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Sample records for zn ions substitution

  1. Magnetic and optical properties of Zn{sup 2+} ion substituted barium hexaferrites

    Energy Technology Data Exchange (ETDEWEB)

    Baykal, A., E-mail: hbaykal@fatih.edu.tr [EYRA Textile Chemicals and Chemical Industry Trade Company, Saraçlar Industrial Zone, No: 3-12, 34490 İkitelli, İstanbul (Turkey); Auwal, I.A. [Department of Chemistry, Sule Lamido University, P.M.B 048, Kafin Hausa, Jigawa State (Nigeria); Güner, S. [Department of Physics, Fatih University, 34500 B.Çekmece, İstanbul (Turkey); Sözeri, H. [TÜBITAK – UME, National Metrology Institute, 41470 Gebze, Kocaeli (Turkey)

    2017-05-15

    Ba{sub 1−x}Zn{sub x}Fe{sub 12}O{sub 19} (0.0≤x≤0.3) hexaferrites were produced via sol-gel auto combustion technique. XRD patterns show that all the samples are single-phase M-type barium hexaferrite (BaM). Scanning electron microscopy (SEM) revealed that grains have a size range of 0.5–2 µm. The magnetic hysteresis (σ-H) loops revealed the ferromagnetic nature of NPs. The average crystallite sizes were calculated by applying Scherrer equation on the base of XRD powder patterns of all samples and found to be in the range of 16.78–48.34 nm. In particular, Ba{sub 1−x}Zn{sub x}Fe{sub 12}O{sub 19} (0.0≤x≤0.3) hexaferrites have suitable magnetic characteristics (saturation magnetization in a range of 63.00–67.70 emu/g and coercive field in a range of 822–1275 Oe) for magnetic recording and permanent magnets. Effective crystalline anisotropy constants (K{sub eff}) are between 4.20×10{sup 5} and 4.84×10{sup 5} Erg/g. Magnetic moment increased by the substitution of non-magnetic Zn{sup 2+} ions. The anisotropy field (H{sub a}) or intrinsic coercivity values above 13255 Oe reveals that all samples are magnetically hard materials. Tauc plots were drawn to specify the direct optical energy band gap (E{sub g}) of NPs. The E{sub g} values are in a narrow range between 1.69 eV and 1.76 eV. - Highlights: • Diamagnetic Zn{sup 2+} ionsubstitution on magnetic and optical properties of barium hexaferrite has been investigated. • All products are ferromagnetic. • The grain sizes are much larger than the critical dimension of 431 nm to exhibit single-domain nature.

  2. Improvement of the magnetic moment of NiZn ferrites induced by substitution of Nd3+ ions for Fe3+ ions

    Science.gov (United States)

    Wu, Xuehang; Chen, Wen; Wu, Wenwei; Wu, Juan; Wang, Qing

    2018-05-01

    Four types of Ni-Zn based ferrites materials having the general formula Ni0.5Zn0.5NdxFe2-xO4 (0.0 ≤ x ≤ 0.12) have been successfully synthesized by calcining oxalates in air and the influence of Nd content on the structure and magnetic properties of Ni0.5Zn0.5NdxFe2-xO4 is studied. X-ray diffraction examination confirms that a high-crystallized Ni0.5Zn0.5NdxFe2-xO4 with cubic spinel structure is obtained when the precursor is calcined at 1000 °C in air for 2 h. The substitutions of Nd3+ ions for partial Fe3+ ions do not change the spinel crystalline structure of MFe2O4. The incorporation of Nd3+ ions in place of Fe3+ ions in Ni-Zn ferrites increases the average crystallite size. Specific saturation magnetization decreases with increase in Nd content. This is because Nd3+ ions with smaller magnetic moment preferentially fill the octahedral sites. In addition, antiferromagnetic FeNdO3 increases with increase in Nd content. In this study, Ni0.5Zn0.5Nd0.08Fe1.92O4, calcined at 1000 °C, exhibits the highest magnetic moment (4.2954 μB) and the lowest coercivity (28.82 Oe).

  3. Zn substitution NiFe{sub 2}O{sub 4} nanoparticles with enhanced conductivity as high-performances electrodes for lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Mao, Junwei [Guang dong Engineering Technology Research Center of Efficient Green Energy and Environmental Protection Materials, Guangzhou 510006 (China); Guang dong Provincial Key Laboratory of Quantum Engineering and Quantum Materials, School of Physics and Telecommunication Engineering, South China Normal University, Guangzhou 510006 (China); Hou, Xianhua, E-mail: houxh@scnu.edu.cn [Guang dong Engineering Technology Research Center of Efficient Green Energy and Environmental Protection Materials, Guangzhou 510006 (China); Guang dong Provincial Key Laboratory of Quantum Engineering and Quantum Materials, School of Physics and Telecommunication Engineering, South China Normal University, Guangzhou 510006 (China); Huang, Fengsi; Shen, Kaixiang [Guang dong Engineering Technology Research Center of Efficient Green Energy and Environmental Protection Materials, Guangzhou 510006 (China); Guang dong Provincial Key Laboratory of Quantum Engineering and Quantum Materials, School of Physics and Telecommunication Engineering, South China Normal University, Guangzhou 510006 (China); Lam, Kwok-ho [Department of Electrical Engineering, The Hong Kong Polytechnic University, Hunghom, Kowloon 999077 (Hong Kong); Ru, Qiang [Guang dong Engineering Technology Research Center of Efficient Green Energy and Environmental Protection Materials, Guangzhou 510006 (China); Guang dong Provincial Key Laboratory of Quantum Engineering and Quantum Materials, School of Physics and Telecommunication Engineering, South China Normal University, Guangzhou 510006 (China); Hu, Shejun, E-mail: husj@scnu.edu.cn [Guang dong Engineering Technology Research Center of Efficient Green Energy and Environmental Protection Materials, Guangzhou 510006 (China); Guang dong Provincial Key Laboratory of Quantum Engineering and Quantum Materials, School of Physics and Telecommunication Engineering, South China Normal University, Guangzhou 510006 (China)

    2016-08-15

    Zn{sup 2+} ion substituted nickel ferrite nanomaterials with the chemical formula Ni{sub 1−x}Zn{sub x}Fe{sub 2}O{sub 4} for x = 0, 0.3, 0.5, 0.7 and 1 have been synthesized by a facile green-chemical hydrothermal method as anode materials in lithium ion battery. The morphology and structure of the samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The physical and electrochemical properties were tested by electrochemical system. Furthermore, the energetic and electronic properties of the samples were investigated by density functional calculations. The results suggest that Zn substitution can affect the conduction performance of the zinc - nickel ferrite. Meanwhile, electrochemical results show that an enhancement in the capacity with increasing Zn concentration is observed especially for x = 0.3 which exhibit high discharge capacity of 1416 mAh g{sup −1}at the end of 100th cycle. Moreover, the theoretical research method with high yield synthesis strategy described in the present work holds promise for the general fabrication of other metallic elements substitution in complex transition metal oxides for high power LIBs. - Highlights: • Ni{sub 1−x}Zn{sub x}Fe{sub 2}O{sub 4} anodes have been synthesized by hydrothermal method. • First principles calculation was used to investigate the conduction performance. • Electrochemical performance was enhanced with Zn substitution.

  4. Zn substitution NiFe_2O_4 nanoparticles with enhanced conductivity as high-performances electrodes for lithium ion batteries

    International Nuclear Information System (INIS)

    Mao, Junwei; Hou, Xianhua; Huang, Fengsi; Shen, Kaixiang; Lam, Kwok-ho; Ru, Qiang; Hu, Shejun

    2016-01-01

    Zn"2"+ ion substituted nickel ferrite nanomaterials with the chemical formula Ni_1_−_xZn_xFe_2O_4 for x = 0, 0.3, 0.5, 0.7 and 1 have been synthesized by a facile green-chemical hydrothermal method as anode materials in lithium ion battery. The morphology and structure of the samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The physical and electrochemical properties were tested by electrochemical system. Furthermore, the energetic and electronic properties of the samples were investigated by density functional calculations. The results suggest that Zn substitution can affect the conduction performance of the zinc - nickel ferrite. Meanwhile, electrochemical results show that an enhancement in the capacity with increasing Zn concentration is observed especially for x = 0.3 which exhibit high discharge capacity of 1416 mAh g"−"1at the end of 100th cycle. Moreover, the theoretical research method with high yield synthesis strategy described in the present work holds promise for the general fabrication of other metallic elements substitution in complex transition metal oxides for high power LIBs. - Highlights: • Ni_1_−_xZn_xFe_2O_4 anodes have been synthesized by hydrothermal method. • First principles calculation was used to investigate the conduction performance. • Electrochemical performance was enhanced with Zn substitution.

  5. Ab initio understanding of magnetic properties in Zn2+ substitution of Fe3O4 ultra-thin film with dilute Zn substitution

    Science.gov (United States)

    Huang, Zhaocong; Chen, Qian; Jiang, Sheng; Dong, Shuai; Zhai, Ya

    2018-05-01

    The mechanism of the magnetic properties on the Zn2+ substituted Fe3O4 film have been investigated based on first principle calculations. It is found that the surface effect plays an important role in the occupation of Zn ion, and in turn changes the magnetic moment. It may also destroy the half metallic behavior of Fe3O4 film even if the Zn2+ concentration only is one Zn2+ per unit cell (4%), which is different from that in bulk material.

  6. Arsenic in ZnO and GaN: substitutional cation or anion sites?

    CERN Document Server

    Wahl, Ulrich; Rita, Elisabete; Marques, Ana Claudia; Alves, Eduardo; Carvalho Soares, José

    2007-01-01

    We have determined the lattice location of ion implanted As in ZnO and GaN by means of conversion electron emission channeling from radioactive $^{73}$As. In contrast to what one might expect from its nature as a group V element, we find that As does not occupy substitutional O sites in ZnO but in its large majority substitutional Zn sites. Arsenic in ZnO is thus an interesting example for an impurity in a semiconductor where the major impurity lattice site is determined by atomic size and electronegativity rather than its position in the periodic system. In contrast, in GaN the preference of As for substitutional cation sites is less pronounced and about half of the implanted As atoms occupy Ga and the other half N sites. Apparently, the smaller size-mismatch between As and N and the chemical similarity of both elements make it feasible that As partly substitutes for N atoms.

  7. Defect dynamics in Li substituted nanocrystalline ZnO: A spectroscopic analysis

    Energy Technology Data Exchange (ETDEWEB)

    Ghosh, S., E-mail: sghoshphysics@gmail.com [Department of Material Science, Indian Association for the Cultivation of Science, 2A and 2B Raja S.C. Mullick Road, Jadavpur, Kolkata 700032 (India); Nambissan, P.M.G.; Thapa, S. [Applied Nuclear Physics Division, Saha Institute of Nuclear Physics, Sector 1, Block AF, Bidhannagar, Kolkata 700064 (India); Mandal, K. [Department of Condensed Matter Physics and Material Sciences, S.N. Bose National Centre for Basic Sciences, Block JD, Sector III, Salt Lake, Kolkata 700098 (India)

    2014-12-01

    Very recently, vacancy-type defects have been found to play a major role in stabilizing d{sup 0} ferromagnetism in various low dimensional ZnO systems. In this context, the evolution of vacancy-type defects within the ZnO nanocrystals due to the doping of ZnO by alkali metal lithium (Li) is investigated using X-ray photoelectron (XPS), photoluminescence (PL) and positron annihilation spectroscopy (PAS). Li-doping is found to have significant effects in modifying the vacancy-type defects, especially the Zn vacancy (V{sub Zn}) defects within the ZnO lattice. XPS measurement indicated that initially the Li{sup 1+} ions substitute at Zn{sup 2+} sites, but when Li concentration exceeds 7 at%, excess Li starts to move through the interstitial sites. The increase in positron lifetime components and the lineshape S-parameter obtained from coincident Doppler broadening spectra with Li-doping indicated an enhancement of V{sub Zn} defect concentration within the doped ZnO lattice. The vacancy type defects, initially of the predominant configuration V{sub Zn+O+Zn} got reduced to neutral ZnO divacancies due to the partial recombination by the doped Li{sup 1+} ions but, when the doping concentration exceeded 7 at% and Li{sup 1+} ions started migrating to the interstitials, positron diffusion is partly impeded and this results in reduced probability of annihilation. PL spectra have shown intense green and yellow-orange emission due to the stabilization of a large number of V{sub Zn} defects and Li substitutional (Li{sub Zn}) defects respectively. Hence Li can be a very useful dopant in stabilizing and modifying significant amount of Zn vacancy-defects which can play a useful role in determining the material behavior.

  8. Defect dynamics in Li substituted nanocrystalline ZnO: A spectroscopic analysis

    International Nuclear Information System (INIS)

    Ghosh, S.; Nambissan, P.M.G.; Thapa, S.; Mandal, K.

    2014-01-01

    Very recently, vacancy-type defects have been found to play a major role in stabilizing d 0 ferromagnetism in various low dimensional ZnO systems. In this context, the evolution of vacancy-type defects within the ZnO nanocrystals due to the doping of ZnO by alkali metal lithium (Li) is investigated using X-ray photoelectron (XPS), photoluminescence (PL) and positron annihilation spectroscopy (PAS). Li-doping is found to have significant effects in modifying the vacancy-type defects, especially the Zn vacancy (V Zn ) defects within the ZnO lattice. XPS measurement indicated that initially the Li 1+ ions substitute at Zn 2+ sites, but when Li concentration exceeds 7 at%, excess Li starts to move through the interstitial sites. The increase in positron lifetime components and the lineshape S-parameter obtained from coincident Doppler broadening spectra with Li-doping indicated an enhancement of V Zn defect concentration within the doped ZnO lattice. The vacancy type defects, initially of the predominant configuration V Zn+O+Zn got reduced to neutral ZnO divacancies due to the partial recombination by the doped Li 1+ ions but, when the doping concentration exceeded 7 at% and Li 1+ ions started migrating to the interstitials, positron diffusion is partly impeded and this results in reduced probability of annihilation. PL spectra have shown intense green and yellow-orange emission due to the stabilization of a large number of V Zn defects and Li substitutional (Li Zn ) defects respectively. Hence Li can be a very useful dopant in stabilizing and modifying significant amount of Zn vacancy-defects which can play a useful role in determining the material behavior

  9. Minority anion substitution by Ni in ZnO

    CERN Document Server

    Pereira, Lino Miguel da Costa; Correia, João Guilherme; Amorim, Lígia Marina; Silva, Daniel José; David-Bosne, Eric; Decoster, Stefan; da Silva, Manuel Ribeiro; Temst, Kristiaan; Vantomme, André

    2013-01-01

    We report on the lattice location of implanted Ni in ZnO using the $\\beta$− emission channeling technique. In addition to the majority substituting for the cation (Zn), a significant fraction of the Ni atoms occupy anion (O) sites. Since Ni is chemically more similar to Zn than it is to O, the observed O substitution is rather puzzling. We discuss these findings with respect to the general understanding of lattice location of dopants in compound semiconductors. In particular, we discuss potential implications on the magnetic behavior of transition metal doped dilute magnetic semiconductors.

  10. Defect dynamics in Li substituted nanocrystalline ZnO: A spectroscopic analysis

    Science.gov (United States)

    Ghosh, S.; Nambissan, P. M. G.; Thapa, S.; Mandal, K.

    2014-12-01

    Very recently, vacancy-type defects have been found to play a major role in stabilizing d0 ferromagnetism in various low dimensional ZnO systems. In this context, the evolution of vacancy-type defects within the ZnO nanocrystals due to the doping of ZnO by alkali metal lithium (Li) is investigated using X-ray photoelectron (XPS), photoluminescence (PL) and positron annihilation spectroscopy (PAS). Li-doping is found to have significant effects in modifying the vacancy-type defects, especially the Zn vacancy (VZn) defects within the ZnO lattice. XPS measurement indicated that initially the Li1+ ions substitute at Zn2+ sites, but when Li concentration exceeds 7 at%, excess Li starts to move through the interstitial sites. The increase in positron lifetime components and the lineshape S-parameter obtained from coincident Doppler broadening spectra with Li-doping indicated an enhancement of VZn defect concentration within the doped ZnO lattice. The vacancy type defects, initially of the predominant configuration VZn+O+Zn got reduced to neutral ZnO divacancies due to the partial recombination by the doped Li1+ ions but, when the doping concentration exceeded 7 at% and Li1+ ions started migrating to the interstitials, positron diffusion is partly impeded and this results in reduced probability of annihilation. PL spectra have shown intense green and yellow-orange emission due to the stabilization of a large number of VZn defects and Li substitutional (LiZn) defects respectively. Hence Li can be a very useful dopant in stabilizing and modifying significant amount of Zn vacancy-defects which can play a useful role in determining the material behavior.

  11. Quinoline-substituted Zinc(II) phthalocyanine for the dual detection of ferric and zinc ions

    Energy Technology Data Exchange (ETDEWEB)

    Gupta, Ankush [Lyallpur Khalsa College of Engineering, Jalandhar (India); Kim, A Rong [Dong-A University, Busan (Korea, Republic of); Kim, Kyung Sub; Na, Kun [The Catholic University, Seoul (Korea, Republic of); Choi, Myung Seok [Konkuk University, Seoul (Korea, Republic of); Park, Jong S. [Pusan National University, Busan (Korea, Republic of)

    2015-09-15

    Here we present the synthesis and properties of quinoline-substituted zinc(II) phthalocyanine, Zn[Pc(O-QN){sub 4} ]. Zn[Pc(O-QN){sub 4} ] can function as a highly selective chemosensor against Fe{sup 3+} and Zn{sup 2+} ions, exhibiting efficient fluorescence quenching and enhancement, respectively. Various characterization techniques were employed to investigate the intermolecular interactions of Zn[Pc(O-QN){sub 4} ] with metal ions. A double-electron exchange and a forbidden photoinduced electron transfer behavior in Zn[Pc(O-QN){sub 4} ] were attributed to such opposite responses. Furthermore, by taking advantage of selectivity, we successfully employed Zn[Pc(O-QN)-4 ] to stain and record confocal fluorescence microscopy images of Chang liver cells in the presence of metal ions.

  12. Influence of iron substitution by selected rare-earth ions on the properties of NiZn ferrite fillers and PVC magneto-polymer composites

    Science.gov (United States)

    Ušák, Elemír; Ušáková, Mariana; Dosoudil, Rastislav; Šoka, Martin; Dobročka, Edmund

    2018-04-01

    Nickel-zinc ferrites are very important soft magnetic materials from the point of view of diverse technical applications (such as, e.g., various electronic devices and components) for their high magnetic permeability and permittivity, low core loss, high resistivity, high Curie temperature as well as mechanical strength and chemical stability. Due to their good absorbing properties, they can be used as microwave absorbing and shielding materials with the aim of decreasing the environmental pollution caused by non-ionizing microwave radiation. The ferrite material incorporated into the polymer matrix creates qualitatively new magneto-polymer composite material taking benefits from both components. The properties typical for polymers (elasticity, mouldability, etc.) are combined with good high-frequency magnetic parameters, thus allowing to utilize these materials, e.g., in high-frequency applications where especially flexibility of composite materials plays a key role. Small amounts of selected rare-earth (RE) ions, in particular Y3+, La3+, Eu3+ and Gd3+ have been embedded into the nickel-zinc ferrite that has been used as the magnetic filler in magnetic polymer composites with polyvinylchloride (PVC) acting as the polymeric matrix. The effect of various types of rare-earth ions on the structural as well as quasi-static and dynamic (electro)magnetic properties of the ferrite fillers as well as ferrite/PVC composites, in particular the frequency dispersion of the complex permeability, has been studied.

  13. Synthesis of Zn{sup 2+} substituted maghemite nanoparticles and investigation of their structural and magnetic properties

    Energy Technology Data Exchange (ETDEWEB)

    Mozaffari, M. [Department of Physics, Faculty of Science, University of Isfahan, Isfahan 81746-73441 (Iran, Islamic Republic of); Shatooti, S. [Department of Physics, Razi University, Kermanshah 67149-67346 (Iran, Islamic Republic of); Jafarzadeh, M., E-mail: mjafarzadeh1027@yahoo.com [Faculty of Chemistry, Razi University, Kermanshah 67149-67346 (Iran, Islamic Republic of); Niyaifar, M. [Department of Physics, Ahvaz Branch, Islamic Azad University, Ahvaz (Iran, Islamic Republic of); Aftabi, A. [Department of Physics, University of Kurdistan, Sanandaj 66177-15175 (Iran, Islamic Republic of); Mohammadpour, H. [Department of Physics, Ahvaz Branch, Islamic Azad University, Ahvaz (Iran, Islamic Republic of); Amiri, Sh. [Department of Physics, Razi University, Kermanshah 67149-67346 (Iran, Islamic Republic of)

    2015-05-15

    Maghemite and Zn{sup 2+} substituted maghemite (γ-Fe{sub 2−y} Zn{sub 3y/2}O{sub 3}, y=0.0, 0.11, 0.24, 0.36, 0.50 and 0.66) nanoparticles were prepared by coprecipitation method. The effect of Zn{sup 2+} substitution on the structural, morphological and magnetic properties of the nanoparitcles were studied by different techniques such as X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, field emission scanning electron microscopy (FESEM), magnetometry, magnetic thermogravimetry and Mössbauer spectroscopy. The results of XRD showed that all samples have spinel structure with an increase in lattice parameter by increasing the content of Zn{sup 2+}. FTIR spectra were proved the synthesis of maghemite and Zn{sup 2+} substituted maghemite with appearance of the related absorption bands and band shift upon Zn{sup 2+} substitution. Morphological studies by FESEM demonstrated that the nanoparticles were uniform and spherical with average particle size in range of 20–24 nm. Room temperature magnetic measurements showed that as Zn{sup 2+} content increases, saturation magnetization initially increase up to 75.34 emu/g for y=0.11 and then decrease to 3.65 emu/g for y=0.66, due to substitution of magnetic Fe{sup 3+} by non-magnetic Zn{sup 2+}. Decrease in Curie temperature of the samples, from 510 for maghemite to 250 °C for y=0.36, by increasing the Zn{sup 2+} substitution was a result of reduction of superexchange interactions between different sites. Then, the Curie temperature increased up to 680 °C for y=0.66 which was due to migration of some Zn{sup 2+} ions from A to B sites in the structure of spinel. Room temperature Mössbauer spectra exhibited that the sample with y=0.0 was superparamagnetic, while by increasing the content of Zn{sup 2+}, relaxation effect increased by weakening of A–B exchange interaction. - Highlights: • Synthesis of Zn{sup 2+}-substituted maghemite via co-precipitation/oxidation method. • Increase in lattice

  14. Mn{sup 2+} ions distribution in doped sol–gel deposited ZnO films

    Energy Technology Data Exchange (ETDEWEB)

    Stefan, Mariana, E-mail: mstefan@infim.ro [National Institute of Materials Physics, P.O. Box MG-7, 077125 Magurele (Romania); Ghica, Daniela; Nistor, Sergiu V.; Maraloiu, Adrian V. [National Institute of Materials Physics, P.O. Box MG-7, 077125 Magurele (Romania); Plugaru, Rodica [National Institute for R & D in Microtechnologies (IMT), Erou Iancu Nicolae Str. 126A, 077190 Bucharest (Romania)

    2017-02-28

    Highlights: • Several Mn{sup 2+} centers observed by EPR in sol–gel ZnO films. • Mn{sup 2+} ions localized at Zn{sup 2+} sites in ZnO grains and disordered ZnO phase. • Sixfold coordinated Mn{sup 2+} ions localized in inter-grain region. • Aggregated Mn in insular-like regions between ZnO grains in the ZnO:5%Mn film. • Aggregated Mn phase presence and distribution observed by EPR and EDX-STEM. - Abstract: The localization and distribution of the Mn{sup 2+} ions in two sol–gel deposited ZnO films doped with different manganese concentrations were investigated by electron paramagnetic resonance spectroscopy and analytical transmission electron microscopy. In the lightly doped sample the Mn{sup 2+} ions are mainly localized substitutionally at isolated tetrahedrally coordinated Zn{sup 2+} sites in both crystalline ZnO nanograins (34%) and surrounding disordered ZnO (52%). In the highly doped ZnO film, a much smaller proportion of manganese substitutes Zn{sup 2+} in the crystalline and disordered ZnO (10%). The main amount (85%) of manganese aggregates in a secondary phase as an insular-like distribution between the ZnO nanograins. The remaining Mn{sup 2+} ions (14% and 5% at low and high doping levels, respectively) are localized at isolated, six-fold coordinated sites, very likely in the disordered intergrain region. Annealing at 600 °C induced changes in the Mn{sup 2+} ions distribution, reflecting the increase of the ZnO crystallization degree, better observed in the lightly doped sample.

  15. Intrinsic magnetism of a series of Co substituted ZnO single crystals

    International Nuclear Information System (INIS)

    Lv Peiwen; Huang Feng; Chu Wangsheng; Lin Zhang; Chen Dagui; Li Wei; Chen Dongliang; Wu Ziyu

    2008-01-01

    Magnetic properties of a series of well-substituted Zn 1-x Co x O (x = 0.018,0.036 and 0.05) single crystals were studied. A typical paramagnetic anisotropy property, which strengthens when x decreases, was found. A magnetization step was observed at 2 K when the magnetic field is parallel to the c axis, indicating that paramagnetic anisotropy is the origin of the strong crystal field effect on Co 2+ ions in ZnO lattices. The Co 2+ single-ion anisotropy parameter 2D is obtained as 7.5 K. The effective moment of Co 2+ takes the values 2.7 μ B , 1.82 μ B , 1.49 μ B when x = 0.018, 0.036 and 0.05, revealing that more antiferromagnetic coupling between Co 2+ ions arises in the perfect crystal when x increases

  16. Effect of Zn and Ni substitution on structural, morphological and magnetic properties of tin oxide nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Bhuvana, S. [Research and Development Centre, Bharathiar University, Coimbatore 641046, Tamilnadu (India); Department of Physics, Dr. NGP Institute of Technology, Coimbatore 641048, Tamilnadu (India); Ramalingam, H.B.; Vadivel, K. [Department of Physics, Government Arts College, Udumalpet 642126, Tamilnadu (India); Ranjith Kumar, E., E-mail: ranjueaswar@gmail.com [Department of Physics, Dr. NGP Institute of Technology, Coimbatore 641048, Tamilnadu (India); Ayesh, Ahmad I. [Department of Math., Stat. and Physics, Qatar University, Doha (Qatar)

    2016-12-01

    Structural, morphological, optical and magnetic properties of Zn and Zn–Ni co-doped tin oxide (SnO{sub 2}) nanoparticles synthesized by sol-gel method. The influence of doping concentration on phase and particle size of the nanoparticles was determined by X-ray diffraction. The XRD study reveals that the lattice constant and crystallite size of the samples decrease with the increase of doping concentration. The change in the band gap energy of SnO{sub 2} nanoparticles influenced more by doping with Zn and Ni. The external morphology and particle size were recorded by SEM and TEM. The results indicated that Ni{sup 2+} ions would uniformly substituted into the Zn{sup 2+} sites of SnO{sub 2} lattice. The substitution of Ni creates a vital change in magnetic properties that has been measured by vibrating sample magnetometer (VSM). - Highlights: • Sn{sub 2-(x+y)} Ni{sub x}Zn{sub y}O{sub 2}, (x=y=0.07 to 0.10) nano particles are prepared by simple sol gel method. • X-ray diffraction data confirms the single phase rutile tetragonal structure. • The VSM was used to confirm, the codoping of (Ni, Zn) increases the magnetic moment of the sample prepared. • Inducing ferromagnetism in sample makes it suitable for future spintronics applications.

  17. Influence of La3+ Substitution on Structure, Morphology and Magnetic Properties of Nanocrystalline Ni-Zn Ferrite.

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    Y K Dasan

    Full Text Available Lanthanum substituted Ni-Zn ferrite nanoparticles (Ni0.5Zn0.5LaxFe1-xO4; 0.00 ≤x≤ 1.00 synthesized by sol-gel method were presented. X-ray diffraction patterns reveal the typical single phase spinel cubic ferrite structure, with the traces of secondary phase for lanthanum substituted nanocrystals. In addition, the structural analysis also demonstrates that the average crystallite size varied in the range of 21-25 nm. FTIR spectra present the two prominent absorption bands in the range of 400 to 600 cm-1 which are the fingerprint region of all ferrites. Surface morphology of both substituted and unsubstituted Ni-Zn ferrite nanoparticle samples was studied using FESEM technique and it indicates a significant increase in the size of spherical shaped particles with La3+ substitution. Magnetic properties of all samples were analyzed using vibrating sample magnetometer (VSM. The results revealed that saturation magnetization (Ms and coercivity (Hc of La3+ substituted samples has decreased as compared to the Ni-Zn ferrite samples. Hence, the observed results affirm that the lanthanum ion substitution has greatly influenced the structural, morphology and magnetic properties of Ni-Zn ferrite nanoparticles.

  18. Doping effects of Co2+ ions on ZnO nanorods and their photocatalytic properties

    International Nuclear Information System (INIS)

    Qiu Xiaoqing; Li Guangshe; Sun Xuefei; Li Liping; Fu Xianzhi

    2008-01-01

    A series of Zn 1-x Co x O nanorods with dopant content ranging from x = 0.00 to 0.10 was prepared by a wet chemical method. All Zn 1-x Co x O samples were investigated by x-ray diffraction, transmission electron microscopy, energy-dispersion x-ray line mapping analysis, and UV-visible absorption spectroscopy. It was found that Co 2+ ions were homogeneously substituted for Zn 2+ ions in ZnO nanorods. Rhodamine B degradation was used as a probe reaction to evaluate the effect of Co 2+ doping on ZnO nanorods and photocatalytic performance under UV light and visible light irradiation. Co 2+ ions acted as the trapping or recombination centers for electrons and holes, leading to a reduction in photodegradation efficiency under UV light illumination. Alternatively, Co 2+ ions enhanced the optical absorption and produced the photoinduced carriers under visible illumination in terms of two charge transfer transitions involving Co 2+ ions. Consequently, Co 2+ ions substituted in the lattice of ZnO nanorods significantly improved the visible light photocatalytic activity

  19. Intrinsic magnetism of a series of Co substituted ZnO single crystals

    Energy Technology Data Exchange (ETDEWEB)

    Lv Peiwen [Laboratory of Materials Chemistry and Physics, Fujian Institute of Research on the Structure of Matter, National Engineering Research Center for Optoelectronic Crystalline Materials, Chinese Academy of Sciences, Fuzhou, Fujian 350002 (China); Huang Feng [Laboratory of Materials Chemistry and Physics, Fujian Institute of Research on the Structure of Matter, National Engineering Research Center for Optoelectronic Crystalline Materials, Chinese Academy of Sciences, Fuzhou, Fujian 350002 (China); Chu Wangsheng [Beijing Synchrotron Radiation Facility, Institute of High Energy Physics, Chinese Academy of Sciences, 100049 Beijing (China); Lin Zhang [Laboratory of Materials Chemistry and Physics, Fujian Institute of Research on the Structure of Matter, National Engineering Research Center for Optoelectronic Crystalline Materials, Chinese Academy of Sciences, Fuzhou, Fujian 350002 (China); Chen Dagui [Laboratory of Materials Chemistry and Physics, Fujian Institute of Research on the Structure of Matter, National Engineering Research Center for Optoelectronic Crystalline Materials, Chinese Academy of Sciences, Fuzhou, Fujian 350002 (China); Li Wei [Laboratory of Materials Chemistry and Physics, Fujian Institute of Research on the Structure of Matter, National Engineering Research Center for Optoelectronic Crystalline Materials, Chinese Academy of Sciences, Fuzhou, Fujian 350002 (China); Chen Dongliang [Beijing Synchrotron Radiation Facility, Institute of High Energy Physics, Chinese Academy of Sciences, 100049 Beijing (China); Wu Ziyu [Beijing Synchrotron Radiation Facility, Institute of High Energy Physics, Chinese Academy of Sciences, 100049 Beijing (China)

    2008-01-23

    Magnetic properties of a series of well-substituted Zn{sub 1-x}Co{sub x}O (x = 0.018,0.036 and 0.05) single crystals were studied. A typical paramagnetic anisotropy property, which strengthens when x decreases, was found. A magnetization step was observed at 2 K when the magnetic field is parallel to the c axis, indicating that paramagnetic anisotropy is the origin of the strong crystal field effect on Co{sup 2+} ions in ZnO lattices. The Co{sup 2+} single-ion anisotropy parameter 2D is obtained as 7.5 K. The effective moment of Co{sup 2+} takes the values 2.7 {mu}{sub B}, 1.82 {mu}{sub B}, 1.49 {mu}{sub B} when x = 0.018, 0.036 and 0.05, revealing that more antiferromagnetic coupling between Co{sup 2+} ions arises in the perfect crystal when x increases.

  20. Effect of neodymium substitutions on electromagnetic properties in low temperature sintered NiCuZn ferrite

    Science.gov (United States)

    Wu, C. P.; Tung, M. J.; Ko, W. S.; Wang, Y. P.; Tong, S. Y.; Yang, M. D.

    2015-11-01

    Nd3+ ions substituted Ni0.37Cu0.14Zn0.52Fe2O4 (Nd3+ ions content=0, 0.01, 0.04, 0.6, 1.5 wt%) were prepared by the usual standard ceramic method at 1030 °C sintering temperature, and the composition dependence of the physical and magnetic properties has been investigated. SEM micrographs and EDX analysis revealed that it is no obvious impurities up to Nd3+ ions content wt%=0.04. For higher Nd3+ ions content samples (0.6 and 1.5 wt%), there are two kind of impurities Cu-rich and Nd-rich iron oxide phase. The saturation magnetization of the 0.01 wt% Nd3+ions content sample is higher as result of that the A-B sites distance and YK-angles are shorter and smaller. The saturation magnetization of 0.04-1.5 wt% Nd3+ ion content sample are reduced, since the total magnetic moments of the AB site are decreased. For the 0.6 wt% sample, the Curie temperature increasing is as result of the Cu-rich iron oxide separating out. The maximum enhancements of permeability μ‧ are improved to 11.2% (0.04 wt%) and 29.2% (0.6 wt%) at the 6.7 and 13.8 MHz, respectively. However, it is notice that small amount substitutions of Nd3+ increase the high frequency electromagnetic characteristics, can be applied to NFC technology and WPT technologies.

  1. Effect of neodymium substitutions on electromagnetic properties in low temperature sintered NiCuZn ferrite

    Energy Technology Data Exchange (ETDEWEB)

    Wu, C.P., E-mail: itria20161@itri.org.tw; Tung, M.J.; Ko, W.S.; Wang, Y.P.; Tong, S.Y.; Yang, M.D.

    2015-11-01

    Nd{sup 3+} ions substituted Ni{sub 0.37}Cu{sub 0.14}Zn{sub 0.52}Fe{sub 2}O{sub 4} (Nd{sup 3+} ions content=0, 0.01, 0.04, 0.6, 1.5 wt%) were prepared by the usual standard ceramic method at 1030 °C sintering temperature, and the composition dependence of the physical and magnetic properties has been investigated. SEM micrographs and EDX analysis revealed that it is no obvious impurities up to Nd{sup 3+} ions content wt%=0.04. For higher Nd{sup 3+} ions content samples (0.6 and 1.5 wt%), there are two kind of impurities Cu-rich and Nd-rich iron oxide phase. The saturation magnetization of the 0.01 wt% Nd{sup 3+}ions content sample is higher as result of that the A–B sites distance and YK-angles are shorter and smaller. The saturation magnetization of 0.04–1.5 wt% Nd{sup 3+} ion content sample are reduced, since the total magnetic moments of the AB site are decreased. For the 0.6 wt% sample, the Curie temperature increasing is as result of the Cu-rich iron oxide separating out. The maximum enhancements of permeability μ′ are improved to 11.2% (0.04 wt%) and 29.2% (0.6 wt%) at the 6.7 and 13.8 MHz, respectively. However, it is notice that small amount substitutions of Nd{sup 3+} increase the high frequency electromagnetic characteristics, can be applied to NFC technology and WPT technologies.

  2. Identification of substitutional Li in n-type ZnO and its role as an acceptor

    Science.gov (United States)

    Johansen, K. M.; Zubiaga, A.; Makkonen, I.; Tuomisto, F.; Neuvonen, P. T.; Knutsen, K. E.; Monakhov, E. V.; Kuznetsov, A. Yu.; Svensson, B. G.

    2011-06-01

    Monocrystalline n-type zinc oxide (ZnO) samples prepared by different techniques and containing various amounts of lithium (Li) have been studied by positron annihilation spectroscopy (PAS) and secondary ion mass spectrometry. A distinct PAS signature of negatively charged Li atoms occupying a Zn-site (LiZn-), so-called substitutional Li, is identified and thus enables a quantitative determination of the content of LiZn. In hydrothermally grown samples with a total Li concentration of ~2×1017cm-3,LiZn is found to prevail strongly, with only minor influence, by other possible configurations of Li. Also in melt grown samples doped with Li to a total concentration as high as 1.5×1019cm-3, a considerable fraction of the Li atoms (at least 20%) is shown to reside on the Zn-site, but despite the corresponding absolute acceptor concentration of ⩾(2-3)×1018cm-3, the samples did not exhibit any detectable p-type conductivity. The presence of LiZn is demonstrated to account for the systematic difference in positron lifetime of 10-15 ps between Li-rich and Li-lean ZnO materials as found in the literature, but further work is needed to fully elucidate the role of residual hydrogen impurities and intrinsic open volume defects.

  3. Two-dimensional electron gases in MgZnO/ZnO and ZnO/MgZnO/ZnO heterostructures grown by dual ion beam sputtering

    Science.gov (United States)

    Singh, Rohit; Arif Khan, Md; Sharma, Pankaj; Than Htay, Myo; Kranti, Abhinav; Mukherjee, Shaibal

    2018-04-01

    This work reports on the formation of high-density (~1013-1014 cm-2) two-dimensional electron gas (2DEG) in ZnO-based heterostructures, grown by a dual ion beam sputtering system. We probe 2DEG in bilayer MgZnO/ZnO and capped ZnO/MgZnO/ZnO heterostructures utilizing MgZnO barrier layers with varying thickness and Mg content. The effect of the ZnO cap layer thickness on the ZnO/MgZnO/ZnO heterostructure is also studied. Hall measurements demonstrate that the addition of a 5 nm ZnO cap layer results in an enhancement of the 2DEG density by about 1.5 times compared to 1.11 × 1014 cm-2 for the uncapped bilayer heterostructure with the same 30 nm barrier thickness and 30 at.% Mg composition in the barrier layer. From the low-temperature Hall measurement, the sheet carrier concentration and mobility are both found to be independent of the temperature. The capacitance-voltage measurement suggests a carrier density of ~1020 cm-3, confined in 2DEG at the MgZnO/ZnO heterointerface. The results presented are significant for the optimization of 2DEG for the eventual realization of cost-effective and large-area MgZnO/ZnO-based high-electron-mobility transistors.

  4. Mixed Zn and O substitution of Co and Mn in ZnO

    CERN Document Server

    Pereira, Lino Miguel da Costa; Decoster, Stefan; Correia, João Guilherme; Amorim, Lígia Marina; da Silva, Manuel Ribeiro; Araújo, João Pedro; Vantomme, André

    2011-01-01

    The physical properties of an impurity atom in a semiconductor are primarily determined by the lattice site it occupies. In general, this occupancy can be correctly predicted based on chemical intuition, but not always. We report on one such exception in the dilute magnetic semiconductors Co- and Mn-doped ZnO, experimentally determining the lattice location of Co and Mn using $\\beta$-emission channeling from the decay of radioactive $^{61}$Co and $^{56}$Mn implanted at the ISOLDE facility at CERN. Surprisingly, in addition to the majority substituting for Zn, we find up to 18% (27%) of the Co (Mn) atoms in O sites, which is virtually unaffected by thermal annealing up to 900 °C. We discuss how this anion site configuration, which had never been considered before for any transition metal in any metal oxide material, may in fact have a low formation energy. This suggests a change in paradigm regarding transition-metal incorporation in ZnO and possibly other oxides and wide-gap semiconductors.

  5. Intrinsic point-defect balance in self-ion-implanted ZnO.

    Science.gov (United States)

    Neuvonen, Pekka T; Vines, Lasse; Svensson, Bengt G; Kuznetsov, Andrej Yu

    2013-01-04

    The role of excess intrinsic atoms for residual point defect balance has been discriminated by implanting Zn or O ions into Li-containing ZnO and monitoring Li redistribution and electrical resistivity after postimplant anneals. Strongly Li-depleted regions were detected in the Zn-implanted samples at depths beyond the projected range (R(p)) upon annealing ≥ 600 °C, correlating with a resistivity decrease. In contrast, similar anneals of the O-implanted samples resulted in Li accumulation at R(p) and an increased resistivity. Control samples implanted with Ar or Ne ions, yielding similar defect production as for the Zn or O implants but with no surplus of intrinsic atoms, revealed no Li depletion. Thus, the depletion of Li shows evidence of excess Zn interstitials (Zn(I)) being released during annealing of the Zn-implanted samples. These Zn(I)'s convert substitutional Li atoms (Li(Zn)) into highly mobile interstitial ones leading to the strongly Li-depleted regions. In the O-implanted samples, the high resistivity provides evidence of stable O(I)-related acceptors.

  6. Mössbauer studies of Sn /Nb substituted Mn–Zn ferrites

    Indian Academy of Sciences (India)

    Unknown

    communications, devices like computers, microprocessor and VCR systems, the use of above said types of power supplies highly increased. Though studies on Mn–Zn ... Hence, the aim of the present paper is to bring out the. Mössbauer studies of Sn/Nb substituted Mn–Zn ferrites. 2. Sample preparation and experimental.

  7. Dual mode antibacterial activity of ion substituted calcium phosphate nanocarriers for bone infections

    Directory of Open Access Journals (Sweden)

    Sampath Kumar eT.S.

    2015-05-01

    Full Text Available Nanotechnology has tremendous potential for the management of infectious diseases caused by multi-drug resistant (MDR bacteria, through the development of newer antibacterial materials and efficient modes of antibiotic delivery. Calcium phosphate (CaP bioceramics are commonly used as bone substitutes due to their similarity to bone mineral and are widely researched upon for the treatment of bone infections associated with bone loss. CaPs can be used as local antibiotic delivery agents for bone infections and can be substituted with antibacterial ions in their crystal structure to have a wide spectrum, sustained antibacterial activity even against drug resistant bacteria. In the present work, a dual mode antibiotic delivery system with antibacterial ion substituted calcium deficient hydroxyapatite (CDHA nanoparticles has been developed. Antibacterial ions such as zinc, silver and strontium have been incorporated into CDHA at concentrations of 6 at. %, 0.25-0.75 at. % and 2.5-7.5 at. % respectively. The samples were found to be phase pure, acicular nanoparticles of length 40-50 nm and width 5-6 nm approximately. The loading and release profile of doxycycline, a commonly used antibiotic, was studied from the nanocarriers. The drug release was studied for five days and the release profile was influenced by the ion concentrations. The release of antibacterial ions was studied over a period of 21 days. The ion substituted CDHA samples were tested for antibacterial efficacy on S.aureus and E.coli by MIC/MBC studies and time-kill assay. AgCDHA and ZnCDHA showed high antibacterial activity against both bacteria while SrCDHA was weakly active against S.aureus. Present study shows that the antibiotic release can provide the initial high antibacterial activity and the sustained ion release can provide a long-term antibacterial activity. Such dual mode antibiotic and antibacterial ion release offers an efficient and potent way to treat an incumbent drug

  8. High temperature dielectric studies of indium-substituted NiCuZn nanoferrites

    Science.gov (United States)

    Hashim, Mohd.; Raghasudha, M.; Shah, Jyoti; Shirsath, Sagar E.; Ravinder, D.; Kumar, Shalendra; Meena, Sher Singh; Bhatt, Pramod; Alimuddin; Kumar, Ravi; Kotnala, R. K.

    2018-01-01

    In this study, indium (In3+)-substituted NiCuZn nanostructured ceramic ferrites with a chemical composition of Ni0.5Cu0.25Zn0.25Fe2-xInxO4 (0.0 ≤ x ≤ 0.5) were prepared by chemical synthesis involving sol-gel chemistry. Single phased cubic spinel structure materials were prepared successfully according to X-ray diffraction and transmission electron microscopy analyses. The dielectric properties of the prepared ferrites were measured using an LCR HiTester at temperatures ranging from room temperature to 300 °C at different frequencies from 102 Hz to 5 × 106 Hz. The variations in the dielectric parameters ε‧ and (tanδ) with temperature demonstrated the frequency- and temperature-dependent characteristics due to electron hopping between the ions. The materials had low dielectric loss values in the high frequency range at all temperatures, which makes them suitable for high frequency microwave applications. A qualitative explanation is provided for the dependences of the dielectric constant and dielectric loss tangent on the frequency, temperature, and composition. Mӧssbauer spectroscopy was employed at room temperature to characterize the magnetic behavior.

  9. Zn2+ in-situ substitution behavior during the formation of BaTiO3 coatings from plasma-sprayed powders collected in liquid nitrogen

    Science.gov (United States)

    Liu, Zhe; Xing, Zhiguo; Wang, Haidou; Xue, Zifan; Chen, Shuying; Cui, Xiufang; Jin, Guo

    2018-04-01

    The dielectric performance of BaTiO3 ceramic coatings is enhanced significantly by the addition of ZnO. In this study, the maximum relative permittivity value (εr ≈ 923) was measured in BaTiO3 coatings with ZnO added at 6 wt%. The Curie temperature (Tc) was in the range of 111 °C-121 °C for all of the ZnO-modified BaTiO3 coatings. Tc shifted to low temperatures as the ZnO content increased. Detailed analyses were performed to determine the phase composition and optical band gaps of powders collected in liquid nitrogen, which showed that the Zn2+ ions were incorporated into the BaTiO3 lattice where they substituted into the Ti4+ sites, and the composite powders (BaTiO3 + 6 wt% ZnO) tolerated high temperatures in the plasma beam. In addition, some residual Zn accumulated in the grain boundary in the form of ZnO. X-ray diffraction and Raman spectroscopy showed that the substitution led to changes in the compositional and structural properties. The red shift in the optical band gap of BaTiO3 indicated that the ZnTi'' defects caused by the dopants acted as carriers in the doped BaTiO3 coatings.

