uanl.edu.mx [Centro de Innovación, Investigación y Desarrollo en Ingeniería y Tecnología, Facultad de Ingeniería Mecánica y Eléctrica, Universidad Autónoma de Nuevo León, Km. 10 de la nueva carretera al Aeropuerto Internacional de Monterrey, PIIT Monterrey, CP 66600 Apodaca, Nuevo León (Mexico); González-González, V.A.; Dzul-Bautista, I.B.; Cienfuegos-Pelaes, R.F. [Centro de Innovación, Investigación y Desarrollo en Ingeniería y Tecnología, Facultad de Ingeniería Mecánica y Eléctrica, Universidad Autónoma de Nuevo León, Km. 10 de la nueva carretera al Aeropuerto Internacional de Monterrey, PIIT Monterrey, CP 66600 Apodaca, Nuevo León (Mexico); Barandiaran, J.M.; Gutierréz, J. [BCMaterials and Universidad del País Vasco (UPV/EHU), Departamento de Electricidad y Electrónica, P.O Box 644, 48080 Bilbao (Spain); Hernández, T. [Facultad de Ciencias Químicas, Universidad Autónoma de Nuevo León, C.P. 66450 San Nicolás de los Garza, Nuevo León (Mexico); and others

    2015-03-01

    Nd{sub x}Bi{sub 1−x}Fe{sub 0.95}Co{sub 0.05}O{sub 3} (x=0, 0.05, 0.10, 0.15) nanopowders were prepared by a combustion-derived method. The Rietvelt fitting of the X-Ray diffraction data from the Nd{sub x}Bi{sub 1−x}Fe{sub 0.95}Co{sub 0.05}O{sub 3} (NBFCO) powders showed nanopowders with rhombohedral BiFeO{sub 3} crystalline structure (R3c) for x≤10 and a partial structural transition to orthorhombic phase (Pnma) for x=0.15. The differential thermal analysis and thermogravimetric analysis (DTA/TGA) showed a crystallization temperature of 180 °C. Transmission electronmicroscopy (TEM) images revealed that the NBFCO nanopowders were composed of fine particles under 60 nm. From Raman spectroscopy, a band of disordered anion lattice was observed at 653 cm{sup −1}. In spite of the antiferromagnetic nature of bulk BiFeO{sub 3}, the NBFCO nanopowders obtained displayed a ferromagnetic hysteresis loop, with coercivity about 0.1 T and remanent magnetization of 1.02–4.33 A m{sup 2}/kg were obtained at room temperature. This ferromagnetic behavior is due to increasing and uncompensated spins at the surface and the canted internal spin by the tilt of FeO{sub 6} octahedral units. We have developed a novel synthetic route for the preparation of ferromagnetic BFO-derived nanopowder materials by a surfactant-assisted combustion-derived method. - Highlights: • The structure of materials obtained is studied. • A new synthesis method was proposed to obtain ferrimagnetic–ferromagnetic BiFeO{sub 3} nanoparticles. • Synthesis temperature does not exceed 200 °C. • The obtained nanoparticles have sizes less than 52 nm.

  11. Synthesis and magnetic characterization of LaMnO{sub 3} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Hernandez, E.; Sagredo, V. [Universidad de Los Andes, Facultad de Ciencias, Laboratorio de Magnetismo, 5101 Merida (Venezuela, Bolivarian Republic of); Delgado, G. E. [Universidad de Los Andes, Facultad de Ciencias, Laboratorio de Cristalografia, 5101 Merida (Venezuela, Bolivarian Republic of)

    2015-07-01

    LaMnO{sub 3} nanoparticles system were prepared by the sol-gel auto-combustion method, in order to analyze the structure and magnetic behavior presented by the compound prepared following a new alternative route of synthesis. Structural characterization, morphology and crystallite size was performed by X-ray diffraction (XRD), infrared spectroscopy (IR) and electron microscopy. The XRD study together with a Rietveld analysis showed that the LaMnO{sub 3} compound crystallized in a perovskite hexagonal structure. The IR spectra showed that the compound has tensile energy bands in the Mn-O-Mn bonds related with the octahedron MnO{sub 6}; which are attributed to a characteristic vibration of the ABO{sub 3} perovskite. An estimated size and morphological analysis was carried out by applying the Scherrer formula and using transmission electron microscopy, revealing non-spherical shape and particle sizes between 13 nm and 18 nm. The magnetic measurements M(T) were performed by using zero field-cooled and field-cooled protocols which revealed a positive Weiss temperature indicating the presence of ferromagnetic interactions with a Curie temperature, T{sub C} = 150 K. (Author)

  12. Layer structured Na{sub 2}Ni(MoO{sub 4}){sub 2} particles as a visible-light-driven photocatalyst for degradation of methylene blue

    Energy Technology Data Exchange (ETDEWEB)

    Lu, Yuting; Chen, Luyang; Huang, Yanlin [College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123 (China); Chen, Cuili; Kim, Sun Il [Department of Physics and Interdisciplinary Program of Biomedical, Mechanical & Electrical Engineering, Pukyong National University, Busan 608-737 (Korea, Republic of); Seo, Hyo Jin, E-mail: hjseo@pknu.ac.kr [Department of Physics and Interdisciplinary Program of Biomedical, Mechanical & Electrical Engineering, Pukyong National University, Busan 608-737 (Korea, Republic of)

    2015-03-15

    Highlights: • Na{sub 2}Ni(MoO{sub 4}){sub 2} nanoparticles were developed by Pechini method. • The nanoparticles show high absorption in UV–vis wavelength region. • Na{sub 2}Ni(MoO{sub 4}){sub 2} has high activity in the MB dye degradation under visible light. • Hexagonal layers with heavily distorted NiO{sub 6} were superiority for photocatalysis. - Abstract: A new visible-light-driven photocatalyst of Na{sub 2}Ni(MoO{sub 4}){sub 2} particle was prepared by the modified Pechini method. The crystal structure was measured by X-ray diffraction (XRD) and the structural refinement. The sample was investigated by scanning electron microscope (SEM), transmission electron microscopy (TEM), and UV–vis absorption spectrum measurements. The average size of Na{sub 2}Ni(MoO{sub 4}){sub 2} particle is about 180 nm. Na{sub 2}Ni(MoO{sub 4}){sub 2} particle have an efficient optical absorption in the UV–visible light wavelength region with a direct allowed electronic transition of 2.06 eV. The effective photodegradation of methylene blue (MB) dye was demonstrated, which benefits from the special crystal structure of Na{sub 2}Ni(MoO{sub 4}){sub 2} particle. This crystal lattice has two infinite chains formed by (Ni,Na)O{sub 6} and MoO{sub 4} polyhedra standing in lines alone with the inner wall of the hexagonal tunnels. This results in the efficient optical absorption and provides more chances for electron–hole separations, which can further react with dye molecules to oxidize the dye pollutant into non-toxic products.

  13. Particle characteristics and reduction behavior of synthetic magnetite

    Energy Technology Data Exchange (ETDEWEB)

    Ramadan, Wegdan [Physics Department, Faculty of Science, Alexandria University, Alexandria 21511 (Egypt); Zaki, Mohamed I., E-mail: mizaki@link.net [Chemistry Department, Faculty of Science, Minia University, El-Minia 61519 (Egypt); Fouad, Nasr E.; Mekhemer, Gamal A.H. [Chemistry Department, Faculty of Science, Minia University, El-Minia 61519 (Egypt)

    2014-04-15

    Two samples (S1 and S2) of magnetite were synthesized, using two different methods, and characterized by means of X-ray powder diffractometry, infrared and Mössbauer spectroscopy, N{sub 2} sorptiometry and electron microscopy. Particles of sample-S1 were found to be loosely agglomerated, micro-sized spheroids (200–350 nm) composed almost solely of highly aggregated (fused) crystallites (size averaged at 35 nm) of cubic-Fe{sub 3}O{sub 4}. In contrast, particles of sample-S2 were strongly agglomerated, nano-sized spheroids (25–30 nm) composed of slightly aggregated crystallites (size averaged at 11 nm) of cubic-Fe{sub 3}O{sub 4} and noncrystalline domains made-up of FeO(OH) species. Temperature-programed reduction (TPR) profiles obtained for the two samples were similar in monitoring two peaks at >450 °C assignable to a two-step reduction of Fe{sub 3}O{sub 4} (→FeO→Fe), but different in monitoring a peak at<450 °C only for the reduction of FeO(OH) (→Fe{sub 3}O{sub 4}) contained in sample-S2. However, curve fitting analysis of the TPR profiles and molecular stoichiometry calculations based on amounts of hydrogen consumed revealed that the two-step reduction of Fe{sub 3}O{sub 4} is not straightforward. That is by resolving two consecutive pathways for each step and, hence, nonstoichiometric intermediate products whose composition was found to be critically controlled by the composition of the reducing gas atmosphere (5 or 80% H{sub 2}/N{sub 2}) and characteristics of the starting sample particles (chemical and phase composition, and, but to lesser extents, the agglomeration and average size). - Highlights: • Nano or micro, pure Fe{sub 3}O{sub 4} particles are H{sub 2}-reduced in two steps (→FeO→Fe) at >450 °C. • FeO(OH)-impure particles exhibit a third reduction step (FeO(OH)→Fe{sub 3}O{sub 4}) at <450 °C. • FeO disproportion and related autocatalytic effects complicate the reduction course. • Consequently, each of the Fe{sub 3}O{sub 4

  14. Preparation and characterization of Ba{sub 0.2}Sr{sub 0.2}La{sub 0.6}MnO{sub 3} nanoparticles and investigation of size & shape effect on microwave absorption

    Energy Technology Data Exchange (ETDEWEB)

    Peymanfar, Reza; Javanshir, Shahrzad, E-mail: shjavan@iust.ac.ir

    2017-06-15

    Highlights: • Hydrothermal synthesis of Ba{sub 0.2}Sr{sub 0.2}La{sub 0.6}MnO{sub 3} performed in the presence of PMMA. • Shape and size-controlled synthesis of NPs over the range 15–50 Nm was explored. • Investigation of shape and size effect of NPs on microwave absorption properties. - Abstract: In this paper, the design and characterization of a radar absorbing material (RAM) was investigated at microwave frequency. Ba{sub 0.2}Sr{sub 0.2}La{sub 0.6}MnO{sub 3} magnetic nanoparticles was synthesized thru a facile hydrothermal method in the presence of polymethyl methacrylate (PMMA) and the possibility of shape and size-controlled synthesis of nanoparticles (NPs) over the range 15–50 Nm was also explored. Afterward, the effect of shape and size of the synthesized Ba{sub 0.2}Sr{sub 0.2}La{sub 0.6}MnO{sub 3} NPs on microwave absorption properties was investigated in KU-band. The crystal structures and morphology of as-synthesized nanoparticles were characterized and confirmed by FESEM, XRD, VSM, FTIR analysis. The RAM samples were prepared by dispersion of magnetic NPs in silicone rubber in an ultrasonic bath. The maximum reflection loss (RL) values NPs were 12.04 dB at 14.82 GHz and a broad absorption band (over 1.22 GHz) with RL values <−10 dB are obtained and the maximum reflection loss (RL) values of decrease and shaped NPs were 22.36 dB at 14.78 GHz and a broad absorption band (over 2.67 GHz) with RL values <−10 dB are obtained. The results indicated that the particle size and shape play a major role on the absorption properties of the composites in the 12.4–18 GHz frequency range. It is observed that microwave absorption properties increased with the decrease in average particle size of NPs.

  15. Synthesis of sub-10 nm VO2 nanoparticles films with plasma-treated glass slides by aqueous sol–gel method

    International Nuclear Information System (INIS)

    Lan, Shi-Di; Cheng, Chih-Chia; Huang, Chi-Hsien; Chen, Jem-Kun

    2015-01-01

    Highlights: • Sub-10 nm VO 2 nanoparticles (VNPs) are synthesized on a plasma-treated glass. • Glass slides generate negative charges sites after plasma treatment to attract VO 2 + . • Doping tungsten with 1 wt% in VNPs did not change particle size significantly. • The particle size of VNP can be tuned by the density of negative charge sites. • Sub-10 nm structured VO 2 particle films exhibited high visible transmittance. - Abstract: This paper describes an aqueous sol–gel synthesis of thermochromic thin films consisted of vanadium dioxide nanoparticles (VNPs) on glass slides. The glass slides were treated by argon/oxygen plasma to generate dispersedly negative charge sites on the surface to attract VO 2 + from a sol–gel solution. After heat treatment in a low-pressure carbon monoxide/carbon dioxide (CO/CO 2 ) atmosphere, the VNPs could be generated in sub-10 nm of particle size on the surface. Various levels of doping were achieved by adding small quantities of a water-soluble tungsten compound to the sol; however, the particle size increased slightly with the tungsten doping levels. The change in electrical conductivity with temperature for VNP films were measured and compared to VO 2 crystalline films. VNP films exhibited the lower transition temperature of the semiconductor to metal phase change; at a doping level of 4 wt% the transition temperature was measured at 32.2 ± 1.2 and 24.1 ± 1.2 °C for the VO 2 and VNP films, respectively. The VNP films showed excellent visible transparency and a large change in transmittance at near-infrared (NIR) wavelengths before and after the metal–insulator phase transition (MIT). The current method is a landmark in the development of nanostructured material toward applications in energy-saving smart windows.

  16. Digestive ripening facilitated atomic diffusion at nanosize regime: Case of AuIn{sub 2} and Ag{sub 3}In intermetallic nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Arora, Neha [Department of Inorganic and Physical Chemistry, Indian Institute of Science, Bangalore 560 012 (India); Jagirdar, Balaji R., E-mail: jagirdar@ipc.iisc.ernet.in [Department of Inorganic and Physical Chemistry, Indian Institute of Science, Bangalore 560 012 (India); Klabunde, Kenneth J. [Department of Chemistry, Kansas State University, Manhattan, KS 66506 (United States)

    2014-10-15

    Highlights: • A digestive ripening facilitated interatomic diffusion process is presented. • Nearly monodisperse AuIn{sub 2} and Ag{sub 3}In intermetallic nanoparticles were synthesized. • Optimization of reaction temperature facilitates interatomic transfer. • Presence of excess ligand plays a crucial role in the digestive ripening process. - Abstract: Monodisperse colloidal gold–indium (AuIn{sub 2}) intermetallic nanoparticles have been synthesized from Au and In colloids using the digestive ripening process. Formation of the intermetallic proceeds via digestive ripening facilitated atomic diffusion of Au and In atoms from the Au and In nanoparticles followed simultaneously by their growth in the solution. Optimization of the reaction temperature was found to be crucial for the formation of AuIn{sub 2} intermetallic from gold and indium nanoparticles. Transmission electron microscopy revealed the presence of nearly monodisperse nanoparticles of Au and AuIn{sub 2} with particle size distribution of 3.7 ± 1.0 nm and 5.0 ± 1.6 nm, respectively. UV–visible spectral studies brought out the absence of SPR band in pure AuIn{sub 2} intermetallic nanoparticles. Optical study and electron microscopy, in combination with powder X-ray diffraction established phase pure AuIn{sub 2} intermetallic nanoparticles unambiguously. The potential of such an unprecedented approach has been further exploited in the synthesis of Ag{sub 3}In intermetallic nanoparticles with the dimension of less than 10 nm.

  17. Electrical characteristics of SrTiO{sub 3}/Al{sub 2}O{sub 3} laminated film capacitors

    Energy Technology Data Exchange (ETDEWEB)

    Peng, Yong; Yao, Manwen, E-mail: yaomw@tongji.edu.cn; Chen, Jianwen; Xu, Kaien; Yao, Xi [Functional Materials Research Laboratory, School of Materials Science and Engineering, Tongji University, Shanghai 200092 (China)

    2016-07-07

    The electrical characteristics of SrTiO{sub 3}/Al{sub 2}O{sub 3} (160 nm up/90 nm down) laminated film capacitors using the sol-gel process have been investigated. SrTiO{sub 3} is a promising and extensively studied high-K dielectric material, but its leakage current property is poor. SrTiO{sub 3}/Al{sub 2}O{sub 3} laminated films can effectively suppress the demerits of pure SrTiO{sub 3} films under low electric field, but the leakage current value reaches to 0.1 A/cm{sup 2} at higher electric field (>160 MV/m). In this study, a new approach was applied to reduce the leakage current and improve the dielectric strength of SrTiO{sub 3}/Al{sub 2}O{sub 3} laminated films. Compared to laminated films with Au top electrodes, dielectric strength of laminated films with Al top electrodes improves from 205 MV/m to 322 MV/m, simultaneously the leakage current maintains the same order of magnitude (10{sup −4} A/cm{sup 2}) until the breakdown occurs. The above electrical characteristics are attributed to the anodic oxidation reaction in origin, which can repair the defects of laminated films at higher electric field. The anodic oxidation reactions have been confirmed by the corresponding XPS measurement and the cross sectional HRTEM analysis. This work provides a new approach to fabricate dielectrics with high dielectric strength and low leakage current.

  18. Synthesis and properties of In{sub 2}O{sub 3} nanoparticles processed in microwave system

    Energy Technology Data Exchange (ETDEWEB)

    Moura, Ana Paula de; Longo, Elson; Berger, Danielle; Varela, Jose A., E-mail: apdemoura@gmail.com [Universidade Estadual Paulista Julio de Mesquita Filho (UNESP), Araraquara, SP (Brazil). Instituto de Quimica; Rosa, Ieda Lucia Viana [Universidade Federal de Sao Carlos (UFSCar), SP (Brazil); Li, Maximo Siu [Universidade de Sao Paulo (USP), Sao Carlos, SP (Brazil). Instituto de Fisica

    2016-07-01

    Full text: Indium oxide (In{sub 2}O{sub 3}), an n-type semiconductor with a wide band gap of about 3.6 eV, has been widely used as a solar cell, a window heater, materials for a flat panel display and gas sensors [1]. The domestic microwave oven (MO) has been successfully employed to obtain materials. In this work, In{sub 2}O{sub 3} powders were synthesized by the co-precipitation method and processed in microwave hydrothermal system at 100 deg C for 1 min, 30 min and 60 min. The materials samples were characterized by X-ray diffraction (XRD), Raman spectroscopy, field-emission scanning electron microscopy (FE-SEM), diffuse reflectance spectroscopy (UV-vis) as well as photoluminescence and photocatalytic properties. XRD patterns showed all peaks were indexed to the In{sub 2}O{sub 3} phase. These values are in agreement with as reported in the standard card (JCPDS No. 71-2194) indicating the single phase formation for all the analyzed samples, also in accordance to the Raman data. FE-SEM show that all materials are composed by spherical and aggregated particle with size of around 50-80 nm. The UV-Vis absorption spectra report was used to obtain a band gap of around 3.49 eV for all materials. PL spectra consist of a broad band at 420-600 nm, corresponding to a near-band edge emission related to the recombination of excitons and level emission related to structural defects. The photocatalytic properties of In{sub 2}O{sub 3} were studied and showed that these materials present good efficiency in the photocatalytic activity for degradation of Rhodamine. Reference: [1] F.V. Motta , R.C. Lima , A.P.A. Marques , E.R. Leite, J.A. Varela, E. Longo, Mater Res Bull 45 (2010) 1703-1706. (author)

  19. Study of cerium doped magnetite (Fe{sub 3}O{sub 4}:Ce)/PMMA nanocomposites

    Energy Technology Data Exchange (ETDEWEB)

    Padalia, Diwakar, E-mail: Padalia.diwakar@gmail.com [Department of Physics, G.B. Pant University of Agriculture and Technology, Pantnagar, Uttrakhand (India); Johri, U.C. [Department of Physics, G.B. Pant University of Agriculture and Technology, Pantnagar, Uttrakhand (India); Zaidi, M.G.H. [Supercritical Fluid Processing Laboratory, Department of Chemistry, G.B. Pant University of Agriculture and Technology, Pantnagar, Uttrakhand (India)

    2012-03-01

    The paper presents the synthesis and properties of polymer nanocomposite material based on cerium doped magnetite (Fe{sub 3}O{sub 4}) as filler material and poly methyl methacrylate (PMMA) as host matrix. The magnetite (Fe{sub 3}O{sub 4}) particles were synthesized by co-precipitation route using stable ferrous and ferric salts with ammonium hydroxide as precipitating agent. Further, they doped by cerium oxide (CeO{sub 2}) non-stoichiometrically. The composite material was fabricated by solvent evaporation method. Here 2.4 GHz microwaves were used to study the effect of microwaves heating on polymerization. The phase and crystal structure is determined by X-ray diffraction (XRD). The average crystallite size of the composites varies from 28 to 35 nm. The chemical structure is confirmed by Fourier transform infrared (FTIR) spectroscopy. The magnetic and thermal properties are investigated by vibrating sample magnetometer (VSM) and differential scanning calorimetry (DSC). The thermal study shows that the microwave heated samples possess higher glass transition temperature (T{sub g}). The magnetic results suggest that coercivity (H{sub C}) and squareness (M{sub r}/M{sub s}) of the loop increases with increasing doping percent of cerium.

  20. Photoluminescence and cathodoluminescence properties of Sr{sub 2}Gd{sub 8}Si{sub 6}O{sub 26}:RE{sup 3+}(RE{sup 3+}=Tb{sup 3+}or Sm{sup 3+}) phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Hussain, Sk. Khaja [Department of Electronics and Radio Engineering, Kyung Hee University, 1 Seocheon-dong, Giheung-gu, Yongin-si, Gyeonggi-do 446-701 (Korea, Republic of); Rao, Gattupalli Manikya [Department of Physics, College of Science and Technology, Andhra University, Visakhapatanam, Andhra Pradesh 53003 (India); Raju, G. Seeta Rama; Krishna Bharat, L. [Department of Electronics and Radio Engineering, Kyung Hee University, 1 Seocheon-dong, Giheung-gu, Yongin-si, Gyeonggi-do 446-701 (Korea, Republic of); Subba Rao, P.S.V., E-mail: raopsvs@rediffmail.com [Department of Physics, College of Science and Technology, Andhra University, Visakhapatanam, Andhra Pradesh 53003 (India); Yu, Jae Su, E-mail: jsyu@khu.ac.kr [Department of Electronics and Radio Engineering, Kyung Hee University, 1 Seocheon-dong, Giheung-gu, Yongin-si, Gyeonggi-do 446-701 (Korea, Republic of)

    2016-10-15

    Trivalent terbium (Tb{sup 3+}) or samarium (Sm{sup 3+}) ions individually activated green and orange emitting Sr{sub 2}Gd{sub 8}Si{sub 6}O{sub 26} (SGSO) phosphors were synthesized by a citrate sol–gel method. The X-ray diffraction patterns of SGSO:Tb{sup 3+} and SGSO:Sm{sup 3+} phosphors exhibited the characteristic diffraction peaks of oxyapatite in a hexagonal lattice structure. The photoluminescence (PL) properties at ultraviolet (UV) or near-UV excitation wavelengths were measured for Tb{sup 3+} or Sm{sup 3+} ions doped SGSO phosphors as a function of its respective concentration. The PL spectra of SGSO:Tb{sup 3+} phosphors revealed the characteristic emission peaks of both Gd{sup 3+} and Tb{sup 3+} ions which are associated with 4f–4f transitions under 274 nm of excitation wavelength. When the concentration of Tb{sup 3+} ions increased over 0.05 mol (5 mol%), the emission intensities of {sup 5}D{sub 3} transitions decreased due to the well-known cross-relaxation process. However, based on the intensities of {sup 5}D{sub 4} transitions, the optimum concentration of Tb{sup 3+} ions was found to be 0.05 mol. Under 404 nm of excitation wavelength, the SGSO:Sm{sup 3+} phosphors exhibited the characteristic orange emission at 600 nm due to the {sup 4}G{sub 5/2}→{sup 6}H{sub 7/2} electronic transition. The optimum concentration of SGSO:Sm{sup 3+} phosphors was found to be 0.02 mol. The decay curves of the optimized SGSO:Tb{sup 3+} and SGSO:Sm{sup 3+} phosphors were well fitted to single exponential functions and their lifetimes were calculated. Furthermore, the optimized phosphor samples showed good thermal stability. Likewise, cathodoluminescence properties were also studied for the optimized samples as a function of filament current and accelerating voltage. The Commission International de I-Eclairage chromaticity coordinates were calculated for the SGSO:Tb{sup 3+} and SGSO:Sm{sup 3+} phosphors.

  1. A novel rare earth zinc germanide, Y b{sub 2}Zn{sub 3}Ge{sub 3.1}; crystal structure and physical properties

    Energy Technology Data Exchange (ETDEWEB)

    Grytsiv, A [Institut fuer Physikalische Chemie, Universitaet Wien, Waehringerstrasse 42, A-1090 Vienna (Austria); Kaczorowski, D [W Trzebiatowski Institute of Low Temperature and Structure Research, Polish Academy of Sciences, P-50-950 Wroclaw, PO Box 1410 (Poland); Rogl, P [Institut fuer Physikalische Chemie, Universitaet Wien, Waehringerstrasse 42, A-1090 Vienna (Austria); Tran, V [W Trzebiatowski Institute of Low Temperature and Structure Research, Polish Academy of Sciences, P-50-950 Wroclaw, PO Box 1410 (Poland); Godart, C [CNRS-UPR209, ISCSA, 2-8 rue Henri Dunant, F94320 Thiais (France); Gofryk, K [W Trzebiatowski Institute of Low Temperature and Structure Research, Polish Academy of Sciences, P-50-950 Wroclaw, PO Box 1410 (Poland); Giester, G [Institut fuer Mineralogie und Kristallographie, Universitaet Wien, Althanstrasse 14, A-1090 Vienna (Austria)

    2005-01-19

    A novel ternary structure type has been determined from single crystals of Y b{sub 2}Zn{sub 3}Ge{sub 3.1} grownfrom zinc flux solvent. Y b{sub 2}Zn{sub 3}Ge{sub 3.1} crystallizes in a novel monoclinic structure type (a = 1.5804(2) nm, b 0.429 70(1) nm, c = 1.1524(1) nm; {beta} = 126.14(1) deg.) with space group C 2/m,Z = 4. The large ytterbium atoms are at the centres of pentagonal pyramids formed by Zn/Ge atoms. Zinc atoms are centred in distorted triangular prisms and polyhedra around germanium atoms are related to octahedra. The void at the centre of the Zn octahedra is only partially (20%) filled by Ge atoms. There are two positions for Yb atoms in the unit cell, which contain ions with valency slightly higher than 2+, as evidenced by x-ray absorption spectroscopy and bulk magnetic measurements. The compound exhibits metallic-like electrical conductivity, and its Seebeck coefficient shows a temperature variation characteristic of metals, being, however, fairly enhanced, as expected for intermediate valence systems.

  2. Transport properties of La{sub 2/3}Sr{sub 1/3}MnO{sub 3}/LaAlO{sub 3}/Pt tunnel junctions

    Energy Technology Data Exchange (ETDEWEB)

    Galceran, R.; Balcells, Ll.; Pomar, A.; Konstantinović, Z.; Sandiumenge, F.; Martínez, B. [Instituto de Ciencia de Materiales de Barcelona - CSIC, Campus UAB, Bellaterra 08193 (Spain)

    2015-03-14

    Magnetotransport properties of La{sub 2/3}Sr{sub 1/3}MnO{sub 3}/LaAlO{sub 3}/Pt tunnel junctions have been thoroughly analyzed, as a function of temperature and magnetic field, to test the suitability of LaAlO{sub 3} for insulating barriers and spin injection processes. The insulating behavior of LaAlO{sub 3} maintained down to 1–2 nm (corresponding to 4–5 unit cells) renders this material useful as tunnel barrier. The temperature dependence of the junction resistance, R(T), down to 200 K confirms direct tunneling as the dominant conduction channel. The barrier parameters of the junctions, φ{sub 0} and s, are estimated using Simmons' model in the intermediate voltage range. The energy of the barrier was estimated to be φ{sub 0} ∼ 0.4 eV at room temperature. The dependence of R(T) and φ{sub 0} on the magnetic field shows an anisotropic tunneling magnetoresistance of ∼4% at low T when changing the direction of the magnetization with respect to the current flow.

  3. Structural and magnetic properties of Ni{sub 0.15}Mg{sub 0.1}Cu{sub 0.3}Zn{sub 0.45}Fe{sub 2}O{sub 4} ferrite prepared by NaOH-precipitation method

    Energy Technology Data Exchange (ETDEWEB)

    Hou, Wei-xiao; Wang, Zhi, E-mail: zhiwang@tju.edu.cn

    2015-09-15

    Highlights: • NiMgCuZn ferrites were successfully prepared by low-temperature sintering. • NiMgCuZn ferrites have the advantages of both NiCuZn and MgCuZn ferrites. • NiMgCuZn ferrites exhibit high Curie temperature & high stability of permeability. - Abstract: The Ni{sub 0.15}Mg{sub 0.1}Cu{sub 0.3}Zn{sub 0.45}Fe{sub 2}O{sub 4} ferrite powders have been prepared by NaOH co-precipitation method and characterized by X-ray diffraction (XRD) and vibrating sample magnetometer (VSM). The XRD patterns confirm the single phase spinel structure of synthesized nanoparticles. The average crystallite size of the particles increases from 12 to 36 nm with calcining temperature (T{sub a}) from 500 to 800 °C. The saturation magnetization (M{sub s}) of the superparamagnetic particles was deduced by Langevin theory. Subsequently, the densification characteristics and magnetic properties of the low-temperature 950 °C-sintered ferrite bulk samples were also investigated. The magnetic measurement showed that the sintered bulk sample of T{sub a} = 600 °C has the highest initial permeability (μ{sub i}), lowest coercivity (H{sub c}), largest saturation magnetization (M{sub s}) and satisfactory thermal stability of μ{sub i}. The microstructures of sintered samples were examined using field emission scanning electric microscope (FESEM). The T{sub a} has significant influence on the bulk density, initial permeability, saturation magnetization and coercivity of Ni{sub 0.15}Mg{sub 0.1}Cu{sub 0.3}Zn{sub 0.45}Fe{sub 2}O{sub 4} ferrite.

  4. Facile Template-Free Fabrication of the hollow sea cucumber-like TbF{sub 3} and luminescent properties

    Energy Technology Data Exchange (ETDEWEB)

    Gao, Yu, E-mail: gaoy777@126.com [College of Materials Science and Engineering, Shenyang University of Chemical Technology, Shenyang, 100142 (China); Shi, Shan; Fang, Qinghong; Yang, Feng [College of Materials Science and Engineering, Shenyang University of Chemical Technology, Shenyang, 100142 (China); Xu, Zhenhe [College of Applied Chemistry, Shenyang University of Chemical Technology, Shenyang, 100142 (China)

    2014-12-15

    Graphical abstract: Hollow sea cucumber-like TbF{sub 3} has been prepared via a facile hydrothermal route. The possible growth mechanism and the luminescent properties of the as-prepared sample have been discussed. - Highlights: • TbF3 particles were prepared by a facile hydrothermal route. • TbF3 product show strong green emission. • This method may be more widely applicable in the design of other rare-earth compounds. - Abstract: Hollow sea cucumber-like TbF{sub 3} was successfully fabricated by a self-assembled hydrothermal method. The crystal structure, morphology and photoluminescence properties of the as-prepared TbF{sub 3} crystals were investigated. The results revealed that the as-prepared TbF{sub 3} sample has orthorhombic structure and composed of monodispersed 3D hollow sea cucumber-like particles. The possible formation mechanism for sea cucumber-like TbF{sub 3} is presented in detail. Additionally, the as-prepared sample possesses property of down-conversion photoluminescence. The excitation spectrum of TbF{sub 3} sample was obtained by monitoring the emission of Tb{sup 3+} at 545 nm was composed of the characteristics f–f transition lines within the Tb{sup 3+} 4f{sup 8} configuration. Under the UV light irradiation, the emission spectrum exhibited four obvious lines centered at 491, 545, 588, and 620 nm, which was corresponding to the {sup 5}D{sub 4} → {sup 7}F{sub J} (J = 6, 5, 4, 3) transitions of the Tb{sup 3+} ions in the TbF{sub 3} nanoparticles.

  5. Efficient and thermally stable red luminescence from nano-sized phosphor of Gd{sub 6}MoO{sub 12}:Eu{sup 3+}

    Energy Technology Data Exchange (ETDEWEB)

    Qin, Lin [Soochow University, College of Chemistry, Chemical Engineering and Materials Science (China); Wei, Donglei [Pukyong National University, Department of Physics and Interdisciplinary Program of Biomedical Engineering (Korea, Republic of); Huang, Yanlin [Soochow University, College of Chemistry, Chemical Engineering and Materials Science (China); Kim, Sun Il [Pukyong National University, Department of Physics and Interdisciplinary Program of Biomedical Engineering (Korea, Republic of); Yu, Young Moon [Pukyong National University, LED-Marin Convergence Technology R and BD Center (Korea, Republic of); Seo, Hyo Jin, E-mail: hjseo@pknu.ac.kr [Pukyong National University, Department of Physics and Interdisciplinary Program of Biomedical Engineering (Korea, Republic of)

    2013-09-15

    A novel red-emitting nano-phosphor of Eu{sup 3+}-doped Gd{sub 6}MoO{sub 12} was successfully synthesized by the Pechini method. The crystalline phase was confirmed by X-ray powder diffraction analysis. The morphology of the nano-phosphor was analyzed by scanning electron microscopy, indicating a good crystallization with particles smaller than 500 nm. The luminescence properties such as photoluminescence spectra and decay curves were investigated. The phosphors can be efficiently excited by near-ultraviolet (near-UV) light and exhibit a bright red luminescence around 613 nm ascribed to the forced electric dipole transition {sup 5}D{sub 0}{yields}{sup 7}F{sub 2} of Eu{sup 3+} ions. The thermal stabilities were investigated from the temperature-dependent luminescence decay curves (lifetimes) and spectra intensities. The luminescence properties in relation to applications in white light-emitting diodes (W-LEDs) such as the absolute luminescence quantum efficiency, excitation wavelength, and color coordinates were discussed. The Gd{sub 6}MoO{sub 12}:Eu{sup 3+} nano-phosphor is a promising red-emitting candidate for the fabrication of W-LEDs with near-UV chips.

  6. Liquid phase surface melting of AA8011 aluminum alloy by addition of Al/Al{sub 2}O{sub 3} nano-composite powders synthesized by high-energy milling

    Energy Technology Data Exchange (ETDEWEB)

    Sohi, M. Heydarzadeh [School of Metallurgy and Materials Engineering, College of Engineering, University of Tehran, Tehran (Iran, Islamic Republic of); Hojjatzadeh, S.M.H., E-mail: Hojatzadeh@yahoo.com [Department of Welding, Science and Research Branch, Azad University, Tehran (Iran, Islamic Republic of); Moosavifar, Sh. S.; Heshmati-Manesh, S. [School of Metallurgy and Materials Engineering, College of Engineering, University of Tehran, Tehran (Iran, Islamic Republic of)

    2014-09-15

    Highlights: • Aluminum matrix composite layers reinforced with alumina particles were fabricated. • Non milled powders caused porosity in the microstructures because of poor wettability. • The ball milling of powders was significantly improved the wettability of nano ceramic particles. • The micro hardness of the layers was approximately 3 times greater than that of the base metal. - Abstract: Poor wettability of particles is an obstacle in formation of sound composite layer via surface melting. Pre-coating of particles with metallic material by different techniques, such as ball milling may enhance the wettability of the particles with molten metal. In this study, composite surface layers containing Al{sub 2}O{sub 3} particles were fabricated on the surface of AA8011 aluminum substrates by tungsten inert gas (TIG) surface melting using preplaced layers of Al/Al{sub 2}O{sub 3} powder mixtures in two different forms: (1) a mixture of 40 wt% Al and 60 wt% of 50 nm Al{sub 2}O{sub 3} powders and (2) a mixture obtained by mechanical alloying of 40 wt% Al and 60 wt% of 60 μm Al{sub 2}O{sub 3} powders. Morphology evolution of powders during ball milling and the microstructure of the fabricated composite layers were studied through conventional characterization techniques, such as optical microscopy, scanning electron microscopy (SEM), and X-ray diffraction (XRD). Microhardness measurements were also performed across the alloyed zone. The results indicated that the layer fabricated by the second route showed a defect free structure with a more uniform distribution of Al{sub 2}O{sub 3} particles in comparison with the layer obtained by the first route. It was also noticed that the uniform dispersion of Al{sub 2}O{sub 3} particles in the fabricated layer increased the hardness to 133 HV which was over 3 times of that of the base metal.

  7. Photoluminescence and thermoluminescence properties of Tb{sup 3+} doped K{sub 3}Gd(PO{sub 4}){sub 2} nanophosphor

    Energy Technology Data Exchange (ETDEWEB)

    Gupta, Palvi; Bedyal, A.K. [School of Physics, Shri Mata Vaishno Devi University, Katra, 182320 Jammu and Kashmir (India); Kumar, Vinay, E-mail: vinaykdhiman@yahoo.com [School of Physics, Shri Mata Vaishno Devi University, Katra, 182320 Jammu and Kashmir (India); Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein ZA9300 (South Africa); Khajuria, Y. [School of Physics, Shri Mata Vaishno Devi University, Katra, 182320 Jammu and Kashmir (India); Lochab, S.P. [Inter University Accelerator Centre, Anura Asaf Ali Marg, P. O. Box 10502, New Delhi 110067 (India); Pitale, S.S. [Crystal Technology Laboratory,TPD, Bhabha Atomic Research Centre Trombay, Mumbai 400085 (India); Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein ZA9300 (South Africa); Ntwaeaborwa, O.M.; Swart, H.C. [Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein ZA9300 (South Africa)

    2014-12-15

    Energy level diagram of Tb{sup 3+} ion in the K{sub 3}Gd(PO{sub 4}){sub 2} host lattice. - Highlights: • First time, a detailed TL and PL study on undoped and Tb{sup 3+} doped K{sub 3}Gd(PO{sub 4}){sub 2} nanophosphor. • Combustion method was employed to synthesize the Tb{sup 3+} doped K{sub 3}Gd(PO{sub 4}){sub 2} nanophosphor. • Mechanism of excitation and emission in undoped and Tb{sup 3+} doped K{sub 3}Gd(PO{sub 4}){sub 2} nanophosphor was given. - Abstract: Tb{sup 3+} doped nanoparticulate K{sub 3}Gd(PO{sub 4}){sub 2} phosphor was prepared by combustion method using urea as a fuel. The structure, optical and luminescent properties of the phosphor were studied by X-ray diffraction (XRD), scanning electron microscopy (SEM), diffuse reflectance spectroscopy (DRS), photoluminescence spectroscopy (PL), and thermoluminescence (TL) spectroscopy. In undoped K{sub 3}Gd(PO{sub 4}){sub 2}, the excitation and emission peaks at 273 nm and 323 nm belongs to the {sup 8}S{sub 7/2} → {sup 6}I{sub J(J=7/2)} and {sup 6}P{sub J(J=7/2)} → {sup 8} S{sub 7/2} transitions of Gd{sup 3+} while green emission was observed in the Tb{sup 3+} doped K{sub 3}Gd(PO{sub 4}){sub 2}. TL study was carried out after exposing the samples to γ-radiations (0.1–5 kGy) in the K{sub 3}Gd(PO{sub 4}){sub 2}:Tb{sup 3+} (1.5 mol%). The calculated kinetic parameters were compared with different methods. The band gap of the phosphor was estimated as 5.80 eV. The green shade of the Tb{sup 3+} ion with the CIE coordinates (x, y) as (0.29, 0.54) was in good agreement with the well known green phosphors.

  8. Laser ablation of nanoscale particles with 193 nm light

    International Nuclear Information System (INIS)

    Choi, J H; Lucas, D; Koshland, C P

    2007-01-01

    Laser interaction with nanoscale particles is distinct and different from laser-bulk material interaction, where a hot plasma is normally created. Here, we review our studies on 193 nm laser ablation of various nanoscale particles including NaCl, soot, polystyrene, and gold. The 20 ns laser beam with fluences up to 0.3 J/cm 2 irradiates nanoparticles in a gas stream at laser repetition rates from 10 to 100 Hz. The particle size distributions before and after irradiation are measured with a scanning mobility particle sizer (SMPS), and particle morphology is examined with electron microscopy. All the nanomaterials studied exhibit a similar disintegration pattern and similar particle formation characteristics. No broadband emission associated with particle heating or optical breakdown is observed. The nanoparticles formed after irradiation have a smaller mean diameter and an order of magnitude higher number concentration with a more spherical shape compared to the original particles. We use the photon-atom ratio (PAR) to interpret the laser-particle interaction energetics

  9. Microwave assisted synthesis of core–shell LiFe{sub 1/3}Mn{sub 1/3}Co{sub 1/3}PO{sub 4}/C nanocomposite cathode for high-performance lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Li, Huanhuan [Automotive Engineering Research Institute, Jiangsu University, 301 Xuefu Road, Zhenjiang 212013 (China); Li, Yunxing [School of Material Science and Engineering, Jiangsu University, Zhenjiang 212013 (China); Chen, Long; Jiang, Haobin [Automotive Engineering Research Institute, Jiangsu University, 301 Xuefu Road, Zhenjiang 212013 (China); Wei, Jinping [Institute of New Energy Material Chemistry, Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Nankai University, Tianjin 300071 (China); Wang, Hongbo [China Aviation Lithium Battery Co. Ltd., Luoyang 471003 (China); Wang, Yaping, E-mail: wangyaping@ujs.edu.cn [School of Material Science and Engineering, Jiangsu University, Zhenjiang 212013 (China)

    2014-12-25

    Highlights: • We firstly report a fast microwave heating way to prepare LiFe{sub 1/3}Mn{sub 1/3}Co{sub 1/3}PO{sub 4}/C. • The reversible discharge capacity of LiFe{sub 1/3}Mn{sub 1/3}Co{sub 1/3}PO{sub 4}/C is about 169 mA h g{sup −1}. • LiFe{sub 1/3}Mn{sub 1/3}Co{sub 1/3}PO{sub 4}/C nanocomposite elucidates excellent cyclic stability. • LiFe{sub 1/3}Mn{sub 1/3}Co{sub 1/3}PO{sub 4}/C nanocomposite exhibits attractive rate capability. - Abstract: A microwave assisted method is developed for synthesizing pure LiFe{sub 1/3}Mn{sub 1/3}Co{sub 1/3}PO{sub 4} and LiFe{sub 1/3}Mn{sub 1/3}Co{sub 1/3}PO{sub 4}/C nanocomposite. Olivine LiFe{sub 1/3}Mn{sub 1/3}Co{sub 1/3}PO{sub 4} coated with uniform amorphous carbon film of ∼5 nm in thickness with an average size of ∼200 nm is successfully obtained. Compared with pure LiFe{sub 1/3}Mn{sub 1/3}Co{sub 1/3}PO{sub 4}, LiFe{sub 1/3}Mn{sub 1/3}Co{sub 1/3}PO{sub 4}/C composite presents enhanced electrochemical Li-ion intercalation performances. It exhibits a high discharge capacity of 169 mA h g{sup −1} at 0.1 C (theoretical capacity is 170 mA h g{sup −1}). The capacity retention is 99% after 30 cycles. Furthermore, the capacities are still retained 101 at 5 C and 76 mA h g{sup −1} and 20 C, respectively. Carbon coating can significantly improve the Li-ion diffusion, the reversibility of lithium extraction/insertion and electrical conductivity of LiCo{sub 1/3}Mn{sub 1/3}Fe{sub 1/3}PO{sub 4}.

  10. Chemiluminescence of the Ce{sup 3+}* ions, and the {sup 1}ГђЕѕ{sub 2} and ({sup 1}ГђЕѕ{sub 2}){sub 2} molecular species of oxygen induced by active surface of the (NH{sub 4}){sub 2}Ce(NO{sub 3}){sub 6} crystals at reduction of Ce{sup 4+} to Ce{sup 3+} by water in heterogeneous system «(NH{sub 4}){sub 2}Ce(NO{sub 3}){sub 6}-C{sub 6}H{sub 6}-H{sub 2}O»

    Energy Technology Data Exchange (ETDEWEB)

    Bulgakov, Ramil G., E-mail: profbulgakov@yandex.ru [Laboratory of Negative Ions Mass Spectrometry, Institute of Molecule and Crystal Physics, Ufa Research Centre of the Russian Academy of Sciences, 71, Oktyabrya Prosp., 450054 Ufa (Russian Federation); Gazeeva, Dilara R., E-mail: galimovdi@mail.ru [Laboratory of High Energy Chemistry and Catalysis, Institute of Petrochemistry and Catalysis Russian Academy of Sciences, 141 Prosp. Oktyabrya, 450075 Ufa (Russian Federation); Galimov, Dim I. [Laboratory of High Energy Chemistry and Catalysis, Institute of Petrochemistry and Catalysis Russian Academy of Sciences, 141 Prosp. Oktyabrya, 450075 Ufa (Russian Federation)

    2017-03-15

    We have discovered an unusual new chemiluminescence (CL) in the title system, which is different from other known CL by unusual combination of various in nature emitters, namely, electronically excited state of the Ce{sup 3+}* ion (λ{sub max}=335 nm), singlet oxygen {sup 1}ГђЕѕ{sub 2} (emission near 1270 nm) and its dimer ({sup 1}ГђЕѕ{sub 2}){sub 2} (λ{sub max}=490, 645, 715 nm). The Ce{sup 3+}* ions and oxygen emitters {sup 1}O{sub 2} and ({sup 1}O{sub 2}){sub 2} are generated in the reaction of Ce{sup 4+} with water and hydrogen peroxide, respectively. CL is generated only in a heterogeneous system «(NH{sub 4}){sub 2}Ce(NO{sub 3}){sub 6}-C{sub 6}H{sub 6}-H{sub 2}O» and completely absent in a homogeneous solution (NH{sub 4}){sub 2}Ce(NO{sub 3}){sub 6} in water containing benzene. This is due to the fact that the redox processes and CL in the «(NH{sub 4}){sub 2}Ce(NO{sub 3}){sub 6}-C{sub 6}H{sub 6}-H{sub 2}O» system are induced by active surface of the (NH{sub 4}){sub 2}Ce(NO{sub 3}){sub 6} crystals. It is through the action of the active surface of the (NH{sub 4}){sub 2}Ce(NO{sub 3}){sub 6} crystals is carried out population of such a high energy level of 5d{sup 1} excited state of Ce{sup 3+}* ion (λ{sub max}=353 nm, 3.7 eV). Discovered CL is the first example of an experimental registration of the Ce{sup 3+}* ion emission in a chemical reaction, because formation of Ce{sup 3+}* ion previously assumed to be in a great many works on the study of CL in reactions of Ce{sup 4+} compounds with various reducing agents, including the reaction with water, initiated by light or catalysts. Possible mechanism generation of new CL in the system under study has been proposed in the paper. - Highlights: • A new chemiluminescence (CL) in the (NH{sub 4}){sub 2}Ce(NO{sub 3}){sub 2}-C{sub 6}H{sub 6}-H{sub 2}O system was discovered. • The emission of the Ce{sup 3+}* ion as a CL emitter has been registered for the first time. • Other emitters of this CL are

  11. Near-infrared photoluminescence in La{sub 0.98}AlO{sub 3}: {sub 0.02}Ln{sup 3+}(Ln = Nd/Yb) for sensitization of c-Si solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Sawala, N. S., E-mail: nssawala@gmail.com; Koparkar, K. A.; Omanwar, S. K. [Department of Physics, SantGadge Baba Amravati University, Amravati - MH, 444602 (India); Bajaj, N. S. [Department of Physics, Toshniwal Art, Commerce and Science College, Sengoan, Hingoli - MH (India)

    2016-05-06

    The host matrix LaAlO{sub 3} was synthesized by conventional solid state reaction method in which the Nd{sup 3+} ions and Yb{sup 3+} ions successfully doped at 2mol% concentrations. The phase purity was confirmed by X ray powder diffraction (XRD) method. The photoluminescence (PL) properties were studied by spectrophotometer in near infra red (NIR) and ultra violet visible (UV-VIS) region. The Nd{sup 3+} ion doped LaAlO{sub 3} converts a visible (VIS) green photon (587 nm) into near infrared (NIR) photon (1070 nm) while Yb{sup 3+} ion doped converts ultra violet (UV) photon (221 nm) into NIR photon (980 nm). The La{sub 0.98}AlO{sub 3}: {sub 0.02}Ln{sup 3+}(Ln = Nd / Yb) can be potentiality used for betterment of photovoltaic (PV) technology. This result further indicates its potential application as a luminescence converter layer for enhancing solar cells performance.

  12. Observation of the domain structures in ferromagnetically coupled (Fe{sub 97}Al{sub 3}){sub 85}N{sub 15}/Al{sub 2}O{sub 3} multilayers

    Energy Technology Data Exchange (ETDEWEB)

    Stobiecki, T.; Zoladz, M. [Department of Electronics, University of Mining and Metallurgy, 30-059 Krakow (Poland); Otto, M.; Roell, K. [Universitaet Gesamthochschule Kassel, Experimentalphysik IV, 34132 Kassel (Germany); Maass, W. [Unaxis GmbH, Alzenau (Germany)

    2003-03-01

    The strength of ferromagnetic (FM) coupling as a function of the spacer thickness of Al{sub 2}O{sub 3} was investigated by means of the Kerr microscopy used for analysis of magnetic domains. It was found that strong FM-coupling, strong uniaxial anisotropy and coherent rotation of the magnetization have been observed for the spacer thickness in the range of 0.2 nm{<=}t{<=}1 nm, however weak FM-coupling, patch domains and 360 -walls occur for the spacer thickness of t=2.5 nm. At a spacer thickness of t{>=}5 nm transition takes place from weak FM-coupling to the decoupled state where complex interlayer interactions and different types of the domain walls were observed. (Abstract Copyright [2003], Wiley Periodicals, Inc.)

  13. Luminescence characterization of sol-gel derived Pr{sup 3+} doped NaGd(WO{sub 4}){sub 2} phosphors for solid state lighting applications

    Energy Technology Data Exchange (ETDEWEB)

    Durairajan, A., E-mail: durairajan.a@gmail.com [Crystal Growth Centre, Anna University, Chennai, 600025 (India); I3N-Aveiro, Department of Physics, University of Aveiro, Aveiro, 3810 193 (Portugal); Thangaraju, D. [Research Institute of Electronics, Shizuoka University, 3-5-1 Johoku, Hamamatsu, Shizuoka, 432-8011 (Japan); Moorthy Babu, S. [Crystal Growth Centre, Anna University, Chennai, 600025 (India); Valente, M.A. [I3N-Aveiro, Department of Physics, University of Aveiro, Aveiro, 3810 193 (Portugal)

    2016-08-15

    In the present work, xPr{sup 3+}:NaGd(WO{sub 4}){sub 2} (0.5 ≤ x ≤ 5.0 mol%) sub-micron phosphors were synthesised by sol-gel method. Low cost precursors of metal nitrates and low temperature thermal treatment was used compared to conventional solid state reaction. The formation of highly crystalline phosphors with tetragonal structure was confirmed by XRD and increase of Pr{sup 3+} ions content in host matrix leads to expansion of the unit cell volume. The surface morphology, size and particle distribution of the phosphors were observed by field emission scanning electron microscopy (FE-SEM). A rectangular shape particle with a size distribution ranging from 400 to 600 nm and tightly packed surface was seen in FE-SEM micrographs. The various internal and external phonon modes vibration corresponding to double tungstate structure was observed in Raman spectra. The optical properties of the synthesised phosphors were explored by ultraviolet visible (UV–Vis) absorption in diffuse reflectance and photoluminescence (PL) measurements. UV–Vis measurements distinguished the host and Pr{sup 3+} absorption and also reveal an increase in optical band gap values with an increase of Pr{sup 3+}. The PL measurements show various emissions from green and red regions under 450 nm. The maximum intensity emission at 489 nm is due to {sup 3}P{sub 0} → {sup 3}H{sub 4} transition of Pr{sup 3+}. From the maximum emission the critical doping concentration was calculated to be at 3.5 mol% and critical distance between two adjacent Pr{sup 3+} ions as 20.43 Å. - Highlights: • A sol-gel method was used to prepare Pr{sup 3+} doped NaGd(WO{sub 4}){sub 2} at low temperature. • Structural, spectroscopic, morphological, and optical and luminescence properties were studied. • The praseodymium ions are in trivalent state, the site symmetry is distorted and S{sub 4} local symmetry with Na{sup +} ions. • Strong green emission was observed under UV and visible excitation.

  14. Recording-media-related morphology and magnetic properties of crystalline CoPt{sub 3} and CoPt{sub 3}-Au core-shell nanoparticles synthesized via reverse microemulsion

    Energy Technology Data Exchange (ETDEWEB)

    Bahmanrokh, Ghazaleh, E-mail: ghazalehbahmanrokh@yahoo.com; Hashim, Mansor; Matori, Khamirul Amin; Kanagesan, Samikannu; Sabbaghizadeh, Rahim; Ezzad Shafie, Mohd Shamsul [Materials Synthesis and Characterization Laboratory, Institute of Advanced Technology, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor (Malaysia); Navasery, Manizheh; Soltani, Nayereh [Department of Physics, Faculty of Science, Universiti Putra Malaysia, 43400 UPM, Serdang, Selangor (Malaysia); Vaziri, Parisa [Department of Medical Physics and Biomedical Engineering, Shahid Beheshti University of Medical Sciences, Tehran (Iran, Islamic Republic of)

    2014-09-07

    A comparative experimental study of the magnetic properties of CoPt{sub 3} and CoPt{sub 3}/Au nanoparticles as well as a detailed study of the structural properties of the samples by X-ray diffraction, Transmission electron microscopy, and vibrating sample magnetometer is presented in this work. In addition, the effect of particle size on the structure and magnetic properties of nanoparticles prepared by microemulsion is studied. The correlation between particle size, crystallinity, and magnetization was studied as well. CoPt nanoparticles have been studied intensively over the last decade because of their increased magnetic anisotropy in the ordered phase that can be interesting for high density magnetic recording. A significant high coercivity for as-prepared CoPt{sub 3} and CoPt{sub 3}-Au nanoparticles was obtained at room temperature and enhanced after annealing. The focused aim of our study is to obtain high coercivity at room temperature that follows the Curie-Weiss law. This indicates an interacting system in which the nanoparticles behave like single domain ferromagnetic materials in the particle size range of 8 to 35 nm. In addition, the interaction increases by cooling the samples to low temperature around 15 K. Temperature dependence 1/M graph was obtained to investigate the behavior of nanoparticles at low temperature and shows the best fit with Curie-Weis mode.

  15. Preparation, patterning and luminescent properties of oxyapatite La sub 9 sub . sub 3 sub 3 (SiO sub 6) sub 4 O sub 2 :A(A = Eu sup 3 sup + , Tb sup 3 sup + , Ce sup 3 sup +) phosphor films by sol-gel soft lithography

    CERN Document Server

    Han, X M; Xing, R B; Fu, J; Wang, S B; Han, Y C

    2003-01-01

    Silicate oxyapatite La sub 9 sub . sub 3 sub 3 (SiO sub 6) sub 4 O sub 2 :A (A = Eu sup 3 sup + , Tb sup 3 sup + and/or Ce sup 3 sup +) phosphor films and their patterning were fabricated by a sol-gel process combined with soft lithography. X-ray diffraction(XRD), Fourier transform infrared spectroscopy, atomic force microscopy, optical microscopy and photoluminescence spectra, as well as lifetimes, were used to characterize the resulting films. The results of XRD indicated that the films began to crystallize at 800 deg. C and the crystallinity increased with the increase in annealing temperatures. Transparent nonpatterned phosphor films were uniform and crack-free, which mainly consisted of rodlike grains with a size between 150 and 210 nm. Patterned thin films with different bandwidths(20, 50 mu m) were obtained by the micromoulding in capillaries technique. The doped rare earth ions(Eu sup 3 sup + , Tb sup 3 sup + and Ce sup 3 sup +) showed their characteristic emission in crystalline La sub 9 sub . sub 3 ...

  16. Optical properties of the Na{sub 2}O-B{sub 2}O{sub 3}-Bi{sub 2}O{sub 3}-MoO{sub 3} glasses

    Energy Technology Data Exchange (ETDEWEB)

    Saddeek, Yasser B. [Physics Department, Faculty of Science, Al-Azhar University, P.O. 71452, Assiut (Egypt); Aly, K.A., E-mail: kamalaly2001@gmail.co [Physics Department, Faculty of Science, Al-Azhar University, P.O. 71452, Assiut (Egypt); Dahshan, A., E-mail: adahshan73@gmail.co [Department of Physics, Faculty of Science, Suez Canal University, Port Said (Egypt); Kashef, I.M.El. [Department of Physics, Faculty of Education, Suez Canal University, Al Arish (Egypt)

    2010-04-02

    Glasses with compositions (100 - x)Na{sub 2}B{sub 4}O{sub 7}-0.5Bi{sub 2}O{sub 3}-0.5MoO{sub 3}, with 0 {<=} x {<=} 40 mol% have been prepared using the melt quenching technique. The optical transmittance and reflectance spectrum of the glasses have been recorded in the wavelength range 300-1100 nm. The values of the optical band gap E{sub g}{sup opt} for indirect transition and refractive index have been determined for 0 {<=} x {<=} 40 mol%. The average electronic polarizability of the oxide ion {alpha}{sub O{sup 2-}} and the optical basicity have been estimated from the calculated values of the refractive indices. The variations in the different physical parameters such as the optical band gap, the refractive index, the average electronic polarizability of the oxide ion and the optical basicity with Bi{sub 2}O{sub 3} and MoO{sub 3} content have been analyzed and discussed in terms of the changes in the glass structure. The results are interpreted in terms of the increase in the number of non-bridging oxygen atoms, substitution of longer bond-lengths of Bi-O, and Mo-O in place of shorter B-O bond and the change in Na{sup +} ion concentration.

  17. Fabrication of magnetic and fluorescent chitin and dibutyrylchitin sub-micron particles by oil-in-water emulsification.

    Science.gov (United States)

    Blanco-Fernandez, Barbara; Chakravarty, Shatadru; Nkansah, Michael K; Shapiro, Erik M

    2016-11-01

    Chitin is a carbohydrate polymer with unique pharmacological and immunological properties, however, because of its unwieldy chemistry, the synthesis of discreet sized sub-micron particles has not been well reported. This work describes a facile and flexible method to fabricate biocompatible chitin and dibutyrylchitin sub-micron particles. This technique is based on an oil-in-water emulsification/evaporation method and involves the hydrophobization of chitin by the addition of labile butyryl groups onto chitin, disrupting intermolecular hydrogen bonds and enabling solubility in the organic solvent used as the oil phase during fabrication. The subsequent removal of butyryl groups post-fabrication through alkaline saponification regenerates native chitin while keeping particles morphology intact. Examples of encapsulation of hydrophobic dyes and nanocrystals are demonstrated, specifically using iron oxide nanocrystals and coumarin 6. The prepared particles had diameters between 300-400nm for dibutyrylchitin and 500-600nm for chitin and were highly cytocompatible. Moreover, they were able to encapsulate high amounts of iron oxide nanocrystals and were able to label mammalian cells. We describe a technique to prepare sub-micron particles of highly acetylated chitin (>90%) and dibutyrylchitin and demonstrate their utility as carriers for imaging. Chitin is a polysaccharide capable of stimulating the immune system, a property that depends on the acetamide groups, but its insolubility limits its use. No method for sub-micron particle preparation with highly acetylated chitins have been published. The only approach for the preparation of sub-micron particles uses low acetylation chitins. Dibutyrylchitin, a soluble chitin derivative, was used to prepare particles by oil in water emulsification. Butyryl groups were then removed, forming chitin particles. These particles could be suitable for encapsulation of hydrophobic payloads for drug delivery and cell imaging, as well as

  18. Structural analysis, optical and dielectric function of [Ba{sub 0.9}Ca{sub 0.1}](Ti{sub 0.9}Zr{sub 0.1})O{sub 3} nanocrystals

    Energy Technology Data Exchange (ETDEWEB)

    Herrera-Pérez, G., E-mail: guillermo.herrera@cimav.edu.mx, E-mail: damasio.morales@cimav.edu.mx [Centro de Investigación en Materiales Avanzados (CIMAV), S. C. Miguel de Cervantes 120, Chihuahua 31136, Chihuahua (Mexico); Physics of Materials Department, Centro de Investigación en Materiales Avanzados (CIMAV), S. C. Miguel de Cervantes 120, Chihuahua 31136, Chihuahua (Mexico); Morales, D., E-mail: guillermo.herrera@cimav.edu.mx, E-mail: damasio.morales@cimav.edu.mx; Paraguay-Delgado, F.; Reyes-Rojas, A.; Fuentes-Cobas, L. E. [Physics of Materials Department, Centro de Investigación en Materiales Avanzados (CIMAV), S. C. Miguel de Cervantes 120, Chihuahua 31136, Chihuahua (Mexico); Borja-Urby, R. [Centro de Nanociencias Micro y Nanotecnologías, Instituto Politécnico Nacional, 07300 México City (Mexico)

    2016-09-07

    This work presents the identification of inter-band transitions in the imaginary part of the dielectric function (ε{sub 2}) derived from the Kramers–Kronig analysis for [Ba{sub 0.9}Ca{sub 0.1}](Ti{sub 0.9}Zr{sub 0.1})O{sub 3} (BCZT) nanocrystals synthesized by the modified Pechini method. The analysis started with the chemical identification of the atoms that conform BCZT in the valence loss energy region of a high energy-resolution of electron energy loss spectroscopy. The indirect band energy (E{sub g}) was determined in the dielectric response function. This result is in agreement with the UV-Vis technique, and it obtained an optical band gap of 3.16 eV. The surface and volume plasmon peaks were observed at 13.1 eV and 26.2 eV, respectively. The X-ray diffraction pattern and the Rietveld refinement data of powders heat treated at 700 °C for 1 h suggest a tetragonal structure with a space group (P4 mm) with the average crystal size of 35 nm. The average particle size was determined by transmission electron microscopy.

  19. Synthesis and PL study of UV emitting phosphor KCa{sub 4}(BO{sub 3}){sub 3}:Pb{sup 2+}

    Energy Technology Data Exchange (ETDEWEB)

    Gawande, A.B., E-mail: gawandeab@gmail.com [Department of Physics, SGB Amravati University, Amravati, Maharashtra (India); Sonekar, R.P., E-mail: sonekar_rp@yahoo.com [Department of Physics, G.S. College, Khamgaon, Buldhana District, Maharashtra (India); Omanwar, S.K. [Department of Physics, SGB Amravati University, Amravati, Maharashtra (India)

    2014-05-01

    Pb{sup 2+} doped KCa{sub 4}(BO{sub 3}){sub 3} materials were prepared by a novel solution combustion synthesis technique which is slight variation of combustion synthesis method. The synthesized materials were characterized by powder XRD and FT-IR. Scanning Electron Microscopy (SEM) observation indicated that the microstructure of the phosphor consisted of irregular grains which get finer and shaped in doped sample as compared to pure. The photoluminescence properties of synthesized materials were investigated using Spectrofluorometer at room temperature. The emission and excitation bands of the synthesized phosphors were observed at 335 nm and 260 nm respectively. The concentration of Pb{sup 2+} for which optimum emission is obtained was found to be 0.005 mol. The critical transfer distance (R{sub 0}) for optimum concentration was determined to be 16.88 Å. The Stokes shift of KCa{sub 4}(BO{sub 3}){sub 3}:Pb{sup 2+} was measured to be 8756 cm{sup −1}. The phosphor could find application in medical and lamp industry. - Highlights: • Inorganic borate phosphor KCa{sub 4}(BO{sub 3}){sub 3}:Pb{sup 2+} has been synthesized by solution combustion synthesis technique. • Structure confirmation of synthesized phosphor done by using powder XRD and FT-IR. • Doping effect on the surface morphology of synthesized material is shown by SEM images. • Stokes shift, optimum concentration and critical transfer distance for optimum concentration in KCa{sub 4}(BO{sub 3}){sub 3}:Pb{sup 2+} have been determined.