  10. Labile Zn ions on octacalcium phosphate-derived Zn-containing hydroxyapatite surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Honda, Yoshitomo; Anada, Takahisa; Morimoto, Shinji [Division of Craniofacial Function Engineering (CFE), Tohoku University Graduate School of Dentistry, Sendai (Japan); Suzuki, Osamu, E-mail: suzuki-o@m.tohoku.ac.jp [Division of Craniofacial Function Engineering (CFE), Tohoku University Graduate School of Dentistry, Sendai (Japan)

    2013-05-15

    We previously synthesized and characterized zinc-containing octacalcium phosphate (OCP) and its hydrolyzed Ca-deficient hydroxyapatite (HA). In the present report, we attempted to define the state of Zn in the OCP-derived Zn-calcium phosphates (CaPs) in relation to the presence of specific amino acids. Zn-containing OCPs were prepared in solutions that included Zn ions up to a concentration of 3.5 mM, and their hydrolyzates [hydrolyzed (hy)-Zn-CaP] were obtained in hot water. The materials were characterized by x-ray diffraction and scanning electron microscopy. The concentration of Ca and Zn ions at room temperature was determined by analyzing the supernatant after incubating the materials in α-minimal essential medium (α-MEM) and HEPES buffer including cysteine, histidine, lysine, aspartic acid, and glutamic acid. Zn ions were more dissolved in α-MEM than HEPES buffer in the absence of amino acids. The inclusion of the amino acids enhanced Zn dissolution by several hundred fold, even in HEPES buffer. Among the amino acids, both cysteine and histidine enhanced the release of Zn. The effect was particularly remarkable with cysteine even in the presence of the other amino acids tested. These results indicate that Zn ions are present as a surface labile pool, which tends to be preferentially desorbed by cysteine, a ubiquitous molecule present in serum.

  11. Photovoltaic Performance of ZnO Nanosheets Solar Cell Sensitized with Beta-Substituted Porphyrin

    Directory of Open Access Journals (Sweden)

    Arumugam Mahesh

    2011-01-01

    Full Text Available The photoanode of dye-sensitized solar cell (DSSC was fabricated using two-dimensional ZnO nanosheets (2D ZnO NSs sensitized with beta-substituted porphyrins photosensitizer, and its photovoltaic performance in solid-state DSSC with TiO2 nanotubes (TiO2 TNs modified poly (ethylene oxide (PEO polymer electrolyte was studied. The ZnO NSs were synthesized through hydrothermal method and were characterized through high-resolution scanning electron microscopy (HRSEM, diffused reflectance spectra (DRS, photoluminescence spectra (PL, and X-ray diffraction (XRD analysis. The crystallinity of the polymer electrolytes was investigated using X-ray diffraction analysis. The photovoltaic performance of the beta-substituted porphyrins sensitized solar cells was evaluated under standard AM1.5G simulated illumination (100 mW cm−2. The efficiency of energy conversion from solar to electrical due to 2D ZnO NSs based DSSCs is 0.13%, which is about 1.6 times higher than that of the control DSSC using ZnO nanoparticles (ZnO NPs as photoanode (0.08%, when TiO2 NTs fillers modified PEO electrolyte was incorporated in the DSSCs. The current-voltage (- and photocurrent-time (- curves proved stable with effective collection of electrons, when the 2D ZnO nanostructured photoanode was introduced in the solid-state DSSC.

  12. Biological responses of brushite-forming Zn- and ZnSr- substituted beta-tricalcium phosphate bone cements

    Directory of Open Access Journals (Sweden)

    S Pina

    2010-09-01

    Full Text Available The core aim of this study was to investigate zinc (Zn- and zinc and strontium (ZnSr-containing brushite-forming beta-tricalcium phosphate (TCP cements for their effects on proliferation and differentiation of osteoblastic-like cells (MC3T3-E1 cell line as well as for their in vivo behaviour in trabecular bone cylindrical defects in a pilot study. In vitro proliferation and maturation responses of MC3T3-E1 osteoblastic-like cells to bone cements were studied at the cellular and molecular levels. The Zn- and Sr-containing brushite cements were found to stimulate pre-osteoblastic proliferation and osteoblastic maturation. Indeed, MC3T3-E1 cells exposed to the powdered cements had increased proliferative rates and higher adhesiveness capacity, in comparison to control cells. Furthermore, they exhibited higher alkaline phosphatase (ALP activity and increased Type-I collagen secretion and fibre deposition into the extracellular matrix. Proliferative and collagen deposition properties were more evident for cells grown in cements doped with Sr. The in vivo osteoconductive propertiesof the ZnCPC and ZnSrCPC cements were also pursued. Histological and histomorphometric analyses were performed at 1 and 2 months after implantation, using carbonated apatite cement (Norian SRS® as control. There was no evidence of cement-induced adverse foreign body reactions, and furthermore ZnCPC and ZnSrCPC cements revealed better in vivo performance in comparison to the control apatite cement. Additionally, the presence of both zinc and strontium resulted in the highest rate of new bone formation. These novel results indicate that the investigated ZnCPC and ZnSrCPC cements are both biocompatible and osteoconductive, being good candidate materials to use as bone substitutes.

  13. Dielectric behaviour of erbium substituted Mn–Zn ferrites

    Indian Academy of Sciences (India)

    Unknown

    Abstract. Dielectric properties such as dielectric constant (ε′) and dielectric loss tangent (tan δ) of mixed. Mn–Zn–Er ferrites having the compositional formula Mn0⋅58Zn0⋅37Fe2⋅05–xErxO4 (where x = 0⋅2, 0⋅4, 0⋅6, 0⋅8 and. 1⋅0) were measured at room temperature in the frequency range 1–13 MHz using a HP ...

  14. Vanadium substitution: A simple and economic way to improve UV sensing in ZnO

    Science.gov (United States)

    Srivastava, Tulika; Bajpai, Gaurav; Rathore, Gyanendra; Liu, Shun Wei; Biring, Sajal; Sen, Somaditya

    2018-04-01

    The UV sensing in pure ZnO is due to oxygen adsorption/desorption process from the ZnO surface. Vanadium doping improves the UV sensitivity of ZnO. The enhancement in UV sensitivity in vanadium-substituted ZnO is attributed to trapping and de-trapping of electrons at V4+ and V5+-related defect states. The V4+ state has an extra electron than the V5+ state. A V4+ to V5+ transformation happens with excitation of this electron to the conduction band, while a reverse trapping process liberates a visible light. An analytic study of response phenomenon reveals this trapping and de-trapping process.

  15. Effect of Ligand Substitution around the Dy(III) on the SMM Properties of Dual-Luminescent Zn-Dy and Zn-Dy-Zn Complexes with Large Anisotropy Energy Barriers: A Combined Theoretical and Experimental Magnetostructural Study.

    Science.gov (United States)

    Costes, Jean Pierre; Titos-Padilla, Silvia; Oyarzabal, Itziar; Gupta, Tulika; Duhayon, Carine; Rajaraman, Gopalan; Colacio, Enrique

    2016-05-02

    The new dinuclear Zn(II)-Dy(III) and trinuclear Zn(II)-Dy(III)-Zn(II) complexes of formula [(LZnBrDy(ovan) (NO3)(H2O)](H2O)·0.5(MeOH) (1) and [(L(1)ZnBr)2Dy(MeOH)2](ClO4) (3) (L and L(1) are the dideprotonated forms of the N,N'-2,2-dimethylpropylenedi(3-methoxysalicylideneiminato and 2-{(E)-[(3-{[(2E,3E)-3-(hydroxyimino)butan-2-ylidene ]amino}-2,2-dimethylpropyl)imino]methyl}-6-methoxyphenol Schiff base compartmental ligands, respectively) have been prepared and magnetostructurally characterized. The X-ray structure of 1 indicates that the Dy(III) ion exhibits a DyO9 coordination sphere, which is made from four O atoms coming from the compartmental ligand (two methoxy terminal groups and two phenoxido bridging groups connecting Zn(II) and Dy(III) ions), other four atoms belonging to the chelating nitrato and ovanillin ligands, and the last one coming to the coordinated water molecule. The structure of 3 shows the central Dy(III) ion surrounded by two L(1)Zn units, so that the Dy(III) and Zn(II) ions are linked by phenoxido/oximato bridging groups. The Dy ion is eight-coordinated by the six O atoms afforded by two L(1) ligands and two O atoms coming from two methanol molecules. Alternating current (AC) dynamic magnetic measurements of 1, 3, and the previously reported dinuclear [LZnClDy(thd)2] (2) complex (where thd = 2,2,6,6-tetramethyl-3,5-heptanedionato ligand) indicate single molecule magnet (SMM) behavior for all these complexes with large thermal energy barriers for the reversal of the magnetization and butterfly-shaped hysteresis loops at 2 K. Ab initio calculations on 1-3 show a pure Ising ground state for all of them, which induces almost completely suppressed quantum tunnelling magnetization (QTM), and thermally assisted quantum tunnelling magnetization (TA-QTM) relaxations via the first excited Kramers doublet, leading to large energy barriers, thus supporting the observation of SMM behavior. The comparison between the experimental and theoretical

  16. Thin Bioactive Zn Substituted Hydroxyapatite Coating Deposited on Ultrafine Grained Titanium Substrate: Structure Analysis

    Science.gov (United States)

    Prosolov, Konstantin A.; Belyavskaya, Olga A.; Muehle, Uwe; Sharkeev, Yurii P.

    2018-02-01

    Nanocrystalline Zn substituted hydroxyapatite coatings were deposited by radiofrequency magnetron sputtering on the surface of ultrafine-grained titanium substrates. Cross section transmission electron microscopy provided information about the morphology and texture of the thin film while in-column energy dispersive X-ray analysis confirmed the presence of Zn in the coating. The Zn substituted hydroxyapatite coating was formed by an equiaxed polycrystalline grain structure. Effect of substrate crystallinity on the structure of deposited coating is discussed. An amorphous TiO2 sublayer of 8 nm thickness was detected in the interface between the polycrystalline coating and the Ti substrate. Its appearance in the amorphous state is attributed to prior to deposition etching of the substrate and subsequent condensation of oxygen-containing species sputtered from the target. This layer contributes to the high coating-to-substrate adhesion. The major P-O vibrational modes of high intensity were detected by Raman spectroscopy. The Zn substituted hydroxyapatite could be a material of choice when antibacterial osteoconductive coating with a possibility of withstanding mechanical stress during implantation and service is needed.

  17. Thin Bioactive Zn Substituted Hydroxyapatite Coating Deposited on Ultrafine-Grained Titanium Substrate: Structure Analysis

    Directory of Open Access Journals (Sweden)

    Konstantin A. Prosolov

    2018-02-01

    Full Text Available Nanocrystalline Zn-substituted hydroxyapatite coatings were deposited by radiofrequency magnetron sputtering on the surface of ultrafine-grained titanium substrates. Cross-section transmission electron microscopy provided information about the morphology and texture of the thin film while in-column energy dispersive X-ray analysis confirmed the presence of Zn in the coating. The Zn-substituted hydroxyapatite coating was formed by an equiaxed polycrystalline grain structure. Effect of substrate crystallinity on the structure of deposited coating is discussed. An amorphous TiO2 sublayer of 8-nm thickness was detected in the interface between the polycrystalline coating and the Ti substrate. Its appearance in the amorphous state is attributed to prior to deposition etching of the substrate and subsequent condensation of oxygen-containing species sputtered from the target. This layer contributes to the high coating-to-substrate adhesion. The major P–O vibrational modes of high intensity were detected by Raman spectroscopy. The Zn-substituted hydroxyapatite could be a material of choice when antibacterial osteoconductive coating with a possibility of withstanding mechanical stress during implantation and service is needed.

  18. Electronic structure and photocatalytic activity of wurtzite Cu–Ga–S nanocrystals and their Zn substitution

    KAUST Repository

    Kandiel, Tarek

    2015-03-23

    Stoichiometric and gallium-rich wurtzite Cu-Ga-S ternary nanocrystals were synthesized via a facile solution-based hot injection method using 1-dodecanethiol as a sulfur source. The use of 1-dodecanethiol was found to be essential not only as a sulfur source but also as a structure-directing reagent to form a metastable wurtzite structure. In addition, the substitution of zinc in the wurtzite gallium-rich Cu-Ga-S nanocrystals was also investigated. The obtained nanocrystals were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), diffuse reflectance spectroscopy (DRS), photoluminescence (PL), and inductively coupled plasma atomic emission spectroscopy (ICP-OES). Electronic structures of pristine and the Zn-substituted Cu-Ga-S system were investigated using density functional theory (DFT) with HSE06 exchange-correlation functional. The calculated bandgaps accurately reflect the measured ones. The allowed electronic transitions occur upon the photon absorption from the (Cu + S) band towards the (Ga + S) one. The Zn substitution was found not to contribute to the band edge structure and hence altered the bandgaps only slightly, the direct transition nature remaining unchanged with the Zn substitution. The photocatalytic activities of H2 evolution from an aqueous Na2S/Na2SO3 solution under visible-light illumination on the synthesized nanocrystals were investigated. While the stoichiometric CuGaS2 exhibited negligible activity, the gallium-rich Cu-Ga-S ternary nanocrystals displayed reasonable activity. The optimum Zn substitution in the gallium-rich Cu-Ga-S ternary nanocrystals enhanced the H2 evolution rate, achieving an apparent quantum efficiency of >6% at 400 nm. © 2015 The Royal Society of Chemistry.

  19. Surface tension alteration on calcite, induced by ion substitution

    DEFF Research Database (Denmark)

    Sakuma, Hiroshi; Andersson, Martin Peter; Bechgaard, Klaus

    2014-01-01

    The interaction of water and organic molecules with mineral surfaces controls many processes in nature and industry. The thermodynamic property, surface tension, is usually determined from the contact angle between phases, but how does one understand the concept of surface tension at the nanoscale...... preferentially as ion pairs at solution-calcite interfaces. Mg2+ incorporation weakens organic molecule adhesion while strengthening water adsorption so Mg2+ substitution renders calcite more water wet. When Mg2+ replaces 10% of surface Ca2+, the contact angle changes dramatically, by 40 to 70, converting...

  20. Defects induced magnetic transition in Co doped ZnS thin films: Effects of swift heavy ion irradiations

    Energy Technology Data Exchange (ETDEWEB)

    Patel, Shiv P., E-mail: shivpoojanbhola@gmail.com [Physics Department, University of Allahabad, Allahabad 211002 (India); Pivin, J.C. [CSNSM, IN2P3-CNRS, Batiment 108, F-91405 Orsay Campus (France); Patel, M.K; Won, Jonghan [Materials Science and Technology Division, MST-8, P.O.Box 1663, Mail Stop G755, Los Alamos National Laboratory, Los Alamos, NM 87545 (United States); Chandra, Ramesh [Nanoscience Laboratory, IIC, Indian Institute of Technology, Roorkee 247667 (India); Kanjilal, D. [Inter University Accelerator Centre, Aruna Asaf Ali Marg, New Delhi 110067 (India); Kumar, Lokendra [Physics Department, University of Allahabad, Allahabad 211002 (India)

    2012-07-15

    The effect of swift heavy ions (SHI) on magnetic ordering in ZnS thin films with Co ions substituted on Zn sites is investigated. The materials have been synthesized by pulsed laser deposition on substrates held at 600 Degree-Sign C for obtaining films with wurtzite crystal structure and it showed ferromagnetic ordering up to room temperature with a paramagnetic component. 120 MeV Ag ions have been used at different fluences of 1 Multiplication-Sign 10{sup 11} ions/cm{sup 2} and 1 Multiplication-Sign 10{sup 12} ions/cm{sup 2} for SHI induced modifications. The long range correlation between paramagnetic spins on Co ions was destroyed by irradiation and the material became purely paramagnetic. The effect is ascribed to the formation of cylindrical ion tracks due to the thermal spikes resulting from electron-phonon coupling. - Highlights: Black-Right-Pointing-Pointer Effect of swift heavy ions on magnetic ordering in Co doped ZnS thin films are presented. Black-Right-Pointing-Pointer Magnetization in the pristine films is composed of ferromagnetic and paramagnetic components. Black-Right-Pointing-Pointer The films become purely paramagnetic after swift heavy ions irradiation. Black-Right-Pointing-Pointer The magnetic transition is ascribed to the formation of ion track (or cylindrical defects) due to the thermal spikes.

  1. ZnMoO4:Er3+,Yb3+ phosphor with controlled morphology and enhanced upconversion through alkali ions doping

    Science.gov (United States)

    Luitel, Hom Nath; Chand, Rumi; Watari, Takanori

    2018-04-01

    A facile hydrothermal method was used to synthesize ZnMoO4:Er3+,Yb3+ nanoparticles. The shapes and sizes of the nanoparticles were well tuned by simply monitoring the pH of the starting solution. Microballs consisting of agglomerated nanograins were observed at strong acidic condition. At mild pH, plates and rectangular particles were realized, while strong basic pH stabilized rods. Further increasing pH to extremely basic conditions (pH > 13), rods changed to fragile hairy structures. The nucleation and growth mechanism of nanograins to form different morphology nanoparticles were studied and illustrated. XRD patterns confirmed well crystalline, triclinic structure despite small amount of aliovalent metal ions doping. Under 980 nm excitation, the ZnMoO4:Er3+,Yb3+ nanophosphor exhibited strong green (centered at 530 and 560 nm) and weak red (centered at 660 nm) upconversion (UC) emissions. Substitution of part of the Zn2+ ions by monovalent alkali ions intensified the UC emission intensities drastically. The order of intensification was K+>Na+>Li+>Rb+>no alkali ion. When Zn2+ ions were substituted with 10 at% K+ ions, the green and red UC emissions intensities increased by more than 50 and 15 folds, respectively. Time dependent measurements confirmed efficient Yb to Er energy transfer in the ZnMoO4:Er3+,Yb3+,K+ nanophosphor. The optimized ZnMoO4:Er3+,Yb3+,K+ phosphor exhibited intense UC emissions with 0.31% quantum yield. The upconverted light is visible to naked eye while pumping by laser of less than 1 mW power and opens door for variety of novel applications.

  2. Lattice dynamics and vibration modes frequencies for substitutional impurities in InP, GaP and ZnS

    International Nuclear Information System (INIS)

    Vandevyver, Michel; Plumelle, Pierre.

    1977-01-01

    The model used is a rigid-ion model with an effective ionic charge including general interactions for nearest and next nearest neighbours and long range Coulomb interactions. It provides a good fit with available neutron data and with infrared absorption results for InP. In this model, no hypothesis is made a priori on the interatomic forces and the eleven parameters given by the model are used. A mathematical model which employs a Green's function technique in the mass defect and the nearest neighbour force constant defect approximation is used to calculate the lattice dynamics of the imperfect crystal. The frequencies of the local modes, the gap modes and the band modes, are given for isolated substitutional impurities. The same calculation is achieved for GaP and ZnS and the results are compared with infrared data [fr

  3. Bond length variation in Zn substituted NiO studied from extended X-ray absorption fine structure

    Science.gov (United States)

    Singh, S. D.; Poswal, A. K.; Kamal, C.; Rajput, Parasmani; Chakrabarti, Aparna; Jha, S. N.; Ganguli, Tapas

    2017-06-01

    Bond length behavior for Zn substituted NiO is determined through extended x-ray absorption fine structure (EXAFS) measurements performed at ambient conditions. We report bond length value of 2.11±0.01 Å for Zn-O of rock salt (RS) symmetry, when Zn is doped in RS NiO. Bond length for Zn substituted NiO RS ternary solid solutions shows relaxed behavior for Zn-O bond, while it shows un-relaxed behavior for Ni-O bond. These observations are further supported by first-principles calculations. It is also inferred that Zn sublattice remains nearly unchanged with increase in lattice parameter. On the other hand, Ni sublattice dilates for Zn compositions up to 20% to accommodate increase in the lattice parameter. However, for Zn compositions more than 20%, it does not further dilate. It has been attributed to the large disorder that is incorporated in the system at and beyond 20% of Zn incorporation in the cubic RS lattice of ternary solid solutions. For these large percentages of Zn incorporation, the Ni and the Zn atoms re-arrange themselves microscopically about the same nominal bond length rather than systematically increase in magnitude to minimize the energy of the system. This results in an increase in the Debye-Waller factor with increase in the Zn concentration rather than a systematic increase in the bond lengths.

  4. Spectrum designation and effect of Al substitution on the luminescence of Cr3+ doped ZnGa2O4 nano-sized phosphors

    International Nuclear Information System (INIS)

    Zhang Weiwei; Zhang Junying; Chen Ziyu; Wang Tianmin; Zheng Shukai

    2010-01-01

    Low-temperature photoluminescent spectra of ZnGa 2 O 4 :Cr 3+ nano-sized phosphors calcined at different temperatures were reported. The fine structure of the emission spectra has been designated to Cr 3+ ions in different sites including ideal octahedral, Zn-interstitial, Ga ZN 4 -Zn Ga 6 sites and Ga 2 O 3 impurity. The vibronic sidebands for both Stokes' and anti-Stokes' sides are related to the host lattice vibrations, which were confirmed by IR and Raman spectra. Al 3+ is substituted in Ga 3+ sites to form Zn(Ga 1-y Al y ) 2 O 4 :Cr 0.01 3+ (0≤y≤0.5). The blue shift and luminescent intensity variations of the charge transfer band and 3d-3d transitions in the spectra caused by Al substitution were related to larger band gap and stronger crystal field, respectively. The calculated crystal-field parameters indicated that Al incorporation enhanced the crystal field strength and induced more trigonal distortion due to different radii of Al 3+ and Ga 3+ .

  5. Effect of bismuth ion substitution on structural properties of zinc ferrite nanoparticles

    Directory of Open Access Journals (Sweden)

    Naraavula Suresh Kumar

    2016-06-01

    Full Text Available Bismuth doped nano zinc ferrite particles having the general formula ZnFe2-xBixO4 (x = 0.00, 0.05, 0.10, 0.15, 0.20 and 0.25 were synthesized by sol-gel combustion method. The effect of bismuth doping on structural properties were investigated. The X-ray diffraction (XRD spectra confirm the single phase cubic spinel structure. The average crystallite sizes of all the samples were determined by Debye-Scherrer equation and are in the range 16–20 nm. The lattice parameter increases with the increase of bismuth ion concentration. This is due to the larger ionic radius of Bi3+ ions substituting smaller Fe3+ ions at octahedral sites (B-sites. The surface morphology of all compounds was studied by scanning electron microscope (SEM. The microstructure analysis and the particle size were examined by transmission electron microscope (TEM. The compositional stoichiometry of these samples was verified by energy dispersive spectroscopy (EDS analysis.

  6. Vacancy defect and defect cluster energetics in ion-implanted ZnO

    Science.gov (United States)

    Dong, Yufeng; Tuomisto, F.; Svensson, B. G.; Kuznetsov, A. Yu.; Brillson, Leonard J.

    2010-02-01

    We have used depth-resolved cathodoluminescence, positron annihilation, and surface photovoltage spectroscopies to determine the energy levels of Zn vacancies and vacancy clusters in bulk ZnO crystals. Doppler broadening-measured transformation of Zn vacancies to vacancy clusters with annealing shifts defect energies significantly lower in the ZnO band gap. Zn and corresponding O vacancy-related depth distributions provide a consistent explanation of depth-dependent resistivity and carrier-concentration changes induced by ion implantation.

  7. Structural and magnetic Properties of TbZn-substituted calcium barium M-type nano-structured hexa-ferrites

    Energy Technology Data Exchange (ETDEWEB)

    Khan, Hasan M. [Department of Physics, Bahauddin Zakariya University, Multan 60800 (Pakistan); Department of Electronics, University of York, York YO10 5DD (United Kingdom); Islam, M.U., E-mail: dr.misbahulislam@bzu.edu.pk [Department of Physics, Bahauddin Zakariya University, Multan 60800 (Pakistan); Xu, Yongbing [Department of Electronics, University of York, York YO10 5DD (United Kingdom); Nanjing–York International Centre of Spintronics and Nano-Engineering, Nanjing University, Nanjing 210093 (China); Asif Iqbal, M. [Department of Physics, Bahauddin Zakariya University, Multan 60800 (Pakistan); National University of Science and Technology, College of E and ME, Islamabad (Pakistan); Ali, Irshad [Department of Physics, Bahauddin Zakariya University, Multan 60800 (Pakistan)

    2014-03-15

    Highlights: • Tb–Zn substituted Ca{sub 0.5}Ba{sub 0.5}Fe{sub 12}O{sub 19} samples exhibit single magnetoplumbite phase. • Lattice parameters a and c have increasing values. • Coercivity can be tuned at lower substitution level • Crystallites size was found in the range 18–25 nm by TEM and by Scherrer formula. • These hexa-ferrites are suitable for microwave devices and magnetic recording media. -- Abstract: Effect of TbZn substitution on the structural and magnetic properties of Ca{sub 0.5}Ba{sub 0.5−x}Tb{sub x}Zn{sub y}Fe{sub 12−y}O{sub 19}, (x = 0.00–0.10; y = 0.00–1.00) ferrites prepared by sol–gel auto combustion is reported. The synthesized samples were characterized by Fourier transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy, transmission electron microscopy and Vibrating Sample magnetometery. The X-ray diffraction analysis confirmed single phase M-type hexa-ferrite structure. The lattice parameters were found to increase as TbZn contents increases, which is attributed to the ionic sizes of the implicated cations. The TbZn seems to be completely soluble in the lattice. The results of scanning electron microscopy and transmission electron microscopy shows that the grain size decreases with increase of TbZn substitution. The coercivity values (1277–2025 Oe) of all samples lies in the range of M-type hexa-ferrite and indicate that an increase of anisotropy was achieved by substitution of TbZn, while the size of nanoparticles was drastically reduced between 18 and 25 nm. The increased anisotropy and fine particle size are useful for many applications, such as improving signal noise ratio of recording devices.

  8. Partial substitution of Zn Effects on the Structural and Electrical Properties of High Temperature Hg0.95Ag0.05Ba2Ca2Cu3O8+δ Superconductors

    Science.gov (United States)

    Abed, Noor S.; Fathi, Sabah J.; Jassim, Kareem A.; Mahdi, Shatha H.

    2018-05-01

    The effect of the Ag partial substitution at Hg site in HgOδ layer and Zn partial substitution at Ca site in CaO layer on the structure,Tc,electrical properties, and oxygen content for Hg-1223 have been studied. Bulk polycrystalline Hg1-xAgxBa2Ca2-yZnyCu3O8+δ compound samples with x=0.05 and y=0.0, 0.05, 0.1, 0.15, 0.2, 0.25, and 0.3, are synthesized by a solid state reaction process. Structural properties are studied by using X-ray powder pattern, the high temperature phase superconductor (Hg-1223) of the tetragonal structure didn't change with the partial substitution of Zn and Ag ions, lattice parameters c,c/a are established to vary with Ag and Zn- substitution. The surface morphology has been studied by using atomic force microscopes (AFM), showed that all specimens have good crystalline and homogeneous surface. Also give a best nano size value is 75.72 nm at x=0.05 and y=0.3. Four probe technique is used to measure Tc. The Tc were found to be increases from 129 K to 147 K and oxygen content were found to be increases with increasing Zn. In addition, dielectric properties (dielectric constant, dielectric loss factor, and the alternating electrical conductivity) are characterized directly by relating with Ag and Zn concentration.

  9. Improvement of in vitro corrosion and cytocompatibility of biodegradable Fe surface modified by Zn ion implantation

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Henan; Zheng, Yang; Li, Yan, E-mail: liyan@buaa.edu.cn; Jiang, Chengbao

    2017-05-01

    Highlights: • Fe{sub 2}O{sub 3}/ZnO oxides were formed on the surface of Zn implanted pure Fe samples. • The corrosion rate of the pure Fe in SBF was increased after Zn implantation. • Cytocompatibility of the pure Fe was improved by Zn ion implantation. - Abstract: Pure Fe was surface-modified by Zn ion implantation to improve the biodegradable behavior and cytocompatibility. Surface topography, chemical composition, corrosion resistance and cytocompatibility were investigated. Atomic force microscopy, auger electron spectroscopy and X-ray photoelectron spectroscopy results showed that Zn was implanted into the surface of pure Fe in the depth of 40–60 nm and Fe{sub 2}O{sub 3}/ZnO oxides were formed on the outmost surface. Electrochemical measurements and immersion tests revealed an improved degradable behavior for the Zn-implanted Fe samples. An approximately 12% reduction in the corrosion potential (E{sub corr}) and a 10-fold increase in the corrosion current density (i{sub corr}) were obtained after Zn ion implantation with a moderate incident ion dose, which was attributed to the enhanced pitting corrosion. The surface free energy of pure Fe was decreased by Zn ion implantation. The results of direct cell culture indicated that the short-term (4 h) cytocompatibility of MC3T3-E1 cells was promoted by the implanted Zn on the surface.

  10. The role of ion exchange in the passivation of In(Zn)P nanocrystals with ZnS

    Science.gov (United States)

    Cho, Deok-Yong; Xi, Lifei; Boothroyd, Chris; Kardynal, Beata; Lam, Yeng Ming

    2016-03-01

    We have investigated the chemical state of In(Zn)P/ZnS core/shell nanocrystals (NCs) for color conversion applications using hard X-ray absorption spectroscopy (XAS) and photoluminescence excitation (PLE). Analyses of the edge energies as well as the X-ray absorption fine structure (XAFS) reveal that the Zn2+ ions from ZnS remain in the shell while the S2- ions penetrate into the core at an early stage of the ZnS deposition. It is further demonstrated that for short growth times, the ZnS shell coverage on the core was incomplete, whereas the coverage improved gradually as the shell deposition time increased. Together with evidence from PLE spectra, where there is a strong indication of the presence of P vacancies, this suggests that the core-shell interface in the In(Zn)P/ZnS NCs are subject to substantial atomic exchanges and detailed models for the shell structure beyond simple layer coverage are needed. This substantial atomic exchange is very likely to be the reason for the improved photoluminescence behavior of the core-shell particles compare to In(Zn)P-only NCs as S can passivate the NCs surfaces.

  11. Exploratory studies of element substitutions in synthetic tetrahedrite. Part II. Selenium and tellurium as anions in Zn-Fe tetrahedrites

    DEFF Research Database (Denmark)

    Karup-Møller, Sven; Makovicky, E.

    1999-01-01

    -free) compositons do not materialize. The substituted Se tetrahedrite coexists with Cu3SbSe3, (iron-bearing) Cu2-xSe, Cu3SbSe4 plus/minus low Zn-sulfide melt. Selenium does not adopt the role of cation and tellurium that of anion in the tetrahedrite structure. The explanation of the severely restricted composition...

  12. Electrical modulus and dielectric behavior of Cr{sup 3+} substituted Mg–Zn nanoferrites

    Energy Technology Data Exchange (ETDEWEB)

    Mansour, S.F.; Abdo, M.A.

    2017-04-15

    The dielectric parameters and ac electrical conductivity of Mg{sub 0.8}Zn{sub 0.2}Cr{sub x}Fe{sub 2−x}O{sub 4}; (0≤x≤0.025) nanoferrites synthesized citrate–nitrate auto-combustion method were studied using the complex impedance technique in the frequency and temperature ranges 4 Hz–5 MHz and 303–873 K respectively. Hopping of charge carriers plus interfacial polarization could interpret the behaviors of dielectric constant (ε′), dielectric loss tangent (tanδ) and ac electrical conductivity (σ{sub ac}) with frequency, temperatures and composition. The up-normal behavior observed in tanδ trend with temperatures confirms the presence of relaxation loss (dipoles losses). Correlated barrier hopping (CBH) of electron is the conduction mechanism of the investigated nanoferrites. Cole-Cole plots at different temperatures emphasize the main role of grain and grain boundaries in the properties of the investigated nanoferrites. Cr{sup 3+} substitution can control the dielectric parameters and ac electrical conductivity of Mg-Zn nanoferrites making it candidates for versatile applications. - Highlights: • The composition dependence of ε′, tanδ, and σ{sub ac} showed the same trend. • CBH model is the conduction mechanism of the investigated nanoferrite. • Cole-Cole plots confirmed the role of grain and grain boundaries in our nanoferrites.

  13. Magnetic, hyperthermic and structural properties of zn substituted CaFe2O4 powders

    Science.gov (United States)

    Kheradmand, Abbas; Vahidi, Omid; Masoudpanah, S. M.

    2018-03-01

    In the present study, we have synthesized single phase Ca1 - x Zn x Fe2O4 powders by hydrothermal method. The cation distribution between the tetrahedral and octahedral sites in the spinel structure and the magnetic properties as a function of the zinc substitution have been investigated by X-ray diffraction (XRD), infrared spectroscopy and vibrating sample magnetometer methods. The obtained XRD pattern indicated that the synthesized particles had single phase cubic spinel structure with no impurity. The magnetic measurements showed that the saturation magnetization increased from 83 to 98 emu/g with the addition of zinc due to the decrease of inversity. The particle size observed by electron microscopy decreased from 1.38 to 0.97 µm with the increase of zinc addition. The Ca0.7Zn0.3Fe2O4 powders exhibited appropriate heating capability for hyperthermia applications with the maximum AC heating temperature of 20 °C and specific loss power of 9.29 W/g.

  14. The O-H Bond Dissociation Energies of Substituted Phenols and Proton Affinities of Substituted Phenoxide Ions: A DFT Study

    Directory of Open Access Journals (Sweden)

    Tadafumi Uchimaru

    2002-04-01

    Full Text Available Abstract: The accurate O-H bond dissociation enthalpies for a series of meta and para substituted phenols (X-C6H4-OH, X=H, F, Cl, CH3, OCH3, OH, NH2, CF3, CN, and NO2 have been calculated by using the (ROB3LYP procedure with 6-311G(d,p and 6-311++G(2df,2p basis sets. The proton affinities of the corresponding phenoxide ions (XC6H4-O- have also been computed at the same level of theory. The effect of change of substituent position on the energetics of substituted phenols has been analyzed. The correlations of Hammett’s substituent constants with the bond dissociation enthalpies of the O-H bonds of phenols and proton affinities of phenoxide ions have been explored.

  15. Effects of site substitution and metal ion addition on doped manganites

    CERN Document Server

    Pradhan, A K; Roul, B K; Sahu, D R; Muralidhar, M

    2002-01-01

    We report transport, magnetization and transmission electron microscopy studies of the effects of A-and B-site substitution, and the addition of metal ions such as Pt, Ag and Sr, on doped ABO sub 3 perovskites, where A = La, Pr etc and B = Mn. Disorder induced by such substitution changes the behaviour of the charge-ordered (CO) state significantly. A-and B-site substitution suppresses the CO phase due to size mismatch and disorder produced by inhomogeneity. On the other hand, addition of metal ions such as Pt and Ag improves several colossal-magnetoresistance properties significantly due to microstructural effects and enhanced current percolation through grain boundaries.

  16. Study of coordinated system Zn(II)- isoleucine-isoleuciante ion; Estudio del sistema coordinado Zn(II)-Isoleucina neutra-ion isolencionato

    Energy Technology Data Exchange (ETDEWEB)

    Ruiz Morales, J.C.; Cuesta Gonzalez, M. de la; Cuesta Sanchez, M.; Rodriguez-Placeres, J.C. [Departamento de Quimica Fisica, Universidad de la Laguna, Tenerife (Spain)

    1996-11-01

    The polarographic method has been applied to the study of the coordinated system Zn(II)-isoleucine-isoleucinate ion, in aqueous medium, l=1.0M(NaClO{sub 4}) and T=25+- 0.05 degree centigree. The stabilization of the coordinated species [Zn(HI)]``2+ (Beta{sub 1}0=1.7), [Zn(I)]``+ (Beta{sub 0}1=5.6.10``4) and [Zn(HI)(I)]``+ (Beta{sub 1}1=1.1.10``5) has been stablished. (Author) 12 refs.

  17. Suppression and enhancement of deep level emission of ZnO on Si4+ & V5+ substitution

    Science.gov (United States)

    Srivastava, T.; Bajpai, G.; Sen, S.

    2018-03-01

    ZnO possess a wide range of tunable properties depending on the type and concentration of dopant. Defects in ZnO due to doped aliovalent ions can generate certain functionalities. Such defects in the lattice do not deteriorate the material properties but actually modifies the material towards infinite number of possibilities. Defects like oxygen vacancies play a significant role in photocatalytic and sensing applications. Depending upon the functionality, defect state of ZnO can be modified by suitable doping. Amount and nature of different dopant has different effect on defect state of ZnO. It depends upon the ionic radii, valence state, chemical stability etc. of the ion doped. Two samples with two different dopants i.e., silicon and vanadium, Zn1-xSixO and Zn1-xVxO, for x=0 & 0.020, were synthesized using solgel method (a citric acid-glycerol route) followed by solid state sintering. A comparison of their optical properties, photoluminescence and UV-Vis spectroscopy, with pure ZnO was studied at room temperature. Silicon doping drastically reduces whereas vanadium doping enhances the green emission as compared with pure ZnO. Suppression and enhancement of defect levels (DLE) is rationalized by the effects of extra charge present on Si4+ & V5+ (in comparison to Zn2+) and formation of new hybrid state (V3d O2p) within bandgap. Reduction of defects in Zn1-xSixO makes it suitable material for opto-electronics application whereas enhancement in defects in Zn1-xVxO makes it suitable material for photocatalytic as well as gas sensing application.

  18. Adsorption behaviour and kinetics of exchange of Zn2+ and Eu3+ ions on a composite ion exchanger

    International Nuclear Information System (INIS)

    Morcos, T.N.

    2007-01-01

    Equilibria and kinetics of exchange of both Zn2+ and Eu3+ ions on a composite ion-exchanger, cobalt hexacyanocobaltate (III) (CoHCC) incorporated in polyacrylonitrile (PAN), has been studied. The apparent capacity of CoHCC-PAN for Zn2+ and Eu3+ was determined and found to be 0.353 and 0.69 meq/g, respectively. The higher capacity for Eu3+ ions than that for Zn2+ ions is due to the higher electrostatic interaction strength of the higher charge ion with the surface. Freundlich and Langmiur adsorption isotherms were used to investigate solute (Zn2+ or Eu3+) exchange phenomenon at the liquid/solid interface. The results indicated that both Langmuir and Freundlich isotherms fit well for both Zn2+ and Eu3+. Sorption data have been also treated with the Dubinin-Radushkevich equation. The kinetics of Zn2+ or Eu3+ sorption on the composite seems to show that the reaction was proceed via two steps. The first one was fast and probably due to adsorption followed by a slow exchange reaction. In view of the data obtained on the effect of particle size and metal ion concentrations on the rate of exchange reaction, it is concluded that the mechanism for both ions was chemical control. Generally, it seems that there are two exchange sites chemically equivalent but present in pores of different sizes which lead to different degrees of dehydration of the ions sorbed on the two sites

  19. Luminescence enhancement of (Sr1-x Mx )2 SiO4 :Eu2+ phosphors with M (Ca2+ /Zn2+ ) partial substitution for white light-emitting diodes.

    Science.gov (United States)

    Wang, Yulong; Zhang, Wentao; Gao, Yang; Long, Jianping; Li, Junfeng

    2017-02-01

    Eu 2 + -doped Sr 2 SiO 4 phosphor with Ca 2 + /Zn 2 + substitution, (Sr 1-x M x ) 2 SiO 4 :Eu 2 + (M = Ca, Zn), was prepared using a high-temperature solid-state reaction method. The structure and luminescence properties of Ca 2 + /Zn 2 + partially substituted Sr 2 SiO 4 :Eu 2 + phosphors were investigated in detail. With Ca 2 + or Zn 2 + added to the silicate host, the crystal phase could be transformed between the α-form and the β-form of the Sr 2 SiO 4 structure. Under UV excitation at 367 nm, all samples exhibit a broad band emission from 420 to 680 nm due to the 4f 6 5d 1  → 4f 7 transition of Eu 2 + ions. The broad emission band consists of two peaks at 482 and 547 nm, which correspond to Eu 2 + ions occupying the ten-fold oxygen-coordinated Sr.(I) site and the nine-fold oxygen-coordinated Sr.(II) site, respectively. The luminescence properties, including the intensity and lifetime of Sr 2 SiO 4 :Eu 2 + phosphors, improved remarkably on Ca 2 + /Zn 2 + addition, and promote its application in white light-emitting diodes. Copyright © 2016 John Wiley & Sons, Ltd. Copyright © 2016 John Wiley & Sons, Ltd.

  20. The Substitution of IVD (Ion Vapor Deposition) Aluminum for Cadmium

    Science.gov (United States)

    1989-08-01

    thus lose the anvantages the substitution nay offer suco as improveu perfornance arc/or the elimination of hazaruous waste production. This report...various processe-s are snown in Tlaole 31. The lVU alumiinum capitai cost includes the cooTter arc ucoicoted equipmient suco as a grit olaster ano glass

  1. A study on photoelectrochemical properties of ZnO@ZnS nanostructures synthesized via facile ion-exchange approach

    Science.gov (United States)

    Sharma, Akash; Sahoo, Pooja; Thangavel, R.

    2018-05-01

    In this work, ZnO nanorods (NRs) were fabricated, on cleaned ITO substrates by using sol-gel spin coating followed by hydrothermal technique. In order to coat zinc sulphide (ZnS) layers on the earlier prepared NRs a facile ion-exchange approach was adopted. The ZnO@ZnS nanostructures so prepared were characterised by using X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), UV-visible spectroscopy and photoelectrochemical study. XRD spectra confirmed the hexagonal wurtzite structure of all the samples along with preferential c-axis orientation. Further it was also observed from the FESEM images that sulfidation process doesn't affect the structure of ZnO NRs arrays. From the absorption spectra it can be clearly observed that the light absorbing property has increased in within the visible range due to the formation of ZnS layer on the ZnO nanostructures, which is not possible for either of the material individually. The cyclic voltammetry results indicates the enhancement in photocurrent density after illumination for the synthesized nanostructures. The electrocatalytic behaviour of ZnO@ZnS electrodes have been studied using a 3-electrode system in presence of 0.1M NaOH electrolyte solution with respect to an Ag/AgCl reference electrode.

  2. PSynthesis, characterization and electromagnetic properties of Zn-substituted CoFe{sub 2}O{sub 4} via sucrose assisted combustion route

    Energy Technology Data Exchange (ETDEWEB)

    Gabal, M.A., E-mail: mgabalabdonada@yahoo.com [Chemistry Department, Faculty of Science, King Abdulaziz University, Jeddah (Saudi Arabia); Al-Juaid, A.A.; Al-Rashed, S.M.; Hussein, M.A. [Chemistry Department, Faculty of Science, King Abdulaziz University, Jeddah (Saudi Arabia); Al-Marzouki, F. [Physics Department, Faculty of Science, King Abdulaziz University, Jeddah (Saudi Arabia)

    2017-03-15

    Nanocrystalline Co{sub 1−x}Zn{sub x}Fe{sub 2}O{sub 4} ferrites (0.0≤x≤0.1) were synthesized via simple, economic and environmentally friend sucrose auto-combustion method. An appropriate mechanism for complexation process as well as ferrites formation was suggested and discussed. The detailed structural studies were estimated through X-ray diffractometer (XRD), Fourier transform infrared spectroscopy (FT-IR) and transmission electron microscopy (TEM) measurements. The results confirmed the formation of mixed spinel phase with cubic structure and exhibited a gradual decrease in the crystal size from 58 nm to 20 nm by the addition of zinc. Based on the obtained structural parameters, an appropriate cation distribution was suggested and reinforced via electrical and magnetic properties measurements. Hysteresis loops measurements, indicated ferromagnetic characteristics, with hard magnetic properties, for the samples with 0.0≤x≤0.6. The samples with higher Zn-content exhibited paramagnetic properties. The changes in the magnetization and coercivity by the addition of zinc can be discussed in the view of the influence of cationic stoichiometry and magneto-crystalline anisotropy, respectively. The huge decrease in the magnetization value at x≥0.8 suggested a shift from ferromagnetic to paramagnetic characteristics. Ac-conductivity as well as dielectric constant behaviors reinforced this magnetic transition. The obtained Curie transition temperatures (T{sub C}) were gradually shifted to lower temperatures by the addition of zinc. The addition of zinc results in the substitution of Co{sup 2+} ions in the octahedral sites thus, decreases B-B hopping probability, decreases conductivity and consequently increases activation energy. The most predominant conduction mechanisms in the ferromagnetic and paramagnetic regions are expected to be due to electron hoppings between different valence state ions and small positive polaron migration, respectively. - Graphical

  3. H passivation of Li on Zn-site in ZnO: Positron annihilation spectroscopy and secondary ion mass spectrometry

    Science.gov (United States)

    Johansen, K. M.; Zubiaga, A.; Tuomisto, F.; Monakhov, E. V.; Kuznetsov, A. Yu.; Svensson, B. G.

    2011-09-01

    The interaction of hydrogen (H) with lithium (Li) and zinc vacancies (VZn) in hydrothermally grown n-type zinc oxide (ZnO) has been investigated by positron annihilation spectroscopy (PAS) and secondary ion mass spectrometry. Li on Zn-site (LiZn) is found to be the dominant trap for migrating H atoms, while the trapping efficiency of VZn is considerably smaller. After hydrogenation, where the LiZn acceptor is passivated via formation of neutral LiZn-H pairs, VZn occurs as the prime PAS signature and with a concentration similar to that observed in nonhydrogenated Li-poor samples. Despite a low efficiency as an H trap, the apparent concentration of VZn in Li-poor samples decreases after hydrogenation, as detected by PAS, and evidence for formation of the neutral VZnH2 complex is presented.

  4. Structural, morphological and electrical properties of Sn-substituted Ni-Zn ferrites synthesized by double sintering technique

    Energy Technology Data Exchange (ETDEWEB)

    Ali, M.A. [Department of Physics, Chittagong University of Engineering and Technology (CUET), Chittagong 4349 (Bangladesh); Uddin, M.M., E-mail: mohi@cuet.ac.bd [Department of Physics, Chittagong University of Engineering and Technology (CUET), Chittagong 4349 (Bangladesh); Khan, M.N.I. [Materials Science Division, Atomic Energy Center, Dhaka 1000 (Bangladesh); Chowdhury, F.U.-Z. [Department of Physics, Chittagong University of Engineering and Technology (CUET), Chittagong 4349 (Bangladesh); Haque, S.M. [Materials Science Division, Atomic Energy Center, Dhaka 1000 (Bangladesh)

    2017-02-15

    The Sn-substituted Ni-Zn ferrites, (0.0≤x≤0.30), have been synthesized by the standard double sintering technique from the oxide nanopowders of Ni, Zn, Fe and Sn. The structural and electrical properties have been investigated by the X-ray diffraction (XRD), scanning electron microscopy (SEM), DC resistivity and dielectric measurements. From XRD data, the single cubic spinel phase has been confirmed for x≤0.1, whereas for x>0.1 an extra intermediate phase has been detected along with the cubic spinel phase of Ni-Zn ferrite. The grain size is increased due to Sn substitution in Ni-Zn ferrites. DC resistivity as a function of temperature has been measured by two probe method. The semiconducting nature has been found operative in the samples. The DC resistivity was found to decrease whilst the dielectric constant increased with increasing Sn content in Ni-Zn ferrites. The unusual behavior of the dielectric loss factor of the ferrites was explained by the Rezlescu model. The electrical relaxation of the ferrites has been studied in terms of electric modulus formalism and the time for dielectric relaxation was calculated. The contribution of grain resistance has been studied from the Cole-Cole plot. The suitability to use the as prepared samples in the miniaturized memory devices based capacitive components or energy storage principles are confirmed from the values of dielectric constant. - Highlights: • Sn-substituted Ni-Zn ferrites with cubic spinel structure have been synthesized. • a{sub th} is calculated and well compared with a{sub expt}. • Dielectric unusual behavior has been successfully explained by the Rezlescu model. • Long τ (ns) is determined, can be utilized for memory and spintronics devices.