  20. Microwave-assisted rapid synthesis of Fe{sub 2}O{sub 3}/ACF hybrid for high efficient As(V) removal

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Huiyun; Lv, Kangle; Du, Ying; Ye, Hengpeng; Du, Dongyun, E-mail: dydu666@mail.scuec.edu.cn

    2016-07-25

    In this paper, an efficient adsorbent, iron-modified activated carbon fiber (Fe{sub 2}O{sub 3}/ACF), was rapidly fabricated by microwave-assisted heating treatment strategy, which is used to remove As(V) from simulated wastewater. The adsorbent was characterized by scanning electron microscopy (SEM), TEM, N{sub 2} sorption, X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). The characterization results showed that rod-like Fe{sub 2}O{sub 3} particles in sizes of about 20 nm × 50 nm were homogeneously anchored on the surface of ACF. The goal of high As(V) removal efficiency was achieved with maximum adsorption capacity of 20.33 mg g{sup −1}. The effects of temperature on thermodynamics and kinetics of As(V) adsorption were systematically studied. It was found that the adsorption of As(V) on the surface of Fe{sub 2}O{sub 3}/ACF is an endothermic process with a standard enthalpy change (ΔH{sup 0}) of 24.79 kJ mol{sup −1}. Batch experimental result showed that almost all of the As(V) with initial concentration of 3.0 mg L{sup −1} can be removed in the presence of Fe{sub 2}O{sub 3}/ACF, where the residual As(V) in filtrate was less than 0.01 mg L{sup −1}, below the tolerance level of drinking water suggested by World Health Organization (WHO). The presence of salt such as NaCl, Na{sub 2}SO{sub 4}, and MgSO{sub 4} showed little effects on the adsorption of As(V), indicating the promising application of Fe{sub 2}O{sub 3}/ACF in industrial wastewater. - Highlights: • Fe{sub 2}O{sub 3}/ACF hybrid was rapidly fabricated using a microwave-assisted heating strategy. • Fe{sub 2}O{sub 3} nanorods in sizes of 20 × 50 nm were homogeneously anchored on the surface of ACF. • The maximum adsorption capacity of 20.33 mg g{sup −1} As (V) on Fe{sub 2}O{sub 3}/ACF was achieved. • The adsorption of As (V) is an endothermic process (ΔH{sup 0} = 24.79 kJ mol{sup −1}). • The presence of salt shows little effect on the adsorption of As (V).

  1. The effects of energy transfer on the Er{sup 3+} 1.54 {mu}m luminescence in nanostructured Y{sub 2}O{sub 3} thin films with heterogeneously distributed Yb{sup 3+} and Er{sup 3+} codopants

    Energy Technology Data Exchange (ETDEWEB)

    Hoang, J.; Chang, J. P. [Department of Chemical and Biomolecular Engineering, University of California, Los Angeles, California 90095 (United States); Schwartz, Robert N.; Wang, Kang L. [Department of Electrical Engineering, University of California, Los Angeles, California 90095 (United States)

    2012-09-15

    We report the effects of heterogeneous Yb{sup 3+} and Er{sup 3+} codoping in Y{sub 2}O{sub 3} thin films on the 1535 nm luminescence. Yb{sup 3+}:Er{sup 3+}:Y{sub 2}O{sub 3} thin films were deposited using sequential radical enhanced atomic layer deposition. The Yb{sup 3+} energy transfer was investigated for indirect and direct excitation of the Yb {sup 2}F{sub 7/2} state using 488 nm and 976 nm sources, respectively, and the trends were described in terms of Forster and Dexter's resonant energy transfer theory and a macroscopic rate equation formalism. The addition of 11 at. % Yb resulted in an increase in the effective Er{sup 3+} photoluminescence (PL) yield at 1535 nm by a factor of 14 and 42 under 488 nm and 976 nm excitations, respectively. As the Er{sub 2}O{sub 3} local thickness was increased to greater than 1.1 A, PL quenching occurred due to strong local Er{sup 3+}{r_reversible} Er{sup 3+} excitation migration leading to impurity quenching centers. In contrast, an increase in the local Yb{sub 2}O{sub 3} thickness generally resulted in an increase in the effective Er{sup 3+} PL yield, except when the Er{sub 2}O{sub 3} and Yb{sub 2}O{sub 3} layers were separated by more than 2.3 A or were adjacent, where weak Yb{sup 3+}{r_reversible} Er{sup 3+} coupling or strong Yb{sup 3+}{r_reversible} Yb{sup 3+} interlayer migration occurred, respectively. Finally, it is suggested that enhanced luminescence at steady state was observed under 488 nm excitation as a result of Er{sup 3+}{yields} Yb{sup 3+} energy back transfer coupled with strong Yb{sup 3+}{r_reversible} Yb{sup 3+} energy migration.

  2. Dual mode emission and harmonic generation in ZnO-CaO-Al{sub 2}O{sub 3}: Er{sup 3+} nano-composite

    Energy Technology Data Exchange (ETDEWEB)

    Verma, R.K. [Laser and Spectroscopy Laboratory, Department of Physics, Banaras Hindu University, Varanasi 221005 (India); Kumar, K. [Laser and Spectroscopy Laboratory, Department of Physics, Banaras Hindu University, Varanasi 221005 (India); Nano-technology Application Centre, University of Allahabad, Allahabad (India); Rai, S.B., E-mail: sbrai49@yahoo.co.i [Laser and Spectroscopy Laboratory, Department of Physics, Banaras Hindu University, Varanasi 221005 (India)

    2011-05-15

    Er{sup 3+} doped ZnO-CaO-Al{sub 2}O{sub 3} nano-composite phosphor has been synthesized through combustion method and its emission and harmonic generation properties have been studied. The X-ray diffraction and thermal analysis techniques have been used to prove the dual phase (ZnO and CaO-Al{sub 2}O{sub 3}) nature of the phosphor. The phosphor has shown up-conversion emission on near-infra-red (976 nm) excitation and down-conversion emission on 355 nm excitation in presence of Er{sup 3+} and thus behaves as a dual mode phosphor. On excitation with 976 nm diode laser, material shows color tunability (calcination of composite material at different temperatures). Formation of ZnO nanocrystals on heat treatment of as-synthesized sample has shown its characteristic emission at 388 nm and also the energy transfer from ZnO to Er{sup 3+} ions. The low temperature emission measurements have been carried out and the results have been discussed. Phosphor has shown strong second harmonic generation (SHG) at 532 nm on 1064 nm and at 266 nm on 532 nm excitation. - Research highlights: {yields} We have synthesized Er{sup 3+} doped composite material by combustion method. The two phases of composites are ZnO and CaO-Al{sub 2}O{sub 3}. {yields} The phosphor has shown up-conversion emission on near-infra-red (976 nm) excitation and down-conversion emission on 355 nm excitation in presence of Er{sup 3+} and thus behaves as a dual mode phosphor. This material also shows colour tenability on excitation of 976 nm diode laser at different temperature calcinations (i.e., As-synthesized to calcinated at 1473 K). {yields} Low temperature effects on Er{sup 3+} as well as ZnO emission have been carried out. We observed that at low temperature the efficiency of Er{sup 3+} increases while in the case of ZnO its intensity increases and also 12 nm shifting observed. {yields} Composite material has shown strong second harmonic generation (SHG) at 532 nm on 1064 nm and at 266 nm on 532 nm

  3. Photoluminescence characteristics of reddish-orange Eu{sup 3+} or Sm{sup 3+} singly-doped and Eu{sup 3+} and Sm{sup 3+} co-doped KZnGd(PO{sub 4}){sub 2} phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Jeong, Jun Ho; Bandi, Vengala Rao; Grandhe, Bhaskar Kumar; Jang, Ki Wan; Lee, Ho Sueb [Changwon National University, Changwon (Korea, Republic of); Yi, Soung Soo [Silla University, Busan (Korea, Republic of); Jeong, Jung Hyun [Pukyong National University, Busan (Korea, Republic of)

    2011-02-15

    Eu{sup 3+} or Sm{sup 3+} singly-doped and Eu{sup 3+} and Sm{sup 3+} co-doped KZnGd(PO{sub 4}){sub 2} phosphors were synthesized by using a conventional solid state reaction method at 750 .deg. C. The emission spectra of KZnGd{sub 1-x}(PO{sub 4}){sub 2}:Eu{sup 3+}{sub x} with {lambda}{sub ex} = 395 nm and KZnGd{sub 1-y}(PO{sub 4}){sub 2}:Sm{sup 3+}{sub y} with {lambda}{sub ex} = 403 nm phosphors showed intense {sup 5}D{sub 0} {yields} {sup 7}F{sub 1}, {sup 4}G{sub 5/2} {yields} {sup 6}H{sub 7/2} emission transitions at 595 nm and 599 nm, respectively. The optimum relative intensity of the KZnGd{sub 1-x-y}(PO{sub 4}){sub 2}:Eu{sup 3+}{sub x} , Sm{sup 3+}{sub y} phosphor was obtained for the doping concentrations of (x = 0.09, y = 0.01). In addition, the temperature dependent luminescence intensity of the synthesized phosphors was investigated and the thermal stability of the KZnGd(PO{sub 4}){sub 2}:Eu{sup 3+} phosphor was found to be higher than that of standard YAG:Ce{sup 3+} and KZnGd{sub 1-x-y}(PO{sub 4}){sub 2}:Eu{sup 3+}{sub x} Sm{sup 3+}{sub y} under near ultra-violet (NUV) light emitting diode excitation (LED). Therefore, we suggest that Eu{sup 3+} or Sm{sup 3+} singly-doped and Eu{sup 3+} and Sm{sup 3+} co-doped KZnGd(PO{sub 4}){sub 2} phosphors should be efficient for different red-color-emitting display device applications and NUV-LED-based white-light-emitting diodes.

  4. A contribution to the kinetic study of the metatectic reaction U+U{sub 3}Si{sub 2}{yields}U{sub 3}Si; Contribucion al Estudio cinetico de la Reaccion Metatectica U+U{sub 3}Si{sub 2} U{sub 3}Si

    Energy Technology Data Exchange (ETDEWEB)

    Arroyo Ruiperez, J; Esteban Hernandez, J A

    1962-07-01

    An experimental study has been made to decide upon the advantages and drawbacks of the different methods and reagents employed in the metallography of U-Si alloys. It has been observed that all samples thermally treated to form the epsilon-phase undergo from the beginning a coalescence of the U{sub 3}Si{sub 2} particles, which makes practically useless any fine state of dispersion that might be present originally, as recommended by some authors. The coalescence of the U{sub 3}Si{sub 2} particle decreases the surface available for reaction and consequently the reaction rate. (Author) 7 refs.

  5. Strong enhancement of the upconversion emission in ZrO{sub 2}: Yb{sup 3+}, Er{sup 3+}, Gd{sup 3+} nanocubes synthesized with Na{sub 2}S

    Energy Technology Data Exchange (ETDEWEB)

    Urbina-Frías, Alejandra; López-Luke, Tzarara; Oliva, Jorge [Centro de Investigaciones en Óptica, A.P. 1-948, León, Guanajuato 37150 (Mexico); Salas, Pedro [Centro de Física Aplicada y Tecnología Avanzada, Universidad Nacional Autónoma de México, A.P. 1-1010, Querétaro 76000 (Mexico); Torres-Castro, Alejandro [Universidad Autónoma de Nuevo León, A.P. 126-F, Monterrey, NeNuevo Leon 66450 (Mexico); De la Rosa, Elder, E-mail: elder@cio.mx [Centro de Investigaciones en Óptica, A.P. 1-948, León, Guanajuato 37150 (Mexico)

    2016-04-15

    In this work, the structural, morphological and luminescent characterization of ZrO{sub 2}:Yb{sup 3+},Er{sup 3+}, Gd{sup 3+} nanocrystals prepared with Na{sub 2}S by precipitation method is reported. The XRD spectra showed a mixture of tetragonal (88%) and monoclinic phases (12%) in samples fabricated with and without Na{sub 2}S. The tetragonal phase (100%) was stabilized by the introduction of the Gd{sup 3+}. According to TEM images, samples showed a cubic morphology with an average size of 150 nm, when both, Na{sub 2}S and Gd{sup 3+} were added. Red (678 nm), green (545 nm) and ultraviolet (275, 285 nm) emissions were obtained as a result of the upconversion process due to the energy transfer between Yb{sup 3+}–Er{sup 3+}–Gd{sup 3+} ions, under 970 nm of excitation. The integrated red band showed an increment of 40% and 125%, for samples prepared with Na{sub 2}S and combined with Gd{sup 3+}, respectively, compared to the ZrO{sub 2}:Yb{sup 3+}–Er{sup 3+} sample. Such increments are explained in terms of the surface pasivation by using Na{sub 2}S during the synthesis process and the role of Gd{sup 3+} as a reservoir of energy from Er{sup 3+}. - Highlights: • ZrO{sub 2}:Yb,Er nanoparticles were synthesized by a precipitation method. • ZrO{sub 2}:Yb,Er nanoparticles were prepared with Na{sub 2}S and sensitized with Gd{sup 3+}. • An increment of 40% in luminescence occurred in samples prepared with Na{sub 2}S. • An increment of 125% were obtained by the synergistic effect between Na{sub 2}S and Gd3{sup +}.

  6. Evaluation of optoelectronic response and Raman active modes in Tb{sup 3+} and Eu{sup 3+}-doped gadolinium oxide (Gd{sub 2}O{sub 3}) nanoparticle systems

    Energy Technology Data Exchange (ETDEWEB)

    Paul, Nibedita [National Institute of Technology Nagaland, Department of Physics, Dimapur, Nagaland (India); Tezpur University, Department of Physics, Tezpur, Assam (India); Mohanta, D. [Tezpur University, Department of Physics, Tezpur, Assam (India)

    2016-09-15

    Rare earth oxide (Tb{sup 3+}:Gd{sub 2}O{sub 3} and Eu{sup 3+}:Gd{sub 2}O{sub 3}) nanophosphors are exploited through spectroscopic and microscopic tools with special emphasis on D-F mediated radiative emission and Raman active vibrational modes. Powder X-ray diffraction measurements have revealed cubic crystal structure of the nanosystems and with an average crystallite size varying between ∝3.2 and 4.8 nm. Photoluminescence (PL) spectra of Tb{sup 3+} doped systems signify intense blue-green (∝490 nm) and green (∝544 nm) emissions mediated by {sup 5}D{sub 4} → {sup 7}F{sub 6} and {sup 5}D{sub 4} → {sup 7}F{sub 5} transitional events; respectively. In the PL responses of Eu{sup 3+} doped nanoparticle systems, we also identify magnetically-driven {sup 5}D{sub 0} → {sup 7}F{sub 1} (∝591 nm) and electrically driven {sup 5}D{sub 0} → {sup 7}F{sub 2} (∝619 nm) radiative features which seem to improve with increasing doping level. However, the magnitude of Judd-Ofelt (J-O) intensity parameters (Ω {sub 2,} {sub 4}), is significantly lowered for the high doping cases. Raman spectra of the undoped and RE doped systems exhibited several A{sub g} and F{sub g} modes in the range of Raman shift ∝100-600 cm{sup -1}. In the Raman spectra, the peaks located at ∝355 cm{sup -1} are assigned to the mixed mode of F{sub g} + A{sub g}, the line width of which was found to increase with RE doping. Moreover, owing to the enhanced defect concentration in the doped systems than its undoped counterpart, we anticipate a faster phonon relaxation and consequently, a suppression of phonon lifetime in the former case. (orig.)

  7. Functional BaTiO{sub 3} nanostructures immobilized onto si-based substrates using sol–gel and reverse micelle techniques

    Energy Technology Data Exchange (ETDEWEB)

    Mamana, Nadia, E-mail: nadia@fceia.unr.edu.ar; Pellegri, Nora [CONICET, FCEIyA, UNR, Laboratorio de Materiales Cerámicos IFIR (Argentina)

    2015-03-15

    The current tendency toward miniaturization of electronic devices has driven the interest in developing ferroelectric materials in low dimensions. In this work, for the preparation of lead-free BaTiO{sub 3} nanoparticles, we used a combination of the sol–gel method with the reverse micelles techniques. Moreover, previously to the thermal treatment, it was necessary to remove the surfactant. For this stage, oleic acid was used to stabilize the nanoparticles in the solution. Then, nanometer-sized particles were deposited on different substrates (Si, Pt/TiO{sub 2}/SiO{sub 2}/Si). The influence of different modes of deposition on particle size, degree of agglomeration, was analyzed. The mean particle size was 10 nm. Finally, the deposition of BaTiO{sub 3} particles on a conductive substrate such as the wafer of platinum (Pt/TiO{sub 2}/SiO{sub 2}/Si) was confirmed by several AFM techniques.

  8. Energy transfer between Tb{sup 3+} and Eu{sup 3+} in co-doped Y{sub 2}O{sub 3} nanocrystals prepared by Pechini method

    Energy Technology Data Exchange (ETDEWEB)

    Back, M., E-mail: m.back@hotmail.it [Universita Ca' Foscari di Venezia and INSTM, Dipartimento di Scienze Molecolari e Nanosistemi (Italy); Boffelli, M. [Kyoto Institute of Technology and Research Institute for Nanoscience (Japan); Massari, A.; Marin, R. [Universita Ca' Foscari di Venezia and INSTM, Dipartimento di Scienze Molecolari e Nanosistemi (Italy); Enrichi, F. [Coordinamento Interuniversitario Veneto per le Nanotecnologie (CIVEN) (Italy); Riello, P., E-mail: riellop@unive.it [Universita Ca' Foscari di Venezia and INSTM, Dipartimento di Scienze Molecolari e Nanosistemi (Italy)

    2013-07-15

    Tb{sup 3+} and Eu{sup 3+} co-doped Y{sub 2}O{sub 3} nanoparticles with a volume-weighted average size of about 30 nm were synthesized via simple Pechini-type sol-gel process. The growth of monocrystalline nanoparticles is investigated via XRD and TEM analysis. The study of energy transfer between Tb{sup 3+} and Eu{sup 3+} ions was carried out by means of PL, PLE, and photoluminescence decay analyses. The energy transfer from Tb{sup 3+} to Eu{sup 3+} is efficient and we show how a resonant type via a dipole-dipole interaction is the most probable mechanism. We compared the energy-transfer efficiencies calculated from the intensities and from the lifetimes of {sup 5}D{sub 4}{yields}{sup 7}F{sub 5} transition of Tb, showing the presence of two populations of Tb, with different local surroundings, in the matrix. Furthermore, the critical distance between Tb{sup 3+} and Eu{sup 3+} ions has been calculated by means of different theories, from a new probabilistic approach based on the discretization of the theory of Chandrasekhar about the distribution of the nearest neighbors in a random distribution of particles, and from the PL data, suggesting a value of about 7 A.

  9. Electrical properties of Pb(Zr{sub 0.52}Ti{sub 0.48})O{sub 3}–BiFeO{sub 3} multilayers on non-platinized silicon substrate

    Energy Technology Data Exchange (ETDEWEB)

    Dutta, Shankar, E-mail: shankardutta77@gmail.com [Solid State Physics Laboratory, DRDO, Lucknow Road, Timarpur, Delhi 110054 (India); Chatterjee, Ratnamala [Department of Physics, IIT Delhi, Hauz Khas, New Delhi 110016 (India)

    2015-08-15

    Highlights: • A Pb(Zr{sub 0.52}Ti{sub 0.48})O{sub 3}/BiFeO{sub 3} multilayer film is deposited on a silicon substrate. • The phase, crystalline structure, and morphology of the film are studied. • The magnetic property of the film is studied. • In the absence of the bottom electrode, interdigitated terminal (IDTs) structures are fabricated on top of the film. • The electrical properties of the film are studied. - Abstract: In this study, a Pb(Zr{sub 0.52}Ti{sub 0.48})O{sub 3}/BiFeO{sub 3} (PZT–BFO) multilayer film is deposited by the sol–gel technique on a silicon substrate. Prior to the multilayer deposition, a ZrO{sub 2} buffer layer is introduced. The multilayer thin film shows the polycrystalline phase-pure perovskite structures of BFO and PZT. Surface morphology study indicates that the grain size of the film varies from 20 to 30 nm. In the absence of the bottom electrode, the electrical properties of the film are studied in-plane by fabricating interdigitated terminals (IDTs) on top of the film. The inter-IDT line gap is kept large (10 μm) to avoid shorting due to unintentional particle contamination. The remnant polarization of the film is found to be ∼35 μC/cm{sup 2} at a 100-V bias. The dielectric constant of the film is found to be 650 at 1 kHz. The film also showed a low leakage current density of ∼4 × 10{sup −9} A/cm{sup 2} at 200 kV/cm.

  10. Study on the electrical transport properties of La{sub 2/3}Ba{sub 1/3}MnO{sub 3}:Ag{sub 0.04}/LaAlO{sub 3} (001) films

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Xiang, E-mail: lxjim@126.com; Zhao, Shuang; Zhang, Shao-Chun

    2017-01-01

    La{sub 2/3}Ba{sub 1/3}MnO{sub 3}: wt%Ag{sub x} (LBMO:Ag{sub x}, x=0.04) films were prepared on single crystalline (001)-orientated LaAlO{sub 3} substrates by pulsed laser deposition technique. All the samples show along the (00l) orientation in rhombohedral structure with R3c space group. The surface roughness (Ra), insulator-metal transition temperature (Tp) and resistivity at Tp (ρ{sub Tp}) of the LBMO:Ag{sub 0.04} films reached optimal values of 3.29 nm, 288 K and 0.033 Ω cm at 740 °C, respectively. The improvement of electrical transport properties in the films are attributed to the optimal growth temperature and Ag-doping improve the microstructure of the surfaces, grain boundaries (GBs) in connectivity and better crystallization. In addition, the electrical conduction behaviors can be well fitted with the grain/domain boundary, electron–electron and magnon scattering mechanisms in the ferromagnetic metallic region (TTp).

  11. Temperature dependent emission characteristics of monoclinic YBO{sub 3}: Eu{sup 3+}/Tb{sup 3+} phosphor

    Energy Technology Data Exchange (ETDEWEB)

    Sharma, Suchinder K., E-mail: suchindersharma@gmail.com [AMO-Physics Division, Physical Research Laboratory, Navrangpura, Ahmedabad 380009 (India); Malik, M. Manzar [Department of Physics, Maulana Azad National Institute of Technology (MANIT), Bhopal (India)

    2016-05-15

    YBO{sub 3}:Eu{sup 3+}/Tb{sup 3+} phosphor samples synthesized by modified combustion method are studied in the present work using powder X-ray diffraction, UV–visible absorption spectroscopy, X-ray excited luminescence spectroscopy and optical parametric oscillator (OPO) based laser excited emission spectroscopy. The temperature dependence of luminescence emission is also studied. The structural analysis suggests that the samples possess monoclinic structure with C2/c space group. The emission maximum was excitation wavelength dependent and prominent emission was observed at 593 nm (241 nm excitation) and 613 nm (300 nm excitation) for YBO{sub 3}:Eu{sup 3+} samples. The prominent magnetic/ electric (593/613 nm) dipole-moment allowed transitions are attributed to the presence of Eu{sup 3+} at different sites. For YBO{sub 3}:Tb{sup 3+} phosphor, 543 nm emission was prominent and had no impact of the cite symmetry. The increase in PL intensity in Eu{sup 3+} doped samples above 225 K is associated with the carrier mobility. An energy level scheme showing the positions of the 4f and 5d energy levels of all divalent and trivalent lanthanide ions relative to the valence and conduction band of the YBO{sub 3} has been constructed opening the possibility of using YBO{sub 3} for other interesting applications. - Highlights: • Synthesis of YBO{sub 3} by modified combustion method using glycine as fuel. • Crystallization in monoclinic phase (rarely investigated). • Eu and Tb doping and investigation of temperature dependent PL. • VRBE diagram generated in YBO{sub 3} to develop new optical materials.

  12. Photodissociation of van der Waals clusters of isoprene with oxygen, C{sub 5}H{sub 8}-O{sub 2}, in the wavelength range 213-277 nm

    Energy Technology Data Exchange (ETDEWEB)

    Vidma, Konstantin V.; Frederix, Pim W. J. M.; Parker, David H. [Institute for Molecules and Materials, Radboud University Nijmegen, Heyendaalseweg 135, 6525 ED Nijmegen (Netherlands); Baklanov, Alexey V. [Institute of Chemical Kinetics and Combustion, Institutskaja Street 3, Novosibirsk 630090 (Russian Federation) and Novosibirsk State University, Pirogova street 2, Novosibirsk 630090 (Russian Federation)

    2012-08-07

    The speed and angular distribution of O atoms arising from the photofragmentation of C{sub 5}H{sub 8}-O{sub 2}, the isoprene-oxygen van der Waals complex, in the wavelength region of 213-277 nm has been studied with the use of a two-color dissociation-probe method and the velocity map imaging technique. Dramatic enhancement in the O atoms photo-generation cross section in comparison with the photodissociation of individual O{sub 2} molecules has been observed. Velocity map images of these 'enhanced' O atoms consisted of five channels, different in their kinetic energy, angular distribution, and wavelength dependence. Three channels are deduced to be due to the one-quantum excitation of the C{sub 5}H{sub 8}-O{sub 2} complex into the perturbed Herzberg III state ({sup 3}{Delta}{sub u}) of O{sub 2}. This excitation results in the prompt dissociation of the complex giving rise to products C{sub 5}H{sub 8}+O+O when the energy of exciting quantum is higher than the complex photodissociation threshold, which is found to be 41740 {+-} 200 cm{sup -1} (239.6{+-}1.2 nm). This last threshold corresponds to the photodissociation giving rise to an unexcited isoprene molecule. The second channel, with threshold shifted to the blue by 1480 {+-} 280 cm{sup -1}, corresponds to dissociation with formation of rovibrationally excited isoprene. A third channel was observed at wavelengths up to 243 nm with excitation below the upper photodissociation threshold. This channel is attributed to dissociation with the formation of a bound O atom C{sub 5}H{sub 8}-O{sub 2}+hv{yields} C{sub 5}H{sub 8}-O{sub 2}({sup 3}{Delta}{sub u}) {yields} C{sub 5}H{sub 8}O + O and/or to dissociation of O{sub 2} with borrowing of the lacking energy from incompletely cooled complex internal degrees of freedom C{sub 5}H{sub 8}{sup *}-O{sub 2}+hv{yields} C{sub 5}H{sub 8}{sup *}-O{sub 2}({sup 3}{Delta}{sub u}) {yields} C{sub 5}H{sub 8}+ O + O. The kinetic energy of the O atoms arising in two other

  13. Electrical and magnetic properties of spherical SmFeO{sub 3} synthesized by aspartic acid assisted combustion method

    Energy Technology Data Exchange (ETDEWEB)

    Yuvaraj, Subramanian [Solid State Ionics and Energy Devices Laboratory, Department of Physics, Bharathiar University, Coimbatore 641 046 (India); Layek, Samar [Department of Physics, Indian Institute of Technology, Kanpur 208016 (India); Vidyavathy, S. Manisha [Department of Ceramic Technology, Anna University, Chennai 600 025 (India); Yuvaraj, Selvaraj [Solid State Ionics and Energy Devices Laboratory, Department of Physics, Bharathiar University, Coimbatore 641 046 (India); Meyrick, Danielle [School of Engineering and Information Technology, Murdoch University, South St. Murdoch, WA 6150 (Australia); Selvan, R. Kalai, E-mail: selvankram@buc.edu.in [Solid State Ionics and Energy Devices Laboratory, Department of Physics, Bharathiar University, Coimbatore 641 046 (India)

    2015-12-15

    Highlights: • SmFeO{sub 3} is synthesized by simple combustion method using aspartic acid as the fuel. • The particles are spherical in shape with the size ranges between 150 and 300 nm. • Cole–Cole plot infers the bulk conduction mechanism. • Room temperature VSM analysis reveal the weak ferromagnetic behaviour of SmFeO{sub 3}. • Mössbauer analysis elucidates the +3 oxidation state of Fe atoms. - Abstract: Samarium orthoferrite (SmFeO{sub 3}) is synthesized by a simple combustion method using aspartic acid as fuel. Phase purity and functional groups are analyzed via X-ray diffraction (XRD) and Fourier transform infrared (FT-IR) analysis, which confirms the single phase formation of orthorhombic SmFeO{sub 3}. Approximately spherical particles with size range 150–300 nm is revealed by scanning electron microscope (SEM). The conductivity of the material is identified by the single semicircle obtained in the solid state impedance spectra at elevated temperatures. The calculated electrical conductivity increases with increasing temperature, inferring the semiconducting nature of SmFeO{sub 3}. A magnetic study at room temperature revealed weak ferromagnetic behaviour in SmFeO{sub 3} due to Dzyaloshinsky–Moriya antisymmetric exchange interaction mechanism. Mössbauer analysis confirmed the +3 oxidation state of iron and magnetic ordering of the sample at room temperature.

  14. Freeze-drying synthesis of Li{sub 3}V{sub 2}(PO{sub 4}){sub 3}/C cathode material for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Qiao, Y.Q. [State Key Laboratory of Silicon Materials, Department of Materials Science and Engineering, Zhejiang University, Hangzhou 310027 (China); Wang, X.L., E-mail: wangxl@zju.edu.cn [State Key Laboratory of Silicon Materials, Department of Materials Science and Engineering, Zhejiang University, Hangzhou 310027 (China); Mai, Y.J.; Xia, X.H.; Zhang, J.; Gu, C.D. [State Key Laboratory of Silicon Materials, Department of Materials Science and Engineering, Zhejiang University, Hangzhou 310027 (China); Tu, J.P., E-mail: tujp@zju.edu.cn [State Key Laboratory of Silicon Materials, Department of Materials Science and Engineering, Zhejiang University, Hangzhou 310027 (China)

    2012-09-25

    Highlights: Black-Right-Pointing-Pointer Li{sub 3}V{sub 2}(PO{sub 4}){sub 3}/C was synthesized by freeze-drying method. Black-Right-Pointing-Pointer A specific capacity of 105.6 mAh g{sup -1} can be obtained at 14.8 C. Black-Right-Pointing-Pointer 93.3 mAh g{sup -1} can be delivered at a higher current density of 29.6 C. Black-Right-Pointing-Pointer The Li{sub 3}V{sub 2}(PO{sub 4}){sub 3}/C electrode shows a good cycling performance. - Abstract: Li{sub 3}V{sub 2}(PO{sub 4}){sub 3}/C cathode material was synthesized by using a freeze-drying method followed by carbon-thermal reduction. This as-prepared material has a uniform particle size distribution and a well carbon coating on the surface of Li{sub 3}V{sub 2}(PO{sub 4}){sub 3} particles. The Li{sub 3}V{sub 2}(PO{sub 4}){sub 3}/C exhibits good electrochemical performance and cycling stability. Between 3.0 and 4.3 V, the composite delivered a reversible capacity of 125.2 mAh g{sup -1} at a charge-discharge rate of 1.48 C (1 C = 133 mA g{sup -1}) and without obviously capacity fading after 100 cycles. Even at 14.8 C and 29.6 C rates, it can still deliver discharge capacities of 105.6 mAh g{sup -1} and 93.3 mAh g{sup -1}, and the discharge capacities of 84.5 and 60.5 mAh g{sup -1} are sustained after 500 cycles, respectively.

  15. Functionalized multimodal ZnO@Gd{sub 2}O{sub 3} nanosystems to use as perspective contrast agent for MRI

    Energy Technology Data Exchange (ETDEWEB)

    Babayevska, Nataliya, E-mail: natbab@amu.edu.pl; Florczak, Patryk; Woźniak-Budych, Marta; Jarek, Marcin; Nowaczyk, Grzegorz; Zalewski, Tomasz; Jurga, Stefan

    2017-05-15

    Highlights: • The multimodal ZnO@Gd{sub 2}O{sub 3} nanostructures were obtained by wet chemistry methods. • FA and Dox have been effectively bonded onto the ZnO nanoparticles surface. • Functionalized ZnO@Gd{sub 2}O{sub 3} NPs are good contrast agents, useful for MR imaging. - Abstract: The main aim of this research was the synthesis of the multimodal hybrid ZnO@Gd{sub 2}O{sub 3} nanostructures as prospective contrast agent for Magnetic Resonance Imaging (MRI) for bio-medical applications. The nanoparticles surface was functionalized by organosilicon compounds (OSC) then, by folic acid (FA) as targeting agent and doxorubicin (Dox) as chemotherapeutic agent. Doxorubicin and folic acid were attached to the nanoparticles surface by amino groups as well as due to attractive physical interactions. The morphology and crystallography of the nanostructures were studied by HRTEM and SAXS techniques. After ZnO nanoparticles surface modification by Gd{sup 3+} and annealing at 900 °C, ZnO@Gd{sub 2}O{sub 3} nanostructures are polydispersed with size 30–100 nm. NMR (Nuclear Magnetic Resonance) studies of ZnO@Gd{sub 2}O{sub 3} were performed on fractionated particles with size up to 50 nm. Fourier transform infrared spectroscopy (FTIR), UV–vis spectroscopy, zeta-potential measurements and energy dispersive X-ray analysis (EDX) showed that functional groups have been effectively bonded onto the nanoparticles surface. The high adsorption capacity of folic acid (up to 20%) and doxorubicin (up to 40%) on nanoparticles was reached upon 15 min of adsorption process in a temperature-dependent manner. The nuclear magnetic resonance (NMR) relaxation measurements confirmed that the obtained ZnO@Gd{sub 2}O{sub 3} nanostructures could be good contrast agents, useful for magnetic resonance imaging.

  16. Statistical evaluation of potential damage to the Al(OH){sub 3} layer on nTiO{sub 2} particles in the presence of swimming pool and seawater

    Energy Technology Data Exchange (ETDEWEB)

    Virkutyte, Jurate [Pegasus Technical Services, Inc (United States); Al-Abed, Souhail R., E-mail: al-abed.souhail@epa.gov [U.S. Environmental Protection Agency, National Risk Management Research Laboratory (United States)

    2012-03-15

    Nanosized TiO{sub 2} particles (nTiO{sub 2}) are usually coated with an Al(OH){sub 3} layer when used in sunscreen to shield against the harmful effects of free radicals that are generated when these particles are exposed to UV radiation. Therefore, it is vital to insure the structural stability of these particles in the environment where the protective layer may be damaged and adverse health and environmental effects can occur. This study utilized X-ray analysis (SEM-EDS) to provide a qualitative and semi-quantitative assessment of the chemical and physical characteristics of Al(OH){sub 3}-coated original and damaged nTiO{sub 2} particles (used in sunscreen lotion formulations) in the presence of both swimming pool and seawater. Also, by utilizing statistical tools, a distribution of Al/Ti (%) on the particle surface was determined and evaluated. It was found that 45 min of treatment with swimming pool and seawater significantly induced the redistribution of Al/Ti (%), which changed the surface characteristics of particles and, therefore, may have induced undesired photo-activity and the consequent formation of free radicals.

  17. Basic characteristics of atmospheric particles, trace gases and meteorology in a relatively clean Southern African Savannah environment

    Directory of Open Access Journals (Sweden)

    L. Laakso

    2008-08-01

    Full Text Available We have analyzed one year (July 2006–July 2007 of measurement data from a relatively clean background site located in dry savannah in South Africa. The annual-median trace gas concentrations were equal to 0.7 ppb for SO<sub>2sub>, 1.4 ppb for NO<sub>x>, 36 ppb for O<sub>3sub> and 105 ppb for CO. The corresponding PM<sub>1sub>, PM<sub>2.5sub> and PM<sub>10sub> concentrations were 9.0, 10.5 and 18.8 μg m3, and the annual median total particle number concentration in the size range 10–840 nm was 2340 cm3. During Easterly winds, influence of industrial sources approximately 150 km away from the measurement site was clearly visible, especially in SO<sub>2sub> and NO<sub>x> concentrations. Of gases, NO<sub>x> and CO had a clear annual, and SO<sub>2sub>, NO<sub>x> and O<sub>3sub> clear diurnal cycle. Atmospheric new-particle formation was observed to take place in more than 90% of the analyzed days. The days with no new particle formation were cloudy or rainy days. The formation rate of 10 nm particles varied in the range of 0.1–28 cm3 s−1 (median 1.9 cm3 s−1 and nucleation mode particle growth rates were in the range 3–21 nm h−1 (median 8.5 nm h−1. Due to high formation and growth rates, observed new particle formation gives a significant contribute to the number of cloud condensation nuclei budget, having a potential to affect the regional climate forcing patterns.

  18. Cold white light generation through the simultaneous emission from Ce{sup 3+}, Dy{sup 3+} and Mn{sup 2+} in 90Al{sub 2}O{sub 3}{center_dot}2CeCl{sub 3}{center_dot}3DyCl{sub 3}{center_dot}5MnCl{sub 2} thin film

    Energy Technology Data Exchange (ETDEWEB)

    Gonzalez, W. [Departamento de Fisica, Universidad Autonoma Metropolitana-Iztapalapa, P.O. Box 55-534, Mexico, D.F. 09340 (Mexico); Alvarez, E. [Departamento de Fisica, Universidad de Sonora (UNISON), Boulevard Luis Encinas y Rosales s/n, Hermosillo, Sonora 83000 (Mexico); Martinez-Martinez, R.; Yescas-Mendoza, E. [Instituto de Fisica y Matematicas, Universidad Tecnologica de la Mixteca, Carretera a Acatlima Km. 2.5, Huajuapan de Leon, Oaxaca 69000 (Mexico); Camarillo, I. [Departamento de Fisica, Universidad Autonoma Metropolitana-Iztapalapa, P.O. Box 55-534, Mexico, D.F. 09340 (Mexico); Caldino, U., E-mail: cald@xanum.uam.mx [Departamento de Fisica, Universidad Autonoma Metropolitana-Iztapalapa, P.O. Box 55-534, Mexico, D.F. 09340 (Mexico)

    2012-08-15

    The photoluminescence of a CeCl{sub 3}, DyCl{sub 3} and MnCl{sub 2} doped aluminum oxide film deposited by ultrasonic spray pyrolysis was characterized by excitation, emission and decay time spectroscopy. A nonradiative energy transfer from Ce{sup 3+} to Dy{sup 3+} and Mn{sup 2+} is observed upon UV excitation at 278 nm (peak emission wavelength of AlGaN-based LEDs). Such energy transfer leads to a simultaneous emission of these ions in the blue, green, yellow and red regions, resulting in white light emission with CIE1931 chromaticity coordinates, x=0.34 and y=0.23, which correspond to cold white light with a color temperature of 4900 K. - Highlights: Black-Right-Pointing-Pointer 90Al{sub 2}O{sub 3}{center_dot}2CeCl{sub 3}{center_dot}3DyCl{sub 3}{center_dot}5MnCl{sub 2} thin film (AOCDM) could be prepared by spray pyrolysis. Black-Right-Pointing-Pointer Non-radiative energy transfer from Ce{sup 3+} to Dy{sup 3+} and Mn{sup 2+} takes place in AOCDM. Black-Right-Pointing-Pointer AOCDM (pumped with 278 nm-UV light) can generate 4900 K cold white light.

  19. Tunable blue-green color emitting phosphors Sr{sub 3}YNa(PO{sub 4}){sub 3}F:Eu{sup 2+}, Tb{sup 3+} based on energy transfer for near-UV white LEDs

    Energy Technology Data Exchange (ETDEWEB)

    Jin, Yahong, E-mail: yhjin@gdut.edu.cn; Lv, Yang; Hu, Yihua, E-mail: huyh@gdut.edu.cn; Chen, Li; Ju, Guifang; Mu, Zhongfei

    2017-05-15

    A series of Eu{sup 2+} and Tb{sup 3+} doped Sr{sub 3}YNa(PO{sub 4}){sub 3}F phosphors have been synthesized via a high temperature solid state reaction method. Eu{sup 2+} activated Sr{sub 3}YNa(PO{sub 4}){sub 3}F phosphors can be efficiently excited by light in the range of 220–420 nm, which matches well with the commercial n-UV LEDs, and show intense blue emission centered at 456 nm. The optimal doping concentration of Eu{sup 2+} is determined to be 1 mol%. The concentration quenching mechanism of Eu{sup 2+} in SYNPF host is mainly attributed to the dipole-dipole interaction. Energy transfer from Eu{sup 2+} to Tb{sup 3+} is observed when Eu{sup 2+} and Tb{sup 3+} are co-doped into Sr{sub 3}YNa(PO{sub 4}){sub 3}F host. Under excitation of 380 nm, the emission color can be varied from blue to green along with the increase of Tb{sup 3+} doping concentration. Based on decay curves, the energy transfer from the Eu{sup 2+} to Tb{sup 3+} ions is demonstrated to be a dipole–dipole mechanism. According to thermal quenching study by yoyo experiments of heating-cooling, Sr{sub 3}YNa(PO{sub 4}){sub 3}F:Eu{sup 2+}, Tb{sup 3+} shows good thermal stability. The thermal quenching mechanism is also discussed. The results indicate that as-prepared samples might be of potential application in w-LEDs.

  20. ANTS-anchored Zn-Al-CO{sub 3}-LDH particles as fluorescent probe for sensing of folic acid

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Pengfei; Liu, Dan; Liu, Yanhuan [State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing 100029 (China); Beijing Key Laboratory of Environmentally Harmful Chemical Analysis, Beijing University of Chemical Technology, Beijing 100029 (China); Li, Lei, E-mail: lilei@mail.buct.edu.cn [State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing 100029 (China); Beijing Key Laboratory of Environmentally Harmful Chemical Analysis, Beijing University of Chemical Technology, Beijing 100029 (China)

    2016-09-15

    A novel fluorescent nanosensor for detecting folic acid (FA) in aqueous media has been developed based on 8-aminonaphthalene-1,3,6-trisulfonate (ANTS) anchored to the surface of Zn-Al-CO{sub 3}-layered double hydroxides (LDH) particles. The nanosensor showed high fluorescence intensity and good photostability due to a strong coordination interaction between surface Zn{sup 2+} ions of Zn-Al-CO{sub 3}-LDH and N atoms of ANTS, which were verified by result of X-ray photoelectron spectroscopy (XPS). ANTS-anchored on the surface of Zn-Al-CO{sub 3}-LDH restricted the intra-molecular rotation leading to ANTS-anchored J-type aggregation emission enhancement. ANTS-anchored Zn-Al-CO{sub 3}-LDH particles exhibited highly sensitive and selective response to FA over other common metal ions and saccharides present in biological fluids. The proposed mechanism was that oxygen atoms of -SO{sub 3} groups in ANTS-anchored on the surface of Zn-Al-CO{sub 3}-LDH were easily collided by FA molecules to form potential hydrogen bonds between ANTS-anchored and FA molecules, which could effectively quench the ANTS-anchored fluorescence. Under the simulated physiological conditions (pH of 7.4), the fluorescence quenching was fitted to Stern-Volmer equation with a linear response in the concentration range of 1 μM to 200 μM with a limit of detection of 0.1 μM. The results indicate that ANTS-anchored Zn-Al-CO{sub 3}-LDH particles can afford a very sensitive system for the sensing FA in aqueous solution. - Highlights: • A novel fluorescent nanosensor has been developed. • The sensor exhibited highly sensitive and selective response to FA. • The fluorescence quenching was fitted to Stern–Volmer equation. • The linear response range was 1–200 μM with a limit of detection of 0.1 μM.

  1. Random telegraph signal amplitudes in sub 100 nm (decanano) MOSFETs: a 3D `Atomistic' simulation study

    OpenAIRE

    Asenov, A.; Balasubramaniam, R.; Brown, A.R.; Davies, J.H.; Saini, S.

    2000-01-01

    In this paper we use 3D simulations to study the amplitudes of random telegraph signals (RTS) associated with the trapping of a single carrier in interface states in the channel of sub 100 nm (decanano) MOSFETs. Both simulations using continuous doping charge and random discrete dopants in the active region of the MOSFETs are presented. We have studied the dependence of the RTS amplitudes on the position of the trapped charge in the channel and on the device design parameters. We have observe...

  2. Synthesis and luminescence enhancement of CaTiO{sub 3}:Bi{sup 3+} yellow phosphor by codoping Al{sup 3+}/B{sup 3+} ions

    Energy Technology Data Exchange (ETDEWEB)

    Cao, Renping, E-mail: jxcrp@163.com; Fu, Ting; Xu, Haidong; Luo, Wenjie; Peng, Dedong; Chen, Zhiquan; Fu, Jingwei

    2016-07-25

    CaTiO{sub 3}:Bi{sup 3+} and CaTiO{sub 3}:Bi{sup 3+}, Al{sup 3+}/B{sup 3+} phosphors are synthesized by solid-state reaction method in air. With excitation 272 and 320 nm, broad PL band peaking at 555 nm with full width at half maximum ∼200 nm is observed in the range of 400–800 nm due to the {sup 3}P{sub 1,0} → {sup 1}S{sub 0} transitions of Bi{sup 3+} ion. PLE spectrum monitored at 555 nm contains two PLE band peaking at ∼272 and 320 nm within the range 230–420 nm owing to metal-to-metal charge-transfer and {sup 1}S{sub 0} → {sup 3}P{sub 1} transition of Bi{sup 3+} ion, respectively. The optimal Bi{sup 3+} doping concentration in CaTiO{sub 3}:Bi{sup 3+} phosphor is about 0.5 mol%. Luminescence properties of CaTiO{sub 3}:Bi{sup 3+} phosphor may be improved obviously by co-doping Al{sup 3+}/B{sup 3+} ions, and its emission intensity can be enhanced 13–15 times after Al{sup 3+} ion is co-doped. Luminous mechanism of CaTiO{sub 3}:Bi{sup 3+} phosphor is analyzed by energy level diagram of Bi{sup 3+} ion. Decay curve and time-resolved spectra confirm that only a single type of Bi{sup 3+} luminescence center exists in CaTiO{sub 3}:Bi{sup 3+} phosphor. - Graphical abstract: PL spectra of CaTiO{sub 3}:Bi{sup 3+} and CaTiO{sub 3}:Bi{sup 3+}, Al{sup 3+}/B{sup 3+} phosphors and the corresponding pictures under 365 nm UV lamp. - Highlights: • CaTiO{sub 3}:Bi{sup 3+} and CaTiO{sub 3}:Bi{sup 3+}, Al{sup 3+}/B{sup 3+} phosphors are synthesized by solid-state reaction in air. • Broadband emission with FWHM ∼200 nm is observed within the range 400–800 nm. • Luminescence properties of CaTiO{sub 3}:Bi{sup 3+} phosphor can be improved by codoping Al{sup 3+}/B{sup 3+} ions. • PL intensity of CaTiO{sub 3}:Bi{sup 3+} phosphor can be enhanced 13–15 times after Al{sup 3+} ion is codoped.

  3. Tapping mode SPM local oxidation nanolithography with sub-10 nm resolution

    International Nuclear Information System (INIS)

    Nishimura, S; Ogino, T; Shirakashi, J; Takemura, Y

    2008-01-01

    Tapping mode SPM local oxidation nanolithography with sub-10 nm resolution is investigated by optimizing the applied bias voltage (V), scanning speed (S) and the oscillation amplitude of the cantilever (A). We fabricated Si oxide wires with an average width of 9.8 nm (V = 17.5 V, S 250 nm/s, A = 292 nm). In SPM local oxidation with tapping mode operation, it is possible to decrease the size of the water meniscus by enhancing the oscillation amplitude of cantilever. Hence, it seems that the water meniscus with sub-10 nm dimensions could be formed by precisely optimizing the oxidation conditions. Moreover, we quantitatively explain the size (width and height) of Si oxide wires with a model based on the oxidation ratio, which is defined as the oxidation time divided by the period of the cantilever oscillation. The model allows us to understand the mechanism of local oxidation in tapping mode operation with amplitude modulation. The results imply that the sub-10 nm resolution could be achieved using tapping mode SPM local oxidation technique with the optimization of the cantilever dynamics

  4. Synthesis and properties of Li{sub 2}SnO{sub 3}/polyaniline nanocomposites as negative electrode material for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Wang Qiufen [School of Science, Northwestern Polytechnical University, Xi' an 710129 (China); School of Physics and Chemistry, Henan Polytechnic University, Jiaozuo 454000 (China); Huang Ying, E-mail: yingh@nwpu.edu.cn [School of Science, Northwestern Polytechnical University, Xi' an 710129 (China); Miao Juan [School of Physics and Chemistry, Henan Polytechnic University, Jiaozuo 454000 (China); Zhao Yang; Wang Yan [School of Science, Northwestern Polytechnical University, Xi' an 710129 (China)

    2012-10-01

    Highlights: Black-Right-Pointing-Pointer Li{sub 2}SnO{sub 3}/polyaniline nanocomposite (40-50 nm) was synthesized by micro emulsion polymerization. Black-Right-Pointing-Pointer Li{sub 2}SnO{sub 3}/PANI exhibits lower initial irreversible capacities than Li{sub 2}SnO{sub 3}. Black-Right-Pointing-Pointer Its capacity retains 569.2 mAh g{sup -1} after 50 cycles. - Abstract: The nanocomposites Li{sub 2}SnO{sub 3}/polyaniline (Li{sub 2}SnO{sub 3}/PANI) have been synthesized by a micro emulsion polymerization method. The structure, morphology and electrochemical properties of the as-prepared materials are characterized by XRD, FTIR, Raman, XPS, TGA, TEM and electrochemical measurements. Results show that Li{sub 2}SnO{sub 3}/PANI nanocomposites are composed of uniform and blocky nano-sized particles (40-50 nm) with clear lattice fringes. Electrochemical measurement suggests that Li{sub 2}SnO{sub 3}/PANI exhibits better cycling properties and lower initial irreversible capacities than Li{sub 2}SnO{sub 3} as negative electrodes materials for lithium-ion batteries. At a current density of 60 mA g{sup -1} in the voltage about 0.05-2.0 V, the initial irreversible capacity of Li{sub 2}SnO{sub 3}/PANI is 563 mAh g{sup -1} while it is 687.5 mAh g{sup -1} to Li{sub 2}SnO{sub 3}. The capacity retained of Li{sub 2}SnO{sub 3}/PANI (569.2 mAh g{sup -1}) is higher than that of Li{sub 2}SnO{sub 3} (510.2 mAh g{sup -1}) after 50 cycles. The PANI in the Li{sub 2}SnO{sub 3}/PANI nanocomposites can buffer the released stress caused by the drastic volume variation during the alloying/de-alloying process of Li-Sn.

  5. Magnetic and superconductivity studies on (In{sub 1−x}Fe{sub x}){sub 2}O{sub 3} thin films

    Energy Technology Data Exchange (ETDEWEB)

    Sai Krishna, N. [Thin Films Laboratory, School of Advanced Sciences, VIT University, Vellore 632 014, Tamil Nadu (India); Kaleemulla, S., E-mail: skaleemulla@gmail.com [Thin Films Laboratory, School of Advanced Sciences, VIT University, Vellore 632 014, Tamil Nadu (India); Amarendra, G. [Materials Science Group, Indira Gandhi Centre for Atomic Research, Kalpakkam 603 102, Tamil Nadu (India); UGC-DAE-CSR, Kalpakkam Node, Kokilamedu 603 104, Tamil Nadu (India); Madhusudhana Rao, N.; Krishnamoorthi, C.; Rigana Begam, M. [Thin Films Laboratory, School of Advanced Sciences, VIT University, Vellore 632 014, Tamil Nadu (India); Omkaram, I. [Department of Electronics and Radio Engineering, Kyung Hee University, Yongin-si Gyeonggi-do 446-701 (Korea, Republic of); Sreekantha Reddy, D. [Department of Physics and Sungkyunkwan Advanced Institute of Nanotechnology (SAINT), Sungkyunkwan University, Suwon 440-746 (Korea, Republic of)

    2015-07-15

    Highlights: • Fe doped In{sub 2}O{sub 3} thin films deposited using electron beam evaporation technique. • Characterization of the samples using XRD, SEM, EDAX, AES, Raman spectroscopy, FT-IR, VSM and magnetoresistance. • All Fe doped In{sub 2}O{sub 3} thin films exhibited the cubic structure of In{sub 2}O{sub 3}. • Pure and Fe doped In{sub 2}O{sub 3} samples exhibited room temperature ferromagnetism and superconductivity at 2 K. - Abstract: Magnetic, magnetoresistivity and superconductivity studies were carried out on (In{sub 1−x}Fe{sub x}){sub 2}O{sub 3} (x = 0.00, 0.03, 0.05 and 0.07) thin films (2D structures) grown on glass substrate by electron beam evaporation technique at 350 °C. The films have an average size of 120 nm particles. All the samples shown soft ferromagnetic hysteresis loops at room temperature and saturation magnetization increased with iron dopant concentration. Observed magnetization could be best interpreted by F-center mediated magnetic exchange interaction in the samples. Temperature dependent resistivity of the sample (x = 0.00 and 0.07) showed metallic behavior down to very low temperatures and superconductivity at 2 K for undoped In{sub 2}O{sub 3} whereas the In{sub 1.86}Fe{sub 0.14}O{sub 3} sample shows superconductivity below 2 K in the absence of magnetic fields. The reduction in transition temperature was attributed to increase electrical disorder with iron doping. Both samples showed positive magnetoresistivity (MR) in superconducting state due to increase of resistivity resulting from breaking of superconducting Cooper pairs upon application of magnetic field. In addition, both the samples show feeble negative MR in normal electrical state. The observed MR in normal state is not due to spin polarized tunneling instead it is due to suppression of scattering of charge carrier by single occupied localized states.

  6. Energy-loss straggling study of proton and alpha-particle beams incident onto ZrO{sub 2} and Al{sub 2}O{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Behar, M.; Fadanelli, R.C. [Instituto de Fisica, Universidade Federal do Rio Grande do Sul, Porto Alegre, 91501-970 (Brazil); Abril, I. [Departamento de Fisica Aplicada, Universitat d' Alacant, 03080 Alacant (Spain); Garcia-Molina, R. [Departamento de Fisica, Centro de Investigacion en Optica y Nanofisica, Universidad de Murcia, 30100 Murcia (Spain); Nagamine, L.C.C. [Instituto de Fisica, Universidade de Sao Paulo, C.P.66318, 05315-970 Sao Paulo (Brazil)

    2011-10-15

    The energy-loss straggling of zirconia (ZrO{sub 2}) and alumina (Al{sub 2}O{sub 3}) has been experimentally determined for proton and alpha-particle beams mainly by means of the Rutherford backscattering technique and in some few cases using the transmission method. The incident energies of the projectiles covers a wide range, from 200 keV up to 2000 keV for H{sup +} and from 200 keV up to 4000 keV for He{sup +} in zirconia films. In the case of alumina films the studied energy range was 100 keV - 3000 keV for H{sup +} and 100 keV - 6000 keV for He{sup +}. Our experimental results compare very well with theoretical calculations based on the dielectric formalism and a suitable description of the electronic excitation spectrum of ZrO{sub 2} and Al{sub 2}O{sub 3} films through their energy-loss function. (authors)

  7. Microstructure of a commercial W–1% La{sub 2}O{sub 3} alloy

    Energy Technology Data Exchange (ETDEWEB)

    Shen, Yinzhong, E-mail: shenyz@sjtu.edu.cn; Xu, Zhiqiang; Cui, Kai; Yu, Jie

    2014-12-15

    W–1% La{sub 2}O{sub 3} alloy is considered as the most promising material for plasma-facing components of fusion reactors. The microstructure of a commercial W–1% La{sub 2}O{sub 3} alloy was investigated using optical and transmission electron microscopes. The microstructure of pure tungsten can be improved significantly by fabrication of W–1% La{sub 2}O{sub 3} alloys. W–1% La{sub 2}O{sub 3} alloys can be produced with no porosities and cracks, and with various oxide phases dispersed in alloy matrix. La{sub 2}O{sub 3} with different crystal structures, La{sub 6}W{sub 2}O{sub 15}, WO{sub 2}, WO{sub 3} and W{sub 3}O{sub 8} phases were identified in as-forged W–1% La{sub 2}O{sub 3} alloy. Long strip-like La{sub 2}O{sub 3} has a very large size, whereas spherical La{sub 6}W{sub 2}O{sub 15}, navicular WO{sub 3}, hexagonal W{sub 3}O{sub 8} and short rod-like La{sub 2}O{sub 3} are smaller particles. Most identified phases have a heterogeneous distribution. Forging leads to a more dispersive distribution of large-sized La{sub 2}O{sub 3} particles but not of fine WO{sub 3} particles compared with rolling. The mechanical properties of the alloys are also discussed.

  8. High critical currents in heavily doped (Gd,Y)Ba{sub 2}Cu{sub 3}O{sub x} superconductor tapes

    Energy Technology Data Exchange (ETDEWEB)

    Selvamanickam, V., E-mail: selva@uh.edu; Gharahcheshmeh, M. Heydari; Xu, A.; Galstyan, E.; Delgado, L. [Department of Mechanical Engineering and Texas Center for Superconductivity, University of Houston, 4800 Calhoun Rd., Houston, Texas 77204-4006 (United States); Cantoni, C. [Oak Ridge National Laboratory, Oak Ridge, Tennessee 37381 (United States)

    2015-01-19

    REBa{sub 2}Cu{sub 3}O{sub x} ((REBCO), RE = rare earth) superconductor tapes with moderate levels of dopants have been optimized for high critical current density in low magnetic fields at 77 K, but they do not exhibit exemplary performance in conditions of interest for practical applications, i.e., temperatures less than 50 K and fields of 2–30 T. Heavy doping of REBCO tapes has been avoided by researchers thus far due to deterioration in properties. Here, we report achievement of critical current densities (J{sub c}) above 20 MA/cm{sup 2} at 30 K, 3 T in heavily doped (25 mol. % Zr-added) (Gd,Y)Ba{sub 2}Cu{sub 3}O{sub x} superconductor tapes, which is more than three times higher than the J{sub c} typically obtained in moderately doped tapes. Pinning force levels above 1000 GN/m{sup 3} have also been attained at 20 K. A composition map of lift factor in J{sub c} (ratio of J{sub c} at 30 K, 3 T to the J{sub c} at 77 K, 0 T) has been developed which reveals the optimum film composition to obtain lift factors above six, which is thrice the typical value. A highly c-axis aligned BaZrO{sub 3} (BZO) nanocolumn defect density of nearly 7 × 10{sup 11 }cm{sup −2} as well as 2–3nm sized particles rich in Cu and Zr have been found in the high J{sub c} films.

  9. Fischer-Tropsch synthesis: Support and cobalt cluster size effects on kinetics over Co/Al{sub 2}O{sub 3} and Co/SiO{sub 2} catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Wenping Ma; Gary Jacobs; Dennis E. Sparks; Muthu K. Gnanamani; Venkat Ramana Rao Pendyala; Chia H. Yen; Jennifer L.S. Klettlinger; Thomas M. Tomsik; Burtron H. Davis [University of Kentucky, Lexington, KY (USA). Center for Applied Energy Research

    2011-02-15

    The influence of support type and cobalt cluster size (i.e., with average diameters falling within the range of 8-40 nm) on the kinetics of Fischer-Tropsch synthesis (FT) were investigated by kinetic tests employing a CSTR and two Co/{gamma}-Al{sub 2}O{sub 3} catalysts having different average pore sizes, and two Co/SiO{sub 2} catalysts prepared on the same support but having different loadings. A kinetic model -r{sub CO}=kP{sup a}{sub co}P{sup b}{sub H2}/(1 + mP{sub H2O}/P{sub H2}) that contains a water effect constant 'm' was used to fit the experimental data obtained with all four catalysts. Kinetic parameters suggest that both support type and average Co particle size impact FT behavior. Cobalt cluster size influenced kinetic parameters such as reaction order, rate constant, and the water effect parameter.Decreasing the average Co cluster diameter by about 30% led to an increase in the intrinsic reaction rate constant k, defined on a per g of catalyst basis, by 62-102% for the {gamma}-Al{sub 2}O{sub 3} and SiO{sub 2}-supported cobalt catalysts. Moreover, less inhibition by adsorbed CO and greater H{sub 2} dissociation on catalysts having smaller Co particles was suggested by the higher a and lower b values obtained for the measured reaction orders. Irrespective of support type, the catalysts having smaller average Co particles were more sensitive to water. Comparing the catalysts having strong interactions between cobalt and support (Co/Al{sub 2}O{sub 3}) to the ones with weak interactions (Co/SiO{sub 2}), the water effect parameters were found to be positive (indicating a negative influence on CO conversion) and negative (denoting a positive effect on CO conversion), respectively. Greater a and a/b values were observed for both Al{sub 2}O{sub 3}-supported Co catalysts, implying greater inhibition of the FT rate by strongly adsorbed CO on Co/Al{sub 2}O{sub 3} relative to Co/SiO{sub 2}. 78 refs., 4 figs., 3 tabs.

  10. Combustion synthesis of CaSc{sub 2}O{sub 4}:Ce{sup 3+} nano-phosphors in a closed system

    Energy Technology Data Exchange (ETDEWEB)

    Peng Wenfang; Zou Shaoyu; Liu Guanxi; Xiao Quanlan; Zhang Rui; Xie Lijuan; Cao Liwei [Department of Chemistry, Jinan University, Guangzhou 510632 (China); Meng Jianxin, E-mail: tmjx@jnu.edu.cn [Institute of Nano-Chemistry, Jinan University, Guangzhou 510632 (China); Liu Yingliang [Institute of Nano-Chemistry, Jinan University, Guangzhou 510632 (China)

    2011-06-09

    Highlights: > CaSc{sub 2}O{sub 4}:Ce{sup 3+} nano-phosphors can be prepared by a single-step combustion method. > The ignition temperature is the lowest in the combustion synthesis of Ce{sup 3+}/Eu{sup 2+} doped phosphors. > The as-prepared nano-phosphors give a uniform particle size in the range of 15-20 nm and have highly dispersity and fluorescence intensity. > It is a convenient method for preparation of monodispersed oxide nano-phosphors, especially those being sensitive to air at high temperature. - Abstract: The CaSc{sub 2}O{sub 4}:Ce{sup 3+} nano-phosphors were successfully prepared by a single-step combustion method at an ignition temperature as low as 200 deg. C in a closed autoclave using glycine as a fuel and PEG4000 as a dispersant. The samples were characterized by X-ray diffraction (XRD), photoluminescence (PL) spectroscopy, scanning electron microscopy (SEM) and transmission electron microscope (TEM). The results revealed that CaSc{sub 2}O{sub 4}:Ce{sup 3+} nano-phosphors can be conveniently prepared at an ignition temperature as low as 200 deg. C, which was much lower than that in the ordinary combustion methods. The optimized ignition temperature was 220 deg. C. The CaSc{sub 2}O{sub 4}:Ce{sup 3+} nano-phosphors give a uniform particle size in the range of 15-20 nm. The low ignition temperature and the addition of PEG4000 dispersant play important roles in the formation of small sized nanoparticles. The as-prepared nano-phosphors were incompact aggregates, but highly dispersed nano-phosphors can be obtained after further ultrasonic treatment. The CaSc{sub 2}O{sub 4}:Ce{sup 3+} nano-phosphors give satisfactory luminescence characteristic benefiting from the closed circumstance, in which cerium atoms can be isolated from the oxidizing atmosphere and non-fluorescent Ce{sup 4+} ions can be ruled out. The present highly dispersed CaSc{sub 2}O{sub 4}:Ce{sup 3+} nano-phosphors with efficient fluorescence are promising in the field of biological labeling

  11. Mechanically activated synthesis of nanocrystalline ternary carbide Fe{sub 3}Mo{sub 3}C

    Energy Technology Data Exchange (ETDEWEB)

    Zakeri, M. [Materials Science Department, Islamic Azad University (Saveh branch), Saveh (Iran, Islamic Republic of)], E-mail: M_zakeri@iau-saveh.ac.ir; Rahimipour, M.R. [Ceramic Department, Materials and Energy Research Center, Tehran (Iran, Islamic Republic of); Khanmohammadian, A. [Materials Science Department, Islamic Azad University (Saveh branch), Saveh (Iran, Islamic Republic of)

    2008-09-25

    In this investigation, Fe{sub 3}Mo{sub 3}C ternary carbide was synthesized from the elemental powders of 3Mo/3Fe/C by mechanical milling and subsequent heat treatment. Structural and morphological evolutions of powders were studied by X-ray diffraction (XRD) and scanning electron microscopy (SEM). Results showed that no phase transformation occurs during milling. A nanostructure Mo (Fe) solid solution obtained after 30 h of milling. With increasing milling time to 70 h no change takes place except grain size reduction to 9 nm and strain enhancement to 0.86%. Milled powders have spheroid shape and very narrow size distribution about 2 {mu}m at the end of milling. Fe{sub 3}Mo{sub 3}C was synthesized during annealing of 70 h milled sample at 700 deg. C. Undesired phases of MoOC and Fe{sub 2}C form at 1100 deg. C. No transformation takes place during annealing of 10 h milled sample at 700 deg. C. Mean grain size and strain get to 69 nm and 0.23% respectively with annealing of 70 h milled sample at 1100 deg. C.