  5. Synthesis, structural investigation and magnetic properties of Zn2+ substituted cobalt ferrite nanoparticles prepared by the sol–gel auto-combustion technique

    International Nuclear Information System (INIS)

    Raut, A.V.; Barkule, R.S.; Shengule, D.R.; Jadhav, K.M.

    2014-01-01

    Structural morphology and magnetic properties of the Co 1−x Zn x Fe 2 O 4 (0.0≤x≥1.0) spinel ferrite system synthesized by the sol–gel auto-combustion technique using nitrates of respective metal ions have been studied. The ratio of metal nitrates to citric acid was taken at 1:3. The as prepared powder of cobalt zinc ferrite was sintered at 600 °C for 12 h after TG/DTA thermal studies. Compositional stoichiometry was confirmed by energy dispersive analysis of the X-ray (EDAX) technique. Single phase cubic spinel structure of Co–Zn nanoparticles was confirmed by XRD data. The average crystallite size (t), lattice constant (a) and other structural parameters of zinc substituted cobalt ferrite nanoparticles were calculated from XRD followed by SEM and FTIR. It is observed that the sol–gel auto-combustion technique has many advantages for the synthesis of technologically applicable Co–Zn ferrite nanoparticles. The present investigation clearly shows the effect of the synthesis method and possible relation between magnetic properties and microstructure of the prepared samples. Increase in nonmagnetic Zn 2+ content in cobalt ferrite nanoparticles is followed by decrease in n B , M s and other magnetic parameters. Squareness ratio for the Co-ferrite was 1.096 at room temperature. - Highlights: • Co–Zn nanoparticles are prepared by sol–gel auto-combustion method. • Structural properties were characterized by XRD, SEM, and FTIR. • Compositional stoichiometry was confirmed by EDAX analysis. • Magnetic parameters were measured by the pulse field hysteresis loop technique

  6. Synthesis, structural investigation and magnetic properties of Zn{sup 2+} substituted cobalt ferrite nanoparticles prepared by the sol–gel auto-combustion technique

    Energy Technology Data Exchange (ETDEWEB)

    Raut, A.V., E-mail: nano9993@gmail.com [Vivekanand Arts and Sardar Dalipsingh Commerce and Science College, Aurangabad, 431004 Maharastra (India); Barkule, R.S.; Shengule, D.R. [Vivekanand Arts and Sardar Dalipsingh Commerce and Science College, Aurangabad, 431004 Maharastra (India); Jadhav, K.M., E-mail: drjadhavkm@gmail.com [Department of Physics, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad, 431004 Maharastra (India)

    2014-05-01

    Structural morphology and magnetic properties of the Co{sub 1−x}Zn{sub x}Fe{sub 2}O{sub 4} (0.0≤x≥1.0) spinel ferrite system synthesized by the sol–gel auto-combustion technique using nitrates of respective metal ions have been studied. The ratio of metal nitrates to citric acid was taken at 1:3. The as prepared powder of cobalt zinc ferrite was sintered at 600 °C for 12 h after TG/DTA thermal studies. Compositional stoichiometry was confirmed by energy dispersive analysis of the X-ray (EDAX) technique. Single phase cubic spinel structure of Co–Zn nanoparticles was confirmed by XRD data. The average crystallite size (t), lattice constant (a) and other structural parameters of zinc substituted cobalt ferrite nanoparticles were calculated from XRD followed by SEM and FTIR. It is observed that the sol–gel auto-combustion technique has many advantages for the synthesis of technologically applicable Co–Zn ferrite nanoparticles. The present investigation clearly shows the effect of the synthesis method and possible relation between magnetic properties and microstructure of the prepared samples. Increase in nonmagnetic Zn{sup 2+} content in cobalt ferrite nanoparticles is followed by decrease in n{sub B}, M{sub s} and other magnetic parameters. Squareness ratio for the Co-ferrite was 1.096 at room temperature. - Highlights: • Co–Zn nanoparticles are prepared by sol–gel auto-combustion method. • Structural properties were characterized by XRD, SEM, and FTIR. • Compositional stoichiometry was confirmed by EDAX analysis. • Magnetic parameters were measured by the pulse field hysteresis loop technique.

  7. The effect of Ce ion substituted OMS-2 nanostructure in catalytic activity for benzene oxidation

    Science.gov (United States)

    Hou, Jingtao; Li, Yuanzhi; Mao, Mingyang; Zhao, Xiujian; Yue, Yuanzheng

    2014-11-01

    The nanostructure of Ce doped OMS-2 plays a very important role in its catalytic property. We demonstrate by density functional theory (DFT) calculations that the unique nanostructure of the Ce ion substituted OMS-2 with Mn vacancy in the framework is beneficial for the improvement of catalytic activity, while the nanostructure of the Ce ion substituted OMS-2 without defects are detrimental to the catalytic activity. We establish a novel and facile strategy of synthesizing these unique Ce ion substituted OMS-2 nanostructure with Mn vacancies in the framework by hydrothermal redox reaction between Ce(NO3)3 and KMnO4 with KMnO4/Ce(NO3)3 at a molar ratio of 3 : 1 at 120 °C. Compared to pure OMS-2, the produced catalyst of Ce ion substituted OMS-2 ultrathin nanorods exhibits an enormous enhancement in the catalytic activity for benzene oxidation, which is evidenced by a significant decrease (ΔT50 = 100 °C, ΔT90 = 129 °C) in the reaction temperature of T50 and T90 (corresponding to the benzene conversion = 50% and 90%), which is considerably more efficient than the expensive supported noble metal catalyst (Pt/Al2O3). We combine both theoretical and experimental evidence to provide a new physical insight into the significant effect due to the defects induced by the Ce ion substitution on the catalytic activity of OMS-2. The formation of unique Ce ion substituted OMS-2 nanostructure with Mn vacancies in the framework leads to a significant enhancement of the lattice oxygen activity, thus tremendously increasing the catalytic activity.The nanostructure of Ce doped OMS-2 plays a very important role in its catalytic property. We demonstrate by density functional theory (DFT) calculations that the unique nanostructure of the Ce ion substituted OMS-2 with Mn vacancy in the framework is beneficial for the improvement of catalytic activity, while the nanostructure of the Ce ion substituted OMS-2 without defects are detrimental to the catalytic activity. We establish a novel

  8. Transport of Zn(OH)4(-2) ions across a polyolefin microporous membrane

    Science.gov (United States)

    Krejci, Ivan; Vanysek, Peter; Trojanek, Antonin

    1993-04-01

    Transport of ZN(OH)4(2-) ions through modified microporous polypropylene membranes (Celgard 3401, 350140) was studied using polarography and conductometry. Soluble Nafion as an ion exchange modifying agent was applied to the membrane by several techniques. The influence of Nafion and a surfactant on transport of zinc ions through the membrane was studied. A relationship between membrane impedance and the rate of Zn(OH)4(2-) transport was found. The found correlation between conductivity, ion permeability and Nafion coverage suggests a suitable technique of membrane preparation to obtain desired zinc ion barrier properties.

  9. Quartz modification by Zn ion implantation and swift Xe ion irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Privezentsev, Vladimir [Institute of Physics and Technology, Russian Academy of Sciences, Moscow (Russian Federation); Kulikauskas, Vaclav [Skobeltsyn Institute of Nuclear Physics, Lomonosov Moscow State University (Russian Federation); Didyk, Alexander; Skuratov, Vladimir [Joint Institute of Nuclear Research, Dubna (Russian Federation); Steinman, Edward; Tereshchenko, Alexey; Kolesnikov, Nikolay [Institute of Solid-State Physics, Russian Academy of Sciences, Chernogolovka (Russian Federation); Trifonov, Alexey; Sakharov, Oleg [National Research University ' ' MIET' ' , Zelenograd, Moscow (Russian Federation); Ksenich, Sergey [National University of Science and Technology ' ' MISiS' ' , Moscow (Russian Federation)

    2017-07-15

    The quartz slides were implanted by {sup 64}Zn{sup +} ions with dose of 5 x 10{sup 16}/cm{sup 2} and energy of 100 keV. After implantation, the amorphous metallic Zn nanoparticles with an average radius of 3.5 nm were created. The sample surface becomes nonuniform, its roughness is increased and its values rise up to 6 nm compared to virgin state, and the roughness maximum is at a value of about 0.8 nm. The surface is made up of valleys and hillocks which have a round shape with an average diameter about 200 nm. At the center of these hillocks are pores with a depth up to 6 nm and a diameter of about 20 nm. After implantation in UV-vis diapason, the optical transmission decreases while PL peak (apparently due to oxygen deficient centers) at wavelength of 400 nm increases. Then the samples were subjected to swift Xe ion irradiation with the fluences of 1 x 10{sup 12}-7.5 x 10{sup 14}/cm{sup 2} and energy of 167 MeV. After Xe irradiation, the sample surface roughness shat down to values of 0.5 nm and the roughness maximum is at a value of about 0.1 nm. Optical transmission in UV-vis diapason increases. The PL peak at wavelength of 400 nm is decreased while a PL peak at wavelength of 660 nm is raised. This peak is presumably due to non-bridging oxygen hole centers or/and NPs with structure Si(core)/SiO{sub 2}(shell). HRTEM image of Zn-implanted quartz subsurface layer. One can see the Zn amorphous nanoparticles, which confirms the electron diffraction pattern (insert). (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  10. Slow positron beam study of hydrogen ion implanted ZnO thin films

    International Nuclear Information System (INIS)

    Hu, Yi; Xue, Xudong; Wu, Yichu

    2014-01-01

    The effects of hydrogen related defect on the microstructure and optical property of ZnO thin films were investigated by slow positron beam, in combination with x-ray diffraction, infrared and photoluminescence spectroscopy. The defects were introduced by 90 keV proton irradiation with doses of 1×10 15 and 1×10 16 ions cm −2 . Zn vacancy and OH bonding (V Zn +OH) defect complex were identified in hydrogen implanted ZnO film by positron annihilation and infrared spectroscopy. The formation of these complexes led to lattice disorder in hydrogen implanted ZnO film and suppressed the luminescence process. - Highlights: • Hydrogen introduced by ion implantation can form hydrogen-related defect complex. • V Zn +OH defect complex is identified by positron annihilation and IR spectroscopy. • Irradiation defects suppress the luminescence process

  11. High temperature superconductivity in Zn and Mn substituted (Tl,Cr)Sr2CaCu2O7

    International Nuclear Information System (INIS)

    Lo, S.V.; Abd Shukor, R.

    1999-01-01

    Samples with nominal starting composition (TICr 0 .15)Sr 2 (Ca 1-x M x )Cu 2 O 7 (TI-1212) for x=0 - 0.7 with M= Zn and Mn have been prepared and investigated by powder X-ray diffraction (XRD) and electrical resistance measurements. All sample showed a mixed phase of 1212 and 1201. Dominant 1212-phase was observed for x=0.0-0.5 and x=0.0-0.4, for Zn and Mn series, respectively. The superconducting transition temperature was suppressed when Zn and Mn are substituted at the Ca site. For the Zn series the normal state behavior is metallic throughout the doping range. For the Mn series the normal state behavior is metallic for 0.1≤x≥0.3 and semiconducting like x>0.3. The suppression of T c and formation of the TI-1212 phase are discussed in terms of the ionic radius and valence state of the substituted elements. (author)

  12. Effects of annealing atmosphere on ZnO{sup -} ions-implanted silica glass: synthesis of Zn and ZnO nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Kuiri, P K [Department of Physics, Achhruram Memorial College, P.O. Jhalda, Purulia 723202 (India); Mahapatra, D P, E-mail: kuiripk@gmail.co [Institute of Physics, Sachivalaya Marg, Bhubaneswar 751005 (India)

    2010-10-06

    The effects of annealing atmosphere (argon or oxygen) on Zn nanoparticles (NPs), embedded in silica glass, synthesized by implanting 50 keV ZnO{sup -} ions to a fluence of 7 x 10{sup 16} cm{sup -2} have been studied. Optical absorption (OA) measurements carried out on the as-implanted samples have been found to result in a surface plasmon resonance (SPR) band centred at {approx}255 nm due to the presence of Zn NPs in the silica glass. An increase in SPR peak intensity with a corresponding reduction of its full width at half maximum have been seen in the OA spectrum taken from the as-implanted sample following annealing in Ar ambient at 700 {sup 0}C for 2 h, indicating a growth in the size of Zn NPs. However, annealing the as-implanted sample in O{sub 2} gas at 700 {sup 0}C for 2 h has been found to result in a steep absorption edge at {approx}364 nm in the OA spectrum which indicates the formation of ZnO NPs. These ZnO NPs show quantum confinement effects due to their small sizes. No observable photoluminescence (PL) emission has been seen from Zn NPs, whereas an excitonic band at {approx}368 nm and three deep-level PL emission bands at {approx}453 nm, {approx}521 nm and {approx}650 nm, respectively, have been seen from ZnO NPs. It was argued that the deep-level PLs were due to the singly ionized oxygen vacancies located at ZnO NPs' surfaces. These observations suggest that ZnO NPs were formed due to oxidation of Zn NPs via interaction with the indiffusing O{sub 2} molecules during annealing in O{sub 2} ambient, but not with the interaction of the implanted oxygen in silica glass.

  13. Spectrum designation and effect of Al substitution on the luminescence of Cr{sup 3+} doped ZnGa{sub 2}O{sub 4} nano-sized phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Zhang Weiwei [Key Laboratory of Micro-nano Measurement, Manipulation and Physics (Ministry of Education), School of Physics and Nuclear Energy Engineering, Beihang University, Beijing 100191 (China); Zhang Junying, E-mail: zjy@buaa.edu.c [Key Laboratory of Micro-nano Measurement, Manipulation and Physics (Ministry of Education), School of Physics and Nuclear Energy Engineering, Beihang University, Beijing 100191 (China); Chen Ziyu; Wang Tianmin [Key Laboratory of Micro-nano Measurement, Manipulation and Physics (Ministry of Education), School of Physics and Nuclear Energy Engineering, Beihang University, Beijing 100191 (China); Zheng Shukai [College of Electronic and Information Engineering, Hebei University, Baoding 071200 (China)

    2010-10-15

    Low-temperature photoluminescent spectra of ZnGa{sub 2}O{sub 4}:Cr{sup 3+} nano-sized phosphors calcined at different temperatures were reported. The fine structure of the emission spectra has been designated to Cr{sup 3+} ions in different sites including ideal octahedral, Zn-interstitial, Ga{sub ZN}{sup 4}-Zn{sub Ga}{sup 6} sites and Ga{sub 2}O{sub 3} impurity. The vibronic sidebands for both Stokes' and anti-Stokes' sides are related to the host lattice vibrations, which were confirmed by IR and Raman spectra. Al{sup 3+} is substituted in Ga{sup 3+} sites to form Zn(Ga{sub 1-y}Al{sub y}){sub 2}O{sub 4}:Cr{sub 0.01}{sup 3+} (0{<=}y{<=}0.5). The blue shift and luminescent intensity variations of the charge transfer band and 3d-3d transitions in the spectra caused by Al substitution were related to larger band gap and stronger crystal field, respectively. The calculated crystal-field parameters indicated that Al incorporation enhanced the crystal field strength and induced more trigonal distortion due to different radii of Al{sup 3+} and Ga{sup 3+}.

  14. Adsorption pertechnetate ions on the substituted Sn-hydroxyapatite

    International Nuclear Information System (INIS)

    Hamarova, A.; Rosskopfova, O.; Pivarciova, L.

    2015-01-01

    Hydroxyapatite is suitable adsorbent for heavy metals and radionuclides due to its large surface area, high stability under redox conditions. SnCl 2 for its reducing properties is used in biomedical applications and industrial technologies, for its reducing properties. The adsorption of TcO 4 - to the HA samples, prepared by wet precipitation method, was studied by the d radio-indication method. Radionuclide 99m Tc was used as radioisotope indicator. The effect of contact time on the adsorption of 99m TcO 4 - ions on the Sn-HA was studied. Sn 2+ ions reduced Tc (VII) to Tc (IV) forming TcO 2 , TcO(OH) 2 or more precisely TcO 2 ·2H 2 O, which can be adsorbed on the surface of the HA, or to form complexes on the surface of the hydroxyapatite. (authors)

  15. Structural interpretation of chemically synthesized ZnO nanorod and its application in lithium ion battery

    International Nuclear Information System (INIS)

    Kundu, Samapti; Sain, Sumanta; Yoshio, Masaki; Kar, Tanusree; Gunawardhana, Nanda; Pradhan, Swapan Kumar

    2015-01-01

    Graphical abstract: - Highlights: • ZnO nanorods are synthesized at room temperature via a simple chemical route. • Growth direction of ZnO nanorods has been determined along 〈0 0 2〉. • ZnO nanorods constructed anode shows a high discharge capacity in first cycle. • It retains good reversible capacity compared to other ZnO morphologies. - Abstract: ZnO nanorods are synthesized at room temperature via a simple chemical route without using any template or capping agent and its importance is evaluated as a suitable candidate for anode material in lithium ion battery. Structural and microstructure characterizations of these nanorods are made by analyzing the X-ray diffraction data employing the Rietveld method of powder structure refinement. It reveals that the ZnO nanorods are grown up with a preferred orientation and elongated along 〈0 0 2〉. FESEM images reveal that these uniform cylindrical shaped nanorods are of different lengths and diameters. These synthesized ZnO nanorods are tested as an anode material for lithium ion batteries. The nano grain size of the ZnO rods results in less volume expansion and/or contraction during the alloying/de-alloying process and causes in good cyclability. In addition, synthesized ZnO nanorods deliver high charge/discharge capacities compared to other reported ZnO materials

  16. Structural interpretation of chemically synthesized ZnO nanorod and its application in lithium ion battery

    Energy Technology Data Exchange (ETDEWEB)

    Kundu, Samapti; Sain, Sumanta [Materials Science Division, Department of Physics, The University of Burdwan, Golapbag, Burdwan 713104, West Bengal (India); Yoshio, Masaki [Advanced Research and Education Centre, Saga University, 1341 Yoga-machi, Saga 840-0047 (Japan); Kar, Tanusree [Department of Materials Science, Indian Association for the Cultivation of Science, Jadavpur, Kolkata 700032, West Bengal (India); Gunawardhana, Nanda, E-mail: nandagunawardhana@pdn.ac.lk [International Research Centre, Senate Building, University of Peradeniya, Peradeniya 20400 (Sri Lanka); Pradhan, Swapan Kumar, E-mail: skpradhan@phys.buruniv.ac.in [Materials Science Division, Department of Physics, The University of Burdwan, Golapbag, Burdwan 713104, West Bengal (India)

    2015-02-28

    Graphical abstract: - Highlights: • ZnO nanorods are synthesized at room temperature via a simple chemical route. • Growth direction of ZnO nanorods has been determined along 〈0 0 2〉. • ZnO nanorods constructed anode shows a high discharge capacity in first cycle. • It retains good reversible capacity compared to other ZnO morphologies. - Abstract: ZnO nanorods are synthesized at room temperature via a simple chemical route without using any template or capping agent and its importance is evaluated as a suitable candidate for anode material in lithium ion battery. Structural and microstructure characterizations of these nanorods are made by analyzing the X-ray diffraction data employing the Rietveld method of powder structure refinement. It reveals that the ZnO nanorods are grown up with a preferred orientation and elongated along 〈0 0 2〉. FESEM images reveal that these uniform cylindrical shaped nanorods are of different lengths and diameters. These synthesized ZnO nanorods are tested as an anode material for lithium ion batteries. The nano grain size of the ZnO rods results in less volume expansion and/or contraction during the alloying/de-alloying process and causes in good cyclability. In addition, synthesized ZnO nanorods deliver high charge/discharge capacities compared to other reported ZnO materials.

  17. Slow positron beam study of hydrogen ion implanted ZnO thin films

    Science.gov (United States)

    Hu, Yi; Xue, Xudong; Wu, Yichu

    2014-08-01

    The effects of hydrogen related defect on the microstructure and optical property of ZnO thin films were investigated by slow positron beam, in combination with x-ray diffraction, infrared and photoluminescence spectroscopy. The defects were introduced by 90 keV proton irradiation with doses of 1×1015 and 1×1016 ions cm-2. Zn vacancy and OH bonding (VZn+OH) defect complex were identified in hydrogen implanted ZnO film by positron annihilation and infrared spectroscopy. The formation of these complexes led to lattice disorder in hydrogen implanted ZnO film and suppressed the luminescence process.

  18. Influence of iron ions on the structural properties of Zn-borosilicate glasses

    International Nuclear Information System (INIS)

    Music, S.; Gotic, M.; Popovic, S.

    1989-01-01

    The objectives of this study were to determine the influence of iron ions on the appearance of crystalline phases in Zn-borosilicate glasses, and to obtain information about valence state and coordination of iron ions. The systems Na 2 O-ZnO-B 2 O 3 -SiO 2 and ZnO-B 2 O 3 -SiO 2 were doped with α-Fe 2 O 3 . X-ray diffraction, IR spectroscopy and 57 Fe Moessbauer spectroscopy were used as experimental techniques. (author) 32 refs.; 5 figs.; 5 tabs

  19. Cation distribution in Ni-substituted Mn{sub 0.5}Zn{sub 0.5}Fe{sub 2}O{sub 4} nanoparticles: A Raman, Mössbauer, X-ray diffraction and electron spectroscopy study

    Energy Technology Data Exchange (ETDEWEB)

    Thota, Suneetha [Microwave Laboratory, Department of Physics, Indian Institute of Technology Delhi, New Delhi 110016 (India); Kashyap, Subhash C., E-mail: skashyap@physics.iitd.ac.in [Microwave Laboratory, Department of Physics, Indian Institute of Technology Delhi, New Delhi 110016 (India); Sharma, Shiv K. [Hawaii Institute of Geophysics and Planetology, University of Hawaii (UH), Honolulu, HI 96822 (United States); Reddy, V.R. [UGC-DAE Consortium for Scientific Research, Khandwa Road, Indore 452017 (India)

    2016-04-15

    Graphical abstract: - Highlights: • Synthesized Mn{sub 0.5−x}Ni{sub x}Zn{sub 0.5}Fe{sub 2}O{sub 4}, nanoparticles (0.05 ≤ x ≤ 0.45) at low temperature. • Raman studies established that Fe and Zn ions occupy A site in equal fraction. • {sup 57}Fe Mossbauer study revealed that Ni and Mn ions occupy nearly 25% of B sites. • Electron spectroscopy (XPS) confirmed that nearly 25% Fe{sup 3+} dwells at A sites. • Diffraction peak intensity (X-ray) quantified cations distribution at A- and B-sites. - Abstract: In this paper we report the structural, vibration, and electronic-structure parameters (bonding and valence of cations) of single phase cubic mixed spinel nanoparticles of (Zn{sub δ}Mn{sub γ}Fe{sub 1−(γ+δ)})[Ni{sub x}Zn{sub 0.5−δ}Mn{sub 0.5−γ−x}Fe{sub 1+(γ+δ)}]O{sub 4} where x = 0.05–0.45 with an aim to determine cation-distribution i.e. δ and γ in these samples. The Raman spectroscopy has established that only Fe and Zn cations occupy tetrahedral interstitial sites in a FCC anion lattice in nearly equal fraction, and Mössbauer spectra have shown that Fe{sup 3+} cations are present at both, tetrahedral and octahedral interstitial sites and Ni{sup 2+} cations are situated at the octahedral sites in all the substituted samples. The photoelectron spectra also revealed the presence of Fe{sup 3+} cations at both the interstitial sites. The best possible cationic distribution in Ni substituted Mn–Zn ferrites has been estimated by reiteratively calculating the intensity ratios of various pairs of X-ray diffraction peaks and matching with the observed intensity ratios.

  20. Ion-substituted calcium phosphate coatings deposited by plasma-assisted techniques: A review.

    Science.gov (United States)

    Graziani, Gabriela; Bianchi, Michele; Sassoni, Enrico; Russo, Alessandro; Marcacci, Maurilio

    2017-05-01

    One of the main critical aspects behind the failure or success of an implant resides in its ability to fast bond with the surrounding bone. To boost osseointegration, the ideal implant material should exhibit composition and structure similar to those of biological apatite. To this aim, the most common approach is to coat the implant surface with a coating of hydroxyapatite (HA), resembling the main component of mineralized tissues. However, bone apatite is a non-stoichiometric, multi-substituted poorly-crystalline apatite, containing significant amounts of foreign ions, with high biological relevance. Ion-substituted HAs can be deposited by so called "wet methods", which are however poorly reproducible and hardly industrially feasible; at the same time bioactive coatings realized by plasma assisted method, interesting for industrial applications, are generally made of stoichiometric (i.e. un-substituted) HA. In this work, the literature concerning plasma-assisted deposition methods used to deposit ion-substituted HA was reviewed and the last advances in this field discussed. The ions taken into exam are those present in mineralized tissues and possibly having biological relevance. Notably, literature about this topic is scarce, especially relating to in vivo animal and clinical trials; further on, available studies evaluate the performance of substituted coatings from different points of view (mechanical properties, bone growth, coating dissolution, etc.) which hinders a proper evaluation of the real efficacy of ion-doped HA in promoting bone regeneration, compared to stoichiometric HA. Moreover, results obtained for plasma sprayed coatings (which is the only method currently employed for deposition at the industrial scale) were collected and compared to those of novel plasma-assisted techniques, that are expected to overcome its limitations. Data so far available on the topic were discussed to highlight advantages, limitations and possible perspectives of these

  1. Improvement of in vitro corrosion and cytocompatibility of biodegradable Fe surface modified by Zn ion implantation

    Science.gov (United States)

    Wang, Henan; Zheng, Yang; Li, Yan; Jiang, Chengbao

    2017-05-01

    Pure Fe was surface-modified by Zn ion implantation to improve the biodegradable behavior and cytocompatibility. Surface topography, chemical composition, corrosion resistance and cytocompatibility were investigated. Atomic force microscopy, auger electron spectroscopy and X-ray photoelectron spectroscopy results showed that Zn was implanted into the surface of pure Fe in the depth of 40-60 nm and Fe2O3/ZnO oxides were formed on the outmost surface. Electrochemical measurements and immersion tests revealed an improved degradable behavior for the Zn-implanted Fe samples. An approximately 12% reduction in the corrosion potential (Ecorr) and a 10-fold increase in the corrosion current density (icorr) were obtained after Zn ion implantation with a moderate incident ion dose, which was attributed to the enhanced pitting corrosion. The surface free energy of pure Fe was decreased by Zn ion implantation. The results of direct cell culture indicated that the short-term (4 h) cytocompatibility of MC3T3-E1 cells was promoted by the implanted Zn on the surface.

  2. Rational design of hierarchical ZnO@Carbon nanoflower for high performance lithium ion battery anodes

    Science.gov (United States)

    liu, Huichao; Shi, Ludi; Li, Dongzhi; Yu, Jiali; Zhang, Han-Ming; Ullah, Shahid; Yang, Bo; Li, Cuihua; Zhu, Caizhen; Xu, Jian

    2018-05-01

    The rational structure design and strong interfacial bonding are crucially desired for high performance zinc oxide (ZnO)/carbon composite electrodes. In this context, micro-nano secondary structure design and strong dopamine coating strategies are adopted for the fabrication of flower-like ZnO/carbon (ZnO@C nanoflowers) composite electrodes. The results show the ZnO@C nanoflowers (2-6 μm) are assembled by hierarchical ZnO nanosheets (∼27 nm) and continuous carbon framework. The micro-nano secondary architecture can facilitate the penetration of electrolyte, shorten lithium ions diffusion length, and hinder the aggregation of the nanosheets. Moreover, the strong chemical interaction between ZnO and coating carbon layer via C-Zn bond improves structure stability as well as the electronic conductivity. As a synergistic result, when evaluated as lithium ion batteries (LIBs) anode, the ZnO@C nanoflower electrodes show high reversible capacity of ca. 1200 mA h g-1 at 0.1 A g-1 after 80 cycles. As well as good long-cycling stability (638 and 420 mA h g-1 at 1 and 5 A g-1 after 500 cycles, respectively) and excellent rate capability. Therefore, this rational design of ZnO@C nanoflowers electrode is a promising anode for high-performance LIBs.

  3. Zn2+ -Ion Sensing by Fluorescent Schiff Base Calix[4]arene Macrocycles.

    Science.gov (United States)

    Ullmann, Steve; Schnorr, René; Handke, Marcel; Laube, Christian; Abel, Bernd; Matysik, Jörg; Findeisen, Matthias; Rüger, Robert; Heine, Thomas; Kersting, Berthold

    2017-03-17

    A macrocyclic ligand (H 2 L) containing two o,o'-bis(iminomethyl)phenol and two calix[4]arene head units has been synthesized and its coordination chemistry towards divalent Ni and Zn investigated. The new macrocycle forms complexes of composition [ML] (M=Zn, M=Ni) and [ZnL(py) 2 ], which were characterized by elemental analysis; IR, UV/Vis, and NMR spectroscopy; electrospray ionization mass spectrometry (ESI-MS); and X-ray crystallography (for [ZnL(py) 2 ] and [NiL]). H 2 L allows the sensitive optical detection of Zn 2+ among a series of biologically relevant metal ions by a dual fluorescence enhancement/quenching effect in solution. The fluorescence intensity of the macrocycle increases by a factor of ten in the presence of Zn 2+ with a detection limit in the lower nanomolar region. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  4. Cation-substituted spinel oxide and oxyfluoride cathodes for lithium ion batteries

    Science.gov (United States)

    Manthiram, Arumugam; Choi, Wonchang

    2010-05-18

    The present invention includes compositions and methods of making cation-substituted and fluorine-substituted spinel cathode compositions by firing a LiMn2-y-zLiyMzO4 oxide with NH4HF2 at low temperatures of between about 300 and 700.degree. C. for 2 to 8 hours and a .eta. of more than 0 and less than about 0.50, mixed two-phase compositions consisting of a spinel cathode and a layered oxide cathode, and coupling them with unmodified or surface modified graphite anodes in lithium ion cells.

  5. Selective Thallium (I Ion Sensor Based on Functionalised ZnO Nanorods

    Directory of Open Access Journals (Sweden)

    Z. H. Ibupoto

    2012-01-01

    Full Text Available Well controlled in length and highly aligned ZnO nanorods were grown on the gold-coated glass substrate by hydrothermal growth method. ZnO nanorods were functionalised with selective thallium (I ion ionophore dibenzyldiaza-18-crown-6 (DBzDA18C6. The thallium ion sensor showed wide linear potentiometric response to thallium (I ion concentrations ( M to  M with high sensitivity of 36.87 ± 1.49 mV/decade. Moreover, thallium (I ion demonstrated fast response time of less than 5 s, high selectivity, reproducibility, storage stability, and negligible response to common interferents. The proposed thallium (I ion-sensor electrode was also used as an indicator electrode in the potentiometric titration, and it has shown good stoichiometric response for the determination of thallium (I ion.

  6. Phytotoxicity of ZnO nanoparticles and the released Zn(II) ion to corn (Zea mays L.) and cucumber (Cucumis sativus L.) during germination.

    Science.gov (United States)

    Zhang, Ruichang; Zhang, Haibo; Tu, Chen; Hu, Xuefeng; Li, Lianzhen; Luo, Yongming; Christie, Peter

    2015-07-01

    Toxicity of engineered nanoparticles on organisms is of concern worldwide due to their extensive use and unique properties. The impacts of ZnO nanoparticles (ZnO NPs) on seed germination and root elongation of corn (Zea mays L.) and cucumber (Cucumis sativus L.) were investigated in this study. The role of seed coats of corn in the mitigation toxicity of nanoparticles was also evaluated. ZnO NPs (1,000 mg L(-1)) reduced root length of corn and cucumber by 17 % (p < 0.05) and 51 % (p < 0.05), respectively, but exhibited no effects on germination. In comparison with Zn(2+), toxicity of ZnO NPs on the root elongation of corn could be attributed to the nanoparticulate ZnO, while released Zn ion from ZnO could solely contribute to the inhibition of root elongation of cucumber. Zn uptake in corn exposed to ZnO NPs during germination was much higher than that in corn exposed to Zn(2+), whereas Zn uptake in cucumber was significantly correlated with soluble Zn in suspension. It could be inferred that Zn was taken up by corn and cucumber mainly in the form of ZnO NPs and soluble Zn, respectively. Transmission electron microscope confirmed the uptake of ZnO NPs into root of corn. Although isolation of the seed coats might not be the principal factor that achieved avoidance from toxicity on germination, seed coats of corn were found to mitigate the toxicity of ZnO NPs on root elongation and prevent approximately half of the Zn from entering into root and endosperm.

  7. Formation of zinc-containing nanoparticles from Zn²⁺ ions in cell culture media: implications for the nanotoxicology of ZnO.

    Science.gov (United States)

    Turney, Terence W; Duriska, Martin B; Jayaratne, Vidura; Elbaz, Abdulkareem; O'Keefe, Sean J; Hastings, Andrew S; Piva, Terrence J; Wright, Paul F A; Feltis, Bryce N

    2012-10-15

    Zinc ions generate a range of poorly soluble Zn-containing nanoparticles when added to commonly used mammalian cell culture media. The formation of these nanoparticles confounds the use of soluble Zn salts as positive controls during cytotoxicity testing of other Zn-containing nanoparticles, such as ZnO. These nanoprecipitates can either be crystalline or amorphous and vary in composition depending upon the concentration of Zn(II) within the medium. The cytotoxicity and immune system response of these nanoparticles in situ are similar to those of 30 nm ZnO nanoparticles. The low residual level of truly soluble Zn species (taken as species passing through a 2 kDa membrane) in cell culture media with serum is insufficient to elicit any appreciable cytotoxicity. These observations highlight the importance of employing appropriate controls when studying ZnO nanoparticle toxicity and suggest a re-evaluation of the conclusions drawn in some previous cytotoxicity studies.

  8. Nanoparticles from Cu-Zn-Al shape memory alloys physically synthesized by ion milling deposition

    Energy Technology Data Exchange (ETDEWEB)

    Pavon, Luis Alberto Lopez [Universidad Autonoma de Nuevo Leon (UANL), Nuevo Leon (Mexico); Cuellara, Enrique Lopez; Castro, Alejandro Torres; Cruza, Azael Martinez de la [Universidad Autonoma de Nuevo Leon (CIIDIT/UANL), Nuevo Leon (Mexico). Centro de Innovacion, Investigacion y Desarrollo en Ingenieria y Tecnologia; Ballesteros, Carmen [Universidad Carlos III de Madrid, Madrid (Spain). Departamento de Fisica; Araujo, Carlos Jose de [Universidade Federal de Campina Grande (UFCG), Campina Grande, PB (Brazil). Departamento de Engenharia Mecanica

    2012-05-15

    In this research, an ion milling equipment was used to elaborate nanoparticles from Cu-Zn-Al alloys with shape memory effect. Two different compositions were used, target A: 75.22Cu-17.12Zn-7.66Al at % with an Ms of -9 deg C and target B: 76.18Cu-15.84Zn-7.98Al with an Ms of 20 degree C. Nanoparticles were characterized by High Resolution Transmission Electron Microscopy, Electron Diffraction and Energy Dispersive X-ray Spectroscopy. The obtained nanoparticles showed a small dispersion, with a size range of 3.2-3.5 nm. Their crystal structure is in good agreement with the bulk martensitic structure of the targets. In this sense, results on morphology, composition and crystal structure have indicated that it is possible to produce nanoparticles of CuZnAl shape memory alloys with martensitic structure in a single process using Ion Milling. (author)

  9. Nanoparticles from Cu-Zn-Al shape memory alloys physically synthesized by ion milling deposition

    International Nuclear Information System (INIS)

    Pavon, Luis Alberto Lopez; Cuellara, Enrique Lopez; Castro, Alejandro Torres; Cruza, Azael Martinez de la; Ballesteros, Carmen; Araujo, Carlos Jose de

    2012-01-01

    In this research, an ion milling equipment was used to elaborate nanoparticles from Cu-Zn-Al alloys with shape memory effect. Two different compositions were used, target A: 75.22Cu-17.12Zn-7.66Al at % with an Ms of -9 deg C and target B: 76.18Cu-15.84Zn-7.98Al with an Ms of 20 degree C. Nanoparticles were characterized by High Resolution Transmission Electron Microscopy, Electron Diffraction and Energy Dispersive X-ray Spectroscopy. The obtained nanoparticles showed a small dispersion, with a size range of 3.2-3.5 nm. Their crystal structure is in good agreement with the bulk martensitic structure of the targets. In this sense, results on morphology, composition and crystal structure have indicated that it is possible to produce nanoparticles of CuZnAl shape memory alloys with martensitic structure in a single process using Ion Milling. (author)

  10. Jahn-Teller coupling of Cr2+ ion with degenerate modes in ZnS, ZnSe, and ZnTe crystals: microscopic treatment

    International Nuclear Information System (INIS)

    Natadze, A.L.; Ryskin, A.I.

    1980-01-01

    The Jahn-Teller (JT) interaction energy is calculated for 5 T 2 and 5 E states of the Cr 2+ ion in ZnS, ZnSe, and ZnTe crystals. The calculations are made within the framework of a particular microscopic model of the crystal field in the distorted crystal (model of point-like exchange charges), the multimode interaction is taken into account. For the 5 T 2 term the energies of interaction with tetragonal and trigonal modes are of the same order of magnitude. This circumstance results in a small height of the barriers that separate various minima of the adiabatic potential and is responsible for the dynamic aspect of the static JT effect in these systems. (author)

  11. Preparation and structure of carbonated calcium hydroxyapatite substituted with heavy rare earth ions

    International Nuclear Information System (INIS)

    Yasukawa, Akemi; Kandori, Kazuhiko; Tanaka, Hidekazu; Gotoh, Keiko

    2012-01-01

    Highlights: ► LnCaHap solid solution particles were prepared using five types of heavy rare earth ions by a precipitation method. ► The length and the crystallinity of the LnCaHap particles first increased and then decreased with increasing Ln 3+ contents. ► A series of YCaHap solid solution particles formed with Y/(Y + Ca) = 0–0.10 were investigated using various methods in detail. -- Abstract: Calcium hydroxyapatite (CaHap) particles substituted five types of heavy rare earth ions (Ln: Y 3+ , Gd 3+ , Dy 3+ , Er 3+ and Yb 3+ ) were synthesized using a precipitation method and characterized using various means. These Ln ions strongly affected the crystal phases and the structures of the products. With increasing Ln/(Ln + Ca) in the starting solution ([X Ln ]), the length and the crystallinity of the particles first increased and then decreased. The rare earth metal-calcium hydroxyapatite (LnCaHap) solid solution particles were obtained at [X Y ] ≤ 0.10 for substituting Y system and at [X Ln ] ≤ 0.01–0.03 for substituting the other Ln systems. LnPO 4 was mixed with LnCaHap at higher [X Ln ] for all Ln systems. A series of yttrium-calcium hydroxyapatite (YCaHap) solid solutions with [X Y ] = 0–0.10 were investigated using XRD, TEM, ICP-AES, IR and TG–DTA in detail.

  12. Adsorption of Pb, Cd, Zn, Cu and Hg ions on Formaldehyde and ...

    African Journals Online (AJOL)

    Adsorption of Pb(II), Cd(II), Zn(II), Cu(II) and Hg(II) ions on formaldehyde and Pyridine modified bean husks were determined. The adsorption capacity of formaldehyde modified bean husks (mg/g) was: Pb2+, 5.01; Cd2+, 3.63; Zn2+, 2.18; Hg2+, 1.82; Cu2+, 1.58 and that of pyridine modified bean husk was: Hg2+, 6.92; Cd2+ ...

  13. Comparative study of ZnO nanorods and thin films for chemical and biosensing applications and the development of ZnO nanorods based potentiometric strontium ion sensor

    Science.gov (United States)

    Khun, K.; Ibupoto, Z. H.; Chey, C. O.; Lu, Jun.; Nur, O.; Willander, M.

    2013-03-01

    In this study, the comparative study of ZnO nanorods and ZnO thin films were performed regarding the chemical and biosensing properties and also ZnO nanorods based strontium ion sensor is proposed. ZnO nanorods were grown on gold coated glass substrates by the hydrothermal growth method and the ZnO thin films were deposited by electro deposition technique. ZnO nanorods and thin films were characterised by field emission electron microscopy [FESEM] and X-ray diffraction [XRD] techniques and this study has shown that the grown nanostructures are highly dense, uniform and exhibited good crystal quality. Moreover, transmission electron microscopy [TEM] was used to investigate the quality of ZnO thin film and we observed that ZnO thin film was comprised of nano clusters. ZnO nanorods and thin films were functionalised with selective strontium ionophore salicylaldehyde thiosemicarbazone [ST] membrane, galactose oxidase, and lactate oxidase for the detection of strontium ion, galactose and L-lactic acid, respectively. The electrochemical response of both ZnO nanorods and thin films sensor devices was measured by using the potentiometric method. The strontium ion sensor has exhibited good characteristics with a sensitivity of 28.65 ± 0.52 mV/decade, for a wide range of concentrations from 1.00 × 10-6 to 5.00 × 10-2 M, selectivity, reproducibility, stability and fast response time of 10.00 s. The proposed strontium ion sensor was used as indicator electrode in the potentiometric titration of strontium ion versus ethylenediamine tetra acetic acid [EDTA]. This comparative study has shown that ZnO nanorods possessed better performance with high sensitivity and low limit of detection due to high surface area to volume ratio as compared to the flat surface of ZnO thin films.

  14. Synthesis of visible light active Gd3+-substituted ZnFe2O4 nanoparticles for photocatalytic and antibacterial activities

    Science.gov (United States)

    Patil, S. B.; Bhojya Naik, H. S.; Nagaraju, G.; Viswanath, R.; Rashmi, S. K.

    2017-08-01

    In the present analysis, we study the assembly of a low-cost and visible light active ZnFe2-xGdxO4 ( x = 0 , 0.3, 0.5 and 0.7) nanoparticles (NPs) photocatalyst. The synthesized samples were characterized by several physicochemical techniques, such as X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), UV-Visible absorption spectroscopy (UV-Vis), scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HRTEM). The phase transition from cubic to orthorhombic was confirmed by XRD patterns. The increase in the concentration of Gd3+ substitution in ZnFe2O4 NPs enhances the redshift of absorption in the visible region of UV-Vis absorption spectra and reduces the band gap. In the photo-Fenton-type reaction, the gadolinium-substituted zinc ferrite (ZGF) NPs exhibit a significant catalytic activity for the degradation of methylene blue (99% in 90 minutes) under visible light (500W xenon lamp) with respect to bare samples (95% in 240 minutes) and they also show an excellent reusability nature. These materials were also screened for antibacterial activity against Gram-negative bacteria strains ( Pseudomonas aeruginosa and Escherichia coli).

  15. On resonance processes in near threshold excitation of resonance lines of Zn+ ion at electron-ion collisions

    International Nuclear Information System (INIS)

    Imre, A.I.; Gomonaj, A.N.; Vukstich, V.S.; Nemet, A.N.

    1998-01-01

    The results of spectroscopic investigation of resonances in excitation of near threshold region of separate components of resonance doublet 4p 2 P 1/2,3/2 0 of Zn + ion by electron impact are given in the present work. The physical basis of their production nature is suggested

  16. Electrical and optical behavior of ZnO nanowires irradiated by ion beam

    DEFF Research Database (Denmark)

    Lisevski, Caroline I.; Fernandes Cauduro, André Luis; Franzen, Paulo L

    2015-01-01

    Zinc oxide nanowires have been attracting much interest due to their potential use in electronics and optoelectonics devices. In this work, we report on the photoluminescence and electrical behavior of ZnO nanowires grown by vapor-liquid-solid method and irradiated with 1.2 MeV He+ ions at several...... doses. The results strongly indicates the existence of an enhanced dynamic annealing effect during the low fluence irradiations allowing it to heal low migration barrier point-defects such as oxygen interstitials (OI), zinc interstitials (ZnI), zinc antisites (ZnO) and oxygen antisites (OZn...

  17. Isotopic exchange kinetics of zinc ions in Zn-A zeolite

    Energy Technology Data Exchange (ETDEWEB)

    Radak, V M; Gal, I J; Salai, J J [Belgrade Univ. (Yugoslavia)

    1976-01-01

    The isotopic exchange kinetics of Zn/sup 2 +/ ions in hydrated Zn-A zeolite of composition (Znsub(5.55)Nasub(0.90)(A10/sub 2/)/sub 12/(Si0/sub 2/)/sub 12/.aq) have been investigated by measuring the fractional attainment of isotopic equilibrium between a ZnCl/sub 2/ solution and a /sup 65/Zn-labelled Zn-A zeolite (30 and 45 ..mu..m particle radii) as a function of time, in the temperature range 25 to 60/sup 0/C. The exchange mechanism is a two-step process which has been resolved, using the Brown-Sherry-Krambeck model (J.Phys.Chem.;75:3846(1971)) into diffusion in the solid particles, with Zn/sup 2 +/ diffusivity of D = 10sup(-3.97 + -0.03) exp(-Esub(D)/RT)m/sup 2/ s/sup -1/, Esub(D) = 67.1 +- 0.5 kJ molee/sup -1/, and an intracrystalline first-order exchange between bound and mobile Zn/sup 2 +/ ions in the network, with a rate constant of k/sub 2/ = 10sup(3.05 +- 0.25) exp(-Esub(k)/RT)s/sup -1/, Esub(k) = 56.5 +- 1.5 kJ mol/sup -1/.

  18. Zinc terephthalates ZnC_8H_4O_4 as anodes for lithium ion batteries

    International Nuclear Information System (INIS)

    Wang, Liping; Zou, Jian; Chen, Shulin; Yang, Jingyi; Qing, Fangzhu; Gao, Peng; Li, Jingze

    2017-01-01

    Graphical abstract: Both of well-crystalline and amorphous zinc terephthalates ZnC_8H_4O_4 are synthesized and amorphous structure demonstrates a higher capacity and better cycling performance. - Highlights: • Crystalline and amorphous ZnC_8H_4O_4 are obtained. • Both crystalline and amorphous ZnC_8H_4O_4 have σ_e of 10"−"7 S m"−"1. • Lithium ion diffusion is the rate-determine process. • Amorphous has a high capacity and durable performance. • Amorphous ZnC_8H_4O_4 has a high apparent lithium ion diffusion coefficient. - Abstract: Organic materials offer the advantages of cost-effective, environmental benignity, and molecular structural diversity as applications of electrode materials for lithium ion batteries. In fact, their lithium storage behaviors in terms of dynamics and kinetics intrinsically lie in ion migration in solids. Thus the solid forms including crystalline and amorphous states are crucial for the properties. In this study, a conventional carbonyl type organic material, namely zinc terephthalate (ZnC_8H_4O_4), is obtained in both well-crystalline and amorphous forms and applied as anodes for lithium ion batteries. ZnC_8H_4O_4 with amorphous structure shows higher lithium storage capacity and better capacity retention compared with that of crystalline one. It is ascribed that the amorphous phase provides a higher lithium ion diffusion coefficient than the crystalline one under the conditions of similar electronic conductivity.