  12. Optimization of La{sub 0.7}Sr{sub 0.3}MnO{sub 3} thin film by pulsed laser deposition for spin injection

    Energy Technology Data Exchange (ETDEWEB)

    Jain, Sourabh, E-mail: sourabhjain@ee.iitb.ac.in [Department of Electrical Engineering, Indian Institute of Technology Bombay, Powai, Mumbai-400076 (India); Sharma, Himanshu [Department of Physics, Indian Institute of Technology Bombay, Powai, Mumbai-400076 (India); Kumar Shukla, Amit [Department of Electrical Engineering, Indian Institute of Technology Bombay, Powai, Mumbai-400076 (India); Tomy, C.V. [Department of Physics, Indian Institute of Technology Bombay, Powai, Mumbai-400076 (India); Palkar, V.R.; Tulapurkar, Ashwin [Department of Electrical Engineering, Indian Institute of Technology Bombay, Powai, Mumbai-400076 (India)

    2014-09-01

    We have investigated low temperature magnetic properties of La{sub 0.7}Sr{sub 0.3}MnO{sub 3} (LSMO) thin films on SrTiO{sub 3} (STO) substrate deposited by pulsed laser deposition (PLD). We observed a large change in the Curie temperature T{sub C} when the LSMO film thickness is reduced from 4 nm (T{sub C}∼280 K) to 2 nm (T{sub C} ∼100 K), which is a result of high strain present at the STO–LSMO interface. The presence of the strain is confirmed by a grazing angle X-ray diffraction (XRD) technique where a particular peak is shifted away from the bulk peak position as we decrease the thickness. In a LSMO/Pb[Zr{sub y}Ti{sub 1−y}]O{sub 3} (PZT)/LSMO magnetic tunnel junction (MTJ), these LSMO thin films can be used for spin injection into the tunnel barrier. Here spin current can be manipulated by changing the strain present at the LSMO–PZT interface by using piezoelectric properties of PZT.

  13. Parametric investigations on the influence of nano-second Nd{sup 3+}:YAG laser wavelength and fluence in synthesizing NiTi nano-particles using liquid assisted laser ablation technique

    Energy Technology Data Exchange (ETDEWEB)

    Patra, Nandini, E-mail: nandinipatra2007@gmail.com [Centre for Material Science and Engineering, Indian Institute of Technology, Indore, Madhya Pradesh, Pin-453441 (India); Akash, K.; Shiva, S.; Gagrani, Rohit; Rao, H. Sai Pranesh; Anirudh, V.R. [Mechatronics and Instrumentation lab, Discipline of Mechanical Engineering, Indian Institute of Technology, Indore, Madhya Pradesh, Pin-453441 (India); Palani, I.A., E-mail: palaniia@iiti.ac.in [Centre for Material Science and Engineering, Indian Institute of Technology, Indore, Madhya Pradesh, Pin-453441 (India); Mechatronics and Instrumentation lab, Discipline of Mechanical Engineering, Indian Institute of Technology, Indore, Madhya Pradesh, Pin-453441 (India); Singh, Vipul [Centre for Material Science and Engineering, Indian Institute of Technology, Indore, Madhya Pradesh, Pin-453441 (India)

    2016-03-15

    Graphical abstract: - Highlights: • Influence of laser wavelengths (1064 nm, 532 nm and 355 nm) and fluences (40 J/cm{sup 2}, 30 J/cm{sup 2} and 20 J/cm{sup 2}) on generation of underwater laser ablated NiTi nanoparticles. • Particle size range of 140–10 nm was generated at varying laser wavelengths. • The alloy formation of NiTi nanoparticles was confirmed from XRD and TEM analysis where the crystalline peaks of NiTi, Ni{sub 4}Ti{sub 3} and Ni{sub 3}Ti were observed from XRD. • Formation efficiency of NiTi nanoparticles was maximum at 1064 nm wavelength and 40 J/cm{sup 2} fluence. - Abstract: This paper investigates the influence of laser wavelengths and laser fluences on the size and quality of the NiTi nanoparticles, generated through underwater solid state Nd:YAG laser ablation technique. The experiments were performed on Ni55%–Ti45% sheet to synthesize NiTi nano-particles at three different wavelengths (1064 nm, 532 nm and 355 nm) with varying laser fluences ranging from 20 to 40 J/cm{sup 2}. Synthesized NiTi nano-particles were characterized through SEM, DLS, XRD, FT-IR, TEM and UV–vis spectrum. It was observed that, maximum particle size of 140 nm and minimum particle size of 10 nm were generated at varying laser wavelengths. The crystallinity and lattice spacing of NiTi alloy nanoparticles were confirmed from the XRD analysis and TEM images, respectively.

  14. Nd{sup 3+}-doped TeO{sub 2}-Bi{sub 2}O{sub 3}-ZnO transparent glass ceramics for laser application at 1.06 μm

    Energy Technology Data Exchange (ETDEWEB)

    Hu, Xiaolin; Luo, Zhiwei; Liu, Taoyong; Lu, Anxian [Central South of University, School of Materials Science and Engineering, Changsha (China)

    2017-04-15

    The high crystallinity transparent glass ceramics based on Nd{sup 3+}-doped 70TeO{sub 2}-15Bi{sub 2}O{sub 3}-15ZnO (TBZ) compositions were successfully prepared by two-step heat treatment process. The effects of Nd{sub 2}O{sub 3} content on the thermal, structural, mechanical, and optical properties of TBZ glass ceramics were studied. The incorporation of Nd{sub 2}O{sub 3} enhanced the crystallization tendency in the matrix glass composition. The crystal phase and morphology of Bi{sub 2}Te{sub 4}O{sub 11} in the glass ceramics were confirmed by X-ray diffraction and field emission scanning electron microscopy. Due to precipitate more crystal phase, the hardness values increased from 3.21 to 3.66 GPa. Eight absorption peaks were observed from 400 to 900 nm and three emission bands appeared in the range of 850-1400 nm. With the increasing of Nd{sub 2}O{sub 3} content from 0.5 to 2.5 wt%, the intensity of absorption peaks enhanced and the emission intensity increased up to 1.0 wt% and then fell down for further dopant concentration. The fluorescence decay lifetime decreased rapidly starting from 1.5 wt% Nd{sub 2}O{sub 3} content due to the obvious energy migration among Nd{sup 3+}. According to the extreme strong emission band around 1062 nm and the optimum Nd{sub 2}O{sub 3} content (1.0 wt%), N10 glass ceramic was considered as a potential material for 1.06 μm laser applications. (orig.)

  15. Photocatalytic decomposition of N{sub 2}O over TiO{sub 2}/g-C{sub 3}N{sub 4} photocatalysts heterojunction

    Energy Technology Data Exchange (ETDEWEB)

    Kočí, K., E-mail: kamila.koci@vsb.cz [Institute of Environmental technologies, VŠB Technical University of Ostrava 17. listopadu 15/2172, 708 00 Ostrava (Czech Republic); Reli, M.; Troppová, I.; Šihor, M. [Institute of Environmental technologies, VŠB Technical University of Ostrava 17. listopadu 15/2172, 708 00 Ostrava (Czech Republic); Kupková, J. [Nanotechnology center, VŠB Technical University of Ostrava 17. listopadu 15/2172, 708 00 Ostrava (Czech Republic); Kustrowski, P. [Faculty of Chemistry, Jagiellonian University in Kraków, ul. Ingardena 3, 30-060 Kraków (Poland); Praus, P. [Institute of Environmental technologies, VŠB Technical University of Ostrava 17. listopadu 15/2172, 708 00 Ostrava (Czech Republic); Department of Chemistry, VŠB Technical University of Ostrava 17. listopadu 15/2172, 708 00 Ostrava (Czech Republic)

    2017-02-28

    Highlights: • TiO{sub 2}/g-C{sub 3}N{sub 4} photocatalysts with the various TiO{sub 2}/g-C{sub 3}N{sub 4} weight ratios. • N{sub 2}O photocatalytic decomposition under UVC and UVA irradiation. • Heterojunction on the TiO{sub 2}/g-C{sub 3}N{sub 4} interface play an important role. • Optimal ratio of TiO{sub 2}:g-C{sub 3}N{sub 4} was 1:2 for the highest activity at UVA irradiation. - Abstract: TiO{sub 2}/g-C{sub 3}N{sub 4} photocatalysts with the various TiO{sub 2}/g-C{sub 3}N{sub 4} weight ratios from 1:2 to 1:6 were fabricated by mechanical mixing in water suspension followed by calcination. Pure TiO{sub 2} was prepared by thermal hydrolysis and pure g-C{sub 3}N{sub 4} was prepared from commercial melamine by thermal annealing at 620 °C. All the nanocomposites were characterized by X-ray powder diffraction, UV–vis diffuse reflectance spectroscopy, Raman spectroscopy, infrared spectroscopy, scanning electron microscopy, transmission electron microscopy, photoelectrochemical measurements and nitrogen physisorption. The prepared mixtures along with pure TiO{sub 2} and g-C{sub 3}N{sub 4} were tested for the photocatalytic decomposition of nitrous oxide under UVC (λ = 254 nm), UVA (λ = 365 nm) and Vis (λ > 400 nm) irradiation. The TiO{sub 2}/g-C{sub 3}N{sub 4} nanocomposites showed moderate improvement compared to pure g-C{sub 3}N{sub 4} but pure TiO{sub 2} proved to be a better photocatalyst under UVC irradiation. However, under UVA irradiation conditions, the photocatalytic activity of TiO{sub 2}/g-C{sub 3}N{sub 4} (1:2) nanocomposite exhibited an increase compared to pure TiO{sub 2}. Nevertheless, further increase of g-C{sub 3}N{sub 4} amount leads/led to a decrease in reactivity. These results are suggesting the nanocomposite with the optimal weight ratio of TiO{sub 2} and g-C{sub 3}N{sub 4} have shifted absorption edge energy towards longer wavelengths and decreased the recombination rate of charge carriers compared to pure g-C{sub 3}N{sub 4}. This is

  16. 3D nanostar dimers with a sub-10-nm gap for single-/few-molecule surface-enhanced raman scattering

    KAUST Repository

    Chirumamilla, Manohar; Toma, Andrea; Gopalakrishnan, Anisha; Das, Gobind; Proietti Zaccaria, Remo; Krahne, Roman; Rondanina, Eliana; Leoncini, Marco; Liberale, Carlo; De Angelis, Francesco De; Di Fabrizio, Enzo M.

    2014-01-01

    Plasmonic nanostar-dimers, decoupled from the substrate, have been fabricated by combining electron-beam lithography and reactive-ion etching techniques. The 3D architecture, the sharp tips of the nanostars and the sub-10 nm gap size promote the formation of giant electric-field in highly localized hot-spots. The single/few molecule detection capability of the 3D nanostar-dimers has been demonstrated by Surface-Enhanced Raman Scattering. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  17. 3D nanostar dimers with a sub-10-nm gap for single-/few-molecule surface-enhanced raman scattering

    KAUST Repository

    Chirumamilla, Manohar

    2014-01-22

    Plasmonic nanostar-dimers, decoupled from the substrate, have been fabricated by combining electron-beam lithography and reactive-ion etching techniques. The 3D architecture, the sharp tips of the nanostars and the sub-10 nm gap size promote the formation of giant electric-field in highly localized hot-spots. The single/few molecule detection capability of the 3D nanostar-dimers has been demonstrated by Surface-Enhanced Raman Scattering. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  18. Amorphous and nanocrystalline fraction calculus for the Fe{sub 73.5}Si{sub 3.5}Ge{sub 10}Nb{sub 3}B{sub 9}Cu{sub 1} alloy

    Energy Technology Data Exchange (ETDEWEB)

    Muraca, D. [Laboratorio de Solidos Amorfos, Departamento de Fisica, Facultad de Ingenieria, Universidad de Buenos Aires (Argentina); Moya, J. [Laboratorio de Solidos Amorfos, Departamento de Fisica, Facultad de Ingenieria, Universidad de Buenos Aires (Argentina); Carrera del Investigador, CONICET (Argentina); Cremaschi, V.J. [Laboratorio de Solidos Amorfos, Departamento de Fisica, Facultad de Ingenieria, Universidad de Buenos Aires (Argentina) and Carrera del Investigador, CONICET (Argentina)]. E-mail: vcremas@fi.uba.ar; Sirkin, H.R.M. [Laboratorio de Solidos Amorfos, Departamento de Fisica, Facultad de Ingenieria, Universidad de Buenos Aires (Argentina); Carrera del Investigador, CONICET (Argentina)

    2007-09-01

    We studied the relationship between the saturation magnetization (M {sub S}) of the Fe{sub 73.5}Si{sub 3.5}Ge{sub 10}Nb{sub 3}B{sub 9}Cu{sub 1} alloy and its nanocrystalline structure. Amorphous ribbons obtained by the melt spinning technique were heat-treated for 1 h at different temperatures. The optimal treatment to obtain a homogeneous structure of Fe{sub 3}(Si,Ge) nanocrystals with a grain size of around 10 nm embedded in an amorphous matrix involved heating at 540 C for 1 h. We calculated the magnetic contribution of the nanocrystals to the heat treated alloy using a linear model and measured the M {sub S} of the Fe{sub 73.5}Si{sub 3.5}Ge{sub 10}Nb{sub 3}B{sub 9}Cu{sub 1} nanocrystalline and of an amorphous alloy of the same composition of the amorphous matrix: Fe{sub 58}Si{sub 0.5}Ge{sub 3.5}Cu{sub 3}Nb{sub 9}B{sub 26}. Using experimental data and theoretical calculations, we obtained the amorphous and crystalline fraction of the heat-treated ribbons.

  19. Surfaces and their effect on the magnetic properties of polycrystalline hollow γ-Mn{sub 2}O{sub 3} and MnO nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Bah, Mohamed A. [Department of Materials Science and Engineering, Newark, DE (United States); Jaffari, G. Hassnain [Department of Physics, Quaid-i-Azam University, Islamabad 45320 (Pakistan); Khan, F.A. [Department of Physics, Bangladesh University of Engineering and Technology, Dhaka 1000 (Bangladesh); Shah, S. Ismat, E-mail: ismat@udel.edu [Department of Materials Science and Engineering, Newark, DE (United States); Department of Physics and Astronomy, Newark, DE (United States)

    2016-07-01

    Graphical abstract: Polycrystalline hollow nanoparticles composed of γ-Mn{sub 2}O{sub 3} and MnO were grown in an inert gas condensation system. Particles where found to range from 15 nm to 30 nm in diameter with different void sizes. Both γ-Mn{sub 2}O{sub 3} and MnO phases were found to exist in a single nanoparticle, and in close proximity. The oxides had different size and random lattice orientations. The morphology of the nanoparticles with the specific oxide is believed to be the leading cause for the observed high coercivity and exchange bias. - Highlights: • Polycrystalline hollow nanoparticles composed of γ-Mn{sub 2}O{sub 3} (ferrimagnetic(FiM)) and MnO (antiferromagnetic(AFM)) crystallites. • γ-Mn{sub 2}O{sub 3} and MnO co-exist in a single nanoparticles. • FC loops exhibited noticeably larger coercivity compared to the ZFC loops. • Compared to the core/shell counter parts, large coercivity and exchange bias, up to 11 kOe and 7 kOe, respectively, were observed at low temperature. • Strong coupling between the FiM and AFM phases. • Large horizontal and vertical shifts. - Abstract: Manganese oxide nanoparticles were prepared in an inert gas condensation system. X-ray Diffraction (XRD) studies revealed presence of multiple manganese oxide phases while high resolution transmission electron microscopy (HRTEM) showed polycrystalline hollow nanoparticle morphology. The additional inner surface of the hollow nanoparticle directly affect the magnetic properties of these particles. Combined physical structure, electronic structure and magnetic susceptibility analyses led to the conclusion that the prepared nanoparticles are polycrystalline and composed of γ-Mn{sub 2}O{sub 3} and MnO crystallites. Magnetic study found a sharp peak around 38 K with no frequency dependence in the AC susceptibility measurement. Large coercivity (H{sub C}) and exchange bias (H{sub EB}) fields, up to 11 kOe and 7 kOe, respectively, were observed below the order

  20. Structural and light up-conversion luminescence properties of Er{sup 3+}-Yb{sup 3+}-W{sup 6+} substituted Bi{sub 4}Ti{sub 3}O{sub 12}

    Energy Technology Data Exchange (ETDEWEB)

    Bokolia, Renuka, E-mail: renuka1274@gmail.com; Chauhan, Lalita; Sreenivas, K. [Department of Physics & Astrophysics, University of Delhi, Delhi-110007 (India); Rai, Vineet K. [Laser & Spectroscopy Laboratory, Department of Applied Physics, Indian School of Mines, Dhanbad 826 004, Jharkhand (India)

    2016-05-23

    The structural and light up-conversion (UC) luminescence properties of W{sup 6+} substituted Bi{sub 3.79}Er{sub 0.03}Yb{sub 0.18}Ti{sub 3-x}W{sub x}O{sub 12} (0 ≤ x ≤ 0.10) ceramics prepared by solid state reaction method have been investigated. X-ray diffraction (XRD) confirms the formation of single phase material with orthorhombic structure. A decrease in the lattice parameters and unit cell volume is observed with increasing W content. Strong UC luminescence at 527, 548 and 662 nm is seen under an excitation of 980 nm for an optimum W content (x = 0.06) and is attributed to the transitions {sup 2}H{sub 11/2} →{sup 4}I{sub 15/2}, {sup 4}S{sub 3/2} →{sup 4}I{sub 15/2} and {sup 4}F{sub 9/2} →{sup 4}I{sub 15/2} respectively. The improved UC luminescence is ascribed to the reduced defects such as oxygen vacancies and change in the crystal field around Er{sup 3+} ions due to B-site (Ti{sup 4+}) substitution with W{sup 6+} ions. Enhanced UC emission is observed for an optimum content of w{sup 6+} in the prepared composition Bi{sub 3.79}Er{sub 0.03}Yb{sub 0.18}Ti{sub 3-x}W{sub x}O{sub 12} for x = 0.06.

  1. Luminescent properties of Sr{sub 2.5-3x/2}Ba{sub 0.5}Sm{sub x}AlO{sub 4}F oxyfluorides

    Energy Technology Data Exchange (ETDEWEB)

    Park, Sangmoon, E-mail: spark@silla.ac.kr [Department of Engineering in Energy and Applied Chemistry, Silla University, Busan 617-736 (Korea, Republic of)

    2012-04-15

    Effective orange Sm{sup 3+}-doped Sr{sub 2.5}Ba{sub 0.5}AlO{sub 4}F phosphors excited at 254 and 408 nm excitation were prepared by the solid-state method. The excitation and emission spectra of Sr{sub 2.5-3x/2}Ba{sub 0.5}Sm{sub x}AlO{sub 4}F and Sr{sub 2.5-3x/2}Ba{sub 0.5}Sm{sub x}AlO{sub 4-{alpha}}F{sub 1-{delta}} (x=0.001{approx}0.1) based on photoluminescence spectroscopy are investigated. The defects in anion-deficient Sr{sub 2.5-3x/2}Ba{sub 0.5}Sm{sub x}AlO{sub 4-{alpha}}F{sub 1-{delta}} (x=0.001, 0.01) are monitored by broad-band photoluminescence emission centered near 480 nm along with the orange emission transitions of Sm{sup 3+}. CIE values and relative luminescent intensities of Sr{sub 2.5-3x/2}Ba{sub 0.5}Sm{sub x}AlO{sub 4}F and Sr{sub 2.5-3x/2}Ba{sub 0.5}Sm{sub x}AlO{sub 4-{alpha}}F{sub 1-{delta}} by changing the Sm{sup 3+} content (x=0.001{approx}0.1) are discussed. - Highlights: Black-Right-Pointing-Pointer Under the excitation of 408 nm competent orange emitting Sr{sub 2.5-3x/2}Ba{sub 0.5}Sm{sub x}AlO{sub 4}F phosphor is initiated. Black-Right-Pointing-Pointer Sm{sup 3+}-activated oxyfluoride phosphor is quite effective to prepare white-emitting light for near-UV LED applications. Black-Right-Pointing-Pointer Defects could be visibly created in the Sr{sub 2.5-3x/2}Ba{sub 0.5}Sm{sub x}Al O{sub 4}F host lattices when Sm{sup 3+} ions are doped less than 5 mol %. Black-Right-Pointing-Pointer The gradual substitution of Sm{sup 3+} contents in oxyfluoride hosts is amenable to change CIE values and desired emitting intensity.

  2. Direct sampling of sub-µm atmospheric particulate organic matter in sub-ng m-3 mass concentrations by proton-transfer-reaction mass spectrometry

    Science.gov (United States)

    Armin, W.; Mueller, M.; Klinger, A.; Striednig, M.

    2017-12-01

    A quantitative characterization of the organic fraction of atmospheric particulate matter is still challenging. Herein we present the novel modular "Chemical Analysis of Aerosol Online" (CHARON) particle inlet system coupled to a new-generation proton-transfer-reaction time-of-flight mass spectrometer (PTR-TOF 6000 X2, Ionicon Analytik, Austria) that quantitatively detects organic analytes in real-time and sub-pptV levels by chemical ionization with hydronium reagent ions. CHARON consists of a gas-phase denuder for stripping off gas-phase analytes (efficiency > 99.999%), an aerodynamic lens for particle collimation combined with an inertial sampler for the particle-enriched flow and a thermodesorption unit for particle volatilization prior to chemical analysis. With typical particle enrichment factors of around 30 for particle diameters (DP) between 120 nm and 1000 nm (somewhat reduced enrichment for 60 nm 6000) and excellent mass accuracies (< 10 ppm) chemical compositions can be assigned and included in further analyses. In addition to a detailed characterization of the CHARON PTR-TOF 6000 X2 we will present first results on the chemical composition of sub-µm particulate organic matter in the urban atmosphere in Innsbruck (Austria).

  3. Fabrication and Luminescent properties of ZnWO{sub 4}:Eu{sup 3+}, Dy{sup 3+} white light-emitting phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Zhai, Yongqing, E-mail: zhaiyongqinghbu@163.com; Wang, Meng; Zhao, Qian; Yu, Jiabao; Li, Xuemin

    2016-04-15

    ZnWO{sub 4}:Eu{sup 3+},Dy{sup 3+} white light-emitting phosphors were prepared by a hydrothermal method followed with calcination process. The as-synthesized phosphors were characterized by X-ray powder diffraction (XRD), Fourier transform infrared (FTIR) spectrum, Raman spectra, scanning electron microscope (SEM), transmission electron microscope (TEM), diffused reflectance spectra, photoluminescence excitation and emission spectra, and photoluminescence decay curves. Furthermore, external quantum efficiency of ZnWO{sub 4}:Eu{sup 3+},Dy{sup 3+} was determined. The results showed that the obtained phosphors have monoclinic wolframite structure. The particles of the phosphors was nearly spherical in shape, and the particle size was about 70–100 nm. Upon excitation at UV light, the white light-emitting can be obtained by combining the blue–green emission of tungstate group and characteristic emission of Eu{sup 3+} and Dy{sup 3+}. Based on the excitation/emission spectra and decay curves, the energy transfer and photoluminescence mechanism for ZnWO{sub 4}:Eu{sup 3+}, Dy{sup 3+} system were discussed.

  4. The Formation of Lithiated Ti-Doped {alpha}-Fe{sub 2}O{sub 3} Nanocrystalline Particles by Mechanical Milling of Ti-Doped Lithium Spinel Ferrite

    Energy Technology Data Exchange (ETDEWEB)

    Widatallah, H. M., E-mail: hisham@ictp.trieste.it [Khartoum University, Department of Physics (Sudan); Gismelseed, A. M.; Bouziane, K. [Sultan Qaboos University, Department of Physics (Oman); Berry, F. J. [Open University, Department of Chemistry (United Kingdom); Al Rawas, A. D.; Al-Omari, I. A.; Yousif, A. A.; Elzain, M. E. [Sultan Qaboos University, Department of Physics (Oman)

    2004-12-15

    The milling of spinel-related Ti-doped Li{sub 0.5}Fe{sub 2.5}O{sub 4} for different times is studied with XRD, Moessbauer spectroscopy and magnetic measurements. Milling converts the material to Li-Ti-doped {alpha}-Fe{sub 2}O{sub 3} nanocrystalline particles via an intermediate {gamma}-LiFeO{sub 2}-related phase. The role played by the dopant Ti-ion in the process is emphasized.

  5. Synthesis, characterization and formaldehyde gas sensitivity of La{sub 0.7}Sr{sub 0.3}FeO{sub 3} nanoparticles assembled nanowires

    Energy Technology Data Exchange (ETDEWEB)

    Yao Pengjun [School of Electronic Science and Technology, Dalian University of Technology, Dalian 116023 (China); School of Educational Technology, Shenyang Normal University, Shenyang 110034 (China); Wang Jing, E-mail: wangjing@dlut.edu.cn [School of Electronic Science and Technology, Dalian University of Technology, Dalian 116023 (China); Du Haiying [School of Electronic Science and Technology, Dalian University of Technology, Dalian 116023 (China); Department of Electromechanical Engineering and Information, Dalian Nationalities University, Dalian 116600 (China); Qi Jinqing [School of Electronic Science and Technology, Dalian University of Technology, Dalian 116023 (China)

    2012-05-15

    Highlights: Black-Right-Pointing-Pointer High aspect ratio La{sub 0.7}Sr{sub 0.3}FeO{sub 3} nanoparticles assembled nanowires were synthesized by a CTAB assisted hydrothermal method. Black-Right-Pointing-Pointer Formaldehyde with low concentration (0.1-100 ppm) was used for gas sensing study. Black-Right-Pointing-Pointer The growth mechanism of La{sub 0.7}Sr{sub 0.3}FeO{sub 3} nanowires was reported. - Abstract: La{sub 0.7}Sr{sub 0.3}FeO{sub 3} nanoparticles assembled nanowires were synthesized by a hydrothermal method assisted with cetyltrimethylammonium bromide (CTAB). The hydrothermal temperature was 180 Degree-Sign C and the annealed temperature was 700 Degree-Sign C. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) were used to characterize the morphology, composition and structural properties of the materials. The results showed that the La{sub 0.7}Sr{sub 0.3}FeO{sub 3} nanoparticles assembled nanowires had a high aspect ratio (the largest aspect ratio >100); the size of the nanoparticles was about 20 nm and the diameter of the nanowires was about 100-150 nm. The growth mechanism of La{sub 0.7}Sr{sub 0.3}FeO{sub 3} nanowires was discussed. Gas sensors were fabricated by using La{sub 0.7}Sr{sub 0.3}FeO{sub 3} nanowires. Formaldehyde gas sensing properties were carried out in the concentration range of 0.1-100 ppm at the optimum operating temperature of 280 Degree-Sign C. The response and recovery times to 20 ppm formaldehyde of the sensor were 110 s and 50 s, respectively. The gas sensing mechanism of La{sub 0.7}Sr{sub 0.3}FeO{sub 3} nanowires was investigated.

  6. Substitution disorder and photoluminescent property of a new rare-earth borate: K{sub 3}TbB{sub 6}O{sub 12}

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Dan; Ma, Fa-Xue; Huang, Min; Chen, Peng-Fei; Zhang, Rong-Hua [Henan Polytechnic Univ., Jiaozuo (China). College of Chemistry and Chemical Engineering; Zhang, Rui-Juan [Henan Polytechnic University, Jiaozuo (China). Academic Affairs Office; Wei, Wei [Capital Normal Univ., Beijing (China). Dept. of Chemistry

    2016-11-01

    A new rare-earth borate K{sub 3}TbB{sub 6}O{sub 12} has been prepared using the high temperature molten salt method and was structurally determined by single crystal X-ray diffraction analyses. The structure features a three-dimensional (3D) framework which is composed of isolated B{sub 5}O{sub 10}, KO{sub 6}, KO{sub 8} and TbO{sub 6} groups. An atom site in the 3{sub 2} screw axis is shared by K and Tb atoms with the molar ratio of 1:1. The self-activated photoluminescence (PL) property of K{sub 3}TbB{sub 6}O{sub 12} was studied. Under the excitation of 378 nm, the emission spectrum exhibits an intense green emission centered at 543-548 nm with the chromaticity coordinates (0.342, 0.590), which can be assigned to the {sup 5}D{sub 4} → {sup 7}F{sub 5} transition of Tb{sup 3+}. The excitation spectra cover a wide range from 330 to 385 nm, which suggests that the K{sub 3}TbB{sub 6}O{sub 12} phosphors can be effectively excited by a near-UV light source. One may expect that compound K{sub 3}TbB{sub 6}O{sub 12} can be used as a green phosphor pumped by near-UV LED chips.

  7. Enhanced dielectric properties of thin Ta{sub 2}O{sub 5} films grown on 65 nm SiO{sub 2}/Si

    Energy Technology Data Exchange (ETDEWEB)

    Kolkovsky, Vl.; Kurth, E.; Kunath, C. [IPMS Fraunhofer, Dresden, Maria-Reiche Str. 2, 01109 Dresden (Germany)

    2016-12-15

    The structural and electrical properties of Ta{sub 2}O{sub 5}/65 nm SiO{sub 2} structures with different thicknesses of Ta{sub 2}O{sub 5} varying in the range of 0-260 nm are investigated. We find that the stack structures grown by the magnetron sputtering technique and annealed at 1220 K in O and Ar atmosphere show one of the highest dielectric constant of Ta{sub 2}O{sub 5}(about 64) among those previously reported in the literature. The structure of the annealed polycrystalline Ta{sub 2}O{sub 5} films is orthorhombic, as obtained from X-ray diffraction measurements and we do not observe any preferential orientation of the annealed films. The Ta{sub 2}O{sub 5} films contain positively charged defects which become mobile at around 400 K and they are tentatively correlated with the oxygen vacancies. The leakage current in the stack structures is a factor of 20 higher compared to that in thin layers with 65 nm SiO{sub 2}. The conduction mechanism in the stack structures can be described by the Fowler-Nordheim model with a barrier height that decreases slightly (<10%) as a function of the thickness of the films. (copyright 2016 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  8. Characterization and luminescent properties of Eu{sup 3+} doped Gd{sub 2}Zr{sub 2}O{sub 7} nanopowders

    Energy Technology Data Exchange (ETDEWEB)

    Rabasovic, M.S., E-mail: majap@ipb.ac.rs [Institute of Physics, University of Belgrade (Serbia); Sevic, D. [Institute of Physics, University of Belgrade (Serbia); Krizan, J. [Faculty for Mechanical Engineering, University of Ljubljana (Slovenia); Terzic, M. [Faculty of Science, University of Novi Sad (Serbia); Mozina, J. [Faculty for Mechanical Engineering, University of Ljubljana (Slovenia); Marinkovic, B.P.; Savic-Sevic, S. [Institute of Physics, University of Belgrade (Serbia); Mitric, M. [Vinča Institute of Nuclear Science, University of Belgrade, P.O. Box 522, 11001 Belgrade (Serbia); Rabasovic, M.D.; Romcevic, N. [Institute of Physics, University of Belgrade (Serbia)

    2015-02-15

    Highlights: • Nanopowders Gd{sub 2}Zr{sub 2}O{sub 7} doped by europium ions (Eu{sup 3+}) have been synthesized. • Their luminescence properties have been measured at room temperature. • The temporal evolution of laser induced phenomena are presented using time-resolved technique. • Lifetime analysis for luminescence bands in emission spectra has been done. - Abstract: Nanopowders based on gadolinium zirconium oxide (Gd{sub 2}Zr{sub 2}O{sub 7}) doped by europium ions (Eu{sup 3+}) were successfully prepared using a flame combustion method. This material is suitable for various optical devices. The structure of prepared materials has been confirmed and characterized using X-ray powder diffraction (XRD), scanning electron microscope (SEM) and photoluminescence (PL) techniques. The luminescence properties of synthesized nanopowders were characterized by emission spectra and luminescence lifetimes by using the streak camera system. PL spectra were obtained at three different excitation wavelengths (Optical Parametric Oscilator (OPO) at 360 nm, laser diode at 365 nm and Ar laser line at 514.5 nm). The strong emission lines at 611 nm and 630 nm corresponding to the {sup 5}D{sub 0} → {sup 7}F{sub 2} long lived transition could be used as a new red light source in optical devices.

  9. Lattice strain estimation for CoAl{sub 2}O{sub 4} nano particles using Williamson-Hall analysis

    Energy Technology Data Exchange (ETDEWEB)

    Aly, Kamal A., E-mail: kamalaly2001@gmail.com [Physics Department, Faculty of Science & Arts, Khulais, University of Jeddah, Jiddah (Saudi Arabia); Physics Department, Faculty of Science, Al-Azhar University, Assiut Branch, Assiut (Egypt); Khalil, N.M. [Chemistry Department, Faculty of Science & Arts, Khulais, University of Jeddah, Jiddah (Saudi Arabia); Refractories, Ceramics and Building Materials Department, National Research Centre, 12311 Cairo (Egypt); Algamal, Yousif [Chemistry Department, Faculty of Science & Arts, Khulais, University of Jeddah, Jiddah (Saudi Arabia); Saleem, Qaid M.A. [Chemistry Department, Faculty of Science & Arts, Khulais, University of Jeddah, Jiddah (Saudi Arabia); Chemistry Department, Faculty of Education, Aden University, Sabwa (Yemen)

    2016-08-15

    CoAl{sub 2}O{sub 4} nanoparticles were prepared via coprecipitation technique through mixing 1:1 M ratio of cobalt nitrate and aluminium nitrate solutions at pH 10. CoAl{sub 2}O{sub 4} crystalline phase was confirmed by X-ray diffraction. Scanning electron microscopy (SEM) result reveals that the particles of CoAl{sub 2}O{sub 4} fired at 900 °C were relatively small (21 nm) and uniform. Increased temperature to 1200 °C gives rise to blocky particles and changes in the powders shape, that because of agglomeration came from the calcination of CoAl{sub 2}O{sub 4}. Furthermore, the particle size increase with increasing the calcinated temperature. The crystalline sizes were evaluated by using X-ray peak broadening analysis suggested by Williamson-Hall (W-H) analysis. It was successfully applied for lattice strain and to calculate mechanical stress and energy density values using different three models namely uniform deformation model (UDM), uniform deformation stress model (UDSM) and uniform deformation energy density model (UDEDM). Also, the root mean square strain was determined. These models gave a different strain values which suggested an isotropic nature of the nanoparticles. Besides, the obtained results W-H analysis are in good agreement with that deduced from SEM analysis and Scherrer's formula. - Highlights: • CoAl{sub 2}O{sub 4} nanoparticles were prepared via coprecipitation technique. • CoAl{sub 2}O{sub 4} nanoparticles were characterized by SEM and XRD. • the lattice size and strain were investigated according to W-H analysis. • The latic size were investigated by W-H analysis, SEM and Sherrar's method. • The root mean square strain was determined.

  10. Comparative study of nano-sized particles CoFe{sub 2}O{sub 4} effects on superconducting properties of Y-123 and Y-358

    Energy Technology Data Exchange (ETDEWEB)

    Slimani, Y.; Hannachi, E.; Ben Salem, M.K.; Hamrita, A. [Laboratory of Physics of Materials-Structures and Properties, Department of Physics, Faculty of Sciences of Bizerte, University of Carthage, 7021 Zarzouna (Tunisia); Varilci, A. [Faculty of Arts and Sciences, Department of Physics, Abant Izzet Baysal University, 14280 Bolu (Turkey); Dachraoui, W. [CINaM-CNRS, Luminy Campus, 13288 Marseille (France); Ben Salem, M., E-mail: salemwiem2005@yahoo.fr [Laboratory of Physics of Materials-Structures and Properties, Department of Physics, Faculty of Sciences of Bizerte, University of Carthage, 7021 Zarzouna (Tunisia); Ben Azzouz, F. [Laboratory of Physics of Materials-Structures and Properties, Department of Physics, Faculty of Sciences of Bizerte, University of Carthage, 7021 Zarzouna (Tunisia); College of Sciences-Girls, Department of Physics, University of Dammam (Saudi Arabia)

    2014-10-01

    The effects of nano-sized CoFe{sub 2}O{sub 4} particles (10 nm) addition on the structural and the normal state resistivity of YBa{sub 2}Cu{sub 3}O{sub 7} (noted Y-123) and Y{sub 3}Ba{sub 5}Cu{sub 8}O{sub 18} (noted Y-358) polycrystalline were systematically studied. Samples were synthesized in oxygen atmosphere using a standard solid state reaction technique by adding CoFe{sub 2}O{sub 4} up to 2 wt%. Phases, microstructure and superconductivity have been systematically investigated using X-ray diffraction (XRD), scanning electron microscopy (SEM) and electrical measurements ρ(T). XRD results reveal that the lattice parameters change for both Y-123 and Y-358 phases. SEM observations reveal that the grain size is reduced with increasing the content of CoFe{sub 2}O{sub 4}. The measurements for the resistivity dependence of temperature show that the depression in superconducting temperature is more pronounced for CoFe{sub 2}O{sub 4} addition in Y-358 compound than in Y-123 one. These results may be attributed to the existence of much more disorder due to a greater number of Cu sites to be substituted by Fe and Co in Y-358 compared to Y-123.

  11. Single-crystalline spherical β-Ga2O3 particles: Synthesis, N-doping and photoluminescence properties

    International Nuclear Information System (INIS)

    Zhang, Tingting; Lin, Jing; Zhang, Xinghua; Huang, Yang; Xu, Xuewen; Xue, Yanming; Zou, Jin; Tang, Chengchun

    2013-01-01

    We report on the synthesis of single-crystalline spherical β-Ga 2 O 3 particles by a simple method in ambient atmosphere. No pre-treatment, catalyst, substrate, or gas flow was required during the synthesis process. The well-dispersed Ga 2 O 3 particles display uniform spherical morphology with an average diameter of ∼200 nm. Photoluminescence studies indicate that the Ga 2 O 3 particles exhibit a broad blue-green light emission and an interesting red light emission at room temperature. The red light emission can be further tuned by post-annealing of the particles in ammonia atmosphere. The present single-crystalline β-Ga 2 O 3 particles with spherical morphology, uniform sub-micrometer sizes and tunable light emission are envisaged to be of high promise for applications in white-LED phosphors and optoelectronic devices. -- Highlights: ► We prepared single-crystalline spherical β-Ga 2 O 3 particles in ambient atmosphere. ► The particles display uniform spherical morphology with an average diameter of ∼200 nm. ► The Ga 2 O 3 particles exhibit a broad blue-green light and an interesting red light emission. ► The red light emission can be further tuned by post-annealing of the particles

  12. An investigation on photoluminescence and energy transfer of Eu{sup 3+}/Sm{sup 3+} single-doped and co-doped Ca{sub 4}YO(BO{sub 3}){sub 3} phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Bandi, Vengala Rao; Grandhe, Bhaskar Kumar [Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Jang, Kiwan, E-mail: kwjang@changwon.ac.kr [Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Shin, Dong-Soo [Department of Chemistry, Changwon National University, Changwon (Korea, Republic of); Yi, Soung-Soo [Department of Photonics, Silla University, Busan (Korea, Republic of); Jeong, Jung-Hyun [Department of Physics, Pukyong National University, Busan (Korea, Republic of)

    2013-07-15

    The present investigation aims to demonstrate the potentiality of Eu{sup 3+}/Sm{sup 3+} single-doped and co-doped Ca{sub 4}YO(BO{sub 3}){sub 3} phosphors, which were prepared by a sol–gel method. The X-ray diffraction (XRD) profiles showed that all the observed peaks could be attributed to the monoclinic phase of Ca{sub 4}YO(BO{sub 3}){sub 3}. From the measured emission profiles, we have noticed that both the single-doped Eu{sup 3+}/Sm{sup 3+} phosphors shows four emission transitions of {sup 5}D{sub 0} → {sup 7}F{sub 0,1,2,3} and {sup 4}G{sub 5/2} → {sup 6}H{sub 5/2,7/2,9/2,11/2} respectively. Among them, the {sup 5}D{sub 0} → {sup 7}F{sub 2} of Eu{sup 3+} and {sup 4}G{sub 5/2} → {sup 6}H{sub 7/2} of Sm{sup 3+} are intense emission transitions, leading to an intense red color emission from the prepared phosphors. The excitation spectra showed that Eu{sup 3+}/Sm{sup 3+} doped samples can be excited efficiently by 394 nm and 402 nm respectively, incidentally which matches well with the characteristic emission from UVLED. The co-doping of Sm{sup 3+} ions can broaden and strengthen the absorption of near UV region and to be efficient to sensitize the emission of the Ca{sub 4}YO(BO{sub 3}){sub 3}:Eu{sup 3+} phosphor. The mechanism involved in the energy transfer between Eu{sup 3+} and Sm{sup 3+} has been explained and elucidated by an energy level diagram. - Highlights: • Eu{sup 3+} or/and Sm{sup 3+}:Ca{sub 4}YO(BO{sub 3}){sub 3} phosphors were prepared by sol–gel method. • The co-doping of Sm{sup 3+} to Ca{sub 4}YO(BO{sub 3}){sub 3}:Eu{sup 3+} extends its absorption of NUV region. • It has intense absorption in NUV region, which is suitable for NUV LED. • The energy transfer process between Eu{sup 3+} and Sm{sup 3+} ions were discussed.

  13. Microstructural characterization and compression properties of TiC{sub 0.61}/Cu(Al) composite synthesized from Cu and Ti{sub 3}AlC{sub 2} powders

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Zhenying, E-mail: zhyhuang@bjtu.edu.cn [Institute of Material Science and Engineering, School of Mechanical and Electronic Control Engineering, Beijing Jiaotong University, Beijing 100044 (China); Institut PPRIME, Département de Physique et Mécanique des Matériaux, CNRS, Université de Poitiers, ENSMA, UPR 3346, SP2MI, Téléport 2 Boulevard Marie et Pierre Curie, BP 30179, F86962 Futuroscope Chasseneuil Cedex (France); Bonneville, Joel [Institut PPRIME, Département de Physique et Mécanique des Matériaux, CNRS, Université de Poitiers, ENSMA, UPR 3346, SP2MI, Téléport 2 Boulevard Marie et Pierre Curie, BP 30179, F86962 Futuroscope Chasseneuil Cedex (France); Zhai, Hongxiang [Institute of Material Science and Engineering, School of Mechanical and Electronic Control Engineering, Beijing Jiaotong University, Beijing 100044 (China); Gauthier-Brunet, Veronique [Institut PPRIME, Département de Physique et Mécanique des Matériaux, CNRS, Université de Poitiers, ENSMA, UPR 3346, SP2MI, Téléport 2 Boulevard Marie et Pierre Curie, BP 30179, F86962 Futuroscope Chasseneuil Cedex (France); and others

    2014-07-25

    Highlights: • Submicro-layered TiC{sub 0.61}/Cu(Al) nanocomposite. • MAX phase. • High yield stress. • Deformation mechanism. - Abstract: A new submicro-layered TiC{sub 0.61}/Cu(Al) composite has been prepared by hot-pressing a mixture of 50 vol.% Ti{sub 3}AlC{sub 2} and 50 vol.% Cu powders at 1150 °C and 30 MPa. It is shown that the initial reinforcement Ti{sub 3}AlC{sub 2} particles have, after synthesis, an unusual microstructure, which consists of submicron-thick layers of TiC{sub 0.61} and Cu(Al) alloy. Both the width of the TiC{sub 0.61} and Cu(Al) layers are ∼150 nm. Thus, the Ti{sub 3}AlC{sub 2} particles are decomposed into the TiC{sub 0.61} phase, while the additional Al atoms provided by Ti{sub 3}AlC{sub 2} diffuse into the molten Cu matrix at high temperature. Compression tests were performed at constant strain rate in the temperature range 20–800 °C. The new designed TiC{sub 0.61}/Cu(Al) composite has both a high yield stress, σ{sub 0.2} measured at 0.2% strain offset, and a high ultimate compressive strength, σ{sub UCS}, which is attributed to strong interface bonding between TiC{sub 0.61} and Cu(Al) phase. For instance, at 20 and 200 °C, σ{sub 0.2} is 770 MPa and 700 MPa, while σ{sub UCS} is 1.18 GPa and 1 GPa, respectively. Plastic deformation takes place in the Cu(Al) matrix. Wavy slip lines are observed indicating that cross-slip could be the dominant deformation mechanism.

  14. Effect of composition on the spontaneous emission probabilities, stimulated emission cross-sections and local environment of Tm{sup 3+} in TeO{sub 2}-WO{sub 3} glass

    Energy Technology Data Exchange (ETDEWEB)

    Oezen, G. E-mail: gozenl@itu.edu.tr; Aydinli, A.; Cenk, S.; Sennaroglu, A

    2003-04-01

    Effect of composition on the structure, spontaneous and stimulated emission probabilities of various 1.0 mol% Tm{sub 2}O{sub 3} doped (1-x)TeO{sub 2}+(x)WO{sub 3} glasses were investigated using Raman spectroscopy, ultraviolet-visible-near-infrared (UV/VIS/NIR) absorption and luminescence measurements. Absorption measurements in the UV/VIS/NIR region were used to determine spontaneous emission probabilities for the 4f-4f transitions of Tm{sup 3+} ions. Six absorption bands corresponding to the absorption of the {sup 1}G{sub 4}, {sup 3}F{sub 2}, {sup 3}F{sub 3} and {sup 3}F{sub 4}, {sup 3}H{sub 5} and {sup 3}H{sub 4} levels from the {sup 3}H{sub 6} ground level were observed. Integrated absorption cross-section of each band except that of {sup 3}H{sub 5} level was found to vary with the glass composition. Luminescence spectra of the samples were measured upon 457.9 nm excitation. Three emission bands centered at 476 nm ({sup 1}G{sub 4}{yields}{sup 3}H{sub 6} transition), 651 nm ({sup 1}G{sub 4}{yields}{sup 3}H{sub 4} transition) and 800 nm ({sup 1}G{sub 4}{yields}{sup 3}H{sub 5} transition) were observed. Spontaneous emission cross-sections together with the luminescence spectra measured upon 457.9 nm excitation were used to determine the stimulated emission cross-sections of these emissions. The effect of glass composition on the Judd-Ofelt parameters and therefore on the spontaneous and the stimulated emission cross-sections for the metastable levels of Tm{sup 3+} ions were discussed in detail. The effect of temperature on the stimulated emission cross-sections for the emissions observed upon 457.9 nm excitation was also discussed.

  15. Y/Gd-free yellow Lu{sub 3}Al{sub 5}O{sub 12}:Ce{sup 3+} phosphor for white LEDs

    Energy Technology Data Exchange (ETDEWEB)

    Park, Kwangwon [Department of Display Science and Engineering, Pukyong National University, Busan 608-737 (Korea, Republic of); Kim, Taehoon; Yu, Youngmoon [LED-Marine Convergence Technology R& BD Center, Pukyong National University, Busan 608−739 (Korea, Republic of); Seo, Kwangil [L-Stone Co. Ltd., Bucheon 421−807 (Korea, Republic of); Kim, Jongsu, E-mail: jsukim@pknu.ac.kr [Department of Display Science and Engineering, Pukyong National University, Busan 608-737 (Korea, Republic of)

    2016-05-15

    Solid solubility limit of Ce{sup 3+} ions into Lu-based garnet, Lu{sub 3(1−x)}Ce{sub 3x}Al{sub 5}O{sub 12}, was determined as below 6.7 mol% (3x<0.2 mol) through Raman spectra and X−ray diffraction patterns. Above the solid solubility limit (3x≥0.2 mol), Lu{sub 3(1−x)}Ce{sub 3x}Al{sub 5}O{sub 12} phosphors showed the significant redshift to the yellow spectral region without Y{sup 3+} and Gd{sup 3+} ions. The redshift was explained in terms of the local compressive strain at the Ce{sup 3+} sites. The optimized sample (3x=0.4 mol) had a dominant emission wavelength of 548 nm, color coordinate of CIEx=0.421, CIEy=0.548, quantum efficiency of 80%, absorbance of 91%, lumen maintenance of 90% and high color stability at 473 K under 450 nm excitation wavelength, suggesting substitutability for the commercial yellow (Y, Gd){sub 3}(Al, Ga){sub 5}O{sub 12}:Ce{sup 3+} phosphor. The measured decay times at higher Ce{sup 3+} concentration are significantly shortened at higher temperature than that of those at lower Ce{sup 3+} concentration. The yellow Lu{sub 2.6}Ce{sub 0.4}Al{sub 5}O{sub 12} and a commercial red (Sr, Ca)AlSiN{sub 3}:Eu{sup 2+} phosphor were applied to the pc-WLED, it gave an excellent luminous efficiency (138 lm/W) with a slightly lower color rendering index (Ra=76.4) under correlated color temperature of 6500 K compared to those of the (Y, Gd){sub 3}(Al, Ga){sub 5}O{sub 12}:Ce{sup 3+}-based one (136 lm/W, Ra=78.7). Especially, the quantities of the used phosphors were significantly decreased by 20% for the yellow LuAG:Ce and by 40% for the red (Sr, Ca)AlSiN{sub 3}:Eu{sup 2+}. Thus, the Y/Gd−free pure LuAG:Ce yellow phosphors can be used as alternative to the commercial yellow YAG:Ce phosphor.

  16. Broadband sensitized white light emission of g-C{sub 3}N{sub 4}/Y{sub 2}MoO{sub 6}:Eu{sup 3+} composite phosphor under near ultraviolet excitation

    Energy Technology Data Exchange (ETDEWEB)

    Han, Bing, E-mail: hanbing@zzuli.edu.cn [School of Material and Chemical Engineering, Zhengzhou University of Light Industry, Zhengzhou 450002 (China); Xue, Yongfei; Li, Pengju [School of Material and Chemical Engineering, Zhengzhou University of Light Industry, Zhengzhou 450002 (China); Zhang, Jingtao [School of Food and Bioengineering, Zhengzhou University of Light Industry, Zhengzhou 450002 (China); Zhang, Jie [School of Material and Chemical Engineering, Zhengzhou University of Light Industry, Zhengzhou 450002 (China); Shi, Hengzhen, E-mail: shihz@zzuli.edu.cn [School of Material and Chemical Engineering, Zhengzhou University of Light Industry, Zhengzhou 450002 (China)

    2015-12-15

    The g-C{sub 3}N{sub 4}/Y{sub 2}MoO{sub 6}:Eu{sup 3+} composite phosphors were synthesized and characterized by X-ray diffraction, Fourier transform-infrared spectroscopy, ultraviolet visible diffuse reflection spectra, photoluminescence spectra and luminescence decay curves. Under the excitation of 360 nm near ultraviolet light, these composite phosphors show tunable emission from blue to red region, in which white light emission can be obtained in term of appropriate quality proportion of Y{sub 2}MoO{sub 6}:Eu{sup 3+} relative to g-C{sub 3}N{sub 4}/Y{sub 2}MoO{sub 6}:Eu{sup 3+}. In addition, the emission color can be also dependent on the excitation wavelength in g-C{sub 3}N{sub 4}/Y{sub 2}MoO{sub 6}:Eu{sup 3+} composite phosphor. - Graphical abstract: Under the excitation of 360 nm near ultraviolet light, the g-C{sub 3}N{sub 4}/Y{sub 2}MoO{sub 6}:Eu{sup 3+} composite phosphors show tunable emission from blue to red region, in which white light emission can be obtained. - Highlights: • The g-C3N4/Y2MoO6:Eu{sup 3+} composite phosphors were synthesized and characterized. • White light emission was realized in the g-C3N4/Y2MoO6:Eu{sup 3+} composites under UV excitation. • A novel idea to realize the broadband sensitized white light emission in phosphors was provided.

  17. Synthesis and characterization particles of Ba{sub 0,50}Sr{sub 0,50}Co{sub 0,80}Fe{sub 0,20}O{sub 3} obtained by the citrate-EDTA technique; Sintese e caracterizacao de particulados de Ba{sub 0,50}Sr{sub 0,50}Co{sub 0,80}Fe{sub 0,20}O{sub 3} obtidos pela tecnica dos citratos-EDTA

    Energy Technology Data Exchange (ETDEWEB)

    Bonturim, E; Vargas, R A; Andreoli, M; Seo, E S.M., [Instituto de Pesquisas Energeticas e Nucleares (CCTM/IPEN/CNEN-SP), Sao Paulo, SP (Brazil). Centro de Ciencia e Tecnologia de Materiais

    2010-07-01

    The Ba{sub (1-x)}Sr{sub (x)}Co{sub (1-y)}Fe{sub (y)}O{sub (3)} (BSCF) has been studied as a cathode material for Intermediate Temperature Solid Oxide Fuel Cell, due to its better ion and electron conduction. This work aims to study the synthesis of the compound obtained from the citrate-EDTA technique. Thermogravimetric analysis indicated the formation of the compound above 800 deg C. The materials calcined at temperatures of 700, 800 and 900 deg C for 5 h showed cubic pseudo-perovskite structure, according to the literature. By analysis of X-ray fluorescence were obtained powders with nominal chemical composition in the temperature range studied. The micrographs obtained by SEM and particle size distribution analysis showed the formation of particle with diameters below 1 micron. (author)

  18. Effects of surface acidities of MCM-41 modified with MoO{sub 3} on adsorptive desulfurization of gasoline

    Energy Technology Data Exchange (ETDEWEB)

    Shao Xinchao, E-mail: sxc86@yahoo.cn [Key Laboratory of Petrochemical Catalytic Science and Technology, Liaoning ShiHua University, Fushun 113001 (China); Zhang Xiaotong; Yu Wenguang; Wu Yuye [Key Laboratory of Petrochemical Catalytic Science and Technology, Liaoning ShiHua University, Fushun 113001 (China); Qin Yucai [Key Laboratory of Petrochemical Catalytic Science and Technology, Liaoning ShiHua University, Fushun 113001 (China); College of Chemistry and Chemical Engineering, China University of Petroleum (East China), Qingdao, Shandong 257061 (China); Sun Zhaolin [Key Laboratory of Petrochemical Catalytic Science and Technology, Liaoning ShiHua University, Fushun 113001 (China); School of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000 (China); Song Lijuan, E-mail: lsong56@263.net [Key Laboratory of Petrochemical Catalytic Science and Technology, Liaoning ShiHua University, Fushun 113001 (China) and College of Chemistry and Chemical Engineering, China University of Petroleum (East China), Qingdao, Shandong 257061 (China)

    2012-12-15

    Highlights: Black-Right-Pointing-Pointer The MoO{sub 3}-MCM-41 samples prepared by spontaneous monolayer dispersion and impregnation with a different MoO{sub 3} filling have been studied. Black-Right-Pointing-Pointer The relative concentration of hydroxyl groups present on before and after containing MoO{sub 3} samples was monitored by in situ FTIR to speculate the bonding style of MoO{sub 3} and MCM-41. Black-Right-Pointing-Pointer The surface acidities of the MoO{sub 3}-MCM-41 adsorbents were investigated systematically and correlated with the desulfurization performance. - Abstract: A series of MCM-41 samples containing molybdenum oxide as active species in the mesoporous channels loaded by spontaneous monolayer dispersion (SMD) and impregnation (IM) have been prepared and characterized using XRD, N{sub 2} adsorption-desorption analysis, Fourier transform infrared spectroscopy (FTIR) and intelligent gravimetric analyzer (IGA). The relative number of hydroxy on the adsorbents was investigated by in situ FTIR. Surface acidities of the adsorbents were studied by infrared spectroscopy of adsorbed pyridine and correlated with reactivity for adsorptive desulfurization. The IGA technique was employed to investigate adsorption behavior of thiophene and benzene on the adsorbents at 303 K. It is shown that MoO{sub 3} can be highly dispersed up to 0.2 g g{sup -1} in the MCM-41 channels by the SMD strategy with the ordered mesoporous structure of the MoMM samples remaining intact. The ordered mesostructure of MCM-41 is, however, destroyed at higher MoO{sub 3} contents of 0.26 and 0.32 g g{sup -1} with particle sizes of 1.2 nm and 3.6 nm, respectively, observed. For the MoMI(0.2) sample prepared by the IM method, the aggregation of the MoO{sub 3} particles takes place with a particle size of 6.5 nm obtained. The results are also revealed that the dispersion extent of the MoO{sub 3} species is related to the abundant surface hydroxy of MCM-41. The host species and guest

  19. Photoluminescence characterization and energy transfer of color-tunable Li{sub 6}Y(BO{sub 3}){sub 3}:Ce{sup 3+},Tb{sup 3+} phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Guan, Anxiang; Zhou, Liya, E-mail: zhouliyatf@163.com; Wang, Guofang; Gao, Fangfang; Wang, Qiuping; Chen, Xueting; Li, Yinghao

    2016-08-01

    Ce{sup 3+} and Tb{sup 3+} singly doped and co-doped Li{sub 6}Y(BO{sub 3}){sub 3} (LYB) phosphors were synthesized through a solid-state reaction. The phosphors were effectively excited by 350 nm, which matched the near-UV emitting InGaN chip. Luminescence spectra and decay lifetime curves of LYB:Ce{sup 3+},Tb{sup 3+} were measured to prove energy transfer from Ce{sup 3+} to Tb{sup 3+}. Through energy transfer, the intensity of the typical emission peak of Tb{sup 3+} at 546 nm in LYB:0.05Ce{sup 3+},0.03Tb{sup 3+} was approximately 1.8 times stronger than that in LYB:0.03Tb{sup 3+}. The mechanism of Ce{sup 3+}→Tb{sup 3+} energy transfer was a dipole–dipole interaction, and the energy transfer efficiency gradually increased to 29.27% with increasing Tb{sup 3+} doping concentration. Furthermore, the emission colors of LYB:Ce{sup 3+},Tb{sup 3+} varied from blue to green by adjusting the Ce{sup 3+}/Tb{sup 3+} ratio, indicating that the phosphors could be used as blue-to-green emitting phosphors for application in ultraviolet light-emitting diodes.

  20. Degradation mechanism of CH{sub 3}NH{sub 3}PbI{sub 3} perovskite materials upon exposure to humid air

    Energy Technology Data Exchange (ETDEWEB)

    Shirayama, Masaki; Kato, Masato; Fujiseki, Takemasa; Hara, Shota; Kadowaki, Hideyuki; Murata, Daisuke; Fujiwara, Hiroyuki, E-mail: fujiwara@gifu-u.ac.jp [Department of Electrical, Electronic and Computer Engineering, Gifu University, 1-1 Yanagido, Gifu 501-1193 (Japan); Miyadera, Tetsuhiko; Sugita, Takeshi; Chikamatsu, Masayuki [Research Center for Photovoltaics, National Institute of Advanced Industrial Science and Technology (AIST), Central 5, 1-1-1 Higashi, Tsukuba, Ibaraki 305-8568 (Japan)

    2016-03-21

    Low stability of organic-inorganic perovskite (CH{sub 3}NH{sub 3}PbI{sub 3}) solar cells in humid air environments is a serious drawback which could limit practical application of this material severely. In this study, from real-time spectroscopic ellipsometry characterization, the degradation mechanism of ultra-smooth CH{sub 3}NH{sub 3}PbI{sub 3} layers prepared by a laser evaporation technique is studied. We present evidence that the CH{sub 3}NH{sub 3}PbI{sub 3} degradation in humid air proceeds by two competing reactions of (i) the PbI{sub 2} formation by the desorption of CH{sub 3}NH{sub 3}I species and (ii) the generation of a CH{sub 3}NH{sub 3}PbI{sub 3} hydrate phase by H{sub 2}O incorporation. In particular, rapid phase change occurs in the near-surface region and the CH{sub 3}NH{sub 3}PbI{sub 3} layer thickness reduces rapidly in the initial 1 h air exposure even at a low relative humidity of 40%. After the prolonged air exposure, the CH{sub 3}NH{sub 3}PbI{sub 3} layer is converted completely to hexagonal platelet PbI{sub 2}/hydrate crystals that have a distinct atomic-scale multilayer structure with a period of 0.65 ± 0.05 nm. We find that conventional x-ray diffraction and optical characterization in the visible region, used commonly in earlier works, are quite insensitive to the surface phase change. Based on results obtained in this work, we discuss the degradation mechanism of CH{sub 3}NH{sub 3}PbI{sub 3} in humid air.

  1. A comparative study of magnetic field induced meta-magnetic transition in nanocrystalline and bulk Pr{sub 0.65}(Ca{sub 0.7}Sr{sub 0.3}){sub 0.35}MnO{sub 3} compound

    Energy Technology Data Exchange (ETDEWEB)

    Saha, Suvayan [CMP Division, Saha Institute of Nuclear Physics, 1/AF, Bidhannagar, Kolkata 700 064 (India); Center for Research in Nanoscience and Nanotechnology, University of Calcutta, JD-2, Salt Lake City, Kolkata 700098, West Bengal (India); Department of Physics, University of Calcutta, 92 A.P.C. Road, Kolkata 700009 (India); Das, Kalipada, E-mail: kalipadadasphysics@gmail.com [Department of Materials Science, Indian Association for the Cultivation of Science, 2A and 2B Raja S.C. Mullick Road, Jadavpur, Kolkata 700032 (India); Bandyopadhyay, Sudipta [Center for Research in Nanoscience and Nanotechnology, University of Calcutta, JD-2, Salt Lake City, Kolkata 700098, West Bengal (India); Department of Physics, University of Calcutta, 92 A.P.C. Road, Kolkata 700009 (India); Das, I. [CMP Division, Saha Institute of Nuclear Physics, 1/AF, Bidhannagar, Kolkata 700 064 (India)

    2017-06-15

    Highlights: • Field induced sharp meta-magnetic transition appears even in nanocrystalline sample. • Magnetic field for the meta-magnetic transition enhances depending upon the cooling field. • This unusual behavior is addressed by the effect of the interfacial strains. - Abstract: In our present study we highlight the observations of external magnetic field induced sharp meta-magnetic transition in polycrystalline bulk as well as nanocrystalline form of Pr{sub 0.65}(Ca{sub 0.7}Sr{sub 0.7}){sub 0.35}MnO{sub 3} compound. Interestingly, such behavior persists in the nanoparticles regardless of the disorder broadened transition. However, higher magnetic field is required for nanoparticles having average particle size ∼40 nm for such meta-magnetic transition, which differs from the general trends of the pure charge ordered nano materials. The interfacial strain between the different magnetic domains plays the important role in magnetic isothermal properties of nanoparticles, when the samples are cooled down in different cooling field. Additionally, both the bulk and nanoparticle compounds exhibit spontaneous phase separation and significantly large magnetoresistance at the low temperature region due to the melting of charge ordered fraction.

  2. Practical Considerations for Detection and Characterization of Sub-Micron Particles in Protein Solutions by Nanoparticle Tracking Analysis.

    Science.gov (United States)

    Gruia, Flaviu; Parupudi, Arun; Polozova, Alla

    2015-01-01

    Nanoparticle Tracking Analysis (NTA) is an emerging analytical technique developed for detection, sizing, and counting of sub-micron particles in liquid media. Its feasibility for use in biopharmaceutical development was evaluated with particle standards and recombinant protein solutions. Measurements of aqueous suspensions of NIST-traceable polystyrene particle standards showed accurate particle concentration detection between 2 × 10(7) and 5 × 10(9) particles/mL. Sizing was accurate for particle standards up to 200 nm. Smaller than nominal value sizes were detected by NTA for the 300-900 nm particles. Measurements of protein solutions showed that NTA performance is solution-specific. Reduced sensitivity, especially in opalescent solutions, was observed. Measurements in such solutions may require sample dilution; however, common sample manipulations, such as dilution and filtration, may result in particle formation. Dilution and filtration case studies are presented to further illustrate such behavior. To benchmark general performance, NTA was compared against asymmetric flow field flow fractionation coupled with multi-angle light scattering (aF4-MALS) and dynamic light scattering, which are other techniques for sub-micron particles. Data shows that all three methods have limitations and may not work equally well under certain conditions. Nevertheless, the ability of NTA to directly detect and count sub-micron particles is a feature not matched by aF4-MALS or dynamic light scattering. Thorough characterization of particulate matter present in protein therapeutics is limited by the lack of analytical methods for particles in the sub-micron size range. Emerging techniques are being developed to bridge this analytical gap. In this study, Nanoparticle Tracking Analysis is evaluated as a potential tool for biologics development. Our results indicate that method performance is molecule-specific and may not work as well under all solution conditions, especially when

  3. Magnetic properties of electron-doped La{sub 0.23}Ca{sub 0.77}MnO{sub 3} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Markovich, V., E-mail: markoviv@bgu.ac.il; Jung, G. [Ben-Gurion University of the Negev, Department of Physics (Israel); Wisniewski, A. [Polish Academy of Sciences, Institute of Physics (Poland); Mogilyansky, D. [Ben-Gurion University of the Negev, Ilse Katz Institute for Nanoscale Science and Technology (Israel); Puzniak, R. [Polish Academy of Sciences, Institute of Physics (Poland); Kohn, A. [Ben-Gurion University of the Negev, Ilse Katz Institute for Nanoscale Science and Technology (Israel); Wu, X. D.; Suzuki, K. [Monash University, Department of Materials Engineering (Australia); Gorodetsky, G. [Ben-Gurion University of the Negev, Department of Physics (Israel)

    2012-09-15

    Magnetic properties of electron-doped La{sub 0.23}Ca{sub 0.77}MnO{sub 3} manganite nanoparticles, with average size of 12 and 60 nm, prepared by the glycine-nitrate method, have been investigated in the temperature range 5-300 K and magnetic fields up to 90 kOe. It is suggested that weak ferromagnetic moment results from ferromagnetic shells of the basically antiferromagnetic nanoparticles and from domains of frustrated disordered phase in the core. Assumption of two distinct sources of ferromagnetism is supported by the appearance of two independent ferromagnetic contributions in the fit of the T{sup 3/2} Bloch law to spontaneous magnetization. The ferromagnetic components, which are more pronounced in smaller particles, occupy only a small fraction of the nanoparticle volume and the antiferromagnetic ground state remains stable. It is found that the magnetic hysteresis loops following field cooled processes, display size-dependent horizontal and vertical shifts, namely, exhibiting exchange bias effect. Time-dependent magnetization dynamics demonstrating two relaxation rates were observed at constant magnetic fields upon cooling to T < 100 K.

  4. Luminescence properties of Sm{sup 3+}-doped Sr{sub 3}Sn{sub 2}O{sub 7} phosphor

    Energy Technology Data Exchange (ETDEWEB)

    Lei Bingfu, E-mail: tleibf@jnu.edu.cn [Department of Physics, Jinan University, Guangzhou 510632 (China); Department of Chemistry and Nanochemistry Institute, Jinan University, Guangzhou 510632 (China); Man Shiqing [Department of Chemistry and Nanochemistry Institute, Jinan University, Guangzhou 510632 (China); Department of Electronic Engineering, Jinan University, Guangzhou 510632 (China); Liu Yingliang [Department of Chemistry and Nanochemistry Institute, Jinan University, Guangzhou 510632 (China); Yue Song [Department of Physics, Jinan University, Guangzhou 510632 (China)

    2010-12-01

    We report on a luminescent phenomenon in Sm{sup 3+}-doped Sr{sub 3}Sn{sub 2}O{sub 7} afterglow phosphor. XRD, photoluminescence, afterglow emission spectra and long-lasting phosphorescence decay curve are used to characterize this phosphor. After irradiation by a 267-nm UV light for 5 min, the Sm{sup 3+}-doped Sr{sub 3}Sn{sub 2}O{sub 7} phosphor emits intense reddish-orange emitting afterglow from the {sup 4}G{sub 5/2} to {sup 6}H{sub J} (J = 5/2, 7/2, 9/2) transitions, and its afterglow can be seen with the naked eye in the dark clearly for more than 1 h after removal of the excitation source. Photoluminescence spectra reveal that the reddish-orange light-emitting long-lasting phosphorescence originate from the mixture of Sm{sup 3+} characteristic transitions. The afterglow decay curve of the Sm{sup 3+}-doped Sr{sub 3}Sn{sub 2}O{sub 7} phosphor contains a fast decay component and another slow decay one. The possible mechanism of this reddish-orange light-emitting LLP phosphor is also discussed based on the experiment results.

  5. Random Telegraph Signal Amplitudes in Sub 100 nm (Decanano) MOSFETs: A 3D 'Atomistic' Simulation Study

    Science.gov (United States)

    Asenov, Asen; Balasubramaniam, R.; Brown, A. R.; Davies, J. H.; Saini, Subhash

    2000-01-01

    In this paper we use 3D simulations to study the amplitudes of random telegraph signals (RTS) associated with the trapping of a single carrier in interface states in the channel of sub 100 nm (decanano) MOSFETs. Both simulations using continuous doping charge and random discrete dopants in the active region of the MOSFETs are presented. We have studied the dependence of the RTS amplitudes on the position of the trapped charge in the channel and on the device design parameters. We have observed a significant increase in the maximum RTS amplitude when discrete random dopants are employed in the simulations.

  6. The effect of Ag layer thickness on the properties of WO{sub 3}/Ag/MoO{sub 3} multilayer films as anode in organic light emitting diodes

    Energy Technology Data Exchange (ETDEWEB)

    Zadsar, Mehdi, E-mail: mehdi_zadsar@yahoo.com [Physics Department, University of Isfahan, Isfahan (Iran, Islamic Republic of); Fallah, Hamid Reza; Mahmoodzadeh, Morteza Haji [Physics Department, University of Isfahan, Isfahan (Iran, Islamic Republic of); Quantum Optics Research Group, University of Isfahan, Isfahan (Iran, Islamic Republic of); Tabatabaei, Seyed Vahid [Physics Department, University of Isfahan, Isfahan (Iran, Islamic Republic of)

    2012-04-15

    Transparent conductive WO{sub 3}/Ag/MoO{sub 3} (WAM) multilayer electrodes were fabricated by thermal evaporation and the effects of Ag layer thickness on the optoelectronic and structural properties of multilayer electrode as anode in organic light emitting diodes (OLEDs) were investigated using different analytical methods. For Ag layers with thickness varying between 5 and 20 nm, the best WAM performances, high optical transmittance (81.7%, at around 550 nm), and low electrical sheet resistance (9.75 {Omega}/cm{sup 2}) were obtained for 15 nm thickness. Also, the WAM structure with 15 nm of Ag layer thickness has a very smooth surface with an RMS roughness of 0.37 nm, which is suitable for use as transparent conductive anode in OLEDs. The current density-voltage-luminance (J-V-L) characteristics measurement shows that the current density of WAM/PEDOT:PSS/TPD/Alq{sub 3}/LiF/Al organic diode increases with the increase in thickness of Ag and WO{sub 3}/Ag (15 nm)/MoO{sub 3} device exhibits a higher luminance intensity at lower voltage than ITO/PEDOT:PSS/TPD/Alq{sub 3}/LiF/Al control device. Furthermore, this device shows the highest power efficiency (0.31 lm/W) and current efficiency (1.2 cd/A) at the current density of 20 mA/cm{sup 2}, which is improved 58% and 41% compared with those of the ITO-based device, respectively. The lifetime of the WO{sub 3}/Ag (15 nm)/MoO{sub 3} device was measured to be 50 h at an initial luminance of 50 cd/m{sup 2}, which is five times longer than 10 h for ITO-based device. - Highlights: Black-Right-Pointing-Pointer Investigation of Ag thickness effect on the properties of WO{sub 3}/Ag/MoO{sub 3} films. Black-Right-Pointing-Pointer Electrical conductivity of multilayer films increases with increasing Ag thickness. Black-Right-Pointing-Pointer Optical transmittance increases by Ag thickness and at 15 nm, reaches 81.7%. Black-Right-Pointing-Pointer Power efficiency of WO{sub 3}/Ag (15 nm)/MoO{sub 3} based devices is higher than that of

  7. Structural, spectroscopic and cytotoxicity studies of TbF{sub 3}@CeF{sub 3} and TbF{sub 3}@CeF{sub 3}@SiO{sub 2} nanocrystals

    Energy Technology Data Exchange (ETDEWEB)

    Grzyb, Tomasz; Runowski, Marcin [Adam Mickiewicz University, Department of Rare Earths, Faculty of Chemistry (Poland); Dabrowska, Krystyna [Polish Academy of Sciences, Bacteriophage Laboratory, Institute of Immunology and Experimental Therapy (Poland); Giersig, Michael; Lis, Stefan, E-mail: blis@amu.edu.pl [Adam Mickiewicz University, Department of Rare Earths, Faculty of Chemistry (Poland)

    2013-10-15

    Terbium fluoride nanocrystals, covered by a shell, composed of cerium fluoride were synthesized by a co-precipitation method. Their complex structure was formed spontaneously during the synthesis. The surface of these core/shell nanocrystals was additionally modified by silica. The properties of TbF{sub 3}@CeF{sub 3} and TbF{sub 3}@CeF{sub 3}@SiO{sub 2} nanocrystals, formed in this way, were investigated. Spectroscopic studies showed that the differences between these two groups of products resulted from the presence of the SiO{sub 2} shell. X-ray diffraction patterns confirmed the trigonal crystal structure of TbF{sub 3}@CeF{sub 3} nanocrystals. High resolution transmission electron microscopy in connection with energy-dispersive X-ray spectroscopy showed a complex structure of the formed nanocrystals. Crystallized as small discs, 'the products', with an average diameter around 10 nm, showed an increase in the concentration of Tb{sup 3+} ions from surface to the core of nanocrystals. In addition to photo-physical analyses, cytotoxicity studies were performed on HSkMEC (Human Skin Microvascular Endothelial Cells) and B16F0 mouse melanoma cancer cells. The cytotoxicity of the nanomaterials was neutral for the investigated cells with no toxic or antiproliferative effect in the cell cultures, either for normal or for cancer cells. This fact makes the obtained nanocrystals good candidates for biological applications and further modifications of the SiO{sub 2} shell.Graphical Abstract.

  8. Beryllium-free β-Rb{sub 2}Al{sub 2}B{sub 2}O{sub 7} as a possible deep-ultraviolet nonlinear optical material replacement for KBe{sub 2}BO{sub 3}F{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Tran, T. Thao; Halasyamani, P. Shiv [Department of Chemistry, University of Houston, TX (United States); Koocher, Nathan Z.; Rondinelli, James M. [Department of Materials Science and Engineering, Northwestern University, Evanston, IL (United States)

    2017-03-06

    A new beryllium-free deep-ultraviolet (DUV) nonlinear optical (NLO) material, β-Rb{sub 2}Al{sub 2}B{sub 2}O{sub 7} (β-RABO), has been synthesized and characterized. The chiral nonpolar acentric material shows second-harmonic generation (SHG) activity at both 1064 and 532 nm with efficiencies of 2 x KH{sub 2}PO{sub 4} and 0.4 x β-BaB{sub 2}O{sub 4}, respectively, and exhibits a short absorption edge below 200 nm. β-Rb{sub 2}Al{sub 2}B{sub 2}O{sub 7} has a three-dimensional structure of corner-shared Al(BO{sub 3}){sub 3}O polyhedra. The discovery of β-RABO shows that through careful synthesis and characterization, replacement of KBe{sub 2}BO{sub 3}F{sub 2} (KBBF) by a Be-free DUV NLO material is possible. (copyright 2017 Wiley-VCH Verlag GmbH and Co. KGaA, Weinheim)

  9. Fabrication of AgFeO{sub 2}/g-C{sub 3}N{sub 4} nanocatalyst with enhanced and stable photocatalytic performance

    Energy Technology Data Exchange (ETDEWEB)

    Tang, Dandan [School of Resources and Environmental Engineering, Wuhan University of Technology, 122 Luoshi Road, Wuhan 430070 (China); Hubei Provincial Collaborative Innovation Center for High Efficient Utilization of Vanadium Resources, Wuhan 430070 (China); Zhang, Gaoke, E-mail: gkzhang@whut.edu.cn [School of Resources and Environmental Engineering, Wuhan University of Technology, 122 Luoshi Road, Wuhan 430070 (China); Hubei Provincial Collaborative Innovation Center for High Efficient Utilization of Vanadium Resources, Wuhan 430070 (China)

    2017-01-01

    Highlights: • AgFeO{sub 2}/g-C{sub 3}N{sub 4} nanocatalyst was synthesized via a facile precipitation method. • The composite displays superior e{sup ∧}/h{sup +} pair separation compared to AgFeO{sub 2} and g-C{sub 3}N{sub 4}. • The composite shows high and stable photocatalytic activity both in water and air. • The active h{sup +} plays the dominate role in the degradation process. - Abstract: This work reported a novel AgFeO{sub 2}/g-C{sub 3}N{sub 4} composite with enhanced photocatalytic activity, which was fabricated by a simple precipitation method. The g-C{sub 3}N{sub 4} sheets with thickness of 2• 4 nm were successfully loaded on the surface of the AgFeO{sub 2} particles. As compared to pure AgFeO{sub 2} and pure g-C{sub 3}N{sub 4}, the as-prepared AgFeO{sub 2}/g-C{sub 3}N{sub 4} photocatalysts exhibited superior absorption in the visible-light region and displayed promising visible-light photocatalytic performance in the degradation of organic contaminations both in water and in air. About 94% of Acid red G (ARG) can be degraded by the optimized AgFeO{sub 2}/g-C{sub 3}N{sub 4} sample, which is ∱/47.5 and ∱/410.7 times higher than that by pure AgFeO{sub 2} and pure g-C{sub 3}N{sub 4}, respectively. Meanwhile, it can also effectively degrade ∱/487% of gaseous formaldehyde to CO{sub 2} within 9 h. The enhanced photocatalytic property and stability of the AgFeO{sub 2}/g-C{sub 3}N{sub 4} composite can be attributed to its specific nanostructure, effective electron-hole separation and the formation of Z-scheme heterostructure between AgFeO{sub 2} and g-C{sub 3}N{sub 4}. This work could provide new and helpful insights into the photocatalytic application of Ag-based delafossite materials.

  10. Chemically deposited Sb{sub 2}S{sub 3} thin films for optical recording

    Energy Technology Data Exchange (ETDEWEB)

    Shaji, S; Arato, A; Castillo, G Alan; Palma, M I Mendivil; Roy, T K Das; Krishnan, B [Facultad de IngenierIa Mecanica y Electrica, Universidad Autonoma de Nuevo Leon, San Nicolas de los Garza, Nuevo Leon, C.P- 66450 (Mexico); O' Brien, J J; Liu, J, E-mail: bkrishnan@fime.uanl.m [Center for Nanoscience and Department of Chemistry and Biochemistry, University of Missouri-St. Louis, One Univ. Blvd., St. Louis, MO - 63121 (United States)

    2010-02-24

    Laser induced changes in the properties of Sb{sub 2}S{sub 3} thin films prepared by chemical bath deposition are described in this paper. Sb{sub 2}S{sub 3} thin films of thickness 550 nm were deposited from a solution containing SbCl{sub 3} and Na{sub 2}S{sub 2}O{sub 3} at 27 {sup 0}C for 5 h. These thin films were irradiated by a 532 nm continuous wave laser beam under different conditions at ambient atmosphere. X-ray diffraction analysis showed amorphous to polycrystalline transformation due to laser exposure of these thin films. Morphology and composition of these films were described. Optical properties of these films before and after laser irradiation were analysed. The optical band gap of the material was decreased due to laser induced crystallization. The results obtained confirm that there is further scope for developing this material as an optical recording media.

  11. Multiferroics BiMn{sub 1−x}Al{sub x}O{sub 3} nanoparticles: Synthesis, characterization and evaluation of various structural, physical, electrical and dielectric parameters

    Energy Technology Data Exchange (ETDEWEB)

    Ahmad, Bashir [Institute of Chemical Sciences, Bahauddin Zakariya University, Multan 60800 (Pakistan); Raissat, Rabia [National Center for Nanoscience and Technology, Beijing (China); Mumtaz, Saleem [Institute of Chemical Sciences, Bahauddin Zakariya University, Multan 60800 (Pakistan); Ahmad, Zahoor [Department of Chemistry, University of Engineering and Technology, Lahore 54890 (Pakistan); Sadiq, Imran [Center for Solid State Physics, University of the Punjab, Lahore (Pakistan); Ashiq, Muhammad Naeem, E-mail: naeembzu@bzu.edu.pk [Institute of Chemical Sciences, Bahauddin Zakariya University, Multan 60800 (Pakistan); Najam-ul-Haq, Muhammad [Institute of Chemical Sciences, Bahauddin Zakariya University, Multan 60800 (Pakistan)

    2017-07-01

    Graphical abstract: Effect of frequency on the dielectric constant of “BiMn{sub 1−x}Al{sub x}O{sub 3}” nanoparticles. - Highlights: • Microemulsion method has been used for the synthesis. • Crystallite size range from 32 to 52 nm. • Electrical resistivity increased from 6 × 10{sup 8} to 8 × 10{sup 9} Ω cm. • The increase in resistivity make these materials for microwave devices. - Abstract: The aluminium substituted bismuth based manganates with nominal composition BiMn{sub 1−x}Al{sub x}O{sub 3} (x = 0.0, 0.2, 0.4, 0.6 and 0.8) were prepared by the simple microemulsion method. The alteration in their structural, electrical and dielectric parameters due to Al substitution has been investigated. The X-ray diffraction analysis (XRD) confirms the formation of single phase orthorhombic with crystallite size ranges from 32 to 52 nm. The morphological features and particle size were determined by using scanning electron microscopy (SEM). The dc electrical resistivity increased from 6 × 10{sup 8} to 8 × 10{sup 9} Ω cm with the increase in substituent concentration. The dielectric constant, dielectric loss tangent and dielectric loss factor decreased with the increase in frequency. The increase in electrical resistivity makes the synthesized materials paramount over other materials and can be useful for technological applications in microwave devices.

  12. Synthesis, characterization, and comparative gas-sensing properties of Fe{sub 2}O{sub 3} prepared from Fe{sub 3}O{sub 4} and Fe{sub 3}O{sub 4}-chitosan

    Energy Technology Data Exchange (ETDEWEB)

    Cuong, Nguyen Duc [Faculty of Hospitality and Tourism, Hue University, 22 Lam Hoang, Vy Da Ward, Hue City (Viet Nam); College of Sciences, Hue University, 77 Nguyen Hue, Phu Nhuan Ward, Hue City (Viet Nam); International Training Institute for Materials Science (ITIMS), Hanoi University of Science and Technology (HUST), Hanoi (Viet Nam); Hoa, Tran Thai; Khieu, Dinh Quang [College of Sciences, Hue University, 77 Nguyen Hue, Phu Nhuan Ward, Hue City (Viet Nam); Lam, Tran Dai [Institute of Materials Science, Vietnamese Academy of Science and Technology, Hanoi (Viet Nam); Hoa, Nguyen Duc [International Training Institute for Materials Science (ITIMS), Hanoi University of Science and Technology (HUST), Hanoi (Viet Nam); Van Hieu, Nguyen, E-mail: hieu@itims.edu.vn [International Training Institute for Materials Science (ITIMS), Hanoi University of Science and Technology (HUST), Hanoi (Viet Nam)

    2012-05-15

    Highlights: Black-Right-Pointing-Pointer We have demonstrated a facile method to prepare Fe{sub 3}O{sub 4} nanoparticles and chitosan-coated Fe{sub 3}O{sub 4} nanoparticles. Black-Right-Pointing-Pointer {alpha}-Fe{sub 2}O{sub 3} sensors prepared from those Fe{sub 3}O{sub 4} materials have been investigated and compared. Black-Right-Pointing-Pointer The results show potential application of {alpha}-Fe{sub 2}O{sub 3} for CO sensors in environmental monitoring. - Abstract: In this paper, Fe{sub 3}O{sub 4} and chitosan (CS)-coated Fe{sub 3}O{sub 4} nanoparticles were synthesized via co-precipitation method and subsequent covalent binding of CS onto the surface for functionalization, respectively. Characterization of the crystal structures and morphologies of as-synthesized nanoparticles by X-ray diffraction, scanning electron microscopy, and transmission electron microscopy demonstrated that Fe{sub 3}O{sub 4} had a cubic spinal structure with irregular shapes and average diameters of 10-20 nm. The surface states and magnetic properties of Fe{sub 3}O{sub 4}-CS nanoparticles were characterized by Fourier transform infrared spectra and vibrating sample magnetometry. Results showed that Fe{sub 3}O{sub 4}-CS nanoparticles possessed super-paramagnetic properties, with saturated magnetization up to 60 emu/g. In addition, Fe{sub 3}O{sub 4} and CS-coated Fe{sub 3}O{sub 4} nanoparticles were used in the fabrication of {alpha}-Fe{sub 2}O{sub 3} based gas sensors. Gas sensing measurements revealed that the {alpha}-Fe{sub 2}O{sub 3} gas sensor prepared from Fe{sub 3}O{sub 4}-CS had a better response to H{sub 2}, CO, C{sub 2}H{sub 5}OH, and NH{sub 3} compared with the device prepared from pristine Fe{sub 3}O{sub 4}. Furthermore, the {alpha}-Fe{sub 2}O{sub 3} sensor prepared from Fe{sub 3}O{sub 4}-CS nanoparticles exhibited the highest response to CO among the test gases, suggesting that it has great potential for practical applications in environmental monitoring.

  13. Bottom-up synthesis of up-converting submicron-sized Er{sup 3+}-doped LiNbO{sub 3} particles

    Energy Technology Data Exchange (ETDEWEB)

    Jardiel, T., E-mail: jardiel@icv.csic.es [Departamento de Electroceramica, Instituto de Ceramica y Vidrio-CSIC, Kelsen 5, 28049 Madrid (Spain); Caballero, A.C. [Departamento de Electroceramica, Instituto de Ceramica y Vidrio-CSIC, Kelsen 5, 28049 Madrid (Spain); Marin-Dobrincic, M.; Cantelar, E.; Cusso, F. [Departamento de Fisica de Materiales, C-04, Facultad de Ciencias, Universidad Autonoma de Madrid, Avda. Francisco Tomas y Valiente 7, 28049 Madrid (Spain)

    2012-08-15

    A new and simple wet chemical synthesis method is proposed to prepare submicron-sized Erbium-doped LiNbO{sub 3} powders. The synthesis procedure comprises the co-precipitation of lithium and erbium ions from common precursors and their subsequent reaction with niobium ethoxide. A systematic characterization by means of X-Ray Diffraction (XRD), X-ray Fluorescence (XRF), Inductively Coupled Plasma (ICP-OES), Atomic Absorption (AAS), Field Emission Scanning Electron Microscopy (FE-SEM), as well as by the examination of the luminescence properties, evidence that with this method a congruent Er{sup 3+}-doped LiNbO{sub 3} single phase material can be obtained without using complex and time-consuming processing steps. The synthesized powders exhibit efficient IR to VIS up-conversion emissions under 974 nm pumping. -- Highlights: Black-Right-Pointing-Pointer A novel chemical route to the preparation of LiNbO{sub 3} powders has been developed. Black-Right-Pointing-Pointer This process avoids complex and time-consuming processing steps. Black-Right-Pointing-Pointer A congruent Er{sup 3+}-doped LiNbO{sub 3} single phase material can be obtained by this way. Black-Right-Pointing-Pointer The luminescence properties are the expected for this composition.

  14. Preparation and catalytic activities for H{sub 2}O{sub 2} decomposition of Rh/Au bimetallic nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Haijun, E-mail: zhanghaijun@wust.edu.cn [Key Laboratory of Integrated Exploitation of Bayan Obo Multi-Metal Resources, Inner Mongolia University of Science and Technology, Baotou 014010 (China); The State Key Laboratory of Refractory and Metallurgy, Wuhan University of Science and Technology, Wuhan 430081 (China); Deng, Xiangong; Jiao, Chengpeng; Lu, Lilin; Zhang, Shaowei [The State Key Laboratory of Refractory and Metallurgy, Wuhan University of Science and Technology, Wuhan 430081 (China)

    2016-07-15

    Graphical abstract: PVP-protected Rh/Au bimetallic nanoparticles (BNPs) were prepared by using hydrogen sacrificial reduction method, the activity of Rh80Au20 BNPs were about 3.6 times higher than that of Rh NPs. - Highlights: • Rh/Au bimetallic nanoparticles (BNPs) of 3∼5 nm in diameter were prepared. • Activity for H{sub 2}O{sub 2} decomposition of BNPs is 3.6 times higher than that of Rh NPs. • The high activity of BNPs was caused by the existence of charged Rh atoms. • The apparent activation energy for H{sub 2}O{sub 2} decomposition over the BNPs was calculated. - Abstract: PVP-protected Rh/Au bimetallic nanoparticles (BNPs) were prepared by using hydrogen sacrificial reduction method and characterized by UV–vis, XRD, FT-IR, XPS, TEM, HR-TEM and DF-STEM, the effects of composition on their particle sizes and catalytic activities for H{sub 2}O{sub 2} decomposition were also studied. The as-prepared Rh/Au BNPs possessed a high catalytic activity for the H{sub 2}O{sub 2} decomposition, and the activity of the Rh{sub 80}Au{sub 20} BNPs with average size of 2.7 nm were about 3.6 times higher than that of Rh monometallic nanoparticles (MNPs) even the Rh MNPs possess a smaller particle size of 1.7 nm. In contrast, Au MNPs with size of 2.7 nm show no any activity. Density functional theory (DFT) calculation as well as XPS results showed that charged Rh and Au atoms formed via electronic charge transfer effects could be responsible for the high catalytic activity of the BNPs.

  15. Synthesis and performance of Li{sub 3}(V{sub 1-x}Mg{sub x}){sub 2}(PO{sub 4}){sub 3} cathode materials

    Energy Technology Data Exchange (ETDEWEB)

    Dai, Changsong; Chen, Zhenyu; Jin, Haizu; Hu, Xinguo [School of Chemical Engineering and Technology, Harbin Institute of Technology, Harbin 150001 (China)

    2010-09-01

    In order to search for cathode materials with better performance, Li{sub 3}(V{sub 1-x}Mg{sub x}){sub 2}(PO{sub 4}){sub 3} (0, 0.04, 0.07, 0.10 and 0.13) is prepared via a carbothermal reduction (CTR) process with LiOH.H{sub 2}O, V{sub 2}O{sub 5}, Mg(CH{sub 3}COO){sub 2}.4H{sub 2}O, NH{sub 4}H{sub 2}PO{sub 4}, and sucrose as raw materials and investigated by X-ray diffraction (XRD), scanning electron microscopic (SEM) and electrochemical impedance spectrum (EIS). XRD shows that Li{sub 3}(V{sub 1-x}Mg{sub x}){sub 2}(PO{sub 4}){sub 3} (x = 0.04, 0.07, 0.10 and 0.13) has the same monoclinic structure as undoped Li{sub 3}V{sub 2}(PO{sub 4}){sub 3} while the particle size of Li{sub 3}(V{sub 1-x}Mg{sub x}){sub 2}(PO{sub 4}){sub 3} is smaller than that of Li{sub 3}V{sub 2}(PO{sub 4}){sub 3} according to SEM images. EIS reveals that the charge transfer resistance of as-prepared materials is reduced and its reversibility is enhanced proved by the cyclic votammograms. The Mg{sup 2+}-doped Li{sub 3}V{sub 2}(PO{sub 4}){sub 3} has a better high rate discharge performance. At a discharge rate of 20 C, the discharge capacity of Li{sub 3}(V{sub 0.9}Mg{sub 0.1}){sub 2}(PO{sub 4}){sub 3} is 107 mAh g{sup -1} and the capacity retention is 98% after 80 cycles. Li{sub 3}(V{sub 0.9}Mg{sub 0.1}){sub 2}(PO{sub 4}){sub 3}//graphite full cells (085580-type) have good discharge performance and the modified cathode material has very good compatibility with graphite. (author)

  16. Synthesis, crystal structure and photoluminescence of a new Eu-doped Sr containing sialon (Sr{sub 0.94}Eu{sub 0.06})(Al{sub 0.3}Si{sub 0.7}){sub 4}(N{sub 0.8}O{sub 0.2}){sub 6}

    Energy Technology Data Exchange (ETDEWEB)

    Yamane, Hisanori, E-mail: yamane@tagen.tohoku.ac.jp [Institute of Multidisciplinary Research for Advanced Materials, Tohoku University 2-1-1 Katahira, Aoba-ku, Sendai 980-8577 (Japan); Shimooka, Satoshi; Uheda, Kyota [Mitsubishi Chemical Group, Science and Technology Research Center, Inc. 1000 Kamoshida-cho, Aoba-ku, Yokohama 227-8502 (Japan)

    2012-06-15

    Colorless transparent platelet single crystals of a novel Eu{sup 2+}-doped strontium silicon aluminum oxynitride, (Sr{sub 0.94}Eu{sub 0.06})(Al{sub 0.3}Si{sub 0.7}){sub 4}(N{sub 0.8}O{sub 0.2}){sub 6}, were prepared at 1800 Degree-Sign C and 0.92 MPa of N{sub 2}. Fundamental reflections of electron and X-ray diffraction of the crystals were indexed with a face-centered orthorhombic unit cell (a=5.8061(5) A, b=37.762(3) A, c=9.5936(9) A). Diffuse streaks elongated in the b-axis direction were observed around the fundamental reflections hkl with h=2n+1 of the electron and X-ray diffraction, indicating stacking faults of (0 1 0)[1 0 0]/2. A crystal structure model without the stacking faults was obtained using the X-ray diffraction data of the fundamental reflections with the space group Fdd2. A SiN{sub 4}-tetrahedron double layer of [SiN{sub 2}]{sub 2} and a Sr/Eu double layer of [(Sr{sub 0.94}Eu{sub 0.06})Al{sub 1.2}Si{sub 0.8}N{sub 0.8} O{sub 1.2}]{sub 2} are stacked alternately along the b-axis direction. The title compound showed an emission with a peak wavelength of 490 nm under 334 nm excitation at room temperature. - Graphical abstract: Single crystals of a novel Eu{sup 2+}-doped strontium silicon aluminum oxynitride, (Sr{sub 0.94}Eu{sub 0.06})(Al{sub 0.3}Si{sub 0.7}){sub 4}(N{sub 0.8}O{sub 0.2}){sub 6}, having stacking faults on the (0 1 0) plane of an orthorhombic cell, were prepared at 1800 Degree-Sign C and 0.92 MPa of N{sub 2}. The compound showed emission with a peak wavelength of 490 nm under 334 nm excitation at room temperature. Highlights: Black-Right-Pointing-Pointer A new compound Eu{sup 2+}-doped (Sr{sub 0.94}Eu{sub 0.06})(Al{sub 0.3}Si{sub 0.7}){sub 4}(N{sub 0.8}O{sub 0.2}){sub 6} was prepared. Black-Right-Pointing-Pointer Stacking faults in the compound were clarified by electron and X-ray diffraction. Black-Right-Pointing-Pointer A basic crystal structure model was obtained based on the X-ray diffraction data. Black-Right-Pointing-Pointer An

  17. Correlation between microstructure and electrical properties of Cu{sub 1.3}Mn{sub 1.7}O{sub 4}/La{sub 2}O{sub 3} composite-coated ferritic stainless steel interconnects

    Energy Technology Data Exchange (ETDEWEB)

    Hosseini, N., E-mail: nazaneen_hosseini@ma.iut.ac.ir [Department of Materials Engineering, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of); Karimzadeh, F.; Abbasi, M.H. [Department of Materials Engineering, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of); Choi, G.M. [Fuel Cell Research Center and Department of Materials Science and Engineering, Pohang University of Science and Technology, Pohang 790-784 (Korea, Republic of)

    2016-07-15

    The goal of this study was to investigate the effect of screen-printed Cu{sub 1.3}Mn{sub 1.7}O{sub 4}/La{sub 2}O{sub 3} composite coating on chromia scale growth and electrical behavior of AISI430 stainless steel interconnects. The coated samples were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy equipped with energy dispersive spectroscopy (FESEM-EDS) and 4-probe area specific resistance (ASR) tests. The results showed that LaCrO{sub 3} conductive perovskite is formed due to the interdiffusion between Cr{sub 2}O{sub 3} and/or CrO{sub 3} and La{sub 2}O{sub 3}. The presence of LaCrO{sub 3} through the composite coating and Cr{sub 2}O{sub 3} sub-scale accompanied by the effective role of spinel phase, acted as a barrier to mitigate the sub-scale growth preventing chromium diffusion through the coating and the cathode. Besides, LaCrO{sub 3} particles within the sub-scale provided suitable conductive paths decreasing ASR from 19.3 mΩ cm{sup 2} for spinel coated sample to 15 mΩ cm{sup 2} for composite coated sample at the end of 500 h oxidation at 750° C. - Highlights: • Cu{sub 1.3}Mn{sub 1.7}O{sub 4}/La{sub 2}O{sub 3} coating was deposited on AISI 430 by screen-printing method. • LaCrO{sub 3} perovskite was formed due to the interdiffusion between Cr species and La{sub 2}O{sub 3}. • LaCrO{sub 3} particles within the chromia provided conductive paths causing ASR reduction. • The co-existence of LaCrO{sub 3} and Cu{sub 1.3}Mn{sub 1.7}O{sub 4} noticeably retarded the chromia growth.

  18. Smooth surfaces in very thin GdBa{sub 2}Cu{sub 3}O{sub 7−δ} films for application in superconducting tunnel junctions

    Energy Technology Data Exchange (ETDEWEB)

    Navarro, H., E-mail: henrynavarro@cab.cnea.gov.ar [Instituto Balseiro, Universidad Nacional de Cuyo & CNEA, 8400 Bariloche (Argentina); Centro Atómico Bariloche, Comisión Nacional de Energía Atómica. Av. Bustillo 9500, 8400 San Carlos de Bariloche (Argentina); Sirena, M. [Instituto Balseiro, Universidad Nacional de Cuyo & CNEA, 8400 Bariloche (Argentina); Centro Atómico Bariloche, Comisión Nacional de Energía Atómica. Av. Bustillo 9500, 8400 San Carlos de Bariloche (Argentina); Kim, Jeehoon [Department of Physics, Pohang University of Science and Technology, Pohang (Korea, Republic of); CALDES, Institute for Basic Science, Pohang (Korea, Republic of); Haberkorn, N. [Instituto Balseiro, Universidad Nacional de Cuyo & CNEA, 8400 Bariloche (Argentina); Centro Atómico Bariloche, Comisión Nacional de Energía Atómica. Av. Bustillo 9500, 8400 San Carlos de Bariloche (Argentina)

    2015-03-15

    Highlights: • A detailed study of the morphological properties of GdBa{sub 2}Cu{sub 3}O{sub 7−δ} thin films was realized. • The inclusion of a very thin SrTiO{sub 3} buffer layer modifies the surface of the SrTiO{sub 3} substrates. • The inclusion of the buffer layer suppress the three dimensional nucleation in the GdBa{sub 2}Cu{sub 3}O{sub 7−δ} film. • GdBa{sub 2}Cu{sub 3}O{sub 7−δ} films with large areas free of topological defects and T{sub c} close to liquid nitrogen can be obtained. - Abstract: This paper provides a systematic analysis of the morphology and the superconducting critical temperature obtained in very thin GdBa{sub 2}Cu{sub 3}O{sub 7−δ} films grown on (0 0 1) SrTiO{sub 3} substrates by DC sputtering. We find that the use of a very thin SrTiO{sub 3} buffer layer (≈2 nm) modify the nucleation of GdBa{sub 2}Cu{sub 3}O{sub 7−δ} on the surface of the substrate reducing the formation of 3 dimensional clusters. Our results demonstrate that 16 nm thick GdBa{sub 2}Cu{sub 3}O{sub 7−δ} films with an average root-mean-square (RMS) smaller than 1 nm and large surface areas (up 10 μm{sup 2}) free of 3 dimensional topological defects can be obtained. In films thinner than 24 nm the onset (zero resistance) of superconducting transition of the films is reduced, being close to liquid nitrogen. This fact can be associated with stress reducing the orthorhombicity and slightly drop in oxygen stoichiometry.

  19. Structure–activity relationships of Pt/Al<sub>2sub>O>3sub> catalysts for CO and NO oxidation at diesel exhaust conditions

    DEFF Research Database (Denmark)

    Boubnov, Alexey; Dahl, Søren; Johnson, Erik

    2012-01-01

    Structure–performance relationships for Pt/Al2O3 catalysts with mean Pt particle sizes of 1, 2, 3, 5 and 10nm are investigated for the catalytic oxidation of CO and NO under lean-burning diesel exhaust conditions. The most active catalysts for CO oxidation exhibit Pt particles of 2–3nm, having...

  20. Chemical bath deposition of Cu{sub 3}BiS{sub 3} thin films

    Energy Technology Data Exchange (ETDEWEB)

    Deshmukh, S.G., E-mail: deshmukhpradyumn@gmail.com; Vipul, Kheraj, E-mail: vipulkheraj@gmail.com [Department of Applied Physics, Sardar Vallabhbhai National Institute of Technology, Ichchhanath, Surat (India); Panchal, A.K. [Department of Electrical Engineering, Sardar Vallabhbhai National Institute of Technology, Ichchhanath, Surat (India)

    2016-05-06

    First time, copper bismuth sulfide (Cu{sub 3}BiS{sub 3}) thin films were synthesized on the glass substrate using simple, low-cost chemical bath deposition (CBD) technique. The synthesized parameters such as temperature of bath, pH and concentration of precursors were optimized for the deposition of uniform, well adherent Cu{sub 3}BiS{sub 3} thin films. The optical, surface morphology and structural properties of the Cu{sub 3}BiS{sub 3} thin films were studied using UV-VIS-NIR spectra, scanning electron microscopy (SEM) and X-ray diffraction (XRD). The as- synthesized Cu{sub 3}BiS{sub 3} film exhibits a direct band gap 1.56 to 1.58 eV having absorption coefficient of the order of 10{sup 5} cm{sup −1}. The XRD declares the amorphous nature of the films. SEM images shows films were composed of close-packed fine spherical nanoparticles of 70-80 nm in diameter. The chemical composition of the film was almost stoichiometric. The optical study indicates that the Cu{sub 3}BiS{sub 3} films can be applied as an absorber layer for thin film solar cells.

  1. Emergence of superconductivity in topological insulator Bi{sub 2}Se{sub 3} by Sr intercalation

    Energy Technology Data Exchange (ETDEWEB)

    Shruti,; Maurya, V. K.; Srivastava, P.; Patnaik, S., E-mail: spatnaik@mail.jnu.ac.in [School of Physical Sciences, Jawaharlal Nehru University, New Delhi-110067 (India)

    2016-05-23

    Recently superconductivity wasreported by Sr intercalation in topological insulator Bi{sub 2}Se{sub 3}. In this report we extensively study anisotropic superconducting properties of Sr{sub 0.1}Bi{sub 2}Se{sub 3} with transition at ~2.9 through resistivity and DC magnetization measurement. We also discuss synthesis methodology for growth of single crystal Sr-Bi{sub 2}Se{sub 3}. The anisotropic properties of Sr{sub 0.1}Bi{sub 2}Se{sub 3} single crystals were studied using transport measurements. Using Ginzburg Landau formulas the upper critical field H{sub c2}(0) comes out to be 2.1 T and 1.4 T for magnetic field applied along the ab-plane and c-axis of the single crystalsand corresponding Ginzburg - Landau coherence lengths are ξ{sub ab} = 15.3 nm and ξ{sub c} = 10.2 nm. The sample shows weak electronic anisotropy Γ = 1.5. Hall resistivity is linear with field at 10 K.

  2. Influence of Al{sub 2}O{sub 3} addition on microstructure and mechanical properties of 3YSZ-Al{sub 2}O{sub 3} composites

    Energy Technology Data Exchange (ETDEWEB)

    Abden, Md. Jaynul [International Islamic Univ., Chittagong (Bangladesh). Dept. of Electrical and Electronic Engineering; Afroze, Jannatul Dil [Noakhali Science and Technology Univ. (Bangladesh). Faculty of Science and Engineering; Gafur, Md. Abdul [Bangladesh Council of Scientific and Industrial Research, Dhaka (Bangladesh). Pilot Plant and Process Development Centre; Chowdhury, Faruque-Uz-Zaman [Chittagong University of Engineering and Technology (Bangladesh). Dept. of Physics

    2015-07-01

    The effect of the amount of Al{sub 2}O{sub 3} content on microstructure, tetragonal phase stability and mechanical properties of 3YSZ-Al{sub 2}O{sub 3} composites are investigated in this study. The ceramic composites are obtained by means of uniaxial compacting at 210 MPa and green compacts are sintered at 1550 C for 3 h in air. The monoclinic zirconia (m-ZrO{sub 2}) phase has completely been transformed into tetragonal zirconia (t-ZrO{sub 2}) phase with corresponding higher Al{sub 2}O{sub 3} content. The t-ZrO{sub 2} grains induce transgranular fracture mode that has contribution in improvement of fracture toughness. The maximum flexural strength of 340 MPa, Vickers hardness value of 14.31 GPa and fracture toughness of 5.1 MPa x m{sup 1/2} in the composition containing 40 wt.-% Al{sub 2}O{sub 3} is attributed to the microstructure with t-ZrO{sub 2} grains as inter- and intragranular particles in the Al{sub 2}O{sub 3} grains, which makes it suitable for dental applications.

  3. Room Temperature Radiolytic Synthesized Cu@CuAlO<sub>2sub>-Al>2sub>O>3sub> Nanoparticles

    Directory of Open Access Journals (Sweden)

    Nayereh Soltani

    2012-09-01

    Full Text Available Colloidal Cu@CuAlO<sub>2sub>-Al>2sub>O>3sub> bimetallic nanoparticles were prepared by a gamma irradiation method in an aqueous system in the presence of polyvinyl pyrrolidone (PVP and isopropanol respectively as a colloidal stabilizer and scavenger of hydrogen and hydroxyl radicals. The gamma irradiation was carried out in a 60Co gamma source chamber with different doses up to 120 kGy. The formation of Cu@CuAlO<sub>2sub>-Al>2sub>O>3sub> nanoparticles was observed initially by the change in color of the colloidal samples from colorless to brown. Fourier transform infrared spectroscopy (FTIR confirmed the presence of bonds between polymer chains and the metal surface at all radiation doses. Results of transmission electron microscopy (TEM, energy dispersive X-ray spectrometry (EDX, and X-ray diffraction (XRD showed that Cu@CuAlO<sub>2sub>-Al>2sub>O>3sub> nanoparticles are in a core-shell structure. By controlling the absorbed dose and precursor concentration, nanoclusters with different particle sizes were obtained. The average particle diameter increased with increased precursor concentration and decreased with increased dose. This is due to the competition between nucleation, growth, and aggregation processes in the formation of nanoclusters during irradiation.

  4. ITO-free organic light-emitting diodes with MoO{sub 3}/Al/MoO{sub 3} as semitransparent anode fabricated using thermal deposition method

    Energy Technology Data Exchange (ETDEWEB)

    Lu, Hsin-Wei; Huang, Ching-Wen [Department of Electrical Engineering, National Cheng Kung University, Tainan 70101, Taiwan (China); Kao, Po-Ching [Department of Electrophysics, National Chiayi University, Chiayi 60004, Taiwan (China); Chu, Sheng-Yuan, E-mail: chusy@mail.ncku.edu.tw [Department of Electrical Engineering, National Cheng Kung University, Tainan 70101, Taiwan (China); Advanced Optoelectronic Technology Center, National Cheng Kung University, Tainan 70101, Taiwan (China)

    2015-08-30

    Highlights: • In this paper, the structure of the proposed devices is substrate (glass; polyethersulfone (PES))/anode (MoO{sub 3}/Al/MoO{sub 3}; MoO{sub 3}/Al)/α-naphthylphenylbiphenyl diamine (NPB) (40 nm)/tris (8-hydroxyquinoline) aluminum (Alq3) (60 nm)/LiF (1 nm)/Al (150 nm). • The optical transmittance of the metal layer was enhanced by depositing metal oxidation (MoO{sub 3}) and metal (Al) layers. • The optimized films show the typical sheet resistance of 7 Ω/sq and a high transmittance of 70% at 550 nm. • The indium-tin-oxide (ITO)-free OLEDs with the fabricated composite anodes on a glass substrate exhibited the high luminance and current efficiency of 21,750 cd/m{sup 2} and 3.18 cd/A, respectively. • The bending effects on PES substrate by depositing metal oxidation (MoO{sub 3}) and metal (Al) layers were also investigated. • MoO{sub 3} covering the Al layer modifies the surface of the electrode and enhances the durability. The surface roughness of the bi-layer films was higher than that of the tri-layer films. Therefore, OLEDs with OMO anode outperform those with bi-layer films anode. - Abstract: In this paper, semitransparent electrodes with the structure substrate/MoO{sub 3}/Al/MoO{sub 3} (OMO) were fabricated via the thermal deposition method for use as the anode in organic light-emitting diodes (OLEDs). The optical transmittance of the metal layer was enhanced by depositing metal oxidation (MoO{sub 3}) and metal (Al) layers. The optimal thickness of the Al thin films was determined to be 15 nm for high optical transmittance and good electrical conductivity. The optimized films show the typical sheet resistance of 7 Ω/sq and a high transmittance of 70% at 550 nm. The indium-tin-oxide (ITO)-free OLEDs with the fabricated composite anodes on a glass substrate exhibited the high luminance and current efficiency of 21,750 cd/m{sup 2} and 3.18 cd/A, respectively. In addition, bending effects on the polyethersulfone (PES) substrate/MoO{sub 3

  5. Nano-grain SnO{sub 2} electrodes for high conversion efficiency SnO{sub 2}-DSSC

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Jung-Hoon; Shin, Yu-Ju [Department of Chemistry, the Catholic University of Korea, Bucheon, Gyeonggi-do 422-743 (Korea, Republic of); Park, Nam-Gyu [School of Chemical Engineering, Sungkyunkwan University, Suwon, Gyeonggi-do 440-746 (Korea, Republic of)

    2011-01-15

    The nano-grain ZnO/SnO{sub 2} composite electrode was prepared by adding 5 w% of the 200-250 nm ZnO particles to the 5 nm SnO{sub 2} colloid in the presence of hydroxypropylcellulose (M.W.=80,000). The nano-grain SnO{sub 2} electrode was obtained by removing the ZnO particles from the composite electrode using acetic acid. The FE-SEM micrographs revealed that both electrodes consisted of interconnected nano-grains that were ca. 800 nm in size, and the large pores between the grains furnished the wide electrolyte diffusion channels within the electrodes. The photovoltaic properties of the nano-grain electrodes were investigated by measuring the I-V behaviors, the IPCE spectra and the ac-impedance spectra. The nano-grain electrodes exhibited remarkably improved conversion efficiencies of 3.96% for the composite and 2.98% for the SnO{sub 2} electrode compared to the value of 1.66% for the usual nano-particle SnO{sub 2} electrode. The improvement conversion efficiencies were mainly attributed to the formation of nano-grains, which facilitated the electron diffusion within the grains. The improved electrolyte diffusion as well as the light-scattering effects enhanced the photovoltaic performance of the SnO{sub 2} electrode. (author)

  6. Radon decay products and 10-1100 nm aerosol particles in Postojna Cave

    Science.gov (United States)

    Bezek, M.; Gregorič, A.; Vaupotič, J.

    2013-03-01

    At the lowest point along the tourist route in Postojna Cave, the activity concentration of radon (222Rn) decay products and the number concentration and size distribution of aerosol particles in the size range of 10-1100 nm were monitored, with the focus on the unattached fraction (fun) of radon decay products (RnDPs), a key parameter in radon dosimetry. The total number concentration of aerosols during visits in summer was lower (700 cm-3) than in winter (2800 cm-3), and was dominated by 50 nm particles (related to the attached RnDPs) in winter. This explains the higher fun values in summer (0.75) and the lower winter measurement (0.04) and, consequently, DCFD values of 43.6 and 13.1 mSv WLM-1 respectively for the calculated dose conversion factors. The difference is caused by an enhanced inflow of fresh outside air, driven in winter by the higher air temperature in the cave compared to outside, resulting in the introduction of outside aerosol particles into the cave.

  7. Interface properties of bilayer structure Alq{sub 3}/Fe{sub 65}Co{sub 35}

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Zhen, E-mail: wangzhen@chd.edu.cn [Department of Applied Physics, Chang’an University, Xi’an 710064 (China); Xu, Chunlong; Wang, Jinguo; Chang, Qiaoli [Department of Applied Physics, Chang’an University, Xi’an 710064 (China); Zuo, Yalu; Xi, Li [Key Laboratory for Magnetism and Magnetic Materials of Ministry of Education, Lanzhou University, Lanzhou 730000 (China)

    2015-04-01

    Highlights: • Bilayer structure of Alq{sub 3}/FeCo was fabricated in a dual ultra high vacuum chamber. • Organic layer reacts partially with the FeCo film. • Electronic injection barrier is 0.76 eV in the interface. • The induced uniaxial anisotropy appears in Alq{sub 3}/FeCo. - Abstract: The interface between the organic and magnetic electrodes is a fundamental problem in organic spintronics devices. Therefore, bilayer structure of Alq{sub 3}/FeCo was fabricated in a dual ultra high vacuum chamber. The electronic structure of Alq{sub 3}–FeCo interface has been studied by X-ray photoelectron spectroscopy and ultraviolet photoelectron spectroscopy with Argon ion etching technique. It was found that organic layer reacts partially with the FeCo film, forming complex binding of metallic carbide and/or oxidation state in the interfacial region. Electronic injection barrier is 0.76 eV in the interface. The structural variation of the contact region is proposed to be one of the possible factors resulting in spin-injection failure. The magnetic properties of FeCo film with different thicknesses on glass substrate and Alq{sub 3} layer are also investigated. The induced uniaxial anisotropy only presents in 3 nm FeCo thickness for glass/FeCo, while it appears in 3–5 nm FeCo for Alq{sub 3}/FeCo.

  8. Enhanced magnetization in V{sub x}Fe{sub 3−x}O{sub 4} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Pool, V.L. [Dept. of Physics, Montana State University, Bozeman, MT 59715 (United States); Kleb, M.T. [Dept. of Chemistry, Montana Tech, Butte, MT 59701 (United States); Ctr. Advanced Supramolecular and Nanoscale Systems, Montana Tech, Butte, MT 59701 (United States); Chorney, C.L. [Dept. of Chemistry, Montana Tech, Butte, MT 59701 (United States); Arenholz, E. [Advanced Light Source, Lawrence Berkeley Nat. Labs, Berkeley, CA 94720 (United States); Idzerda, Y.U., E-mail: Idzerda@montana.edu [Dept. of Physics, Montana State University, Bozeman, MT 59715 (United States)

    2015-12-15

    Nanoparticles of V{sub x}Fe{sub 3−x}O{sub 4} with up to 33% vanadium doping (x=0 to 1) and a 9 nm diameter are investigated in order to determine the site preference of the vanadium and the magnetic behavior of the nanoparticles. The iron and vanadium L{sub 23}-edge X-ray absorption spectroscopy (XAS) and X-ray magnetic circular dichroism (MCD) spectra are used to identify that vanadium initially substitutes into the tetrahedral iron site as V{sup 3+} and that the average iron moment is observed to increase with vanadium concentration up to 12.5% (x=.375). When the vanadium incorporation exceeds 12.5%, the XAS and MCD show that the vanadium begins substituting as V{sup 2+} in the octahedral coordination. This coincides with a rapid reduction of the average moment to zero by 25% (x=.75). The frequency-dependent alternating-current magnetic susceptibility (ACMS) displays a substantial increase in blocking temperature with vanadium concentration and indicated substantial variation in the strength of inter-particle interactions. - Highlights: • Vanadium initially substitutes into the tetrahedral iron site as V{sup 3+}. • The average iron moment increases with vanadium concentration up to 12.5% vanadium (x=.375). • There is a substantial increase in blocking temperature with vanadium concentration. • Above 12.5% vanadium doping, the vanadium substitutes as V{sup 2+} in the octahedral coordination.

  9. Optical and magnetic properties of solid solutions of In{sub 2-x}Mn{sub x}O{sub 3} (0.05, 0.10 and 0.15) nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Khatoon, Sarvari [Nanochemistry Laboratory, Department of Chemistry, Jamia Millia Islamia, New Delhi 110025 (India); Coolahan, Kelsey; Lofland, Samuel E. [Department of Physics and Astronomy, Rowan University, 201 Mullica Hill Road, Glassboro, NJ 08028 (United States); Ahmad, Tokeer, E-mail: tahmad3@jmi.ac.in [Nanochemistry Laboratory, Department of Chemistry, Jamia Millia Islamia, New Delhi 110025 (India)

    2012-12-25

    Highlights: Black-Right-Pointing-Pointer Monophasic Mn-doped In{sub 2}O{sub 3} nanoparticles by solvothermal method for first time. Black-Right-Pointing-Pointer Plausible reaction mechanism and kinetics study using thermogravimetric analysis. Black-Right-Pointing-Pointer Highest surface area obtained so far as compared to the literature report. Black-Right-Pointing-Pointer Particle size decreases with increasing Mn concentration. Black-Right-Pointing-Pointer High degree of optical transparency ({approx}95%) is observed. - Abstract: Mn-doped indium oxide (In{sub 2-x}Mn{sub x}O{sub 3}) nanoparticles (7-12 nm) with x = 0.05, 0.10 and 0.15 have been synthesized by solvothermal method using oxalate precursor route for the first time. Powder X-ray diffraction studies showed the formation of monophasic cubic structure of In{sub 2-x}Mn{sub x}O{sub 3} solid solutions. X-ray diffraction and UV-visible reflectance studies revealed that Mn{sup 2+} ions are doped into the In{sub 2}O{sub 3} lattice. Reflectance measurements showed red shift in an energy band gap which decreases with an increase in the Mn concentration. Maximum surface area of 768 m{sup 2} g{sup -1} is obtained for In{sub 1.85}Mn{sub 0.15}O{sub 3} nanoparticles. Magnetization measurement revealed that all the samples are paramagnetic in nature with very weak antiferromagnetic interactions.

  10. On the mechanisms of titanium particle reactions in O{sub 2}/N{sub 2} and O{sub 2}/Ar atmospheres

    Energy Technology Data Exchange (ETDEWEB)

    Andrzejak, Timothy A.; Shafirovich, Evgeny; Varma, Arvind [School of Chemical Engineering, Purdue University, West Lafayette, IN (United States)

    2009-02-15

    Combustion of titanium particles in air may potentially be used for the in situ synthesis of nanoscale TiO{sub 2} particles, which can photocatalytically degrade chemical and biological air pollutants. The knowledge of Ti particle reactions in O{sub 2}-containing atmospheres is required to develop this method. In the present work, large ({proportional_to}3 mm) single Ti particles were heated by a laser in O{sub 2}/N{sub 2} and O{sub 2}/Ar environments. High-speed digital video recording, thermocouple measurements and quenching at different stages of the process were used for diagnostics. Analysis of the obtained temperature-time curves and quenched particles does not show a significant influence of nitrogen on the oxidation of solid Ti. In all experiments, noticeable surface oxidation started at temperatures between {proportional_to}850 and {proportional_to}950 C, leading to a sharp temperature rise at {proportional_to}1400 C. During prolonged heating at the Ti melting point (1670 C), a liquid TiO{sub 2} bead formed and, after an induction period, ejected fragments. It was shown that this phenomenon may result from an excess of oxygen in the liquid bead. Fragment ejection in O{sub 2}/N{sub 2} atmospheres was more intense than in O{sub 2}/Ar, indicating that N{sub 2} accelerates the oxidation of liquid Ti. (Abstract Copyright [2009], Wiley Periodicals, Inc.)

  11. Sub-10 nm colloidal lithography for circuit-integrated spin-photo-electronic devices

    Directory of Open Access Journals (Sweden)

    Adrian Iovan

    2012-12-01

    Full Text Available Patterning of materials at sub-10 nm dimensions is at the forefront of nanotechnology and employs techniques of various complexity, efficiency, areal scale, and cost. Colloid-based patterning is known to be capable of producing individual sub-10 nm objects. However, ordered, large-area nano-arrays, fully integrated into photonic or electronic devices have remained a challenging task. In this work, we extend the practice of colloidal lithography to producing large-area sub-10 nm point-contact arrays and demonstrate their circuit integration into spin-photo-electronic devices. The reported nanofabrication method should have broad application areas in nanotechnology as it allows ballistic-injection devices, even for metallic materials with relatively short characteristic relaxation lengths.

  12. Photoluminescence characteristics of Sm{sup 3+}-doped Ba{sub 2}CaWO{sub 6} as new orange–red emitting phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Ruiijn [College of Science, Northwest A and F University, Yangling, Shaanxi 712100 (China); Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of); Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Mi Noh, Hyeon; Kee Moon, Byung; Chun Choi, Byung [Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of); Hyun Jeong, Jung, E-mail: jhjeong@pknu.ac.kr [Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of); Sueb Lee, Ho [Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Jang, Kiwan, E-mail: kwjang@changwon.ac.kr [Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Soo Yi, Soung [Department of Electronic Material Engineering, Silla University, Busan 617-736 (Korea, Republic of)

    2014-08-01

    The orange–red emitting Ba{sub 2}CaWO{sub 6}:xSm{sup 3+} (0.01≤x≤0.25) phosphors were synthesized via solid state reaction process. The crystal structure of the phosphor was characterized by XRD. The photoluminescence excitation and emission spectra, concentration effect were investigated. The results show an efficient energy transfer from WO{sub 6}{sup 6−} group to Sm{sup 3+} occurs. The emission spectra of the Ba{sub 2}CaWO{sub 6}:Sm{sup 3+} phosphors consisted of some sharp emission peaks of Sm{sup 3+} ions centre at 579 nm, 618 nm, 625 nm, and 675 nm. The strongest one is located at 610 nm due to {sup 4}G{sub 5/2}→{sup 6}H{sub 7/2} transition of Sm{sup 3+}, generating bright orange–red light. The optimum dopant concentration of Sm{sup 3+} ions in Ba{sub 2}CaWO{sub 6}:xSm{sup 3+} is around 5 mol% and the critical transfer distance of Sm{sup 3+} is calculated as 18 Å. The fluorescence lifetime of Sm{sup 3+} in Ba{sub 2}CaWO{sub 6}:0.05Sm{sup 3+} is 2.36 ms. The Ba{sub 2}CaWO{sub 6}:Sm{sup 3+} phosphors may be potentially used as orange–red phosphors for white light-emitting diodes. - Highlights: • A new host-sensitized Sm{sup 3+}-doped Ba{sub 2}CaWO{sub 6} phosphor was firstly synthesized. • Its structure, luminescent properties are well studied and characterized. • There exists an efficient energy transfer from WO{sub 6}{sup 6−} group to Sm{sup 3+}. • The thermal quenching properties of Ba{sub 2}CaWO{sub 6}:Sm{sup 3+} was firstly evaluated.

  13. Fabrication of full high-T sub c superconducting YBa sub 2 Cu sub 3 O sub 7 sub - sub x trilayer junctions using a polishing technique

    CERN Document Server

    Kuroda, K; Takami, T; Ozeki, T

    2003-01-01

    We have successfully fabricated full high-T sub c superconducting YBa sub 2 Cu sub 3 O sub 7 sub - sub x (YBCO)/PrBa sub 2 Cu sub 3 O sub 7 sub - sub x (PBCO)/YBCO trilayer junctions, which have a simple device structure, such as a Pb-alloy-based Josephson tunneling junction. It has been demonstrated that a polishing technique is extremely useful in the fabrication process: it is effective in smoothing a coarse surface and gentling the slopes of the edges, or decreasing the slope angles. Owing to the polishing technique, the PBCO barrier layer and the upper YBCO layer have been notably thinned: the thicknesses of these layers are 10 nm and 250 nm, respectively. Junctions with the dimensions of 5 mu m x 5 mu m showed resistively shunted junction-like current-voltage curves with a typical critical current density of 110 A/cm sup 2 at 4.2 K. Furthermore, the operation of superconducting quantum interference devices has been demonstrated. (author)

  14. Fabrication of graphene oxide decorated with Fe{sub 3}O{sub 4}@SiO{sub 2} for immobilization of cellulase

    Energy Technology Data Exchange (ETDEWEB)

    Li, Yue; Wang, Xiang-Yu; Jiang, Xiao-Ping; Ye, Jing-Jing; Zhang, Ye-Wang, E-mail: zhangyewang@ujs.edu.cn [Jiangsu University, School of Pharmacy (China); Zhang, Xiao-Yun, E-mail: zhangxiaoyungu@126.com [Jiangsu University, School of Food and Biological Engineering (China)

    2015-01-15

    Fe{sub 3}O{sub 4}@SiO{sub 2}–graphene oxide (GO) composites were successfully fabricated by chemical binding of functional Fe{sub 3}O{sub 4}@SiO{sub 2} and GO and applied to immobilization of cellulase via covalent attachment. The prepared composites were further characterized by transmission electron microscopy and Fourier transform infrared spectroscopy. Fe{sub 3}O{sub 4} nanoparticles (NPs) were monodisperse spheres with a mean diameter of 17 ± 0.2 nm. The thickness of SiO{sub 2} layer was calculated as being 6.5 ± 0.2 nm. The size of Fe{sub 3}O{sub 4}@SiO{sub 2} NPs was 24 ± 0.3 nm, similar to that of Fe{sub 3}O{sub 4}@SiO{sub 2}–NH{sub 2}. Fe{sub 3}O{sub 4}@SiO{sub 2}–GO composites were synthesized by linking of Fe{sub 3}O{sub 4}@SiO{sub 2}–NH{sub 2} NPs to GO with the catalysis of EDC and NHS. The prepared composites were used for immobilization of cellulase. A high immobilization yield and efficiency of above 90 % were obtained after the optimization. The half-life of immobilized cellulase (722 min) was 3.34-fold higher than that of free enzyme (216 min) at 50 °C. Compared with the free cellulase, the optimal temperature of the immobilized enzyme was not changed; but the optimal pH was shifted from 5.0 to 4.0, and the thermal stability was enhanced. The immobilized cellulase could be easily separated and reused under magnetic field. These results strongly indicate that the cellulase immobilized onto the Fe{sub 3}O{sub 4}@SiO{sub 2}–GO composite has potential applications in the production of bioethanol.