  19. Hydrogen substituted graphdiyne as carbon-rich flexible electrode for lithium and sodium ion batteries.

    Science.gov (United States)

    He, Jianjiang; Wang, Ning; Cui, Zili; Du, Huiping; Fu, Lin; Huang, Changshui; Yang, Ze; Shen, Xiangyan; Yi, Yuanping; Tu, Zeyi; Li, Yuliang

    2017-10-27

    Organic electrodes are potential alternatives to current inorganic electrode materials for lithium ion and sodium ion batteries powering portable and wearable electronics, in terms of their mechanical flexibility, function tunability and low cost. However, the low capacity, poor rate performance and rapid capacity degradation impede their practical application. Here, we concentrate on the molecular design for improved conductivity and capacity, and favorable bulk ion transport. Through an in situ cross-coupling reaction of triethynylbenzene on copper foil, the carbon-rich frame hydrogen substituted graphdiyne film is fabricated. The organic film can act as free-standing flexible electrode for both lithium ion and sodium ion batteries, and large reversible capacities of 1050 mAh g -1 for lithium ion batteries and 650 mAh g -1 for sodium ion batteries are achieved. The electrode also shows a superior rate and cycle performances owing to the extended π-conjugated system, and the hierarchical pore bulk with large surface area.

  20. Sodium ions as substitutes for protons in the gastric H,K-ATPase

    International Nuclear Information System (INIS)

    Polvani, C.; Sachs, G.; Blostein, R.

    1989-01-01

    In view of the striking homology among various ion-translocating ATPases including Na,K-ATPase, Ca-ATPase, and H,K-ATPase, and the recent evidence that protons can replace cytoplasmic sodium as well as potassium in the reaction mechanism of the Na,K-ATPase (Polvani, C., and Blostein, R. (1988) J. Biol. Chem. 263, 16757-16763), we studied the role of sodium as a substitute for protons in the H,K-ATPase reaction. Using hog gastric H,K-ATPase-rich inside-out membrane vesicles we observed 22Na+ influx which was stimulated by intravesicular potassium ions (K+i) at pH 8.5 but not at pH 7.1. This sodium influx was observed in medium containing ATP and was inhibited by vanadate and SCH28080, a selective inhibitor of the gastric H,K-ATPase. At least 2-fold accumulation of sodium was observed at pH 8.5. Experiments aimed to determine the sidedness of the alkaline pH requirement for K+i-dependent sodium influx showed that K+i-activated sodium influx depends on pHout and is unaffected by changes in pHin. These results support the conclusion that sodium ions substitute for protons in the H,K-ATPase reaction mechanism and provide evidence for a similarity in ion selectivity and/or binding domains of the Na,K-ATPase and the gastric H,K-ATPase enzymes

  1. Suppression of the internal electric field effects in ZnO/Zn0.7Mg0.3O quantum wells by ion-implantation induced intermixing

    International Nuclear Information System (INIS)

    Davis, J A; Dao, L V; Wen, X; Ticknor, C; Hannaford, P; Coleman, V A; Tan, H H; Jagadish, C; Koike, K; Sasa, S; Inoue, M; Yano, M

    2008-01-01

    Strong suppression of the effects caused by the internal electric field in ZnO/ZnMgO quantum wells following ion-implantation and rapid thermal annealing, is revealed by photoluminescence, time-resolved photoluminescence, and band structure calculations. The implantation and annealing induces Zn/Mg intermixing, resulting in graded quantum well interfaces. This reduces the quantum-confined Stark shift and increases electron-hole wavefunction overlap, which significantly reduces the exciton lifetime and increases the oscillator strength

  2. A selective iodide ion sensor electrode based on functionalized ZnO nanotubes.

    Science.gov (United States)

    Ibupoto, Zafar Hussain; Khun, Kimleang; Willander, Magnus

    2013-02-04

    In this research work, ZnO nanotubes were fabricated on a gold coated glass substrate through chemical etching by the aqueous chemical growth method. For the first time a nanostructure-based iodide ion selective electrode was developed. The ZnO nanotubes were functionalized with miconazole ion exchanger and the electromotive force (EMF) was measured by the potentiometric method. The iodide ion sensor exhibited a linear response over a wide range of concentrations (1 × 10-6 to 1 × 10-1 M) and excellent sensitivity of -62 ± 1 mV/decade. The detection limit of the proposed sensor was found to be 5 × 10-7 M. The effects of pH, temperature, additive, plasticizer and stabilizer on the potential response of iodide ion selective electrode were also studied. The proposed iodide ion sensor demonstrated a fast response time of less than 5 s and high selectivity against common organic and the inorganic anions. All the obtained results revealed that the iodide ion sensor based on functionalized ZnO nanotubes may be used for the detection of iodide ion in environmental water samples, pharmaceutical products and other real samples.

  3. A Selective Iodide Ion Sensor Electrode Based on Functionalized ZnO Nanotubes

    Directory of Open Access Journals (Sweden)

    Magnus Willander

    2013-02-01

    Full Text Available In this research work, ZnO nanotubes were fabricated on a gold coated glass substrate through chemical etching by the aqueous chemical growth method. For the first time a nanostructure-based iodide ion selective electrode was developed. The ZnO nanotubes were functionalized with miconazole ion exchanger and the electromotive force (EMF was measured by the potentiometric method. The iodide ion sensor exhibited a linear response over a wide range of concentrations (1 × 10−6 to 1 × 10−1 M and excellent sensitivity of –62 ± 1 mV/decade. The detection limit of the proposed sensor was found to be 5 × 10−7 M. The effects of pH, temperature, additive, plasticizer and stabilizer on the potential response of iodide ion selective electrode were also studied. The proposed iodide ion sensor demonstrated a fast response time of less than 5 s and high selectivity against common organic and the inorganic anions. All the obtained results revealed that the iodide ion sensor based on functionalized ZnO nanotubes may be used for the detection of iodide ion in environmental water samples, pharmaceutical products and other real samples.

  4. Microwave Characterization of Ba-Substituted PZT and ZnO Thin Films.

    Science.gov (United States)

    Tierno, Davide; Dekkers, Matthijn; Wittendorp, Paul; Sun, Xiao; Bayer, Samuel C; King, Seth T; Van Elshocht, Sven; Heyns, Marc; Radu, Iuliana P; Adelmann, Christoph

    2018-05-01

    The microwave dielectric properties of (Ba 0.1 Pb 0.9 )(Zr 0.52 Ti 0.48 )O 3 (BPZT) and ZnO thin films with thicknesses below were investigated. No significant dielectric relaxation was observed for both BPZT and ZnO up to 30 GHz. The intrinsic dielectric constant of BPZT was as high as 980 at 30 GHz. The absence of strong dielectric dispersion and loss peaks in the studied frequency range can be linked to the small grain diameters in these ultrathin films.

  5. Interaction of divalent metal ions with Zn(2+)-glycerophosphocholine cholinephosphodiesterase from ox brain.

    Science.gov (United States)

    Lee, K J; Kim, M R; Kim, Y B; Myung, P K; Sok, D E

    1997-12-01

    The effect of divalent metal ions on the activity of glycerophosphocholine cholinephosphodiesterse from ox brain was examined. Zn(2+)- and Co(2+)-glycerophosphocholine cholinephosphodiesterases were prepared from the exposure of apoenzyme to Zn2+ and Co2+, respectively, and the properties of two metallo-phosphodiesterases were compared to those of native phosphodiesterase. Although two metallo-enzymes were similar in expressing Km value, optimum pH or sensitivity to Cu2+, they differed in the susceptibility to the inhibition by thiocholine or tellurite; while Co(2+)-phosphodiesterase was more sensitive to tellurites, Zn(2+)-phosphodiesterase was more susceptible to inhibition by thiocholine. In addition, Zn(2+)-phosphodiesterase was more thermo-stable than Co2+ enzyme. Separately, when properties of native phosphodiesterase were compared to those of each metallo-phosphodiesterase, native phosphodiesterase was found to be quite similar to Zn(2+)-phosphodiesterase in many respects. Even in thermo-stability, native enzyme resembled Zn(2+)-phosphodiesterase rather than Co(2+)-enzyme. Consistent with this, the stability of native phosphodiesterase was maintained in the presence of Zn2+, but not Co2+, Mn2+ was also as effective as Zn2+ in the stabilization of the enzyme. Noteworthy, the native enzyme was found to be inhibited competitively by Cu2+ with a Ki value of 20 microM, and its inhibitory action was antagonized effectively by Zn2+ or Co2+. Also, choline, another competitive inhibitor of the enzyme, appeared to antagonize the inhibitory action of Cu2+. Taken together, it is suggested that there may be multiple binding sites for divalent metal ions in the molecule of glycerophosphocholine cholinephosphodiesterase.

  6. 4D-π-1A type β-substituted ZnII-porphyrins: ideal green sensitizers for building-integrated photovoltaics.

    Science.gov (United States)

    Covezzi, A; Orbelli Biroli, A; Tessore, F; Forni, A; Marinotto, D; Biagini, P; Di Carlo, G; Pizzotti, M

    2016-10-18

    Two novel green β-substituted Zn II -porphyrins, G1 and G2, based on a 4D-π-1A type substitution pattern have been synthesized. Their enhanced push-pull character, by reduction of H-L energy gaps, promotes broadening and red-shifting of absorption bands. The effective synthetic pathway and the remarkable spectroscopic properties make G2 ideal for BIPV application.

  7. Highly flexible transparent and conductive ZnS/Ag/ZnS multilayer films prepared by ion beam assisted deposition

    Science.gov (United States)

    Yu, Zhinong; Leng, Jian; Xue, Wei; Zhang, Ting; Jiang, Yurong; Zhang, Jie; Zhang, Dongpu

    2012-01-01

    ZnS/Ag/ZnS (ZAZ) multilayer films were prepared on polyethene terephthalate (PET) by ion beam assisted deposition at room temperature. The structural, optical and electrical characteristics of ZAZ multilayers dependent on the thickness of silver layer were investigated. The ZAZ multilayers exhibit a low sheet resistance of about 10 Ω/sq., a high transmittance of 92.1%, and the improved resistance stabilities when subjected to bending. When the inserted Ag thickness is over 12 nm, the ZAZ multilayers show good resistance stabilities due to the existence of a ductile Ag metal layer. The results suggest that ZAZ film has better optoelectrical and anti-deflection characteristics than conventional indium tin oxide (ITO) single layer.

  8. Optimal Zn-Modified Ca–Si-Based Ceramic Nanocoating with Zn Ion Release for Osteoblast Promotion and Osteoclast Inhibition in Bone Tissue Engineering

    Directory of Open Access Journals (Sweden)

    Jiangming Yu

    2017-01-01

    Full Text Available We investigated the slow release of Zn ion (Zn2+ from nanocoatings and compared the in vitro response of osteoblasts (MC3T3-E1 and proosteoclasts (RAW 264.7 cultured on Ca2ZnSi2O7 nanocoated with different Zn/Ca molar ratios on a Ti-6Al-4V (i.e., Ti substrate to optimize cell behaviors and molecule levels. Significant morphology differences were observed among samples. By comparing with pure Ti and CaSiO3 nanocoating, the morphology of Ca2ZnSi2O7 ceramic nanocoatings was rough and contained small nanoparticles or aggregations. Slow Zn2+ release from nanocoatings was observed and Zn2+ concentration was regulated by varying the Zn/Ca ratios. The cell-response results showed Ca2ZnSi2O7 nanocoating at different Zn/Ca molar ratios for osteoblasts and osteoclasts. Compared to other nanocoatings and Ti, sample Zn/Ca (0.3 showed the highest cell viability and upregulated expression of the osteogenic differentiation genes ALP, COL-1, and OCN. Additionally, sample Zn/Ca (0.3 showed the greatest inhibition of RAW 264.7 cell growth and decreased the mRNA levels of osteoclast-related genes OAR, TRAP, and HYA1. Therefore, the optimal Zn-Ca ratio of 0.3 in Ca2ZnSi2O7 ceramic nanocoating on Ti had a dual osteoblast-promoting and osteoclast-inhibiting effect to dynamically balance osteoblasts/osteoclasts. These optimal Zn-Ca ratios are valuable for Ca2ZnSi2O7 ceramic nanocoating on Ti-coated implants for potential applications in bone tissue regeneration.

  9. Halogeno-substituted 2-aminobenzoic acid derivatives for negative ion fragmentation studies of N-linked carbohydrates.

    Science.gov (United States)

    Harvey, David J

    2005-01-01

    Negative ion electrospray mass spectra of high-mannose N-linked glycans derivatised with 2-aminobenzoic acids and ionised from solutions containing ammonium hydroxide gave prominent [M-H](-) ions accompanied by weaker [M-2H](2-) ions. Fragmentation of both types of ions gave prominent singly charged glycosidic cleavage ions containing the derivatised reducing terminus and ions from the non-reducing terminus that appeared to be products of cross-ring cleavages. Differentiation of these two groups of ions was conveniently achieved in a single spectrum by use of chloro- or bromo-substituted benzoic acids in order to label ions containing the derivative with an atom with a distinctive isotope pattern. Fragmentation of the doubly charged ions gave more abundant fragments, both singly and doubly charged, than did fragmentation of the singly charged ions, but information of chain branching was masked by the appearance of prominent ions produced by internal cleavages. Copyright (c) 2005 John Wiley & Sons, Ltd.

  10. X-ray and magnetic studies of Zn substituted Ni–Pb ferrites

    Indian Academy of Sciences (India)

    Unknown

    nic applications such as transformers, choke coils, noise filters, recording heads etc. Nickel ferrites and Zn2+ sub- stituted nickel-ferrites are widely used in electronics and electrical industries as they exhibit interesting variations in the electrical and magnetic properties. Electrical and magnetic properties are influenced by ...

  11. A P2-Type Layered Superionic Conductor Ga-Doped Na2 Zn2 TeO6 for All-Solid-State Sodium-Ion Batteries.

    Science.gov (United States)

    Li, Yuyu; Deng, Zhi; Peng, Jian; Chen, Enyi; Yu, Yao; Li, Xiang; Luo, Jiahuan; Huang, Yangyang; Zhu, Jinlong; Fang, Chun; Li, Qing; Han, Jiantao; Huang, Yunhui

    2018-01-24

    Here, a P2-type layered Na 2 Zn 2 TeO 6 (NZTO) is reported with a high Na + ion conductivity ≈0.6×10 -3  S cm -1 at room temperature (RT), which is comparable to the currently best Na 1+n Zr 2 Si n P 3-n O 12 NASICON structure. As small amounts of Ga 3+ substitutes for Zn 2+ , more Na + vacancies are introduced in the interlayer gaps, which greatly reduces strong Na + -Na + coulomb interactions. Ga-substituted NZTO exhibits a superionic conductivity of ≈1.1×10 -3  S cm -1 at RT, and excellent phase and electrochemical stability. All solid-state batteries have been successfully assembled with a capacity of ≈70 mAh g -1 over 10 cycles with a rate of 0.2 C at 80 °C. 23 Na nuclear magnetic resonance (NMR) studies on powder samples show intra-grain (bulk) diffusion coefficients D NMR on the order of 12.35×10 -12  m 2  s -1 at 65 °C that corresponds to a conductivity σ NMR of 8.16×10 -3  S cm -1 , assuming the Nernst-Einstein equation, which thus suggests a new perspective of fast Na + ion conductor for advanced sodium ion batteries. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  12. Smoothing of ZnO films by gas cluster ion beam

    International Nuclear Information System (INIS)

    Chen, H.; Liu, S.W.; Wang, X.M.; Iliev, M.N.; Chen, C.L.; Yu, X.K.; Liu, J.R.; Ma, K.; Chu, W.K.

    2005-01-01

    Planarization of wide-band-gap semiconductor ZnO surface is crucial for thin-film device performance. In this study, the rough initial surfaces of ZnO films deposited by r.f. magnetron sputtering on Si substrates were smoothed by gas cluster ion beams. AFM measurements show that the average surface roughness (R a ) of the ZnO films could be reduced considerably from 16.1 nm to 0.9 nm. Raman spectroscopy was used to monitor the structure of both the as-grown and the smoothed ZnO films. Rutherford back-scattering in combination with channeling effect was used to study the damage production induced by the cluster bombardment

  13. Effect of Mg substitution on the magnetic properties of Ni–Zn ferrites

    Indian Academy of Sciences (India)

    Y Ramesh Babu

    2017-05-31

    May 31, 2017 ... C for 6h in air to investigate their structural and magnetic properties. X-ray diffraction ... The tetrava- lent substitutions have been found to improve the .... ducted on ferrites prepared by ceramic method [11] and wet chemical ...

  14. Enhanced magnetic domain relaxation frequency and low power losses in Zn{sup 2+} substituted manganese ferrites potential for high frequency applications

    Energy Technology Data Exchange (ETDEWEB)

    Praveena, K., E-mail: praveenaou@gmail.com [Department of Physics, National Taiwan Normal University, Taipei, 11677, Taiwan (China); Chen, Hsiao-Wen [Department of Physics, National Taiwan Normal University, Taipei, 11677, Taiwan (China); Liu, Hsiang-Lin, E-mail: hliu@ntnu.edu.tw [Department of Physics, National Taiwan Normal University, Taipei, 11677, Taiwan (China); Sadhana, K., E-mail: sadhana@osmania.ac.in [Department of Physics, Osmania University, Saifabad, Hyderabad, 500004 (India); Murthy, S.R. [Department of Physics, Osmania University, Hyderabad, 500007 (India)

    2016-12-15

    Nowadays electronic industries prerequisites magnetic materials, i.e., iron rich materials and their magnetic alloys. However, with the advent of high frequency applications, the standard techniques of reducing eddy current losses, using iron cores, were no longer efficient or cost effective. Current market trends of the switched mode power supplies industries required even low energy losses in power conversion with maintenance of adequate initial permeability. From the above point of view, in the present study we aimed at the production of Manganese–Zinc ferrites prepared via solution combustion method using mixture of fuels and achieved low loss, high saturation magnetization, high permeability, and high magnetic domain relaxation frequency. The as-synthesized Zn{sup 2+} substituted MnFe{sub 2}O{sub 4} were characterized by X-ray diffractometer (XRD) and transmission electron microscopy (TEM). The fractions of Mn{sup 2+}, Zn{sup 2+} and Fe{sup 2+} cations occupying tetrahedral sites along with Fe occupying octahedral sites within the unit cell of all ferrite samples were estimated by Raman scattering spectroscopy. The magnetic domain relaxation was investigated by inductance spectroscopy (IS) and the observed magnetic domain relaxation frequency (f{sub r}) was increased with the increase in grain size. The real and imaginary part of permeability (μ′ and μ″) increased with frequency and showed a maximum above 100 MHz. This can be explained on the basis of spin rotation and domain wall motion. The saturation magnetization (M{sub s}), remnant magnetization (M{sub r}) and magneton number (µ{sub B}) decreased gradually with increasing Zn{sup 2+} concentration. The decrease in the saturation magnetization was discussed with Yafet–Kittel (Y–K) model. The Zn{sup 2+} concentration increases the relative number of ferric ions on the A sites, reduces the A–B interactions. The frequency dependent total power losses decreased as the zinc concentration increased

  15. On the substitution of Sr ions at Y sites in YBa2Cu3O7-d

    International Nuclear Information System (INIS)

    Siddiqi, S.A.; Sreedhar, K.; Drobac, D.; Infante, C.; Matacotta, F.C.; Ganguly, P.

    1989-10-01

    The effect of Sr substitution at the Ba sites in YBa 2 Cu 3 O 7-d has been studied, attempts to substitute Sr exclusively at Y sites have not been successful. We have been able to substitute Sr at Y sites only when the Ba ions are simultaneously substituted by Sr to give solid solutions of the type Y 1-x Sr x Ba 2-2x Sr 2x Cu 3 O 7- x /2-d . These examples show superconducting transitions higher than 78K without significant deterioration in the magnitude of the ac susceptibility. The substitutions are best understood in terms of site constraints on the ions occupying the Y and Ba sites. 4 refs, 2 figs, 2 tabs

  16. Elimination of Cu (II) and Zn (II) ions in mono-element and the bi ...

    African Journals Online (AJOL)

    Elimination of Cu (II) and Zn (II) ions in mono-element and the bi-element aqueous solutions by adsorption on natural clay of Bikougou (Gabon) ... The modeling of the experimental results is better achieved by application of. Freundlich adsorption isotherm and Langmuir adsorption isotherm concerning the adsorption of Cu ...

  17. Removal of Zn(II) and Pb (II) ions Using Rice Husk in Food Industrial ...

    African Journals Online (AJOL)

    Michael Horsfall

    The removal of mentioned heavy metal ions from aqueous solutions was studied by batch ... The binding process was strongly affected by pH and the optimum. pH for Zn2+ and .... on the rice husks are protonated and positively-charged, their.

  18. Surface modification of TiO2 coatings by Zn ion implantation for ...

    Indian Academy of Sciences (India)

    ions such as silver (Ag), zinc (Zn) and copper (Cu) have been developed to improve ... nism of Ag raises concerns about their potential cytotoxicity. [20–22]. ... circulating water to keep the sample temperature at 25◦C. 2.3 Coating .... S. aureus and the effect is obvious and dose dependent. The ... In this work, the mechanisms.

  19. Effect of swift heavy ion irradiation on bare and coated ZnS quantum dots

    International Nuclear Information System (INIS)

    Chowdhury, S.; Hussain, A.M.P.; Ahmed, G.A.; Singh, F.; Avasthi, D.K.; Choudhury, A.

    2008-01-01

    The present study compares structural and optical modifications of bare and silica (SiO 2 ) coated ZnS quantum dots under swift heavy ion (SHI) irradiation. Bare and silica coated ZnS quantum dots were prepared following an inexpensive chemical route using polyvinyl alcohol (PVA) as the dielectric host matrix. X-ray diffraction (XRD) and transmission electron microscopy (TEM) study of the samples show the formation of almost spherical ZnS quantum dots. The UV-Vis absorption spectra reveal blue shift relative to bulk material in absorption energy while photoluminescence (PL) spectra suggests that surface state and near band edge emissions are dominating in case of bare and coated samples, respectively. Swift heavy ion irradiation of the samples was carried out with 160 MeV Ni 12+ ion beam with fluences 10 12 to 10 13 ions/cm 2 . Size enhancement of bare quantum dots after irradiation has been indicated in XRD and TEM analysis of the samples which has also been supported by optical absorption spectra. However similar investigations on irradiated coated quantum dots revealed little change in quantum dot size and emission. The present study thus shows that the coated ZnS quantum dots are stable upon SHI irradiation compared to the bare one

  20. Enhanced exciton emission from ZnO nano-phosphor induced by Yb3+ ions

    CSIR Research Space (South Africa)

    Kabongo, GL

    2014-01-01

    Full Text Available In this work, the sol–gel method was used to prepare Ytterbium (Yb(sup3+)) doped ZnO nano-phosphors with different concentrations of Yb(sup3+) ions. Their structural, morphological, photoluminescence, electronic states and the chemical composition...

  1. Effect for hydrogen, nitrogen, phosphorous, and argon ions irradiation on ZnO NWs

    International Nuclear Information System (INIS)

    Ishaq, A.; Usman, M.; Dee, C. F.; Khurram, A. A.; Yan, L.; Zhou, X. T.; Nadeem, A.; Naseem, S.; Rafique, H. M.; Majlis, B. Y.

    2013-01-01

    Zinc oxide (ZnO) nanowires (NWs) are exposed to energetic proton (H + ), nitrogen (N + ), phosphorus (P + ), and argon (Ar + ) ions to understand the radiation hardness and structural changes induced by these irradiations. High-resolution transmission electron microscopy is utilized to see the irradiation effects in NWs. Multiple doses and energies of radiation at different temperatures are used for different set of samples. The study reveals that wurtzite (crystalline)-structured ZnO NWs experience amorphization, degradation, and morphological changes after the irradiation. At room temperature, deterioration of the crystalline structure is observed under high fluence of H + , N + , and P + ions. While for ZnO NWs, bombarded by Ar + and P + ions, nano-holes are produced. The ZnO NWs surfaces also show corrugated morphology full of nano-humps when irradiated by Ar + ions at 400 °C. The corrugated surface could serve as tight-holding interface when interconnecting it with other NWs/nanotubes. These nano-humps may have the function of increasing the surface for surface-oriented sensing applications in the future.

  2. Effect for hydrogen, nitrogen, phosphorous, and argon ions irradiation on ZnO NWs

    Energy Technology Data Exchange (ETDEWEB)

    Ishaq, A., E-mail: ishaq_ah@yahoo.com; Usman, M. [National Centre for Physics, Quaid-i-Azam University, Experimental Physics Labs (Pakistan); Dee, C. F. [Universiti Kebangsaan Malaysia (UKM), Institute of Microengineering and Nanoelectronics (IMEN) (Malaysia); Khurram, A. A. [National Centre for Physics, Quaid-i-Azam University, Experimental Physics Labs (Pakistan); Yan, L., E-mail: yanlong@sinap.ac.cn; Zhou, X. T. [Chinese Academy of Sciences, Shanghai Institute of Applied Physics (China); Nadeem, A.; Naseem, S. [University of the Punjab, Centre of Excellence in Solid State Physics (Pakistan); Rafique, H. M. [University of the Punjab, Department of Physics (Pakistan); Majlis, B. Y. [Universiti Kebangsaan Malaysia (UKM), Institute of Microengineering and Nanoelectronics (IMEN) (Malaysia)

    2013-04-15

    Zinc oxide (ZnO) nanowires (NWs) are exposed to energetic proton (H{sup +}), nitrogen (N{sup +}), phosphorus (P{sup +}), and argon (Ar{sup +}) ions to understand the radiation hardness and structural changes induced by these irradiations. High-resolution transmission electron microscopy is utilized to see the irradiation effects in NWs. Multiple doses and energies of radiation at different temperatures are used for different set of samples. The study reveals that wurtzite (crystalline)-structured ZnO NWs experience amorphization, degradation, and morphological changes after the irradiation. At room temperature, deterioration of the crystalline structure is observed under high fluence of H{sup +}, N{sup +}, and P{sup +} ions. While for ZnO NWs, bombarded by Ar{sup +} and P{sup +} ions, nano-holes are produced. The ZnO NWs surfaces also show corrugated morphology full of nano-humps when irradiated by Ar{sup +} ions at 400 Degree-Sign C. The corrugated surface could serve as tight-holding interface when interconnecting it with other NWs/nanotubes. These nano-humps may have the function of increasing the surface for surface-oriented sensing applications in the future.

  3. Preparation and structure of carbonated calcium hydroxyapatite substituted with heavy rare earth ions

    Energy Technology Data Exchange (ETDEWEB)

    Yasukawa, Akemi, E-mail: yasukawa@cc.hirosaki-u.ac.jp [School of Home Economics, Faculty of Education, Hirosaki University, 1-bunkyo, Hirosaki, Aomori 036-8560 (Japan); Kandori, Kazuhiko [School of Chemistry, Osaka University of Education, 4-698-1 Asahigaoka, Kashiwara, Osaka 582-8582 (Japan); Tanaka, Hidekazu [Department of Material Science, Faculty of Science and Engineering, Shimane University, 1060 Nishikawatsu, Matsue, Shimane 690-8504 (Japan); Gotoh, Keiko [Faculty of Human Life and Environment, Nara Women' s University, Kita-uoya-nishi, Nara 630-8506 (Japan)

    2012-05-15

    Highlights: Black-Right-Pointing-Pointer LnCaHap solid solution particles were prepared using five types of heavy rare earth ions by a precipitation method. Black-Right-Pointing-Pointer The length and the crystallinity of the LnCaHap particles first increased and then decreased with increasing Ln{sup 3+} contents. Black-Right-Pointing-Pointer A series of YCaHap solid solution particles formed with Y/(Y + Ca) = 0-0.10 were investigated using various methods in detail. -- Abstract: Calcium hydroxyapatite (CaHap) particles substituted five types of heavy rare earth ions (Ln: Y{sup 3+}, Gd{sup 3+}, Dy{sup 3+}, Er{sup 3+} and Yb{sup 3+}) were synthesized using a precipitation method and characterized using various means. These Ln ions strongly affected the crystal phases and the structures of the products. With increasing Ln/(Ln + Ca) in the starting solution ([X{sub Ln}]), the length and the crystallinity of the particles first increased and then decreased. The rare earth metal-calcium hydroxyapatite (LnCaHap) solid solution particles were obtained at [X{sub Y}] {<=} 0.10 for substituting Y system and at [X{sub Ln}] {<=} 0.01-0.03 for substituting the other Ln systems. LnPO{sub 4} was mixed with LnCaHap at higher [X{sub Ln}] for all Ln systems. A series of yttrium-calcium hydroxyapatite (YCaHap) solid solutions with [X{sub Y}] = 0-0.10 were investigated using XRD, TEM, ICP-AES, IR and TG-DTA in detail.

  4. Binder-free ZnO@ZnSnO3 quantum dots core-shell nanorod array anodes for lithium-ion batteries

    Science.gov (United States)

    Tan, Hsiang; Cho, Hsun-Wei; Wu, Jih-Jen

    2018-06-01

    In this work, ZnSnO3 quantum dots (QDs), instead of commonly used conductive carbon, are grown on the ZnO nanorod (NR) array to construct the binder-free ZnO@ZnSnO3 QDs core-shell NR array electrode on carbon cloth for lithium-ion battery. The ZnO@ZnSnO3 QDs core-shell NR array electrode exhibits excellent lithium storage performance with an improved cycling performance and superior rate capability compared to the ZnO NR array electrode. At a current density of 200 mAg-1, 15.8% capacity loss is acquired in the ZnO@ZnSnO3 QDs core-shell NR array electrode after 110 cycles with capacity retention of 1073 mAhg-1. Significant increases in reversible capacities from 340 to 545 mAhg-1 and from 95 to 390 mAhg-1 at current densities of 1000 and 2000 mAg-1, respectively, are achieved as the ZnO NR arrays are coated with the ZnSnO3 QD shells. The remarkably improved electrochemical performances result from that the configuration of binder-free ZnO@ZnSnO3 QDs core-shell NR array electrode not only facilitates the charge transfer through the solid electrolyte interface and the electronic/ionic conduction boundary as well as lithium ion diffusion but also effectively accommodates the volume change during repeated charge/discharge processes.

  5. Dansyl - Substituted Aza Crown Ethers: Complexation with Alkali, Alkaline Earth Metal Ions and Ammonium

    Science.gov (United States)

    Deiab, Shihab; Archibong, Edikan; Tasheva, Donka; Mochona, Bereket; Gangapuram, Madhavi; Redda, Kinfe

    2011-01-01

    The present study investigates the binding properties of four dansyl substituted aza-crown ethers with alkali, alkaline earth metal ions and ammonium. The influence of the solvent polarity and protonation on the photophysical properties of the compounds was studied by UV/Vis and fluorescence methods. The host species caused only slight changes on the absorption spectra of the ligands. The fluorescence changes were more pronounced and concentration dependent thus allowing to calculate the binding constants of the process. The most stable complex under our working conditions was the one between Ba2+ and DNS18C6. PMID:21738561

  6. Effect of the oxygen isoelectronic substitution in Cu2ZnSnS4 and its photovoltaic application

    International Nuclear Information System (INIS)

    Tablero, C.

    2012-01-01

    The optoelectronic properties of Cu 2 ZnSnS 4 and environmental considerations have attracted significant interest for photovoltaics. Using first-principles, we analyze the possible improvement of this material as a photovoltaic absorber via the isoelectronic substitution of S with O atoms. The evolution of the acceptor level is analyzed with respect to the atomic position of the nearest neighbors of the O atom. We estimate the maximum efficiency of this compound when used as a light absorber. The presence of the sub-band gap level below the conduction band could increases the solar-energy conversion with respect to the host. - Highlights: ► Cu 2 ZnSnS 4 is a promising material for low cost thin film solar cell technology. ► Its optoelectronic properties could be improved by states in the band gap. ► The oxygen to give rise to deep traps. ► Maximum efficiency can be larger than the host semiconductor.

  7. Moessbauer studies of 57Fe substitution of Cu ions in superconducting oxides

    International Nuclear Information System (INIS)

    Saitovitch, E.B.

    1988-01-01

    Since the discovery of high-T c superconductivity in YBa 2 Cu 3 O 7 oxides several studies of metal ions substitutions were reported. The observed depression on T c without a systematic correlation with the charge and magnetic moment of Cu substituents claims for more detailed information about its local properties as can be revealed by 57 Fe Moessbauer spectroscopy. The results for different iron concentrations combined with modifications of the superconducting transition are discussed concerning the presence of magnetic moments on the Fe ions and the preferential occupation of Cu(1) sites, recently confirmed by neutron and electron diffraction experiments. The oxygen coordination for the different iron species are proposed on the basis of their dependence on Fe concentration, their behavior at high temperatures as well as the electron diffraction and electron microscopy measurements reported for Fe: YBa 2 Cu 3 O 7 samples. (author) [pt

  8. A Method for Selective Depletion of Zn(II) Ions from Complex Biological Media and Evaluation of Cellular Consequences of Zn(II) Deficiency

    Science.gov (United States)

    Richardson, Christopher E. R.; Cunden, Lisa S.; Butty, Vincent L.; Nolan, Elizabeth M.; Lippard, Stephen J.; Shoulders, Matthew D.

    2018-01-01

    We describe the preparation, evaluation, and application of an S100A12 protein-conjugated solid support, hereafter the “A12-resin,” that can remove 99% of Zn(II) from complex biological solutions without significantly perturbing the concentrations of other metal ions. The A12-resin can be applied to selectively deplete Zn(II) from diverse tissue culture media and from other biological fluids, including human serum. To further demonstrate the utility of this approach, we investigated metabolic, transcriptomic, and metallomic responses of HEK293 cells cultured in medium depleted of Zn(II) using S100A12. The resulting data provide insight into how cells respond to acute Zn(II) deficiency. We expect that the A12-resin will facilitate interrogation of disrupted Zn(II) homeostasis in biological settings, uncovering novel roles for Zn(II) in biology. PMID:29334734

  9. N+ ion-implantation-induced defects in ZnO studied with a slow positron beam

    International Nuclear Information System (INIS)

    Chen, Z Q; Sekiguchi, T; Yuan, X L; Maekawa, M; Kawasuso, A

    2004-01-01

    Undoped ZnO single crystals were implanted with multiple-energy N + ions ranging from 50 to 380 keV with doses from 10 12 to 10 14 cm -2 . Positron annihilation measurements show that vacancy defects are introduced in the implanted layers. The concentration of the vacancy defects increases with increasing ion dose. The annealing behaviour of the defects can be divided into four stages, which correspond to the formation and recovery of large vacancy clusters and the formation and disappearance of vacancy-impurity complexes, respectively. All the implantation-induced defects are removed by annealing at 1200 deg. C. Cathodoluminescence measurements show that the ion-implantation-induced defects act as nonradiative recombination centres to suppress the ultraviolet (UV) emission. After annealing, these defects disappear gradually and the UV emission reappears, which coincides with positron annihilation measurements. Hall measurements reveal that after N + implantation, the ZnO layer still shows n-type conductivity

  10. Origins of low resistivity in Al ion-implanted ZnO bulk single crystals

    Science.gov (United States)

    Oga, T.; Izawa, Y.; Kuriyama, K.; Kushida, K.; Kinomura, A.

    2011-06-01

    The origins of low resistivity in Al ion-implanted ZnO bulk single crystals are studied by combining Rutherford backscattering spectroscopy (RBS), nuclear reaction analysis (NRA), photoluminescence (PL), and Van der Pauw methods. The Al-ion implantation (peak concentration: 2.6 × 1020cm-3) into ZnO is performed using a multiple-step energy. The resistivity decreases from ˜104 Ω cm for un-implanted ZnO to 1.4 × 10-1 Ω cm for as-implanted, and reaches 6.0 × 10-4 Ω cm for samples annealed at 1000 °C. RBS and NRA measurements for as-implanted ZnO suggest the existence of the lattice displacement of Zn (Zni) and O (Oi), respectively. After annealing at 1000 °C, the Zni related defects remain and the Oi related defects disappear. The origin of the low resistivity in the as-implanted sample is attributed to the Zni (˜30 meV [Look et al., Phys. Rev. Lett. 82, 2552 (1999)]). In contrast, the origin of the low resistivity in the sample annealed at 1000 °C is assigned to both of the Zni related defects and the electrically activated Al donor. A new PL emission appears at around 3.32 eV after annealing at 1000 °C, suggesting electrically activated Al donors.

  11. Electrochemical performance of CuNCN for sodium ion batteries and comparison with ZnNCN and lithium ion batteries

    Science.gov (United States)

    Eguia-Barrio, A.; Castillo-Martínez, E.; Klein, F.; Pinedo, R.; Lezama, L.; Janek, J.; Adelhelm, P.; Rojo, T.

    2017-11-01

    Transition metal carbodiimides (TMNCN) undergo conversion reactions during electrochemical cycling in lithium and sodium ion batteries. Micron sized copper and zinc carbodiimide powders have been prepared as single phase as confirmed by PXRD and IR and their thermal stability has been studied in air and nitrogen atmosphere. CuNCN decomposes at ∼250 °C into CuO or Cu while ZnNCN can be stable until 400 °C and 800 °C in air and nitrogen respectively. Both carbodiimides were electrochemically analysed for sodium and lithium ion batteries. The electrochemical Na+ insertion in CuNCN exhibits a relatively high reversible capacity (300 mAh·g-1) which still indicates an incomplete conversion reaction. This incomplete reaction confirmed by ex-situ EPR analysis, is partly due to kinetic limitations as evidenced in the rate capability experiments and in the constant potential measurements. On the other hand, ZnNCN shows incomplete conversion reaction but with good capacity retention and lower hysteresis as negative electrode for sodium ion batteries. The electrochemical performance of these materials is comparable to that of other materials which operate through displacement reactions and is surprisingly better in sodium ion batteries in comparison with lithium ion batteries.

  12. Study the effect of Gd{sup 3+} incorporation into nanocrystalline (Ni–Ti) substituted Mn–Zn ferrites on its structure and functional properties

    Energy Technology Data Exchange (ETDEWEB)

    Rady, K.E., E-mail: k_rady_2001@yahoo.com [Engineering Basic Sciences Department, Faculty of Engineering, Menoufia University, Shebin El-El, Kom (Egypt); Shams, M.S. [Department of Physics and Engineering Mathematics, Faculty of Electronic Engineering, Menoufia University, Menouf (Egypt)

    2017-03-15

    Ferrite samples with general chemical formula Mn{sub 0.9}Zn{sub 0.1}Ni{sub 0.05}Ti{sub 0.05}Gd{sub t}Fe{sub 1.9−t}O{sub 4}; (0.0≤ t≤0.05; step 0.01) were prepared using solid state reaction technique and the effect of Gd{sup 3+} ions incorporation on its physical properties has been studied. From the obtained results, XRD analysis reveals that the samples have a cubic spinel single phase structure for 0.0≤ t≤0.02; while for t≥0.03 a small peak of secondary phase (Gd{sub 3}Fe{sub 5}O{sub 12}) appears and becomes more noticeable with increasing Gd content. The lattice parameter (a) of the prepared samples was found to be initially increases and then decreases with increasing Gd content which may be attributed to the difference in the ionic radii of the cations involved and the solubility limit of Gd{sup 3+} ions. The crystallite size of the samples was estimated using Scherrer's equation and ranged from 96 nm to 107 nm. A vibrating sample magnetometer (VSM) was used at room temperature in order to study the effect of Gd content on the magnetic hysteresis parameters of the prepared ferrites such as saturation magnetization and coercivity. DC molar magnetic susceptibility (χ{sub M}) for the prepared samples was measured using Faraday's method as a function of temperature and the Curie temperature was calculated from the magnetic susceptibility measurements. Also the DC resistivity of the samples was measured at room temperature. The obtained results show that, the substitution by Gd{sup 3+} ions improves the electrical properties of the samples by increasing it DC electrical resistivity by 118% and consequently decreases it eddy current loss while the saturation magnetization slightly decreased by 14% only. The sample of t=0.01 shows a high dc magnetic susceptibility, high saturation magnetization (43.1 emu/g), high electric resistivity 12×10{sup 3} Ω.m and high Curie temperature (496 K), which is useful in some technological applications such

  13. A selective potentiometric copper (II) ion sensor based on the functionalized ZnO nanorods.

    Science.gov (United States)

    Khun, K; Ibupoto, Z H; Liu, X; Nur, O; Willander, M; Danielsson, B

    2014-09-01

    In this work, ZnO nanorods were hydrothermally grown on the gold-coated glass substrate and characterized by field emission scanning electron microscopy (FESEM) and X-ray diffraction (XRD) techniques. The ZnO nanorods were functionalized by two different approaches and performance of the sensor electrode was monitored. Fourier transform infrared spectroscopy (FTIR) was carried out for the confirmation of interaction between the ionophore molecules and ZnO nanorods. In addition to this, the surface of the electrode was characterized by X-ray photoelectron spectroscopy (XPS) showing the chemical and electronic state of the ionophore and ZnO nanorod components. The ionophore solution was prepared in the stabilizer, poly vinyl chloride (PVC) and additives, and then functionalized on the ZnO nanorods that have shown the Nernstian response with the slope of 31 mV/decade. However, the Cu2+ ion sensor was fabricated only by immobilizing the selective copper ion ionophore membrane without the use of PVC, plasticizers, additives and stabilizers and the sensor electrode showed a linear potentiometric response with a slope of 56.4 mV/decade within a large dynamic concentration range (from 1.0 x 10(-6) to 1.0 x 10(-1) M) of copper (II) nitrate solutions. The sensor showed excellent repeatability and reproducibility with response time of less than 10 s. The negligible response to potentially interfering metal ions such as calcium (Ca2+), magnesium (Mg2+), potassium (K+), iron (Fe3+), zinc (Zn2+), and sodium (Na+) allows this sensor to be used in biological studies. It may also be used as an indicator electrode in the potentiometric titration.

  14. The preparation of Zn-ferrite epitaxial thin film from epitaxial Fe3O4:ZnO multilayers by ion beam sputtering deposition

    International Nuclear Information System (INIS)

    Su, Hui-Chia; Dai, Jeng-Yi; Liao, Yen-Fa; Wu, Yu-Han; Huang, J.C.A.; Lee, Chih-Hao

    2010-01-01

    A new method to grow a well-ordered epitaxial ZnFe 2 O 4 thin film on Al 2 O 3 (0001) substrate is described in this work. The samples were made by annealing the ZnO/Fe 3 O 4 multilayer which was grown with low energy ion beam sputtering deposition. Both the Fe 3 O 4 and ZnO layers were found grown epitaxially at low temperature and an epitaxial ZnFe 2 O 4 thin film was formed after annealing at 1000 o C. X-ray diffraction shows the ZnFe 2 O 4 film is grown with an orientation of ZnFe 2 O 4 (111)//Al 2 O 3 (0001) and ZnFe 2 O 4 (1-10)//Al 2 O 3 (11-20). X-ray absorption spectroscopy studies show that Zn 2+ atoms replace the tetrahedral Fe 2+ atoms in Fe 3 O 4 during the annealing. The magnetic properties measured by vibrating sample magnetometer show that the saturation magnetization of ZnFe 2 O 4 grown from ZnO/Fe 3 O 4 multilayer reaches the bulk value after the annealing process.

  15. Magnetic versus nonmagnetic ion substitution effects on Tc in the La-Sr-Cu-O and Nd-Ce-Cu-O systems

    International Nuclear Information System (INIS)

    Tarascon, J.M.; Wang, E.; Kivelson, S.; Bagley, B.G.; Hull, G.W.; Ramesh, R.

    1990-01-01

    The effects of a substitution for Cu by other 3d metals (Ni, Co, and Zn) on T c in the Nd-Ce-Cu-O system was studied and compared with effects of the same ions on T c in the La-Sr-Cu-O system. We found (1) Zn suppresses T c more slowly in the Nd than in the La systems, so the disorder produced by the nonmagnetic ions is less important in the Nd system, (2) Ni and Co depress T c more quickly in the Nd than in the La system, showing that the magnetic pair breaking is stronger in the Nd system, and (3) in the La system the magnetism of the dopant has no effect on T c . Thus, within the same chemical system (cuprates) we find that as the correlation length is increased one obtains more familiar BCS-type behavior. We suggest that much of the behavior of the various high-T c oxides may be simply a function of the correlation length

  16. Calculation of the substitutional fraction of ion-implanted He in an α-Fe target

    Science.gov (United States)

    Erhart, Paul; Marian, Jaime

    2011-07-01

    Ion-implantation is a useful technique to study irradiation damage in nuclear materials. To study He effects in nuclear fusion conditions, He is co-implanted with damage ions to reproduce the correct He/dpa ratios in the desired or available depth range. However, the short-term fate of these He ions, i.e. over the time scales of their own collisional phase, has not been yet unequivocally established. Here we present a computational study of the short-term evolution of He implantation in an Fe substrate at 700 K to approximate the conditions encountered in dual ion-implantation studies in ferritic materials. Using a combination of SRIM, molecular dynamics and kinetic Monte Carlo (kMC), we calculate the fraction of He atoms that end up in substitutional sites shortly after implantation, i.e. before they contribute to long-term microstructural evolution. We find that fractions of at most 3% should be expected for most implantation studies. Additionally, to inform the kMC calculations, we carry out an exhaustive calculation of interstitial He migration energy barriers in the vicinity of matrix vacancies and find that they vary from approximately 20-60 meV depending on the separation and orientation of the He-vacancy pair.

  17. Calculation of the substitutional fraction of ion-implanted He in an α-Fe target

    International Nuclear Information System (INIS)

    Erhart, Paul; Marian, Jaime

    2011-01-01

    Ion-implantation is a useful technique to study irradiation damage in nuclear materials. To study He effects in nuclear fusion conditions, He is co-implanted with damage ions to reproduce the correct He/dpa ratios in the desired or available depth range. However, the short-term fate of these He ions, i.e. over the time scales of their own collisional phase, has not been yet unequivocally established. Here we present a computational study of the short-term evolution of He implantation in an Fe substrate at 700 K to approximate the conditions encountered in dual ion-implantation studies in ferritic materials. Using a combination of SRIM, molecular dynamics and kinetic Monte Carlo (kMC), we calculate the fraction of He atoms that end up in substitutional sites shortly after implantation, i.e. before they contribute to long-term microstructural evolution. We find that fractions of at most 3% should be expected for most implantation studies. Additionally, to inform the kMC calculations, we carry out an exhaustive calculation of interstitial He migration energy barriers in the vicinity of matrix vacancies and find that they vary from approximately 20-60 meV depending on the separation and orientation of the He-vacancy pair.

  18. Ion-implantation induced defects in ZnO studied by a slow positron beam

    International Nuclear Information System (INIS)

    Chen, Z.Q.; Maekawa, M.; Kawasuso, A.; Sekiguchi, T.; Suzuki, R.

    2004-01-01

    Introduction and annealing behavior of defects in Al + -implanted ZnO have been studied using an energy variable slow positron beam. Vacancy clusters are produced after Al + -implantation. With increasing ion dose above 10 14 Al + /cm 2 the implanted layer is amorphized. Heat treatment up to 600 C enhances the creation of large voids that allow the positronium formation. The large voids disappear accompanying the recrystallization process by further heat treatment above 600 C. Afterwards, implanted Al impurities are completely activated to contribute to the n-type conduction. The ZnO crystal quality is also improved after recrystallization. (orig.)

  19. Ion-implantation induced defects in ZnO studied by a slow positron beam

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Z.Q.; Maekawa, M.; Kawasuso, A. [Japan Atomic Energy Research Institute, Gunma (Japan); Sekiguchi, T. [National Inst. for Materials Science, Tsukuba, Ibaraki (Japan); Suzuki, R. [National Inst. of Advanced Industrial Science and Technology, Tsukuba, Ibaraki (Japan)

    2004-07-01

    Introduction and annealing behavior of defects in Al{sup +}-implanted ZnO have been studied using an energy variable slow positron beam. Vacancy clusters are produced after Al{sup +}-implantation. With increasing ion dose above 10{sup 14} Al{sup +}/cm{sup 2} the implanted layer is amorphized. Heat treatment up to 600 C enhances the creation of large voids that allow the positronium formation. The large voids disappear accompanying the recrystallization process by further heat treatment above 600 C. Afterwards, implanted Al impurities are completely activated to contribute to the n-type conduction. The ZnO crystal quality is also improved after recrystallization. (orig.)

  20. Effect of trivalent transition metal ion substitution in Dy2O3 system

    International Nuclear Information System (INIS)

    Dhilip, M.; Saravana Kumar, K.; Anbarasu, V.

    2015-01-01

    One of the very promising approaches to create novel materials is to combine different physical properties in one material to achieve rich functionality. Magnetoelectric multiferroics are attracting attention for fundamental physics due to their unique coupling behaviour between ferroelectricity, ferromagnetism and ferroelasticity and also because of their promising applications for devices in spintronics, information storage, sensing and actuation. The existence of spontaneous magnetization in the perovskite like phase (layer of perovskite) has encouraged exploring the possibility of fabrication of a multiferroic material for multifunctional devices using the concept of magnetoelectric effect. The rare earth orthoferrites (LnFeO 3 where, Ln = La, Sm, Gd, Dy, Er and Yb) are a class of materials having potential for various applications. These compounds and metal ion substituted ferrites crystallising in perovskite structure show promise as catalysts gas separators, cathodes in solid oxide fuel cells, sensor materials, magneto-optic materials and as spin valves. In this present work, Fe substituted in Dysprosium Oxide compounds were prepared by standard solid state reaction at a temperature of 1300℃. The structural analysis of the prepared samples was characterized with powder X-Ray Diffraction technique and the lattice parameters were calculated with PodwerX indexing software. The structural analysis reveals that the substitution of Fe in Dy 2 O 3 system leads to change of crystalline structure from Cubic to Tetragonal. Further, decreasing trend of volume of the unit cell confirms the occupation of smaller ionic radii element Fe in the Dy site of Dy 2 O 3 system. Hence the possibilities of incorporation of trivalent transition metal ion in to the host Dy 2 O 3 site were analyzed. (author)

  1. The Influence of Oxygen Substitution on the Optoelectronic Properties of ZnTe

    Directory of Open Access Journals (Sweden)

    Imad Khan

    2016-01-01

    Full Text Available We communicate theoretical results of the structural, electronic, and optical properties of ZnOxTe1-x (0≤x≤1 in the zincblende structure. The calculations are performed using full potential linearized augmented plane waves (FP-LAPW method, based on density functional theory (DFT. The structural properties are calculated with simple GGA (PBEsol, while the electronic and optical properties are calculated using mBJ-GGA. The mBJ-GGA is used to properly treat the active d-orbital in their valence shell. The ZnOTe alloy is highly lattice mismatched and consequently the lattice constants and bulk moduli largely deviate from the linear behavior. The calculated bandgaps are in agreement with the experimentally measured values, where the nature of bandgaps is direct for the whole range of x except at x=0.25. We also calculate the bandgap bowing parameter from our accurate bandgaps and resolve the existing controversy in this parameter.

  2. Surface and local electronic structure modification of MgO film using Zn and Fe ion implantation

    Science.gov (United States)

    Singh, Jitendra Pal; Lim, Weon Cheol; Lee, Jihye; Song, Jonghan; Lee, Ik-Jae; Chae, Keun Hwa

    2018-02-01

    Present work is motivated to investigate the surface and local electronic structure modifications of MgO films implanted with Zn and Fe ions. MgO film was deposited using radio frequency sputtering method. Atomic force microscopy measurements exhibit morphological changes associated with implantation. Implantation of Fe and Zn ions leads to the reduction of co-ordination geometry of Mg2+ ions in host lattice. The effect is dominant at bulk of film rather than surface as the large concentration of implanted ions resides inside bulk. Moreover, the evidences of interaction among implanted ions and oxygen are not being observed using near edge fine structure measurements.

  3. Structural and magnetic properties of Gd{sup 3+} ion substituted magnesium ferrite nanopowders

    Energy Technology Data Exchange (ETDEWEB)

    Elkady, Ashraf S. [Department of Physics, Faculty of Science, King Abdulaziz University, Jeddah (Saudi Arabia); Department of Reactor Physics, NRC, Atomic Energy Authority, Cairo (Egypt); Hussein, Shaban I. [Department of Reactor Physics, NRC, Atomic Energy Authority, Cairo (Egypt); Rashad, Mohamed M., E-mail: rashad133@yahoo.com [Central Metallurgical Research and Development Institute, Helwan, Cairo 11421 (Egypt)

    2015-07-01

    Nanocrystalline MgGd{sub x}Fe{sub 2−x}O{sub 4} powders (where x=0, 0.05, 0.1, 0.2, 0.25, 0.3) have been synthesized by the ethylene diamine tetraacetic acid (EDTA)-based sol–gel combustion method. X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, high resolution transmission electron microscopy (HRTEM) and vibrating sample magnetometer (VSM) were applied in order to study the effect of variation of Gd{sup 3+} ion substitution and its impact on crystal structure, crystallite size, lattice parameters, nanostructure and magnetic properties of the formed powders. XRD indicated that, after doping and calcination at 400 °C for 2 h, all samples have two spinel ferrite structures namely cubic and tetragonal phases, which are dependent on Gd{sup 3+} ion concentration. The cubic phase is found to increase with increasing the Gd{sup 3+} ion molar ratio up to 0.1, compared to pure MgFe{sub 2}O{sub 4} and higher Gd{sup 3+} content samples. Indeed, with increasing Gd{sup 3+} ion, the crystallite size was almost unchanged whereas the lattice parameter was found to increase. FT-IR spectrum showed broadening of the ν{sub 2} band and the presence of another band in the range (465–470 cm{sup −1}) upon adding Gd{sup 3+} ion, which confirm the presence of Gd{sup 3+} ion in addition to Fe{sup 3+} ion at octahedral site. Besides, these bands were assigned to the formation of (Gd{sup 3+}–O{sup 2−}) complexes at B-sites. HRTEM images showed that the studied samples consist of nanocrystallites having average particle sizes around 9 nm for pure MgFe{sub 2}O{sub 4} up to 27 and 42 nm for the Gd{sup 3+} ion substituted MgFe{sub 2}O{sub 4} of molar ratio 0.05 and 0.30, respectively. An examination of the magnetic properties revealed an increase in saturation magnetization with increasing Gd concentration incorporation up to x=0.1, as a result of the change of cubic and tetragonal spinel ratio and lattice parameters. Meanwhile, the formed powders exhibited

  4. Preparation and electrochemical performance of bramble-like ZnO array as anode materials for lithium-ion batteries

    International Nuclear Information System (INIS)

    Yan, Junfeng; Wang, Gang; Wang, Hui; Zhang, Zhiyong; Ruan, Xiongfei; Zhao, Wu; Yun, Jiangni; Xu, Manzhang

    2015-01-01

    A bramble-like ZnO array with a special three-dimensional (3D) nanostructure was successfully fabricated on Zn foil through a facile two-step hydrothermal process. A possible growth mechanism of the bramble-like ZnO array was proposed. In the first step of hydrothermal process, the crystal nucleus of Zn(OH) 4 2− generated by the zinc atoms and OH − ions fold together preferentially along the positive polar (0001) to form the needle-like ZnO array. In the second step of hydrothermal process, the crystal nuclei of Zn(OH) 4 2− adjust their posture to keep their c-axes vertical to the perching sites due to the sufficient environmental force and further grow preferentially along the (0001) direction so as to form bramble-like ZnO array. The electrochemical properties of the needle- and bramble-like ZnO arrays as anode materials for lithium-ion batteries were investigated and compared. The results show that the bramble-like ZnO material exhibits much better lithium storage properties than the needle-like ZnO sample. Reasons for the enhanced electrochemical performance of the bramble-like ZnO material were investigated

  5. Microwave-assisted aqueous synthesis of transition metal ions doped ZnSe/ZnS core/shell quantum dots with tunable white-light emission

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Jie [Laboratory of Advanced Materials, Fudan University, Shanghai 200438 (China); Chen, Qiuhang; Zhang, Wanlu; Mei, Shiliang; He, Liangjie; Zhu, Jiatao [Engineering Research Center of Advanced Lighting Technology, Ministry of Education, Institute for Electric Light Sources, Fudan University, Shanghai 200433 (China); Chen, Guoping [School of Information Science and Technology, Fudan University, Shanghai 200433 (China); Guo, Ruiqian, E-mail: rqguo@fudan.edu.cn [Engineering Research Center of Advanced Lighting Technology, Ministry of Education, Institute for Electric Light Sources, Fudan University, Shanghai 200433 (China)

    2015-10-01

    Highlights: • ZnSe-based QDs were formed via a microwave-assisted aqueous approach. • The stabilizer, ZnS coats and UV irradiation played a role in the PL enhancement. • Tunable white-light-emitting Mn:ZnSe QDs and Cu,Mn:ZnSe/ZnS QDs were synthesized. • The formation mechanism of Cu,Mn:ZnSe QDs was clarified. • The corresponding CIE color coordinates of different PL spectra were obtained. - Abstract: Synthesis of bright white-light emitting Mn and Cu co-doped ZnSe/ZnS core/shell quantum dots (QDs) (Cu,Mn:ZnSe/ZnS) was reported. Water-soluble ZnSe-based QDs with Mn and Cu doping were prepared using a versatile hot-injection method in aqueous solution with a microwave-assisted approach. Influence of the Se/S ratio, stabilizer, refluxing time and the concentration of Cu/Mn dopant ions on the particle size and photoluminescence (PL) were investigated. The as-prepared QDs in the different stages of growth were characterized by X-ray powder diffractometer (XRD), high-resolution transmission electron microscopy (HRTEM), UV–visible (UV–vis) spectrophotometer, and fluorescence spectrophotometer. It is found that these ZnSe-based QDs synthesized under mild conditions exhibit emission in the range of 390–585 nm. The PL quantum yield (QY) of the as-prepared water-soluble ZnSe QDs can be up to 24.3% after the UV-irradiation treatment. The band-gap emission of ZnSe is effectively restrained through Mn and Cu doping. The refluxing time influences the doping of not only Mn, but also Cu, which leads to the best refluxing time of Mn:ZnSe and the red-shift of the emission of Cu:ZnSe d-dots. Co-doping induced white-light emission (WLE) from Cu,Mn:ZnSe/ZnS core/shell QDs were obtained, which can offer the opportunity for future-generation white-light emitting diodes (LEDs)

  6. Novel water soluble morpholine substituted Zn(II) phthalocyanine: Synthesis, characterization, DNA/BSA binding, DNA photocleavage and topoisomerase I inhibition.

    Science.gov (United States)

    Barut, Burak; Demirbaş, Ümit; Özel, Arzu; Kantekin, Halit

    2017-12-01

    In this study, novel peripherally tetra 3-morpholinophenol substituted zinc(II) phthalocyanine (4) and its water soluble form quaternized zinc(II) phthalocyanine (ZnQ) were synthesized for the first time. These novel compounds were characterized by a combination of different spectroscopic techniques such as FT-IR, 1 H NMR, 13 C NMR, UV-vis and mass. The DNA binding of ZnQ was investigated using UV-vis absorption titration, competitive ethidium bromide, thermal denaturation and viscosity experiments that the ZnQ bound to CT-DNA via intercalation mode. ZnQ indicated photocleavage activity on supercoiled pBR322 plasmid DNA via formation of singlet oxygen under irradiation at 700nm. Besides, the topoisomerase I inhibitory effect experiments showed that ZnQ inhibited topoisomerase I enzyme in a concentration-dependent manner. The bovine serum albumin (BSA) binding experiments indicated that ZnQ bound to proteins through a static quenching mechanism. All of these results claim that ZnQ has potential agent for photodynamic therapy owing to its nucleic acid interactions and photobiological or photochemical properties. Copyright © 2017 Elsevier B.V. All rights reserved.

  7. Improved Optical and Morphological Properties of Vinyl-Substituted Hybrid Silica Materials Incorporating a Zn-Metalloporphyrin

    Directory of Open Access Journals (Sweden)

    Zoltán Dudás

    2018-04-01

    Full Text Available This work is focused on a novel class of hybrid materials exhibiting enhanced optical properties and high surface areas that combine the morphology offered by the vinyl substituted silica host, and the excellent absorption and emission properties of 5,10,15,20-tetrakis(N-methyl-4-pyridylporphyrin-Zn(II tetrachloride as a water soluble guest molecule. In order to optimize the synthesis procedure and the performance of the immobilized porphyrin, silica precursor mixtures of different compositions were used. To achieve the requirements regarding the hydrophobicity and the porous structure of the gels for the successful incorporation of porphyrin, the content of vinyltriacetoxysilane was systematically changed and thoroughly investigated. Substitution of the silica gels with organic groups is a viable way to provide new properties to the support. An exhaustive characterization of the synthesized silica samples was realised by complementary physicochemical methods, such as infrared spectroscopy (FT-IR, absorption spectroscopy (UV-Vis and photoluminescence, nuclear magnetic resonance spectroscopy (29Si-MAS-NMR transmission and scanning electron microscopy (TEM and SEM, nitrogen absorption (BET, contact angle (CA, small angle X ray and neutron scattering (SAXS and SANS. All hybrids showed an increase in emission intensity in the wide region from 575 to 725 nm (Q bands in comparison with bare porphyrin. By simply tuning the vinyltriacetoxysilane content, the hydrophilic/hydrophobic profile of the hybrid materials was changed, while maintaining a high surface area. Good control of hydrophobicity is important to enhance properties such as dispersion, stability behaviour, and resistance to water, in order to achieve highly dispersible systems in water for biomedical applications.

  8. Optical and magnetic properties of Yb ion-doped cobalt-based ZnO ...

    Indian Academy of Sciences (India)

    Administrator

    The X-ray photoelectron spectral peaks for Yb 4f ions ... temperature with high coercivity due to the contribution of both 3d and 4f exchange interaction with the host ... Mn,4,5 Co,6–9 Ni2,10 Fe11–13 and Cu,2,14 and reported to .... water separately under stirring. .... different concentrations of Yb added ZnO : Co, nanopar-.

  9. Effect of neodymium substitution on the electric and dielectric properties of Mn-Ni-Zn ferrite

    Science.gov (United States)

    Agami, W. R.

    2018-04-01

    Ferrite samples of Mn0.5Ni0.1Zn0.4NdxFe2-xO4 (x = 0.0, 0.01, 0.02, 0.05, 0.075 and 0.1) have been prepared by usual ceramic method. The temperature and composition dependences of the dc electric resistivity (ρdc) were studied. The frequency and composition dependences of the ac electric resistivity (ρac) and dielectric parameters (dielectric constant ε' and dielectric loss ε'') have been investigated. ρdc was found to decrease with temperature for all samples while it increases with increasing Nd3+ concentration. On the other hand, ρac and the dielectric properties were found to decrease with increasing the frequency while ρac increases and both ε' and ε'' decrease with increasing Nd3+ concentration. These results were explained by the Maxwell-Wagner two-layer model and Koops's theory. The improvement in dc and ac electric resistivities shows that these prepared materials are valid for decreasing the eddy current losses at high frequencies, so they can be used in the fabrication of multilayer chip inductor (MLCI) devices.

  10. Reactivity of two hydrate forms of europium(3) ethylenediaminetetraacetate in the processes of central ion substitution

    International Nuclear Information System (INIS)

    Nikitenko, S.I.; Martynenko, L.I.; Pechurova, N.I.

    1985-01-01

    Kinetics of central ion substitution in the system EuA - -Cu 2+ , where A 4- -ethylenediaminetetraacetate (pH 6.0, t=25-55 deg C), has been studied spectrophotometrically. It is shown, that the form EuA(H 2 O) 3 - is more reactive as compared with EuA(H 2 O) 2 - . It is found, that equilibrium constant of the process EuA(H 2 O) 3 - reversible EuA(H 2 O) 2 - (1) equals 1 at t=36.2 deg C. The values ΔH and ΔS of the process (1), constituting 13.0+-3.2 kJ/mol and 41.8+-5.5 J/molxdeg respectively, are calculated

  11. Hydronium-Ion-Catalyzed Elimination Pathways of Substituted Cyclohexanols in Zeolite H-ZSM5

    Energy Technology Data Exchange (ETDEWEB)

    Hintermeier, Peter H. [Department; Eckstein, Sebastian [Department; Mei, Donghai [Institute; Olarte, Mariefel V. [Institute; Camaioni, Donald M. [Institute; Baráth, Eszter [Department; Lercher, Johannes A. [Department; Institute

    2017-10-02

    Hydronium ions in the pores of zeolite H-ZSM5 show high catalytic activity in the elimination of water from cyclohexanol in aqueous phase. Substitution induces subtle changes in rates and reaction pathways, which are concluded to be related to steric effects. Exploring the reaction pathways of 2-, 3-, and 4-methylcyclohexanol (2-McyOH, 3-McyOH, and 4-McyOH), 2- and 4-ethylcyclohexanol (2-EcyOH and 4-EcyOH), 2-n-propylcyclohexanol (2-PcyOH), and cyclohexanol (CyOH) it is shown that the E2 character increases with closer positioning of the alkyl and hydroxyl groups. Thus, 4-McyOH dehydration proceeds via an E1-type elimination, while cis-2-McyOH preferentially reacts via an E2 pathway. The entropy of activation decreased with increasing alkyl chain length (ca. 20 J mol-1 K-1 per CH2 unit) for 2-substituted alcohols, which is concluded to result from constraints influencing the configurational entropy of the transition states.

  12. How Hot are Your Ions Really? A Threshold Collision-Induced Dissociation Study of Substituted Benzylpyridinium "Thermometer" Ions

    Science.gov (United States)

    Carpenter, John E.; McNary, Christopher P.; Furin, April; Sweeney, Andrew F.; Armentrout, P. B.

    2017-09-01

    The first absolute experimental bond dissociation energies (BDEs) for the main heterolytic bond cleavages of four benzylpyridinium "thermometer" ions are measured using threshold collision-induced dissociation in a guided ion beam tandem mass spectrometer. In this experiment, substituted benzylpyridinium ions are introduced into the apparatus using an electrospray ionization source, thermalized, and collided with Xe at varied kinetic energies to determine absolute cross-sections for these reactions. Various effects are accounted for, including kinetic shifts, multiple collisions, and internal and kinetic energy distributions. These experimentally measured 0 K BDEs are compared with computationally predicted values at the B3LYP-GD3BJ, M06-GD3, and MP2(full) levels of theory with a 6-311+G(2d,2p) basis set using vibrational frequencies and geometries determined at the B3LYP/6-311+G(d,p) level. Additional dissociation pathways are observed for nitrobenzylpyridinium experimentally and investigated using these same levels of theory. Experimental BDEs are also compared against values in the literature at the AM1, HF, B3LYP, B3P86, and CCSD(T) levels of theory. Of the calculated values obtained in this work, the MP2(full) level of theory with counterpoise corrections best reproduces the experimental results, as do the similar literature CCSD(T) values. Lastly, the survival yield method is used to determine the characteristic temperature (Tchar) of the electrospray source prior to the thermalization region and to confirm efficient thermalization. [Figure not available: see fulltext.

  13. Synthesis, characterization and magnetic properties of MWCNTs decorated with Zn-substituted MnFe{sub 2}O{sub 4} nanoparticles using waste batteries extract

    Energy Technology Data Exchange (ETDEWEB)

    Gabal, M.A., E-mail: mgabalabdonada@yahoo.com [Chemistry Department, Faculty of Science, King Abdulaziz University, Jeddah (Saudi Arabia); Al-Harthy, E.A. [Chemistry Department, Faculty of Science, King Abdulaziz University, Jeddah (Saudi Arabia); Center of Excellence in Environmental Studies, King Abdulaziz University, PO Box 80216, Jeddah 21589 (Saudi Arabia); Al Angari, Y.M.; Abdel Salam, M.; Asiri, A.M. [Chemistry Department, Faculty of Science, King Abdulaziz University, Jeddah (Saudi Arabia)

    2016-06-01

    Mn{sub 1−x}Zn{sub x}Fe{sub 2}O{sub 4} (x=0.2–0.8) nano-crystals, synthesized from recycling of Zn–C batteries, were successfully self-assembled alongside multi-walled carbon nanotubes (MWCNTs) via an environmentally friend sucrose auto-combustion method. The effect of Zn-content on structural and magnetic properties were investigated and discussed. XRD revealed the formation of single-phase ferrites. DTA–TG experiment showed that the auto-combustion reaction finished at about 350 {sup °}C. TEM exhibited that the MWCNTs are well decorated with ferrite particles. Hysteresis loop measurements revealed ferromagnetic behavior, with saturation magnetization decrease by the addition of MWCNTs or increasing Zn-Content. The kinetics of methylene blue dye (MB) removal using MWCNTs/Mn{sub 0.8}Zn{sub 0.2}Fe{sub 2}O nano-composite was investigated and discussed. - Graphical abstract: TEM image of MWCNTs/Mn{sub 0.8}Zn{sub 0.2}Fe{sub 2}O{sub 4} nano-composite showed that the MWCNTs were completely decorated with magnetic nanoparticles. The decoration passed through nucleation and growth processes in which nucleation of ferrite nanoparticles first takes place on the surface of MWCNTs followed by a subsequent growth of these nuclei. - Highlights: • Mn-Zn-ferrites were obtained via recycling process of spent Zn-C batteries. • Mn1−xZnxFe2O4/MWCNTS nano-composites were synthesized via sucrose combustion route. • Zn-substitution effect on structural and magnetic properties was investigated. • MWCNTs/Mn0.8Zn0.2Fe2O4 was investigated to remove MB dye from aqueous media.

  14. HYDROTALSIT Zn-Al-EDTA SEBAGAI ADSORBEN UNTUK POLUTAN ION Pb(II DI LINGKUNGAN Zn-Al-EDTA Hydrotalcite as Adsorbent for Pb(II Ion Pollutant in The Environment

    Directory of Open Access Journals (Sweden)

    Roto Roto

    2015-07-01

    Full Text Available ABSTRAK Polusi ion Pb(II di dalam lingkungan perairan cenderung naik seiring peningkatan jumlah industri smelter dan daur ulang aki bekas. Penelitian ini bertujuan untuk menguji kemampuan hidrotalsit Zn-Al-EDTA sebagai adsorben ion Pb(II dalam air secara mendalam. Hidrotalsit Zn-Al-NO3 disintesis dengan metode kopresipitasi dan hidrotermal pada temperatur 100 °C selama 15 jam. Hidrotalsit Zn-Al-EDTA diperoleh dengan penukaran ion. Keasaman larutan, kinetika dan kapasitas adsorpsi diteliti. Hidrotalsit Zn-Al-EDTA memiliki d003 sebesar 14,52 Å sementara Zn-Al-NO3 sebesar 8,90 Å. Spektra FTIR menunjukkan keberadaan serapan gugus C=O pada bilangan gelombang 1684,77 cm-1. Kondisi optimum adsorpsi ion Pb(II terjadi pada pH 4, waktu kontak 60 menit dan kapasitas adsorpsi diperoleh 2,07 mg/g pada konsentrasi awal 10 mg/L dengan berat adsorben 0,100 g. Adsorpsi ion Pb(II oleh hidrotalsit Zn-Al-EDTA mengikuti reaksi pseudo orde dua dengan tetapan laju adsorpsi sebesar 8,90 g mmol-1min-1. Adsorpsi ion Pb(II oleh Zn-Al-EDTA terjadi karena  pembentukan khelat Pb-EDTA di dalam struktur hidrotalsit. Hasil ini diharapkan mampu memberikan kontribusi yang lebih luas di dalam pengendalian konsentrasi Pb(II di lingkungan. ABSTRACT Polution by Pb(II ion in the water environment tends to increase due the increase in the number of lead smelter and lead acid battery recycling industries. This work aims at studying in details the ability of Zn-Al-EDTA hydrotalcite as adsorbent for Pb(II ion in the environment. The Zn-Al-NO3 hydrotalcite was synthesized first by coprecipitation method followed by hydrothermal treatment at 100 °C for 15 h. The Zn-Al-EDTA hydrotalcite was later obtained by ion exchange process. The solution pH, kinetics and adsorption capacity were studied. The XRD data showed that Zn-Al-EDTA and Zn-Al-NO3 hydrotalcites have d003 of 14.52 and 8.90 Å, respectively. The FTIR spectra suggested that C=O group was observed with absorption band at 1684

  15. ANTIMICROBIAL ACTIVITY OF Ag+, Cu2+, Zn2+, Mg2+ IONS DOPED CHITOSAN NANOPARTICLES

    Directory of Open Access Journals (Sweden)

    Sukhodub LB

    2015-04-01

    Full Text Available Modification by polymers and inorganic ions of the bioactive materials for orthopedic implants with the purpose of initiating controlled reactions in tissues that surround the implant, is one of the modern approaches in medical materials. A key feature of functional polymers is their ability to form complexes with various metal ions in solution. Chitosan is natural biopolymer with pronounced affinity to transition metal ions. Some researches prove the higher antimicrobial activity of Chitosan-metal complexes compared with pure Chitosan. The purpose of this work was the study of antimicrobial activity of Chitosan nanoparticles modified by metal ions Ag+, Cu2+, Zn2+, Mg2+ against reference strains S. aureus 25923 ATSS, E. coli ATCC 25922, C. albicans ATCC 885653 for their further use as components of the composite biomaterials for medical purpose.Chitosan nanoparticles suspension was prepared by known method based on the ionotropic gelation between chitosan and sodium tripolyphosphate.To obtain Chitosan-metal nanoparticles to the Chitosan suspension were added the corresponding metal ions aqueous solutions in quantity to match the concentration of metal ions of 200 ppm . Antibacterial activities of Ag+, Cu2+, Zn2+, Mg2+ ions doped Chitosan nanoparticles, pure Chitosan nanoparticles, metal ions and 1% (v/v acetic acid solution (it was used as solvent for Chitosan against bacteria were evaluated by determination of minimum inhibitory concentration (MIC and minimum bactericidal concentration (MBC in vitro. Muller– Hinton (MH broth and MH agar (Russia were used as growth media. The bacteria suspension for further use was prepared with concentration that corresponded 0,5units by McFarland scale. The MIC was determined by a broth dilution method. The results were read after 24 hours of experimental tubes incubation at 37 oC as equivalent to the concentration of the tube without visible growth. To evaluate MBC, a sample of 0,1 ml was transferred from

  16. Understanding lattice defects to influence ferromagnetic order of ZnO nanoparticles by Ni, Cu, Ce ions

    Energy Technology Data Exchange (ETDEWEB)

    Verma, Kuldeep Chand, E-mail: dkuldeep.physics@gmail.com [Department of Physics, Panjab University, Chandigarh 160014 (India); Kotnala, R.K., E-mail: rkkotnala@gmail.com [CSIR-National Physical Laboratory, New Delhi 110012 (India)

    2017-02-15

    Future spintronics technologies based on diluted magnetic semiconductors (DMS) will rely heavily on a sound understanding of the microscopic origins of ferromagnetism in such materials. It remains unclear, however, whether the ferromagnetism in DMS is intrinsic - a precondition for spintronics - or due to dopant clustering. For this, we include a simultaneous doping from transition metal (Ni, Cu) and rare earth (Ce) ions in ZnO nanoparticles that increase the antiferromagnetic ordering to achieve high-T{sub c} ferromagnetism. Rietveld refinement of XRD patterns indicate that the dopant ions in ZnO had a wurtzite structure and the dopants, Ni{sup 2+}, Cu{sup 2+}, Ce{sup 3+} ions, are highly influenced the lattice constants to induce lattice defects. The Ni, Cu, Ce ions in ZnO have nanoparticles formation than nanorods was observed in pure sample. FTIR involve some organic groups to induce lattice defects and the metal-oxygen bonding of Zn, Ni, Cu, Ce and O atoms to confirm wurtzite structure. Raman analysis evaluates the crystalline quality, structural disorder and defects in ZnO lattice with doping. Photoluminescence spectra have strong near-band-edge emission and visible emission bands responsible for defects due to oxygen vacancies. The energy band gap is calculated using Tauc relation. Room temperature ferromagnetism has been described due to bound magnetic polarons formation with Ni{sup 2+}, Cu{sup 2+}, Ce{sup 3+} ions in ZnO via oxygen vacancies. The zero field and field cooling SQUID measurement confirm the strength of antiferromagnetism in ZnO. The field cooling magnetization is studied by Curie-Weiss law that include antiferromagnetic interactions up to low temperature. The XPS spectra have involve +3/+4 oxidation states of Ce ions to influence the observed ferromagnetism. - Graphical abstract: The lattice defects/vacancies attributed by Ni and Ce ions in the wurtzite ZnO structure are responsible in high T{sub c} -ferromagnetism due to long-range magnetic

  17. Single and binary adsorption of Cd (Ⅱ) and Zn (Ⅱ) ions from aqueous solutions onto bottom ash

    Energy Technology Data Exchange (ETDEWEB)

    Sukpreabprom, Hatairat; Arqueropanyo, Orn-anong; Naksata, Wimol; Janhom, Sorapong [Chiang Mai University, Chiang Mai (Thailand); Sooksamiti, Ponlayuth [The Office of Primary Industries and Mines Region 3, Chiang Mai (Thailand)

    2015-05-15

    Bottom ash, a waste obtained from coal-burning power plant, was used as a low cost adsorbent for the removal of Cd (Ⅱ) and Zn (Ⅱ) ions from single and binary systems in batch experiments. The results of adsorption capacity showed that bottom ash could be considered as a potential adsorbent. The uptake of Zn (Ⅱ) ion was greater than that of Cd (Ⅱ) ion. For single adsorption, based on the correlation coefficient (R{sup 2}) values, both Langmuir and Freundlich isotherms suitably described the adsorption equilibrium data in the initial metal ion concentration range of 10-50 mg/L. The multicomponent isotherms, including the extended Langmuir and IAST-Freundlich isotherms, were used to predict the binary adsorption of Cd (Ⅱ) and Zn (Ⅱ) ions. Furthermore, the appropriate multicomponent isotherm was investigated by minimizing the average relative error (ARE) function. It should be confirmed that the extended Langmuir isotherm fitted the binary adsorption equilibrium data satisfactorily.

  18. Resonantly enhanced spin-lattice relaxation of Mn2 + ions in diluted magnetic (Zn,Mn)Se/(Zn,Be)Se quantum wells

    Science.gov (United States)

    Debus, J.; Ivanov, V. Yu.; Ryabchenko, S. M.; Yakovlev, D. R.; Maksimov, A. A.; Semenov, Yu. G.; Braukmann, D.; Rautert, J.; Löw, U.; Godlewski, M.; Waag, A.; Bayer, M.

    2016-05-01

    The dynamics of spin-lattice relaxation in the magnetic Mn2 + ion system of (Zn,Mn)Se/(Zn,Be)Se quantum-well structures are studied using optical methods. Pronounced cusps are found in the giant Zeeman shift of the quantum-well exciton photoluminescence at specific magnetic fields below 10 T, when the Mn spin system is heated by photogenerated carriers. The spin-lattice relaxation time of the Mn ions is resonantly accelerated at the cusp magnetic fields. Our theoretical analysis demonstrates that a cusp occurs at a spin-level mixing of single Mn2 + ions and a quick-relaxing cluster of nearest-neighbor Mn ions, which can be described as intrinsic cross-relaxation resonance within the Mn spin system.

  19. Efficiencies of Eu{sup 3+} ions and hydrogen atoms as donors in ZnO thin films

    Energy Technology Data Exchange (ETDEWEB)

    Akazawa, Housei, E-mail: akazawa.housei@lab.ntt.co.jp [NTT Device Innovation Center, NTT Corporation, 3-1 Morinosato Wakamiya, Atsugi, Kanagawa 243-0198 (Japan)

    2016-09-15

    The donor efficiencies of Eu{sup 3+} ions and hydrogen atoms in ZnO crystalline films were investigated with reference to that of Ga{sup 3+} ions. It was found that Eu{sup 3+} ions acted as extrinsic donors in ZnO:Eu films, yielding a resistivity of 1.8 × 10{sup −3} Ω cm at a doping level of 1 at. %. This value is comparable to one for intrinsic donors in undoped ZnO films. The conductivity was maintained as the deposition temperature was increased to 200 °C, and this is evidence for the contribution of extrinsic donors. Deposition of Ga-doped and Eu-doped ZnO films in an H{sub 2}O gas flow produced oxyhydrogenated ZnO:(Ga, H) and ZnO:(Eu, H) films in which the Ga{sup 3+} and Eu{sup 3+} donors were deactivated by oxidization. Nevertheless, hydrogen donors contributed to electrical conduction yielding a resistivity of 1 × 10{sup −2} Ω cm. Postannealing in an H{sub 2} gas ambient alleviated the excessive oxidization of the films and thereby reactivated the donor action of Ga{sup 3+} and Eu{sup 3+} ions, causing the resistivity to recover to 10{sup −3} Ω cm for ZnO:(Ga, H) and 10{sup −2} Ω cm for ZnO:(Eu, H). In contrast, vacuum annealing of ZnO:(Ga, H) and ZnO:(Eu, H) films increased resistivity through removal of hydrogen donors while not affecting the oxidized condition of the samples.

  20. Current transport studies of ZnO/p-Si heterostructures grown by plasma immersion ion implantation and deposition

    International Nuclear Information System (INIS)

    Chen, X.D.; Ling, C.C.; Fung, S.; Beling, C.D.; Mei, Y.F.; Fu, Ricky K.Y.; Siu, G.G.; Chu, Paul K.

    2006-01-01

    Rectifying undoped and nitrogen-doped ZnO/p-Si heterojunctions were fabricated by plasma immersion ion implantation and deposition. The undoped and nitrogen-doped ZnO films were n type (n∼10 19 cm -3 ) and highly resistive (resistivity ∼10 5 Ω cm), respectively. While forward biasing the undoped-ZnO/p-Si, the current follows Ohmic behavior if the applied bias V forward is larger than ∼0.4 V. However, for the nitrogen-doped-ZnO/p-Si sample, the current is Ohmic for V forward 2 for V forward >2.5 V. The transport properties of the undoped-ZnO/p-Si and the N-doped-ZnO/p-Si diodes were explained in terms of the Anderson model and the space charge limited current model, respectively

  1. Charge compensation mechanisms in favor of the incorporation of the Eu3+ ion into the ZnO host lattice

    Science.gov (United States)

    Baira, M.; Bekhti-Siad, A.; Hebali, K.; Bouhani-Benziane, H.; Sahnoun, M.

    2018-05-01

    Eu3+ doped phosphors with charge compensation are potential candidates of red emitting phosphors for lamp applications. Charge compensation improves the luminescence performance of the material. The charge compensation can most probably be achieved by three possible mechanisms: (a) two Zn2+ ions are replaced by one Eu3+ ions and one monovalent cation, 2Zn2+ →Eu3++ Li+, where Li+ is acting as a charge compensator; (b) the charge compensation is provided by a zinc vacancy (VZn) defects, 3Zn2+ → 2Eu3++ VZn, the subscript Zn denotes an ion in a normal zinc site in the lattice; (c) two Zn2+ ions are replaced by one Eu3+ ions with the presence of interstitial oxygen (Oi), 2Zn2+ → 2Eu3++ Oi. Electronic structures of the crystals corresponding to the three models are evaluated by the first-principles quantum mechanical calculations based on the density functional theory. It is found that the charge compensator defects make Eu3+ doping in ZnO energetically more favorable. They break the local symmetry around the Eu3+ ion and lead to deep states below the empty upper band, the conduction band that could facilitate intra-4f shell transitions, which can obviously improve the emission intensity of Eu3+-doped ZnO. Therefore, the effect of these defects on the host crystals electronic band states relative to the Eu3+ states is reported, since both electron transfer and electronically energy transfer processes enhance the performance of optoelectronic devices based on this material. These theoretical insights are helpful for designing rare-earth doped oxide materials with high photoluminescence (PL) performance.

  2. Influence of high-energy ion implantation on the microstructure of Sn - 9,8 wt. % Zn alloy

    International Nuclear Information System (INIS)

    Gusakova, O.V.

    2016-01-01

    The results of investigation of influence of Xe ion implantation on the microstructure of Sn - 9,8 wt. % Zn alloy are represented/ Analysis of the experimental results shows that the high-energy ion implantation of Xe causes a change in the particle size of zinc. (authors)

  3. Excitation spectra and forward injection electroluminescence of Er/sup 3+/ ions in ZnS

    International Nuclear Information System (INIS)

    Jiaqi, Y.; Tianren, Z.; Wenlian, L.

    1985-01-01

    Trivalent rare earth ions (RE/sup 3+/) are efficient luminescent centers for electroluminescence (EL) of thin films of II-VI compounds, which are promising display materials and attract more and more attention. The mechanism of all EL devices of RE/sup 3+/ available so far is hot electron impact excitation. Based on the analysis of excitation spectra of RE/sup 3+/ in ZnS, the authors have pointed out the possibility of a new type of EL of RE/sup 3+/ - forward injection EL, which have potential of reducing operation voltage and raising efficiency. The forward injection EL of RE/sup 3+/ has been observed and experimentally proven in ZnS:Er/sup 3+/ diode for the first time

  4. Synthesis and properties of Pr-substituted MgZn ferrites for core materials and high frequency applications

    Energy Technology Data Exchange (ETDEWEB)

    Mukhtar, Muhammad Waqas; Irfan, Muhammad [Department of Physics, Federal Urdu University of Arts, Science and Technology, Islamabad 44000 (Pakistan); Ahmad, Ishtiaq; Ali, Ihsan [Department of Physics, Bahauddin Zakariya University, Multan 60800 (Pakistan); Akhtar, Majid Niaz [Department of Physics, COMSATS Institute of Information Technology, Lahore (Pakistan); Khan, Muhammad Azhar [Department of Physics, Islamia University, Bahawalpur (Pakistan); Abbas, Ghazanfar [Department of Physics, COMSATS Institute of Information Technology, Islamabad 44000 (Pakistan); Rana, M.U. [Center of Excellence in Solid State Physics, University of the Punjab, Lahore (Pakistan); Ali, Akbar [Department of Basic Sciences, Riphah International University, Islamabad-44000 (Pakistan); Ahmad, Mukhtar, E-mail: ahmadmr25@yahoo.com [Department of Physics, COMSATS Institute of Information Technology, Islamabad 44000 (Pakistan)

    2015-05-01

    A series of single phase spinel ferrites having chemical formula Mg{sub 0.5}Zn{sub 0.5}Pr{sub x}Fe{sub 2−x}O{sub 4} (x=0.00, 0.05, 0.10, 0.15, 0.20, 0.25) were prepared using the sol–gel technique after sintering at 700 °C. The thermal decomposition behavior of an as prepared powder was investigated by means of DTA/TGA analyses. The sintered powders were then characterized by Fourier transform infrared spectroscope, X-ray diffraction, scanning electron microscope, energy dispersive X-ray spectroscope and vibrating sample magnetometer. X-ray diffraction patterns confirm the single phase spinel structure of prepared ferrites without the presence of any impurity phase. The value of lattice parameter (a) increases with the increase of Pr contents (x) into the spinel lattice. The grain size estimated from electron microscope images is in the range of 2.75–5.4 µm which confirms the spinel crystalline nature of the investigated samples. The saturation magnetization (M{sub s}) decreases whereas coercivity (H{sub c}) increases with the increase of Pr contents (x). The measured parameters suggest that these materials are favorable for high frequency applications and as core materials. - Highlights: • Pr-substituted spinel ferrites synthesized by autocombustion route have been investigated. • The average grain size was in the range of 2.75–5.4 µm estimated by SEM technique. • The (M{sub s}) decreases whereas (H{sub c}) increases with the increase of Pr contents (x). • These parameters are favorable for high frequency applications and as core materials.

  5. Synthesis and properties of Pr-substituted MgZn ferrites for core materials and high frequency applications

    International Nuclear Information System (INIS)

    Mukhtar, Muhammad Waqas; Irfan, Muhammad; Ahmad, Ishtiaq; Ali, Ihsan; Akhtar, Majid Niaz; Khan, Muhammad Azhar; Abbas, Ghazanfar; Rana, M.U.; Ali, Akbar; Ahmad, Mukhtar

    2015-01-01

    A series of single phase spinel ferrites having chemical formula Mg 0.5 Zn 0.5 Pr x Fe 2−x O 4 (x=0.00, 0.05, 0.10, 0.15, 0.20, 0.25) were prepared using the sol–gel technique after sintering at 700 °C. The thermal decomposition behavior of an as prepared powder was investigated by means of DTA/TGA analyses. The sintered powders were then characterized by Fourier transform infrared spectroscope, X-ray diffraction, scanning electron microscope, energy dispersive X-ray spectroscope and vibrating sample magnetometer. X-ray diffraction patterns confirm the single phase spinel structure of prepared ferrites without the presence of any impurity phase. The value of lattice parameter (a) increases with the increase of Pr contents (x) into the spinel lattice. The grain size estimated from electron microscope images is in the range of 2.75–5.4 µm which confirms the spinel crystalline nature of the investigated samples. The saturation magnetization (M s ) decreases whereas coercivity (H c ) increases with the increase of Pr contents (x). The measured parameters suggest that these materials are favorable for high frequency applications and as core materials. - Highlights: • Pr-substituted spinel ferrites synthesized by autocombustion route have been investigated. • The average grain size was in the range of 2.75–5.4 µm estimated by SEM technique. • The (M s ) decreases whereas (H c ) increases with the increase of Pr contents (x). • These parameters are favorable for high frequency applications and as core materials

  6. Calibration of shahid's analytical method for adulterated Zn-edta fertilizers by ion chromatography and atomic absorption spectroscopy

    International Nuclear Information System (INIS)

    Khan, M.S.A.; Akram, M.; Qazi, M.A.

    2010-01-01

    Chelated zinc fertilizers are usually recommended in calcareous alkaline soils to provide Zn nutrition in order to prevent possible Zn precipitation. In Punjab (Pakistan), Zn EDTA products are being manufactured, and marketed to meet the zinc requirement of various crops grown in Zn deficient soils. Under fertilizer control order, 1973 (amended), their quality has to be monitored by the Agriculture Department, Government of the Punjab. None of the traditional method was found suitable which can separate the mineral fraction from that of chelated adulterated fertilizer except for those methods based on ion chromatography. Calibration of ion chromatography method was carried out by determining the mineral Zn fraction leading to estimate remaining Zn EDTA fraction in fertilizer samples of adulterated nature i.e. mixture of chelated and mineral fraction. In order to achieve the objective atomic absorption spectroscopy was coupled with ion chromatography. The method offers a specific, reliable technique for determination of chelated zinc in fertilizers. In the first step chelation was broken down with concentrated sulphuric acid treatment and total zinc contents were determined by atomic absorption spectroscopy. In second step, non-chelated (mineral) portion of zinc was determined by ion chromatography using cation column and conductivity detector. Chelated zinc was calculated by subtracting non-chelated (mineral) fraction from total zinc contents. (author)

  7. Synthesis, characterization, and application of novel Zn(II)-ionic imprinted polymer for preconcentration of Zn(II) ions from aqueous solution

    Science.gov (United States)

    Wirawan, T.; Supriyanto, G.; Soegianto, A.

    2018-04-01

    Preparation of a new Zn2+ ion-imprinted polymer (Zn-IIP) is presented in this report. The Zn-IIP are prepared by precipitation polymerization using 8-hydroxyquinoline (8HQ) as a ligand, methacrylic acid (MAA) as functional monomer, and ethylene glycol dimethacrylate (EGDMA) as a cross-linker has been prepared. The benzoyl peroxide and ethanol/acetonitrile (2:1) mixture were used as initiator and porogen, respectively. Precipitation polymerization was carried out by heating in a water bath at 60°C for 8 hours. After polymerization, cavities in the polymer particles corresponding to the Zn2+ ions were created by leaching the polymer with 2 mol L-1 HNO3. The polymer was washed with aquabidest and dried in an oven at the temperature of 60°C for 24 hours. The Zn-IIP was characterized by Fourier Transform Infrared Spectrophotometry (FT-IR) and Scanning Electron Microscopy (SEM). The synthesized Zn-IIP was used as a new adsorbent for solid phase extraction (SPE) of Zn(II) prior to Flame Atomic Absorption Spectrometry (FAAS) determination. The experimental parameters for SPE, such as pH of the sample, loading rate, and elution volume, have been optimized. The effect of pH of the sample on the extraction of analyte was studied in batch mode. The effects of loading rate and elution volume on the extraction of analyte were studied in dynamic mode by loading of the sample through IIP-SPE cartridge containing 100 mg of the synthesized Zn-IIP. The imprinted polymer (Zn-IIP) have bands at 3433.06 cm-1 (O-H), 1508.23 cm-1 (C=N aromatics), 1284.5 cm-1 (C-N aromatics), 1056.9 cm-1 (C-O phenol), 1724.24 cm-1 (C=O), and 1639.38 cm-1 (conjugated C=O with C=C). The Scanning Electron Microscopy (SEM) images of IIP and IIP show that the IIP is seen to have more cavities than NIP. The optimum pH for quantitative Zn(II) retention was 5.5, and the elution was completed with 2 mL of 1.0 mol L-1 nitric acid. The optimum loading rate was 0.5 mL min-1. The recovery of Zn(II) from solution

  8. Structural characterization of CdSe/ZnS quantum dots using medium energy ion scattering

    Science.gov (United States)

    Sortica, M. A.; Grande, P. L.; Radtke, C.; Almeida, L. G.; Debastiani, R.; Dias, J. F.; Hentz, A.

    2012-07-01

    In the present work, we have analyzed CdSe/ZnS core-shell quantum dots by medium energy ion scattering (MEIS), which is a powerful technique to explore the synthesis, formation, stability, and elemental distribution of such core-shell structures, along with other auxiliary analytical techniques. By comparing different quantum-dot structural models spectra with the experimental MEIS data, we were able to obtain some sample structural information. We found that, despite the well known non stoichiometric Cd:Se ratio, the core is stoichiometric, and there is an excess of cadmium distributed in the shell.

  9. Composition-structure-property (Zn2+ and Ca2+ ion release) evaluation of Si-Na-Ca-Zn-Ce glasses: Potential components for nerve guidance conduits

    International Nuclear Information System (INIS)

    Zhang, X.F.; Kehoe, S.; Adhi, S.K.; Ajithkumar, T.G.; Moane, S.; O'Shea, H.; Boyd, D.