  15. Fabrication of Y{sub 2}Ti{sub 2}O{sub 7}:Yb{sup 3+},Ho{sup 3+} nanoparticles by a gel-combustion approach and upconverting luminescent properties

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Zhongsheng, E-mail: zhshcheng@ecit.cn [State Key Laboratory Breeding Base of Nuclear Resources and Environment, East China Institute of Technology, Nanchang, Jiangxi 330013 (China); Wang, Min; Wang, Haiqing; Le, Zhanggao; Huang, Guolin; Zou, Lixia; Liu, Zhirong [State Key Laboratory Breeding Base of Nuclear Resources and Environment, East China Institute of Technology, Nanchang, Jiangxi 330013 (China); Wang, Dianyuan; Wang, Qingkai [College of Science, Jiujiang University, Jiujiang, Jiangxi 332005 (China); Gong, Weiping [Electronic Science Department, Huizhou University, Huizhou, Guangdong 516001 (China)

    2014-09-01

    Highlights: • Co-doped (Y{sub 0.99−x}Ho{sub 0.01}Yb{sub x}){sub 2}Ti{sub 2}O{sub 7} nanophosphors were fabricated by gel-combustion method. • The effect of calcination and Yb{sup 3+} doping on upconverting spectra of nanophosphors was studied. • The dependence of upconverting intensity on the excitation power was examined. - Abstract: Yb{sup 3+}, Ho{sup 3+} co-doped pyrochlore-structured (Y{sub 0.99−x}Ho{sub 0.01}Yb{sub x}){sub 2}Ti{sub 2}O{sub 7} (x = 0, 2.5, 5.0, 7.5, 10.0 and 12.5 mol%) nanoparticles (NPs) were successfully fabricated via a gel-combustion approach. The products as-obtained were characterized by various techniques, i.e. X-ray diffraction, transmission electron microscope, Fourier transformed infrared spectra and upconverting spectra. The results indicate that the bright green (∼540 nm) and red (∼660 nm) emissions are observed in Y{sub 2}Ti{sub 2}O{sub 7}:Ho{sup 3+},Yb{sup 3+} NPs under the 980 nm excitation, which is ascribed to the radiative transitions ({sup 5}F{sub 4},{sup 5}S{sub 2}) → {sup 5}I{sub 8} and {sup 5}F{sub 5} → {sup 5}I{sub 8} of Ho{sup 3+} ions, respectively. It is also found that the calcining temperature and Yb{sup 3+} ion doping level have a great influence on the upconverting spectra of (Y{sub 0.99−x}Ho{sub 0.01}Yb{sub x}){sub 2}Ti{sub 2}O{sub 7} NPs. The emission intensities increase initially and then fall down from 800 to 1000 °C. The optimum doping level of Yb{sup 3+} ions is 7.5 mol%, and the intensity of upconverting emissions for (Y{sub 0.915}Ho{sub 0.01}Yb{sub 0.075}){sub 2}Ti{sub 2}O{sub 7} NPs is enhanced by the fold of 32 compared to the Yb{sup 3+}-free samples. The dependence of upconverting intensity on the excitation power reveals the contribution of two photons to both the green and red upconverting process under lower excitation power, and the possible upconverting mechanisms have been proposed accordingly.

  16. Self-reduction process and enhanced blue emission in SrAl{sub 2}Si{sub 2}O{sub 8}: Eu, Tb via electron transfer from Tb{sup 3+} to Eu{sup 3+}

    Energy Technology Data Exchange (ETDEWEB)

    Xu, Hongwei; Wang, Lili; Li, Minhong; Ran, Weiguang; Deng, Zhihan; Houzong, Ruizhi; Shi, Jinsheng [Department of Chemistry and Pharmaceutical Science, Qingdao Agricultural University, Qingdao 266109, Shandong, (China)

    2017-06-15

    Eu, Tb co-doped SrAl{sub 2}Si{sub 2}O{sub 8} luminescent materials were synthesized via a high-temperature solid-state reaction. Excitation spectra of SrAl{sub 2}Si{sub 2}O{sub 8}: Eu{sup 2+} gives two broad excitation bands maximizing at 270 and 330 nm, resulting from splitting Eu{sup 2+} energy levels in octahedral crystal field. Eu single doped SrAl{sub 2}Si{sub 2}O{sub 8} luminescent material exhibits two emission bands at about 406 and 616 nm. Intensity of the blue emission from Eu{sup 2+} is always strong, compared with that of the red emission band of Eu{sup 3+}. Reduction from Eu{sup 3+} to Eu{sup 2+} can be explained with the model of charge compensation. Blue emission in SrAl{sub 2}Si{sub 2}O{sub 8}: xEu was strengthened after incorporation of Tb, which can be explained by electron transfer from Tb{sup 3+} to Eu{sup 3+} (Tb{sup 3+} + Eu{sup 3+} → Tb{sup 4+} + Eu{sup 2+}). Under 230 nm excitation, intensity of Tb{sup 3+} emission was nearly unchanged and that of Eu{sup 2+} was increased, obviously due to the delivery of more electrons to Eu{sup 3+}. The strongest emission of Eu{sup 2+} in 0.09Eu/0.06Tb co-doped SrAl{sub 2}Si{sub 2}O{sub 8} and excited at 270 and 330 nm was remarkably enhanced by about four times compared to that of 0.15Eu Single doped SrAl{sub 2}Si{sub 2}O{sub 8}. All of the results indicate that SrAl{sub 2}Si{sub 2}O{sub 8}:xEu, yTb are potential blue emitting luminescent materials for UV-LEDs. More importantly, this research may provide a new perspective in designing broad band blue luminescent materials. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  17. A simple large-scale synthesis of mesoporous In{sub 2}O{sub 3} for gas sensing applications

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Su; Song, Peng, E-mail: mse_songp@ujn.edu.cn; Yan, Huihui; Yang, Zhongxi; Wang, Qi, E-mail: mse_wangq@ujn.edu.cn

    2016-08-15

    Graphical abstract: Large-scale mesoporous In{sub 2}O{sub 3} nanostructures for gas-sensing applications were successfully fabricated via a facile Lewis acid catalytic the furfural alcohol resin template route. - Highlights: • Mesoporous In{sub 2}O{sub 3} nanostructures with high-yield have been successfully fabricated via a facile strategy. • The microstructure and formation mechanism of mesoporous In{sub 2}O{sub 3} nanostructures were discussed based on the experimental results. • The as-prepared In{sub 2}O{sub 3} samples exhibited high response, short response-recovery times and good selectivity to ethanol gas. - Abstract: In this paper, large-scale mesoporous In{sub 2}O{sub 3} nanostructures were synthesized by a facile Lewis acid catalytic the furfural alcohol resin (FAR) template route for the high-yield. Their morphology and structure were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), differential thermal and thermogravimetry analysis (DSC-TG) and the Brunauer-Emmett-Teller (BET) approach. The as-obtained mesoporous In{sub 2}O{sub 3} nanostructures possess excellent mesoporous and network structure, which increases the contact area with the gases, it is conducive for adsorption-desorption of gas on the surface of In{sub 2}O{sub 3}. The In{sub 2}O{sub 3} particles and pores were both about 15 nm and very uniform. In gas-sensing measurements with target gases, the gas sensor based on mesoporous In{sub 2}O{sub 3} nanostructures showed a good response, short response-recovery time, good selectivity and stability to ethanol. These properties are due to the large specific surface area of mesoporous structure. This synthetic method could use as a new design concept for functional mesoporous nanomaterials and for mass production.

  18. Syngas production from CO{sub 2}-reforming of CH{sub 4} over sol-gel synthesized Ni-Co/Al{sub 2}O{sub 3}-MgOZrO{sub 2} nanocatalyst: effect of ZrO{sub 2} precursor on catalyst properties and performance

    Energy Technology Data Exchange (ETDEWEB)

    Sajjadi, Seyed Mehdi; Haghighi, Mohammad; Rahmani, Farhad, E-mail: haghighi@sut.ac.ir [Reactor and Catalysis Research Center, Sahand University of Technology, Tabriz (Iran, Islamic Republic of)

    2015-05-15

    Ni-Co/Al{sub 2}O{sub 3}-MgO-ZrO{sub 2} nanocatalyst with utilization of two different zirconia precursors, namely, zirconyl nitrate hydrate (ZNH) and zirconyl nitrate solution (ZNS), was synthesized via the sol-gel method. The physiochemical properties of nanocatalysts were characterized by XRD, FESEM, EDX, BET and FTIR analyses and employed for syngas production from CO{sub 2}-reforming of CH{sub 4}. XRD patterns, exhibiting proper crystalline structure and homogeneous dispersion of active phase for the nanocatalyst ZNS precursor employed (NCAMZ-ZNS). FESEM and BET results of NCAMZ-ZNS presented more uniform morphology and smaller particle size and consequently higher surface areas. In addition, average particle size of NCAMZ-ZNS was 15.7 nm, which is close to the critical size for Ni-Co catalysts to avoid carbon formation. Moreover, FESEM analysis indicated both prepared samples were nanoscale. EDX analysis confirmed the existence of various elements used and also supported the statements made in the XRD and FESEM analyses regarding dispersion. Based on the excellent physiochemical properties, NCAMZ-ZNS exhibited the best reactant conversion across all of the evaluated temperatures, e.g. CH{sub 4} and CO{sub 2} conversions were 97.2 and 99% at 850 °C, respectively. Furthermore, NCAMZZNS demonstrated a stable yield with H{sub 2}/CO close to unit value during the 1440 min stability test. (author)

  19. Preparation and characterization of sol-gel derived 4%La{sub 2}O{sub 3}-Al{sub 2}O{sub 3} ceramic membrane on clay-based supports

    Energy Technology Data Exchange (ETDEWEB)

    Ersoy, B. [Afyon Kocatepe Univ., Mining Engineering Dept., AFYON (Turkey); Gunay, V. [TUBITAK-MRC, MCTRI, Gebze-KOCAELI (Turkey)

    2004-07-01

    In this work, {gamma}-Al{sub 2}O{sub 3} membrane layer (4 wt% La{sub 2}O{sub 3}+96% Al{sub 2}O{sub 3}) was coated on the clay based porous support by using the sol-gel coating. The coating solution was prepared by using boehmite (AlOOH), La-nitrate (La{sub 2}(NO{sub 3}){sub 3}.6H{sub 2}O), PVA, distilled water and HNO{sub 3}. The thickness of the {gamma}-Al{sub 2}O{sub 3} membrane layer was between 5-7 {mu}m. Two unprocessed clay samples which were supplied from Kutahya and Balikesir regions, were used to produce supports for the membranes. Porosities of the supports were varied from 25 to 40% depending on sintering temperatures. Mean pore diameter of the supports were between 0.01-1{mu}m. The mean pore diameter of 4wt%La{sub 2}O{sub 3} - Al{sub 2}O{sub 3} membrane layer was around 11 nm and total pore area was 113 m{sup 2} / g at 1000 C for 1 hour. (orig.)

  20. Thermoluminescence response of K{sub 2}Ca{sub 2}(SO{sub 4}){sub 3} nanophosphor Co-doped with Eu and Ce for gamma ray dosimetry

    Energy Technology Data Exchange (ETDEWEB)

    Patil, B. J. [Dept. of Physics, Abasaheb Garware College, Pune-411004 (India); Bhadane, Mahesh S.; Dahiwale, S. S.; Bhoraskar, V. N.; Dhole, S. D., E-mail: sanjay@physics.unipune.ac.in [Department of Physics, University of Pune, Pune 411007 (India); Mandlik, N. T. [Dept. of Physics, Fergusson College, Pune-411004 (India); Kulkarni, M. S. [Radiation Safety Systems Division, Bhabha Atomic Research Centre, Mumbai 400 085 (India); Bhatt, B. C. [Radiological Physics and Advisory Division, Bhabha Atomic Research Centre, Mumbai 400 085 (India)

    2015-06-24

    K{sub 2}Ca{sub 2}(SO{sub 4}){sub 3} nanophosphors co-doped with Eu and Ce were synthesized by the chemical co-precipitation method. These samples were further annealed at 700 °C structural reformation. The structural and morphological characteristics were studied using XRD and TEM techniques. The particle size calculated from XRD spectra was around 35 nm. The as synthesized sample shows cubic structure annealed at 700 °C. The as synthesized and annealed sample of K{sub 2}Ca{sub 2}(SO{sub 4}){sub 3}: EuCe were irradiated with Co{sup 60} gamma rays for the doses from 2Gy to 1kGy. The TL characteristic sample of co-doped were studied for the dosimetric application by gamma radiation. The TL spectrum of annealed sample has single peaked at 160 °C. The Eu doped sample has a high TL sensitivity than Ce doped sample. But after co-doping with Eu and Ce, TL intensity observed to be decreased. The decrees in TL peak intensity of the phosphor on co-doping of Eu and Ce gives an insight into the emission mechanism of the phosphor which involves energy transfer from Eu to Ce. The TL response of all the samples were found to be linear for the dose from 2 Gy to 1 KGy. Therefore, K{sub 2}Ca{sub 2}(SO{sub 4}){sub 3}: EuCe nanophosphor can be used for the measurement of high dose of gamma radiation.

  1. Synthesis and photoluminescent properties of Sr{sub (1−x)}Si{sub 2}O{sub 2}N{sub 2}: xEu{sup 2+} phosphor prepared by polymer metal complex method for WLEDs applications

    Energy Technology Data Exchange (ETDEWEB)

    Hassan, Dhia A., E-mail: dhia_hassan@yahoo.com [Department of Materials Science and Engineering, College of Materials, Xiamen University, Xiamen 361005 (China); Department of Chemistry, College of Education for Pure Science, University of Basrah, Basrah 61004 (Iraq); Xu, Jian; Chen, Yibin; Li, Langkai [Department of Materials Science and Engineering, College of Materials, Xiamen University, Xiamen 361005 (China); Zeng, Renjie, E-mail: rjzeng@xmu.edu.cn [Department of Materials Science and Engineering, College of Materials, Xiamen University, Xiamen 361005 (China); Fujian Key Lab of Advanced Special Materials, Xiamen University, Xiamen 361005 (China)

    2016-07-15

    Highlights: • SrSi{sub 2}O{sub 2}N{sub 2}: Eu{sup 2+} phosphor was prepared by polymer metal complex (pechini method). • The annealing time was decreased from 6 h in solid state method to 3 h. • The particles are crystalline and dispersed well with average size 6.5 μm. - Abstract: Green emitting Sr{sub (1−x)}Si{sub 2}O{sub 2}N{sub 2}: xEu{sup 2+} (x = 0, 0.02, 0.04, 0.06, 0.08 and 0.1) phosphors were synthesized by polymer metal complex or pechini method. The XRD results confirm the formation of a pure phase at 1400 °C for 3 h. The SEM and particles size results indicate that the prepared phosphor consists of a polyhedral crystalline shape with well dispersed and the average particle size around 6.5 μm. The maximum PL intensity was found at 0.04% Eu{sup 2+} with a wide emission band between 460 and 640 nm and a green emission peak at 531.4 nm. The external quantum efficiency of 0.04% Eu{sup 2+} sample was 43.13%. The results indicate that pechini method is an alternative way and close in efficiency to the solid state method to prepare SrSi{sub 2}O{sub 2}N{sub 2} phosphor with higher homogeneity and more uniform size distribution for near UV and blue region applications for white light emitting diodes WLEDs.

  2. Monodispersed MnO nanoparticles with epitaxial Mn{sub 3}O{sub 4} shells

    Energy Technology Data Exchange (ETDEWEB)

    Berkowitz, A E; Rodriguez, G F [Department of Physics, University of California, San Diego La Jolla, CA 92093 (United States); Hong, J I; Fullerton, E E [Center for Magnetic Recording Research, University of California-San Diego La Jolla, CA 92093 (United States); An, K; Hyeon, T [National Creative Research Initiative Center for Oxide Nanocrystalline Materials, Seoul National University, Seoul 151-744 (Korea, Republic of); Agarwal, N; Smith, D J [School of Materials and Department of Physics, Arizona State University, Tempe, AZ 85287 (United States)

    2008-07-07

    We report the microstructural and magnetic properties of monodispersed nanoparticles (NPs) of antiferromagnetic MnO (T{sub N} = 118 K), with epitaxial ferrimagnetic Mn{sub 3}O{sub 4} (T{sub C} = 43 K) shells. Above T{sub C}, an unusually large magnetization is present, produced by the uncompensated spins (UCSs) on the surface of the MnO particles. These spins impart a net anisotropy to the MnO particles that is approximately three orders of magnitude larger than the bulk value. As a result, an anomalously high blocking temperature is exhibited by the MnO particles, and finite coercivity and exchange bias are present above T{sub C}. When field cooled below T{sub C}, a strong exchange bias was established in the Mn{sub 3}O{sub 4} shells as a result of high net anisotropy of the MnO particles. A large coercivity was also observed. Models of several aspects of the behaviour of this unusual system emphasized the essential role of the UCSs on the surfaces of the MnO NPs.

  3. Sol-gel synthesis of Bi{sub 3.25}La{sub 0.75}Ti{sub 3}O{sub 12} nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Wang Wen, E-mail: wangwen@hit.edu.cn [Institute for Advanced Ceramics, School of Materials Science and Engineering, Harbin Institute of Technology, No. 92 West Da-Zhi Street, Harbin 150001, Heilongjiang (China); Hua, Ke; Jiancun, Rao; Jinbiao, Feng; Ming, Feng; Dechang, Jia; Yu, Zhou [Institute for Advanced Ceramics, School of Materials Science and Engineering, Harbin Institute of Technology, No. 92 West Da-Zhi Street, Harbin 150001, Heilongjiang (China)

    2011-04-07

    Research highlights: > One-dimensional (1D) ferroelectrics have been successfully synthesized. The sol-gel template synthesis is a versatile and inexpensive technique for producing nanostructures, and particularly facilitates the fabrication of complex oxide nanotubes or nanowires. Compared with the synthesis of the general nanotubes such as carbon nanotubes with simple crystal structure, the synthesis of ferroelectric compound is difficult due to the multielement and the complex crystal structures of these ferroelectrics. Herein, we report the synthesis of one-dimensional BLT nanotubes on anodic alumina (AAO) templates by immersing a template membrane in sol without polymeric additive. - Abstract: Ferroelectric Bi{sub 3.25}La{sub 0.75}Ti{sub 3}O{sub 12} (BLT) nanotubes were synthesized by sol-gel technique using nanochannel porous anodic aluminum oxide (AAO) templates, and were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM) and high resolution transmission electron microscopy (HRTEM). BLT nanotubes with diameter of around 240 nm and the wall thickness of about 25 nm exhibited a single orthorhombic perovskite structure and highly preferential crystal growth along the [1 1 7] orientation, which have smooth wall morphologies and well-defined diameters corresponding to the diameter of the applied template. The formation mechanism of BLT nanotubes was discussed.

  4. Size dependent magnetic and magneto-optical properties of Ni{sub 0.2}Zn{sub 0.8}Fe{sub 2}O{sub 4} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Li, Oksana A., E-mail: log85@mail.ru [Department of Applied Physics, National Pingtung University, Pingtung 90003, Taiwan (China); Siberian Federal University, Krasnoyarsk 660041 (Russian Federation); Lin, Chun-Rong, E-mail: crlin@mail.nptu.edu.tw [Department of Applied Physics, National Pingtung University, Pingtung 90003, Taiwan (China); Chen, Hung-Yi; Hsu, Hua-Shu [Department of Applied Physics, National Pingtung University, Pingtung 90003, Taiwan (China); Shih, Kun-Yauh [Department of Applied Chemistry, National Pingtung University, Pingtung 90003, Taiwan (China); Edelman, Irina S. [L.V. Kirensky Institute of Physics, SB RAS, Krasnoyarsk 660036 (Russian Federation); Wu, Kai-Wun; Tseng, Yaw-Teng [Department of Applied Physics, National Pingtung University, Pingtung 90003, Taiwan (China); Ovchinnikov, Sergey G. [Siberian Federal University, Krasnoyarsk 660041 (Russian Federation); L.V. Kirensky Institute of Physics, SB RAS, Krasnoyarsk 660036 (Russian Federation); Lee, Jiann-Shing [Department of Applied Physics, National Pingtung University, Pingtung 90003, Taiwan (China)

    2016-06-15

    Ni{sub 0.2}Zn{sub 0.8}Fe{sub 2}O{sub 4} spinel nanoparticles have been synthesized by combustion method. Average particles size varies from 15.5 to 50.0 nm depending on annealing temperature. Correlations between particles size and magnetic and magneto-optical properties are investigated. Magnetization dependences on temperature and external magnetic field correspond to the sum of paramagnetic and superparamagnetic response. Critical size of single-domain transition is found to be 15.9 nm. Magnetic circular dichroism (MCD) studies of nickel zinc spinel are presented here for the first time. The features in magnetic circular dichroism spectrum are assigned to the one-ion d–d transitions in Fe{sup 3+} and Ni{sup 2+} ions, as well to the intersublattice and intervalence charge transfer transitions. The MCD spectrum rearrangement was revealed with the change of the nanoparticles size. - Highlights: • Ni{sub 0.2}Zn{sub 0.8}Fe{sub 2}O{sub 4} nanoparticles were synthesized by combustion method. • Structure and magnetic properties are studied. • Magnetic circular dichroism (MCD) of nickel zinc spinel was measured for the first time. • The MCD spectrum rearrangement was revealed with the change of the nanoparticles size.

  5. Effect of fabrication conditions on phase formation and properties of epitaxial (PbMg{sub 1/3}Nb{sub 2/3}O{sub 3}){sub 0.67}-(PbTiO{sub 3}){sub 0.33} thin films on (001) SrTiO{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Boota, Muhammad [MESA+ Institute for Nanotechnology, Faculty of Science and Technology, University of Twente, P.O. Box 217, 7500AE Enschede (Netherlands); Engineering Department, University of Rome “ROMA TRE”, Via della Vasca Navale 79, 00146 Rome (Italy); Houwman, Evert P., E-mail: e.p.houwman@utwente.nl; Nguyen, Minh D.; Rijnders, Guus [MESA+ Institute for Nanotechnology, Faculty of Science and Technology, University of Twente, P.O. Box 217, 7500AE Enschede (Netherlands); Lanzara, Giulia [Engineering Department, University of Rome “ROMA TRE”, Via della Vasca Navale 79, 00146 Rome (Italy)

    2016-05-15

    The pulsed laser deposition process of 300 nm thick films of Pb(Mg{sub 1/3}Nb{sub 2/3})O{sub 3}){sub 0.67}-(PbTiO{sub 3}){sub 0.33} on (001)-oriented SrTiO{sub 3} was studied by varying deposition pressure, substrate deposition temperature, laser fluence on the target and target-substrate distance. Perovskite phase pure, (001)-oriented, epitaxial smooth films were obtained in a narrow range of deposition parameters. The ferroelectric and dielectric properties of films fabricated within this parameter range still vary significantly. This shows the sensitivity of the system for growth conditions. The best film has a polarization value close to that expected for a (001) poled, stress free single crystal film. All films show deposition conditions dependent variations in the self-bias field. The self-bias is very stable during long cycling for films made at optimum deposition conditions. The piezoelectric coefficients of the films are strongly reduced with respect to bulk single crystal values due to the film clamping. The properties variations are ascribed to changes in the grain boundary properties in which film defects are expected to accumulate. Notably slight off-stoichiometry may cause localized screening charges, affecting specifically the polarization and dielectric constant.

  6. Frequency upconversion fluorescence studies of Er{sup 3+}/Yb{sup 3+}-codoped KNbO{sub 3} phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Balakrishnaiah, R. [Department of Electronic Materials Engineering, Silla University, Busan 617-736 (Korea, Republic of); Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Kim, Dong Woo [Department of Electronic Materials Engineering, Silla University, Busan 617-736 (Korea, Republic of); Yi, Soung Soo, E-mail: ssyi@silla.ac.k [Department of Electronic Materials Engineering, Silla University, Busan 617-736 (Korea, Republic of); Kim, Kwang Duk; Kim, Sung Hoon [Department of Engineering in Energy and Applied Chemistry, Silla University, Busan 617-736 (Korea, Republic of); Jang, Kiwan; Lee, Ho Sueb [Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Jeong, Jung Hyun [Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of)

    2009-05-29

    Different concentrations of Er{sup 3+} and Yb{sup 3+} ions-doped potassium niobate (K{sub 0.9}NbO{sub 3}:Yb{sub (x)}Er{sub (0.1-x)} for x = 0, 0.01, 0.05, 0.09 and 0.1) polycrystalline powder phosphors were prepared by the conventional solid state reaction method and were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM) techniques. Energy transfer and upconversion fluorescence properties of the Yb{sup 3+} and Er{sup 3+}-codoped phosphors have been discussed. The XRD data has shown mono-phase for pure KNbO{sub 3} while the doped samples represented additional phase formation. The SEM micrographs represented the rectangular crystal growth habit for the KNbO{sub 3} phosphors when doped with 0.1 mol of Er{sup 3+} ions. An intense green emission at 557 nm along with a red emission at 674 nm was observed when the doped samples were excited with 975 nm IR radiation. The upconversion mechanism has been discussed based on the excited state absorption and energy transfer mechanisms.

  7. Thermoluminescence and optically stimulated luminescence properties of Dy{sup 3+}-doped CaO–Al{sub 2}O{sub 3}–B{sub 2}O{sub 3}-based glasses

    Energy Technology Data Exchange (ETDEWEB)

    Yahaba, T., E-mail: takuma.yahaba.s1@dc.tohoku.ac.jp [Department of Applied Chemistry, Graduate School of Engineering, Tohoku University, 6-6-07 Aramaki Aza Aoba, Aoba-ku, Sendai 980-8579 (Japan); Fujimoto, Y. [Department of Applied Chemistry, Graduate School of Engineering, Tohoku University, 6-6-07 Aramaki Aza Aoba, Aoba-ku, Sendai 980-8579 (Japan); Yanagida, T. [Nara Institute of Science and Technology (NAIST), 8916-5 Takayama, Ikoma 630-0192 (Japan); Koshimizu, M.; Tanaka, H.; Saeki, K.; Asai, K. [Department of Applied Chemistry, Graduate School of Engineering, Tohoku University, 6-6-07 Aramaki Aza Aoba, Aoba-ku, Sendai 980-8579 (Japan)

    2017-02-01

    We developed Dy{sup 3+}-doped CaO–Al{sub 2}O{sub 3}–B{sub 2}O{sub 3} based glasses with Dy concentrations of 0.5, 1.0, and 2.0 mol% using a melt-quenching technique. The as-synthesized glasses were applicable as materials exhibiting thermoluminescence (TL) and optically stimulated luminescence (OSL). The optical and radiation response properties of the glasses were characterized. In the photoluminescence (PL) spectra, two emission bands due to the {sup 4}F{sub 9/2} → {sup 6}H{sub 15/2} and {sup 4}F{sub 9/2} → {sup 6}H{sub 13/2} transitions of Dy{sup 3+} were observed at 480 and 580 nm. In the OSL spectra, the emission band due to the {sup 4}F{sub 9/2} → {sup 6}H{sub 15/2} transition of Dy{sup 3+} was observed. Excellent TL and OSL responses were observed for dose ranges of 0.1–90 Gy. In addition, TL fading behavior was better than that of OSL in term of the long-time storage. These results indicate that the Dy{sup 3+}-doped CaO–Al{sub 2}O{sub 3}–B{sub 2}O{sub 3}-based glasses are applicable as TL materials.

  8. (Pt{sub 1–x}Cu{sub x}){sub 3}Cu{sub 2}B and Pt{sub 9}Cu{sub 3}B{sub 5}, the first examples of copper platinum borides. Observation of superconductivity in a novel boron filled β-Mn-type compound

    Energy Technology Data Exchange (ETDEWEB)

    Salamakha, Leonid P. [Institute of Solid State Physics, TU Wien, A-1040 Wien (Austria); Sologub, Oksana, E-mail: oksana.sologub@univie.ac.at [Institute of Solid State Physics, TU Wien, A-1040 Wien (Austria); Stöger, Berthold [Institute of Chemical Technologies and Analytics, TU Wien, A-1040 Wien (Austria); Michor, Herwig; Bauer, Ernst [Institute of Solid State Physics, TU Wien, A-1040 Wien (Austria); Rogl, Peter F. [Institute of Physical Chemistry, University of Vienna, A-1090 Wien (Austria)

    2015-09-15

    New ternary copper platinum borides have been synthesized by arc melting of pure elements followed by annealing at 600 °C. The structures have been studied by X-ray single crystal and powder diffraction. (Pt{sub 1−x}Cu{sub x}){sub 3}Cu{sub 2}B (x=0.33) forms a B-filled β-Mn-type structure (space group P4{sub 1}32; a=0.6671(1) nm). Cu atoms are distributed preferentially on the 8c atom sites, whereas the 12d site is randomly occupied by Pt and Cu atoms (0.670(4) Pt±0.330(4) Cu). Boron is located in octahedral voids of the parent β-Mn-type structure. Pt{sub 9}Cu{sub 3}B{sub 5} (space group P-62m; a=0.9048(3) nm, c=0.2908(1) nm) adopts the Pt{sub 9}Zn{sub 3}B{sub 5–δ}-type structure. It has a columnar architecture along the short translation vector exhibiting three kinds of [Pt{sub 6}] trigonal prism columns (boron filled, boron semi-filled and empty) and Pt channels with a pentagonal cross section filled with Cu atoms. The striking structural feature is a [Pt{sub 6}] cluster in form of an empty trigonal prism at the origin of the unit cell, which is surrounded by coupled [BPt{sub 6}] and [Pt{sub 6}] trigonal prisms, rotated perpendicularly to the central one. There is no B–B contact as well as Cu–B contact in the structure. The relationships of Pt{sub 9}Cu{sub 3}B{sub 5} structure with the structure of Ti{sub 1+x}Os{sub 2−x}RuB{sub 2} as well as with the structure families of metal sulfides and aluminides have been elucidated. (Pt{sub 1–x}Cu{sub x}){sub 3}Cu{sub 2}B (x=0.3) (B-filled β-Mn-type structure) is a bulk superconductor with a transition temperature of about 2.06 K and an upper critical field μ{sub 0}H{sub C2}(0){sup WHH} of 1.2 T, whereas no superconducting transition has been observed up to 0.3 K in Pt{sub 9}Cu{sub 3}B{sub 5} (Pt{sub 9}Zn{sub 3}B{sub 5–δ}-type structure) from electrical resistivity measurements. - Highlights: • First two copper platinum borides, (Pt{sub 0.67}Cu{sub 0.33}){sub 3}Cu{sub 2}B and Pt{sub 9}Cu{sub 3}B{sub

  9. Scintillation and optical properties of Ce{sup 3+}-doped CaGdAl{sub 3}O{sub 7} single crystals

    Energy Technology Data Exchange (ETDEWEB)

    Mori, Masaki, E-mail: masaki.mori.mz4@ms.naist.jp [Graduate School of Materials Science, Nara Institute of Science and Technology (NAIST), 8916-5 Takayama-cho, Ikoma-shi, Nara 630-0192 (Japan); Nakauchi, Daisuke; Okada, Go [Graduate School of Materials Science, Nara Institute of Science and Technology (NAIST), 8916-5 Takayama-cho, Ikoma-shi, Nara 630-0192 (Japan); Fujimoto, Yutaka [Department of Applied Chemistry, Graduate School of Engineering, Tohoku University, 6-6-07 Aoba, Aramaki, Aoba-ku, Sendai, 980-8579 (Japan); Kawaguchi, Noriaki [Graduate School of Materials Science, Nara Institute of Science and Technology (NAIST), 8916-5 Takayama-cho, Ikoma-shi, Nara 630-0192 (Japan); Koshimizu, Masanori [Department of Applied Chemistry, Graduate School of Engineering, Tohoku University, 6-6-07 Aoba, Aramaki, Aoba-ku, Sendai, 980-8579 (Japan); Yanagida, Takayuki [Graduate School of Materials Science, Nara Institute of Science and Technology (NAIST), 8916-5 Takayama-cho, Ikoma-shi, Nara 630-0192 (Japan)

    2017-06-15

    The single crystals of 0, 0.6, 1, 1.6 and 2 mol% Ce doped CaGdAl{sub 3}O{sub 7} (Ce:CGAM) were grown by the Floating Zone method, and investigated on photoluminescence (PL) and scintillation properties. In the PL spectra, a broad emission appeared over 380–500 nm under 280 and 360 nm excitations with the quantum yield of 33.8–38.8%. Under a vacuum ultraviolet excitation (90 nm) using a synchrotron source, non-doped CGAM single crystal showed broad emissions over 250–650 nm. The PL decay time profiles followed a monotonic exponential decay with a decay time constant of around 33 ns. The scintillation spectra were similar to those of PL. All of the samples exhibited a clear photoabsorption peak and Compton edge in the pulse height spectra measured under {sup 137}Cs γ-ray irradiation, and the absolute scintillation light yield (LY) was highest for the 2% Ce-doped sample with the value of 3300±300 ph/MeV. The scintillation decay profiles were approximated by a third order exponential decay function, and the extracted decay time of Ce{sup 3+} emission component was around 36–44 ns. Among all the samples, 2%Ce:CGAM single crystal sample showed the best afterglow level as a scintillator under X-ray irradiation. - Highlights: •Ce{sup 3+}-doped CaGdAl{sub 3}O{sub 7} single crystals were synthesized by the FZ method. •Optical and scintillation properties of Ce{sup 3+}-doped CaGdAl{sub 3}O{sub 7} were investigated. •Photoabsorption peak in a pulse height spectrum was clearly observed under γ-rays.

  10. Scalability of Ferroelectric Tunnel Junctions to Sub-100 nm Dimensions

    Science.gov (United States)

    Abuwasib, Mohammad

    The ferroelectric tunnel junction (FTJ) is an emerging low-power device that has potential application as a non-volatile memory and logic element in beyond-CMOS circuits. As a beyond- CMOS device, it is necessary to investigate the device scaling limit of FTJs to sub-50 nm dimensions. In addition to the fabrication of scaled FTJs, the integration challenges and CMOS compatibility of the device needs to be addressed. FTJ device performance including ON/OFF ratio, memory retention time, switching endurance, write /read speed and power dissipation need to be characterized for benchmarking of this emerging device, compared to its charge-based counterparts such as DRAM, NAND/NOR flash, as well as to other emerging memory devices. In this dissertation, a detailed investigation of scaling of BaTiO3 (BTO) based FTJs was performed, from full-scale integration to electrical characterization. Two types of FTJs with La0.67Sr0.33MnO3 (LSMO) and SrRuO3 (SRO) bottom electrodes were investigated in this work namely; Co/BTO/LSMO and Co/BTO/SRO. A CMOS compatible fabrication process for integration of Co/BTO/LSMO FTJ devices ( 3x3 microm 2) was demonstrated for the first time using standard photolithography and self-aligned RIE technique. The fabricated FTJ device showed switching behavior, however, degradation of the LSMO contact was observed during the fabrication process. A detailed investigation of the contact properties of bottom electrode materials (LSMO, SRO) for BTO-based FTJs was performed. The process and thermal stability of different contact overlayers (Ti, Pt) was explained to understand the nature of the ohmic contacts for metal to SRO and LSMO layers. Noble metals-to-SRO was found to form the most stable contacts for FTJs. Based on this study, a systematic scalability study of Co/BTO/SRO FTJs was carried out from micron ( 3x3 microm2) to submicron ( 200x200 nm2) dimensions. Positive UP Negative Down (PUND) measurement confirms the ferroelectric properties of the BTO

  11. Efficient conversion from UV light to near-IR emission in Yb{sup 3+}-doped triple-layered perovskite CaLaNb{sub 3}O{sub 10}

    Energy Technology Data Exchange (ETDEWEB)

    Lu, Yuting; Li, Yuze; Qin, Lin; Huang, Yanlin [College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123 (China); Qin, Chuanxiang, E-mail: qinchuanxiang@suda.edu.cn [College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123 (China); Tsuboi, Taiju [Jiangsu-Singapore Joint Research Center for Organic/Bio-Electronics & Information Displays and Institute of Advanced Materials (IAM), Nanjing Tech University, Nanjing 211816 (China); Huang, Wei, E-mail: wei-huang@njtech.edu.cn [Jiangsu-Singapore Joint Research Center for Organic/Bio-Electronics & Information Displays and Institute of Advanced Materials (IAM), Nanjing Tech University, Nanjing 211816 (China)

    2015-04-15

    Graphical abstract: CaRNb{sub 3}O{sub 10} is a self-activated oxide due to charge transfer transition in octahedral NbO{sub 6} groups. CaLaNb{sub 3}O{sub 10}:Yb{sup 3+} presents intense IR emission due to the cooperative energy transfer from host (NbO{sub 6}) to Yb{sup 3+} is responsible. It could be expected to be potentially applicable for enhancing photovoltaic conversion efficiency of Si-based solar cells. - Abstract: Yb{sup 3+}-doped triple-layered perovskite CaLaNb{sub 3}O{sub 10} micro-particles were synthesized via the solid-state reaction method. The crystal structure and morphology of the polycrystalline samples were investigated by X-ray powder diffraction (XRD) and scanning electron microscopy (SEM) measurements, respectively. The reflectance spectra, photoluminescence (PL) excitation and emission spectra, the decay curves, and the absolute quantum efficiency (QE) of the near-infrared (NIR) emission (910–1100 nm) were measured. Under excitation of UV light, Yb{sup 3+}-doped perovskite shows an intense NIR emission attributed to the {sup 2}F{sub 5/2} → {sup 2}F{sub 7/2} transitions of Yb{sup 3+} ions, which could match maximum spectral response of a Si-based solar cell. This is beneficial for its possible application in an enhancement of the photovoltaic conversion efficiency of solar energy utilization. The efficient energy transfer in Yb{sup 3+}-doped CaLaNb{sub 3}O{sub 10} from NbO{sub 6} groups into Yb{sup 3+} ions was confirmed by the spectra and fluorescent decay measurements. Cooperative energy transfer (CET) was supposed to be the NIR emission mechanism.

  12. Phase transformations in the rapidly solidified Ti{sub 40}Zr{sub 20}Hf{sub 20}Pd{sub 20} alloy

    Energy Technology Data Exchange (ETDEWEB)

    Chen, N. [Division of Engineering Materials, Department of Mechanical Engineering, Tsinghua University, Beijing 100084 (China); Yao Kefu [Division of Engineering Materials, Department of Mechanical Engineering, Tsinghua University, Beijing 100084 (China)], E-mail: kfyao@tsinghua.edu.cn; Louzguine-Luzgin, D.V. [Institute for Materials Research, Tohoku University, Katahira 2-1-1, Aoba-Ku, Sendai 980-8577 (Japan); Qiu Shengbao [Division of Engineering Materials, Department of Mechanical Engineering, Tsinghua University, Beijing 100084 (China); Ranganathan, S. [Department of Metallurgy, Indian Institute of Science, Bangalore 560 012 (India); Inoue, A. [Institute for Materials Research, Tohoku University, Katahira 2-1-1, Aoba-Ku, Sendai 980-8577 (Japan)

    2007-10-15

    We report that an approximant phase was initially obtained in amorphous Ti{sub 40}Zr{sub 20}Hf{sub 20}Pd{sub 20} alloy. In the initial stage of the devitrification process, the approximant phase transforms into an icosahedral (I) phase with a high thermal stability while the cF96 Zr{sub 2}Ni-type (space group Fd3-bar m with a=1.25nm and 96 atoms cell{sup -1}) particles precipitate from the amorphous matrix. Eventually the I phase grows to several hundred nanometers when annealed at about 1000K and then transforms into the Zr{sub 2}Ni-type phase with an endothermic reaction.

  13. Controlled synthesis of La{sub 1−x}Sr{sub x}CrO{sub 3} nanoparticles by hydrothermal method with nonionic surfactant and their ORR activity in alkaline medium

    Energy Technology Data Exchange (ETDEWEB)

    Choi, Bo Hyun; Park, Shin-Ae [Energy System Major, School of Mechanical Engineering, Pusan National University, Busan 609-735 (Korea, Republic of); Park, Bong Kyu [GIFT Center, Pusan National University, Busan, 609-735 (Korea, Republic of); Chun, Ho Hwan, E-mail: chunahh@pusan.ac.kr [Global Core Research Center for Ships and Offshore Plants(GCRC-SOP), Pusan National University, Busan, 609-735 (Korea, Republic of); Kim, Yong-Tae, E-mail: yongtae@pusan.ac.kr [Energy System Major, School of Mechanical Engineering, Pusan National University, Busan 609-735 (Korea, Republic of)

    2013-10-15

    Graphical abstract: We demonstrate that Sr-doped LaCrO{sub 3} nanoparticles were successfully prepared by the hydrothermal synthesis method using the nonionic surfactant Triton X-100 and the applicability of La{sub 1−x}Sr{sub x}CrO{sub 3} to oxygen reduction reaction (ORR) electrocatalysis in an alkaline medium. Compared with the nanoparticles synthesized by the coprecipitation method, they showed enhanced ORR activity. - Highlights: • Sr-doped LaCrO{sub 3} nanoparticles were successfully prepared by the hydrothermal method using the nonionic surfactant. • Homogeneously shaped and sized Sr-doped LaCrO{sub 3} nanoparticles were readily obtained. • Compared with the nanoparticles synthesized by the coprecipitation method, they showed an enhanced ORR activity. • The main origin was revealed to be the decreased particle size due to the nonionic surfactant. - Abstract: Sr-doped LaCrO{sub 3} nanoparticles were prepared by the hydrothermal method with the nonionic surfactant Triton X-100 followed by heat treatment at 1000 °C for 10 h. The obtained perovskite nanoparticles had smaller particle size (about 100 nm) and more uniform size distribution than those synthesized by the conventional coprecipitation method. On the other hand, it was identified with the material simulation that the electronic structure change by Sr doping was negligible, because the initially unfilled e{sub g}-band was not affected by the p-type doping. Finally, the perovskite nanoparticles synthesized by hydrothermal method showed much higher ORR activity by over 200% at 0.8 V vs. RHE than those by coprecipitation method.

  14. Investigation of the structural, optical and dielectric properties of highly (1 0 0)-oriented (Pb{sub 0.60}Ca{sub 0.20}Sr{sub 0.20})TiO{sub 3} thin films on LaNiO{sub 3} bottom electrode

    Energy Technology Data Exchange (ETDEWEB)

    Pontes, D.S.L. [Laboratorio Interdisciplinar de Eletroquimica e Cerâmica, Department of Chemistry, Universidade Federal de São Carlos, Via Washington Luiz, Km 235, P.O. Box 676, 13565-905 São Carlos, São Paulo (Brazil); Pontes, F.M., E-mail: fenelon@fc.unesp.br [Department of Chemistry, Universidade Estadual Paulista, P.O. Box 473, 17033-360 Bauru, São Paulo (Brazil); Chiquito, A.J. [NanO LaB, Transporte Eletrônico em Nanoestruturas, Department of Physics, Universidade Federal de São Carlos, Via Washington Luiz, Km 235, P.O. Box 676, 13565-905 São Carlos, São Paulo (Brazil); Longo, E. [Laboratorio Interdisciplinar de Eletroquimica e Cerâmica, Department of Chemistry, Universidade Federal de São Carlos, Via Washington Luiz, Km 235, P.O. Box 676, 13565-905 São Carlos, São Paulo (Brazil); Institute of Chemistry, Universidade Estadual Paulista, Araraquara, São Paulo (Brazil)

    2014-07-01

    Highlights: • Highly (h 0 0) oriented LNO and PCST thin films were grown on LAO(1 0 0) substrate. • PCST/LNO/LAO structure shown classic ferroelectric–paraelectric phase transition. • PCST/LNO/LAO structure shows superior dielectric properties. • PCST/LAO films showed a direct allowed optical transition. - Abstract: Highly (1 0 0)-oriented Pb{sub 0.60}Ca{sub 0.20}Sr{sub 0.20}TiO{sub 3}/LNO/LAO structure was fabricated using a chemical deposition process via spin-coating technique. XRD revealed that both LNO and Pb{sub 0.60}Ca{sub 0.20}Sr{sub 0.20}TiO{sub 3} films grown on LAO(1 0 0) substrate and LNO/LAO(1 0 0) structure were crystallized to be highly (h 0 0)-oriented, respectively. AFM images revealed smooth surfaces, spherical-shaped grains and a crack-free surface with a roughness of about 3–7 nm. The tetragonal perovskite phase was confirmed by Raman spectroscopy for Pb{sub 0.60}Ca{sub 0.20}Sr{sub 0.20}TiO{sub 3}/LNO/LAO and Pb{sub 0.60}Ca{sub 0.20}Sr{sub 0.20}TiO{sub 3}/LAO structures. The optical transmittance of 340 nm thick Pb{sub 0.60}Ca{sub 0.20}Sr{sub 0.20}TiO{sub 3} films on a LAO(1 0 0) substrate exhibited an average transmittance above 80% in the wavelength range of 500–1000 nm and an optical band gap E{sub g} of 3.56 and 2.87 eV for the direct and indirect transition processes, respectively. The Au/Pb{sub 0.60}Ca{sub 0.20}Sr{sub 0.20}TiO{sub 3}/LNO/LAO structure has a hysteresis loop with remnant polarization, P{sub r}, of 12 μC/cm{sup 2}, and a coercive field, E{sub c}, of 46 kV/cm for an electric field at 370 kV/cm along with a dielectric constant over 1200.

  15. Enhanced visible-light photocatalytic activities of Ag{sub 3}PO{sub 4}/MWCNT nanocomposites fabricated by facile in situ precipitation method

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Bo [Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, School of Petrochemical Engineering, Changzhou University, Changzhou 213164 (China); Li, Zhongyu, E-mail: zhongyuli@mail.tsinghua.edu.cn [Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, School of Petrochemical Engineering, Changzhou University, Changzhou 213164 (China); Changzhou Expansion New Stuff Technology Limited Company, Changzhou 213122 (China); Jilin Institute of Chemical Technology, Jilin 132022 (China); Xu, Song, E-mail: cyanine123@163.com [Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, School of Petrochemical Engineering, Changzhou University, Changzhou 213164 (China); Han, Dandan; Lu, Dayong [Jilin Institute of Chemical Technology, Jilin 132022 (China)

    2014-05-01

    Highlights: • Ag{sub 3}PO{sub 4}/MWCNT composites were facilely fabricated via in situ precipitation method. • Ag{sub 3}PO{sub 4}/MWCNT composites exhibited enhanced visible-light photocatalytic activity. • Ag{sub 3}PO{sub 4}/MWCNT composites showed good photostability compared with Ag{sub 3}PO{sub 4} particles. • Possible photocatalytic mechanism under visible-light irradiation was proposed. - Abstract: The Ag{sub 3}PO{sub 4}/MWCNT nanocomposites were facilely fabricated via in situ precipitation method by adding (NH{sub 4}){sub 2}HPO{sub 4} into the mixture of multi-walled carbon nanotube (MWCNT) and AgNO{sub 3} solution under stirring. The as-prepared Ag{sub 3}PO{sub 4}/MWCNT nanocomposites were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), Raman spectroscopy, field emission scanning electron microscopy (FE-SEM), the Brunauer–Emmett–Teller surface area (BET) and UV–vis diffuse reflectance spectroscopy. The TEM results showed that the Ag{sub 3}PO{sub 4} nanoparticles were distributed on the surface of MWCNT uniformly with an average diameter of 70 nm, indicating excellent loading result. The photocatalytic activities of Ag{sub 3}PO{sub 4}/MWCNT nanocomposites were investigated by degrading methylene blue (MB) and malachite green (MG) under visible-light irradiation. It was found that the Ag{sub 3}PO{sub 4}/MWCNT nanocomposite exhibited excellent photocatalytic performance with enhanced photocatalytic efficiency and good photostability compared with bare Ag{sub 3}PO{sub 4}. Furthermore, a possible mechanism for the photocatalytic oxidative degradation was also discussed.

  16. Cyclic electrical conductivity in BaTiO{sub 3}–PbTiO{sub 3}–V{sub 2}O{sub 5} glass-ceramic nanocomposite

    Energy Technology Data Exchange (ETDEWEB)

    Bahgat, A.A., E-mail: alaabahgat@hotmail.com; Heikal, Sh.; Mahdy, Iman A.; Abd-Rabo, A.S.; Abdel Ghany, A.

    2014-08-15

    In this present work a glass of the composition 22.5 BaTiO{sub 3}+7.5 PbTiO{sub 3}+70 V{sub 2}O{sub 5} was prepared by applying the conventional melt quashing technique. Isothermal annealing of the glass was applied at 732 K following differential scanning calorimetric analysis. The annealing was performed during different time intervals in the range of 0.25–24.0 h. X-ray diffraction and transmission electron microscopy were used to identify different phases as well as particle size precipitated during the annealing process. Nanocomposite glass-ceramic precipitation was recognized with nonperiodic cyclic particle sizes as a function of the annealing period. DC electrical conductivity, on the other hand, was conducted in the temperature range from 300 to 625 K. Electrical conductivity enhancement of the order 3×10{sup 3} times after 2.5 h of annealing was observed. Nonperiodic cyclic DC electrical conductivity behavior was also observed and which was encountered in a reverse manner with particle size development. Furthermore, the analysis of the electrical conduction mechanism predicts that both adiabatic and nonadiabatic small polaron hopping trend may describe the experimental data depending on the particle size.

  17. Luminescent, optical and electronic properties of La{sub 3}Ta{sub 0.5}Ga{sub 5.5}O{sub 14} single crystals grown in different atmospheres

    Energy Technology Data Exchange (ETDEWEB)

    Spassky, D.A., E-mail: deris2002@mail.ru [National University of Science and Technology (MISiS), Leninsky Prospekt, 4, Moscow 119049 (Russian Federation); Institute of Physics, University of Tartu, Ravila 14c, Tartu 50411 (Estonia); Skobeltsyn Institute of Nuclear Physics, M.V. Lomonosov Moscow State University, 119991 Moscow (Russian Federation); Brik, M.G. [Institute of Physics, University of Tartu, Ravila 14c, Tartu 50411 (Estonia); College of Sciences, Chongqing University of Posts and Telecommunications, Chongqing 400065 (China); Institute of Physics, Jan Dlugosz University, Armii Krajowej 13/15, PL-42200 Czestochowa (Poland); Kozlova, N.S.; Kozlova, A.P.; Zabelina, E.V. [National University of Science and Technology (MISiS), Leninsky Prospekt, 4, Moscow 119049 (Russian Federation); Buzanov, O.A. [Fomos-Materials, Buzheninova 16, Moscow 107023 (Russian Federation); Belsky, A. [Institute of Light and Matter, CNRS, University Lyon1, Villeurbanne 69622 (France)

    2016-09-15

    Luminescent, optical and electronic properties of La{sub 3}Ta{sub 0.5}Ga{sub 5.5}O{sub 14} single crystals grown in different atmospheres are presented. The absorption bands at 255, 290, 350 and 480 nm were detected; the intensity of bands increases with the concentration of oxygen in the growth atmosphere. It is shown that the shift of the fundamental absorption edge with the temperature obeys Urbach rule. The corresponding fitting allowed to estimate the slope coefficient σ=0.35, which implies self-trapping of excitons in La{sub 3}Ta{sub 0.5}Ga{sub 5.5}O{sub 14}. Calculations of the band structure, partial densities of states and reflectivity spectra were performed. The bandgap of La{sub 3}Ta{sub 0.5}Ga{sub 5.5}O{sub 14} was determined as E{sub g}=5.6 eV. The luminescence properties under UV, VUV and X-ray excitation were studied. Intrinsic emission band at 440–450 nm is attributed to the excitons self-trapped at TaO{sub 6} molecular complexes. Extrinsic emission bands at 410, 440 and 550 nm are attributed to the emission of excitons trapped by antisite defects, F-centers and oxygen deficient oxyanionic complexes.

  18. Preparation and tribological properties of surface-modified nano-Y{sub 2}O{sub 3} as additive in liquid paraffin

    Energy Technology Data Exchange (ETDEWEB)

    Yu Lin, E-mail: gych@gdut.edu.cn [School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou 510006 (China); Zhang Lin; Ye Fei; Sun Ming; Cheng Xiaoling; Diao Guiqiang [School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou 510006 (China)

    2012-12-15

    Highlights: Black-Right-Pointing-Pointer Nano-Y{sub 2}O{sub 3} was for the first time used as lubricant additive in liquid paraffin. Black-Right-Pointing-Pointer The nano-Y{sub 2}O{sub 3} modified by a coupling-grafting method shows good dispersibility in liquid paraffin. Black-Right-Pointing-Pointer The surface-modified nano-Y{sub 2}O{sub 3} considerably improves the tribological performances of liquid paraffin. - Abstract: Surface-modified nano-Y{sub 2}O{sub 3} was prepared by a coupling-grafting method with vinyl methylerichlorosilane and methyl methacrylate as the coupling agent and grafting agent, respectively. The prepared samples were characterized by X-ray diffraction (XRD), Fourier transform infrared spectra (FT-IR), transmission electron micrograph (TEM) and thermal gravimetric analysis (TGA). The tribological properties of the surface-modified nano-Y{sub 2}O{sub 3} as additive in liquid paraffin were evaluated with a four-ball tester. The results show that the nano-Y{sub 2}O{sub 3} keeps its original crystalline structure after surface modification, and the modified nano-Y{sub 2}O{sub 3} forms a core-shell structure with an average particle size of 24.5 nm. The maximum non-seizure load (P{sub B} value) and sintered load (P{sub D} value) increase by 25% and 26.9%, respectively, when compared with those of liquid paraffin, and the wear scar diameter (WSD) also decrease by 21% when 0.10% surface-modified nano-Y{sub 2}O{sub 3} was added. The protective inorganic-organic film formed by nano-Y{sub 2}O{sub 3} and organic modifiers plays an important role in the improved tribological properties of liquid paraffin.

  19. Synthesis and luminescence properties of ZnAl{sub 2}O{sub 4}:RE{sup 3+} (RE = Eu, Sm) phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Seung Jin; Cho, Shin Ho [Silla University, Busan (Korea, Republic of)

    2014-01-15

    ZnAl{sub 2}O{sub 4}:RE{sup 3+} (RE = Eu or Sm) phosphor powders were synthesized with different concentrations of activator ions by using the conventional solid-state reaction method. The effects of the concentration of activator ions on the structural, morphological, and luminescent properties of zinc aluminate phosphors were investigated. The X-ray diffraction patterns revealed that the phosphors synthesized with different concentrations of activator ions showed mixed phases of ZnAl{sub 2}O{sub 4}, ZnO, and Al{sub 2}O{sub 3}. The crystallite size was estimated using the Scherrer formula, and the maximum size was obtained for 0.20 mol of Eu{sup 3+} ions. The emission spectra of of Eu{sup 3+}-doped ZnAl{sub 2}O{sub 4} phosphors under excitation at 303 nm exhibited one intense green band at approximately 520 nm and three weak bands centered at 590, 621, and 701 nm, respectively. The intensity of all the emission bands reached a maximum for 0.05 mol of Eu{sup 3+} ions. For the Sm{sup 3+}-doped ZnAl{sub 2}O{sub 4} phosphors, a broad emission band peak at 526 nm and several weak lines in the range 470 - 700 nm were observed. The results suggest that the luminescent intensity of the phosphors can be enhanced by controlling the amount of activator ions incorporated into the host lattice.

  20. Improved superconducting properties of La{sub 3}Co{sub 4}Sn{sub 13} with indium substitution

    Energy Technology Data Exchange (ETDEWEB)

    Neha, P.; Srivastava, P. [School of Physical Sciences, Jawaharlal Nehru University, New Delhi 110067 (India); Jha, R. [School of Physical Sciences, Jawaharlal Nehru University, New Delhi 110067 (India); National Physical Laboratory, New Delhi 110012 (India); Shruti [School of Physical Sciences, Jawaharlal Nehru University, New Delhi 110067 (India); Awana, V.P.S. [National Physical Laboratory, New Delhi 110012 (India); Patnaik, S., E-mail: spatnaik@mail.jnu.ac.in [School of Physical Sciences, Jawaharlal Nehru University, New Delhi 110067 (India)

    2016-04-25

    We report two fold increase in superconducting transition temperature of La{sub 3}Co{sub 4}Sn{sub 13} by substituting indium at the tin site. The transition temperature of this skutterudite related compound is observed to increase from 2.5 K to 5.1 K for 10% indium substituted sample. The band structure and density of states calculations also indicate such a possibility. The compounds exhibit type-II superconductivity and the values of lower critical field (H{sub c1}), upper critical field (H{sub c2}), Ginzburg–Landau coherence length (ξ), penetration depth (λ) and GL parameter (κ) are estimated to be 0.0028 T, 0.68 T, 21.6 nm, 33.2 nm and 1.53 respectively for La{sub 3}Co{sub 4}Sn{sub 11.7}In{sub 1.3}. Hydrostatic external pressure leads to decrease in transition temperature and the calculated pressure coefficient is −0.311 K/GPa. Flux pinning and vortex activation energies also improved with indium addition. Only positive frequencies are observed in phonon dispersion curve that relate to the absence of charge density wave or structural instability in the normal state. - Highlights: • Superconducting transition temperature of La{sub 3}Co{sub 4}Sn{sub 13} increases two fold by indium substitution. • Band structure and all basic superconducting parameters (e.g,. H{sub c1}, H{sub c2}, ξ,λ and κ are ascertained. • Dependence of superconducting properties under external pressure is studied.

  1. Preparation of RGO/Fe{sub 3}O{sub 4}/poly (acrylic acid) hydrogel nanocomposites with improved magnetic, thermal and electrochemical properties

    Energy Technology Data Exchange (ETDEWEB)

    Didehban, K.H., E-mail: Didehban95@gmail.com; Mohammadi, L.; Azimvand, J.

    2017-07-01

    A hydrogel nanocomposite composed of reduced graphene oxide (RGO), iron oxide (Fe{sub 3}O{sub 4}) nanoparticles, and polyacrylic acid (PAA) was prepared using radical polymerization. Different percentages of RGO, Fe{sub 3}O{sub 4}, and PAA were used to prepare the nanocomposite. Fourier transform infrared spectroscopy (FTIR) results confirmed the formation of the nanocomposite’s chemical structure. X-ray power diffraction (XRD) patterns revealed the principal peak’s 2θ value to be 77.39° with the size of the nanocomposite particles estimated at 96 nm. Results indicated that the electrochemical capacity of the nanocomposites was controlled by the weight percentage of RGO. Increases to the potential scan rate reduced porosity and surface area, thereby decreasing the electrochemical capacity of the nanocomposites. Moreover, increasing the percentage of Fe{sub 3}O{sub 4} nanoparticles in the nanocomposites improved their magnetic characteristics and thermal properties. The latter also improved when the RGO percentage increased. - Highlights: • A hydrogel nanocomposite composed of RGO/Fe{sub 3}O{sub 4}/PAA was synthesized successfully. • Increasing the percentage of iron nanoparticles improved magnetic properties. • Increasing the percentage of RGO improved thermal and electrochemical capacity. • The Fe{sub 3}O{sub 4} nanoparticles directly affected magnetic properties.

  2. Interfacial microstructure of Si{sub 3}N{sub 4}/Si{sub 3}N{sub 4} brazing joint with Cu-Zn-Ti filler alloy

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, J. [School of Materials Science and Engineering, Harbin Institute of Technology, Harbin 150001 (China)], E-mail: hitzhangjie@hit.edu.cn; Zhang, X.M.; Zhou, Y. [School of Materials Science and Engineering, Harbin Institute of Technology, Harbin 150001 (China); Naka, M. [Joining and Welding Research Institute, Osaka University, Ibaraki, Osaka 567-0047 (Japan); Svetlana, Atroshenko [Faculty of Mathematics and Mechanics, Saint-Petersburg State University (Russian Federation)

    2008-11-15

    In this study, Si{sub 3}N{sub 4} ceramic was jointed by a brazing technique with a Cu-Zn-Ti filler alloy. The interfacial microstructure between Si{sub 3}N{sub 4} ceramic and filler alloy in the Si{sub 3}N{sub 4}/Si{sub 3}N{sub 4} joint was observed and analyzed by using electron-probe microanalysis, X-ray diffraction and transmission electron microscopy. The results indicate that there are two reaction layers at the ceramic/filler interface in the joint, which was obtained by brazing at a temperature and holding time of 1223 K and 15 min, respectively. The layer nearby the Si{sub 3}N{sub 4} ceramic is a TiN layer with an average grain size of 100 nm, and the layer nearby the filler alloy is a Ti{sub 5}Si{sub 3}N{sub x} layer with an average grain size of 1-2 {mu}m. Thickness of the TiN and Ti{sub 5}Si{sub 3}N{sub x} layers is about 1 {mu}m and 10 {mu}m, respectively. The formation mechanism of the reaction layers was discussed. A model showing the microstructure from Si{sub 3}N{sub 4} ceramic to filler alloy in the Si{sub 3}N{sub 4}/Si{sub 3}N{sub 4} joint was provided as: Si{sub 3}N{sub 4} ceramic/TiN reaction layer/Ti{sub 5}Si{sub 3}N{sub x} reaction layer/Cu-Zn solution.

  3. Synthesis, characterization, photocatalytic activity and ethanol-sensing properties of In{sub 2}O{sub 3} and Eu{sup 3+}:In{sub 2}O{sub 3} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Anand, Kanica; Thangaraj, R., E-mail: rthangaraj@rediffmail.com [Semiconductors Laboratory, Department of Physics, GND University, Amritsar (India); Kumar, Praveen [Department of Physics, DAV University, Jalandhar (India); Kaur, Jasmeet; Singh, R. C. [Laboratory for sensors and physical education, Department of Physics, GND University, Amritsar (India)

    2015-05-15

    In the present endeavor, Indium oxide (In{sub 2}O{sub 3}) and Europium doped In{sub 2}O{sub 3} (In{sub 2}O{sub 3}:0.5%Eu{sup 3+} and In{sub 2}O{sub 3}:5%Eu{sup 3+}) nanoparticles were prepared by co-precipitation method. Synthesized nanoparticles were characterized using X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM) and UV-Visible spectrophotometry (UV-vis). XRD revealed that nanoparticles were of pure bixbyite-type cubic phase and the crystallite size decreased with the Eu{sup 3+} doping. SEM micrographs showed that particles were spherical in shape. Synthesized nanoparticles were used for photo degradation of methylene blue (MB) dye under sunlight and the results clearly showed that In{sub 2}O{sub 3}:5%Eu{sup 3+} nanoparticles exhibited higher activity than pure In{sub 2}O{sub 3} nanoparticles. For gas sensing characteristics, the nanoparticles were applied as thick film onto alumina substrate and tested at different operating temperatures. The results showed that the optimum operating temperature of the gas sensors prepared from synthesized nanoparticles is 300°C. The investigations revealed that the addition of Eu{sup 3+} as a dopant enhanced the sensing response of In{sub 2}O{sub 3} nanoparticles appreciably.

  4. ALD Produced B{sub 2}O{sub 3}, Al{sub 2}O{sub 3} and TiO{sub 2} Coatings on Gd{sub 2}O{sub 3} Burnable Poison Nanoparticles and Carbonaceous TRISO Coating Layers

    Energy Technology Data Exchange (ETDEWEB)

    Weimer, Alan

    2012-11-26

    This project will demonstrate the feasibility of using atomic layer deposition (ALD) to apply ultrathin neutron-absorbing, corrosion-resistant layers consisting of ceramics, metals, or combinations thereof, on particles for enhanced nuclear fuel pellets. Current pellet coating technology utilizes chemical vapor deposition (CVD) in a fluidized bed reactor to deposit thick, porous layers of C (or PyC) and SiC. These graphitic/carbide materials degrade over time owing to fission product bombardment, active oxidation, thermal management issues, and long-term irradiation effects. ALD can be used to deposit potential ceramic barrier materials of interest, including ZrO{sub 2}, Y{sub 2}O{sub 3}:ZrO{sub 2} (YSZ), Al{sub 2}O{sub 3}, and TiO{sub 2}, or neutron-absorbing materials, namely B (in BN or B{sub 2}O{sub 3}) and Gd (in Gd{sub 2}O{sub 3}). This project consists of a two-pronged approach to integrate ALD into the next-generation nuclear plant (NGNP) fuel pellet manufacturing process:

  5. Anti-bombing insensitivity life of molybdenum cathode doped with La{sub 2}O{sub 3} and Y{sub 2}O{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Wang Jinshu [School of Materials Science and Engineering, Beijing University of Technology, Beijing 100022 (China)]. E-mail: wangjsh@bjut.edu.cn; Wang Yiman [School of Materials Science and Engineering, Beijing University of Technology, Beijing 100022 (China); Zhou Meiling [School of Materials Science and Engineering, Beijing University of Technology, Beijing 100022 (China)

    2006-03-15

    Anti-bombing insensitivity of La{sub 2}O{sub 3}-Y{sub 2}O{sub 3}-Mo secondary emitter has been studied in this paper. The variation of maximum secondary emission coefficient {delta} {sub max} with time was measured. The cathode after life experiment was analyzed by means of HRM, SEM, EDS and XRD. The results showed that {delta} {sub max} of La{sub 2}O{sub 3}-Y{sub 2}O{sub 3}-Mo cathode operating at 1100 deg. C under continuous electron bombardment of 300 W/cm{sup 2} was still about 2.5 after 1000 h operation, indicating that this kind of cathode had good anti-bombing insensitivity. In the internal part of the cathode, RE{sub 2}O{sub 3} (rare earth oxide) and molybdenum grains distributed alternately and there existed a certain relationship between crystallographic orientation of RE{sub 2}O{sub 3} and that of molybdenum. It was found that a RE{sub 2}O{sub 3} layer was formed on the surface after operation. The high {delta} {sub max} of La{sub 2}O{sub 3}-Y{sub 2}O{sub 3}-Mo cathode was related to the RE{sub 2}O{sub 3} layer on the surface and the amount of nanosized La{sub 2}O{sub 3} particles on the Y{sub 2}O{sub 3} layer.

  6. Dysprosium doping induced shape and magnetic anisotropy of Fe{sub 3−x}Dy{sub x}O{sub 4} (x=0.01–0.1) nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Jain, Richa [School of Sciences, Indira Gandhi National Open University, Maidan Garhi, New Delhi 110068 (India); Department of Physics, ARSD college, University of Delhi, New Delhi 110021 (India); Luthra, Vandna [Department of Physics, Gargi College, Siri Fort Road, New Delhi 110049 (India); Gokhale, Shubha, E-mail: sgokhale@ignou.ac.in [School of Sciences, Indira Gandhi National Open University, Maidan Garhi, New Delhi 110068 (India)

    2016-09-15

    The effect of dysprosium doping on evolution of structural and magnetic properties of magnetite (Fe{sub 3}O{sub 4}) nanoparticles is reported. A standard route of co-precipitation was used for the synthesis of undoped and doped magnetite nanoparticles Fe{sub 3−x}Dy{sub x}O{sub 4} (x=0.0–0.1). Transmission electron microscopy (TEM) shows formation of round shaped particles with diameter in the range of 8–14 nm for undoped sample. On doping beyond x=0.01, the formation of rod like structures is initiated along with the round shaped particles. The number of rods is found to increase with increasing doping concentration. Magnetic characterization using Vibrating Sample Magnetometer (VSM) revealed doping dependent magnetic properties which can be correlated with the crystallite size as determined from X-ray diffraction (XRD). Enhancement in the saturation magnetization in the initial stages of doping can be explained on the basis of incorporation of Dy{sup 3+} ions in the inverse spinel structure at the octahedral site in place of Fe{sup 3+} ions. Subsequent decrease in saturation magnetization observed beyond x=0.03 could be attributed to precipitation of excess Dy in form of dysprosium ferrite phase. - Highlights: • Report on formation of nanorods in magnetite prompted by Dy doping. • Observation of anisotropic magnetic behaviour emanating from the shape anisotropy. • Evidence of Dy{sup 3+} ions occupying octahedral site in place of Fe{sup 3+} ions. • Nanorods envisaged to be useful as catalysts and in biomedical applications.

  7. Optimization of α-Fe{sub 2}O{sub 3}@Fe{sub 3}O{sub 4} incorporated N-TiO{sub 2} as super effective photocatalysts under visible light irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Mohamed, Mohamed Mokhtar, E-mail: mohmok2000@yahoo.com [Benha University, Faculty of Science, Chemistry Department, Benha (Egypt); Bayoumy, W.A. [Benha University, Faculty of Science, Chemistry Department, Benha (Egypt); Goher, M.E. [National Institute of Oceanography & Fisheries, Environmental Chemistry, Cairo (Egypt); Abdo, M.H., E-mail: mh_omr@yahoo.com [National Institute of Oceanography & Fisheries, Environmental Chemistry, Cairo (Egypt); Mansour El-Ashkar, T.Y. [National Institute of Oceanography & Fisheries, Environmental Chemistry, Cairo (Egypt)

    2017-08-01

    Highlights: • The α-Fe{sub 2}O{sub 3}/Fe{sub 3}O{sub 4} doped n-TiO{sub 2} was synthesized via deposition-self assembly technique. • The photocatalyst 1%α-Fe{sub 2}O{sub 3}/Fe{sub 3}O{sub 4}/n-TiO{sub 2} show a remarkable performance while MB degradation. • The strong interaction between α-Fe{sub 2}O{sub 3}/Fe{sub 3}O{sub 4} and n-TiO{sub 2} plays an important role. • It exhibits a unique textural, optical and charge transfer properties. - Abstract: Well dispersed α-Fe{sub 2}O{sub 3}@Fe{sub 3}O{sub 4} nanoparticles (7 nm) supported on mesoporous nitrogen doped titanium dioxide (N-TiO{sub 2}) are synthesized by deposition self-assembly route and their performances as photocatalysts toward methylene blue (MB) degradation are evaluated. The results illustrate that the spherical yolk-shell structure of α-Fe{sub 2}O{sub 3}@Fe{sub 3}O{sub 4}@N-TiO{sub 2} at the loading of 1%; of excellent S{sub BET} (187 m{sup 2} g{sup −1}) and pore volume (0.50 cm{sup 3} g{sup −1}), achieved high photocatalytic performance for the MB degradation (20 ppm, λ > 420 nm, lamp power = 160 W) under visible light illumination (k = 0.059 min{sup −1}). The influence of the interface formation between α-Fe{sub 2}O{sub 3}@Fe{sub 3}O{sub 4} and n-TiO{sub 2} affects severely the charges separation efficiency and enhances the electron transfer to keep on the existence of Fe{sup 3+}/Fe{sup 2+} moieties; those take significant role in the reaction mechanism. The existence of the latter junction is affirmed via XRD, TEM-SAED, Raman and FTIR techniques whereas, the photogenerated charges, their separation together with their transport and recombination rates are depicted via photoluminescence, electrical conductivity, incident photon to current efficiency (IPCE), cyclic voltammetry (CV) and impedance (EIS) measurements. The catalyst loading, zero point charge, pH variation, total organic carbon (TOC%) and the effect of lamps power are thoroughly investigated. The 1%α-Fe{sub 2}O{sub 3

  8. Monoclinic β-Li{sub 2}TiO{sub 3} nanocrystalline particles employing novel urea assisted solid state route: Synthesis, characterization and sintering behavior

    Energy Technology Data Exchange (ETDEWEB)

    Tripathi, Biranchi M., E-mail: biranchi.barc@gmail.com [Powder Metallurgy Division, Bhabha Atomic Research Centre, Vashi Complex, Navi Mumbai 400705 (India); Mohanty, Trupti; Prakash, Deep [Powder Metallurgy Division, Bhabha Atomic Research Centre, Vashi Complex, Navi Mumbai 400705 (India); Tyagi, A.K. [Chemistry Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400085 (India); Sinha, P.K. [Powder Metallurgy Division, Bhabha Atomic Research Centre, Vashi Complex, Navi Mumbai 400705 (India)

    2017-07-15

    Pure phase monoclinic nano-crystalline Li{sub 2}TiO{sub 3} powder was synthesized by a novel urea assisted solid state synthesis method using readily available and economical precursors. A single phase and well crystalline Li{sub 2}TiO{sub 3} powder has been obtained at slightly lower temperature (600–700 °C) and shorter duration (2 h) as compared to the conventional solid state method. The proposed method has significant advantages in comparison to other viable methods mainly in terms of phase purity, powder properties and sinterability. Analysis of chemical composition using inductively coupled plasma atomic emission spectroscopy (ICP-AES) shows no loss of lithium from Li{sub 2}TiO{sub 3} in the proposed method. The emergence of monoclinic Li{sub 2}TiO{sub 3} phase was confirmed by X-ray diffraction (XRD) pattern of as-synthesized powder. The crystallite size of Li{sub 2}TiO{sub 3} powder was calculated to be in the range of 15–80 nm, which varied as a function of urea composition and temperature. The morphology of as-prepared Li{sub 2}TiO{sub 3} powders was examined by scanning electron microscope (SEM). The effect of urea composition on phase and morphology was investigated so as to delineate the role of urea. Upon sintering at < 1000 °C temperature, the Li{sub 2}TiO{sub 3} powder compact attained about 98% of the theoretical density with fine grained (grain size: 2–3 μm) microstructure. It indicates excellent sinter-ability of Li{sub 2}TiO{sub 3} powder synthesized by the proposed method. The fine grained structure is desirable for better tritium breeding performance of Li{sub 2}TiO{sub 3}. Electrochemical impedance spectroscopy at variable temperature showed good electrical properties of Li{sub 2}TiO{sub 3}. The proposed method is simple, anticipated to be cost effective and convenient to realise for large scale production of phase pure nanocrystalline and having significantly enhanced sinter-ability Li{sub 2}TiO{sub 3} powder.

  9. Particle size effect on microwave absorbing of La{sub 0.67}Ba{sub 0.33}Mn{sub 0.94}Ti{sub 0.06}O{sub 3} powders prepared by mechanical alloying with the assistance of ultrasonic irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Saptari, Sitti Ahmiatri, E-mail: siti-ahmiatri@yahoo.co.id [Faculty of Science and Technology, State Islamic University, Jakarta (Indonesia); Manaf, Azwar; Kurniawan, Budhy [Departement of Physics, University of Indonesia, Depok (Indonesia)

    2016-03-11

    Doped manganites have attracted substantial interest due to their unique chemical and physics properties, which makes it possible to be used for microwave absorbing materials. In this paper we report synthesizes and characterization of La{sub 0.67}Ba{sub 0.33}Mn{sub 0.94}Ti{sub 0.06}O{sub 3} powders prepared by mechanical alloying with the assistance of a high power ultrasonic treatment. After solid state reaction, the presence of single phase was confirmed by X-ray Diffraction (XRD). Refinement results showed that samples are single phase with monoclinic structure. It was found that powder materials derived from mechanical alloying results in large variation in the particle size. A significant improvement was obtained upon subjecting the mechanically milled powder materials to an ultrasonication treatment for a relatively short period of time. As determined by particle size analyzer (PSA), the mean particle size gradually decreased from the original size of 5.02 µm to 0.36 µm. Magnetic properties were characterized by VSM, and hysteresis loops results showed that samples are soft magnetic. It was found that when the mean particle size decreases, saturation was increases and coersitivity was decreases. Microwave absorption properties were investigated in the frequency range of 8-12 GHz using vector network analyzer. An optimal reflection loss of 24.44 dB is reached at 11.4 GHz.

  10. Electrochemical impedance spectroscopy and corrosion behaviour of Al{sub 2}O{sub 3}-Ni nano composite coatings

    Energy Technology Data Exchange (ETDEWEB)

    Ciubotariu, Alina-Crina [Dunarea de Jos, University of Galati, Metallurgy and Materials Science Faculty, Competences Center Interfaces-Tribocorrosion-Electrochemical Systems, CC-ITES, 47 Domneasca Street, 80008 Galati (Romania)], E-mail: Alina.Ciubotariu@ugal.ro; Benea, Lidia [Dunarea de Jos, University of Galati, Metallurgy and Materials Science Faculty, Competences Center Interfaces-Tribocorrosion-Electrochemical Systems, CC-ITES, 47 Domneasca Street, 80008 Galati (Romania); Lakatos-Varsanyi, Magda [Bay Zoltan Foundation, Institute for Materials Science and Technology, Budapest H-1116 (Hungary); Dragan, Viorel [Dunarea de Jos, University of Galati, Metallurgy and Materials Science Faculty, Competences Center Interfaces-Tribocorrosion-Electrochemical Systems, CC-ITES, 47 Domneasca Street, 80008 Galati (Romania)

    2008-05-20

    In this paper, the results on the electrochemical impedance spectroscopy and corrosion properties of electrodeposited nanostructured Al{sub 2}O{sub 3}-Ni composite coatings are presented. The nanocomposite coatings were obtained by codeposition of alumina nanoparticles (13 nm) with nickel during plating process. The coating thickness was 50 {mu}m on steel support and an average of nano Al{sub 2}O{sub 3} particles inside of coatings at 15 vol.% was present. The structure of the coatings was investigated by scanning electron microscopy (SEM). It has been found that the codeposition of Al{sub 2}O{sub 3} particles with nickel disturbs the nickel coating's regular surface structure. The electrochemical behavior of the coatings in the corrosive solutions was investigated by polarization potentiodynamic and electrochemical impedance spectroscopy methods. As electrochemical test solutions 0.5 M sodium chloride and 0.5 M potassium sulphate were used in a three electrode open cell. The corrosion potential is shifted to more negative values for nanostructured coatings in 0.5 M sodium chloride. The polarization resistance in 0.5 M sodium chloride decreases in 24 h, but after that increases slowly. In 0.5 M potassium sulphate solution the polarization resistance decreases after 2 h and after 30 h of immersion the polarization resistance is higher than that of the beginning value. The corrosion rate calculated by polarization potentiodynamic curves obtained after 30 min from immersion in solution is smaller for nanostructured coatings in 0.5 M potassium sulphate (4.74 {mu}m/year) and a little bit bigger in 0.5 M sodium chloride (5.03 {mu}m/year)

  11. Energy transfer and downconversion near-infrared material of Tb{sup 3+} and Yb{sup 3+} doped Ca{sub 5}(BO{sub 3}){sub 3}F

    Energy Technology Data Exchange (ETDEWEB)

    Hou, Dejian; Li, Jin-Yan [School of Metallurgy and Chemistry Engineering, Jiangxi University of Science and Technology, Ganzhou 341000, Jiangxi (China); Lin, Huihong, E-mail: linhh@hstc.edu.cn [School of Chemical and Environmental Engineering, Hanshan Normal University, Chaozhou 521041, Guangdong (China); Zhang, Jingxiang [School of Chemical and Environmental Engineering, Hanshan Normal University, Chaozhou 521041, Guangdong (China)

    2016-11-01

    Yb{sup 3+} and Tb{sup 3+} singly doped and Tb{sup 3+}–Yb{sup 3+} co-doped Ca{sub 5}(BO{sub 3}){sub 3}F phosphors were prepared by a solid state reaction method. The luminescence emission and excitation spectra as well as the luminescence decay curves were investigated. The emission bands of Yb{sup 3+} ion are located around 1000 nm, matching well with the optimal response of Si-based solar cells. Tb{sup 3+} can be a sensitizer for Yb{sup 3+} in the host. The energy transfer from Tb{sup 3+} to Yb{sup 3+} was investigated, the energy transfer mechanism was proposed as cooperative energy transfer. Tb{sup 3+} concentration dependent quantum efficiency was calculated and the maximum efficiency approached 115.5%.

  12. Preparation and characterization of the electrodeposited Cr-Al{sub 2}O{sub 3}/SiC composite coating

    Energy Technology Data Exchange (ETDEWEB)

    Gao Jifeng, E-mail: readlot@tom.com [State Key Laboratory of Mould Technology, Institute of Materials Science and Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China); Suo Jinping, E-mail: jpsuo@yahoo.com.cn [State Key Laboratory of Mould Technology, Institute of Materials Science and Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China)

    2011-09-01

    To increase the SiC content in Cr-based coatings, Cr-Al{sub 2}O{sub 3}/SiC composite coatings were plated in Cr(VI) baths which contained Al{sub 2}O{sub 3}-coated SiC powders. The Al{sub 2}O{sub 3}-coated SiC composite particles were synthesized by calcining the precursor prepared by heterogeneous deposition method. The transmission electron microscopy analysis of the particles showed that the nano-SiC particle was packaged by alumina. The zeta potential of the particles collected from the bath was up to +23 mV, a favorable condition for the co-deposition of the particles and chromium. Pulse current was used during the electrodeposition. Scanning Electron Microscopy (SEM) indicated that the coating was compact and combined well with the substrate. Energy dispersive X-ray analysis of Cr-Al{sub 2}O{sub 3}/SiC coatings demonstrated that the concentration of SiC in the coating reached about 2.5 wt.%. The corrosion behavior of the composite coating was studied by potentiodynamic polarization and electrochemical impedance spectroscopy techniques. The data obtained suggested that the Al{sub 2}O{sub 3}/SiC particles significantly enhanced the corrosion resistance of the composite coating in 0.05 M HCl solution.

  13. Investigations of percutaneous uptake of ultrafine TiO{sub 2} particles at the high energy ion nanoprobe LIPSION

    Energy Technology Data Exchange (ETDEWEB)

    Menzel, F. E-mail: fmenzel@physik.uni-leipzig.de; Reinert, T.; Vogt, J.; Butz, T

    2004-06-01

    Micronised TiO{sub 2} particles with a diameter of about 15 nm are used in sunscreens as physical UV filter. Due to the small particle size it may be supposed that TiO{sub 2} particles can pass through the uppermost horny skin layer (stratum corneum) via intercellular channels and penetrate into deeper vital skin layers. Accumulations of TiO{sub 2} particles in the skin can decrease the threshold for allergies of the immune system or cause allergic reactions directly. Spatially resolved ion beam analysis (PIXE, RBS, STIM and secondary electron imaging) was carried out on freeze-dried cross-sections of biopsies of pig skin, on which four different formulations containing TiO{sub 2} particles were applied. The investigations were carried out at the high energy ion nanoprobe LIPSION in Leipzig with a 2.25 MeV proton beam, which was focused to a diameter of 1 {mu}m. The analysis concentrated on the penetration depth and on pathways of the TiO{sub 2} particles into the skin. In these measurements a penetration of TiO{sub 2} particles through the s. corneum into the underlying stratum granulosum via intercellular space was found. Hair follicles do not seem to be important penetration pathways because no TiO{sub 2} was detected inside. The TiO{sub 2} particle concentration in the stratum spinosum was below the minimum detection limit of about 1 particle/{mu}m{sup 2}. These findings show the importance of coating the TiO{sub 2} particles in order to prevent damage of RNA and DNA of skin cells by photocatalytic reactions of the penetrated particles caused by absorption of UV light.

  14. Capture and alignment of phi29 viral particles in sub-40 nanometer porous alumina membranes.

    Science.gov (United States)

    Moon, Jeong-Mi; Akin, Demir; Xuan, Yi; Ye, Peide D; Guo, Peixuan; Bashir, Rashid

    2009-02-01

    Bacteriophage phi29 virus nanoparticles and its associated DNA packaging nanomotor can provide for novel possibilities towards the development of hybrid bio-nano structures. Towards the goal of interfacing the phi29 viruses and nanomotors with artificial micro and nanostructures, we fabricated nanoporous Anodic Aluminum Oxide (AAO) membranes with pore size of 70 nm and shrunk the pores to sub 40 nm diameter using atomic layer deposition (ALD) of Aluminum Oxide. We were able to capture and align particles in the anodized nanopores using two methods. Firstly, a functionalization and polishing process to chemically attach the particles in the inner surface of the pores was developed. Secondly, centrifugation of the particles was utilized to align them in the pores of the nanoporous membranes. In addition, when a mixture of empty capsids and packaged particles was centrifuged at specific speeds, it was found that the empty capsids deform and pass through 40 nm diameter pores whereas the particles packaged with DNA were mainly retained at the top surface of the nanoporous membranes. Fluorescence microscopy was used to verify the selective filtration of empty capsids through the nanoporous membranes.

  15. Optical microcavities and enhanced electroluminescence from electroformed Al-Al{sub 2}O{sub 3}-Ag diodes

    Energy Technology Data Exchange (ETDEWEB)

    Hickmott, T. W. [Department of Physics, State University of New York at Albany, Albany, New York 12222 (United States)

    2013-12-21

    Electroluminescence (EL) and electron emission into vacuum (EM) occur when a non-destructive dielectric breakdown of Al-Al{sub 2}O{sub 3}-Ag diodes, electroforming, results in the development of a filamentary region in which current-voltage (I-V) characteristics exhibit voltage-controlled negative resistance. The temperature dependence of I-V curves, EM, and, particularly, EL of Al-Al{sub 2}O{sub 3}-Ag diodes with anodic Al{sub 2}O{sub 3} thicknesses between 12 nm and 30 nm, has been studied. Two filters, a long-pass (LP) filter with transmission of photons with energies less than 3.0 eV and a short-pass (SP) filter with photon transmission between 3.0 and 4.0 eV, have been used to characterize EL. The voltage threshold for EL with the LP filter, V{sub LP}, is ∼1.5 V. V{sub LP} is nearly independent of Al{sub 2}O{sub 3} thickness and of temperature and is 0.3–0.6 V less than the threshold voltage for EL for the SP filter, V{sub SP}. EL intensity is primarily between 1.8 and 3.0 eV when the bias voltage, V{sub S} ≲ 7 V. EL in the thinnest diodes is enhanced compared to EL in thicker diodes. For increasing V{sub S}, for diodes with the smallest Al{sub 2}O{sub 3} thicknesses, there is a maximum EL intensity, L{sub MX}, at a voltage, V{sub LMX}, followed by a decrease to a plateau. L{sub MX} and EL intensity at 4.0 V in the plateau region depend exponentially on Al{sub 2}O{sub 3} thickness. The ratio of L{sub MX} at 295 K for a diode with 12 nm of Al{sub 2}O{sub 3} to L{sub MX} for a diode with 25 nm of Al{sub 2}O{sub 3} is ∼140. The ratio of EL intensity with the LP filter to EL intensity with the SP filter, LP/SP, varies between ∼3 and ∼35; it depends on Al{sub 2}O{sub 3} thickness and V{sub S}. Enhanced EL is attributed to the increase of the spontaneous emission rate of a dipole in a non-resonant optical microcavity. EL photons interact with the Ag and Al films to create surface plasmon polaritons (SPPs) at the metal-Al{sub 2}O{sub

  16. A study of luminescence from Eu{sup 3+}, Ce{sup 3+}, Tb{sup 3+} and Ce{sup 3+}/Tb{sup 3+} in new potassium gadolinium phosphate K{sub 3}Gd{sub 5}(PO{sub 4}){sub 6}

    Energy Technology Data Exchange (ETDEWEB)

    Meng, Fangui; Zhang, Hongzhi [School of Materials Science and Engineering, Central South University of Forestry and Technology, Changsha 410004 (China); Chen, Cuili; Kim, Sun Il [Department of Physics and Interdisciplinary Program of Biomedical, Mechanical & Electrical Engineering, Pukyong National University, Busan 608-737 (Korea, Republic of); Seo, Hyo Jin, E-mail: hjseo@pknu.ac.kr [Department of Physics and Interdisciplinary Program of Biomedical, Mechanical & Electrical Engineering, Pukyong National University, Busan 608-737 (Korea, Republic of); Zhang, Xinmin, E-mail: xmzhuga@163.com [School of Materials Science and Engineering, Central South University of Forestry and Technology, Changsha 410004 (China)

    2016-06-25

    New potassium gadolinium phosphate [K{sub 3}Gd{sub 5}(PO{sub 4}){sub 6}] doped with Eu{sup 3+}, Ce{sup 3+}, Tb{sup 3+} and co-doped with Ce{sup 3+} and Tb{sup 3+} phosphors were prepared by high temperature solid state synthesis. Phase purity of the powders was checked by X-ray powder diffraction. Luminescence and excitation spectra of samples were reported. In particular, the interaction mechanism between Eu{sup 3+} ions was investigated in terms of the Inokuti–Hirayama model; it was found that the interactions between Eu{sup 3+} can be assigned to dipole–dipole interaction. K{sub 3}Gd{sub 5}(PO{sub 4}){sub 6}:Eu{sup 3+} could act as a candidate for solid state lighting due to its strong absorption band in the near-UV region (350–400 nm). The energy transfer from Ce{sup 3+} to Tb{sup 3+} was confirmed and the mechanism was studied using Dexter's theory; it is concluded that electric dipole–dipole interaction predominates in the energy transfer process from Ce{sup 3+} to Tb{sup 3+} in the K{sub 3}Gd{sub 5}(PO{sub 4}){sub 6} host. The energy transfer efficiency and critical distance were also investigated. - Highlights: • Optical properties of K{sub 3}Gd{sub 5}(PO{sub 4}){sub 6}:RE{sup 3+} are investigated for the first time. • The interaction mechanism between Eu{sup 3+} ions is attributed to dipole–dipole type. • K{sub 3}Eu{sub 5}(PO{sub 4}){sub 6} is a candidate phosphor for application to solid state lighting. • There exists an efficient energy transfer from Ce{sup 3+} to Tb{sup 3+} (η is up to 95%). • The mechanism of energy transfer process is electric dipole–dipole interaction.

  17. Controllable synthesis and field emission enhancement of Al{sub 2}O{sub 3} coated In{sub 2}O{sub 3} core-shell nanostructures

    Energy Technology Data Exchange (ETDEWEB)

    Wang Yang; Li Yawei; Yu Ke; Zhu Ziqiang, E-mail: yk5188@263.net [Key Laboratory of Polar Materials and Devices (Ministry of Education of China), Department of Electronic Engineering, East China Normal University, Shanghai 200241 (China)

    2011-03-16

    Four types of indium oxide (In{sub 2}O{sub 3}) nanostructures were synthesized on Au-catalysed silicon substrate via a VLS method. A rod-like In{sub 2}O{sub 3} nanostructure was chosen to fabricate In{sub 2}O{sub 3}-Al{sub 2}O{sub 3} core-shell nanostructures with different shell thicknesses via a two-step method. Core-shell nanostructures with shell thickness of 30 nm are reprocessed by annealing and H{sub 2} plasma treating. Field emission (FE) properties of all the samples were measured and compared. It is found that Al{sub 2}O{sub 3} coatings remarkably decrease the effective work function and improve the FE capabilities of In{sub 2}O{sub 3} nanostructures (turn-on field decreases from 1.34 to 1.26 V {mu}m{sup -1}, threshold field decreases from 3.60 to 2.64 V {mu}m{sup -1}). Annealing and H{sub 2} plasma treating can promote the improvement even further (turn-on field 1.23 V {mu}m{sup -1}, 1.21 V {mu}m{sup -1} and threshold field 2.50 V {mu}m{sup -1}, 2.14 V {mu}m{sup -1}, respectively). The FE enhancement is attributed to the electron accumulation in the insulating Al{sub 2}O{sub 3} nanostructure and the electron redistribution at the heterojunction.

  18. Effect of pH variation on the stability and structural properties of In(OH){sub 3} nanoparticles synthesized by co-precipitation method

    Energy Technology Data Exchange (ETDEWEB)

    Goh, Kian Wei; Wong, Yew Hoong [University of Malaya, Department of Mechanical Engineering, Faculty of Engineering, Kuala Lumpur (Malaysia); Johan, Mohd Rafie [University of Malaya, Department of Mechanical Engineering, Faculty of Engineering, Kuala Lumpur (Malaysia); University of Malaya, Nanotechnology and Catalysis Research Centre, Kuala Lumpur (Malaysia)

    2016-10-15

    Indium hydroxide (In(OH){sub 3}) nanoparticles were synthesized at various pH values (8-11) by co-precipitation method. Its properties were characterized by X-ray diffractometer, Fourier transform infrared spectroscopy, Raman spectroscopy and transmission electron microscope. The electrostatic stability of nanoparticles is carried out through zeta potential measurement. The crystallite size of nanoparticles calculated by Scherrer equation has similar trend with the values obtained from William-Hall plot. TEM images show that the particles size is within the range of 11.76-20.76 nm. The maximum zeta potential is 3.68 mV associated with the smallest particle size distribution of 92.6 nm occurred at pH 10. Our work clearly confirms the crystallite size, stability and the morphology of In(OH){sub 3} NPs are strongly depending on the pH of precursor solution. (orig.)

  19. Near room temperature approaches for the preparation of air-stable and crystalline CH{sub 3}NH{sub 3}PbI{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Gujarathi, Yogini D.; Haram, Santosh K., E-mail: haram@chem.unipune.ac.in

    2016-04-15

    This work demonstrates an exotic role of CH{sub 2}Cl{sub 2} in a formation of stable phase of highly crystalline CH{sub 3}NH{sub 3}PbI{sub 3} perovskite, on a bulk scale. In the first method, a partially-reacted product obtained after co-grinding of precursors viz. CH{sub 3}NH{sub 3}I and PbI{sub 2}was sonicated in CH{sub 2}Cl{sub 2} to form pure phase of CH{sub 3}NH{sub 3}PbI{sub 3}. In second method, the precursors in γ-Butyrolactone were treated with CH{sub 2}Cl{sub 2} to form crystalline and phase-pure CH{sub 3}NH{sub 3}PbI{sub 3}. X-ray Diffraction analysis confirmed the formation of stable and highly crystalline tetragonal phase of CH{sub 3}NH{sub 3}PbI{sub 3} perovskite having space group I4cm. Well-defined rhombo-hexagonal dodecahedron crystals were seen in SEM and TEM images. Exceptional air stability of CH{sub 3}NH{sub 3}PbI{sub 3} so forms are attributed to adsorption of CH{sub 2}Cl{sub 2}. Optical band gaps obtained from the diffused reflectance spectra (Kubelka–Munk analysis), matched very well with the one estimated from Cyclic Voltammetry (CV). Valence band and conduction band edge positions estimated from the CV analysis are in good agreement with the one reported from UV photoelectron spectroscopy. Both the samples gave steady state fluorescence at ca. 750 nm with quantum yields in the range 15–35.5%. - Highlights: • A role of CH{sub 2}Cl{sub 2} is brought out in formation of stable CH{sub 3}NH{sub 3}PbI{sub 3} perovskite. • Cyclic voltammetry has been used to estimate the band edge positions. • Excellent fluorescence quantum yield, underlines the minimal structural defects.

  20. Oxidant effect of La(NO{sub 3}){sub 3}·6H{sub 2}O solution on the crystalline characteristics of nanocrystalline ZrO{sub 2} films grown by atomic layer deposition

    Energy Technology Data Exchange (ETDEWEB)

    Oh, Nam Khen [Graduate School of Energy Science and Technology, Chungnam National University, 99 Daehak-ro, Yuseong-gu, Daejeon 34134 (Korea, Republic of); Vacuum Center, Korea Research Institute of Standards and Science (KRISS), 267 Gajeong-ro, Yuseong-gu, Daejeon 34113 (Korea, Republic of); Kim, Jin-Tae [Vacuum Center, Korea Research Institute of Standards and Science (KRISS), 267 Gajeong-ro, Yuseong-gu, Daejeon 34113 (Korea, Republic of); Department of Nanomaterials Science and Engineering, University of Science and Technology, 217 Gajeong-ro, Yuseong-gu, Daejeon 34113 (Korea, Republic of); Kang, Goru; An, Jong-Ki; Nam, Minwoo [Vacuum Center, Korea Research Institute of Standards and Science (KRISS), 267 Gajeong-ro, Yuseong-gu, Daejeon 34113 (Korea, Republic of); Kim, So Yeon [Graduate School of Energy Science and Technology, Chungnam National University, 99 Daehak-ro, Yuseong-gu, Daejeon 34134 (Korea, Republic of); Park, In-Sung, E-mail: parkis77@hanyang.ac.kr [Institute of Nano Science and Technology, Hanyang University, 222 Wangsimni-ro, Seongdong-gu, Seoul 04763 (Korea, Republic of); Yun, Ju-Young, E-mail: jyun@kriss.re.kr [Vacuum Center, Korea Research Institute of Standards and Science (KRISS), 267 Gajeong-ro, Yuseong-gu, Daejeon 34113 (Korea, Republic of); Department of Nanomaterials Science and Engineering, University of Science and Technology, 217 Gajeong-ro, Yuseong-gu, Daejeon 34113 (Korea, Republic of)

    2017-02-01

    Highlights: • The La(NO{sub 3}){sub 3}·6H{sub 2}O aqua solution is introduced as an oxidant in ALD process. • The H{sub 2}O and La(NO{sub 3}){sub 3}·6H{sub 2}O lead different crystalline properties of ZrO{sub 2} films. • Concentration of La(NO{sub 3}){sub 3}·6H{sub 2}O solution minimally influences crystalline status. - Abstract: Nanocrystalline ZrO{sub 2} films were synthesized by atomic layer deposition method using CpZr[N(CH{sub 3}){sub 2}]{sub 3} (Cp = C{sub 5}H{sub 5}) as the metal precursor and La(NO{sub 3}){sub 3}·6H{sub 2}O solution as the oxygen source. La element in the deposited ZrO{sub 2} films could not be detected as its content was below the resolution limit of the X-ray photoelectron spectroscopy. The alternative introduction of La(NO{sub 3}){sub 3}·6H{sub 2}O solution to conventionally used H{sub 2}O as the oxidant effectively altered the crystalline structure, grain size, and surface roughness of the grown ZrO{sub 2} films. Specifically, the crystalline structure of the ZrO{sub 2} film changed from a mixture of tetragonal and monoclinic phases to monoclinic phase. The average grain size also increased, and the resulting film surface became rougher. The average grain sizes of the ZrO{sub 2} films prepared from La(NO{sub 3}){sub 3}·6H{sub 2}O solution at concentrations of 10, 20, 30, and 40% were 280, 256, 208, and 200 nm, respectively, whereas that prepared using H{sub 2}O oxidant was 142 nm. However, the concentration of La(NO{sub 3}){sub 3}·6H{sub 2}O solution minimally influenced the crystalline characteristics of the nanocrystalline ZrO{sub 2} films i.e., the crystalline structure, grain size, and surface roughness except for crystallite size.

  1. Optical and structural study of In{sub 2}S{sub 3} thin films growth by co-evaporation and chemical bath deposition (CBD) on Cu{sub 3}BiS{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Mesa, F., E-mail: fgmesar@unal.edu.co [Unidad de Estudios Universitarios, Colegio Mayor de Nuestra Señora del Rosario, Cra. 24 N° 63C-69, Bogotá (Colombia); Chamorro, W. [Université de Lorraine, Institut Jean Lamour, Nancy (France); Hurtado, M. [Departamento de Quimica, Universidad Nacional de Colombia, Cra. 30 N° 45-03, Bogotá (Colombia); Departamento de Física, Universidad de los Andes, Calle 21 No. 1-20, Bogotá (Colombia)

    2015-09-30

    Highlights: • In{sub 2}S{sub 3} thin films usually grow like an ultrathin. • Samples grown by CBD have a higher degree of coverage of the substrate unlike co-evaporation method. • Solar cells of Al/TCO/In{sub 2}S{sub 3}/Cu{sub 3}BiS{sub 3}/Mo structure. • In{sub 2}S{sub 3} thin films were deposited on Cu{sub 3}BiS{sub 3} (CBS), with of In{sub 2}S{sub 3} β-phase with tetragonal structure. - Abstract: We present the growth of In{sub 2}S{sub 3} onto Cu{sub 3}BiS{sub 3} layers and soda-lime glass (SLG) substrates by using chemical bath deposition (CBD) and physical co-evaporation. The results reveal that the microstructure and the optical properties of the In{sub 2}S{sub 3} films are highly dependent on the growth method. X-ray diffractrograms show that In{sub 2}S{sub 3} films have a higher crystallinity when growing by co-evaporation than by CBD. In{sub 2}S{sub 3} thin films grown by CBD with a thickness below 170 nm have an amorphous structure however when increasing the thickness the films exhibit two diffraction peaks associated to the (1 0 3) and (1 0 7) planes of the β-In{sub 2}S{sub 3} tetragonal structure. It was also found that the In{sub 2}S{sub 3} films present an energy bandgap (E{sub g}) of about 2.75 eV, regardless of the thickness of the samples.

  2. Pulse radiolysis study of NaNO/sub 2/ and NaNO/sub 3/ solutions. [Electrons

    Energy Technology Data Exchange (ETDEWEB)

    Broszkiewicz, R K [Institute of Nuclear Research, Warsaw (Poland)

    1976-01-01

    The pulse radiolysis of aqueous solutions of NaNO/sub 2/ and NaNO/sub 3/ has been done. In the nitrate solutions the transient species NO/sup 2 -//sub 2/ and NO/sub 2/ have been observed, the former reacting with water to produce NO, the latter dimerizing to N/sub 2/O/sub 4/. In the presence of O/sub 2/ and unidentified species with absorption maximum at 280 nm, probably a peroxy compound, is being formed. The radiolytic processes occurring in the nitrite solution do not depend on /NO/sub 02// and no effect of the direct energy absorption by NO/sup -//sub 2/ has been noticed. Transient species in the diluted nitrate solution are NO/sup 2 -//sub 3/ and the pernitrous ion; in concentrated solutions NO/sub 3/ is the main transient product. NO/sub 3/ is formed by the direct energy absorption by NO/sup -//sub 3/. Participation in tha effect of the cation should not be disregarded. There is evidence that the 340 nm peak in the transient spectrum is probably connected with N/sub 2/O/sub 4/ and not with NO/sub 3/. The tranient spectra, extinction coefficients of products and rate constants of relevant reactions are given.

  3. A facile approach to fabricate of photothermal functional Fe{sub 3}O{sub 4}@CuS microspheres

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Baolong; Shan, Yan, E-mail: shanyan@qust.edu.cn; Chen, Kezheng, E-mail: kchen@qust.edu.cn

    2017-06-01

    Photothermal functional Fe{sub 3}O{sub 4}@CuS microspheres have been prepared successfully by a simple chemical deposition method. The adsorption of cetyltrimethyl-ammonium bromide (CTAB) on the magnetic microspheres plays an important role in forming the structure of the composites. The present materials are characterized with XRD, TEM, SEM, FTIR, and UV-VIS-NIR spectrophotometer. The results show that Fe{sub 3}O{sub 4} microspheres are coated by CuS layer with thickness of 10 nm. The saturation magnetization value of Fe{sub 3}O{sub 4}@CuS core-shell microspheres is 27 emu/g at room temperature and the sample possesses excellent magnetic response in the presence of applied magnetic field. Moreover, these microspheres exhibit good dispersion, suitable size and significant photothermal conversion efficiency up to 20.7% at 808 nm laser irradiation. Fluctuation value of the highest temperature of Fe{sub 3}O{sub 4}@CuS dispersion over four times LASER ON/OFF indicates that photothermal stability of Fe{sub 3}O{sub 4}@CuS microspheres is good. - Highlights: • The Fe{sub 3}O{sub 4} microspheres have been coated with CuS and the thickness of CuS layer is about 10 nm. • The Fe{sub 3}O{sub 4}@CuS microspheres are ferromagnetism, and possess good photothermal conversion efficiency and photostability. • The materials have great potential application for photothermal therapy.

  4. A Novel Synthetic Route for Green-emitting Zn{sub 2-x}Mn{sub x}SiO{sub 4} Phosphor using Colloidal Silica

    Energy Technology Data Exchange (ETDEWEB)

    Kang, Seong Gu [Hoseo University, Asan (Korea, Republic of); Park, Jung Chul [Silla University, Busan (Korea, Republic of)

    2010-11-15

    We have synthesized Mn-doped Zn{sub 2}SiO{sub 4} phosphors by solgel method using colloidal silica. The adsorption characteristics of the citric acid molecules onto the silica surfaces enables us to use colloidal silica as a Si-source instead of TEOS which is generally utilized for the fine particle synthesis of the silicate based compounds. At a very low temperature (800 .deg. C), we could obtain the single phase of Zn{sub 2}SiO{sub 4}, which is remarkable compared to that of the solid state reaction (about 1300 .deg. C). The mean size of particles prepared at 800 .deg. C, 900 .deg. C, and 1000 .deg. C is 100 nm, 200 nm, and 400 nm, respectively. The PL intensity of Zn{sub 1.92}Mn{sub 0.08}SiO{sub 4} prepared at different temperature between 800 .deg. C and 1200 .deg. C, increases as the synthetic temperature rises up. Moreover, the PL intensity of Zn{sub 1.92}Mn{sub 0.08}SiO{sub 4} prepared at 1200 .deg. C is remarkable compared to that of the commercial Zn{sub 2}SiO{sub 4} : Mn (Kasei company, Japan). The PL intensity for Zn{sub 1.92}Mn{sub 0.08}SiO{sub 4} as a function of colloidal silica content, do not induces a considerable change in PL intensity, but a considerable modification in the morphology of particles. It might be said that colloidal silica is a promising chemical as a Si-source for the synthesis of fine particle of silicate compounds, instead of TEOS. The Mn{sup 2+}-doped Zn{sub 2}SiO{sub 4} phosphor has been used as a luminescent material for lamp and plasma panel display because of its high-luminescent efficiency and chemical stability. The emission of the Zn{sub 2-x}Mn{sub x}SiO{sub 4} at 520 nm is attributed to d-level spin-forbidden transition for Mn(II). According to the earlier literatures, the photoluminescence (PL) process of Zn{sub 2-x}Mn{sub x}SiO{sub 4} phosphors has been characterized by the transition of 3d{sup 5} electrons in the manganese ion acting as an activation center in the willemite structure. In particular, the transition

  5. Radon decay products and 10–1100 nm aerosol particles in Postojna Cave

    Directory of Open Access Journals (Sweden)

    M. Bezek

    2013-03-01

    Full Text Available At the lowest point along the tourist route in Postojna Cave, the activity concentration of radon (222Rn decay products and the number concentration and size distribution of aerosol particles in the size range of 10–1100 nm were monitored, with the focus on the unattached fraction (fun of radon decay products (RnDPs, a key parameter in radon dosimetry. The total number concentration of aerosols during visits in summer was lower (700 cm−3 than in winter (2800 cm−3, and was dominated by 50 nm particles (related to the attached RnDPs in winter. This explains the higher fun values in summer (0.75 and the lower winter measurement (0.04 and, consequently, DCFD values of 43.6 and 13.1 mSv WLM−1 respectively for the calculated dose conversion factors. The difference is caused by an enhanced inflow of fresh outside air, driven in winter by the higher air temperature in the cave compared to outside, resulting in the introduction of outside aerosol particles into the cave.

  6. Study on the Heating Behavior of Fe{sub 3}O{sub 4}-Embedded Thermoplastic Polyurethane Adhesive Film via Induction heating

    Energy Technology Data Exchange (ETDEWEB)

    Bae, Duck Hwan; Shon, Min Young [Pukyong National University, Busan (Korea, Republic of); Oh, Sang Taek; Kim, Gu Ni [Korea Institute of Footwear and Leather Technology, Busan (Korea, Republic of)

    2016-08-15

    The heating behavior of thermoplastic polyurethane adhesive (TPU) embedded by nanometer or micrometer Fe{sub 3}O{sub 4} particle is examined by induction heating. The effects of the size and the amount of Fe{sub 3}O{sub 4} particle, TPU film thickness, and input power of the induction heater were examined on heating behaviors of TPU. The quantity of heat generated in the TPU films increased with the amount of Fe{sub 3}O{sub 4} particles, film thickness, or input power. On the other hand, the quantity of heat generation of TPU is decreased with increasing Fe{sub 3}O{sub 4} size. We confirmed that the mechanism of hysteresis led to heat loss in the nanometer and micrometer-sized Fe{sub 3}O{sub 4} particles, and it was the key controller of the quantity of heat generated in the Fe{sub 3}O{sub 4} particle-embedded TPU films by induction heating.

  7. Reverse micellar synthesis, structural characterization and dielectric properties of Sr-doped BaZrO{sub 3} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Ahmad, Tokeer, E-mail: tahmad3@jmi.ac.in [Nanochemistry Laboratory, Department of Chemistry, Jamia Millia Islamia, New Delhi, 110025 (India); Ubaidullah, Mohd [Nanochemistry Laboratory, Department of Chemistry, Jamia Millia Islamia, New Delhi, 110025 (India); Department of Chemistry, Banasthali University, Tonk, Rajasthan, 304022 (India); School of Science and Technology, Glocal University, Mirzapur, Saharanpur, 247121, Uttar Pradesh (India); Shahazad, Mohd [Nanochemistry Laboratory, Department of Chemistry, Jamia Millia Islamia, New Delhi, 110025 (India); Kumar, Dinesh [Department of Chemistry, Banasthali University, Tonk, Rajasthan, 304022 (India); Al-Hartomy, Omar A. [Department of Physics, Faculty of Science, King Abdulaziz University, Jeddah, 21589 (Saudi Arabia)

    2017-01-01

    Sr-doped BaZrO{sub 3} nanoparticles with strontium content varying from 5 to 20 mol % were successfully synthesized by reverse micellar method at 900 °C for the first time. Systematic studies have been carried out to establish the structural and electrical properties of the as prepared nanoparticles. These nanoparticles were characterized using powder X-ray diffraction, transmission electron microscopy, BET surface area and dielectric measurements. X-ray diffraction analysis showed the formation of monophasic and highly crystalline nanoparticles which could be indexed in cubic BaZrO{sub 3} with contraction of lattice on strontium substitution. A monotonic shift of diffraction pattern towards higher angel confirms the formation of solid solutions of Ba{sub 1−x}Sr{sub x}ZrO{sub 3} (0.05 ≤ x ≤ 0.20) which was corroborating well with lattice parameter studies. Transmission electron microscopic studies showed the formation of cubic, spherical and hexagonal nanoparticles with an average grain size of 40–65 nm. Energy dispersive X-ray spectroscopic studies confirmed the presence of dopant (Sr{sup 2+}) in the BaZrO{sub 3} matrix and estimated chemical species corroborate well with the loaded composition. Specific surface area of the solid solution comes out to be in the range of 104–244 m{sup 2} g{sup -1}. Smallest particle of size 40 nm shows highest surface area 244 m{sup 2} g{sup -1} for 20 mol% Sr-doped BaZrO{sub 3}. Dielectric and impedance studies were also carried out as a function of frequency and temperature to explore the electrical properties of Sr-doped BaZrO{sub 3}. The dielectric constant of Ba{sub 1−x}Sr{sub x}ZrO{sub 3} (0.05 ≤ x ≤ 0.20) was found to be in the range of 13–25 for x = 0.05 to x = 0.20 with nearly similar dielectric loss of the order of 0.02. The conductance increases linearly with increase in frequency at room temperature, however the impedance has an inverse effect. - Highlights: • Monophasic nanocrystalline Ba{sub 1−x}Sr{sub

  8. Sub-10 nm low current resistive switching behavior in hafnium oxide stack

    Energy Technology Data Exchange (ETDEWEB)

    Hou, Y., E-mail: houyi@pku.edu.cn, E-mail: lfliu@pku.edu.cn [Institute of Microelectronics, Peking University, 100871 Beijing (China); IMEC, Kapeldreef 75, B-3001 Heverlee (Belgium); Department of Physics and Astronomy, KU Leuven, Celestijnenlaan 200D, B-3001 Heverlee (Belgium); Celano, U.; Xu, Z.; Vandervorst, W. [IMEC, Kapeldreef 75, B-3001 Heverlee (Belgium); Department of Physics and Astronomy, KU Leuven, Celestijnenlaan 200D, B-3001 Heverlee (Belgium); Goux, L.; Fantini, A.; Degraeve, R.; Youssef, A.; Jurczak, M. [IMEC, Kapeldreef 75, B-3001 Heverlee (Belgium); Liu, L., E-mail: houyi@pku.edu.cn, E-mail: lfliu@pku.edu.cn; Cheng, Y.; Kang, J. [Institute of Microelectronics, Peking University, 100871 Beijing (China)

    2016-03-21

    In this letter, a tip-induced cell relying on the conductive atomic force microscope is proposed. It is verified as a referable replica of an integrated resistive random access memory (RRAM) device. On the basis of this cell, the functionality of sub-10 nm resistive switching is confirmed in hafnium oxide stack. Moreover, the low current switching behavior in the sub-10 nm dimension is found to be more pronounced than that of a 50 × 50 nm{sup 2} device. It shows better ON/OFF ratio and low leakage current. The enhanced memory performance is ascribed to a change in the shape of the conductive filament as the device dimensions are reduced to sub-10 nm. Therefore, device downscaling provides a promising approach for the resistance optimization that benefits the RRAM array design.

  9. Photon up-converting (Yb,Er){sub 2}O{sub 3} thin films by atomic layer deposition

    Energy Technology Data Exchange (ETDEWEB)

    Tuomisto, Minnea [Department of Chemistry, University of Turku (Finland); Doctoral Programme in Physical and Chemical Sciences, University of Turku Graduate School (UTUGS), Turku (Finland); Giedraityte, Zivile; Karppinen, Maarit [Department of Chemistry and Materials Science, School of Chemical Engineering, Aalto University (Finland); Lastusaari, Mika [Department of Chemistry, University of Turku (Finland); Turku University Centre for Materials and Surfaces (MatSurf), Turku (Finland)

    2017-06-15

    We report up-converting (Yb,Er){sub 2}O{sub 3} thin films grown with the atomic layer deposition (ALD) technique. The films are crystalline and show a homogeneous morphology with a roughness less than 1 nm for 40 nm thick films. High-intensity near-infrared (NIR) to green and red two-photon up-conversion emission is obtained with 974 nm excitation through an absorption by Yb{sup 3+}, followed by a Yb{sup 3+}-Er{sup 3+} energy transfer and emission from Er{sup 3+}. The ALD technique promises to be excellent for producing up-converting films for many applications such as near-infrared radiation absorbing layers for solar cells and sensors in point-of-care biomedical diagnostics. Schematic picture of the ALD-grown (Yb,Er){sub 2}O{sub 3} thin film including the up-conversion emission spectra. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  10. Optimization and complexing agent-assisted synthesis of green SrAl{sub 2}O{sub 4}: Eu{sup 2+}, Dy{sup 3+} phosphors through sol–gel process

    Energy Technology Data Exchange (ETDEWEB)

    Du, Hongli; Shan, Wenfei; Wang, Liying; Xu, De; Yin, Hao [School of Chemistry and Chemical Engineering, Hunan University, Changsha 410082 (China); Chen, Yanwen [Hunan Labour Protection Institute of Nonferrous Metals, Changsha 410014 (China); Guo, Dongcai, E-mail: dcguo2001@hnu.edu.cn [School of Chemistry and Chemical Engineering, Hunan University, Changsha 410082 (China); Hunan Provincial Key Laboratory for Cost-effective Utilization of Fossil Fuel Aimed at Reducing Carbon-dioxide Emissions, Changsha 410082 (China)

    2016-08-15

    A novel Eu{sup 2+}–Dy{sup 3+}co-doped strontium aluminate green long-lasting phosphors were synthesized via conventional sol–gel method with citric acid and polyethylene glycol used as chelating agent, respectively. Orthogonal experiments were employed to optimize the main synthesis conditions and obtain the optimum technological parameters. Subsequently, the crystal structure, morphology, decay curve and luminescence property of the composites were characterized. X-ray diffraction (XRD) showed that the samples were composed of single-phase SrAl{sub 2}O{sub 4}. Scanning electron microscopy (SEM) revealed that the resultant nanoparticles performed graininess with a size of 100 nm around. The excitation and emission spectra indicated that, excitation broadband chiefly lay in the ultraviolet range, and nanocrystalline particles emitted strong light at 510 nm, which corresponding to the typical characteristic 5d–4f transition of Eu{sup 2+} ion excited at around 360 nm. The long afterglow photoluminescence of nanoparticles SrAl{sub 2}O{sub 4}: Eu{sup 2+}, Dy{sup 3+} (denoted as SAO: ED) was observed in the dark with the naked eye even after the removal of the excitation light. The luminescence properties suggested that SAO: ED phosphor may be regarded as a potential green phosphor candidate for near-UV and blue light-emitting diodes (LEDs).

  11. Large-scale lithography for sub-500nm features

    International Nuclear Information System (INIS)

    Pelzer, R L; Steininger, T; Belier, Benoit; Julie, Gwenaelle

    2006-01-01

    The interest in micro- and nanotechnologies has grown rapidly in the last years. The applications are versatile and different techniques found its way into several research domains as optics, electronics, magnetism, fluidics, etc. In all of these fields integration of more and more functions on steadily decreasing device dimensions lead to an increase in structural density and feature size. Expensive and slow processes utilizing projection steppers or e-beam direct writer equipment are used to fabricate nm features today. A high throughput and cost effective method adapted on a standard mask aligner will be demonstrated, making features of below 300nm available on wafer-level. We will demonstrate results of 4 different resists exposed on a DUV proximity aligner and plasma etched for optical and biological applications in the sub-300nm range

  12. Large-scale lithography for sub-500nm features

    Energy Technology Data Exchange (ETDEWEB)

    Pelzer, R L [Technology group, EV Group, DI Erich Thallner Str. 1, A-4780 Schaerding (Austria); Steininger, T [Technology group, EV Group, DI Erich Thallner Str. 1, A-4780 Schaerding (Austria); Belier, Benoit [CNRS, Institut d' Electronique Fondamentale, Universite Paris-Sud Bat 220, F- 91405 Orsay Cedex (France); Julie, Gwenaelle [CNRS, Institut d' Electronique Fondamentale, Universite Paris-Sud Bat 220, F- 91405 Orsay Cedex (France)

    2006-04-01

    The interest in micro- and nanotechnologies has grown rapidly in the last years. The applications are versatile and different techniques found its way into several research domains as optics, electronics, magnetism, fluidics, etc. In all of these fields integration of more and more functions on steadily decreasing device dimensions lead to an increase in structural density and feature size. Expensive and slow processes utilizing projection steppers or e-beam direct writer equipment are used to fabricate nm features today. A high throughput and cost effective method adapted on a standard mask aligner will be demonstrated, making features of below 300nm available on wafer-level. We will demonstrate results of 4 different resists exposed on a DUV proximity aligner and plasma etched for optical and biological applications in the sub-300nm range.

  13. Luminescent properties of codoping Y{sub 2}O{sub 3}: Eu, Me (Me = Mg, Ca) nanorods

    Energy Technology Data Exchange (ETDEWEB)

    Liu Zhilong; Wang Qin; Yang Yuming; Tao Chunyan; Yang Hua, E-mail: huayang86@sina.co [Jilin University, College of Chemistry (China)

    2010-08-15

    Phosphors of nanorods Y{sub 2}O{sub 3}: Eu (Mg, Ca) have been prepared by the hydrothermal method. The effect of Mg, Ca co-dopants on the Y{sub 2}O{sub 3}: Eu phosphor photoluminescence (PL) property was investigated. Upon excitation with ultraviolet (UV) irradiation, it is shown that there is a strong emission at around 610 nm corresponding to the forced electric dipole {sup 5}D{sub 0}-{sup 7}F{sub 2} transition of Eu{sup 3+}. At a certain concentration, Mg, Ca ions' doping effectively enhanced the luminescent properties of Y{sub 2}O{sub 3}: Eu{sup 3+} nanorods and did not change the cubic phase of the host. The structure of Y{sub 2}O{sub 3}: Eu{sup 3+} (Mg, Ca) phosphors was characterized by X-Ray diffraction (XRD). From XRD patterns, it is indicated that the phosphor Y{sub 2}O{sub 3}:(Eu, Ca) forms without impurity phase. From SEM, TEM images, it is shown that the crystal size of the nanorods phosphors is about 1-2 {mu}m in length and 30-50 nm in diameter.

  14. Luminescence properties of Sr{sub 3-x-3y/2}M{sub x}Ce{sub y}AlO{sub 4}F (M=Ca, Ba, 0{<=}x{<=}0.9, 0.001{<=}y{<=}0.05) phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Choi, Hye-Min [Department of Engineering in Energy and Applied Chemistry, Silla University, Busan 617-736 (Korea, Republic of); Park, Sangmoon, E-mail: spark@silla.ac.kr [Department of Engineering in Energy and Applied Chemistry, Silla University, Busan 617-736 (Korea, Republic of)

    2012-09-15

    Luminescent materials composed of Sr{sub 3-x-3y/2}M{sub x}Ce{sub y}AlO{sub 4}F (M=Ca, Ba, 0{<=}x{<=}0.9, 0.001{<=}y{<=}0.05) were prepared by the solid-state reaction method. X-ray diffraction (XRD) patterns of the obtained oxyfluorides are exhibited for indexing peak positions. Dynamic excitation and emission spectra of the Ce{sup 3+}-activated oxyfluoride phosphors are clearly monitored. The critical emission quenching as a function of Ce{sup 3+} contents in Sr{sub 2.5-3y/2}M{sub 0.5}Ce{sub y}AlO{sub 4}F phosphors is revealed at quite low concentrations of the activator. CIE coordinates of blue and green Sr{sub 2.5-3y/2}M{sub 0.5}Ce{sub y}AlO{sub 4}F phosphors are clearly measured. The relative quantum efficiency of Sr{sub 2.4985}Ca{sub 0.5}Ce{sub 0.005}AlO{sub 4}F based on the integrated emission is determined. The Sr{sub 3-x-3y/2}M{sub x}Ce{sub y}AlO{sub 4}F phosphors excited near 410 nm light could be prominent phosphors in applications of NUV-LED. - Highlights: Black-Right-Pointing-Pointer Blue and green emitting oxyfluoride phosphors are excitated near 410 nm Black-Right-Pointing-Pointer Ce{sup 3+}-activated oxyfluoride phosphors are quite effective to prepare white light for near-UV LED applications. Black-Right-Pointing-Pointer Gradual substitution of Ce{sup 3+} content in the oxyfluoride hosts changes CIE values.

  15. Erbium-ion implantation into various crystallographic cuts of Al{sub 2}O{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Nekvindova, P. [Department of Inorganic Chemistry, Institute of Chemical Technology, Technicka 5, 166 28 Prague 6 (Czech Republic); Mackova, A.; Malinsky, P. [Nuclear Physics Institute of the Academy of Sciences of the Czech Republic v.v.i., 250 68 Rez (Czech Republic); Department of Physics, Faculty of Science, J.E. Purkinje University, Ceske mladeze 8, 400 96 Usti nad Labem (Czech Republic); Cajzl, J.; Svecova, B. [Department of Inorganic Chemistry, Institute of Chemical Technology, Technicka 5, 166 28 Prague 6 (Czech Republic); Oswald, J. [Institute of Physics, Academy of Sciences of the Czech Republic, v.v.i., Cukrovarnicka 10, 162 53 Prague (Czech Republic); Wilhelm, R.A. [Institute of Ion Beam Physics and Materials Research, Helmholtz-Zentrum Dresden-Rossendorf, 01314 Dresden (Germany); Technische Universität Dresden, 01062 Dresden (Germany)

    2015-12-15

    This paper reports on the importance of crystallographic cuts with a different orientation on the luminescent properties and structural changes of Al{sub 2}O{sub 3} implanted with Er{sup +} ions at 190 keV and with a fluence of 1.0 × 10{sup 16} cm{sup −2}. Post-implantation annealing at 1000 °C in oxygen atmosphere was also done. The chemical compositions and erbium concentration-depth profiles of implanted layers were studied by Rutherford Backscattering Spectrometry (RBS) and compared to SRIM simulations. The same value of the maximum erbium concentration (up to 2 at.%) was observed at a depth of about 40 nm for all crystallographic cuts. The structural properties of the prepared layers were characterised by RBS/channelling. The relative amount of disordered atoms of 70–80% was observed in the prepared implanted layers and discussed for various cuts. It has been found that erbium is positioned randomly in the Al{sub 2}O{sub 3} crystalline matrix, and no preferential positions appeared even after the annealing procedure. Erbium luminescence properties were measured in the wavelength range of 1440–1650 nm for all samples. As-implanted Al{sub 2}O{sub 3} samples had a significant luminescence band at 1530 nm. The best luminescence was repeatedly observed in the 〈0 0 0 1〉 cut of Al{sub 2}O{sub 3}. The annealing procedure significantly improved the luminescent properties.

  16. Preparation of spherical and cubic Fe{sub 55}Co{sub 45} microstructures for studying the role of particle morphology in magnetorheological suspensions

    Energy Technology Data Exchange (ETDEWEB)

    Arief, Injamamul; Mukhopadhyay, P.K., E-mail: pkm@bose.res.in

    2014-06-01

    Cubic and spherical Fe{sub 55}Co{sub 45} alloyed microstructures were synthesized by borohydride reduction from aqueous solutions of metallic precursors, using stabilizers and polymer. Monosodium citrate, sodium acetate and PEG 6000 were utilized as electrostatic stabilizers and polymeric surface modifier. Suitable reaction conditions were maintained for synthesis of predominantly larger particles (0.7 µm to 1.2 µm), that facilitates use in magnetorheological fluids. Surface morphological studies by scanning electron microscopy revealed well shaped cubic and spherical geometry for the citrate and polymer-stabilized Fe{sub 55}Co{sub 45} alloys, while the alloy compositions remained nearly the same for both. X-ray diffractions of the as-prepared and annealed samples under various temperatures showed high degree of crystallinity with increasing temperatures. Studies of D.C. magnetization of the systems reveal that the particles have a core–shell structure, with inner magnetic core having a diameter around 30 nm with a log-normal distribution. Magnetorheological studies were performed with 8 vol% suspensions of as-synthesized particles dispersed in silicone oil (viscosity 30 mPa s at 25 °C) under different magnetic fields. Detailed studies of the magnetorheological properties were studied on these systems for practical use.

  17. Integration of gas phase condensed nanoparticles in YBa{sub 2}Cu{sub 3}O{sub 7-δ} multilayers; Integration von gasphasenkondensierten Nanopartikeln in YBa{sub 2}Cu{sub 3}O{sub 7-δ}-Multilagen

    Energy Technology Data Exchange (ETDEWEB)

    Sparing, Maria

    2012-07-01

    The control and targeted variation of nanoparticles properties is a central challenge in research on particle induced defects in YBa{sub 2}Cu{sub 3}O{sub 7-δ}. Using a combined Sputter-PLD system with inert gas condensation particle size and density integrated into the YBCO multilayers were varied independently. The cooling process influences the electrical properties of the multilayers. The effect of HfO2 and FePt nanoparticles on the structural and electrical properties was studied.

  18. The germanides Er{sub 5}Pd{sub 4}Ge{sub 8} and Tm{sub 5}Pd{sub 4}Ge{sub 8}. 3D [Pd{sub 4}Ge{sub 8}] polyanions with Ge{sub 2} dumb-bells and Ge{sub 4} chains in cis-conformation

    Energy Technology Data Exchange (ETDEWEB)

    Heying, Birgit; Rodewald, Ute C.; Poettgen, Rainer [Muenster Univ. (Germany). Inst. fuer Anorganische und Analytische Chemie

    2017-07-01

    Tm{sub 5}Pd{sub 4}Ge{sub 8} was synthesized by melting of the elements in an arc-melting furnace. The new germanide was characterized by powder and single-crystal X-ray diffraction: own structure type, P2{sub 1}/m, a=574.3(1), b=1380.4(3), c=836.4(1) pm, β=107.57(2) , V=0.6321 nm{sup 3}, wR2=0.0578, 2533 F{sup 2} values, 86 variables. The palladium and germanium atoms built up a three-dimensional [Pd{sub 4}Ge{sub 8}]{sup 15-} polyanionic network which contains a unique germanium substructure composed of the Zintl anions Ge{sub 2}{sup 6-} dumb-bells and Ge{sub 4}{sup 10-} chains in cis-conformation. The palladium atoms within the network have distorted square pyramidal germanium coordination. The three crystallographically independent thulium atoms have coordination numbers 15, 16 and 17 with partial motifs of the Frank-Kasper type polyhedra. The isotypic germanide Er{sub 5}Pd{sub 4}Ge{sub 8} forms only after annealing the arc-melted sample at 1070 K for 1 week: a=575.14(9), b=1386.3(3), c=838.4(1) pm, β=107.51(2) , V=0.6375 nm{sup 3}.