    2011-01-01

    Bioactive glasses have demonstrated tailored therapeutic ion release, primarily with respect to the augmentation of hard tissues. However, controlled degradation and release of therapeutic ions from biomaterials may also play an important role in soft tissue regeneration such as repair of peripheral nerve discontinuities. In this study, three silica based glasses (0.5SiO 2 -0.2CaO-0.13ZnO-XNa 2 O-(0.17-X) CeO 2 ) where, (0.04 29 Si isotope was probed for each glass using 29 Si MAS-NMR, whilst the thermal characteristics of each glass were examined using DTA. Following these analyses, ion release profiles for Ca 2+ and Zn 2+ were evaluated; an equivalent specific surface area of 1 m 2 of each glass powder was incubated (37 deg. C) in 10 ml of citric acid buffer and TRIS-HCI buffer solution (pH 3.0 and pH 7.4 respectively) for incubation periods of up to 30 days. The Zn 2+ concentration of each filtrate was analysed using flame Atomic Absorption Spectroscopy (Varian AA240FS Fast Sequential AAS) and the Ca 2+ concentration of each filtrate was determined using Inductively Coupled Plasma-Mass Spectrometer (Varian 820 ICP-MS). Results obtained from the 29 Si MAS-NMR spectra indicated Q 2 structures pervading the network. An analytical model was proposed to analyse the ion release profiles for each glass, and indicated heterogeneous dissolution of glass networks. The ion release data demonstrates that ion release in the range (19.26-3130 ppm) for Ca 2+ and in the range (5.97-4904 ppm) for Zn 2+ occurred. Release of such elements, at appropriate levels, from peripheral nerve guidance conduits may be advantageous with respect to the repair of peripheral nerve discontinuities.

  10. Effect of ion beam irradiation on the structure of ZnO films deposited by a dc arc plasmatron.

    Science.gov (United States)

    Penkov, Oleksiy V; Lee, Heon-Ju; Plaksin, Vadim Yu; Ko, Min Gook; Joa, Sang Beom; Yim, Chan Joo

    2008-02-01

    The deposition of polycrystalline ZnO film on a cold substrate was performed by using a plasmatron in rough vacuum condition. Low energy oxygen ion beam generated by a cold cathode ion source was introduced during the deposition process. The change of film property on the ion beam energy was checked. It is shown that irradiation by 200 eV ions improves crystalline structure of the film. Increasing of ion beam energy up to 400 eV leads to the degradation of a crystalline structure and decreases the deposition rate.

  11. Formation and characterization of ZnO : Tm+ optical waveguides fabricated by Tm+ and O+ ion implantation

    International Nuclear Information System (INIS)

    Ming Xianbing; Lu Fei; Liu Hanping; Chen Ming; Wang Lei

    2009-01-01

    Planar optical waveguides were formed in ZnO crystal by Tm + and O + ion implantation. The distributions of Tm + in as-implanted and annealed ZnO samples were investigated by the RBS technique. A shift of the Tm + peak towards the sample surface and out diffusion were observed after thermal treatment and subsequent O + ion implantation. Waveguide formation was determined after O + implantation in Tm + -implanted ZnO crystal. By using the prism-coupling method two guided modes were detected. The refractive index profile in the implanted waveguide was reconstructed according to the SRIM and RCM simulation. The RBS/channelling measurements show that the lattice structure of ZnO did not suffer detectable damage after O + implantation.

  12. Facile Synthesis of Graphene/ZnO Composite as an Anode with Enhanced Performance for Lithium Ion Batteries

    Directory of Open Access Journals (Sweden)

    Yanhong Zhao

    2014-01-01

    Full Text Available Graphene/ZnO composites with different contents of ZnO have been successfully synthesized via a liquid phase route. The structure, morphology, and electrochemical performances of the composites are investigated by XRD, Raman, SEM, TEM, AFM, and electrochemical measurement. The results reveal that ZnO nanoparticles wedged on the surface of the graphene nanosheets. The initial capacity of graphene/ZnO (1 : 1 reached 1155.27 mAh g−1, which increased 162.87 mAh g−1 compared with the initial capacity of graphene. This could be attributed to the unique structure of the prepared composite and synergies of graphene and ZnO in the lithium ion storage.

  13. Gallium ion implantation greatly reduces thermal conductivity and enhances electronic one of ZnO nanowires

    Directory of Open Access Journals (Sweden)

    Minggang Xia

    2014-05-01

    Full Text Available The electrical and thermal conductivities are measured for individual zinc oxide (ZnO nanowires with and without gallium ion (Ga+ implantation at room temperature. Our results show that Ga+ implantation enhances electrical conductivity by one order of magnitude from 1.01 × 103 Ω−1m−1 to 1.46 × 104 Ω−1m−1 and reduces its thermal conductivity by one order of magnitude from 12.7 Wm−1K−1 to 1.22 Wm−1K−1 for ZnO nanowires of 100 nm in diameter. The measured thermal conductivities are in good agreement with those in theoretical simulation. The increase of electrical conductivity origins in electron donor doping by Ga+ implantation and the decrease of thermal conductivity is due to the longitudinal and transverse acoustic phonons scattering by Ga+ point scattering. For pristine ZnO nanowires, the thermal conductivity decreases only two times when its diameter reduces from 100 nm to 46 nm. Therefore, Ga+-implantation may be a more effective method than diameter reduction in improving thermoelectric performance.

  14. Preconcentration of Zn2+ and Cu2+ ions from food and vegetable samples using modified activated carbon.

    Science.gov (United States)

    Ghaedi, M; Tavallali, H; Montazerozohori, M; Zahedi, E; Amirineko, M; Khodadoust, S; Karimipour, G

    2012-11-01

    In this work, two N/S-containing chelating agents 2-(4-methoxybenzylideneamino)thiophenol (2-4-MBAT) and 2-(4-chlorobenzylideneamino) benzenethiol (2-4-CBABT) were synthesized as new sorbents and were used for preconcentration of Zn(2+) and Cu(2+) ions in food and vegetable samples. In the proposed procedure, the trace amount of Zn(2+) and Cu(2+) ions from 250 mL of sample solution at pH = 5.0 was preconcentrated by 1 g of activated carbon (AC) loaded with 15 mg of 2-4-MBAT and 2-4-CBABT separately. The breakthrough volumes (maximum sample volume that their metal ions quantitatively can be enriched) for solid-phase extraction (SPE) procedure based on the AC modified with 2-4-MBAT and 2-4-CBABT were 800 and 750 mL, respectively. The sorbed Zn(2+) and Cu(2+) ions were efficiently eluted by 8 mL of 4 mol L(-1) HNO(3) and preconcentration factor of 112.5 and 93.7 and experimental enhancement factor of 30 and 35 ions were obtained for Zn(2+) and Cu(2+), respectively. The application of this enrichment procedure allowed the extraction of trace metal ions with recoveries exceeding of 90%.

  15. Dielectric relaxation behavior and impedance studies of Cu2+ ion doped Mg - Zn spinel nanoferrites

    Science.gov (United States)

    Choudhary, Pankaj; Varshney, Dinesh

    2018-03-01

    Cu2+ substituted Mg - Zn nanoferrites is synthesized by low temperature fired sol gel auto combustion method. The spinel nature of nanoferrites was confirmed by lab x-ray technique. Williamson - Hall (W-H) analysis estimate the average crystallite size (22.25-29.19 ± 3 nm) and micro strain induced Mg0.5Zn0.5-xCuxFe2O4 (0.0 ≤ x ≤ 0.5). Raman scattering measurements confirm presence of four active phonon modes. Red shift is observed with enhanced Cu concentration. Dielectric parameters exhibit a non - monotonous dispersion with Cu concentration and interpreted with the support of hopping mechanism and Maxwell-Wagner type of interfacial polarization. The ac conductivity of nanoferrites increases with raising the frequency. Complex electrical modulus reveals a non - Debye type of dielectric relaxation present in nanoferrites. Reactive impedance (Z″) detected an anomalous behavior and is related with resonance effect. Complex impedance demonstrates one semicircle corresponding to the intergrain (grain boundary) resistance and also explains conducting nature of nanoferrites. For x = 0.2, a large semicircle is observed revealing the ohmic nature (minimum potential drop at electrode surface). Dielectric properties were improved for nanoferrites with x = 0.2 and is due to high dielectric constant, conductivity and minimum loss value (∼0.009) at 1 MHz.

  16. Trace amounts of Cu{sup 2+} ions influence ROS production and cytotoxicity of ZnO quantum dots

    Energy Technology Data Exchange (ETDEWEB)

    Moussa, Hatem [CNRS and Université de Lorraine, Laboratoire Réactions et Génie des Procédés (LRGP), CNRS UMR 7274, 1 rue Grandville, 54001 Nancy (France); Laboratoire de Biosurveillance de l' Environnement, Université de Carthage, Faculté des Sciences de Bizerte, 7021 Jarzouna, Bizerte (Tunisia); Merlin, Christophe [CNRS and Université de Lorraine, Laboratoire de Chimie Physique et Microbiologie pour l' Environnement (LCPME), CNRS UMR 7564, 15 Avenue du Charmois, 54500 Vandoeuvre-lès-Nancy (France); Dezanet, Clément [CNRS and Université de Lorraine, Laboratoire Réactions et Génie des Procédés (LRGP), CNRS UMR 7274, 1 rue Grandville, 54001 Nancy (France); Balan, Lavinia [Institut de Science des Matériaux de Mulhouse (IS2M), CNRS UMR 7361, 15 rue Jean Starcky, 68093 Mulhouse (France); Medjahdi, Ghouti [CNRS and Université de Lorraine, Institut Jean Lamour (IJL), UMR CNRS 7198, BP 70239, 54506 Vandoeuvre-lès-Nancy Cedex (France); Ben-Attia, Mossadok [Laboratoire de Biosurveillance de l' Environnement, Université de Carthage, Faculté des Sciences de Bizerte, 7021 Jarzouna, Bizerte (Tunisia); and others

    2016-03-05

    Highlights: • Chemisorbed Cu{sup 2+} ions on ZnO QDs enhance ROS production. • A mechanism combining excited electrons and holes and Fenton reactions is proposed. • ZnO@APTMS/Cu QDs were found to be the most deleterious to E. coli cells. - Abstract: 3-Aminopropyltrimethoxysilane (APTMS) was used as ligand to prepare ZnO@APTMS, Cu{sup 2+}-doped ZnO (ZnO:Cu@APTMS) and ZnO quantum dots (QDs) with chemisorbed Cu{sup 2+} ions at their surface (ZnO@APTMS/Cu). The dots have a diameter of ca. 5 nm and their crystalline and phase purities and composition were established by X-ray diffraction, transmission electron microscopy, UV-visible and fluorescence spectroscopies and by X-ray photoelectron spectroscopy. The effect of Cu{sup 2+} location on the ability of the QDs to generate reactive oxygen species (ROS) under light irradiation was investigated. Results obtained demonstrate that all dots are able to produce ROS (·OH, O{sub 2}·{sup −}, H{sub 2}O{sub 2} and {sup 1}O{sub 2}) and that ZnO@APTMS/Cu QDs generate more ·OH and O{sub 2}·{sup −} radicals and H{sub 2}O{sub 2} than ZnO@APTMS and ZnO:Cu@APTMS QDs probably via mechanisms associating photo-induced charge carriers and Fenton reactions. In cytotoxicity experiments conducted in the dark or under light exposure, ZnO@APTMS/Cu QDs appeared slightly more deleterious to Escherichia coli cells than the two other QDs, therefore pointing out the importance of the presence of Cu{sup 2+} ions at the periphery of the nanocrystals. On the other hand, with the lack of photo-induced toxicity, it can be inferred that ROS production cannot explain the cytotoxicity associated to the QDs. Our study demonstrates that both the production of ROS from ZnO QDs and their toxicity may be enhanced by chemisorbed Cu{sup 2+} ions, which could be useful for medical or photocatalytic applications.

  17. Doping properties of ZnO thin films for photovoltaic devices grown by URT-IP (ion plating) method

    International Nuclear Information System (INIS)

    Iwata, K.; Sakemi, T.; Yamada, A.; Fons, P.; Awai, K.; Yamamoto, T.; Matsubara, M.; Tampo, H.; Sakurai, K.; Ishizuka, S.; Niki, S.

    2004-01-01

    The Uramoto-gun with Tanaka magnetic field (URT)-ion plating (IP) method is a novel ion plating technique for thin film deposition. This method offers the advantage of low-ion damage, low deposition temperatures, large area deposition and high growth rates. Ga-doped ZnO thin films were grown using the URT-IP method, and the doping properties were evaluated. The opposing goals of low Ga composition and low resistivity are required for industrial applications of transparent conductive oxide (TCO). We have carried out a comparison between the carrier concentration and Ga atomic concentration in Ga-doped ZnO thin films and found the trade-off point for optimal TCO performance. The optimum growth conditions were obtained using a 3% Ga 2 O 3 content ZnO target

  18. Synthesis and properties of ZnTe and Eu3+ ion co-doped glass nanocomposites

    International Nuclear Information System (INIS)

    Rahaman Molla, Atiar; Tarafder, Anal; Dey, Chirantan; Karmakar, Basudeb

    2014-01-01

    In this study, ZnTe (II-VI) semiconductor and Eu +3 -ion co-doped borosilicate glass has been prepared in the SiO 2 -K 2 O-CaO-BaO-B 2 O 3 glass system followed by controlled heat-treatment to produce glass nanocomposites. Glass transition temperature and crystallization peak temperature have been evaluated using DSC analysis. Dilatometric studies were carried out to evaluate thermal expansion co-efficient, glass transition temperature, and dilatometric softening temperature and found to be 10.7 × 10 −6 /K, 580° C and 628° C, respectively. TEM micrographs demonstrate formation of nano sized crystallites of less than 50 nm. The ZnTe crystal formation also established through selected area electron diffraction (SAED) analysis and high resolution images obtained through TEM studies. With increasing heat treatment time, optical transmission cut-off wavelength (λ cut-off ) shifted towards higher wavelength. Excitation spectra were recorded by monitoring emission at 613 nm corresponding to the 5 D 0 → 7 F 2 transition. An intense 394 nm excitation band corresponding to the 7 F 0 → 5 L 6 transition was observed. Emission spectra were then recorded by exciting the glass samples at 394 nm. When the glass is heat-treated for 30 min at 610° C, a 6-fold increase in the intensity of the red emission at 612 nm has been observed, which is attributed to the segregation of Eu 3+ ions into the low phonon energy ZnTe crystallites and as the size of the nanocrystals is smaller than the size of the exciton, quantum confinement effect is visible. Further increase in heat-treatment duration led to decrease in luminescence intensity due to the growth of larger size crystals. 5 D 1 → 7 F 0 transition is visible only in the samples heat-treated for 30 min and 1 h, which is a characteristic of presence of Eu 3+ ions in the low phonon energy ZnTe crystal sites. The micro hardness of the precursor glass and glass nanocomposites was evaluated; base glass shows

  19. Full solar spectrum light driven thermocatalysis with extremely high efficiency on nanostructured Ce ion substituted OMS-2 catalyst for VOCs purification

    Science.gov (United States)

    Hou, Jingtao; Li, Yuanzhi; Mao, Mingyang; Yue, Yuanzheng; Greaves, G. Neville; Zhao, Xiujian

    2015-01-01

    The nanostructured Ce ion substituted cryptomelane-type octahedral molecular sieve (OMS-2) catalyst exhibits strong absorption in the entire solar spectrum region. The Ce ion substituted OMS-2 catalyst can efficiently transform the absorbed solar energy to thermal energy, resulting in a considerable increase of temperature. By combining the efficient photothermal conversion and thermocatalytic activity of the Ce ion substituted OMS-2 catalyst, we carried out full solar spectrum, visible-infrared, and infrared light driven catalysis with extremely high efficiency. Under the irradiation of full solar spectrum, visible-infrared, and infrared light, the Ce ion substituted OMS-2 catalyst exhibits extremely high catalytic activity and excellent durability for the oxidation of volatile organic pollutants such as benzene, toluene, and acetone. Based on the experimental evidence, we propose a novel mechanism of solar light driven thermocatalysis for the Ce ion substituted OMS-2 catalyst. The reason why the Ce ion substituted OMS-2 catalyst exhibits much higher catalytic activity than pure OMS-2 and CeO2/OMS-2 nano composite under the full solar spectrum irradiation is discussed.The nanostructured Ce ion substituted cryptomelane-type octahedral molecular sieve (OMS-2) catalyst exhibits strong absorption in the entire solar spectrum region. The Ce ion substituted OMS-2 catalyst can efficiently transform the absorbed solar energy to thermal energy, resulting in a considerable increase of temperature. By combining the efficient photothermal conversion and thermocatalytic activity of the Ce ion substituted OMS-2 catalyst, we carried out full solar spectrum, visible-infrared, and infrared light driven catalysis with extremely high efficiency. Under the irradiation of full solar spectrum, visible-infrared, and infrared light, the Ce ion substituted OMS-2 catalyst exhibits extremely high catalytic activity and excellent durability for the oxidation of volatile organic pollutants

  20. Effect of substituting cerium-rich mischmetal with lanthanum on high temperature properties of die-cast Mg-Zn-Al-Ca-RE alloys

    International Nuclear Information System (INIS)

    Anyanwu, Ifeanyi A.; Gokan, Yasuhiro; Suzuki, Atsuya; Kamado, Shigeharu; Kojima, Yo; Takeda, Suguru; Ishida, Taketoshi

    2004-01-01

    Mg-Zn-Al-Ca-RE alloys have been found to be promising materials for substituting aluminum alloys used for automatic transmission case applications in the automobile industry. Particularly, Mg-0.5%Zn-6%Al-1%Ca-3%RE (ZAXE05613) alloy exhibits comparable creep resistance as ADC12 die-casting aluminum alloy that is currently used for automatic transmission case applications. Changing the rare earth (RE) content of the alloy from mischmetal to lanthanum gives a further improvement in the creep properties of the alloy. Lanthanum addition results in the crystallization of a large amount of acicular Al 11 RE 3 (Al 11 La 3 ) compound along the grain boundaries as well as across the grain boundaries and this effectively controls grain boundary sliding and dislocation motion in the vicinity of the grain boundaries. As a result, die-cast ZAXLa05613 alloy exhibits a higher creep resistance than that of ZAXE05613 alloy

  1. Structural and optical characterization of Mn doped ZnS nanocrystals elaborated by ion implantation in SiO2

    International Nuclear Information System (INIS)

    Bonafos, C.; Garrido, B.; Lopez, M.; Romano-Rodriguez, A.; Gonzalez-Varona, O.; Perez-Rodriguez, A.; Morante, J.R.; Rodriguez, R.

    1999-01-01

    Mn doped ZnS nanocrystals have been formed in SiO 2 layers by ion implantation and thermal annealing. The structural analysis of the processed samples has been performed mainly by Secondary Ion Mass Spectroscopy (SIMS) and Transmission Electron Microscopy (TEM). The data show the precipitation of ZnS nanocrystals self-organized into two layers parallel to the free surface. First results of the optical analysis of samples co-implanted with Mn show the presence of a yellow-green photoluminescence depending on the Mn concentration and the size of the nanocrystals, suggesting the doping with Mn of some precipitates

  2. Structural and optical properties of ZnMgO nanostructures formed by Mg in-diffused ZnO nanowires

    International Nuclear Information System (INIS)

    Pan, C.-J.; Hsu, H.-C.; Cheng, H.-M.; Wu, C.-Y.; Hsieh, W.-F.

    2007-01-01

    ZnMgO nanostructures with wurtzite phase were prepared by thermal diffusion of Mg into the ZnO nanowires. As ZnO light-emitting devices have been operated by using ZnMgO layers as energy barrier layers to confine the carriers, it is essential to realize the characterization of ZnMgO particularly. In this work, the Mg content in Zn 1 -x Mg x O alloy determined by X-ray diffraction (XRD) and photoluminescence (PL) shows a good coincidence. The variation of lattice constant and the blueshift of near-band-edge emission indicate that Zn 2+ ions are successfully substituted by Mg 2+ ions in the ZnO lattice. In Raman-scattering studies, the change of E 2 (high) phonon line shape in ZnO:Mg nanostructures reveals the microscopic substitutional disorder. In addition to the host phonons of ZnO, two additional bands around 383 and 510 cm -1 are presumably attributed to the Mg-related vibrational modes. - Graphical abstract: We reported the synthesis of the ZnMgO nanostructures prepared by a simple vapor transport method. Magnesium-related anomalous modes are observed by Raman spectra for the first time in ZnMgO system

  3. Multifunctions of dual Zn/Mg ion co-implanted titanium on osteogenesis, angiogenesis and bacteria inhibition for dental implants.

    Science.gov (United States)

    Yu, Yiqiang; Jin, Guodong; Xue, Yang; Wang, Donghui; Liu, Xuanyong; Sun, Jiao

    2017-02-01

    In order to improve the osseointegration and long-term survival of dental implants, it is urgent to develop a multifunctional titanium surface which would simultaneously have osteogeneic, angiogeneic and antibacterial properties. In this study, a potential dental implant material-dual Zn/Mg ion co-implanted titanium (Zn/Mg-PIII) was developed via plasma immersion ion implantation (PIII). The Zn/Mg-PIII surfaces were found to promote initial adhesion and spreading of rat bone marrow mesenchymal stem cells (rBMSCs) via the upregulation of the gene expression of integrin α1 and integrin β1. More importantly, it was revealed that Zn/Mg-PIII could increase Zn 2+ and Mg 2+ concentrations in rBMSCs by promoting the influx of Zn 2+ and Mg 2+ and inhibiting the outflow of Zn 2+ , and then could enhance the transcription of Runx2 and the expression of ALP and OCN. Meanwhile, Mg 2+ ions from Zn/Mg-PIII increased Mg 2+ influx by upregulating the expression of MagT1 transporter in human umbilical vein endothelial cells (HUVECs), and then stimulated the transcription of VEGF and KDR via activation of hypoxia inducing factor (HIF)-1α, thus inducing angiogenesis. In addition to this, it was discovered that zinc in Zn/Mg-PIII had certain inhibitory effects on oral anaerobic bacteria (Pg, Fn and Sm). Finally, the Zn/Mg-PIII implants were implanted in rabbit femurs for 4 and 12weeks with Zn-PIII, Mg-PIII and pure titanium as controls. Micro-CT evaluation, sequential fluorescent labeling, histological analysis and push-out test consistently demonstrated that Zn/Mg-PIII implants exhibit superior capacities for enhancing bone formation, angiogenesis and osseointegration, while consequently increasing the bonding strength at bone-implant interfaces. All these results suggest that due to the multiple functions co-produced by zinc and magnesium, rapid osseointegration and sustained biomechanical stability are enhanced by the novel Zn/Mg-PIII implants, which have the potential

  4. Structural and dielectric properties of Zr and Cu co-substituted Ni{sub 0.5}Zn{sub 0.5}Fe{sub 2}O{sub 4}

    Energy Technology Data Exchange (ETDEWEB)

    Jalaiah, K., E-mail: kjalu4u@gmail.com [Department of Physics, Andhra University, Visakhapatnam 530 003 (India); Chandra mouli, K. [Department of Engineering Physics, Andhra University, Visakhapatnam 530 003 (India); Subba Rao, P.S.V. [Department of Physics, Andhra University, Visakhapatnam 530 003 (India); Sreedhar, B. [IICT, Hyderabad (India)

    2017-06-15

    Highlights: • The porosity was increased with increasing dopant concentration of Zr and Cu from the 10.57% to 20.11%. • The force constant and wave numbers in octahedral and tetrahedral site is increased with increasing the dopant concentration of Zr and Cu. • The compositional dielectric constant at 100 kHz is increased from the 9.85 to 86.53, with increasing dopant concentration of Zr and Cu. - Abstract: Zr and Cu Ni{sub 0.5}Zn{sub 0.5}Fe{sub 2}O{sub 4} ferrites have been prepared by the sol-gel auto combustion method using the nitrates. The ethylene glycol and citric acid were mixed as the combustion agents. The synthesized powders were calcinate at 800 °C for 3 h and they are pressed in desired shaped and sintered at 1200 °C for 2 h in air atmosphere. The X-ray diffraction analysis confirms the single phase cubic spinel structure. The SEM pictures revels that the substitution of higher valence ions results fine grained intragranular pore free microstructure. The dielectric properties of substituted ferrites exhibits decreasing trend at lower frequencies up to 1000 Hz beyond which it should in stable response. All the results are explained in terms of compositional and frequency variation.

  5. Perfluoroalkyl-substituted ethylene carbonates: Novel electrolyte additives for high-voltage lithium-ion batteries

    Science.gov (United States)

    Zhu, Ye; Casselman, Matthew D.; Li, Yan; Wei, Alexander; Abraham, Daniel P.

    2014-01-01

    A new family of polyfluoroalkyl-substituted ethylene carbonates is synthesized and tested as additives in lithium-ion cells containing EC:EMC + LiPF6-based electrolyte. The influence of these compounds is investigated in Li1.2Ni0.15Mn0.55Co0.1O2//graphite cells via a combination of galvanostatic cycling and electrochemical impedance spectroscopy (EIS) tests. Among the four additives studied in this work (4-(trifluoromethyl)-1,3-dioxolan-2-one (TFM-EC), 4-(perfluorobutyl)-1,3-dioxolan-2-one (PFB-EC), 4-(perfluorohexyl)-1,3-dioxolan-2-one (PFH-EC), and 4-(perfluorooctyl)-1,3-dioxolan-2-one (PFO-EC)), small amounts (0.5 wt%) of PFO-EC is found to be most effective in lessening cell performance degradation during extended cycling. Linear sweep voltammetry (LSV), X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy are used to further characterize the effects of PFO-EC on the positive and negative electrodes. LSV data from the electrolyte, and XPS analyses of electrodes harvested after cycling, suggest that PFO-EC is oxidized on the cathode forming surface films that slow electrode/cell impedance rise. Differential capacity (dQ/dV) plots from graphite//Li cells suggest that PFO-EC is involved in solid electrolyte interphase (SEI) formation. Raman data from anodes after cycling suggest that structural disordering of graphite is reduced by the addition of PFO-EC, which may explain the improved cell capacity retention.

  6. A facile strategy for fabrication of nano-ZnO/yeast composites and their adsorption mechanism towards lead (II) ions

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Wei; Meng, Lingyin [College of Science, Sichuan Agricultural University, Yaan 625014 (China); Mu, Guiqin [Maize Research Institute of Sichuan Agricultural University, Wenjiang 611130 (China); Zhao, Maojun; Zou, Ping [College of Science, Sichuan Agricultural University, Yaan 625014 (China); Zhang, Yunsong, E-mail: yaanyunsong@126.com [College of Science, Sichuan Agricultural University, Yaan 625014 (China)

    2016-08-15

    Highlights: • Nano-ZnO/yeast composites were fabricated by alkali hydrothermal method. • Nano-ZnO was in-situ achieved and anchored on the yeast surface. • Alkali and hydrothermal process cause more exposed funcitional groups on yeast. • Nano-ZnO/yeast composites show higher Pb{sup 2+} adsorption ability than pristine yeast. • Nano-ZnO and exposed functional groups synergistically participate in adsorption. - Abstract: Nano-ZnO/yeast composites were successfully fabricated by one-step alkali hydrothermal method, and their adsorption properties for Pb{sup 2+} ions were also evaluated. Various influencing parameters of nano-ZnO/yeast composites, such as initial pH, contact time and initial Pb{sup 2+} concentration were investigated, respectively. The maximum adsorption capacity of nano-ZnO/yeast composites for Pb{sup 2+} (31.72 mg g{sup −1}) is 2.03 times higher than that of pristine yeast (15.63 mg g{sup −1}). The adsorption mechanism of nano-ZnO/yeast composites was studied by a series of techniques. Scanning electron microscopy (SEM) showed that nano-ZnO is evenly deposited on yeast surface. Atomic force microscopy (AFM) analysis exhibited that the yeast surface is rougher than that of pristine yeast. Energy dispersive X-ray detector (EDX) and X-ray diffraction (XRD) indicated the existence of nano-ZnO on yeast surface. Additionally, X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR) measurements further illustrated that alkali hydrothermal method causes not only the generation and anchorage of nano-ZnO on yeast surface but also the exposure of more functional groups (such as amino, carboxyl groups etc.) on yeast surface, both of which could adsorb Pb{sup 2+} via synergistic effect.

  7. A facile strategy for fabrication of nano-ZnO/yeast composites and their adsorption mechanism towards lead (II) ions

    International Nuclear Information System (INIS)

    Zhang, Wei; Meng, Lingyin; Mu, Guiqin; Zhao, Maojun; Zou, Ping; Zhang, Yunsong

    2016-01-01

    Highlights: • Nano-ZnO/yeast composites were fabricated by alkali hydrothermal method. • Nano-ZnO was in-situ achieved and anchored on the yeast surface. • Alkali and hydrothermal process cause more exposed funcitional groups on yeast. • Nano-ZnO/yeast composites show higher Pb"2"+ adsorption ability than pristine yeast. • Nano-ZnO and exposed functional groups synergistically participate in adsorption. - Abstract: Nano-ZnO/yeast composites were successfully fabricated by one-step alkali hydrothermal method, and their adsorption properties for Pb"2"+ ions were also evaluated. Various influencing parameters of nano-ZnO/yeast composites, such as initial pH, contact time and initial Pb"2"+ concentration were investigated, respectively. The maximum adsorption capacity of nano-ZnO/yeast composites for Pb"2"+ (31.72 mg g"−"1) is 2.03 times higher than that of pristine yeast (15.63 mg g"−"1). The adsorption mechanism of nano-ZnO/yeast composites was studied by a series of techniques. Scanning electron microscopy (SEM) showed that nano-ZnO is evenly deposited on yeast surface. Atomic force microscopy (AFM) analysis exhibited that the yeast surface is rougher than that of pristine yeast. Energy dispersive X-ray detector (EDX) and X-ray diffraction (XRD) indicated the existence of nano-ZnO on yeast surface. Additionally, X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR) measurements further illustrated that alkali hydrothermal method causes not only the generation and anchorage of nano-ZnO on yeast surface but also the exposure of more functional groups (such as amino, carboxyl groups etc.) on yeast surface, both of which could adsorb Pb"2"+ via synergistic effect.

  8. Impact of ZnO substitution on magnetic response and microwave absorption capability of strontium-natural nanoferrites

    Directory of Open Access Journals (Sweden)

    W. Widanarto

    2015-01-01

    Full Text Available Ferrite being a compound derived from iron oxides including magnetite and hematite possesses similar properties as ceramics which are hard and brittle. Certainly, the mounting demand for electronics has been a major factor driving the exponential growth of ferrite based materials. ZnO doped strontium-natural nanoferrites of composition (80 − xFe2O3:xZnO:20SrCO3, where x = 0, 10, 20 mol% are synthesized and sintered via the solid state reaction scheme. Samples are characterized by SEM, XRD, VSM, and VNA measurements to determine the impact of ZnO contents’ variation on the surface morphology, structure, magnetic and microwave absorption properties. The Nicolson–Ross–Weir method is applied to evaluate samples’ reflection loss. The average grain size of the strontium ferrite is found to reduce with the increase in ZnO concentration. Materials sintered at 1100 °C without ZnO incorporation are composed of hexagonal SrFe12O19. Meanwhile, the addition of ZnO produces cubic ZnFe2O4 and SrFeO2 phases. Insertion of ZnO results in reduction of magnetic parameters and reflection loss. Furthermore, the anisotropy magnetic field of strontium natural ferrites displays a rapid drop from 350 kA/m to 79.6 kA/m with the increase in ZnO. Strontium ferrite containing 20 mol% of ZnO exhibits superior microwave absorption with reflection loss within −45 dB to −55.94 dB in the frequency range of 7–13 GHz. This facilely synthesized a new class of materials which is believed to be economically promising for microwave absorption applications in the GHz range.

  9. Highly sensitive luminescent sensor for cyanide ion detection in aqueous solution based on PEG-coated ZnS nanoparticles.

    Science.gov (United States)

    Mehta, Surinder K; Salaria, Khushboo; Umar, Ahmad

    2013-03-15

    Using polyethylene glycol (PEG) coated ZnS nanoparticles (NPs), a novel and highly sensitive luminescent sensor for cyanide ion detection in aqueous solution has been presented. ZnS NPs have been used to develop efficient luminescence sensor which exhibits high reproducibility and stability with the lowest limit of detection of 1.29×10(-6) mol L(-1). The observed limit of detection of the fabricated sensor is ~6 times lower than maximum value of cyanide permitted by United States Environmental Protection Agency for drinking water (7.69×10(-6) mol L(-1)). The interfering studies show that the developed sensor possesses good selectivity for cyanide ion even in presence of other coexisting ions. Importantly, to the best of our knowledge, this is the first report which demonstrates the utilization of PEG- coated ZnS NPs for efficient luminescence sensor for cyanide ion detection in aqueous solution. This work demonstrates that rapidly synthesized ZnS NPs can be used to fabricate efficient luminescence sensor for cyanide ion detection. Copyright © 2013 Elsevier B.V. All rights reserved.

  10. Structural, dielectric and gas sensing behavior of Mn substituted spinel MFe{sub 2}O{sub 4} (M=Zn, Cu, Ni, and Co) ferrite nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Ranjith Kumar, E., E-mail: ranjueaswar@gmail.com [Department of Physics, Dr. NGP Institute of Technology, Coimbatore 641048, Tamil Nadu (India); Siva Prasada Reddy, P.; Sarala Devi, G. [Inorganic and Physical Chemistry Division, Indian Institute Chemical Technology, Hyderabad 500607 (India); Sathiyaraj, S. [Department of Chemistry, Dr. NGP Institute of Technology, Coimbatore 641048, Tamil Nadu (India)

    2016-01-15

    Spinel ferrite (MnZnFe{sub 2}O{sub 4}, MnCuFe{sub 2}O{sub 4}, MnNiFe{sub 2}O{sub 4} and MnCoFe{sub 2}O{sub 4}) nanoparticles have been prepared by evaporation method. The annealing temperature plays an important role on changing particle size of the spinel ferrite nanoparticles was found out by X-ray diffraction and transmission electron microscopy. The role of manganese substitution in the spinel ferrite nanoparticles were also analyzed for different annealing temperature. The substitution of Mn also creates a vital change in dielectric properties have been measured in the frequency range of 100 kHz to 5 MHz. These spinel ferrites are decomposed to α-Fe{sub 2}O{sub 3} after annealing above 550 °C in air. Through the characterization of the prepared powder, the effect of annealing temperature, chemical composition and preparation technique on the microstructure, particle size and dielectric properties of the Mn substituted spinel ferrite nanoparticles are discussed. Furthermore, Conductance response of Mn substituted MFe{sub 2}O{sub 4} ferrite nanoparticles were measured by exposing the materials to reducing gas like liquefied petroleum gas (LPG). - Highlights: • The egg white support to achieve sample with shorter reaction time. • Manganese plays a significant role in sensor response. • Nature of the ferrites was affected with increasing annealing temperature.

  11. Structural, dielectric and gas sensing behavior of Mn substituted spinel MFe2O4 (M=Zn, Cu, Ni, and Co) ferrite nanoparticles

    Science.gov (United States)

    Ranjith Kumar, E.; Siva Prasada Reddy, P.; Sarala Devi, G.; Sathiyaraj, S.

    2016-01-01

    Spinel ferrite (MnZnFe2O4, MnCuFe2O4, MnNiFe2O4 and MnCoFe2O4) nanoparticles have been prepared by evaporation method. The annealing temperature plays an important role on changing particle size of the spinel ferrite nanoparticles was found out by X-ray diffraction and transmission electron microscopy. The role of manganese substitution in the spinel ferrite nanoparticles were also analyzed for different annealing temperature. The substitution of Mn also creates a vital change in dielectric properties have been measured in the frequency range of 100 kHz to 5 MHz. These spinel ferrites are decomposed to α-Fe2O3 after annealing above 550 °C in air. Through the characterization of the prepared powder, the effect of annealing temperature, chemical composition and preparation technique on the microstructure, particle size and dielectric properties of the Mn substituted spinel ferrite nanoparticles are discussed. Furthermore, Conductance response of Mn substituted MFe2O4 ferrite nanoparticles were measured by exposing the materials to reducing gas like liquefied petroleum gas (LPG).

  12. Amendment of saturation magnetization, blocking temperature and particle size homogeneity in Mn-ferrite nanoparticles using Co-Zn substitution

    Energy Technology Data Exchange (ETDEWEB)

    Eltabey, M.M. [Basic Engineering Science Department, Faculty of Engineering, Menoufiya University (Egypt); Physics Department, Faculty of Science, Jazan University, Jazan (Saudi Arabia); Massoud, A.M., E-mail: Amassouda1@yahoo.com [Physics Department, Faculty of Science, Ain Shams University, Abbassia 11566, Cairo (Egypt); Radu, Cosmin [Lake Shore Cryotronics, Inc., Westerville, OH (United States)

    2017-01-15

    Nanocrystalline particles of compositions (CoZn){sub x}Mn{sub 1−x}Fe{sub 2}O{sub 4} were prepared by the coprecipitation method from stoichiometric aqueous solutions, where x varies from 0 to 0.3 in steps of 0.05. The synthesized powders were characterized by X-ray diffraction (XRD), transmission electron microscope (TEM) and Fourier transform infrared spectroscopy (FT-IR). A vibrating sample magnetometer (VSM) was used to measure the hysteresis parameters at 300 and 6 K. Zero field cooling (ZFC) and field cooling (FC) curves were obtained at the temperature range 6–400 K and the blocking temperature values were determined. XRD analysis confirmed the formation of the obtained powder in a single cubic spinel phase and it showed also that the lattice parameter is decreasing with the increase of (Co-Zn) content. FT-IR measurements between 160 and 650 cm{sup −1} also confirmed the intrinsic cation vibrations of the spinel structure. The magnetic measurements showed that the saturation magnetization, coercivity and the values of blocking temperatures were increased with the (Co-Zn) content. TEM micrographs declared the improvement of particle size homogeneity with the increase of (Co-Zn) content without remarkable change in the average particle size. The obtained results were discussed in view of A-B sublattices interaction and superparamagnetic phenomenon. - Highlights: • Nanocrystalline particles of compositions (CoZn){sub x}Mn{sub 1-x}Fe{sub 2}O{sub 4} were prepared by the coprecipitation method. • XRD analysis showed that the lattice parameter is decreased with the increase of (Co,Zn) content. • The saturation magnetization is improved with the (Co,Zn) content. • Particle size homogeneity is enhanced with (Co,Zn) content. • The values of blocking temperatures are enhanced with increasing (Co,Zn) content.

  13. Full Solar Spectrum Light Driven Thermocatalysis with Extremely High Efficiency on Nanostructured Ce Ion Substituted OMS-2 Catalyst for VOCs Purification

    DEFF Research Database (Denmark)

    Hou, J.T.; Li, Y.Z.; Mao, M.Y.

    2015-01-01

    solar spectrum, visible-infrared, and infrared light, the Ce ion substituted OMS-2 catalyst exhibits extremely high catalytic activity and excellent durability for the oxidation of volatile organic pollutants such as benzene, toluene, and acetone. Based on the experimental evidence, we propose a novel...... in a considerable increase of temperature. By combining the efficient photothermal conversion and thermocatalytic activity of the Ce ion substituted OMS-2 catalyst, we carried out full solar spectrum, visible-infrared, and infrared light driven catalysis with extremely high efficiency. Under the irradiation of full...... mechanism of solar light driven thermocatalysis for the Ce ion substituted OMS-2 catalyst. The reason why the Ce ion substituted OMS-2 catalyst exhibits much higher catalytic activity than pure OMS-2 and CeO2/OMS-2 nano composite under the full solar spectrum irradiation is discussed....

  14. Ga+ focused-ion-beam implantation-induced masking for H2 etching of ZnO films

    International Nuclear Information System (INIS)

    Fang, Hsin-Chiao; Huang, Jun-Han; Chu, Wen-Huei; Liu, Chuan-Pu

    2010-01-01

    Gallium implantation of ZnO by a focused-ion beam is used to create a mask for ZnO dry etching with hydrogen. Effects of Ga + fluence on the etch stop properties and the associated mechanisms are investigated. The fluence of 2.8 x 10 16 cm -2 is determined to be optimum to render the best mask quality. While lower fluences would cause less etching selectivity, higher fluences would cause erosion of the surface and particles to be precipitated on the surface after H 2 treatment at high temperature. In contrast to the commonly adopted gallium oxide formation on Si, transmission electron microscopy analysis reveals that, for the fluences ≤ 2.8 x 10 16 cm -2 , Ga + ions are incorporated as dopants into ZnO without any second phases or precipitates, indicating the Ga-doped ZnO layer behaves as a mask for H 2 etching due to the higher electronegativity of Ga + towards oxygen. However, for the fluences ≥ 4.6 x 10 16 cm -2 , the surface particles are responsible for the etch stop and are identified as ZnGa 2 O 4 . We finally demonstrate a complicated pattern of 'NCKU' on ZnO by using this technique. The study not only helps clarify the related mechanisms, but also suggests a feasible extension of the etch stop process that can be applied to more functional material.

  15. Low-temperature synthesis of hexagonal transition metal ion doped ZnS nanoparticles by a simple colloidal method

    International Nuclear Information System (INIS)

    Wang, Liping; Huang, Shungang; Sun, Yujie

    2013-01-01

    A general route to synthesize transition metal ions doped ZnS nanoparticles with hexagonal phase by means of a conventional reverse micelle at a low temperature is developed. The synthesis involves N,N-dimethylformamide, Zn(AC) 2 solution, thiourea, ammonia, mercaptoacetic acid, as oil phase, water phase, sulfide source, pH regulator, and surfactant, respectively. Thiourea, ammonia and mercaptoacetic acid are demonstrated crucial factors, whose effects have been studied in detail. In addition, the FT-IR spectra suggest that mercaptoacetic acid may form complex chelates with Zn 2+ in the preparation. In the case of Cu 2+ as a doped ion, hexagonal ZnS:Cu 2+ nanoparticles were synthesized at 95 °C for the first time. The X-ray diffraction (XRD) and transmission electron microscope (TEM) measurements show that the ZnS:Cu 2+ nanoparticles are polycrystalline and possess uniform particle size. The possible formation mechanism of the hexagonal doped ZnS is discussed.

  16. Intrinsic labeling of alpha-fetoprotein with 65Zn

    International Nuclear Information System (INIS)

    Preiss, I.L.

    1994-01-01

    Many enzymes, proteins, and large molecules bind a variety of inorganic ions. The replacement of a specific metal ion with another element can disrupt the biodistribution and biochemistry of the host molecule. Alpha-fetoprotein (AFP) is a known oncofetal antigen. The authors have demonstrated that the substitution of Cu or Pb on AFP inhibits the transplacental migration of AFP and may lead to fetal demise. It is evident that in labeling with a radiotracer in order to observe the true distribution of a molecule, one must select a radioisotope of an element which is naturally bound to the host molecule. It has been demonstrated that AFP binds Zn in vivo. Thus, substituting 65 Zn for natural Zn produces an intrinsic label for AFP. The authors discuss the methodology for stripping and labeling of AFP with 65 Zn. The biodistribution of labeled AFP is compared with that of 65 Zn 2+ in healthy and diseased (hepatoma) animals

  17. Effects of oxygen gas flow rates and Ga contents on structural properties of Ga-doped ZnO films prepared by ion-plating with a DC arc discharge

    International Nuclear Information System (INIS)

    Terasako, Tomoaki; Nomoto, Junichi; Makino, Hisao; Yamamoto, Naoki; Shirakata, Sho; Yamamoto, Tetsuya

    2015-01-01

    Structural properties of highly c-axis oriented polycrystalline Ga-doped ZnO (GZO) films prepared by ion-plating with a DC arc discharge were studied in terms of the oxygen gas flow rate (F O2 ) introduced into the chamber during the deposition process and the Ga 2 O 3 content in the GZO sintered pellet. The X-ray diffraction (XRD) measurements revealed that the GZO films have the residual compressive stress along the a-axis direction (in-plane) and the tensile stress along the c-axis direction (out-of-plane). The increase in F O2 or the increase in Ga 2 O 3 content was effective for relaxing the in-plane compressive stress induced by the so-called atomic peening effect. The positive correlation between the carrier concentration (n) and the primitive cell volume (V) would be due to the incorporation of Ga atoms substituting Zn sites (Ga Zn s) together with the generation of n-type intrinsic defects or complex defects. - Highlights: • Films of Ga-doped ZnO (GZO) films were deposited by ion-plating with a DC arc discharge. • Structural properties of GZO films were examined by X-ray diffraction measurements. • GZO films had the residual compressive stress along the a-axis direction. • There was the correlation between the carrier concentration and the cell volume.

  18. Effects of oxygen gas flow rates and Ga contents on structural properties of Ga-doped ZnO films prepared by ion-plating with a DC arc discharge

    Energy Technology Data Exchange (ETDEWEB)

    Terasako, Tomoaki, E-mail: terasako.tomoaki.mz@ehime-u.ac.jp [Graduate School of Science and Engineering, Ehime University, 3 Bunkyo-cho, Matsuyama-shi, Ehime 790-8577 (Japan); Nomoto, Junichi; Makino, Hisao; Yamamoto, Naoki [Research Institute, Kochi University of Technology, 185 Miyanokuchi, Tosayamada-cho, Kami-shi, Kochi 782-8502 (Japan); Shirakata, Sho [Graduate School of Science and Engineering, Ehime University, 3 Bunkyo-cho, Matsuyama-shi, Ehime 790-8577 (Japan); Yamamoto, Tetsuya [Research Institute, Kochi University of Technology, 185 Miyanokuchi, Tosayamada-cho, Kami-shi, Kochi 782-8502 (Japan)

    2015-12-01

    Structural properties of highly c-axis oriented polycrystalline Ga-doped ZnO (GZO) films prepared by ion-plating with a DC arc discharge were studied in terms of the oxygen gas flow rate (F{sub O2}) introduced into the chamber during the deposition process and the Ga{sub 2}O{sub 3} content in the GZO sintered pellet. The X-ray diffraction (XRD) measurements revealed that the GZO films have the residual compressive stress along the a-axis direction (in-plane) and the tensile stress along the c-axis direction (out-of-plane). The increase in F{sub O2} or the increase in Ga{sub 2}O{sub 3} content was effective for relaxing the in-plane compressive stress induced by the so-called atomic peening effect. The positive correlation between the carrier concentration (n) and the primitive cell volume (V) would be due to the incorporation of Ga atoms substituting Zn sites (Ga{sub Zn}s) together with the generation of n-type intrinsic defects or complex defects. - Highlights: • Films of Ga-doped ZnO (GZO) films were deposited by ion-plating with a DC arc discharge. • Structural properties of GZO films were examined by X-ray diffraction measurements. • GZO films had the residual compressive stress along the a-axis direction. • There was the correlation between the carrier concentration and the cell volume.

  19. Kinetic study of the isotopic exchange of Na+ and Zn2+ ions on iron and chromium titanates

    International Nuclear Information System (INIS)

    Zakaria, E.S.; Ali, I.M.; Aly, H.F.