  19. Phosphorescence behavior and photoluminescence mechanism of Dy{sup 3+} sensitized β-Zn{sub 3}(PO{sub 4}){sub 2}: Mn{sup 2+} phosphor

    Energy Technology Data Exchange (ETDEWEB)

    Xie, Ting; Guo, Hongxu [School of Chemistry & Environment, Minnan Normal University, Zhangzhou 363000, Fujian (China); Zhang, Junying [Department of Physics, Beihang University, Beijing 100191 (China); Odetola, Christopher [Department of Chemistry, University of Ontario Institute of Technology, Ontario L1H 7K4 (Canada); He, Yuneng; Lin, Heng; Chen, Guoliang [School of Chemistry & Environment, Minnan Normal University, Zhangzhou 363000, Fujian (China); Zheng, Zishan, E-mail: Z.Zheng@mnnu.edu.cn [School of Chemistry & Environment, Minnan Normal University, Zhangzhou 363000, Fujian (China)

    2015-09-05

    Highlights: • A red long persistent phosphor of β-Zn{sub 3}(PO{sub 4}){sub 2}: Mn{sup 2+}, Dy{sup 3+} was synthesized. • Dy{sup 3+} as a sensitizer transfers its energy to the luminescent center of Mn{sup 2+}. • The three factors are responsible for the improvement of LPP properties. - Abstract: A red long persistent phosphor (LPP) of β-Zn{sub 3}(PO{sub 4}){sub 2}: Mn{sup 2+}, Dy{sup 3+} was synthesized conventionally via homogeneous coprecipitation and conventional solid-state sintering methods. The emission peak of phosphor was found at 620 nm, which can be assigned to the {sup 4}T{sub 1g} → {sup 6}A{sub 1g} transition of Mn{sup 2+}. The decay curves of phosphors show that Dy{sup 3+} ions co-doping can largely improve the performance of the red LLP of β-Zn{sub 3}(PO{sub 4}){sub 2}: Mn{sup 2+}. This red long-persistent luminescence was observed for about 4 h in the limit of light perception for naked eyes when excited under 254 nm UV light for 5 min. Thermoluminescence analysis indicates that the dopant of Dy{sup 3+} ions produced suitable trap depth of defects that enhanced the luminescence of LPP. It is hypothesized that Dy{sup 3+} as a sensitizer transfers its energy to the luminescent center of Mn{sup 2+}. We propose that the emission mechanism of LPP experiences a series process of electron–hole pairs: production, release, movement and combination. The decay time of LPP has close relationship with the life span of electron–hole pairs during their releasing time from traps and moving length on their path.

  20. Secondary phase formation in YBa{sub 2}Cu{sub 3}O{sub 7-{delta}} thin films and YBa{sub 2}Cu{sub 3}O{sub 7-{delta}}/SrTiO{sub 3} superlattices

    Energy Technology Data Exchange (ETDEWEB)

    Johnson, C.N.L.

    1996-06-01

    Studies of YBa{sub 2}Cu{sub 3}O{sub 7-{delta}} (YBCO) thin films and YBCO/STO superlattices has been performed. The dc magnetron sputtered YBCO single layer investigation concerned the dependence of the secondary phase formation and superconducting transport properties on sputtering target and ambient gas composition. YBCO/STO superlattices, grown by dc and rf magnetron sputtering, respectively, were analyzed with respect to microstructure and formation of secondary phases. The main characterization techniques used in this study have been x-ray diffraction to identify phases and to obtain orientational relationships, scanning electron microscopy to study surface morphology, transmission electron microscopy for microstructural characterization, and energy-dispersive x-ray spectroscopy for chemical characterization. With the aim to reduce or avoid the formation of copper-rich surface particles and still maintain satisfactory superconducting transport properties, YBCO films were deposited using copper-poor or yttrium-rich sputtering targets in an Ar:O{sub 2} or Ar:O{sub 2}:N{sub 2}O sputtering gas mixture. It was found that the use of yttrium-rich targets and N{sub 2}O in the sputtering gas is a reliable way to achieve smooth films without surface particles and with satisfactory superconducting properties, while the use of copper-poor targets and N{sub 2}O deteriorates those properties. Based on the previous results, YBCO/STO superlattices were grown using yttrium-rich YBCO targets and stoichiometric STO targets, respectively, in a Ar:O{sub 2}:N{sub 2}O sputtering gas mixture. The superlattices were found to have sharp interfaces and no indications of interface reactions were detected. 61 refs, 18 figs, 3 tabs

  1. Study on upconversion luminescence and thermal properties of Ho{sup 3+}/Yb{sup 3+} co-doped La{sub 2}O{sub 3}–TiO{sub 2}–ZrO{sub 2} glasses

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Minghui; Wen, Haiqin [State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai, 200050 (China); Yu, Huimei [Analysis and Testing Center of Inorganic Materials, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai, 200050 (China); Ai, Fei [State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai, 200050 (China); Shao, Hui [School of Materials Science and Engineering, Jiangsu University of Science and Technology, Zhenjiang, 212003 (China); Pan, Xiuhong; Tang, Meibo; Yu, Jianding; Gai, Lijun [State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai, 200050 (China); Liu, Yan, E-mail: liuyan@mail.sic.ac.cn [State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai, 200050 (China)

    2016-07-05

    Bulk Ho{sup 3+}/Yb{sup 3+} co-doped La{sub 2}O{sub 3}–TiO{sub 2}–ZrO{sub 2} glass spheres were fabricated by aerodynamic levitation method. High concentration of Yb{sup 3+} ions was successfully doped in glasses. The effects of Yb{sup 3+} concentration on mechanical properties, Raman, absorption spectra, thermal stability, and glass forming ability were studied systematically. Green, red, and infrared emissions centered at 550, 662, and 758 nm were obtained at 980 nm excitation. Yellow light from glass spheres can be easily observed by naked eyes. As Yb{sup 3+} concentration increases, the upconversion luminescence can be improved obviously. The upconversion luminescence mechanism is a two-photon process of energy transfer, excited state absorption, and energy back transfer. The emission intensity can be enhanced in the samples with high Yb{sup 3+} concentration, since the absorption for the incident laser and the energy transfer efficiency are increased, and the nonradiative relaxation probability is reduced. The light color referring to the ratio for red to green emissions can be tuned by Yb{sup 3+} concentration. Ho{sup 3+}/Yb{sup 3+} co-doped La{sub 2}O{sub 3}–TiO{sub 2}–ZrO{sub 2} glasses show promising comprehensive properties and are helpful to speed the application of upconversion luminescence materials. - Highlights: • Ho{sup 3+}/Yb{sup 3+} doped titanate glasses are prepared by containerless processing. • The effects of Yb{sup 3+} on thermal and mechanical properties have been studied. • High concentration of Yb{sup 3+} is favorable to upconversion luminescence. • The mechanisms are energy transfer, excited state absorption, energy back transfer.

  2. Investigation of Al{sub 2}O{sub 3} barrier film properties made by atomic layer deposition onto fluorescent tris-(8-hydroxyquinoline) aluminium molecular films

    Energy Technology Data Exchange (ETDEWEB)

    Maindron, Tony; Aventurier, Bernard [LETI/DOPT/SCOOP/Laboratoire des Composants pour la Visualisation, CEA-LETI, MINATEC Campus, 17 rue des Martyrs, F-38054 Grenoble Cedex 9 (France); Ghazouani, Ahlem; Jullien, Tony [LETI/DTSI/SDEP/Laboratoire Dépôt Equipe 2, CEA-LETI, MINATEC Campus, 17 rue des Martyrs, F-38054 Grenoble Cedex 9 (France); Rochat, Névine [LETI/DTSI/Service de Caractérisation des Matériaux et Composants, CEA-LETI, MINATEC Campus, 17 rue des Martyrs, F-38054 Grenoble Cedex 9 (France); Simon, Jean-Yves; Viasnoff, Emilie [LETI/DOPT/SCOOP/Laboratoire des Composants pour la Visualisation, CEA-LETI, MINATEC Campus, 17 rue des Martyrs, F-38054 Grenoble Cedex 9 (France)

    2013-12-02

    Al{sub 2}O{sub 3} films have been deposited at 85 °C by atomic layer deposition onto single 100 nm thick tris-(8-hydroxyquinoline) aluminium (AlQ{sub 3}) films made onto silicon wafers. It has been found that a thick ALD-deposited Al{sub 2}O{sub 3} layer (> 11 nm) greatly prevents the photo-oxidation of AlQ{sub 3} films when exposed to continuous UV irradiation (350 mW/cm{sup 2}). Thin Al{sub 2}O{sub 3} thicknesses (< 11 nm) on the contrary yield lower barrier performances. Defects in the Al{sub 2}O{sub 3} layer have been easily observed as non-fluorescent AlQ{sub 3} singularities, or black spots, under UV light on the system Si/AlQ{sub 3}/Al{sub 2}O{sub 3} stored into laboratory conditions (22 °C/50% Relative Humidity (RH)) for long time scale (∼ 2000 h). Accelerated aging conditions in a climatic chamber (85 °C/85% RH) also allow faster visualization of the same defects (168 h). The black spot density grows upon time and the black spot density occurrence rates have been calculated to be 0.024 h{sup −1}·cm{sup −2} and 0.243 h{sup −1}·cm{sup −2} respectively for the two testing conditions. A detailed investigation of these defects did show that they cannot be ascribed to the presence of a detectable particle. In that sense they are presumably the consequence of the existence of nanometre-scaled defects which cannot be detected onto fresh samples. Interestingly, an additional overcoating of ebeam-deposited SiO{sub 2} onto the Si/AlQ{sub 3}/Al{sub 2}O{sub 3} sample helps to decrease drastically the black spot density occurrence rates down to 0.004 h{sup −1}·cm{sup −2} and 0.04 h{sup −1}·cm{sup −2} respectively for 22 °C/50% RH and 85 °C/85% RH testing conditions. These observations highlight the moisture sensitivity of low temperature ALD-deposited Al{sub 2}O{sub 3} films and confirm the general idea that a single Al{sub 2}O{sub 3} ALD film performs as an ultra-high barrier but needs to be overprotected from water condensation by an

  3. Characterization investigations during mechanical alloying and sintering of Ni-W solid solution alloys dispersed with WC and Y{sub 2}O{sub 3} particles

    Energy Technology Data Exchange (ETDEWEB)

    Genc, Aziz, E-mail: agenc@itu.edu.t [Particulate Materials Laboratories, Department of Metallurgical and Materials Engineering, Istanbul Technical University, Maslak, 34469 Istanbul (Turkey); Luetfi Ovecoglu, M. [Particulate Materials Laboratories, Department of Metallurgical and Materials Engineering, Istanbul Technical University, Maslak, 34469 Istanbul (Turkey)

    2010-10-15

    Research highlights: {yields} Characterization investigations on the Ni-W solid solution alloys fabricated via mechanical alloying and the evolution of the properties of the powders with increasing MA durations. {yields} Reinforcement of the selected Ni-W powders with WC and Y{sub 2}O{sub 3} particles and further MA together for 12 h. {yields} There is no reported literature on the development and characterization of Ni-W solid solution alloys matrix composites fabricated via MA. {yields} Sintering of the developed composites and the characterization investigations of the sintered samples. {yields} Identification of new 'pomegranate-like' structures in the bulk of the samples. - Abstract: Blended elemental Ni-30 wt.% W powders were mechanically alloyed (MA'd) for 1 h, 3 h, 6 h, 12 h, 24 h, 36 h and 48 h in a Spex mixer/mill at room temperature in order to investigate the effects of MA duration on the solubility of W in Ni and the grain size, hardness and particle size. Microstructural and phase characterizations of the MA'd powders were carried out using X-ray diffractometer (XRD), scanning electron microscope (SEM) and transmission electron microscope (TEM). On the basis of achieved saturation on the solid solubility, hardness and particle size, the Ni-30 wt.% W powders MA'd for 48 h were chosen as the matrix which was reinforced with different amounts of WC and/or with 1 wt.% Y{sub 2}O{sub 3} particles. The reinforced powders were further MA'd for 12 h. The MA'd powders were sintered at 1300 {sup o}C for 1 h under Ar and H{sub 2} gas flowing conditions. Microstructural characterizations of the sintered samples were conducted via XRD and SEM. Sintered densities were measured by using the Archimedes' method. Vickers microhardness tests were performed on both MA'd powders and the sintered samples. Sliding wear experiments were done in order to investigate wear behaviors of the sintered samples.

  4. Theoretical study of the absorption spectrum and the thermochemistry of the CF{sub 3}OSO{sub 3} radical

    Energy Technology Data Exchange (ETDEWEB)

    Cobos, Carlos J.; Croce, Adela E. [Inst. de Investigaciones Fisicoquimicas Teoricas y Aplicadas (INIFTA), Univ. Nacional de La Plata, CCT La Plata-CONICET (Argentina)

    2010-08-15

    The UV-visible absorption spectrum of the recently reported CF{sub 3}OSO{sub 3} radical has been studied by using the time-dependent generalization of the density functional theory (TDDFT). For this a set of eleven hybrid functionals combined with the 6-311+G(3df) basis set were employed. The main features of the three experimental absorption bands of CF{sub 3}OSO{sub 3} recorded over the 220-530 nm range are well reproduced by the calculations. A dissociation enthalpy for the CF{sub 3}OSO{sub 3} bond of 19.1 kcal mol{sup -1} is predicted at the BAC-G3MP2//B3LYP/6-311+G(3df) level of theory. (orig.)

  5. Tunable luminescence and energy transfer properties of KSr{sub 4}(BO{sub 3}){sub 3}:Dy{sup 3+}, Eu{sup 3+} phosphors for near-UV warm-white LEDs

    Energy Technology Data Exchange (ETDEWEB)

    Leng, Zhihua; Li, Linlin; Liu, Yali; Zhang, Nannan; Gan, Shucai, E-mail: gansc@jlu.edu.cn

    2016-05-15

    Dy{sup 3+} and Eu{sup 3+} codoped KSr{sub 4}(BO{sub 3}){sub 3} phosphors were successfully synthesized by solid-state reaction process. Under near-ultraviolet (near-UV) excitation, individual Dy{sup 3+} or Eu{sup 3+} ion activated sample exhibits characteristic emissions in their respective regions. In KSr{sub 4}(BO{sub 3}){sub 3}:Dy{sup 3+}, xEu{sup 3+} phosphors, the energy transfer from Dy{sup 3+} to Eu{sup 3+} was revealed to be resonant type by dipole–dipole mechanism. And the critical distance R{sub Dy–Eu} was calculated to be 13.95 Å. The energy transfer efficiency of KSr{sub 4}(BO{sub 3}){sub 3}:Dy{sup 3+}, xEu{sup 3+} reached about 20% when the concentration of Eu{sup 3+} was 0.035. Moreover, the emitting colors of Dy{sup 3+} and Eu{sup 3+} codoped samples can be adjusted from the edge of white area to warm white via tuning the activator (Eu{sup 3+}) doped concentration. More significantly, the chromaticity coordinates (0.334, 0.351) of KSr{sub 4}(BO{sub 3}){sub 3}:0.005Dy{sup 3+}, 0.015Eu{sup 3+} sample are extremely adjacent to standard white light (0.33, 0.33). The quantum efficiency of the KSr{sub 4}(BO{sub 3}){sub 3}:0.005Dy{sup 3+}, 0.015Eu{sup 3+} phosphor with 389 nm excitation is found to be 42%, demonstrating that the obtained single-component white-emitting phosphor exhibits potential applications for solid state lighting.

  6. Deformation Behavior of Sub-micron and Micron Sized Alumina Particles in Compression.

    Energy Technology Data Exchange (ETDEWEB)

    Sarobol, Pylin; Chandross, Michael E.; Carroll, Jay; Mook, William; Boyce, Brad; Kotula, Paul Gabriel; McKenzie, Bonnie Beth; Bufford, Daniel Charles; Hall, Aaron Christopher.

    2014-09-01

    The ability to integrate ceramics with other materials has been limited due to high temperature (>800degC) ceramic processing. Recently, researchers demonstrated a novel process , aerosol deposition (AD), to fabricate ceramic films at room temperature (RT). In this process, sub - micro n sized ceramic particles are accelerated by pressurized gas, impacted on the substrate, plastically deformed, and form a dense film under vacuum. This AD process eliminates high temperature processing thereby enabling new coatings and device integration, in which ceramics can be deposited on metals, plastics, and glass. However, k nowledge in fundamental mechanisms for ceramic particle s to deform and form a dense ceramic film is still needed and is essential in advancing this novel RT technology. In this wo rk, a combination of experimentation and atomistic simulation was used to determine the deformation behavior of sub - micron sized ceramic particle s ; this is the first fundamental step needed to explain coating formation in the AD process . High purity, singl e crystal, alpha alumina particles with nominal size s of 0.3 um and 3.0 um were examined. Particle characterization, using transmission electron microscopy (TEM ), showed that the 0.3 u m particles were relatively defect - free single crystals whereas 3.0 u m p articles were highly defective single crystals or particles contained low angle grain boundaries. Sub - micron sized Al 2 O 3 particles exhibited ductile failure in compression. In situ compression experiments showed 0.3um particles deformed plastically, fractured, and became polycrystalline. Moreover, dislocation activit y was observed within the se particles during compression . These sub - micron sized Al 2 O 3 particles exhibited large accum ulated strain (2 - 3 times those of micron - sized particles) before first fracture. I n agreement with the findings from experimentation , a tomistic simulation s of nano - Al 2 O 3 particles showed dislocation slip and

  7. The calcium and rare earth oxo-borates, Ca{sub 4}ReO(BO{sub 3}){sub 3} (Re = Gd, Y, La): synthesis and investigations of new non-critical phase matching configurations for frequency conversion at specific laser wavelengths; Les oxoborates de calcium et de lanthanide, Ca{sub 4}LnO(BO{sub 3}){sub 3} (Ln = Gd, Y, La): synthese et recherche d'angles d'accord de phase non critique pour la conversion de frequence de longueurs d'onde Laser specifiques

    Energy Technology Data Exchange (ETDEWEB)

    Reino, E

    2002-12-15

    Visible and UV lasers are currently investigated for many applications as data storage, medicine, etc. Intracavity frequency doubling appears as a good solution. Thus, the non-linear family Ca{sub 4}REO(BO{sub 3}){sub 3} (RE = rare earth, RECOB) has shown a considerable interest to produce compact visible laser. In addition, it is possible to tune the compositions of RECOB by partial substitutions in order to achieve non-critical phase matching (NCPM). In the present work, various cationic substitutions have been studied in solid solutions as Gd{sub 1-x}Y{sub x}COB, Gd{sub 1-x}La{sub x}COB, Gd{sub 1-x}Sc{sub x}COB (for the first time), Re{sub 1-x}Bi{sub x}COB (REe = Gd or Y) and (Ca{sub 1-x}Sr{sub x}){sub 4}GdO(BO{sub 3}){sub 3} in order to investigate their crystal growth and adjust the NCPM wavelength by composition. The wavelength range is related to neodymium doped laser materials emitting on the 4F3/2-4I9/2 transition, for example Nd:YAP (YAlO{sub 3}) at 930 nm, Nd:YAG (Y{sub 3}Al{sub 5}O{sub 12}) at 946 nm or Nd:ASL (Sr{sub 1-x}Nd{sub y}La{sub x-y}Mg{sub x}Al{sub 11-x}O{sub 19}) at 900 nm. We have also demonstrated that the compositions for NCPM can be determined from the refractive index of both lattices M{sub 1-x}M'{sub x}COB (M, M' RE) with x = 0 or 1, using the Clausius-Mosotti relation. Two new blue laser systems, constituted of a laser crystal and a non-linear crystal optimized for type-I NCPM second harmonic generation, were achieved: a 946 nm Nd:YAG laser with Gd{sub 0.87}Y{sub 0.13}COB and a 900 nm Nd:ASL laser with Gd{sub 0.56}Y{sub 0.44}COB. Moreover, we have performed for the first time a CW laser action at 900 nm with Nd:ASL. (author)

  8. Investigation of the molecular motions in Cd(NH/sub 3/)/sub 6/Cl/sub 2/ by NMR spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Pislewski, N [Polska Akademia Nauk, Poznan. Inst. Fizyki Molekularnej; Ferris, L T.H. [University Coll., London (UK). Dept. of Chemistry

    1981-07-01

    NMR results are reported for intramolecular motion in Cd(NH/sub 3/)/sub 6/Cl/sub 2/. Below the 180 K phase transition, the motion of the NH/sub 3/ groups is well described by the Hilt-Hubbard theory with an activation energy of 9.63 kJ/mol. The inter-proton distance in NH/sub 3/ determined from relaxational measurements is 0.161 nm. Several K below and above the transition point, two phases with different spin-lattice relaxation times coexist.

  9. Conversion of green emission into white light in Gd{sub 2}O{sub 3} nanophosphors

    Energy Technology Data Exchange (ETDEWEB)

    Jayasimhadri, M.; Ratnam, B.V. [Department of Physics, Changwon National University, Changwon, 641-773 (Korea, Republic of); Jang, Kiwan, E-mail: kwjang@changwon.ac.k [Department of Physics, Changwon National University, Changwon, 641-773 (Korea, Republic of); Lee, Ho Sueb [Department of Physics, Changwon National University, Changwon, 641-773 (Korea, Republic of); Yi, Soung-Soo [Department of Photonics, Silla University, Busan (Korea, Republic of); Jeong, Jung-Hyun [Department of Physics, Pukyong National University, Busan (Korea, Republic of)

    2010-09-01

    Gd{sub 2}O{sub 3} nanophosphors were prepared by combustion synthesis with and without doping of Dy{sup 3+} ions. The X-ray powder diffraction patterns indicate that as-prepared Gd{sub 2}O{sub 3} and 0.1 mol% Dy{sub 2}O{sub 3} doped Gd{sub 2}O{sub 3} nanophosphors have monoclinic structures. The transmission electron microscope (TEM) studies revealed that the as-prepared phosphors had an average crystallite sizes around 37 nm. The excitation and emission properties have been investigated for Dy{sup 3+} doped and undoped Gd{sub 2}O{sub 3} nanophosphors. New emission bands were observed in the visible region for Gd{sub 2}O{sub 3} nanophosphors without any rare earth ion doping under different excitations. A tentative mechanism for the origin of luminescence from Gd{sub 2}O{sub 3} host was discussed. Emission properties also measured for 0.1 mol% Dy{sup 3+} doped Gd{sub 2}O{sub 3} nanophosphors and found the characteristic Dy{sup 3+} visible emissions at 489 and 580 nm due to {sup 4}F{sub 9/2} {yields} {sup 6}H{sub 15/2} and {sup 4}F{sub 9/2} {yields} {sup 6}H{sub 13/2} transitions, respectively. The chromaticity coordinates were calculated based on the emission spectra of Dy{sup 3+} doped and undoped Gd{sub 2}O{sub 3} nanophosphors and analyzed with Commission Internationale de l'Eclairage (CIE) chromaticity diagram. These nanophosphors exhibit green color in undoped Gd{sub 2}O{sub 3} and white color after adding 0.1 mol% Dy{sub 2}O{sub 3} to Gd{sub 2}O{sub 3} nanophosphors under UV excitation. These phosphors could be a promising phosphor for applications in flat panel displays.

  10. Nanofibers obtained by electrospinning of BaTiO3 particles dispersed in polyvinyl alcohol and ethylcellulose

    Energy Technology Data Exchange (ETDEWEB)

    Avila, Humar A.; Reboredo, Maria M.; Castro, Miriam; Parra, Rodrigo, E-mail: havila@fi.mdp.edu.ar [Instituto de Investigaciones en Ciencia y Tecnologia de Materiales - INTEMA, Consejo Nacional de Investigaciones Cientificas y Tecnicas - CONICET, Universidad Nacional de Mar del Plata - UNMdP, Mar del Plata (Argentina)

    2013-11-01

    Barium titanate particles (100-300 nm) synthesized by hydrothermal method were dispersed in both polyvinyl alcohol (PVA) and ethylcellulose (EC) solutions. These suspensions were processed by electrospinning. When no particles were added, homogeneous polymeric nanofibers were obtained. Under certain conditions, polymeric suspensions of barium titanate particles were electrospun generating polymeric fibers with BT particles. The effect of a surfactant was also assessed over the formation of nanofibers. The BaTiO{sub 3} particles synthesized by hydrothermal method were characterized by X-Ray diffraction (XRD), field emission-scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM) and Raman spectroscopy. Fibers were characterized by scanning electron microscopy (SEM). (author)

  11. Coherent 3D nanostructure of γ-Al{sub 2}O{sub 3}: Simulation of whole X-ray powder diffraction pattern

    Energy Technology Data Exchange (ETDEWEB)

    Pakharukova, V.P., E-mail: verapakh@catalysis.ru [Boreskov Institute of Catalysis SB RAS, Pr. Lavrentieva 5, 630090 Novosibirsk (Russian Federation); Novosibirsk State University, Pirogova Street 2, 630090 Novosibirsk (Russian Federation); Research and Educational Center for Energy Efficient Catalysis, Novosibirsk State University, Novosibirsk 630090 (Russian Federation); Yatsenko, D.A. [Boreskov Institute of Catalysis SB RAS, Pr. Lavrentieva 5, 630090 Novosibirsk (Russian Federation); Novosibirsk State University, Pirogova Street 2, 630090 Novosibirsk (Russian Federation); Gerasimov, E. Yu.; Shalygin, A.S.; Martyanov, O.N.; Tsybulya, S.V. [Boreskov Institute of Catalysis SB RAS, Pr. Lavrentieva 5, 630090 Novosibirsk (Russian Federation); Novosibirsk State University, Pirogova Street 2, 630090 Novosibirsk (Russian Federation); Research and Educational Center for Energy Efficient Catalysis, Novosibirsk State University, Novosibirsk 630090 (Russian Federation)

    2017-02-15

    The structure and nanostructure features of nanocrystalline γ-Al{sub 2}O{sub 3} obtained by dehydration of boehmite with anisotropic platelet-shaped particles were investigated. The original models of 3D coherent nanostructure of γ-Al{sub 2}O{sub 3} were constructed. The models of nanostructured γ-Al{sub 2}O{sub 3} particles were first confirmed by a direct simulation of powder X–Ray diffraction (XRD) patterns using the Debye Scattering Equation (DSE) with assistance of high-resolution transmission electron microscopy (HRTEM) study. The average crystal structure of γ-Al{sub 2}O{sub 3} was shown to be tetragonally distorted. The experimental results revealed that thin γ-Al{sub 2}O{sub 3} platelets were heterogeneous on a nanometer scale and nanometer-sized building blocks were separated by partially coherent interfaces. The XRD simulation results showed that a specific packing of the primary crystalline blocks in the nanostructured γ-Al{sub 2}O{sub 3} particles with formation of planar defects on (001), (100), and (101) planes nicely accounted for pronounced diffuse scattering, anisotropic peak broadening and peak shifts in the experimental XRD pattern. The identified planar defects in cation sublattice seem to be described as filling cation non-spinel sites in existing crystallographic models of γ-Al{sub 2}O{sub 3} structure. The overall findings provided an insight into the complex nanostructure, which is intrinsic to the metastable γ-Al{sub 2}O{sub 3} oxide. - Highlights: • Thin plate-like crystallites of γ-Al{sub 2}O{sub 3} were obtained. • Models of 3D coherent nanostructure of γ-Al{sub 2}O{sub 3} were constructed. • Models were verified by simulating XRD patterns using the Debye Scattering Equation. • Specific broadening of XRD peaks was explained in terms of planar defects. • Primary crystalline blocks in γ-Al{sub 2}O{sub 3} are separated by partially coherent interfaces.

  12. Synthesis and characterization of nanostructured CaZrO{sub 3} and BaZrO{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Ibiapino, Amanda Laura; Figueiredo, Laysa Pires de [Departamento de Quimica, Instituto de Ciencias Exatas e da Terra, Universidade Federal do Mato Grosso, MT (Brazil); Lascalea, Gustavo E. [LISAMEN/CONICET, Ciudad de Mendoza (Argentina); Prado, Rogerio Junqueira, E-mail: rjprado@ufmt.br [Instituto de Fisica, Universidade Federal do Mato Grosso, Cuiaba - MT (Brazil)

    2013-09-01

    In this work, nanostructured samples of barium zirconate (BaZrO{sub 3}) and calcium zirconate (CaZrO{sub 3}) were synthesized by the gel-combustion method, using glycine as fuel. The ceramic powders were calcined at 550 Degree-Sign C for 2 h and subsequently heat treated at 1350 Degree-Sign C for 10 min (fast-firing). The X-ray diffraction technique was employed to identify and characterize the crystalline phases present in the synthesized powders, using the Rietveld method. Monophasic nanostructured samples of BaZrO{sub 3} and CaZrO{sub 3} presenting average crystallite sizes of around 8.5 and 10.3 nm, respectively, were found after fast-firing. (author)

  13. Up-conversion routines of Er{sup 3+}–Yb{sup 3+} doped Y{sub 6}O{sub 5}F{sub 8} and YOF phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Park, Sangmoon, E-mail: spark@silla.ac.kr [Center for Green Fusion Technology and Department of Engineering in Energy & Applied Chemistry, Silla University, Busan 617-736 (Korea, Republic of); Yang, Wonseok; Park, Chu-Young; Noh, Minhee; Choi, Seulki [Center for Green Fusion Technology and Department of Engineering in Energy & Applied Chemistry, Silla University, Busan 617-736 (Korea, Republic of); Park, Dahye; Jang, Ho Seong; Cho, So-Hye [Center for Materials Architecturing, Institute of Multidisciplinary Convergence of Materials, Korea Institute of Science and Technology, Seoul 130-650 (Korea, Republic of)

    2015-11-15

    Highlights: • Single-phase optical materials of Y{sub 6}O{sub 5}F{sub 8}:Er and YOF:Er were prepared. • Effective spectral converting properties were observed in Y{sub 6}O{sub 5}F{sub 8}:Er,Yb. • 980 nm diode laser was irradiated for up-converting analysis. • A multi-photon process in the phosphors was investigated. - Abstract: Optical materials composed of a Y{sub 6(1−p−q)}Er{sub 6p}Yb{sub 6q}O{sub 5}F{sub 8} (p = 0.001–0.1, q = 0.005–0.1) solid solution with Y{sub 0.99}Er{sub 0.01}OF were prepared via a solid-state reaction using excess NH{sub 4}F flux at 950 °C for 30 min. X-ray diffraction patterns of Y{sub 6(1−p−q)}Er{sub 6p}Yb{sub 6q}O{sub 5}F{sub 8} and Y{sub 0.99}Er{sub 0.01}OF were compared upon altering the synthesis temperature and the molar ratio of the NH{sub 4}F flux to the Y{sup 3+} (Er{sup 3+}, Yb{sup 3+}) ions. The effective spectral-conversion properties of Er{sup 3+} and Er{sup 3+}–Yb{sup 3+} ions in Y{sub 6}O{sub 5}F{sub 8} phosphors were monitored during excitation with a 980 nm wavelength diode-laser. Selection of appropriate Er{sup 3+} and/or Yb{sup 3+} concentrations in the Y{sub 6}O{sub 5}F{sub 8} structure led to achievement of the desired up-conversion emission, from the green to the red regions of the spectra. Furthermore, the mechanism of up-conversion in the phosphors was described by an energy-level schematic. Up-conversion emission spectra and the dependence of the emission intensity on pump power (between 193 and 310 mW) in the Y{sub 6(0.995−q)}Er{sub 0.03}Yb{sub 6q}O{sub 5}F{sub 8} phosphors were also investigated.

  14. Silicon MIS diodes with Cr{sub 2}O{sub 3} nanofilm: Optical, morphological/structural and electronic transport properties

    Energy Technology Data Exchange (ETDEWEB)

    Erdogan, Ibrahim Y. [Bingoel University, Faculty of Sciences and Arts, Department of Chemistry, 12000- Bingoel (Turkey); Guellue, O., E-mail: omergullu@gmail.com [Batman University, Faculty of Sciences and Arts, Department of Physics, 72060- Batman (Turkey)

    2010-04-15

    In this work we report the optical, morphological and structural characterization and diode application of Cr{sub 2}O{sub 3} nanofilms grown on p-Si substrates by spin coating and annealing process. X-ray diffraction (XRD), non-contact mode atomic force microscopy (NC-AFM), ultraviolet-visible (UV-vis) spectroscopy and photoluminescence (PL) spectroscopy were used for characterization of nanofilms. For Cr{sub 2}O{sub 3} nanofilms, the average particle size determined from XRD and NC-AFM measurements was approximately 70 nm. Structure analyses of nanofilms demonstrate that the single phase Cr{sub 2}O{sub 3} on silicon substrate is of high a crystalline structure with a dominant in hexagonal (1 1 0) orientation. The morphologic analysis of the films indicates that the films formed from hexagonal nanoparticles are with low roughness and uniform. UV-vis absorption measurements indicate that the band gap of the Cr{sub 2}O{sub 3} film is 3.08 eV. The PL measurement shows that the Cr{sub 2}O{sub 3} nanofilm has a strong and narrow ultraviolet emission, which facilitates potential applications in future photoelectric nanodevices. Au/Cr{sub 2}O{sub 3}/p-Si metal/interlayer/semiconductor (MIS) diodes were fabricated for investigation of the electronic properties such as current-voltage and capacitance-voltage. Ideality factor and barrier height for Au//Cr{sub 2}O{sub 3}/p-Si diode were calculated as 2.15 eV and 0.74 eV, respectively. Also, interfacial state properties of the MIS diode were determined. The interface-state density of the MIS diode was found to vary from 2.90 x 10{sup 13} eV{sup -1} cm{sup -2} to 8.45 x 10{sup 12} eV{sup -1} cm{sup -2}.

  15. Colossal elastoresistance, electroresistance and magnetoresistance in Pr{sub 0.5}Sr{sub 0.5}MnO{sub 3} thin films

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Liping, E-mail: chenliping0003@163.com [Department of Physics, Zhejiang Normal University, Jinhua 321004 (China); Department of Physics, Hong Kong University, Hong Kong (China); Guo, Xuexiang [Department of Physics, Zhejiang Normal University, Jinhua 321004 (China); Gao, J. [Department of Physics, Hong Kong University, Hong Kong (China)

    2016-05-01

    Pr{sub 0.5}Sr{sub 0.5}MnO{sub 3} thin films on substrates of (001)-oriented LaAlO{sub 3} were epitaxially grown by pulsed laser deposition. It was found that a substrate-induced strain of ~1.3% brings a great resistivity change of ~98% at 25 K. We studied the dependence of resistivity on the applied electric current and magnetic field. In the greatly strained films of 60 nm thickness the electroresistance ER=[ρ(I{sub 1} {sub μA})−ρ(I{sub 1000} {sub μA})]/ρ(I{sub 1} {sub μA}) reaches ~70% at T=25 K, much higher than ER~7% in the strain-relaxed films of 400 nm thickness, implying the strain effect on ER. Also the magnetoresistance of the film falls with strain-relaxation. Therefore the electric properties of the film could be efficiently modified by strain, electric current and magnetic field. All of them may be explained by the effect on the percolative phase separation and competition in the half-doped manganite material. The manganite films located at phase boundary are expected to be an ideal compound for providing practical colossal effects of elastoresistance, electroresistance and magnetoresistance due to the multiphase coexistence. - Highlights: • The electric current-induced electroresistance (ER) and magnetoresistance (MR)studies on PLD grown Pr{sub 0.5}Sr{sub 0.5}MnO{sub 3}/(001) LaAlO{sub 3} films were found to be greatly sensitive to the film thickness arising from the strain. • It is shown that, 60 nm film exhibit compressive in-plane strain which leads to phase separation and hence colossal MR and ER. • Our results suggest that the manganites located at phase boundary may be an ideal compound for providing practical colossal effects of elastoresistance, electroresistance and magnetoresistance.

  16. Synthesis and photoluminescence properties of microcrystalline Sr{sub 2}ZnWO{sub 6}:RE{sup 3+} (RE = Eu, Dy, Sm and Pr) phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Dabre, K.V. [Department of Physics, Arts, Commerce and Science College, Koradi, Nagpur 441111 (India); Park, K. [Faculty of Nanotechnology and Advanced Materials Engineering, Sejong University, Seoul 143-747 (Korea, Republic of); Dhoble, S.J., E-mail: sjdhoble@rediffmail.com [Department of Physics, R.T.M. Nagpur University, Nagpur 440033 (India)

    2014-12-25

    Graphical abstract: CIE chromaticity coordinate diagram (1931) indicating different colors of Sr{sub 2}ZnWO{sub 6}:RE{sup 3+} (RE = Eu (a), Dy (b and c), Sm (d–f) and Pr (g and h)) phosphor under different excitation 466 nm (a), 312 nm (b), 454 nm (c), 313 nm (d), 408 nm (e), 482 nm (f), 315 nm (g) and 450 nm (h). - Highlights: • Microcrystalline Sr{sub 2}ZnWO{sub 6}:RE{sup 3+} (RE = Eu, Dy, Sm and Pr) phosphors were synthesized by solid state method. • Photoluminescence properties of phosphor were investigated. • Color of the phosphor for different excitation has been verified by chromaticity diagram. • The host absorption and energy transfer were investigated. - Abstract: The novel microcrystalline Sr{sub 2}ZnWO{sub 6}:RE{sup 3+} (RE = Eu, Dy, Sm and Pr) phosphors were synthesized by solid-state reaction method at 1250 °C and their photoluminescence properties were investigated. The Eu{sup 3+} and Dy{sup 3+} activated phosphors show intense red (616 nm) and yellow (574 nm) emission respectively; which indicate that the rare earth ions are substituted at non-centrosymmetric site in the host lattice. Near white (Dy{sup 3+}) and reddish-orange (Sm{sup 3+}) emissions of rare earth ions in the host lattice show strong host absorption and energy transfer from the host to activator ion. Pr{sup 3+} activated phosphor shows a series of emission peaks in the visible region with the most intense peak in the blue region at 491 and 499 nm.

  17. Monodisperse Ni{sub x}Fe{sub 3-x}O{sub 4} nanospheres: Metal-ion-steered size/composition control mechanism, static magnetic and enhanced microwave absorbing properties

    Energy Technology Data Exchange (ETDEWEB)

    Jiang, Kedan, E-mail: 17858961652@163.com [College of Chemistry and Life Sciences, Zhejiang Normal University, Jinhua 321004 (China); Liu, Yun, E-mail: liuyun650403@163.com [State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070 (China); Pan, Yefei, E-mail: 3083780256@qq.com [College of Chemistry and Life Sciences, Zhejiang Normal University, Jinhua 321004 (China); Wang, Ru, E-mail: 631081137@qq.com [College of Chemistry and Life Sciences, Zhejiang Normal University, Jinhua 321004 (China); Hu, Panbing, E-mail: 1036855954@qq.com [College of Chemistry and Life Sciences, Zhejiang Normal University, Jinhua 321004 (China); He, Rujia, E-mail: 634185782@qq.com [College of Chemistry and Life Sciences, Zhejiang Normal University, Jinhua 321004 (China); Zhang, Lingli, E-mail: 786510121@qq.com [College of Chemistry and Life Sciences, Zhejiang Normal University, Jinhua 321004 (China); Tong, Guoxiu, E-mail: tonggx@zjnu.cn [College of Chemistry and Life Sciences, Zhejiang Normal University, Jinhua 321004 (China)

    2017-05-15

    Highlights: • A metal-ion-steered solvothermal method for synthesizing Ni{sub x}Fe{sub 3-x}O{sub 4} nanospheres. • Proposing an in situ-reduction, coordination-precipitation transformation mechanism. • Investigating size- and composition-dependent static magnetic properties. • Investigating size- and composition-dependent microwave absorbing properties. - Abstract: An easy metal-ion-steered solvothermal method was developed for the one-step synthesis of monodisperse, uniform Ni{sub x}Fe{sub 3-x}O{sub 4} polycrystalline nanospheres with tunable sphere diameter (40–400 nm) and composition (0 ≤ x ≤ 0.245) via changing just Ni{sup 2+}/Fe{sup 3+} molar ratio (γ). With g increased from 0:1 to 2:1, sphere diameter gradually decreased and crystal size exhibited an inversed U-shaped change tendency, followed by increased Ni/Fe atom ratio from 0% to 0.0888%. An in situ-reduction, coordination-precipitation transformation mechanism was proposed to interpret the metal-ion-steered growth. Size- and composition-dependent static magnetic and microwave absorbing properties were systematically investigated. Saturation magnetization declines with g in a Boltzmann model due to the changes of crystal size, sphere diameter, and Ni content. The coercivity reaches a maximum at γ = 0.75:1 because of the critical size of Fe{sub 3}O{sub 4} single domain (25 nm). Studies on microwave absorption reveal that 150–400 nm Fe{sub 3}O{sub 4} nanospheres mainly obey the quarter-wavelength cancellation model with the single-band absorption; 40–135 nm Ni{sub x}Fe{sub 3-x}O{sub 4} nanospheres (0 ≤ x ≤ 0.245) obey the one and three quarter-wavelength cancellation model with the multi-band absorption. 150 nm Fe{sub 3}O{sub 4} nanospheres exhibit the optimal EM wave-absorbing property with an absorbing band of 8.94 GHz and the maximum R{sub L} of −50.11 dB.

  18. Fabrication, structure, and properties of Fe{sub 3}O{sub 4}-C encapsulated with YVO{sub 4}:Eu{sup 3+} composites

    Energy Technology Data Exchange (ETDEWEB)

    Shi Jianhui; Tong Lizhu; Liu Deming; Yang Hua, E-mail: huayang86@sina.com [Jilin University, College of Chemistry (China)

    2012-03-15

    The use of carbon shells offers many advantages in surface coating or surface modification due to their surface with activated carboxyl and carbonyl groups. In this study, the Fe{sub 3}O{sub 4}-C-YVO{sub 4}:Eu{sup 3+} composites were prepared through a simple sol-gel process. Reactive carbon interlayer was introduced as a key component, which separates lanthanide-based luminescent component from the magnetite, more importantly, it effectively prevent oxidation of the Fe{sub 3}O{sub 4} core during the whole preparation process. The morphology, structure, magnetic, and luminescent properties of the composites were characterized by transmission electron microscopy (TEM), high-resolution TEM, X-ray diffraction, X-ray photoelectron spectra, VSM, and photoluminescent spectrophotometer. As a result, the Fe{sub 3}O{sub 4}-C/YVO{sub 4}:Eu{sup 3+} composites with well-crystallized and core-shell structure were prepared and the YVO{sub 4}:Eu{sup 3+} luminescent layer decorating the Fe{sub 3}O{sub 4}-C core-shell microspheres are about 10 nm. In addition, the Fe{sub 3}O{sub 4}-C-YVO{sub 4}:Eu{sup 3+} composites have the excellent magnetic and luminescent properties, which allow them great potential for bioapplications such as magnetic bioseparation, magnetic resonance imaging, and drug/gene delivery.

  19. Synthesis, crystal structure and characterizations of a new red phosphor K{sub 3}EuB{sub 6}O{sub 12}

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Dan, E-mail: iamzd1996@163.com [College of Chemistry and Chemical Engineering, Henan Polytechnic University, Jiaozuo, Henan, 454000 (China); State Key Laboratory of Structural Chemistry, Fuzhou, Fujian, 350002 (China); Ma, Fa-Xue; Wu, Zhi-Qiang; Zhang, Lei [College of Chemistry and Chemical Engineering, Henan Polytechnic University, Jiaozuo, Henan, 454000 (China); Wei, Wei, E-mail: wwei@cnu.edu.cn [Department of Chemistry, Capital Normal University, Beijing, 100048 (China); Yang, Juan; Zhang, Rong-Hua; Chen, Peng-Fei; Wu, Shan-Xuan [College of Chemistry and Chemical Engineering, Henan Polytechnic University, Jiaozuo, Henan, 454000 (China)

    2016-10-01

    A new potassium europium borate K{sub 3}EuB{sub 6}O{sub 12} has been prepared using a high temperature molten salt method and structurally characterized by single crystal X-ray diffraction (SC-XRD) analyses. Its structure features a three-dimensional (3D) framework composed of isolated [B{sub 5}O{sub 10}]{sup 5−} anions that are bridged by K{sup +} and Eu{sup 3+} ions. In this structure, one crystallographic distinct atom site is mixed occupied by K/Eu at a molar ratio of 1:1. The self-activated photoluminescence (PL) of K{sub 3}EuB{sub 6}O{sub 12} was studied. The excitation spectrum covers a wide range from 322 to 466 nm, which suggests that the K{sub 3}EuB{sub 6}O{sub 12} phosphors can be effectively excited by a near-UV light source. The emission spectrum consists of groups of lines in the red spectral region due to the {sup 5}D{sub 0}→{sup 7}F{sub j} (j = 1, 2, 3, 4) electronic transitions of Eu{sup 3+} ions, with the most intense line at 611 nm. We may expect that K{sub 3}EuB{sub 6}O{sub 12} has the potential to be a red phosphor pumped by near-UV LED chips. - Highlights: • A new red phosphor K{sub 3}EuB{sub 6}O{sub 12} was prepared. • The crystal structure of K{sub 3}EuB{sub 6}O{sub 12} was determined for the first time. • The photoluminescence properties of K{sub 3}EuB{sub 6}O{sub 12} are studied. • K{sub 3}EuB{sub 6}O{sub 12} show intense self-activated red emission under near-UV light excitation.

  20. Temperature dependence of the coercive field of gas atomized Fe{sub 73.5}Si{sub 13.5}B{sub 9}Nb{sub 3}Cu{sub 1}

    Energy Technology Data Exchange (ETDEWEB)

    Garcia-Escorial, A., E-mail: age@cenim.csic.es [CENIM-CSIC, Avda, Gregorio del Amo, 8, 28040 Madrid (Spain); Lieblich, M. [CENIM-CSIC, Avda, Gregorio del Amo, 8, 28040 Madrid (Spain); Hernando, A.; Aragon, A.; Marin, P. [Instituto de Magnetismo Aplicado, IMA, P.O. Box 155, 28230 Madrid (Spain)

    2012-09-25

    Highlights: Black-Right-Pointing-Pointer An anomalous thermal dependence of the coercive field of gas atomized Fe{sub 73.5}Si{sub 13.5}B{sub 9}Nb{sub 3}Cu{sub 1} powder particles under 25 {mu}m powder particle, increasing Hc as temperature increases. Black-Right-Pointing-Pointer It is proposed that Cu rich regions at inter-grain boundaries could act as exchange decoupling regions contributing to the thermal increase of coercivity. Black-Right-Pointing-Pointer This anomalous thermal dependence points out that tailoring microstructure and size, by controlling the cooling rate of more adequate multiphase systems, could be a promising procedure to develop soft or hard magnets, avoiding Rare Earths metals that is nowadays an important target for the engineering of magnetic materials. - Abstract: In this work, the dependence of the coercive field of Fe{sub 73.5}Si{sub 13.5}B{sub 9}Nb{sub 3}Cu{sub 1} gas atomized powder with the temperature for different particle sizes has been studied, observing an anomalous behavior in the under 25 powder particle size fraction. This unusual behavior is related with the microstructure of the powder, and is attributed to the presence of a multiphase magnetic system, with non-magnetic regions decoupling the ferromagnetic domains.

  1. SU-F-T-662: Feasibility Study of Fe3O4/TaOx Nano Particles as a Radiosensitizer for Radiation Therapy

    Energy Technology Data Exchange (ETDEWEB)

    Ahn, S [Department of Health Sciences and Technology, Samsung Advanced Institute for Health Sciences and Technology, Sungkyunkwan University (Korea, Republic of); Lee, N [School of Advanced Materials Engineering College of Engineering, Kookmin Uiniversity (Japan); Shin, S; Choi, C; Han, Y; Park, H; Choi, D; Lim, D [Samsung Medical Center, Sungkyunkwan University School of Medicine radiation oncology (Korea, Republic of)

    2016-06-15

    Purpose: To investigate the feasibility of using multifunctional Fe{sub 3}O{sub 4}/TaOx(core / shell) nano particles developed for CT and MRI contrast agent as dose enhancing radiosensitizers. Methods: Firstly, to verify the imaging detectability of Fe{sub 3}O{sub 4}/TaOx nano particles, in-vivo tests were conducted. Approximately 600 mg/kg of 19 nm diameter Fe{sub 3}O{sub 4}/TaOx nano particles dispersed in phosphate buffered saline(PBS) were injected to ten nude Balb/c mice through the tail vein. Difference between pre- and post-injection images was analyzed by computing the pixel histogram and correlation coefficient factor using MATLAB in the user defined ROI. Secondly, to quantify the potential therapeutic enhancement with nano materials, DER (Dose Enhancement Ratio) and number of SER (Secondary Electron Ratio) were computed using TOPAS(ver.2.0 P-03) MC simulation. Results: In CT, MRI imaging, the aorta, the blood vessel, and the liver were clearly visualized after intravenous injection of Fe{sub 3}O{sub 4}/TaOx nano particles. There was large different between pre and post-injection images of Histogram data and Coefficients of correlation factor in CT and MR are 0.006, 0.060, respectively. When 70 MeV protons were irradiated for a Gold, Tantalum, TaOx, Fe{sub 3}O{sub 4}/TaOx, Fe{sub 3}O{sub 4} nano particle, DER was 2.59, 2.41, 1.68, 1.54 and 1.36 respectively. Similarly, SER increment was 2.31, 2.15, 1.56, 1.46, and 1.27 for Gold, Tantalum, TaOx, Fe{sub 3}O{sub 4}/TaOx, Fe{sub 3}O{sub 4} nano particle, respectively. Conclusion: Fe{sub 3}O{sub 4}/TaOx nano particles have potential as a multifunctional agent which enhances the accuracy in cancer detection through visualization of developed tumor lesion and increases the therapeutic effect in proton therapy. The dose enhancement with Fe{sub 3}O{sub 4}/TaOx was estimated as half of the Gold. However, tumor targeting such as combined with magnetic field may overcome the low DER. This research was supported by the

  2. Facile synthesis of Ca{sub 0.68}Si{sub 9}Al{sub 3}(ON){sub 16}:Eu{sup 2+} microbelts mat with the enhanced fluorescence and mechanical performance

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Hailei; Cui, Bo [State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Donghua University, Shanghai 201620 (China); Wang, Hongzhi, E-mail: wanghz@dhu.edu.cn [State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Donghua University, Shanghai 201620 (China); Zhang, Qinghong [Engineering Research Center of Advanced Glasses Manufacturing Technology, MOE, College of Materials Science and Engineering, Donghua University, Shanghai 201620 (China); Li, Yaogang, E-mail: yaogang_li@dhu.edu.cn [Engineering Research Center of Advanced Glasses Manufacturing Technology, MOE, College of Materials Science and Engineering, Donghua University, Shanghai 201620 (China)

    2016-01-15

    Yellow-emitting phosphor mat consisting of Ca{sub 0.68}Si{sub 9}Al{sub 3}(ON){sub 16}:Eu{sup 2+} microbelts was prepared by electrospinning and subsequent nitridation. The as-prepared fiber precursor is smooth and uniform with diameter of 800 to 900 nm. After removing organic templates and nitridation, the morphology of the fiber is well retained and thus a smooth microbelts phosphor mat was obtained. X-ray diffraction and the photoluminescence (PL) spectra reveals that a relatively pure Ca{sub 0.68}Si{sub 9}Al{sub 3}(ON){sub 16} phase and the highest spectral intensity could be obtained at a relatively low temperature of 1500 °C and Eu{sup 2+} doping molar concentration of 0.1. The excitation spectra exhibits a broad band, ranging from 300 to 550 nm, which could be excited by blue LED chip at room temperature. The emission spectra of all exhibits a single broad band in the 400 to 700 nm region, with the maximum intensity always being at 580 nm. The Ca{sub 0.68}Si{sub 9}Al{sub 3}(ON){sub 16}:Eu{sup 2+} microbelts phosphor mat has the bending strength about 4.5 MPa with a photoluminescence quantum yield as high as 65%. By employing it as yellow phosphor, a high-performance warm white LED could be fabricated with low correlated color temperature (2985 K), high-color-rendering index (Ra=86) and luminous efficacy of 129.5 lm W{sup −1}. Different color temperatures also could be tuned by employing microbelts phosphor mats with different thicknesses. - Graphical abstract: Yellow-emitting phosphor mat consisting of Ca{sub 0.68}Si{sub 9}Al{sub 3}(ON){sub 16}:Eu{sup 2+} microbelts fibers were prepared by electrospinning the fiber precursor and subsequent nitridation. Because the good mechanical strength it could be utilized to realize LEDs remote packaging. By employing it as yellow phosphor, a high-performance warm white LED could be fabricated. Different color temperatures also could be tuned by employing microbelts phosphor mats with different thicknesses

  3. Phase formation, morphology and magnetic properties of MgFe{sub 2}O{sub 4} nanoparticles synthesized by hydrothermal technique

    Energy Technology Data Exchange (ETDEWEB)

    Nonkumwong, Jeeranan [Department of Chemistry, Faculty of Science, Chiang Mai University, Chiang Mai 50200 (Thailand); Ananta, Supon [Department of Physics and Materials Science, Faculty of Science, Chiang Mai University, Chiang Mai 50200 (Thailand); Jantaratana, Pongsakorn [Department of Physics, Faculty of Science, Kasetsart University, Bangkok 11900 (Thailand); Phumying, Santi; Maensiri, Santi [Advanced Materials Physics Laboratory (Amp.), School of Physics, Institute of Science, Suranaree University of Technology, Nakhon Ratchasima 30000 (Thailand); Srisombat, Laongnuan, E-mail: slaongnuan@yahoo.com [Department of Chemistry, Faculty of Science, Chiang Mai University, Chiang Mai 50200 (Thailand)

    2015-05-01

    In the present work, the processing conditions for obtaining monodispersed magnesium ferrite (MgFe{sub 2}O{sub 4}) nanoparticles with the desired morphology and relatively high saturation magnetization via hydrothermal technique were developed. For the first time, the effects of base type and reaction conditions (i.e. temperature and time) on phase formation, morphology and magnetic properties of the obtained products were determined by using a combination of XRD, TEM/EDX and VSM techniques. It is seen that the saturation magnetization of the particles can be increased by employing lower reaction temperature and/or shorter reaction time, while narrow size distribution of the particles can be maintained. In addition, it was found that pure phase of superparamagnetic MgFe{sub 2}O{sub 4} nanoparticles with the smallest size of about 65 nm was obtained by using CH{sub 3}COONa as a base at 180 °C for 14 h. - Highlights: • Preparation of MgFe{sub 2}O{sub 4} nanoparticles by hydrothermal method. • Effects of base and reaction conditions on formation and morphology MgFe{sub 2}O{sub 4} particles. • Producing the 65 nm MgFe{sub 2}O{sub 4} nanoparticles with superparamagnetic property.

  4. Effects of 20–100 nm particles on liquid clouds in the clean summertime Arctic

    Directory of Open Access Journals (Sweden)

    W. R. Leaitch

    2016-09-01

    Full Text Available Observations addressing effects of aerosol particles on summertime Arctic clouds are limited. An airborne study, carried out during July 2014 from Resolute Bay, Nunavut, Canada, as part of the Canadian NETCARE project, provides a comprehensive in situ look into some effects of aerosol particles on liquid clouds in the clean environment of the Arctic summer. Median cloud droplet number concentrations (CDNC from 62 cloud samples are 10 cm−3 for low-altitude cloud (clouds topped below 200 m and 101 cm−3 for higher-altitude cloud (clouds based above 200 m. The lower activation size of aerosol particles is  ≤  50 nm diameter in about 40 % of the cases. Particles as small as 20 nm activated in the higher-altitude clouds consistent with higher supersaturations (S for those clouds inferred from comparison of the CDNC with cloud condensation nucleus (CCN measurements. Over 60 % of the low-altitude cloud samples fall into the CCN-limited regime of Mauritsen et al. (2011, within which increases in CDNC may increase liquid water and warm the surface. These first observations of that CCN-limited regime indicate a positive association of the liquid water content (LWC and CDNC, but no association of either the CDNC or LWC with aerosol variations. Above the Mauritsen limit, where aerosol indirect cooling may result, changes in particles with diameters from 20 to 100 nm exert a relatively strong influence on the CDNC. Within this exceedingly clean environment, as defined by low carbon monoxide and low concentrations of larger particles, the background CDNC are estimated to range between 16 and 160 cm−3, where higher values are due to activation of particles  ≤  50 nm that likely derive from natural sources. These observations offer the first wide-ranging reference for the aerosol cloud albedo effect in the summertime Arctic.

  5. Controlled synthesis, formation mechanism, and carbon oxidation properties of Ho{sub 2}Cu{sub 2}O{sub 5} nanoplates prepared with a coordination-complex method

    Energy Technology Data Exchange (ETDEWEB)

    Guo, Rui [School of Resources and Materials, Northeastern University at Qinhuangdao 066004 (China); School of Metallurgy, Northeastern University, Shenyang 110004 (China); You, Junhua [School of Materials Science and Engineering, Shenyang University of Technology, Shenyang 110870 (China); Han, Fei; Li, Chaoyang; Zheng, Guiyuan; Xiao, Weicheng [School of Resources and Materials, Northeastern University at Qinhuangdao 066004 (China); Liu, Xuanwen, E-mail: lxw@mail.neuq.edu.cn [School of Resources and Materials, Northeastern University at Qinhuangdao 066004 (China); School of Metallurgy, Northeastern University, Shenyang 110004 (China)

    2017-02-28

    Highlights: • The crystallization mechanism relies on Ho{sup 3+} and Cu{sup 2+} diffusion. • The Ho{sub 2}Cu{sub 2}O{sub 5} particles are refined by the coordination complex method under N{sub 2} environment. • The catalytic oxidation activity of Ho{sub 2}Cu{sub 2}O{sub 5} samples for carbon is enhanced. - Abstract: Ho{sub 2}Cu{sub 2}O{sub 5} nanoplates with perovskite structures were synthesized via a simple solution method (SSM) and a coordination-complex method (CCM) using [HoCu(3,4-pdc){sub 2}(OAc)(H{sub 2}O){sub 3}]·8H{sub 2}O (L = 3,4-pyridinedicarboxylic acid) as a precursor. The CCM was also performed in an N{sub 2} environment (CCMN) under various calcination conditions. The crystallization processes were characterized using X-ray diffraction, scanning electron microscopy, and high-resolution transmission electron microscopy. Ho{sub 2}Cu{sub 2}O{sub 5} formed through the diffusion of CuO into Ho{sub 2}O{sub 3} particles. Cu{sup 2+} diffused faster than Ho{sup 3+} during this process. The initial products of CCMN (along with the thermal decomposition products) were initially laminarized in the N{sub 2} atmosphere, which prevented the growth of CuO particles and decreased the size of the Ho{sub 2}Cu{sub 2}O{sub 5} particles. The final Ho{sub 2}Cu{sub 2}O{sub 5} particles from CCMN had a nanoplate morphology with an average thickness of 75 nm. The decomposition of organic molecules and protection from N{sub 2} played important roles in determining the morphology of the resulting Ho{sub 2}Cu{sub 2}O{sub 5}. The catalytic oxidation activity of Ho{sub 2}Cu{sub 2}O{sub 5} samples for carbon was characterized using a specific surface area measurement and thermogravimetric analysis, which revealed that the samples produced by CCMN had the highest catalytic activity.

  6. Infrared absorption of CH{sub 3}OSO and CD{sub 3}OSO radicals produced upon photolysis of CH{sub 3}OS(O)Cl and CD{sub 3}OS(O)Cl in p-H{sub 2} matrices

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Yu-Fang; Kong, Lin-Jun [Department of Applied Chemistry and Institute of Molecular Science, National Chiao Tung University, 1001 Ta-Hsueh Rd., Hsinchu 30010, Taiwan (China); Lee, Yuan-Pern [Department of Applied Chemistry and Institute of Molecular Science, National Chiao Tung University, 1001 Ta-Hsueh Rd., Hsinchu 30010, Taiwan (China); Institute of Atomic and Molecular Sciences, Academia Sinica, Taipei 10617, Taiwan (China)

    2012-03-28

    Irradiation at 239 {+-} 20 nm of a p-H{sub 2} matrix containing methoxysulfinyl chloride, CH{sub 3}OS(O)Cl, at 3.2 K with filtered light from a medium-pressure mercury lamp produced infrared (IR) absorption lines at 3028.4 (attributable to {nu}{sub 1}, CH{sub 2} antisymmetric stretching), 2999.5 ({nu}{sub 2}, CH{sub 3} antisymmetric stretching), 2950.4 ({nu}{sub 3}, CH{sub 3} symmetric stretching), 1465.2 ({nu}{sub 4}, CH{sub 2} scissoring), 1452.0 ({nu}{sub 5}, CH{sub 3} deformation), 1417.8 ({nu}{sub 6}, CH{sub 3} umbrella), 1165.2 ({nu}{sub 7}, CH{sub 3} wagging), 1152.1 ({nu}{sub 8}, S=O stretching mixed with CH{sub 3} rocking), 1147.8 ({nu}{sub 9}, S=O stretching mixed with CH{sub 3} wagging), 989.7 ({nu}{sub 10}, C-O stretching), and 714.5 cm{sup -1} ({nu}{sub 11}, S-O stretching) modes of syn-CH{sub 3}OSO. When CD{sub 3}OS(O)Cl in a p-H{sub 2} matrix was used, lines at 2275.9 ({nu}{sub 1}), 2251.9 ({nu}{sub 2}), 2083.3 ({nu}{sub 3}), 1070.3 ({nu}{sub 4}), 1056.0 ({nu}{sub 5}), 1085.5 ({nu}{sub 6}), 1159.7 ({nu}{sub 7}), 920.1 ({nu}{sub 8}), 889.0 ({nu}{sub 9}), 976.9 ({nu}{sub 10}), and 688.9 ({nu}{sub 11}) cm{sup -1} appeared and are assigned to syn-CD{sub 3}OSO; the mode numbers correspond to those used for syn-CH{sub 3}OSO. The assignments are based on the photolytic behavior and a comparison of observed vibrational wavenumbers, infrared intensities, and deuterium isotopic shifts with those predicted with the B3P86/aug-cc-pVTZ method. Our results extend the previously reported four transient IR absorption bands of gaseous syn-CH{sub 3}OSO near 2991, 2956, 1152, and 994 cm{sup -1} to 11 lines, including those associated with C-O, O-S, and S=O stretching modes. Vibrational wavenumbers of syn-CD{sub 3}OSO are new. These results demonstrate the advantage of a diminished cage effect of solid p-H{sub 2} such that the Cl atom, produced via UV photodissociation of CH{sub 3}OS(O)Cl in situ, might escape from the original cage to yield isolated CH{sub 3}OSO

  7. Thickness dependence of dynamic and static magnetic properties of pulsed laser deposited La{sub 0.7}Sr{sub 0.3}MnO{sub 3} films on SrTiO{sub 3}(001)

    Energy Technology Data Exchange (ETDEWEB)

    Monsen, Åsmund [Department of Physics, NTNU, 7491 Trondheim (Norway); Boschker, Jos E. [Department of Electronics and Telecommunications, NTNU, 7491 Trondheim (Norway); Macià, Ferran [Department of Physics, New York University, 4 Washington Place, New York, NY 10003 (United States); Wells, Justin W. [Department of Physics, NTNU, 7491 Trondheim (Norway); Nordblad, Per [Department of Engineering Sciences, Uppsala University, Box 534, SE-751 21 Uppsala (Sweden); Kent, Andrew D. [Department of Physics, New York University, 4 Washington Place, New York, NY 10003 (United States); Mathieu, Roland [Department of Engineering Sciences, Uppsala University, Box 534, SE-751 21 Uppsala (Sweden); Tybell, Thomas [Department of Electronics and Telecommunications, NTNU, 7491 Trondheim (Norway); Wahlström, Erik, E-mail: erik.wahlstrom@ntnu.no [Department of Physics, NTNU, 7491 Trondheim (Norway)

    2014-11-15

    We present a comprehensive study of the thickness dependence of static and magneto-dynamic magnetic properties of La{sub 0.7}Sr{sub 0.3}MnO{sub 3}. Epitaxial pulsed laser deposited La{sub 0.7}Sr{sub 0.3}MnO{sub 3}/SrTiO{sub 3}(001) thin films in the range from 3 unit cell (uc) to 40 uc (1.2–16 nm) have been investigated through ferromagnetic resonance (FMR) spectroscopy and SQUID magnetometry at variable temperature. Magnetodynamically, three different thickness, d, regimes are identified: 20 uc ≲d uc where the system is bulk like, a transition region 8 uc ≤d≲20 uc where the FMR linewidth and the position depend on thickness and d=6 uc which displays significantly altered magnetodynamic properties, while still displaying bulk magnetization. Magnetization and FMR measurements are consistent with a nonmagnetic volume corresponding to ∼4 uc. We observe a reduction of Curie temperature (T{sub C}) with decreasing thickness, which is coherent with a mean field model description. The reduced ordering temperature also accounts for the thickness dependence of the magnetic anisotropy constants and resonance fields. The damping of the system is strongly thickness dependent, and is for thin films dominated by thickness dependent anisotropies, yielding both a strong two-magnon scattering close to T{sub c} and a low temperature broadening. For the bulk like samples a large part of the broadening can be linked to spread in magnetic anisotropies attributed to crystal imperfections/domain boundaries of the bulk like film. - Highlights: • Thickness dependent magnetodynamic anisotropy constants and line-widths have been measured. • For thicknesses >8nm the films are bulk-like. • Thin film line-widths are dominated by surface/interface imperfections. • Thick film line-widths are dominated by crystal imperfections/domain boundaries.