    2004-01-01

    Iron(III) (FeTi) and chromium (III) titanates (CrTi) were prepared as cation exchange materials in a granular form. The rate of the isotopic exchange of Na + /*Na + and Zn 2+ /*Zn 2+ between aqueous solution and iron(III) and chromium(III) titanates in Na + or Zn 2+ form has been carried out radiometrically in the 25-60 deg C temperature range. The exchange rate is controlled by a particle diffusion mechanism and experimental and theoretical approaches have been used to obtain the rate of diffusion through the spherical particles of the exchangers. The values of self diffusion (D-bar) of Na + and Zn 2+ ions were measured at different operation conditions, particle size, reaction temperatures and drying temperatures of the matrix. The values of kinetic and thermodynamic parameters were calculated and their significance discussed. (author)

  20. Studies of adsorption and desorption of zinc ions on zeolites by means of 65Zn

    International Nuclear Information System (INIS)

    Foeldesova, M.; Dillinger, P.; Lukac, P.

    2001-01-01

    The uptake of different metals by natural and chemically modified ion-exchangers, including zeolites, were studied in order to minimize the contamination of environment with metals in ionic form. In recent years considerable attention has been devoted to the studies of chemically modified zeolites their properties and applications. The used zeolite originated from the deposit Nizny Hrabovec, eastern Slovakia (NH) and from deposit of Ukraine (U). The zeolite from Slovakia is a clinoptilolite /40 -70%/ type, the zeolite from Ukraine is a mixed mordenite /75%/ and clinoptilolite /25%/ type. A fraction of 1.5 -2.5 mm was separated from the grained zeolite by sieving. The sedimentary zeolites, being the siliceous zeolites, should exhibit substantial non-selectivity for the divalent cations having a high hydration enthalpy , including zinc ( -2026 kJ/g). Zinc is an essential trace element in all-living systems from bacteria to humans. The toxicity of zinc and most of zinc compounds is generally low, however, sometimes industrial and household wastes contain zinc in concentrations, which can be harmful to the environment. The zinc-accompanying impurities, such as cadmium and lead, are of much greater danger .The main source of zinc are waste waters and continuous emission from the production and processing of zinc, other nonferrous smelters, from coal power plants and fossil combustion. The static radio-exchange method using model radioactive solutions was utilized for the determination of the sorption of Zn by the mentioned above zeolitic materials. For this purpose the aqueous solution of 5 · 10 -2 mol dm -3 ZnCl 2 labelled with 65 Zn was used. The areas of application of natural zeolites have been well defined. However, their use can become more efficient after chemical modification. The zeolites acquire new valuable properties, while retaining their original ones. The obtained results make these materials excellent candidates for their potential use for waste water

  1. Removal of uranium ions from synthetic wastewater using ZnO/Na-clinoptilolite nanocomposites

    International Nuclear Information System (INIS)

    Aghadavoud, Azadeh; Saraee, Khadijeh Rezaee Ebrahim; Shakur, Hamid Reza; Sayyari, Rasol

    2016-01-01

    Uranium is one of the heavy metals that is found in industrial wastewater and is very toxic for human and environment. In this work, natural clinoptilolite is used as a low-cost adsorbent for uranium removal from aqueous solutions. The sodium form of clinoptilolite and ZnO/Na-clinoptilolite nanocomposite were prepared. The sample sorption capacities for uranium removal from simulated drinking water in the presence of other anions and cations were investigated. Natural zeolite and its modified forms were characterized by XRD, XRF, FTIR, TEM and BET. Batch experiments were used to determine the best adsorption conditions. The effects of various parameters such as contact time, pH, initial uranium concentration, temperature and mass sorbent on the removal efficiency of uranium ions were studied. The equilibration was attained after 2 and 6 h for the Na-clinoptilolite and ZnO/Na-clinoptilolite nanocomposite, respectively. Both adsorbents showed relatively fast adsorption. Effective removal of uranium was demonstrated at pH values of 4-8 for both forms of zeolite. Temperature had no significant effect on adsorption. The maximum removal efficiency of uranium by the ZnO/Na-clinoptilolite nanocomposite in pH=7.2 and room temperature was 98.55%. Langmuir, Freundlich and Sips models were used for describing the equilibrium isotherms for uranium uptake. The Sips model corresponded well with the experimental data. The thermodynamic parameters, such as ΔG , ΔH and ΔS , have been calculated and interpreted. The pseudo-first order and pseudo-second order models were applied to describe the kinetic data. The pseudo-second order kinetic model had excellent kinetic data fitting (R2=1).

  2. Removal of uranium ions from synthetic wastewater using ZnO/Na-clinoptilolite nanocomposites

    Energy Technology Data Exchange (ETDEWEB)

    Aghadavoud, Azadeh; Saraee, Khadijeh Rezaee Ebrahim; Shakur, Hamid Reza [Isfahan Univ. (Iran, Islamic Republic of). Dept. of Nuclear Engineering; Sayyari, Rasol

    2016-07-01

    Uranium is one of the heavy metals that is found in industrial wastewater and is very toxic for human and environment. In this work, natural clinoptilolite is used as a low-cost adsorbent for uranium removal from aqueous solutions. The sodium form of clinoptilolite and ZnO/Na-clinoptilolite nanocomposite were prepared. The sample sorption capacities for uranium removal from simulated drinking water in the presence of other anions and cations were investigated. Natural zeolite and its modified forms were characterized by XRD, XRF, FTIR, TEM and BET. Batch experiments were used to determine the best adsorption conditions. The effects of various parameters such as contact time, pH, initial uranium concentration, temperature and mass sorbent on the removal efficiency of uranium ions were studied. The equilibration was attained after 2 and 6 h for the Na-clinoptilolite and ZnO/Na-clinoptilolite nanocomposite, respectively. Both adsorbents showed relatively fast adsorption. Effective removal of uranium was demonstrated at pH values of 4-8 for both forms of zeolite. Temperature had no significant effect on adsorption. The maximum removal efficiency of uranium by the ZnO/Na-clinoptilolite nanocomposite in pH=7.2 and room temperature was 98.55%. Langmuir, Freundlich and Sips models were used for describing the equilibrium isotherms for uranium uptake. The Sips model corresponded well with the experimental data. The thermodynamic parameters, such as ΔG , ΔH and ΔS , have been calculated and interpreted. The pseudo-first order and pseudo-second order models were applied to describe the kinetic data. The pseudo-second order kinetic model had excellent kinetic data fitting (R2=1).

  3. Beyond the Nernst-limit with dual-gate ZnO ion-sensitive field-effect transistors

    NARCIS (Netherlands)

    Spijkman, M.; Smits, E.C.P.; Cillessen, J.F.M.; Biscarini, F.; Blom, P.W.M.; Leeuw, D.M. de

    2011-01-01

    The sensitivity of conventional ion-sensitive field-effect transistors (ISFETs) is limited to 59 mV/pH, which is the maximum detectable change in electrochemical potential according to the Nernst equation. Here we demonstrate a transducer based on a ZnO dual-gate field-effect transistor that

  4. Ag{sup +12} ion induced modifications of structural and optical properties of ZnO-PMMA nanocomposite films

    Energy Technology Data Exchange (ETDEWEB)

    Sharma, Sarla; Vijay, Y. K. [Department of Physics, University of Rajasthan, Jaipur-302055 (India); Vyas, Rishi [Department of Physics, Malaviya National Institute of Technology, Jaipur-302017 (India)

    2013-02-05

    The influence of swift heavy ion (SHI) irradiation on structural and photoluminescence (PL) properties of ZnO-PMMA nanocomposite films, prepared by solution casting method, was studied. The ZnO-PMMA nanocomposite films were irradiated using 120 MeV Ag{sup +12} ions at different fluences varying from 1 Multiplication-Sign 10{sup 11} to 1 Multiplication-Sign 10{sup 13} ions/cm{sup 2}. The intensity of the X-ray diffraction peaks is increased at the high fluence, without evolution of any new peak. A shift in absorption edge (i.e. shift in optical band gap) towards higher wavelength was observed after irradiation and PL from ZnO-PMMA nanocomposite films is found to increase up to a critical fluence and then found to be suppressed for higher fluence (1 Multiplication-Sign 10{sup 12} ion/cm{sup 2}). The change in photoluminescence after irradiation can be attributed to the change in microstructure of PMMA matrix as well as the agglomeration of ZnO nanoparticles.

  5. Ag+12 ion induced modifications of structural and optical properties of ZnO-PMMA nanocomposite films

    International Nuclear Information System (INIS)

    Sharma, Sarla; Vijay, Y. K.; Vyas, Rishi

    2013-01-01

    The influence of swift heavy ion (SHI) irradiation on structural and photoluminescence (PL) properties of ZnO-PMMA nanocomposite films, prepared by solution casting method, was studied. The ZnO-PMMA nanocomposite films were irradiated using 120 MeV Ag +12 ions at different fluences varying from 1×10 11 to 1×10 13 ions/cm 2 . The intensity of the X-ray diffraction peaks is increased at the high fluence, without evolution of any new peak. A shift in absorption edge (i.e. shift in optical band gap) towards higher wavelength was observed after irradiation and PL from ZnO-PMMA nanocomposite films is found to increase up to a critical fluence and then found to be suppressed for higher fluence (1×10 12 ion/cm 2 ). The change in photoluminescence after irradiation can be attributed to the change in microstructure of PMMA matrix as well as the agglomeration of ZnO nanoparticles.

  6. Fabrication of electrospun ZnMn2O4 nanofibers as anode material for lithium-ion batteries

    International Nuclear Information System (INIS)

    Luo, Lei; Qiao, Hui; Chen, Ke; Fei, Yaqian; Wei, Qufu

    2015-01-01

    Highlights: • ZnMn 2 O 4 nanofibers were successfully synthesized by a facile electrospinning and calcination method for lithium-ion batteries. • The as-prepared ZnMn 2 O 4 nanofibers, containing PVP and PAN with ratio of 1:9, exhibited a high initial discharge capacity of 1274 mAh g −1 , and the stabilized capacity was as high as 603 mAh g −1 after 60 cycles at a current density of 50 mA g −1 . • The as-prepared ZnMn 2 O 4 anode material showed good lithium storage performances and excellent rate capability and can be a promising electrode material for lithium-ion batteries in the future. - Abstract: In this paper, ZnMn 2 O 4 nanofibers were synthesized by a facile electrospinning and calcination method. Electrochemical properties of the nanofiber anode material for lithium-ion batteries were investigated. The as-prepared ZnMn 2 O 4 nanofibers, containing PVP and PAN with ratio of 1:9, exhibited a high initial discharge capacity of 1274 mAh g −1 , and the stabilized capacity was as high as 603 mAh g −1 after 60 cycles at a current density of 50 mA g −1 . Besides the high specific capacity and good cyclability, the electrode also showed good rate capability. Even at 2000 mA g −1 , the electrode could deliver a capacity of as high as 352 mAh g −1 . The results suggest a promising application of the electrospun ZnMn 2 O 4 nanofibers as anode material for lithium-ion batteries

  7. Room-temperature ferromagnetic properties of Cu-doped ZnO rod ...

    Indian Academy of Sciences (India)

    We have investigated properties of the Cu-doped ZnO crystalline film synthesized by the hydrothermal method. X-ray diffraction and X-ray ... DMSs are semiconducting alloys whose lattice is made up in part of substitutional magnetic ... investigate Cu-doped ZnO system (Hou et al 2007a, b), as. Cu is a potential magnetic ion ...

  8. Structural and optical properties of DC magnetron sputtered ZnO films on glass substrate and their modification by Ag ions implantation

    Science.gov (United States)

    Ahmad, R.; Afzal, Naveed; Amjad, U.; Jabbar, S.; Hussain, T.; Hussnain, A.

    2017-07-01

    This work is focused on investigating the effects of deposition time and Ag ions implantation on structural and optical properties of ZnO film. The ZnO film was prepared on glass substrate by pulsed DC magnetron sputtering of pure Zn target in reactive oxygen environment for 2 h, 3 h, 4 h and 5 h respectively. X-ray diffraction results revealed polycrystalline ZnO film whose crystallinity was improved with increase of the deposition time. The morphological features indicated agglomeration of smaller grains into larger ones by increasing the deposition time. The UV-vis spectroscopy analysis depicted a small decrease in the band gap of ZnO from 3.36 eV to 3.27 eV with increase of deposition time. The Ag ions implantation in ZnO films deposited for 5 h on glass was carried out by using Pelletron Accelerator at different ions fluences ranging from 1  ×  1011 ions cm-2 to 2  ×  1012 ions cm-2. XRD patterns of Ag ions implanted ZnO did not show significant change in crystallite size by increasing ions fluence from 1  ×  1011 ions cm-2 to 5  ×  1011 ions cm-2. However, with further increase of the ions fluence, the crystallite size was decreased. The band gap of Ag ions implanted ZnO indicated anomalous variations with increase of the ions fluence.

  9. Energy Transfer Efficiency from ZnO-Nanocrystals to Eu3+ Ions Embedded in SiO₂ Film for Emission at 614 nm.

    Science.gov (United States)

    Mangalam, Vivek; Pita, Kantisara

    2017-08-10

    In this work, we study the energy transfer mechanism from ZnO nanocrystals (ZnO-nc) to Eu 3+ ions by fabricating thin-film samples of ZnO-nc and Eu 3+ ions embedded in a SiO₂ matrix using the low-cost sol-gel technique. The time-resolved photoluminescence (TRPL) measurements from the samples were analyzed to understand the contribution of energy transfer from the various ZnO-nc emission centers to Eu 3+ ions. The decay time obtained from the TRPL measurements was used to calculate the energy transfer efficiencies from the ZnO-nc emission centers, and these results were compared with the energy transfer efficiencies calculated from steady-state photoluminescence emission results. The results in this work show that high transfer efficiencies from the excitonic and Zn defect emission centers is mostly due to the energy transfer from ZnO-nc to Eu 3+ ions which results in the radiative emission from the Eu 3+ ions at 614 nm, while the energy transfer from the oxygen defect emissions is most probably due to the energy transfer from ZnO-nc to the new defects created due to the incorporation of the Eu 3+ ions.

  10. Metallic ions catalysis for improving bioleaching yield of Zn and Mn from spent Zn-Mn batteries at high pulp density of 10.

    Science.gov (United States)

    Niu, Zhirui; Huang, Qifei; Wang, Jia; Yang, Yiran; Xin, Baoping; Chen, Shi

    2015-11-15

    Bioleaching of spent batteries was often conducted at pulp density of 1.0% or lower. In this work, metallic ions catalytic bioleaching was used for release Zn and Mn from spent ZMBs at 10% of pulp density. The results showed only Cu(2+) improved mobilization of Zn and Mn from the spent batteries among tested four metallic ions. When Cu(2+) content increased from 0 to 0.8 g/L, the maximum release efficiency elevated from 47.7% to 62.5% for Zn and from 30.9% to 62.4% for Mn, respectively. The Cu(2+) catalysis boosted bioleaching of resistant hetaerolite through forming a possible intermediate CuMn2O4 which was subject to be attacked by Fe(3+) based on a cycle of Fe(3+)/Fe(2+). However, poor growth of cells, formation of KFe3(SO4)2(OH)6 and its possible blockage between cells and energy matters destroyed the cycle of Fe(3+)/Fe(2+), stopping bioleaching of hetaerolite. The chemical reaction controlled model fitted best for describing Cu(2+) catalytic bioleaching of spent ZMBs. Copyright © 2015 Elsevier B.V. All rights reserved.

  11. Experimental and numerical optical characterization of plasmonic copper nanoparticles embedded in ZnO fabricated by ion implantation and annealing

    Energy Technology Data Exchange (ETDEWEB)

    Le, Khai Q. [Faculty of Science and Technology, Hoa Sen University, Ho Chi Minh City (Viet Nam); Department of Physics, Faculty of Science, Jazan University, P.O. Box 114, 45142 Jazan (Saudi Arabia); Nguyen, Hieu P.T. [Department of Electrical and Computer Engineering, New Jersey Institute of Technology, NJ 07102 (United States); Ngo, Quang Minh [Institute of Material Sciences, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet Road, Cau Giay, Hanoi (Viet Nam); Canimoglu, Adil [Nigde University, Faculty of Arts and Sciences, Physics Department, Nigde (Turkey); Can, Nurdogan, E-mail: cannurdogan@yahoo.com [Celal Bayar University, Faculty of Arts and Sciences, Department of Physics, Muradiye, Manisa (Turkey); Department of Physics, Faculty of Science, Jazan University, P.O. Box 114, 45142 Jazan (Saudi Arabia)

    2016-06-05

    Here we describe the successfully fabrication of metal nanoparticle crystals by implanting copper (Cu) ions into single zinc oxide (ZnO) crystals with ion energy of 400 keV at ion doses of 1 × 10{sup 16} to 1 × 10{sup 17} ions/cm{sup 2}. After implantation and post-annealing treatment, the Cu implanted ZnO produces a broad range of luminescence emissions, ranging from green to yellow. A green luminescence peak at 550 nm could be ascribed to the isolated Cu ions. The changes in luminescence emission bands between the initial implant and annealed suggest that the implants give rise to clustering Cu nanoparticles in the host matrix but that the annealing process dissociates these. Numerical modelling of the Cu nanoparticles was employed to simulate their optical properties including the extinction cross section, electron energy loss spectroscopy and cathodoluminescence. We demonstrate that the clustering of nanoparticles generates Fano resonances corresponding to the generation of multiple resonances, while the isolation of nanoparticles results in intensity amplification. - Highlights: • We present the fabrication of metal nanoparticle crystals by implanting Cu into ZnO. • The luminescence properties were studied at different annealing temperature. • Numerical modelling of the Cu nanoparticles was employed. • We demonstrate that the clustering of nanoparticles generates Fano resonances.

  12. Study of chemically synthesized ZnO nano particles under a bio template using radioactive ion beam

    CERN Multimedia

    This is a project proposal to study nano sized semiconductor ZnO system, useful in biology and medicinal purposes, using radioactive ion beam from ISOLDE. Doping of the nano particles with Cu, Cd and Ga ions (in their variable valancy states) are expected to impart changes in the electrical structure and properties in the said system under study. The morphological changes, chemical environment, micro structure, electrical and optical properties of the nano size particles of ZnO system (developed under a bio template of folic acid) after the interaction with radioactive ion beam will be studied. The provision of perturbed angular correlation (PAC) study with respect to the changes in chemical environment, where ever possible will be attempted.

  13. 50 MeV, Li"3"+ - ion irradiation effect on magnetic ordering of Y"3"+ - substituted yttrium iron garnet

    International Nuclear Information System (INIS)

    Sharma, P. U.; Zankat, K. B.; Dolia, S. N.; Modi, K. B.

    2016-01-01

    This communication presents the effect of non-magnetic Y"3"+ ions substitution for magnetic Fe"3"+ ions and 50 MeV, Li"3"+ ion irradiation (fluence: 5 × 10"1"3 ions/cm"2) on magnetic ordering and Neel temperature of Y_3_+_xFe_5_-_xO_1_2 (x = 0.0, 0.2, 0.4 and 0.6) garnet system, studied by means of X-ray powder diffractometry and thermal variation of low field (0.5 Oe) ac susceptibility measurements. The un-irradiated compositions exhibit normal ferrimagnetic behavior with decrease in transition temperature (T_N) on increasing Y"3"+-concentration (x). The irradiated counterparts are characterized by tailing effect indicative of non-uniform effect of irradiation and lower value of T_N. The results have been discussed based on the weakening of magnetic exchange interactions and cumulative effect of redistribution of cations and fractional creation of localized paramagnetic centers resulting from swift heavy ion irradiation. The Neel temperatures and exchange integrals have been calculated theoretically.

  14. An excellent performance anode of ZnFe2O4/flake graphite composite for lithium ion battery

    International Nuclear Information System (INIS)

    Yao, Lingmin; Hou, Xianhua; Hu, Shejun; Tang, Xiaoqin; Liu, Xiang; Ru, Qiang

    2014-01-01

    Highlights: • ZnFe 2 O 4 /flake graphite composite was synthesized by hydrothermal method. • The ZnFe 2 O 4 /flake graphite anode demonstrated high initial coulombic efficiency of 87.7%. • The initial discharge /charge capacity was 848 mA h g −1 and 744 mA h g −1 . • The high capacity retention of 98% was obtained for the ZnFe 2 O 4 /flake graphite anode. -- Abstract: An approach of hydrothermal reaction for lithium ion battery was adopted, by which ZnFe 2 O 4 /flake graphite composites with excellent performance could be prepared as anode materials for lithium ion batteries. With nano-sized ZnFe 2 O 4 particles coating on the electrochemical active matrix of flake graphite, the special composites allowed improved electronic conductivity and constructed an expressway for the transport of charges and lithium ions. Thus the ZnFe 2 O 4 /flake graphite anode became a compromise between capacity and cycle ability. The initial discharge–charge capacity was 848 mA h g −1 and 744 mA h g −1 at a constant current density of 100 mA g −1 , respectively. As high as 87.7% of the initial coulombic efficiency was obtained. Additionally, the charge capacity maintained constantly in the range of 720–735 mA h g −1 in following cycles. And a high reversible charge capacity of 730 mA h g −1 could be attained after 100 cycles, with the reversible capacity retention of 98%

  15. Iron (III Ion Sensor Based on the Seedless Grown ZnO Nanorods in 3 Dimensions Using Nickel Foam Substrate

    Directory of Open Access Journals (Sweden)

    Mazhar Ali Abbasi

    2013-01-01

    Full Text Available In the present work, the seedless, highly aligned and vertical ZnO nanorods in 3 dimensions (3D were grown on the nickel foam substrate. The seedless grown ZnO nanorods were characterised by field emission scanning electron microscopy (FESEM, high resolution transmission electron microscopy (HRTEM, and X-ray diffraction (XRD techniques. The characterised seedless ZnO nanorods in 3D on nickel foam were highly dense, perpendicular to substrate, grown along the (002 crystal plane, and also composed of single crystal. In addition to this, these seedless ZnO nanorods were functionalized with trans-dinitro-dibenzo-18-6 crown ether, a selective iron (III ion ionophore, along with other components of membrane composition such as polyvinyl chloride (PVC, 2-nitopentylphenyl ether as plasticizer (NPPE, and tetrabutyl ammonium tetraphenylborate (TBATPB as conductivity increaser. The sensor electrode has shown high linearity with a wide range of detection of iron (III ion concentrations from 0.005 mM to 100 mM. The low limit of detection of the proposed ion selective electrode was found to be 0.001 mM. The proposed sensor also described high storage stability, selectivity, reproducibility, and repeatability and a quick response time of less than 10 s.

  16. Defects induced by swift heavy ions in the 18R martensite of Cu-Zn-Al alloy

    International Nuclear Information System (INIS)

    Zelaya, Eugenia; Tolley, Alfredo; Condo, Adriana; Lovey, Francisco; Schumacher, G

    2003-01-01

    The swift heavy ion incidence over the surface of a given material produces a strong energy deposition in a nanometric scale.Swift heavy ions, of the order of one thousand of MeV, deposit their energy as electronic excitations.This highly localized deposition can induce metastable transformations within the material. For example, in martensitic NiTi alloys irradiated with swift heavy ions, it has been observed changes on the martensitic transformation temperature and amorphous areas induced by the irradiation.In this work, the effects produced by swift heavy ions on the martensitic 18R structure of Cu-Zn-Al alloy (Cu - 12.17 Zn - 17.92 Al, in %at) were analyzed.Crystalline samples were irradiated in a direction close to the [2 1 0] of 18R with Xe + 230 MeV, Au + of 350 MeV and Kr + of 200 MeV ion beams.Defects of the order of nanometers induced by the irradiation were observed by transmission electron microscopy (TEM) and high resolution electron microscopy (HREM).It was also observed, that the average size of the irradiation defects induced by Au + ion is larger than those induced by Xe + and Kr + ions.In this case, no relationship between the observed defects and the energy deposition was found in the 23 keV/nn to 48 keV/nn range

  17. Cycling behaviour of sponge-like nanostructured ZnO as thin-film Li-ion battery anodes

    International Nuclear Information System (INIS)

    Garino, Nadia; Lamberti, Andrea; Gazia, Rossana; Chiodoni, Angelica; Gerbaldi, Claudio

    2014-01-01

    Highlights: • Zn is thermally oxidized in ambient air to obtain sponge-like ZnO film. • Polycrystalline, transparent, porous thin film is obtained. • Film exhibits stabile specific capacity (∼300 mAh g −1 ) after prolonged cycling. • Sponge-like ZnO film shows promising prospects as Li-ion battery anode. - Abstract: Single phase wurtzitic porous ZnO thin films are obtained by a simple two-step method, involving the sputtering deposition of a sponge-like metallic Zn layer, followed by a moderately low temperature treatment for the complete zinc oxidation. Thanks to its 3D nanostructuration, the superimposition of small branches able to grow in length almost isotropically and forming a complex topography, sponge-like ZnO can combine the fast transport properties of one dimensional material and the high surface area usually provided by nanocrystalline electrodes. When galvanostatically tested in lithium cell, after the initial decay, it can provide an almost stable specific capacity higher than 50 μAh cm −2 after prolonged cycling at estimated 0.7 C, with very high Coulombic efficiency

  18. Cycling behaviour of sponge-like nanostructured ZnO as thin-film Li-ion battery anodes

    Energy Technology Data Exchange (ETDEWEB)

    Garino, Nadia, E-mail: nadia.garino@iit.it [Center for Space Human Robotics @Polito, Istituto Italiano di Tecnologia, Corso Trento, 21, 10129 Turin (Italy); Lamberti, Andrea; Gazia, Rossana; Chiodoni, Angelica [Center for Space Human Robotics @Polito, Istituto Italiano di Tecnologia, Corso Trento, 21, 10129 Turin (Italy); Gerbaldi, Claudio, E-mail: claudio.gerbaldi@polito.it [Center for Space Human Robotics @Polito, Istituto Italiano di Tecnologia, Corso Trento, 21, 10129 Turin (Italy); 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: • Zn is thermally oxidized in ambient air to obtain sponge-like ZnO film. • Polycrystalline, transparent, porous thin film is obtained. • Film exhibits stabile specific capacity (∼300 mAh g{sup −1}) after prolonged cycling. • Sponge-like ZnO film shows promising prospects as Li-ion battery anode. - Abstract: Single phase wurtzitic porous ZnO thin films are obtained by a simple two-step method, involving the sputtering deposition of a sponge-like metallic Zn layer, followed by a moderately low temperature treatment for the complete zinc oxidation. Thanks to its 3D nanostructuration, the superimposition of small branches able to grow in length almost isotropically and forming a complex topography, sponge-like ZnO can combine the fast transport properties of one dimensional material and the high surface area usually provided by nanocrystalline electrodes. When galvanostatically tested in lithium cell, after the initial decay, it can provide an almost stable specific capacity higher than 50 μAh cm{sup −2} after prolonged cycling at estimated 0.7 C, with very high Coulombic efficiency.

  19. Indirect Determination of Mercury Ion by Inhibition of a Glucose Biosensor Based on ZnO Nanorods

    Directory of Open Access Journals (Sweden)

    Magnus Willander

    2012-11-01

    Full Text Available A potentiometric glucose biosensor based on immobilization of glucose oxidase (GOD on ZnO nanorods (ZnO-NRs has been developed for the indirect determination of environmental mercury ions. The ZnO-NRs were grown on a gold coated glass substrate by using the low temperature aqueous chemical growth (ACG approach. Glucose oxidase in conjunction with a chitosan membrane and a glutaraldehyde (GA were immobilized on the surface of the ZnO-NRs using a simple physical adsorption method and then used as a potentiometric working electrode. The potential response of the biosensor between the working electrode and an Ag/AgCl reference electrode was measured in a 1mM phosphate buffer solution (PBS. The detection limit of the mercury ion sensor was found to be 0.5 nM. The experimental results provide two linear ranges of the inhibition from 0.5 × 10−6 mM to 0.5 × 10−4 mM, and from 0.5 × 10−4 mM to 20 mM of mercury ion for fixed 1 mM of glucose concentration in the solution. The linear range of the inhibition from 10−3 mM to 6 mM of mercury ion was also acquired for a fixed 10 mM of glucose concentration. The working electrode can be reactivated by more than 70% after inhibition by simply dipping the used electrode in a 10 mM PBS solution for 7 min. The electrodes retained their original enzyme activity by about 90% for more than three weeks. The response to mercury ions was highly sensitive, selective, stable, reproducible, and interference resistant, and exhibits a fast response time. The developed glucose biosensor has a great potential for detection of mercury with several advantages such as being inexpensive, requiring minimum hardware and being suitable for unskilled users.

  20. Indirect determination of mercury ion by inhibition of a glucose biosensor based on ZnO nanorods.

    Science.gov (United States)

    Chey, Chan Oeurn; Ibupoto, Zafar Hussain; Khun, Kimleang; Nur, Omer; Willander, Magnus

    2012-11-06

    A potentiometric glucose biosensor based on immobilization of glucose oxidase (GOD) on ZnO nanorods (ZnO-NRs) has been developed for the indirect determination of environmental mercury ions. The ZnO-NRs were grown on a gold coated glass substrate by using the low temperature aqueous chemical growth (ACG) approach. Glucose oxidase in conjunction with a chitosan membrane and a glutaraldehyde (GA) were immobilized on the surface of the ZnO-NRs using a simple physical adsorption method and then used as a potentiometric working electrode. The potential response of the biosensor between the working electrode and an Ag/AgCl reference electrode was measured in a 1mM phosphate buffer solution (PBS). The detection limit of the mercury ion sensor was found to be 0.5 nM. The experimental results provide two linear ranges of the inhibition from 0.5 × 10(-6) mM to 0.5 × 10(-4) mM, and from 0.5 × 10(-4) mM to 20 mM of mercury ion for fixed 1 mM of glucose concentration in the solution. The linear range of the inhibition from 10(-3) mM to 6 mM of mercury ion was also acquired for a fixed 10 mM of glucose concentration. The working electrode can be reactivated by more than 70% after inhibition by simply dipping the used electrode in a 10 mM PBS solution for 7 min. The electrodes retained their original enzyme activity by about 90% for more than three weeks. The response to mercury ions was highly sensitive, selective, stable, reproducible, and interference resistant, and exhibits a fast response time. The developed glucose biosensor has a great potential for detection of mercury with several advantages such as being inexpensive, requiring minimum hardware and being suitable for unskilled users.

  1. Coordination geometries of Zn(II) and Cd(II) in phosphotriesterase: Influence of water molecules in the active site

    DEFF Research Database (Denmark)

    Krauss, M; Olsen, Lars; Antony, J

    2002-01-01

    Models of the metal ion binding sites of native ZnZn and of cadmium-substituted ZnCd and CdCd phosphotriesterase, including full amino acid side chains, were geometry optimized with quantum mechanical methods, with effective fragment potentials (EFP) representing the protein environment surroundi...... to the Od1 of the carboxylate of the first-shell aspartate designated M 1, but the energy difference between Cd1Zn2 and the lowest energy Zn1Cd2 structure is only about 2 kcal/mol and decreasing with the addition of water molecules. The Zn1Cd2 arrangement is found experimentally....

  2. The role of ion irradiation in activating silent Raman modes via tuning in plasmonic behaviour and surface disorder of Au/ZnO/Pt NFG system

    Science.gov (United States)

    Singh, Udai B.; Gautam, Subodh K.; Kumar, Sunil; Ojha, Sunil; Ghosh, Santanu; Singh, Fouran

    2017-09-01

    The perceptible progression of Raman modes of zinc oxide (ZnO) is studied in nanostructures film gap (Au (10 nm)/ZnO (70 nm)/Pt (50 nm)) system with 1.2 MeV Xe ion irradiation. Unattainable silent Raman modes of ZnO turn out to be strongly visible after ion irradiation. The creation of ion-beam-induced lattice disorder, defects, and impurities in a ZnO layer leads to breakdown the translational crystal symmetry that results in the origin of silent modes. The formation of hot-spots in the ZnO layer of the NFG system also supports the enhancement of the intensity of Raman modes. Overall results are attributed to combined effects of lattice disorder, defects, and impurities along with plasmonic effect and explained in the framework of elastic-thermal-spike formation.

  3. Calculation of the substitutional fraction of ion-implanted He in an Fe target

    OpenAIRE

    Erhart, Paul; Marian, Jaime

    2010-01-01

    Ion-implantation is a useful technique to study irradiation damage in nuclear materials. To study He effects in nuclear fusion conditions, He is co-implanted with damage ions to reproduce the correct He/dpa ratios in the desired or available depth range. However, the short-term fate of these He ions, i.e over the time scales of their own collisional phase, has not been yet unequivocally established. Here we present an atomistic study of the short-term evolution of He implantation in an Fe sub...

  4. Modelling Zn(II) sorption onto clayey sediments using a multi-site ion-exchange model

    International Nuclear Information System (INIS)

    Tertre, E.; Beaucaire, C.; Coreau, N.; Juery, A.

    2009-01-01

    In environmental studies, it is necessary to be able to predict the behaviour of contaminants in more or less complex physico-chemical contexts. The improvement of this prediction partly depends on establishing thermodynamic models that can describe the behaviour of these contaminants and, in particular, the sorption reactions on mineral surfaces. In this way, based on the mass action law, it is possible to use surface complexation models and ion exchange models. Therefore, the aim of this study is (i) to develop an ion-exchange model able to describe the sorption of transition metal onto pure clay minerals and (ii) to test the ability of this approach to predict the sorption of these elements onto natural materials containing clay minerals (i.e. soils/sediments) under various chemical conditions. This study is focused on the behaviour of Zn(II) in the presence of clayey sediments. Considering that clay minerals are cation exchangers containing multiple sorption sites, it is possible to interpret the sorption of Zn(II), as well as competitor cations, by ion-exchange equilibria with the clay minerals. This approach is applied with success to interpret the experimental data obtained previously in the Zn(II)-H + -Na + -montmorillonite system. The authors' research team has already studied the behaviour of Na + , K + , Ca 2+ and Mg 2+ versus pH in terms of ion exchange onto pure montmorillonite, leading to the development of a thermodynamic database including the exchange site concentrations associated with montmorillonite and the selectivity coefficients of Na + , K + , Ca 2+ , Mg 2+ , and Zn 2+ versus H + . In the present study, experimental isotherms of Zn(II) on two different sediments in batch reactors at different pH and ionic strengths, using NaCl and CaSO 4 as electrolytes are reported. Assuming clay minerals are the main ion-exchanging phases, it is possible to predict Zn(II) sorption onto sediments under different experimental conditions, using the previously

  5. Absence of intrinsic ferromagnetism in Zn1-xMnxO alloys

    International Nuclear Information System (INIS)

    Zhang Huawei; Shi Erwei; Chen Zhizhan; Liu Xuechao; Xiao Bing

    2006-01-01

    Zn 1-x Mn x O alloys, with different Mn concentrations, were prepared by the hydrothermal method. X-ray diffraction and electron paramagnetic resonance spectra demonstrate that Zn 2+ ions are homogeneously substituted by Mn 2+ ions without changing the ZnO wurtzite structure. The x = 0.02 and 0.04 samples are paramagnetic. When the Mn concentrations are increased to x = 0.08 and 0.10, the samples exhibit some ferromagnetism due to a secondary phase (Zn,Mn)Mn 2 O 4 . (letter to the editor)

  6. The pi Complex of the Hydronium Ion Frozen on the Pathway of Electrophilic Aromatic Substitution

    Czech Academy of Sciences Publication Activity Database

    Růžičková, Z.; Holub, Josef; Melichar, Petr; Moncol, J.; Wann, D. A.; Fanfrlík, Jindřich; Růžička, A.; Hnyk, Drahomír

    2016-01-01

    Roč. 2016, č. 26 (2016), s. 4473-4475 ISSN 1434-193X R&D Projects: GA ČR(CZ) GBP208/12/G016 Institutional support: RVO:61388980 ; RVO:61388963 Keywords : Anions * Pi complexes * Electrophilic substitution * Quantum mechanics * Structure elucidation Subject RIV: CA - Inorganic Chemistry; CF - Physical ; Theoretical Chemistry (UOCHB-X) Impact factor: 2.834, year: 2016

  7. Paracrystalline Disorder from Phosphate Ion Orientation and Substitution in Synthetic Bone Mineral.

    Science.gov (United States)

    Marisa, Mary E; Zhou, Shiliang; Melot, Brent C; Peaslee, Graham F; Neilson, James R

    2016-12-05

    Hydroxyapatite is an inorganic mineral closely resembling the mineral phase in bone. However, as a biological mineral, it is highly disordered, and its composition and atomistic structure remain poorly understood. Here, synchrotron X-ray total scattering and pair distribution function analysis methods provide insight into the nature of atomistic disorder in a synthetic bone mineral analogue, chemically substituted hydroxyapatite. By varying the effective hydrolysis rate and/or carbonate concentration during growth of the mineral, compounds with varied degrees of paracrystallinity are prepared. From advanced simulations constrained by the experimental pair distribution function and density functional theory, the paracrystalline disorder prevalent in these materials appears to result from accommodation of carbonate in the lattice through random displacement of the phosphate groups. Though many substitution modalities are likely to occur in concert, the most predominant substitution places carbonate into the mirror plane of an ideal phosphate site. Understanding the mineralogical imperfections of a biologically analogous hydroxyapatite is important not only to potential bone grafting applications but also to biological mineralization processes themselves.

  8. Influence of Al3+ substitution on the electrical resistivity and dielectric behavior of Ni0.25Cu0.20Zn0.55AlxFe2-xO4 ferrites synthesized by solid state reaction technique

    Science.gov (United States)

    Rahman, K. R.; Chowdhury, F.-U.-Z.; Khan, M. N. I.

    2017-12-01

    In this paper, the effect of Al3+ substitution on the electrical and dielectric properties of Ni0.25Cu0.20Zn0.55AlxFe2-xO4 ferrites with x = 0.0, 0.05. 0.10, 0.15 and 0.20, synthesized by solid state reaction has been reported. Using two probe method, the DC resistivity has been investigated in the temperature range from 30 °C to 300 °C. Activation energy was calculated from the Arrhenius plot. The electrical conduction is explained on the basis of the hopping mechanism. The frequency dependent dielectric properties of these spinel ferrites have been studied at room temperature by measuring AC resistivity, conductivity (σac), dielectric constant and dielectric loss tangent (tan δ) in the frequency range between 1 kHz and 120 MHz. The study of dielectric properties showed that the dielectric constant and dielectric loss increased with increasing non-magnetic Al ions. The dependence of dielectric constant with frequency has been explained by Maxwell-Wagner interfacial polarization. Cole-Cole plots show semicircular arc(s) for the samples, and equivalent RC circuits have been proposed to clarify the phenomena involved therein. The analysis of complex impedance spectroscopy has been used to distinguish between the grain and grain boundary contribution to the total resistance.

  9. Technical feasibility for commercialization of lithium ion battery as a substitute dry battery for motorcycle

    Science.gov (United States)

    Kurniyati, Indah; Sutopo, Wahyudi; Zakaria, Roni; Kadir, Evizal Abdul

    2017-11-01

    Dry battery on a motorcycle has a rapid rate of voltage drop, life time is not too long, and a long charging time. These are problems for users of dry battery for motorcycle. When the rate in the voltage decreases, the energy storage in the battery is reduced, then at the age of one to two years of battery will be dead and cannot be used, it makes the user should replace the battery. New technology development of a motorcycle battery is lithium ion battery. Lithium ion battery has a specification that has been tested and possible to replace dry battery. Characteristics of lithium ion battery can answer the question on the dry battery service life, the rate of decrease in voltage and charging time. This paper discusses about the technical feasibility for commercialization of lithium ion battery for motorcycle battery. Our proposed methodology of technical feasibility by using a goldsmith commercialization model of the technical feasibility and reconfirm the technical standard using the national standard of motorcycle battery. The battery has been through all the stages of the technical feasibility of the goldsmith model. Based on the results of the study, lithium ion batteries have the minimum technical requirements to be commercialized and has been confirmed in accordance with the standard motorcycle battery. This paper results that the lithium ion battery is visible to commercialized by the technical aspect.

  10. Differential sensing of fluoride and cyanide ions by using Dicyano substituted benzimidazole probe

    Energy Technology Data Exchange (ETDEWEB)

    Gupta, Akul Sen; Garg, Aparna; Paul, Kamaldeep; Luxami, Vijay, E-mail: vluxami@thapar.edu

    2016-05-15

    Excited State Intramolecular Proton Transfer based benzimidazole derivative having push–pull effect has been synthesized and investigated their photophysical behavior towards various anions. The probe 2 has been used for selective estimation of F{sup −} and CN{sup −} anions and signaled the binding event through formation of new absorption band at 465 nm. The probe 2 opens different emission channels at 425 nm in the presence of CN{sup −} ions and two new emission bands at 435 nm and 365 nm in case of F{sup −} ions. The probe 2 behaved as chemodosimeter for CN{sup −} ions which have been proved by {sup 1}H NMR and whereas fluoride caused hydrogen bonding interactions with probe 2 and restricted the ESIPT emission at 505 nm from OH to nitrogen of benzimidazole moiety to release its enol emission. The differential behavior of F{sup −} ions and CN{sup −} have been confirmed through DFT calculations. - Graphical abstract: The probe 2 binds chemodosimetrically with cyanide ions and act as chemosensor for fluoride ion.

  11. Differential sensing of fluoride and cyanide ions by using Dicyano substituted benzimidazole probe

    International Nuclear Information System (INIS)

    Gupta, Akul Sen; Garg, Aparna; Paul, Kamaldeep; Luxami, Vijay

    2016-01-01

    Excited State Intramolecular Proton Transfer based benzimidazole derivative having push–pull effect has been synthesized and investigated their photophysical behavior towards various anions. The probe 2 has been used for selective estimation of F − and CN − anions and signaled the binding event through formation of new absorption band at 465 nm. The probe 2 opens different emission channels at 425 nm in the presence of CN − ions and two new emission bands at 435 nm and 365 nm in case of F − ions. The probe 2 behaved as chemodosimeter for CN − ions which have been proved by 1 H NMR and whereas fluoride caused hydrogen bonding interactions with probe 2 and restricted the ESIPT emission at 505 nm from OH to nitrogen of benzimidazole moiety to release its enol emission. The differential behavior of F − ions and CN − have been confirmed through DFT calculations. - Graphical abstract: The probe 2 binds chemodosimetrically with cyanide ions and act as chemosensor for fluoride ion.

  12. Removal of thorium (IV) ions from aqueous solution by a novel nanoporous ZnO: Isotherms, kinetic and thermodynamic studies.

    Science.gov (United States)

    Kaynar, Ümit H; Ayvacıklı, Mehmet; Hiçsönmez, Ümran; Kaynar, Sermin Çam

    2015-12-01

    The adsorption of thorium (IV) from aqueous solutions onto a novel nanoporous ZnO particles prepared by microwave assisted combustion was studied using batch methods under different experimental conditions. The effect of contact time, solution pH, initial concentration and temperature on adsorption process was studied. The ability of this material to remove Th (IV) from aqueous solution was characterises by Langmuir, Freunlinch and Temkin adsorption isotherms. The adsorption percent and distribution coefficient for nanoporous ZnO powders in optimum conditions were 97% ± 1.02; 8080 L kg(-1)for Th (IV), respectively. Based on the Langmuir model, the maximum adsorption capacity of nanoporous ZnO for Th (IV) was found to be 1500 g kg(-1). Thermodynamic parameters were determined and discussed. The results indicated that nanoporous ZnO was suitable as sorbent material for recovery and adsorption of Th (IV) ions from aqueous solutions. The radioactive Th (VI) in surface water, sea water and waste waters from technologies producing nuclear fuels, mining (uranium and thorium) and laboratories working with radioactive materials (uranium and thorium) can be removed with this nanoporous ZnO. Copyright © 2015 Elsevier Ltd. All rights reserved.

  13. Adsorption Isotherms of Cs+, Co2+, Zn2+ and Eu3+ on Zirconium Vanadate Ion-Exchanger

    International Nuclear Information System (INIS)

    Shady, S.A.; El-Ashery, S.M.; El-Naggar, I.M.

    2009-01-01

    Zirconium vanadate had been prepared by the dropwise addition of 0.1 M sodium vanadate and 0.1 M zirconyl chloride by molar ratio of zirconium/vanadium 2. Exchange isotherms for Cs + /H + , Co 2+ /H + ,Zn 2+ /H + and Eu 3+ /H + have been determined at 25, 40 and 60 degree C. Besides, it was proved that cesium, cobalt, zinc and europium are chemically adsorbed. Moreover, the heat of adsorption of these ions on zirconium vanadate had been calculated and indicated that zirconium vanadate is of endothermic behavior towards these ions

  14. Enhancement of photo sensor properties of nanocrystalline ZnO thin film by swift heavy ion irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Mahajan, S. V.; Upadhye, D. S.; Bagul, S. B. [Department of Nanotechnology, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad-431004 (India); Shaikh, S. U.; Birajadar, R. B.; Siddiqui, F. Y.; Huse, N. P. [Thin film and Nanotechnology Laboratory, Department of Physics, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad-431004 (India); Sharma, R. B., E-mail: ramphalsharma@yahoo.com, E-mail: rps.phy@gmail.com [Thin film and Nanotechnology Laboratory, Department of Physics, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad-431004 (India); Department of Nanotechnology, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad-431004 (India)

    2015-06-24

    Nanocrystalline Zinc Oxide (ZnO) thin film prepared by Low cost Successive Ionic Layer Adsorption and Reaction (SILAR) method. This film was irradiated by 120 MeV Ni{sup 7+} ions with the fluence of 5x10{sup 12}ions/cm{sup 2}. The X-ray diffraction study was shows polycrystalline nature with wurtzite structure. The optical properties as absorbance were determined using UV-Spectrophotometer and band gap was also calculated. The Photo Sensor nature was calculated by I-V characteristics with different sources of light 40W, 60W and 100W.

  15. Structural and morphological evolution in magnetron co-sputtered (Zn, Cr)O films

    International Nuclear Information System (INIS)

    Hu, Y M; Chiou, J W; Han, T C; Chen, Y T; Hsu, C W; Chen, G J; Chou, W Y; Chang, J; Hsu, J Y; Yu, Y C

    2008-01-01

    In this study, x-ray diffraction, scanning electron microscopy, micro-Raman spectroscopy, x-ray absorption near-edge structure and particle-induced x-ray emission are used to characterize the microstructure of (Zn, Cr)O films prepared using a co-sputtering method. We found that the Cr ions did not substitute for the Zn sites but instead formed Cr nano-particles and secondary oxide phases (SOPs) of Cr 2 O 3 and/or ZnCr 2 O 4 in co-sputtered Zn 1-x Cr x O films with Cr content x ≥ 0.1. Evidence is presented for the evolution of SOPs formed in (Zn, Cr)O films with increasing Cr sputtering power. Based on the inspection of the Cr and Zn contents in (Zn, Cr)O films, we conclude that the formation of the Cr 2 O 3 phase is driven by a substantial increase in the atomic ratio of Cr/Zn, followed by the formation of a ZnCr 2 O 4 phase promoted by a higher content of Cr than of Zn in film with increasing Cr sputtering power. It seems that a strong preference of Cr for octahedral rather than tetrahedral coordination with oxygen would trigger the formation of SOPs rather than the substitution of Cr into Zn sites and could be an obstacle for achieving a real Cr-substituted ZnO dilute magnetic oxide.