  8. Magnetic and magneto-optical characteristics of spin coated Co{sub 0.6}Zn{sub 0.4}Fe{sub 1.7}Mn{sub 0.3}O{sub 4} thin films on Pt (1 1 1) coated Si substrate

    Energy Technology Data Exchange (ETDEWEB)

    Gupta, Arti, E-mail: artigupta80@gmail.com [Department of Physics and Astrophysics, University of Delhi, Delhi110007 (India); Dutta, Shankar [Solid State Physics Laboratory, DRDO, Lucknow Road, Timarpur, Delhi110054 (India); Tandon, Ram Pal [Department of Physics and Astrophysics, University of Delhi, Delhi110007 (India)

    2016-05-15

    Highlights: • Properties of Co{sub 0.6}Zn{sub 0.4}Mn{sub 0.3}Fe{sub 1.7}O{sub 4} thin films on Pt-Si substrate are reported. • Reduction in thickness ∼27% with increased annealing temperature was found. • Partial (3 3 3) plane textured orientation was noted for these films. - Abstract: This paper reports magnetic and magneto-optical properties of Co{sub 0.6}Zn{sub 0.4}Fe{sub 1.7}Mn{sub 0.3}O{sub 4} nanocrystalline thin films (thickness ∼140–200 nm) deposited on Pt (1 1 1)/Ti/SiO{sub 2}/Si substrates by spin coating technique. Deposited films are then annealed at 600 °C and 700 °C for 60 min (significant reduction in film thickness from 200 nm to 140 nm was noted with the increase in post deposition annealing temperature). The X ray diffraction patterns confirmed the spinel cubic structure of Co{sub 0.6}Zn{sub 0.4}Fe{sub 1.7}Mn{sub 0.3}O{sub 4} films with polycrystalline phase and also indicated a partial <3 3 3> texture orientation. Deposited films showed magnetic anisotropy as evidenced from magnetic and magneto-optical measurements. Higher in plane remnant magnetization and low coercivity values as compared to out of plane ones were observed for both samples, indicating in plane alignment of easy axis of magnetization.

  9. Fabrication of Au{sub nanoparticle}@mSiO{sub 2}@Y{sub 2}O{sub 3}:Eu nanocomposites with enhanced fluorescence

    Energy Technology Data Exchange (ETDEWEB)

    Li, Huiqin [Key Laboratory of Synthetic and Natural Functional Molecule Chemistry (Ministry of Education), Shaanxi Key Laboratory of Physico-Inorganic Chemistry, College of Chemistry & Materials Science, Northwest University, Xi' an, 710069 (China); College of Chemistry & Chemical Engineering, Baoji University of Arts & Sciences, Baoji, 721013 (China); Kang, Jianmiao [Key Laboratory of Synthetic and Natural Functional Molecule Chemistry (Ministry of Education), Shaanxi Key Laboratory of Physico-Inorganic Chemistry, College of Chemistry & Materials Science, Northwest University, Xi' an, 710069 (China); Yang, Jianhui, E-mail: jianhui@nwu.edu.cn [Key Laboratory of Synthetic and Natural Functional Molecule Chemistry (Ministry of Education), Shaanxi Key Laboratory of Physico-Inorganic Chemistry, College of Chemistry & Materials Science, Northwest University, Xi' an, 710069 (China); Wu, Biao, E-mail: wubiao@nwu.edu.cn [Key Laboratory of Synthetic and Natural Functional Molecule Chemistry (Ministry of Education), Shaanxi Key Laboratory of Physico-Inorganic Chemistry, College of Chemistry & Materials Science, Northwest University, Xi' an, 710069 (China)

    2016-07-15

    Herein, Au{sub nanoparticle}@mSiO{sub 2}@Y{sub 2}O{sub 3}:Eu nanocomposites are synthesized through layer-by-layer assembly technology. Au{sub nanoparticle}@mSiO{sub 2} core–shell nanospheres were prepared at first in the presence of CTAB in aqueous solution system by the modified one-pot method. A chemical precipitation method and a succeeding calcination process were adopted to the growth of Y{sub 2}O{sub 3}:Eu shells on the surfaces of Au{sub nanoparticle}@mSiO{sub 2} core–shell nanospheres. The structure, morphology and composition of the nanocomposites were confirmed by XRD, TEM and UV–vis absorption spectrum. The prepared Au{sub nanoparticle}@mSiO{sub 2}@Y{sub 2}O{sub 3}:Eu nanocomposites have showed the emission intensity enhances to 6.23 times at 30 nm thickness of the silica spacer between the core of Au nanoparticle and the shell of Y{sub 2}O{sub 3}:Eu. According to the observations of fluorescent lifetime and the modeling of local electric field, the metal-enhanced and quenched fluorescence is closely related with the enhancement of excitation and radiative decay rate and the quenching by NRET comes as a result of competition between the distance-dependent mechanisms. This kind of multifunctional inorganic material will be widely used in electronics, biology and medical drug loading, etc. - Highlights: • Fabrication of Au{sub nanoparticle}@mSiO{sub 2}@Y{sub 2}O{sub 3}:Eu nanocomposites with core-spacer-shell structure. • The controllable fluorescence is achieved by adjusting the spacer thickness of silica. • The fluorescence enhancement is 6.23-fold at an optimal spacer thickness about 30 nm. • The metal-enhanced fluorescence mechanism is proposed.

  10. Strong red-emission of Eu{sup 3+}:Li{sub 4}Ti{sub 5}O{sub 12} powders for phosphor applications

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Yan [Kazuo Inamori School of Engineering, New York State College of Ceramics, Alfred University, Alfred, NY 14802 (United States); Jiménez, José A. [Department of Chemistry, University of North Florida, Jacksonville, FL 32224 (United States); Wu, Yiquan, E-mail: wuy@alfred.edu [Kazuo Inamori School of Engineering, New York State College of Ceramics, Alfred University, Alfred, NY 14802 (United States)

    2016-08-15

    The synthesis and photoluminescence properties of trivalent europium doped lithium titanate (Eu{sup 3+}:Li{sub 4}Ti{sub 5}O{sub 12}) with different Eu{sup 3+} concentrations (0.1 mol%, 0.3 mol%, 1.0 mol%, 3.0 mol%) are reported and analyzed as a phosphor. Europium (III) nitrate (Eu(NO{sub 3}){sub 3}) was employed as Eu{sup 3+} source, while lithium acetate dihydrate (CH{sub 3}COOLi·2H{sub 2}O) and titanium n-butoxide (Ti(OC{sub 4}H{sub 9}){sub 4}) were adopted as raw materials to synthesize the host lithium titanate with a Li:Ti stoichiometry of 4.5:1. Phase identification was performed using X-ray diffraction (XRD), and morphology was examined using scanning electron microscopy (SEM). Eu{sup 3+}:Li{sub 4}Ti{sub 5}O{sub 12} powders showed strong red emission at 612 nm, corresponding to the {sup 5}D{sub 0}–{sup 7}F{sub 2} transition, with the strongest excitation peak observed in the blue light region at 464 nm. Decay time analyses revealed relatively short lifetimes accompanying typical exponential decay rates. The effect of Eu{sup 3+} concentration (0.1 mol%, 0.3 mol%, 1.0 mol%, 3.0 mol%) on photoluminescence intensity and decay time was explored, and is reported here. It was determined that the CIE color coordinates (0.66, 0.34) of the doped Li{sub 4}Ti{sub 5}O{sub 12} powders were independent of Eu{sup 3+} concentration, and that the coordinates are very similar to the ideal red chromaticity (0.67, 0.33) designated by the National Television Standard Committee (NTSC) system.

  11. Synthesis and characterization of Fe{sub 3}O{sub 4} nanoparticles coated with fucan polysaccharides

    Energy Technology Data Exchange (ETDEWEB)

    Silva, V.A.J.; Andrade, P.L. [Programa de Pós-Graduação em Ciências de Materiais, Centro de Ciências Exatas e da Natureza, Universidade Federal de Pernambuco, 50670-901 Recife-PE (Brazil); Laboratório de Imunopatologia Keizo Asami (LIKA), Universidade Federal de Pernambuco, 50670-901 Recife-PE (Brazil); Silva, M.P.C. [Laboratório de Imunopatologia Keizo Asami (LIKA), Universidade Federal de Pernambuco, 50670-901 Recife-PE (Brazil); Departamento de Bioquímica, Universidade Federal de Pernambuco, 50670-420 Recife-PE (Brazil); Bustamante D, A. [Laboratorio de Cerámicos y Nanomateriales, Facultad de Ciencias Físicas, Universidad Nacional Mayor de San Marcos, Ap. Postal 14-0149 Lima (Peru); De Los Santos Valladares, Luis [Laboratório de Imunopatologia Keizo Asami (LIKA), Universidade Federal de Pernambuco, 50670-901 Recife-PE (Brazil); Cavendish Laboratory, University of Cambridge, J.J. Thomson Avenue, Cambridge CB3 0HE (United Kingdom); Albino Aguiar, J., E-mail: albino@df.ufpe.br [Programa de Pós-Graduação em Ciências de Materiais, Centro de Ciências Exatas e da Natureza, Universidade Federal de Pernambuco, 50670-901 Recife-PE (Brazil); Departamento de Física, Universidade Federal de Pernambuco, 50670-901 Recife-PE (Brazil)

    2013-10-15

    In this work we report the preparation of fucan-coated magnetite (Fe{sub 3}O{sub 4}) nanoparticles by the co-precipitation method. These nanoparticles were characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, Mössbauer spectroscopy and magnetic measurements. The nanoparticles showed quasi-spherical morphology with mean sizes around 10 nm. XRD and FT-IR confirmed the functionalization of the Fe{sub 3}O{sub 4} nanoparticles with the fucan polysaccharide. Room temperature magnetization measurements and Mössbauer spectroscopy showed that the nanoparticles exhibited superparamagnetic behavior at 300 K and the magnetic properties of the Fe{sub 3}O{sub 4} are partly screened by the coating preventing aggregation. - Highlights: • Syntheses of fucan-coated Fe{sub 3}O{sub 4} nanoparticles were made by co-precipitation method. • The efficiency of polysaccharide coated was analyzed by XRD and FT-IR. • The magnetic nanoparticles mean size was 10–20 nm. • The fucan-coated magnetite nanoparticles showed superparamagnetic behavior.

  12. Preliminary observation of self-reduction of Eu ions in α-Ca{sub 3}(PO{sub 4}){sub 2} phosphors prepared in air condition

    Energy Technology Data Exchange (ETDEWEB)

    Tong, Chao [College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123 (China); Zhu, Yangguang; Xu, Chuanyan [Suzhou Biomaterials and Advanced Manufacture Engineering Technology Research Center, Suzhou Dingan Technology Co., Ltd, Suzhou 215200 (China); Li, Yadong, E-mail: liyadong@suda.edu.cn [College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123 (China)

    2016-11-01

    A series of Eu doped α-Ca{sub 3}(PO{sub 4}){sub 2} phosphors were synthesized by a high-temperature solid-state reaction in air atmosphere. The crystal structures, photoluminescence properties of the phosphors were systematically studied. The emission spectra showed a broad emission band centered at 492 nm attributed to the typical 4f{sup 6}5d{sup 1}→4f{sup 7} transition of Eu{sup 2+}ions, and several sharp peaks from 560 to 750 nm attributed to the 5D{sub 0}→7F{sub J}(J=0,1,2,3,4) transition of Eu{sup 3+}ions. The results, combined with the X-ray photoelectron spectroscopy measurements, demonstrate self-reduction of Eu{sup 3+}to Eu{sup 2+}occurred in α-Ca{sub 3}(PO{sub 4}){sub 2} matrix for the first time. This suggested that the Eu{sup 2+}ions in α-Ca{sub 3}(PO{sub 4}){sub 2}could serve as a spectroscopic probe to detect the content of α-Ca{sub 3}(PO{sub 4}){sub 2}in phase transition process.

  13. Removal of heavy metals from aqueous solutions using Fe{sub 3}O{sub 4}, ZnO, and CuO nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Mahdavi, Shahriar, E-mail: smahdaviha@yahoo.com; Jalali, Mohsen, E-mail: jalali@basu.ac.ir [College of Agriculture, Bu-Ali Sina University, Department of Soil Science (Iran, Islamic Republic of); Afkhami, Abbas, E-mail: afkhami@basu.ac.ir [College of Chemistry, Bu-Ali Sina University, Department of Analytical Chemistry (Iran, Islamic Republic of)

    2012-08-15

    This study investigated the removal of Cd{sup 2+}, Cu{sup 2+}, Ni{sup 2+}, and Pb{sup 2+} from aqueous solutions with novel nanoparticle sorbents (Fe{sub 3}O{sub 4}, ZnO, and CuO) using a range of experimental approaches, including, pH, competing ions, sorbent masses, contact time, scanning electron microscopy, transmission electron microscopy, and X-ray diffraction. The images showed that Fe{sub 3}O{sub 4}, ZnO, and CuO particles had mean diameters of about 50 nm (spheroid), 25 nm (rod shape), and 75 nm (spheroid), respectively. Tests were performed under batch conditions to determine the adsorption rate and uptake at equilibrium from single and multiple component solutions. The maximum uptake values (sum of four metals) in multiple component solutions were 360.6, 114.5, and 73.0 mg g{sup -1}, for ZnO, CuO, and Fe{sub 3}O{sub 4}, respectively. Based on the average metal removal by the three nanoparticles, the following order was determined for single component solutions: Cd{sup 2+} > Pb{sup 2+} > Cu{sup 2+} > Ni{sup 2+}, while the following order was determined in multiple component solutions: Pb{sup 2+} > Cu{sup 2+} > Cd{sup 2+} > Ni{sup 2+}. Sorption equilibrium isotherms could be described using the Freundlich model in some cases, whereas other isotherms did not follow this model. Furthermore, a pseudo-second order kinetic model was found to correctly describe the experimental data for all nanoparticles. Scanning electron microscopy, energy dispersive X-ray before and after metal sorption, and soil solution saturation indices showed that the main mechanism of sorption for Cd{sup 2+} and Pb{sup 2+} was adsorption, whereas both Cu{sup 2+} and Ni{sup 2+} sorption were due to adsorption and precipitation. These nanoparticles have potential for use as efficient sorbents for the removal of heavy metals from aqueous solutions and ZnO nanoparticles were identified as the most promising sorbent due to their high metal uptake.

  14. Comparison of Y{sub 2}O{sub 3}:Bi{sup 3+} phosphor thin films fabricated by the spin coating and radio frequency magnetron techniques

    Energy Technology Data Exchange (ETDEWEB)

    Jafer, R.M.; Yousif, A. [Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein ZA 9300 (South Africa); Department of Physics, Faculty of Education, University of Khartoum, P.O. Box 321, Postal Code 11115 Omdurman (Sudan); Kumar, Vinod [Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein ZA 9300 (South Africa); Photovoltaic Laboratory, Centre for Energy Studies, Indian Institute of Technology Delhi, New Delhi 110016 (India); Pathak, Trilok Kumar [Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein ZA 9300 (South Africa); Semiconductor Physics Lab, Department of Physics, Gurukula Kangri University, Haridwar (India); Purohit, L.P. [Semiconductor Physics Lab, Department of Physics, Gurukula Kangri University, Haridwar (India); Swart, H.C., E-mail: swarthc@ufs.ac.za [Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein ZA 9300 (South Africa); Coetsee, E., E-mail: CoetseeE@ufs.ac.za [Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein ZA 9300 (South Africa)

    2016-09-15

    The reactive radio-frequency (RF) magnetron sputtering and spin coating fabrication techniques were used to fabricate Y{sub 2−x}O{sub 3}:Bi{sub x=0.5%} phosphor thin films. The two techniques were analysed and compared as part of investigations being done on the application of down-conversion materials for a Si solar cell. The morphology, structural and optical properties of these thin films were investigated. The X-ray diffraction results of the thin films fabricated by both techniques showed cubic structures with different space groups. The optical properties showed different results because the Bi{sup 3+} ion is very sensitive towards its environment. The luminescence results for the thin film fabricated by the spin coating technique is very similar to the luminescence observed in the powder form. It showed three obvious emission bands in the blue and green regions centered at about 360, 410 and 495 nm. These emissions were related to the {sup 3}P{sub 1}–{sup 1}S{sub 0} transition of the Bi{sup 3+} ion situated in the two different sites of the Y{sub 2}O{sub 3} matrix with I a-3(206) space group. Whereas the thin film fabricated by the radio frequency magnetron technique showed a broad single emission band in the blue region centered at about 416 nm. This was assigned to the {sup 3}P{sub 1}–{sup 1}S{sub 0} transition of the Bi{sup 3+} ion situated in one of the Y{sub 2}O{sub 3} matrix's sites with a Fm-3 (225) space group. The spin coating fabrication technique is suggested to be the best technique to fabricate the Y{sub 2}O{sub 3}:Bi{sup 3+} phosphor thin films. - Highlights: • RF sputtering and spin coating were used to fabricate Y{sub 2−x}O{sub 3}:Bi{sub x=0.5%} phosphor thin films. • XRD results of the two films showed cubic structures with different space groups. • PL showed different emission for the Bi{sup 3+} ions in the two films. • Three emission bands in the blue and green regions centered at about 360, 410 and 495 nm. • RF

  15. Crystallization of 21.25Gd{sub 2}O{sub 3}-63.75MoO{sub 3}-15B{sub 2}O{sub 3} glass induced by femtosecond laser at the repetition rate of 250 kHz

    Energy Technology Data Exchange (ETDEWEB)

    Zhong, M.J.; Han, Y.M. [Department of Physics, Shanghai University, 99 Shangda Road, Shanghai 200444 (China); Liu, L.P. [Hunan Biological and Electromechanical Polytechnic, Changsha 410126 (China); Zhou, P.; Du, Y.Y.; Guo, Q.T. [Department of Physics, Shanghai University, 99 Shangda Road, Shanghai 200444 (China); Ma, H.L., E-mail: mahl@staff.shu.edu.cn [Department of Physics, Shanghai University, 99 Shangda Road, Shanghai 200444 (China); Dai, Y. [Department of Physics, Shanghai University, 99 Shangda Road, Shanghai 200444 (China)

    2010-12-01

    We report the formation of {beta}'-Gd{sub 2}(MoO{sub 4}){sub 3} (GMO) crystal on the surface of the 21.25Gd{sub 2}O{sub 3}-63.75MoO{sub 3}-15B{sub 2}O{sub 3} glass, induced by 250 kHz, 800 nm femtosecond laser irradiation. The morphology of the modified region in the glass was clearly examined by scanning electron microscopy (SEM). By micro-Raman spectra, the laser-induced crystals were confirmed to be GMO phases and it is found that these crystals have a strong dependence on the number and power of the femtosecond laser pulses. When the irradiation laser power was 900 mW, not only the Raman peaks of GMO crystals but also some new peaks at 214 cm{sup -1}, 240 cm{sup -1}, 466 cm{sup -1}, 664 cm{sup -1} and 994 cm{sup -1}which belong to the MoO{sub 3} crystals were observed. The possible mechanisms are proposed to explain these phenomena.

  16. Structure and crystallization behavior of La{sub 2}O{sub 3}⋅3B{sub 2}O{sub 3} metaborate glasses doped with Nd{sup 3+} or Eu{sup 3+} ions

    Energy Technology Data Exchange (ETDEWEB)

    Pytalev, D.S., E-mail: pytalev@isan.troitsk.ru [Institute of Spectroscopy, Russian Academy of Sciences, 5 Fizicheskaya St., 142190 Troitsk, Moscow (Russian Federation); Caurant, D.; Majérus, O.; Trégouët, H. [Institut de Recherche de Chimie Paris, CNRS – Chimie ParisTech, 11 Rue Pierre et Marie Curie, 75005 Paris (France); Charpentier, T. [CEA, IRAMIS, NIMBE, CEA-CNRS UMR 3299, Laboratoire de Structure et Dynamique par Résonance Magnétique, 91191 Gif-sur-Yvette (France); Mavrin, B.N. [Institute of Spectroscopy, Russian Academy of Sciences, 5 Fizicheskaya St., 142190 Troitsk, Moscow (Russian Federation)

    2015-08-25

    Highlights: • The structure and crystallization behavior of the La{sub 2}O{sub 3}⋅3B{sub 2}O{sub 3} glass are studied. • LaB{sub 3}O{sub 6} crystallizes congruently without intermediate but only from glass surface. • The structure of the amorphous and the crystalline phases differ significantly. • The activation energy of LaB{sub 3}O{sub 6} crystal growth is determined. - Abstract: The local structure and crystallization behavior of the stoichiometric La{sub 2}O{sub 3}⋅3B{sub 2}O{sub 3} (LaMB) metaborate glass doped with Nd{sup 3+} or Eu{sup 3+} ions are studied using differential thermal analysis (DTA), X-ray diffraction (XRD), Raman scattering and {sup 11}B magic-angle spinning nuclear magnetic resonance (MAS NMR), optical absorbance and luminescence techniques. In the crystallized samples, XRD, NMR and Raman spectroscopy have detected the formation of only one crystalline phase (congruent crystallization of LaB{sub 3}O{sub 6}). No intermediate metastable crystalline phase has been detected before LaB{sub 3}O{sub 6} crystals formation (single stage crystallization process). The observation of heat treated glass samples by scanning electron microscopy (SEM) and optical microscopy coupled with the study of the effect of varying the glass particle size on the DTA curves have both revealed that LaB{sub 3}O{sub 6} crystallization only occurs by a heterogeneous nucleation mechanism (needle-shape crystals) from glass surface. The activation energy E{sub c} of crystal growth has been determined by performing DTA experiments at different heating rates with the Kissinger (784 kJ/mol) and Ozawa (801 kJ/mol) equations than can be used for surface crystallization processes. The heterogeneous crystallization behavior and the spectroscopic results obtained in this work by comparing the LaMB glass with the LaB{sub 3}O{sub 6} crystalline phase suggest the existence of significant structural differences between the amorphous and the crystalline phases contrary to what

  17. Strain control of Urbach energy in Cr-doped PrFeO{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Kumar, Anil; Warshi, M.K.; Mishra, Vikash; Saxena, Shailendra K.; Kumar, Rajesh; Sagdeo, Pankaj R. [Indian Institute of Technology Indore, Material Research Laboratory, Discipline of Physics and MEMS, Indore (India)

    2017-09-15

    Polycrystalline samples of PrFe{sub 1-x}Cr{sub x}O{sub 3} having average particle size of ∝90 nm have been prepared by wet chemical route. The structural phase purity of the prepared samples is confirmed by powder X-ray diffraction followed by Rietveld refinements. It is observed that with Cr doping, the Urbach energy (E{sub u}) increases. The E{sub u} is measure of the various disorders present in the sample, such as chemical and structural. To understand the contribution to the E{sub u} due to chemical and structural disorders, we have probed the chemical and structural disorders in the samples by elemental mappings and through X-ray diffraction experiments, respectively. Elemental mapping confirms chemical homogeneity of prepared samples. It is observed that with Cr doping the crystallographic strain increases and Urbach energy shows the similar scaling. (orig.)

  18. Near-UV and blue wavelength excitable Mg{sub 0.6}Ca{sub 2.16}Mo{sub 0.2}W{sub 0.8}O{sub 6}: Eu{sub 0.12}{sup 3+}/Na{sub 0.12}{sup +} high efficiency red phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Khanna, A. [Smart Lighting Engineering Research Center, Rensselaer Polytechnic Institute, Troy, NY 12180 (United States); Electrical Computer and Systems Engineering, Rensselaer Polytechnic Institute, Troy, NY 12180 (United States); Dutta, P.S., E-mail: duttap@rpi.edu [Smart Lighting Engineering Research Center, Rensselaer Polytechnic Institute, Troy, NY 12180 (United States); Electrical Computer and Systems Engineering, Rensselaer Polytechnic Institute, Troy, NY 12180 (United States)

    2015-05-15

    Red phosphors with narrow emission around 615 nm (with FWHM~5–10 nm) having chemical compositions of A{sub 0.6}Ca{sub 2.16}Mo{sub 0.2}W{sub 0.8}O{sub 6}: Eu{sub 0.12}{sup 3+}/Na{sub 0.12}{sup +} (A=Mg, Sr) have been found to exhibit the highest luminescence amongst the molybdate–tungstate family when excited by sources in the 380–420 nm wavelength range. Thus they are most suitable for enhancing color rendering index and lowering color temperature in phosphor converted white LEDs (pc-WLEDs) with near-UV/blue LED excitation sources. The excitation band edge in the near UV/blue wavelength in the reported phosphor has been attributed to the coordination environment of the transition metal ion (Mo{sup 6+}, W{sup 6+}) and host crystal structure. Furthermore the quantum efficiency of the phosphors has been enhanced by adjusting activator concentration, suitable compositional alloying using substitutional alkaline earth metal cations and charge compensation mechanisms. - Graphical abstract: The charge transfer excitation of orthorhombic Mg{sub 0.6}Ca{sub 2.16}Mo{sub 0.2}W{sub 0.8}O{sub 6}: Eu{sub 0.12}{sup 3+}/Na{sub 0.12}{sup +} is significantly higher than tetragonal CaMoO{sub 4}: Eu{sup 3+} phosphors making Mg{sub 0.6}Ca{sub 2.16}Mo{sub 0.2}W{sub 0.8}O{sub 6}: Eu{sub 0.12}{sup 3+}/Na{sub 0.12}{sup +} prime candidates for fabrication of warm white phosphor-converted LEDs. - Highlights: • LED excitable Mg{sub 0.6}Ca{sub 2.16}Mo{sub 0.2}W{sub 0.8}O{sub 6}: Eu{sub 0.12}{sup 3+}/Na{sub 0.12}{sup +} phosphors were synthesized. • These phosphors are 10 times more intense than CaMoO{sub 4}: Eu{sup 3+} red phosphors. • Their intensity and efficiency were enhanced by materials optimization techniques. • Such techniques include compositional alloying, charge compensation, etc.

  19. Optical properties of WO{sub 3} thin films using surface plasmon resonance technique

    Energy Technology Data Exchange (ETDEWEB)

    Paliwal, Ayushi; Sharma, Anjali; Gupta, Vinay, E-mail: drguptavinay@gmail.com, E-mail: vgupta@physics.du.ac.in [Department of Physics and Astrophysics, University of Delhi, Delhi 110007 (India); Tomar, Monika [Department of Physics, Miranda House, University of Delhi, Delhi 110007 (India)

    2014-01-28

    Indigenously assembled surface plasmon resonance (SPR) technique has been exploited to study the thickness dependent dielectric properties of WO{sub 3} thin films. WO{sub 3} thin films (80 nm to 200 nm) have been deposited onto gold (Au) coated glass prism by sputtering technique. The structural, optical properties and surface morphology of the deposited WO{sub 3} thin films were studied using X-ray diffraction, UV-visible spectrophotometer, Raman spectroscopy, and Scanning electron microscopy (SEM). XRD analysis shows that all the deposited WO{sub 3} thin films are exhibiting preferred (020) orientation and Raman data indicates that the films possess single phase monoclinic structure. SEM images reveal the variation in grain size with increase in thickness. The SPR reflectance curves of the WO{sub 3}/Au/prism structure were utilized to estimate the dielectric properties of WO{sub 3} thin films at optical frequency (λ = 633 nm). As the thickness of WO{sub 3} thin film increases from 80 nm to 200 nm, the dielectric constant is seen to be decreasing from 5.76 to 3.42, while the dielectric loss reduces from 0.098 to 0.01. The estimated value of refractive index of WO{sub 3} film is in agreement to that obtained from UV-visible spectroscopy studies. The strong dispersion in refractive index is observed with wavelength of incident laser light.

  20. Sub 20nm particle inspection on EUV mask blanks

    NARCIS (Netherlands)

    Bussink, P.G.W.; Volatier, J.B.; Walle, P. van der; Fritz, E.C.; Donck, J.C.J. van der

    2016-01-01

    The Rapid Nano is a particle inspection system developed by TNO for the qualification of EUV reticle handling equipment. The detection principle of this system is dark-field microscopy. The performance of the system has been improved via model-based design. Through our model of the scattering

  1. Dual mode NIR long persistent phosphorescence and NIR-to-NIR Stokes luminescence in La{sub 3}Ga{sub 5}GeO{sub 14}: Cr{sup 3+}, Nd{sup 3+} phosphor

    Energy Technology Data Exchange (ETDEWEB)

    Wu, Yiling; Li, Yang, E-mail: msliyang@scut.edu.cn; Qin, Xixi; Chen, Ruchun; Wu, Dakun; Liu, Shijian; Qiu, Jianrong, E-mail: qjr@scut.edu.cn

    2015-11-15

    Recently, long persistent phosphors (LPPs) have been considered to be the most prominent candidates for biomedical applications. However, the LPPs suffer from a dramatic decrease in luminescence intensity after incorporation into the tissue. Therefore, it is very necessary to develop the more competitive LPPs and acquire the reproducible tissue imaging. Here, we propose and experimentally demonstrate an effective bifunctional La{sub 3}Ga{sub 5}GeO{sub 14}: Cr{sup 3+}, Nd{sup 3+} phosphor with the interesting characteristic of near-infrared long persistent phosphorescence and NIR-to-NIR Stokes luminescence. Cr{sup 3+} and Nd{sup 3+} ions are simultaneously selected as the emission centers in order to take advantage of the remarkable phosphorescence properties of Cr{sup 3+}, and the appropriate energy level characteristic of NIR-excitation band (808 nm) and NIR-emission (1064 nm), and the ability as the brilliant auxiliary to create more efficient defects of Nd{sup 3+}. The efficient dual-modal emission is, accordingly utilized to realize the convenient, high-resolution global detection and local imaging. - Highlights: • Dual mode phosphor with NIR long afterglow and NIR-to-NIR Stokes luminescence. • Increasing the persistent duration due to the codoping of Nd. • Avoiding the noteworthy overheating effect due to the strong absorption at 980 nm.

  2. Scintillation properties of (C sub 6 H sub 1 sub 3 NH sub 3) sub 2 PbI sub 4 Exciton luminescence of an organic/inorganic multiple quantum well structure compound induced by 2.0 MeV protons

    CERN Document Server

    Shibuya, K; Takeoka, Y; Asai, K

    2002-01-01

    We report a new type of scintillator especially suitable for pulse-radiation detection. Thin films of organic/inorganic perovskite compound (n-C sub 6 H sub 1 sub 3 NH sub 3) sub 2 PbI sub 4 , which is characterized by a multiple quantum well structure, were bombarded by 2.0 MeV protons, and their radiation-induced emission spectra were obtained. A single and sharp emission peak due to an exciton was observed at the wavelength of 524 nm. This emission was clearly detected even at room temperature, and its quantum efficiency was very high. The line shape of this emission did not change, retaining its sharpness, and no other emissions appeared throughout the irradiation. The optical response of (n-C sub 6 H sub 1 sub 3 NH sub 3) sub 2 PbI sub 4 is very fast. (n-C sub 6 H sub 1 sub 3 NH sub 3) sub 2 PbI sub 4 is a promising scintillator material, meeting requirements not satisfied by conventional scintillators.

  3. Mechanochemical and combustion synthesis of CeB{sub 6}

    Energy Technology Data Exchange (ETDEWEB)

    Akguen, Baris [Roketsan Missiles Inc., Ankara (Turkey); Sevinc, Naci; Topkaya, Yavuz [Middle East Technical Univ., Ankara (Turkey). Dept. of Metallurgical and Materials Engineerung; Camurlu, H. Erdem [Akdeniz Univ., Antalya (Turkey). Dept. of Mechanical Engineering

    2013-04-15

    CeB{sub 6} powder was prepared via combustion synthesis (CS) and mechanochemical processing (MCP) methods starting from CeO{sub 2}, B{sub 2}O{sub 3} and Mg powder mixtures. In CS, reactant mixtures were ignited in a preheated pot furnace under argon atmosphere. Products contained CeB{sub 6}, MgO and Mg{sub 3}B{sub 2}O{sub 6}, as revealed by X-ray diffraction analysis. After leaching in 1 M HCl for 15h, MgO was removed but Mg{sub 3}B{sub 2}O{sub 6} could not be removed from the products. Ball milling of products in ethanol prior to leaching made the removal of Mg{sub 3}B{sub 2}O{sub 6} possible by leaching. Yield of CeB{sub 6} was 68.6% in CS. MCP was performed in a stainless steel vial with a planetary ball mill at 300 rpm for 30h. MCP products contained CeB{sub 6}, MgO and small amount of Fe. Leaching in 1 M HCl for 30min was sufficient to remove MgO. Yield of CeB{sub 6} was 84.4% in MCP. According to scanning electron microscopy examinations, particles of CeB6 prepared by CS and MCP had submicrometer size. Average particle sizes were determined as 290nm and 240nm, respectively.

  4. Properties of Er{sub 2}O{sub 3} nanoparticles synthesized by a modified co-precipitation method

    Energy Technology Data Exchange (ETDEWEB)

    Castaneda C, J.; Maranon R, V. F.; Perez Ladron de G, H.; Rodriguez R, R. A.; Chiu Z, R. [Universidad de Guadalajara, Centro Universitario de los Lagos, Av. Enrique Diaz de Leon s/n, Lagos de Moreno 47460, Jalisco (Mexico); Meneses N, M. A., E-mail: jcc050769@yahoo.com.mx [Centro de Investigaciones en Optica, A. C., Apdo. Postal 1-948, Leon, Guanajuato (Mexico)

    2015-07-01

    Er{sub 2}O{sub 3} nanoparticles were synthesized by co-precipitation with the addition of ascorbate as stabilizing agent. The nanoparticles had spherical shapes with a mean diameter of 32 nm and were allocated in clusters, as determined by X-ray diffraction, atomic force microscopy and optical microscopy. Characteristic green and red emissions from Er{sup 3+} were recorded by pumping the nanoparticles at 525 nm, 805 nm and 975 nm. However, the luminescence spectra show an enhancement of red emission for Nir pump wavelengths. We proposed this behavior was due to phonon-assisted depopulation mechanisms and energy transfer processes related to the different excitation schemes. (Author)

  5. Noticeable red emission and Raman active modes in nanoscale gadolinium oxyfluoride (Gd{sub 4}O{sub 3}F{sub 6}) systems with Eu{sup 3+} inclusion

    Energy Technology Data Exchange (ETDEWEB)

    Hazarika, Samiran; Mohanta, Dambarudhar [Tezpur University, Nanoscience and Soft Matter Laboratory, Department of Physics, Tezpur, Assam (India)

    2017-05-15

    Eu{sup 3+} doped gadolinium oxyfluoride (Gd{sub 4}O{sub 3}F{sub 6}, GOF) nanoscale systems have been synthesized following a modified Pechini method. While exhibiting a tetragonal crystal structure, the GOF nanosystem gave an average crystallite size (d) of ∝21-26 nm. The Lotgering factor (L{sub F}), which is a measure of orientation of crystallites along the preferred direction was found to vary between 0.22 and 0.48. In the photoluminescence spectra, ∝595 and ∝613 nm peaks were identified as magnetically driven ({sup 5}D{sub 0} → {sup 7}F{sub 1}) and electrically driven ({sup 5}D{sub 0} → {sup 7}F{sub 2}) transitions with latter (red emission) being strongly manifested with Eu{sup 3+} doping concentration and intrinsic defects. Moreover, several Raman active modes have been probed in the Raman spectra with low frequency peaks (<300 cm{sup -1}) and moderate frequency peaks (∝481 and 567 cm{sup -1}) assigned to observable vibration of heavy atom Gd-Gd pairs and Gd-O groups, respectively. Apart from manifestation of phononic features, inclusion of Eu{sup 3+} in the host lattice would bring new insight on improving the red emission response prior to concentration quenching. (orig.)

  6. Synthesis and photoluminescence properties of Ba{sub 2}CaZn{sub 2}Si{sub 6}O{sub 17}:Eu{sup 3+} red phosphors for white LED applications

    Energy Technology Data Exchange (ETDEWEB)

    Annadurai, G.; Kennedy, S. Masilla Moses, E-mail: kennedysmm@ssn.edu.in

    2016-01-15

    Novel pellyite type Ba{sub 2}CaZn{sub 2}Si{sub 6}O{sub 17}:Eu{sup 3+} red emitting phosphors with different Eu{sup 3+} contents were synthesized by the solid state reaction method. The crystal structure, photoluminescence properties and concentration quenching of Ba{sub 2}CaZn{sub 2}Si{sub 6}O{sub 17}:Eu{sup 3+} phosphors were investigated. Powder X-ray diffraction measurements confirmed the structure of the samples. The photoluminescence emission (PL) and excitation (PLE) spectra were measured. The results showed that the dominant hypersensitive red emission peak of the phosphors Ba{sub 2}CaZn{sub 2}Si{sub 6}O{sub 17}:Eu{sup 3+} was located at 613 nm attributed to the Eu{sup 3+} transition ({sup 5}D{sub 0}→{sup 7}F{sub 2}) which could be effectively excited by 395 nm (near-UV). The latter band matched well with the emission from the near-UV LED chips. The intensity ratio of {sup 5}D{sub 0}→{sup 7}F{sub 2} to {sup 5}D{sub 0}→{sup 7}F{sub 1} transition showed slight variation with Eu{sup 3+} concentrations. The Eu{sup 3+} emission intensity was maximum for 9 mol%. The luminescence quantum efficiency was determined and also the decay profiles were obtained and analyzed. In addition, the Commission International del'Eclairage (CIE) chromaticity coordinates of Ba{sub 2}CaZn{sub 2}Si{sub 6}O{sub 17}:0.09Eu{sup 3+} phosphor were calculated to be 0.637 and 0.362. The experimental results demonstrated that the Ba{sub 2}CaZn{sub 2}Si{sub 6}O{sub 17}:Eu{sup 3+} red emitting phosphor is a potential candidate for white light emitting diodes (WLEDs) pumped by near-UV chip. - Highlights: • A novel Ba{sub 2}CaZn{sub 2}Si{sub 6}O{sub 17}:Eu{sup 3+} red phosphor was synthesized. • The samples yielded a dominant PL emission of Eu{sup 3+} at 613 nm. • Eu{sup 3+} concentration was optimized to be 9 mol% in Ba{sub 2}CaZn{sub 2}Si{sub 6}O{sub 17.} • CIE chromaticity coordinates were estimated from the emission spectrum.

  7. Color-tunable and luminescence properties of phosphors of Ce{sup 3+} and Tb{sup 3+} co-doped La{sub 5}Si{sub 3}O{sub 12}N for UV w-LEDs

    Energy Technology Data Exchange (ETDEWEB)

    Deng, Junru; Chen, Jian; Liu, Yangai, E-mail: liuyang@cugb.edu.cn

    2016-02-15

    A series of Ce{sup 3+}, Tb{sup 3+} and Ce{sup 3+}/Tb{sup 3+} co-doped in La{sub 5}Si{sub 3}O{sub 12}N phosphors were synthesized by conventional high temperature solid state reaction method. With the increase of Tb{sup 3+}, the green emission was realized in (La{sub 0.94−y}Ce{sub 0.06}Tb{sub y}){sub 5}Si{sub 3}O{sub 12}N phosphors on the basis of the efficient energy transfer from Ce{sup 3+} to Tb{sup 3+} with an efficiency (η{sub T}) over 58.72%. The room temperature PL decay curves of the Ce{sup 3+} ions in (La{sub 0.94−y}Ce{sub 0.06}Tb{sub y}){sub 5}Si{sub 3}O{sub 12}N phosphors monitored at 460 nm with an excitation at 365 nm indicated that the energy transfer process between Ce{sup 3+} and Tb{sup 3+} indeed took place. The CIE chromaticity diagrams for (La{sub 0.94−y}Ce{sub 0.06}Tb{sub y}){sub 5}Si{sub 3}O{sub 12}N phosphors were also observed, which shows the color tuned from blue to blue-greenish to green with the increase of Tb{sup 3+} concentration from 0.01 to 0.08. These results demonstrated that Tb{sup 3+} ion with low 4f–4f absorption efficiency in near UV region can play the role of an activator in narrow green-emitting phosphor through efficient energy feeding by allowing 4f–5d absorption of Ce{sup 3+} with high oscillator strength. All the results indicated that the Ce{sup 3+} and Tb{sup 3+} activated La{sub 5}Si{sub 3}O{sub 12}N phosphor may be good candidates for blue-green components in n-UV white LEDs. - Highlights: • A series of Ce{sup 3+}, Tb{sup 3+} and Ce{sup 3+}/Tb{sup 3+} co-doped in La{sub 5}Si{sub 3}O{sub 12}N phosphors were synthesized by high temperature solid state reaction method. • The green emission was realized in (La{sub 0.94−y}Ce{sub 0.06}Tb{sub y})Si{sub 3}O{sub 12}N phosphors on the basis of the highly efficient energy transfer. • The Ce{sup 3+} and Tb{sup 3+} activated La{sub 5}Si{sub 3}O{sub 12}N phosphor may be good candidates for blue-green components in n-UV white LEDs.

  8. Surface and spectral studies of green emitting Sr{sub 3}B{sub 2}O{sub 6}:Tb{sup 3+} phosphor

    Energy Technology Data Exchange (ETDEWEB)

    Neharika [School of Physics, Shri Mata Vaishno Devi University, Katra 182320, J& K (India); Kumar, Vinay, E-mail: vinaykumar@smvdu.ac.in [School of Physics, Shri Mata Vaishno Devi University, Katra 182320, J& K (India); Sharma, J.; Singh, Vivek K. [School of Physics, Shri Mata Vaishno Devi University, Katra 182320, J& K (India); Ntwaeaborwa, O.M.; Swart, H.C. [Department of Physics, University of the Free State, PO Box 339, Bloemfontein ZA9300 (South Africa)

    2016-01-15

    Highlights: • XPS technique has been used to study the surface composition of the phosphor. • The phosphor is synthesized by combustion method using urea as fuel. • Multipole–multipole interaction was found to play a key role for concentration quenching of Tb{sup 3+} doped Sr{sub 3}B{sub 2}O{sub 6} phosphor. - Abstract: In this paper, we report the synthesis of trivalent Tb{sup 3+} doped Sr{sub 3}B{sub 2}O{sub 6} phosphor by combustion method using urea as an organic fuel. The structure of the product has been verified by X-ray diffraction study which shows a rhombohedral phase with a space group of R-3c having lattice constants a = 9.064 Å, b = 9.064 Å, c = 12.611 Å. X-ray photoelectron spectroscopy has been used to study the elemental composition and electronic states of the Tb{sup 3+} doped Sr{sub 3}B{sub 2}O{sub 6} phosphor. Photoluminescence spectra showed that the phosphor emits in the greenish region (with the main peak at 544 nm) of color gamut under UV excitation. The diffuse reflectance spectra of the Sr{sub 3}B{sub 2}O{sub 6} phosphor were studied. Lifetime and band gap of the phosphors were calculated to be 2.55 ms and 5.25 ± 0.02 eV, respectively.

  9. Synthesis and photoluminescence properties of Eu{sup 3+}, Sm{sup 3+} and Pr{sup 3+} doped Ca{sub 2}ZnWO{sub 6} phosphors for phosphor converted LED

    Energy Technology Data Exchange (ETDEWEB)

    Dabre, K.V. [Department of Physics, Arts, Commerce and Science College, Koradi, Nagpur-441111, Maharashtra (India); Dhoble, S.J., E-mail: sjdhoble@rediffmail.com [Department of Physics, R.T.M. Nagpur University, Nagpur-440033, Maharashtra (India)

    2014-06-01

    In this work, we report on the synthesis and photoluminescence (PL) properties of rare earth (Eu{sup 3+}, Sm{sup 3+} and Pr{sup 3+}) doped double perovskite tungstate Ca{sub 2}ZnWO{sub 6} phosphor. The phosphors were synthesized by two step modified solid state method. Phase purity and formation of phosphor were confirmed by XRD technique. PL spectra of Eu{sup 3+}, Sm{sup 3+} and Pr{sup 3+} doped phosphor show intense emission peaks in red region at 615, 604 and 650 nm respectively, upon the visible excitation of 466 nm (Eu{sup 3+}), 410 nm (Sm{sup 3+}) and 491 nm (Pr{sup 3+}). The CIE coordinates of the phosphors are in the yellow (Sm{sup 3+} doped sample) and orange (Eu{sup 3+} and Pr{sup 3+} doped sample) regions near the edge of color space which confirms their applicability in LEDs. -- Highlights: •Eu{sup 3+}, Sm{sup 3+} and Pr{sup 3+} doped and undoped samples of Ca{sub 2}ZnWO{sub 6} phosphor synthesized by Solid state method. •The phosphors have intense excitation in violet and blue region of visible spectrum. •Phosphors show intense emission peaks in red region. •CIE coordinates of phosphors are lie in yellow (Sm{sup 3+} doped phosphor) and orange (Eu{sup 3+} and Pr{sup 3+} doped phosphor) region near to edge of color space.

  10. The synthesis and luminescence properties of a novel red-emitting phosphor. Eu{sup 3+}-doped Ca{sub 9}La(PO{sub 4}){sub 7}

    Energy Technology Data Exchange (ETDEWEB)

    Liang, Zehui [Guangdong University of Technology, Experimental Teaching Department, Guangzhou (China); Guangdong University of Technology, School of Chemical Engineering and Light Industry, Guangzhou (China); Mu, Zhongfei; Zhu, Daoyun [Guangdong University of Technology, Experimental Teaching Department, Guangzhou (China); Wang, Qiang; Wu, Fugen [Guangdong University of Technology, School of Materials and Energy, Guangzhou (China)

    2017-10-15

    A series of novel red-emitting phosphors Ca{sub 9}La{sub 1-x}(PO{sub 4}){sub 7}: xEu{sup 3+} were synthesized by high-temperature solid state reactions. The photoluminescence excitation and photoluminescence spectra of these phosphors were investigated in detail. O{sup 2-}-Eu{sup 3+} charge transfer band peaking at about 261 nm is dominant in the PLE spectra of Eu{sup 3+}-doped Ca{sub 9}La(PO{sub 4}){sub 7}, indicating that the phosphors are suitable for tricolor fluorescent lamps. The phosphors also show a good absorption in near ultraviolet (around 395 nm) and blue (around 465 nm) spectral region, which indicates that it can be pumped with NUV and blue chips for white light-emitting diodes. The transition of {sup 5}D{sub 0} → {sup 7}F{sub 2} of Eu{sup 3+} in this lattice can emit bright red light. Ca{sub 9}La(PO{sub 4}){sub 7} could accommodate a large amount of Eu{sup 3+} with an optimal concentration of 60 mol%. The dipole-dipole interaction between Eu{sup 3+} is the dominant mechanism for concentration quenching of Eu{sup 3+}. The calculated color coordinates lie in red region (x = 0.64, y = 0.36), which is close to Y{sub 2}O{sub 3}: 0.05Eu{sup 3+} (x = 0.65, y = 0.34). The integral emission intensity of Ca{sub 9}La{sub 0.4}(PO{sub 4}){sub 7}: 0.6Eu{sup 3+} is 1.9 times stronger than that of widely used commercial red phosphor Y{sub 2}O{sub 3}: 0.05Eu{sup 3+}. All these results indicate that Eu{sup 3+}-doped Ca{sub 9}La(PO{sub 4}){sub 7} is a promising red-emitting phosphor which can be used in tricolor fluorescent lamps and white light-emitting diodes. (orig.)

  11. Growth behavior of LiMn{sub 2}O{sub 4} particles formed by solid-state reactions in air and water vapor

    Energy Technology Data Exchange (ETDEWEB)

    Kozawa, Takahiro, E-mail: t-kozawa@jwri.osaka-u.ac.jp [Joining and Welding Research Institute, Osaka University, 11–1 Mihogaoka, Ibaraki, Osaka 567-0047 (Japan); Yanagisawa, Kazumichi [Research Laboratory of Hydrothermal Chemistry, Faculty of Science, Kochi University, 2–5-1 Akebono-cho, Kochi 780-8520 (Japan); Murakami, Takeshi; Naito, Makio [Joining and Welding Research Institute, Osaka University, 11–1 Mihogaoka, Ibaraki, Osaka 567-0047 (Japan)

    2016-11-15

    Morphology control of particles formed during conventional solid-state reactions without any additives is a challenging task. Here, we propose a new strategy to control the morphology of LiMn{sub 2}O{sub 4} particles based on water vapor-induced growth of particles during solid-state reactions. We have investigated the synthesis and microstructural evolution of LiMn{sub 2}O{sub 4} particles in air and water vapor atmospheres as model reactions; LiMn{sub 2}O{sub 4} is used as a low-cost cathode material for lithium-ion batteries. By using spherical MnCO{sub 3} precursor impregnated with LiOH, LiMn{sub 2}O{sub 4} spheres with a hollow structure were obtained in air, while angulated particles with micrometer sizes were formed in water vapor. The pore structure of the particles synthesized in water vapor was found to be affected at temperatures below 700 °C. We also show that the solid-state reaction in water vapor is a simple and valuable method for the large-scale production of particles, where the shape, size, and microstructure can be controlled. - Graphical abstract: This study has demonstrated a new strategy towards achieving morphology control without the use of additives during conventional solid-state reactions by exploiting water vapor-induced particle growth. - Highlights: • A new strategy to control the morphology of LiMn{sub 2}O{sub 4} particles is proposed. • Water vapor-induced particle growth is exploited in solid-state reactions. • The microstructural evolution of LiMn{sub 2}O{sub 4} particles is investigated. • The shape, size and microstructure can be controlled by solid-state reactions.

  12. Measurements of the London penetration depths in YBa sub 2 Cu sub 3 O sub x by means of muon spin rotation (. mu. SR) experiments

    Energy Technology Data Exchange (ETDEWEB)

    Puempin, B.; Keller, H.; Kuendig, W.; Odermatt, W.; Savic, I.M.; Schneider, J.W.; Simmler, H.; Zimmermann, P. (Physik-Inst., Univ. Zuerich (Switzerland)); Bednorz, J.G.; Maeno, Y.; Mueller, K.A.; Rossel, C. (IBM Research Div., Zuerich Research Lab., Rueschlikon (Switzerland)); Kaldis, E.; Rusiecki, S. (Lab. fuer Festkoerperphysik, ETH Zuerich (Switzerland)); Assmus, W.; Kowalewski, J. (Physikalisches Inst., Univ. Frankfurt (Germany, F.R.))

    1989-12-01

    To get accurate values of the London penetration depths in YBa{sub 2}Cu{sub 3}O{sub x}, {mu}SR measurements were performed on a high quality, sintered sample and a c-axis-oriented polycrystal. For the sintered sample the temperature dependence of the effective penetration depth {lambda}{sub eff} is well described by the two-fluid model, with {lambda}{sub eff}(0) = 155(10) nm. This behavior of {lambda}{sub eff}(T) is consistent with conventional s-wave pairing. The anisotropy ratio {lambda}{sub c}/{lambda}{sub ab} {approx equal} 5(1) was determined from measurements on the polycrystal. These results were used to calculate {lambda}{sub ab}(0) = 130(10) nm and {lambda}{sub c}(0) {approx equal} 500-800 nm. (orig.).

  13. Controlled synthesis and photoluminescence properties of In{sub 2}O{sub 3} rods with dodecahedron In{sub 2}O{sub 3} microcrystals on top

    Energy Technology Data Exchange (ETDEWEB)

    Ouacha, Hassan [King Abdullah Institute for Nanotechnology, King Saud University, Riyadh (Saudi Arabia); Hendaoui, Ali [Department of Physics, College of Science and General Studies, Alfaisal University, Riyadh (Saudi Arabia); Kleineberg, Ulf [Faculty of Physics, Ludwig Maximilian University of Munich, Garching (Germany); Albrithen, Hamad; Azzeer, Abdallah [Physics and Astronomy Department, King Saud University, Riyadh (Saudi Arabia)

    2017-10-15

    In{sub 2}O{sub 3} rods with dodecahedron In{sub 2}O{sub 3} microcrystals on top were synthesized in an electrical furnace via Au-catalyzed vapor transport process. A catalyst-assisted selective vapor-solid (VS) growth was proposed to explain the formation of the dodecahedron In{sub 2}O{sub 3} microcrystal, while the self-catalytic VS growth mechanism dominated the subsequent one-dimensional (1D) growth of the In{sub 2}O{sub 3} rod underneath the In{sub 2}O{sub 3} microcrystal. The structural evolution of these structures was carefully examined during the synthesis process by controlling the growth parameters. The morphologies, crystalline structures and surface chemistry were characterized by scanning electron microscopy (SEM), X-ray diffraction technique (XRD), and X-ray photoelectron spectroscopy (XPS), respectively. The photoluminescence (PL) spectrum at room temperature of the as-grown In{sub 2}O{sub 3} structures exhibited both UV and blue luminescence emission under one excitation at 260 nm, which may be related to the existence of oxygen vacancies. The synthesized multifaceted In{sub 2}O{sub 3} microcrystal has shown to contain a large number of vertices and may find many applications in developing three-dimensional (3D) resonators. This work will not only enrich the synthesis science but also will open doors for applications of such structures in optical devices. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  14. Characterization of the yttria-stabilized zirconia thin film electrophoretic deposited on La{sub 0.8}Sr{sub 0.2}MnO{sub 3} substrate

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Koho [Department of Mold and Die Engineering, National Kaohsiung University of Applied Sciences, 415 Chien-Kung Rode, Kaohsiung 80782, Taiwan (China); Shen, Jung-Hsiung [Department of Mold and Die Engineering, National Kaohsiung University of Applied Sciences, 415 Chien-Kung Rode, Kaohsiung 80782, Taiwan (China); Yang, Kai-Yun [Department of Materials Science and Engineering, National Chen Kung University, 1 Ta-Hsueh Road, Tainan 70101, Taiwan (China); Hung, I-Ming [Department of Materials Science and Engineering, National Chen Kung University, 1 Ta-Hsueh Road, Tainan 70101, Taiwan (China); Department of Chemical Engineering and Materials Science, Yuan Ze University, 135 Yuan-Tung Road, Chungli, Taoyunn 320, Taiwan (China); Fung, Kuan-Zong [Department of Materials Science and Engineering, National Chen Kung University, 1 Ta-Hsueh Road, Tainan 70101, Taiwan (China); Wang, Moo-Chin [Faculty of Fragrance and Cosmetics, Kaohsiung Medical University, 100 Shi-Chuan 1st Road, Kaohsiung 807, Taiwan (China)]. E-mail: mcwang@kmu.edu.tw

    2007-06-14

    The yttria-stabilized zirconia (YSZ) thin films electrophoretic deposited on the La{sub 0.8}Sr{sub 0.2}MnO{sub 3} (LSM) substrate have been characterized by using zeta potential analysis, X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The La{sub 2}Zr{sub 2}O{sub 7} (LZ) formed at the interface between the YSZ thin film and LSM substrate, after sintered at 1400 {sup o}C for 52 h, are identified by XRD. The zeta potential of the YSZ particles in pure ethanol-acetone is about 7.8 mV, but when the I{sub 2} concentration is greater than 0.6 g/1, the zeta potential attains a constant value, 46 mV. The relation between deposit weight of the YSZ films and the applied voltage shows a non-linear behavior. Thickness of the YSZ thin film deposited on the LSM substrate by electrophoretic deposition is controlled by a diffusion process. A larger LZ with the thickness of 200 nm is formed at the interface between the YSZ film and the LSM substrate.

  15. Effect of nano-TiO{sub 2} particles size on the corrosion resistance of alkyd coating

    Energy Technology Data Exchange (ETDEWEB)

    Deyab, M.A., E-mail: hamadadeiab@yahoo.com; Keera, S.T.

    2014-08-01

    The coating system containing various sizes (∼10, 50, 100, 150 nm) of nano-TiO{sub 2} were prepared and investigated for corrosion protection of carbon steel in 1.0 M H{sub 2}SO{sub 4} using polarization, EIS and transmission electron microscopy (TEM) techniques. It was found that nano-TiO{sub 2} particles improved the corrosion resistance of alkyd coatings. The corrosion resistance occurs via physical adhesion on the metal surface. O{sub 2} and H{sub 2}O permeability of coating decreased with decrease in the nano-TiO{sub 2} size. The inhibition efficiency was found to increase with decreasing the size of nano-TiO{sub 2} and with decreasing the temperature. - Highlights: • Nano-TiO{sub 2} coating were prepared and used for corrosion protection of C-steel. • Nano-TiO{sub 2} particles in coating are effective to improve the corrosion resistance. • Nano-TiO{sub 2} coating inhibit both anodic and cathodic reactions. • Corrosion inhibition efficiency increases with decrease in the size of nano-TiO{sub 2}. • O{sub 2} and H{sub 2}O permeability of coating decreased with decrease in the nano-TiO{sub 2} size.

  16. Synthesis and luminescent properties of Eu{sup 3+}-activated Na{sub 0.5}Gd{sub 0.5}MoO{sub 4}: A strong red-emitting phosphor for LED and FED applications

    Energy Technology Data Exchange (ETDEWEB)

    Du, Peng; Yu, Jae Su, E-mail: jsyu@khu.ac.kr

    2016-11-15

    A series of Eu{sup 3+}-activated Na{sub 0.5}Gd{sub 0.5}MoO{sub 4} phosphors were prepared by a typical sol–gel method. The as-prepared samples possessed a single tetragonal phase and consisted of closely-packed particles. Under the excitation of 395 nm, all the phosphors exhibited the characteristic emissions of Eu{sup 3+} ions corresponding to the {sup 5}D{sub 0}→ {sup 7}F{sub J} transitions. The photoluminescence (PL) emission intensities were enhanced with the increment of Eu{sup 3+} ion concentration and the optimum doping concentration was 0.25 mol. The energy transfer mechanism between the Eu{sup 3+} ions was dominated by dipole–dipole interaction and the critical distance was found to be 8.45 Å. Furthermore, the temperature-dependent PL emission spectra suggested that the obtained phosphors had good thermal stability (60.4% of the initial intensity at 150 °C). In addition, the color purity, chromatic and cathodoluminescence (CL) properties of the Na{sub 0.5}Gd{sub 0.5}MoO{sub 4}:0.25Eu{sup 3+} phosphor were also investigated. The results indicated that the Eu{sup 3+}-activated Na{sub 0.5}Gd{sub 0.5}MoO{sub 4} phosphors with excellent PL and CL properties may have potential applications in white light-emitting diodes and field-emission displays.

  17. Synthesis of the lithium metatitanate, Li{sub 2}TiO{sub 3}, by the modified combustion method; Sintesis del metatitanato de litio, Li{sub 2}TiO{sub 3}, por el metodo modificado de combustion

    Energy Technology Data Exchange (ETDEWEB)

    Cruz, D.; Bulbulian, S. [ININ, 52045 Ocoyoacac, Estado de Mexico (Mexico); Pfeiffer, H. [IIM-UNAM, A.P. 70-360, 04510 Mexico D.F. (Mexico)]. e-mail: sb@nuclear.inin.mx

    2005-07-01

    A modified combustion method to obtain Li{sub 2}TiO{sub 3} it was used, a compound to be used in fusion reactors like tritium generator material. To obtain Li{sub 2}TiO{sub 3} were proven different molar ratios of lithium hydroxide (LiOH), titanium oxide (TiO{sub 2}) and urea (CO(NH{sub 2}){sub 2}), as well as different heating temperatures (550, 650 and 750 C). The characterization of the products it was carried out using X-ray diffraction, Scanning electron microscopy and Thermal gravimetric analysis. The sample prepared with a molar ratio Li: Ti: urea = 2.75: 1: 3 was the one that presented as only product the Li{sub 2}TiO{sub 3}. The particle size and the morphology found in the Li{sub 2}TiO{sub 3}, showed similar particle size and morphology to the TiO{sub 2} used as precursor. (Author)

  18. In situ trace gas and particle measurements in the summer lower stratosphere during STREAM II. Implications for O{sub 3} production

    Energy Technology Data Exchange (ETDEWEB)

    Bregman, A; Lelieveld, J; Scheeren, H A [Institute for Marine and Atmospheric Sciences, Utrecht (Netherlands); Arnold, F; Buerger, V; Schneider, J [Max-Planck-Inst. for Nuclear Physics, Heidelberg (Germany); Fischer, H; Waibel, A [Max-Planck-Inst. fuer Chemie, Mainz (Germany); Siegmund, P C; Wauben, W M.F. [Koninklijk Nederlands Meteorologisch Inst., De Bilt (Netherlands); Stroem, J [Stockholm Univ. (Sweden). Dept. of Meteorology

    1998-12-31

    In situ aircraft measurements of O{sub 3}, CO, HNO{sub 3}, and aerosol particles are presented, performed over the North Sea region in the summer lower stratosphere during the STREAM-II campaign (Stratosphere Troposphere Experiments by Aircraft Measurements). Elevated CO mixing ratios are attributed to mixing of polluted tropospheric air into the lowermost extra-tropical stratosphere. Model calculations illustrate that the O{sub 3} production efficiency of NO{sub x} is smaller than previously assumed, under conditions with relatively high HNO{sub 3} mixing ratios, as observed during STREAM-II. The model simulations further suggest a relatively high O{sub 3} production efficiency from CO oxidation, as a result of the relatively high ambient HNO{sub 3} and NO{sub x} concentrations, implying that upward transport of CO rich air enhances O{sub 3} production in the lowermost stratosphere. (author) 13 refs.

  19. In situ trace gas and particle measurements in the summer lower stratosphere during STREAM II. Implications for O{sub 3} production

    Energy Technology Data Exchange (ETDEWEB)

    Bregman, A.; Lelieveld, J.; Scheeren, H.A. [Institute for Marine and Atmospheric Sciences, Utrecht (Netherlands); Arnold, F.; Buerger, V.; Schneider, J. [Max-Planck-Inst. for Nuclear Physics, Heidelberg (Germany); Fischer, H.; Waibel, A. [Max-Planck-Inst. fuer Chemie, Mainz (Germany); Siegmund, P.C.; Wauben, W.M.F. [Koninklijk Nederlands Meteorologisch Inst., De Bilt (Netherlands); Stroem, J. [Stockholm Univ. (Sweden). Dept. of Meteorology

    1997-12-31

    In situ aircraft measurements of O{sub 3}, CO, HNO{sub 3}, and aerosol particles are presented, performed over the North Sea region in the summer lower stratosphere during the STREAM-II campaign (Stratosphere Troposphere Experiments by Aircraft Measurements). Elevated CO mixing ratios are attributed to mixing of polluted tropospheric air into the lowermost extra-tropical stratosphere. Model calculations illustrate that the O{sub 3} production efficiency of NO{sub x} is smaller than previously assumed, under conditions with relatively high HNO{sub 3} mixing ratios, as observed during STREAM-II. The model simulations further suggest a relatively high O{sub 3} production efficiency from CO oxidation, as a result of the relatively high ambient HNO{sub 3} and NO{sub x} concentrations, implying that upward transport of CO rich air enhances O{sub 3} production in the lowermost stratosphere. (author) 13 refs.

  20. Megasonic cleaning strategy for sub-10nm photomasks

    Science.gov (United States)

    Hsu, Jyh-Wei; Samayoa, Martin; Dress, Peter; Dietze, Uwe; Ma, Ai-Jay; Lin, Chia-Shih; Lai, Rick; Chang, Peter; Tuo, Laurent

    2016-10-01

    One of the main challenges in photomask cleaning is balancing particle removal efficiency (PRE) with pattern damage control. To overcome this challenge, a high frequency megasonic cleaning strategy is implemented. Apart from megasonic frequency and power, photomask surface conditioning also influences cleaning performance. With improved wettability, cleanliness is enhanced while pattern damage risk is simultaneously reduced. Therefore, a particle removal process based on higher megasonic frequencies, combined with proper surface pre-treatment, provides improved cleanliness without the unintended side effects of pattern damage, thus supporting the extension of megasonic cleaning technology into 10nm half pitch (hp) device node and beyond.