  16. Synthesis and electrochemical properties of ZnMn_2O_4 anode for lithium-ion batteries

    International Nuclear Information System (INIS)

    Feng, Chuanqi; Wang, Wei; Chen, Xiao; Wang, Shiquan; Guo, Zaiping

    2015-01-01

    Graphical abstract: ZnMn_2O_4 nanoparticles were prepared through the rheological phase reaction method (R-ZMO) or the mixed solvothermal method(M-ZMO). The particles of M-ZMO were clustered together to form uniform microspheres morphology. The M-ZMO behaved higher reversible capacity and better cycle performance than that of R-ZMO. - Highlights: • ZnMn_2O_4 nanoparticles were prepared through the rheological phase reaction method (R-ZMO) or the mixed solvothermal method (M-ZMO). • The M-ZMO behaved higher reversible capacity and better cycle performance than that of R-ZMO. • The morphology and cell parameters of ZnMn_2O_4 are important effects on its electrochemical properties. • The diffusion coefficient of Li"+ in M-ZMO is beneficial for M-ZMO to be used an anode. - Abstract: The precursors of ZnMn_2O_4 were synthesized by different methods (the rheological phase reaction method or the mixed solvothermal method). The precursors were heat-treated at a suitable temperature to obtain the expected product (ZnMn_2O_4). The synthesized samples were characterized by X-ray diffraction, scanning electron microscopy, and transmission electron microscopy. The electrochemical properties of the samples were also investigated. The results show that ZnMn_2O_4 was synthesized successfully. The particles of ZnMn_2O_4 were irregular quasi-spheres with sizes of about 50 nm. The ZnMn_2O_4 nanoparticles synthesized through the mixed solvothermal method were clustered together to form microspheres about 1 μm in diameter. The electrochemical testing results showed that the ZnMn_2O_4 synthesized through the mixed solvothermal method featured higher reversible capacity and better cycling performance than the sample synthesized by the rheological phase reaction method. The ZnMn_2O_4 synthesized through the mixed solvothermal method could be a promising anode material for lithium ion battery application.

  17. Quantum electrodynamics effects in the 4s-4p transitions in Cu-like and Zn-like ions

    International Nuclear Information System (INIS)

    Cheng, K.; Wagner, R.A.

    1987-01-01

    Multiconfiguration Dirac-Fock energies are compared with experiment for the 4s-4p transitions in Cu-like ions and the 4s 2 1 S 0 --4s4p 1 P 1 transition in Zn-like ions for Au, Pb, Bi, Th, and U. The Coulomb, Breit, and QED contributions to these transitions are tabulated for selected ions in the range Z = 50--92. Results show that the agreement between theory and experiment is good enough to show the importance of QED corrections in the spectra of these highly stripped ions. Contrary to earlier findings by Seely et al. [Phys. Rev. Lett. 57, 2924 (1986)] we find no significant differences between the observed and calculated transition energies after finite-nuclear-size corrections are included

  18. Ion species dependence of the implantation-induced defects in ZnO studied by a slow positron beam

    International Nuclear Information System (INIS)

    Chen, Z.Q.; Maekawa, M.; Kawasuso, A.; Naramoto, H.

    2007-01-01

    In this work, we implanted B + , O + , Al + , and P + ions into ZnO with energy of 50-380 keV and total doses of 4 x 10 15 cm -2 for each ion. The implantation-induced defects and their thermal recovery were studied using a slow positron beam. Vacancy clusters are produced in all the implanted samples. It is found that the thermal recovery of these vacancies induced by different ions shows much difference. In case of B + and Al + -implantation, the vacancy clusters agglomerate to much larger size and might evolve to microvoids during annealing. However, for O + and P + ions, which are heavier than B + and Al + , the vacancies show a much weaker agglomeration process. The mechanism of such difference is discussed. (copyright 2007 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  19. Intercalation of Molybdate Ions into Ni/Zn Layered Double Hydroxide Salts: Synthesis, Characterization, and Preliminary Catalytic Activity in Methyl Transesterification of Soybean Oil

    OpenAIRE

    Colombo, Kamila; Maruyama, Swami A.; Yamamoto, Carlos I.; Wypych, Fernando

    2017-01-01

    This study reports the synthesis and characterization of a Ni/Zn layered double hydroxide salt intercalated with acetate ions and the subsequent replacement of the acetate ions with molybdate ions via an ion exchange reaction, conducted at two different pH values. Regardless of the pH employed during the synthesis, the basal spacing in the Ni/Zn layered double hydroxide salt decreased from 13.08 Å to approximately 9.5 Å, which agreed with intercalation of hydrated molybdate anions. The non-ca...

  20. Effect of substitution of 1 at% Ni for Zn on the microstructure and mechanical properties of Mg{sub 94}Y{sub 4}Zn{sub 2} alloy

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Huan, E-mail: liuhuanseu@hotmail.com [Jiangsu Key Lab of Advanced Metallic Materials, School of Material Science and Engineering, Southeast University, Nanjing 211189 (China); Xue, Feng, E-mail: xuefeng@seu.edu.cn [Jiangsu Key Lab of Advanced Metallic Materials, School of Material Science and Engineering, Southeast University, Nanjing 211189 (China); Bai, Jing; Zhou, Jian [Jiangsu Key Lab of Advanced Metallic Materials, School of Material Science and Engineering, Southeast University, Nanjing 211189 (China); Liu, Xiaodao [Nanjing Yunhai Special Metals Co., Ltd., Nanjing 211200 (China)

    2013-11-15

    The microstructure and mechanical properties of Mg{sub 94}Y{sub 4}Zn{sub 2} and Mg{sub 94}Y{sub 4}Zn{sub 1}Ni{sub 1} alloys have been systematically investigated by optical microscopy (OM), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and an electronic universal testing machine. The as-cast WZ42 alloy is composed of α-Mg matrix, 18R LPSO (long period stacking ordered) phase and a small fraction of Mg{sub 24}(Y,Zn){sub 5} phases. With the replacement of 1 at% Ni atoms, the phase structures in WZN411 alloy remain unchanged, but their chemical compositions vary obviously. A great number of stacking faults exist in α-Mg grains of WZ42 alloy, while they are barely observed in WZN411 alloy. After annealing at 500 °C for 12 h, there are plenty of 14H LPSO lamellas formed in WZ42 alloy and many nano-scale α-Mg slices generated between 18R phases. In contrast, the 18R in WZN411 alloy is thermally stable, and both the formation of α-Mg slices and 14H lamellas are restricted for annealed WZN411 alloy. Tensile tests indicate that the as-extruded WZ42 alloy exhibits ultimate tensile strength of 390 MPa, tensile yield strength of 246 MPa and elongation of 2.8% at room temperature. With the replacement of 1 at% Ni, the UTS and TYS of WZN411 alloy increase by 20 MPa and the ductility improves as well. The improvement of comprehensive mechanical properties could be ascribed to the substitution of 1 at% Ni element, which could enhance the degree of solid-solution strengthening and stimulate the thermal stability of 18R phase during annealing and extrusion processes.

  1. Effect of 1.2 MeV argon ions irradiation on magnetic properties of ZnO

    International Nuclear Information System (INIS)

    Mishra, D.K.; Mohapatra, Jyoshnarani; Mahato, Banashree; Kumar, P.; Mitra, Amitav; Singh, S.K.; Kanjilal, D.

    2013-01-01

    Room temperature ferromagnetism in 1.2 MeV argon ions irradiated polycrystalline ZnO has been observed. The magnetic contribution in form of saturation magnetization is higher in sample irradiated with ion fluence of 1 × 10 15 ions/cm 2 . However, annealing of the defects at higher fluences of 5 × 10 15 ions/cm 2 reduce the magnetic contribution in comparison to the magnetic contribution of the lower fluences. The X-ray diffraction reveals that the degree of crystallinity decreases with the increase of ion fluences upto 1 × 10 15 ions/cm 2 and further it increases at a fluence of 5 × 10 15 ions/cm 2 . The inhomogeneous arrangement of grains and changes in their sizes with increasing ion fluences decrease the magnetic ordering of the system. The electron probe microstructure analyses and micro-Raman spectra of irradiated samples show in-homogeneity in zinc and oxygen ratio which is one of the causes to show ferromagnetism.

  2. Substitutional HCN- molecular ions in KCN crystal: a paramagnetic probe in a ferroelastic material

    International Nuclear Information System (INIS)

    Weid, J.P. von der; Carmo, L.C.S. do; Ribeiro, S.C.

    1978-01-01

    The HCN - molecular ion was produced in single crystals of KCN: 10 -2 OH - irradiated by UV light at 77 K. The spin Hamiltonian parameters were measured at 60 K and the temperature dependence of the spectrum was investigated between 60 K and 170 K. This temperature dependence is explained by the rapid motion of the molecule with the increasing temperature and the elastic interaction of the molecule with the surrounding ions. Using the similarity between the paramagnetic HCN - molecule and the CN - ions of the host lattice a qualitative picture of the local phenomena occuring in the ferroelastic phase of KCN could be made and the energy of the elastic interaction between CN - was estimated of the order of 7 meV [pt

  3. Emission channeling studies on transition-metal doped GaN and ZnO: Cation versus anion substitution

    CERN Document Server

    AUTHOR|(CDS)2070176; Wahl, Ulrich; Martins Correia, Joao; Amorim, Lígia; Silva, Daniel; Decoster, Stefan; Castro Ribeiro Da Silva, Manuel; Temst, Kristiaan; Vantomme, André

    2014-01-01

    The magnetic and electric properties of impurities in semiconductors are strongly dependent on the lattice sites which they occupy. While the majority site can often be predicted based on chemical similarities with the host elements and is usually simple to confirm experimentally, minority sites are far more complicated to predict, detect and identify. We have carried out extensive beta− emission channeling studies on the lattice location of transition metal impurities in wide-gap dilute magnetic semiconductors, namely Co and Mn in GaN and ZnO, making use of radioactive 61Co and 56Mn implanted at the ISOLDE facility at CERN. In addition to the majority occupation of cation (Ga, Zn) sites, we located significant fractions (of the order of 20%) of the Co and Mn impurities in anion (N, O) sites, which are virtually unaffected by thermal annealing up to 900 °C. Here, we present the beta− emission channeling experiments on 61Co-implanted GaN. We discuss these results in the context of our recent reports of mi...

  4. Reactivity and selectivity of the electrophile aromatic substitution in the gas phase by positive 80Br and 125I decay ions

    International Nuclear Information System (INIS)

    Knust, E.J.

    1975-02-01

    The nuclear isomeric transition sup(80m)Br(IT) 80 Br or the electron capture decay 125 Xe(EC) 125 I in the presence of high concentrations of a noble gas such as Ar or Xe are suitable for the study of the electrophilic substitution of bromium or iodonium ions in the gas phase. By using this nuclear method, which, unlike physical methods, also allows the determination of the isomer distribution, the electrophilic aromatic bromation and iodation of mono-substituted benzene compounds through unsolvated positive bromine or iodine ions could be investigated for the first time using radio-gas chromatographic techniques. (orig./LH) [de

  5. Electron transfer rates and equilibria between substituted phenoxide ions and phenoxyl radicals

    International Nuclear Information System (INIS)

    Steenken, S.; Neta, P.

    1979-01-01

    The rate constants for electron transfer from a series of substituted isomeric dihydroxy- and diaminobenzenes to different substituted phenoxyl radicals were measured by observing the decay or buildup of one of the radicals invoved. In many cases the electron transfer reactions were reversible and the equilibrium constants could be calculated from the individual rate constants for attainment of equilibrium and from the concentrations of the species involved at equilibrium. From the equilibrium constants the one-electron redox potentials for 15 individual Q - ./Q 2- pairs were determined, using the value for hydroquinone (23 mV at pH 13.5) as a reference. The potential for catechol (43 mV) is near that of hydroquinone; resorcinol is oxidized much less readily (300 mV), while phenol is even a weaker reductant (>500mV). Methyl, methoxy, and hydroxy substituents decrease the redox potentials while acetyl and carboxyl substituents increase these values. Ascorbate has a potential (15mV) similar to that of hydroquinone, while TMPD (82mV) and p-phenylenediamine (183mV) are less easily oxidized

  6. Facile Synthesis of ZnO Nanoparticles on Nitrogen-Doped Carbon Nanotubes as High-Performance Anode Material for Lithium-Ion Batteries

    Directory of Open Access Journals (Sweden)

    Haipeng Li

    2017-09-01

    Full Text Available ZnO/nitrogen-doped carbon nanotube (ZnO/NCNT composite, prepared though a simple one-step sol-gel synthetic technique, has been explored for the first time as an anode material. The as-prepared ZnO/NCNT nanocomposite preserves a good dispersity and homogeneity of the ZnO nanoparticles (~6 nm which deposited on the surface of NCNT. Transmission electron microscopy (TEM reveals the formation of ZnO nanoparticles with an average size of 6 nm homogeneously deposited on the surface of NCNT. ZnO/NCNT composite, when evaluated as an anode for lithium-ion batteries (LIBs, exhibits remarkably enhanced cycling ability and rate capability compared with the ZnO/CNT counterpart. A relatively large reversible capacity of 1013 mAh·g−1 is manifested at the second cycle and a capacity of 664 mAh·g−1 is retained after 100 cycles. Furthermore, the ZnO/NCNT system displays a reversible capacity of 308 mAh·g−1 even at a high current density of 1600 mA·g−1. These electrochemical performance enhancements are ascribed to the reinforced accumulative effects of the well-dispersed ZnO nanoparticles and doping nitrogen atoms, which can not only suppress the volumetric expansion of ZnO nanoparticles during the cycling performance but also provide a highly conductive NCNT network for ZnO anode.

  7. Cathode and ion-luminescence of Eu:ZnO thin films prepared by reactive magnetron sputtering and plasma decomposition of non-volatile precursors

    Energy Technology Data Exchange (ETDEWEB)

    Gil-Rostra, Jorge [Instituto de Ciencia de Materiales de Sevilla, CSIC, Univ. Sevilla, C/Américo Vespucio 49, E-41092 Sevilla (Spain); Ferrer, Francisco J. [Centro Nacional de Aceleradores, CSIC, Univ. Sevilla, Av. Thomas A. Edison 7, E-41092 Sevilla (Spain); Martín, Inocencio R. [Departamento de Física Fundamental y Experimental, Electrónica y Sistemas, U. La Laguna, C/Astrofísico Francisco Sánchez s/n, E-38206 La Laguna, Santa Cruz de Tenerife (Spain); González-Elipe, Agustín R.; Yubero, Francisco [Instituto de Ciencia de Materiales de Sevilla, CSIC, Univ. Sevilla, C/Américo Vespucio 49, E-41092 Sevilla (Spain)

    2016-10-15

    This paper reports the luminescent behavior of Eu:ZnO thin films prepared by an one-step procedure that combines reactive magnetron sputtering deposition of ZnO with the plasma activated decomposition of a non-volatile acetylacetonate precursor of Eu sublimated in an effusion cell. Chemical composition and microstructure of the Eu:ZnO thin films have been characterized by several methods and their photo-, cathode- and ion-luminescent properties studied as a function of Eu concentration. The high transparency and well controlled optical properties of the films have demonstrated to be ideal for the development of cathode- and ion- luminescence sensors.

  8. Modulatory effects of Zn2+ ions on the toxicity of citrate- and PVP-capped gold nanoparticles towards freshwater algae, Scenedesmus obliquus.

    Science.gov (United States)

    Iswarya, V; Johnson, J B; Parashar, Abhinav; Pulimi, Mrudula; Chandrasekaran, N; Mukherjee, Amitava

    2017-02-01

    Gold nanoparticles (GNPs) are widely used for medical purposes, both in diagnostics as well as drug delivery, and hence are prone to release and distribution in the environment. Thus, we have explored the effects of GNPs with two distinct surface capping (citrate and PVP), and three different sizes (16, 27, and 37 nm) at 0.01-, 0.1-, and 1-mg L -1 concentrations on a predominant freshwater alga Scenedesmus obliquus in the sterile freshwater matrix. We have also investigated how an abundant metal ion from freshwater, i.e., Zn 2+ ions may modulate the effects of the selected GNPs (40 nm, citrate, and PVP capped). Preliminary toxicity results revealed that gold nanoparticles were highly toxic in comparison to zinc ions alone. A significant modulation in the toxicity of Zn ions was not noticed in the presence of GNPs. In contrast, zinc ions minimized the toxicity produced by GNPs (both CIT-37 and PVP-37), despite its individual toxicity. Approximately, about 42, 33, and 25% toxicity reduction was noted at 0.05-, 0.5-, and 5-mg L -1 Zn ions, respectively, for CIT-37 GNPs, while 31% (0.05 mg L -1 ), 24% (0.5 mg L -1 ), and 9% (5 mg L -1 ) of toxicity reduction were noted for PVP-37 GNPs. Maximum toxicity reduction was seen at 0.05 mg L -1 of Zn ions. Abbott modeling substantiated antagonistic effects offered by Zn 2+ ions on GNPs. Stability and sedimentation data revealed that the addition of zinc ions gradually induced the aggregation of NPs and in turn significantly reduced the toxicity of GNPs. Thus, the naturally existing ions like Zn 2+ have an ability to modulate the toxicity of GNPs in a real-world environment scenario.

  9. Adsorption of Zn(II) and Cd(II) ions in batch system by using the Eichhornia crassipes.

    Science.gov (United States)

    Módenes, A N; Espinoza-Quiñones, F R; Borba, C E; Trigueros, D E G; Lavarda, F L; Abugderah, M M; Kroumov, A D

    2011-01-01

    In this work, the displacement effects on the sorption capacities of zinc and cadmium ions of the Eichornia crassipes-type biosorbent in batch binary system has been studied. Preliminary single metal sorption experiments were carried out. An improvement on the Zn(II) and Cd(II) ions removal was achieved by working at 30 °C temperature and with non-uniform biosorbent grain sizes. A 60 min equilibrium time was achieved for both Zn(II) and Cd(II) ions. Furthermore, it was found that the overall kinetic data were best described by the pseudo second-order kinetic model. Classical multi-component adsorption isotherms have been tested as well as a modified extended Langmuir isotherm model, showing good agreement with the equilibrium binary data. Around 0.65 mequiv./g maximum metal uptake associated with the E. crassipes biosorbent was attained and the E. crassipes biosorbent has shown higher adsorption affinity for the zinc ions than for the cadmium ones in the binary system.

  10. Solubilization of insoluble zinc compounds by Gluconacetobacter diazotrophicus and the detrimental action of zinc ion (Zn2+) and zinc chelates on root knot nematode Meloidogyne incognita.

    Science.gov (United States)

    Saravanan, V S; Kalaiarasan, P; Madhaiyan, M; Thangaraju, M

    2007-03-01

    To examine the zinc (Zn) solubilization potential and nematicidal properties of Gluconacetobacter diazotrophicus. Atomic Absorption Spectrophotometer, Differential Pulse Polarography and Gas Chromatography Coupled Mass Spectrometry were used to estimate the total Zn and Zn(2+) ions and identify the organic acids present in the culture supernatants. The effect of culture filtrate of Zn-amended G. diazotrophicus PAl5 on Meloidogyne incognita in tomato was examined under gnotobiotic conditions. Gluconacetobacter diazotrophicus PAl5 effectively solubilized the Zn compounds tested and 5-ketogluconic acid was identified as the major organic acid aiding the solubilization of zinc oxide. The presence of Zn compounds in the culture filtrates of G. diazotrophicus enhanced the mortality and reduced the root penetration of M. incognita under in vitro conditions. 5-ketogluconic acid produced by G. diazotrophicus mediated the solubilization process and the available Zn(2+) ions enhanced the nematicidal activity of G. diazotrophicus against M. incognita. Zn solubilization and enhanced nematicidal activity of Zn-amended G. diazotrophicus provides the possibility of exploiting it as a plant growth promoting bacteria.

  11. Aggregation of dialkyl-substituted diphosphonic acids and its effect on metal ion extraction.

    Energy Technology Data Exchange (ETDEWEB)

    Chiarizia, R.; Barrans, R. E., Jr.; Ferraro, J. R. Herlinger, A. W.; McAlister, D. R.

    1999-10-22

    Solvent extraction reagents containing the diphosphonic acid group exhibit an extraordinary affinity for tri-, tetra- and hexavalent actinides. Their use has been considered for actinide separation and pre-concentration procedures. Solvent extraction data obtained with P,P{prime}-di(2-ethylhexyl) methane-, ethane- and butanediphosphonic acids exhibit features that are difficult to explain without Knowledge of the aggregation state of the extractants. Information about the aggregation of the dialkyl-substituted diphosphonic acids in aromatic diluents has been obtained using the complementary techniques of vapor pressure osmometry (VPO), small angle neutron scattering (SANS), infrared spectroscopy and molecular mechanics. The results from these techniques provide an understanding of the aggregation behavior of these extractants that is fully compatible with the solvent extraction data. The most important results and their relevance to solvent extraction are reviewed in this paper.

  12. The fraction of substitutional boron in silicon during ion implantation and thermal annealing

    International Nuclear Information System (INIS)

    Caturla, M.J.; Johnson, M.D.; Diaz de la Rubia, T.

    1998-01-01

    We present results from a kinetic Monte Carlo simulation of boron transient enhanced diffusion (TED) in silicon. Our approach avoids the use of phenomenological fits to experimental data by using a complete and self-consistent set of values for defect and dopant energetics derived mostly from ab initio calculations. The results predict that, during annealing of 40 keV B-implanted Si at 800 degree C, there exists a time window during which all the implanted boron atoms are substitutional. At earlier or later times, the interactions between free silicon self-interstitials and boron atoms drive the growth of boron clusters and result in an inactive boron fraction. The results show that the majority of boron TED takes place during the growth period of interstitial clusters and not during their dissolution. copyright 1998 American Institute of Physics

  13. Transient negative ions in benzene. Some N-heterocyclic and mono-substituted derivatives

    International Nuclear Information System (INIS)

    Nenner, Irene

    1975-01-01

    Electron transmission spectroscopy is used to study transient negative ions or shape resonances in various benzene derivatives. Because of the long lifetime of these ions (τ > 10 -14 S) the vibrational structure of their first two electronic states is observed superposed on the total electron cross section curves in the energy range 0-6 eV and the corresponding adiabatic electron affinities are determined. The comparison of the first electron affinity with the first ionization potential and the energy on the first excited state of each of the derivatives is used to characterize the 'donor' substituents on the benzene ring. As a complementary study, these derivatives are studied in the liquid phase using polarography (cyclic voltametry). The linear correlation established between polarographic potentials measured in dimethyl formamide and the electron affinities was used to deduce electron affinities for several molecules which are difficult to measure in the gas phase. (author) [fr

  14. Synthesis and properties of the diluted magnetic semiconductor ZnO doped with nickel ions by combustion reaction; Sintese e propriedades do semicondutor magnetico diluido ZnO dopado com ions de niquel por meio da reacao de combustao

    Energy Technology Data Exchange (ETDEWEB)

    Morais, A.; Torquato, R.A.; Costa, A.C.F.M, E-mail: m.artur@hotmail.com.br [Universidade Federal da Paraiba (UFPB), Joao Pessoa, PB (Brazil). Departamento de Engenharia de Materiais; Universidade Federal de Campina Grande (UFCG), PB (Brazil). Departamento de Engenharia de Materiais

    2017-10-01

    One of the greatest challenges for the development of the spintronics this creation of materials having semiconductivity and magnetism at above room temperatures, enabling the creation of devices with greater processing speeds. This work aims to synthesize by combustion reaction semiconductor ZnO doped with nickel ions at a concentration of 0.08 mol for applications such as diluted magnetic semiconductor (DMS). The combustion reaction is quite simple and promising in obtaining single-phase materials at the nanoscale. The obtained powder was subjected to the characterizations of X-ray diffraction (XRD), X-ray fluorescence, vibrating sample magnetometry (VSM), and UV-vis spectroscopy. The crystalline material exhibits ZnO crystalline structure and coercive field of 161,36 Oe, showing that the material exhibits the properties of an SMD. (author)

  15. Highly selective and sensitive fluorescence detection of Zn(2+) and Cd(2+) ions by using an acridine sensor.

    Science.gov (United States)

    Visscher, A; Bachmann, S; Schnegelsberg, C; Teuteberg, T; Mata, R A; Stalke, D

    2016-04-07

    Fluorescence spectroscopy investigations of the new acridine derivative bis(N,N-dimethylaminemethylene)acridine (3) show remarkable selectivity and sensitivity towards Zn(2+) and Cd(2+) ions in methanol and for the latter even in water. Through the chelation of the metal ions the present PET effect is quenched, significantly enhancing the emission intensity of the fluorophore. In solution, the bonding situation is studied by fluorescence and NMR spectroscopy, as well as ESI-TOF mass-spectrometry measurements. The solid state environment is investigated by X-ray diffraction and computational calculations. Here, we can show the complexation of the zinc and cadmium ions by the methylene bridged amine receptors as well as by the nitrogen atom of the acridine system.

  16. Band-gap tuning and magnetic properties of heterovalent ions (Ba, Sr and Ca) substituted BiFeO_3 nanoparticles

    International Nuclear Information System (INIS)

    Chauhan, Sunil; Kumar, Manoj; Katyal, S. C.

    2016-01-01

    A Comparative study of heterovalent Ba, Sr and Ca ions substitution on the structural, vibrational, optical and magnetic properties of BiFeO_3 nanoparticles was carried out. The distorted rhombohedral structure was confirmed from both X-ray diffraction and Raman spectroscopy techniques in pure BiFeO_3 and Bi_0_._8_5A_0_._1_5FeO_3 (A= Ba, Sr and Ca) samples. UV-Visible spectroscopy results show that the band-gap of BiFeO_3 nanoparticles can be tuned by heterovalent ions substitution from 2.12 eV for BiFeO_3 to 2.10, 2.06 and 2.03 eV for Ca, Sr and Ba substituted BiFeO_3 nanoparticles respectively. The magnetic measurements indicate enhancement in magnetization for heterovalent A"2"+ substituted BiFeO_3 samples and the magnetization increases with increase of ionic radius of the substituted ions.

  17. Preparation of Carbon-Encapsulated ZnO Tetrahedron as an Anode Material for Ultralong Cycle Life Performance Lithium-ion Batteries

    International Nuclear Information System (INIS)

    Ren, Zhimin; Wang, Zhiyu; Chen, Chao; Wang, Jia; Fu, Xinxin; Fan, Chenyao; Qian, Guodong

    2014-01-01

    Highlights: • A novel architecture of 3D carbon framework to encapsulate ZnO nanocrystals was prepared. • The ZnO@C exhibits ultralong cycle life and high specific capacity when was used as anode. • The in situ carbonization leads to a strong connection between the carbon and ZnO. - ABSTRACT: In this paper we report a novel architecture of three-dimension (3D) carbon framework to encapsulate tetrahedron ZnO nanocrystals that serves as an anode material for lithium-ion batteries (LIBs). The ZnO@C composites are prepared via a simple internal-reflux method combined with subsequent calcination in argon. The amorphous carbon is formed on the surface of the ZnO crystals by in situ carbonization of the surfactant, which leads to a strong connection between the carbon framework and the active materials and guarantees faster charge transfer on the electrode. The ZnO crystal calcined at 500°C (ZnO@C-5) possesses regular tetrahedron shape with a side length of 150-200 nm and all of them are uniformly anchored among the network of amorphous carbon. The developed ZnO@C structures not only improve the electronic conductivity of the electrode, but they also offer a larger volume expansion of ZnO during cycling. As a result, the ZnO@C-5 demonstrates a higher reversible capacity, ultralong cycle life and better rate capability than that of the ZnO@C-7 and pure ZnO crystals. After 300 cycles, the ZnO@C-5 demonstrates a high capacity of 518 mAhg −1 at a current density of 110.7 mAg −1 . Moreover, this simple approach prepared the 3D composites architecture could shed light on the design and synthesis of other transition metal oxides for energy storage

  18. Fine structure study on low concentration zinc substituted hydroxyapatite nanoparticles

    International Nuclear Information System (INIS)

    Hu, Wei; Ma, Jun; Wang, Jianglin; Zhang, Shengmin

    2012-01-01

    The fine structure of zinc substituted hydroxyapatite was studied using experimental analysis and first-principles calculations. The synthetic hydroxyapatite nanoparticles containing low Zn concentration show rod-like morphology. The crystallite sizes and unit-cell volumes tended to decrease with the increased Zn concentration according to X-ray diffraction patterns. The Zn K-edge X-ray absorption spectra and fitting results suggest that the hydroxyapatite doped with 0.1 mole% zinc is different in the zinc coordination environments compared with that containing more zinc. The density function theory calculations were performed on zinc substituted hydroxyapatite. Two mechanisms included replacing calcium by zinc and inserting zinc along the hydroxyl column and were investigated, and the related substitution energies were calculated separately. It is found that the substitution energies are negative and lowest for inserting zinc between the two oxygen atoms along the hydroxyl column (c-axis). Combined with the spectral analysis, it is suggested that the inserting mechanism is favored for low concentration zinc substituted hydroxyapatite. Highlights: ► We investigate the fine structure of hydroxyapatite with low content of Zn. ► XANES spectra are similar but a little different at low zinc content. ► Zinc ions influence hydroxyapatite crystal formation and lattice parameters. ► Formation energies are calculated according to plane-wave density function theory. ► Low content of zinc prefers to locate at hydroxyl column in hydroxyapatite lattice.

  19. Comparative energies of Zn(II) cation localization as a function of the distance between two forming cation position aluminium ions in high-silica zeolites

    NARCIS (Netherlands)

    Kachurovskaya, N.A.; Zhidomirov, G.M.; van Santen, R.A.

    2004-01-01

    Periodical calcns. of Zn(II) metal cation stabilization in cationic positions with distantly placed aluminum ions has been performed for high-silica ferrierite. It was found that decrease of the stabilization energy at large distances between Al ions (more than 10 .ANG.) is about of 2 eV in

  20. Zn and Ni substitutional effects on spin fluctuations in YBa sub 2 Cu sub 3 O sub 7 by sup 6 sup 3 sup , sup 6 sup 5 Cu NQR

    CERN Document Server

    Han, K S; Mean, B J; Lee, K H; Seo, S W; Lee, M H; Lee, W C

    2000-01-01

    We have prepared Zn- and Ni-substituted YBa sub 2 Cu sub 3 O sub 7 (YBa sub 2 Cu sub 3 sub - sub x M sub x O sub 7 , M=Zn or Ni, x=0.00 approx 0.09) and performed sup 6 sup 3 sup , sup 6 sup 5 Cu nuclear quadrupole resonance (NQR) measurements for the plane site at 300 and 100 K. Substitutional effects on the relaxation rates are markedly different. Both the spin-lattice and the spin-spin relaxation rates decrease for Zn-doped YBCO. However, those increase for Ni-doped YBCO. This contrast in local electronic dynamics provides clear microscopic evidence that Zn forms no local moment while Ni develops a local moment. Consequently, the antiferromagnetic spin fluctuation is suppressed by Zn doping whereas it is preserved by Ni doping. This is also confirmed by the ratio of the sup 6 sup 3 sup , sup 6 sup 5 Cu spin-lattice relaxation rates for the plane coppers.

  1. The effect of FR enhancement in reactive ion beam sputtered Bi, Gd, Al-substituted iron- garnets: Bi2O3 nanocomposite films

    OpenAIRE

    Berzhansky, V.; Shaposhnikov, A.; Karavainikov, A.; Prokopov, A.; Mikhailova, T.; Lukienko, I.; Kharchenko, Yu.; Miloslavskaya, O.; Kharchenko, N.

    2012-01-01

    The effect of considerable Faraday rotation (FR) and figure of merit (Q) enhancement in Bi, Gd, Al-substituted iron garnets: Bi2O3 nano-composite films produced by separate reactive ion beam sputtered Bi:YIG and Bi2O3 films was found. It reached threefold enhancement of the FR and twofold of the Q one on GGG substrates.

  2. Hydrothermal synthesis and magnetic properties of Mn doped ZnS nanoparticles

    Science.gov (United States)

    Rashad, M. M.; Rayan, D. A.; El-Barawy, K.

    2010-01-01

    Nanocrystallite Mn doped Zn1-XS (X = 0 to 0.4) powders have been synthesized through a hydrothermal route. The effect of the hydrothermal temperature and Mn2+ ions substitution on the crystal structure, crystallite size, microstructure and magnetic properties were investigated using (XRD), (SEM) and (VSM). The results revealed that wurtzite zinc sulfide phase was formed using thiourea as a sulfur source at temperature 150- 200oC for 24 h. The crystallite size was (7.9-15.1 nm) was obtained at the same conditions. The doping of Mn2+ ions decreased the crystallite size of the formed ZnS wurtzite phase was in the range between 7.9 and 3.8 nm. SEM micrographs showed that the produced ZnS and Mn doped ZnS particles were appeared as spherical shape. The magnetic properties were improved by substitution of Mn2+ ions up to 0.2.

  3. Hydrothermal synthesis and magnetic properties of Mn doped ZnS nanoparticles

    International Nuclear Information System (INIS)

    Rashad, M M; Rayan, D A; El-Barawy, K

    2010-01-01

    Nanocrystallite Mn doped Zn 1-X S (X = 0 to 0.4) powders have been synthesized through a hydrothermal route. The effect of the hydrothermal temperature and Mn 2+ ions substitution on the crystal structure, crystallite size, microstructure and magnetic properties were investigated using (XRD), (SEM) and (VSM). The results revealed that wurtzite zinc sulfide phase was formed using thiourea as a sulfur source at temperature 150- 200 o C for 24 h. The crystallite size was (7.9-15.1 nm) was obtained at the same conditions. The doping of Mn 2+ ions decreased the crystallite size of the formed ZnS wurtzite phase was in the range between 7.9 and 3.8 nm. SEM micrographs showed that the produced ZnS and Mn doped ZnS particles were appeared as spherical shape. The magnetic properties were improved by substitution of Mn 2+ ions up to 0.2.

  4. Photo catalytic degradation of nitrobenzene using nanocrystalline TiO{sub 2} photo catalyst doped with Zn ions

    Energy Technology Data Exchange (ETDEWEB)

    Reynoso S, E. A.; Perez S, S.; Reyes C, A. P.; Castro R, C. L.; Felix N, R. M.; Lin H, S. W. [Instituto Tecnologico de Tijuana, Centro de Graduados e Investigacion, Apdo. Postal 1166, 22000 Tijuana, Baja California (Mexico); Paraguay D, F. [Centro de Investigacion en Materiales Avanzados, Apdo. Postal 311109, Chihuahua (Mexico); Alonso N, G. [UNAM, Centro de Nanociencias y Nanotecnologia, Carretera Tijuana-Ensenada Km 107, Apdo. Postal 356, 22800 Ensenada, Baja California (Mexico)

    2013-07-01

    Photo catalysis is a method widely used in the degradation of organic pollutants of the environment. The development of new materials is very important to improve the photo catalytic properties and to find new applications for TiO{sub 2} as a photo catalyst. In this article we reported the synthesis of a photo catalyst based on TiO{sub 2} doped with Zn{sup 2+} ions highly efficient in the degradation of nitrobenzene. The results of photo catalytic activity experiments showed that the Zn{sup 2+} doped TiO{sub 2} is more active that un-doped TiO{sub 2} catalyst with an efficiency of 99% for the nitrobenzene degradation at 120 min with an apparent rate constant of 35 x 10{sup -3} min{sup -1}. For the characterization of photo catalyst X-ray diffraction, transmission electron microscopy and Raman spectroscopy were used. (Author)

  5. Photo catalytic degradation of nitrobenzene using nanocrystalline TiO2 photo catalyst doped with Zn ions

    International Nuclear Information System (INIS)

    Reynoso S, E. A.; Perez S, S.; Reyes C, A. P.; Castro R, C. L.; Felix N, R. M.; Lin H, S. W.; Paraguay D, F.; Alonso N, G.

    2013-01-01

    Photo catalysis is a method widely used in the degradation of organic pollutants of the environment. The development of new materials is very important to improve the photo catalytic properties and to find new applications for TiO 2 as a photo catalyst. In this article we reported the synthesis of a photo catalyst based on TiO 2 doped with Zn 2+ ions highly efficient in the degradation of nitrobenzene. The results of photo catalytic activity experiments showed that the Zn 2+ doped TiO 2 is more active that un-doped TiO 2 catalyst with an efficiency of 99% for the nitrobenzene degradation at 120 min with an apparent rate constant of 35 x 10 -3 min -1 . For the characterization of photo catalyst X-ray diffraction, transmission electron microscopy and Raman spectroscopy were used. (Author)

  6. Effect of Dy3+ substitution on structural and magnetic properties of nanocrystalline Ni-Cu-Zn ferrites

    Science.gov (United States)

    Kabbur, S. M.; Ghodake, U. R.; Nadargi, D. Y.; Kambale, Rahul C.; Suryavanshi, S. S.

    2018-04-01

    Nanocrystalline Ni0.25Cu0.30Zn0.45DyxFe2-xO4 (x = 0.0, 0.025, 0.05, 0.075, 0.1 and 0.125 mol.) ferrimagnetic oxides have been synthesized by sol-gel autocombustion route. X-ray diffraction study reveals the formation of spinel cubic structure with an expansion of the unit cell by Dy addition. Bertaut method was employed to propose the site occupancy i.e. cation distribution for elements at A-tetrahedral and B-octahedral sites of spinel lattice. The intrinsic vibrational absorption bands i.e. υ1 (712-719 cm-1) and υ2 (496-506 cm-1) are observed for tetrahedral and octahedral sites respectively. The microstructural aspect confirms the formation of an average grain size (∼7-99 nm) with presence of expected elements. Magnetization studies reveal that the magnetic moments are no longer linear but exhibit canting effect due to spin frustration. The frequency dispersion spectrum of initial permeability has been explained based on grain size, saturation magnetization and anisotropy constant. Thermal hysteresis curve (initial permeability versus temperature) indicates magnetic disordering to paramagnetic state at Néel temperature (TN). High values of TN show that the present ferrite samples are cation-ordered with d-electrons contributing towards the magnetic interaction at the sublattice.

  7. The role of praseodymium substituted ions on electrical and magnetic properties of Mg spinel ferrites

    Energy Technology Data Exchange (ETDEWEB)

    Farid, Muhammad Tahir, E-mail: tahirfaridbzu@gmail.com; Ahmad, Ishtiaq; Kanwal, Muddassara; Murtaza, Ghulam; Ali, Irshad; Khan, Sajjad Ahmad

    2017-04-15

    Spinel ferrites with composition MgPr{sub y}Fe{sub 2−y}O{sub 4} (y=0.0, 0.025, 0.05, 0.075, 0.10) were successfully synthesized using sol-gel auto-combustion technique. The structural prisoperties of a prepared sintered powder were characterized with the help of X-ray Diffraction (XRD) and then also by using Scanning electron microscopy (SEM). Electrical measurements demonstrate that resistivity and activation energy increases with the Praseodymium substitution while dc resistivity decreases with the rise of temperature showing the semiconductor nature of the synthesized ferrites. Remanence and the saturation magnetization (M{sub s}) decrease while coercivity (H{sub c}) also increases with the increase in praseodymium contents. Anisotropic constant is observed to exhibit similar behavior as H{sub C}. The above mentioned parameters suggest that the synthesized samples are favorable for microwave absorbing purposes. - Highlights: • Magnesium based spinel ferrites were successfully synthesized by sol-gel method. • The spinel phase has been observed in all samples. • The dc resistivity are found to increase with increasing Pr content • The samples with high resistivity have high values of activation energy. • The Ms Decreases with increasing Pr contents while Hc increases.

  8. Absence of intrinsic ferromagnetism in Zn{sub 1-x}Mn{sub x}O alloys

    Energy Technology Data Exchange (ETDEWEB)

    Zhang Huawei [Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050 (China); Shi Erwei [Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050 (China); Chen Zhizhan [Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050 (China); Liu Xuechao [Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050 (China); Xiao Bing [Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050 (China)

    2006-10-04

    Zn{sub 1-x}Mn{sub x}O alloys, with different Mn concentrations, were prepared by the hydrothermal method. X-ray diffraction and electron paramagnetic resonance spectra demonstrate that Zn{sup 2+} ions are homogeneously substituted by Mn{sup 2+} ions without changing the ZnO wurtzite structure. The x = 0.02 and 0.04 samples are paramagnetic. When the Mn concentrations are increased to x = 0.08 and 0.10, the samples exhibit some ferromagnetism due to a secondary phase (Zn,Mn)Mn{sub 2}O{sub 4}. (letter to the editor)

  9. SnO2/ZnO composite structure for the lithium-ion battery electrode

    International Nuclear Information System (INIS)

    Ahmad, Mashkoor; Yingying, Shi; Sun, Hongyu; Shen, Wanci; Zhu, Jing

    2012-01-01

    In this article, SnO 2 /ZnO composite structures have been synthesized by two steps hydrothermal method and investigated their lithium storage capacity as compared with pure ZnO. It has been found that these composite structures combining the large specific surface area, stability and catalytic activity of SnO 2 micro-crystals, demonstrate the higher initial discharge capacity of 1540 mA h g −1 with a Coulombic efficiency of 68% at a rate of 120 mA h g −1 between 0.02 and 2 V and found much better than that of any previously reported ZnO based composite anodes. In addition, a significantly enhanced cycling performance, i.e., a reversible capacity of 497 mA h g −1 is retained after 40 cycles. The improved lithium storage capacity and cycle life is attributed to the addition of SnO 2 structure, which act as good electronic conductors and better accommodation of the large volume change during lithiation/delithiation process. - Graphical abstract: SnO 2 /ZnO composite structures demonstrate the improved lithium storage capacity and cycle life as compared with pure ZnO nanostructure. Highlights: ► Synthesis of SnO 2 /ZnO composite structures by two steps hydrothermal approach. ► Investigation of lithium storage capacity. ► Excellent lithium storage capacity and cycle life of SnO 2 /ZnO composite structures.

  10. Water soluble and efficient amino acid Schiff base receptor for reversible fluorescence turn-on detection of Zn2+ ions: Quantum chemical calculations and detection of bacteria

    Science.gov (United States)

    Subha, L.; Balakrishnan, C.; Natarajan, Satheesh; Theetharappan, M.; Subramanian, Balanehru; Neelakantan, M. A.

    2016-01-01

    An amino acid Schiff base (R) capable of recognizing Zn2+ ions selectively and sensitively in an aqueous medium was prepared and characterized. Upon addition of Zn2+ ions, the receptor exhibits fluorescence intensity enhancements ( 40 fold) at 460 nm (quantum yield, Φ = 0.05 for R and Φ = 0.18 for R-Zn2+) and can be detected by naked eye under UV light. The receptor can recognize the Zn2+ (1.04 × 10- 8 M) selectively for other metal ions in the pH range of 7.5-11. The Zn2+ chelation with R decreases the loss of energy through non-radiative transition and leads to fluorescence enhancement. The binding mode of the receptor with Zn2+ was investigated by 1H NMR titration and further validated by ESI-MS. The elemental color mapping and SEM/EDS analysis were also used to study the binding of R with Zn2+. Density functional theory calculations were carried out to understand the binding mechanism. The receptor was applied as a microbial sensor for Escherichia coli and Staphylococcus aureus.

  11. pH-dependence of the specific binding of Cu(II) and Zn(II) ions to the amyloid-β peptide

    International Nuclear Information System (INIS)

    Ghalebani, Leila; Wahlström, Anna; Danielsson, Jens; Wärmländer, Sebastian K.T.S.; Gräslund, Astrid

    2012-01-01

    Highlights: ► Cu(II) and Zn(II) display pH-dependent binding to the Aβ(1–40) peptide. ► At pH 7.4 both metal ions display residue-specific binding to the Aβ peptide. ► At pH 5.5 the binding specificity is lost for Zn(II). ► Differential Cu(II) and Zn(II) binding may help explain metal-induced AD toxicity. -- Abstract: Metal ions like Cu(II) and Zn(II) are accumulated in Alzheimer’s disease amyloid plaques. The amyloid-β (Aβ) peptide involved in the disease interacts with these metal ions at neutral pH via ligands provided by the N-terminal histidines and the N-terminus. The present study uses high-resolution NMR spectroscopy to monitor the residue-specific interactions of Cu(II) and Zn(II) with 15 N- and 13 C, 15 N-labeled Aβ(1–40) peptides at varying pH levels. At pH 7.4 both ions bind to the specific ligands, competing with one another. At pH 5.5 Cu(II) retains its specific histidine ligands, while Zn(II) seems to lack residue-specific interactions. The low pH mimics acidosis which is linked to inflammatory processes in vivo. The results suggest that the cell toxic effects of redox active Cu(II) binding to Aβ may be reversed by the protective activity of non-redox active Zn(II) binding to the same major binding site under non-acidic conditions. Under acidic conditions, the protective effect of Zn(II) may be decreased or changed, since Zn(II) is less able to compete with Cu(II) for the specific binding site on the Aβ peptide under these conditions.

  12. Carbon-coated ZnO mat passivation by atomic-layer-deposited HfO2 as an anode material for lithium-ion batteries.

    Science.gov (United States)

    Jung, Mi-Hee

    2017-11-01

    ZnO has had little consideration as an anode material in lithium-ion batteries compared with other transition-metal oxides due to its inherent poor electrical conductivity and large volume expansion upon cycling and pulverization of ZnO-based electrodes. A logical design and facile synthesis of ZnO with well-controlled particle sizes and a specific morphology is essential to improving the performance of ZnO in lithium-ion batteries. In this paper, a simple approach is reported that uses a cation surfactant and a chelating agent to synthesize three-dimensional hierarchical nanostructured carbon-coated ZnO mats, in which the ZnO mats are composed of stacked individual ZnO nanowires and form well-defined nanoporous structures with high surface areas. In order to improve the performance of lithium-ion batteries, HfO 2 is deposited on the carbon-coated ZnO mat electrode via atomic layer deposition. Lithium-ion battery devices based on the carbon-coated ZnO mat passivation by atomic layer deposited HfO 2 exhibit an excellent initial discharge and charge capacities of 2684.01 and 963.21mAhg -1 , respectively, at a current density of 100mAg -1 in the voltage range of 0.01-3V. They also exhibit cycle stability after 125 cycles with a capacity of 740mAhg -1 and a remarkable rate capability. Copyright © 2017 Elsevier Inc. All rights reserved.

  13. N{sup +} ion-implantation-induced defects in ZnO studied with a slow positron beam

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Z Q [Japan Atomic Energy Research Institute, 1233 Watanuki, Takasaki, Gunma 370-1292, Japan (Japan); Sekiguchi, T [Nanomaterials Laboratory, National Institute for Materials Science, 1-2-1 Sengen, Tsukuba, Ibaraki 305-0047 (Japan); Yuan, X L [Nanomaterials Laboratory, National Institute for Materials Science, 1-2-1 Sengen, Tsukuba, Ibaraki 305-0047 (Japan); Maekawa, M [Japan Atomic Energy Research Institute, 1233 Watanuki, Takasaki, Gunma 370-1292, Japan (Japan); Kawasuso, A [Japan Atomic Energy Research Institute, 1233 Watanuki, Takasaki, Gunma 370-1292, Japan (Japan)

    2004-01-21

    Undoped ZnO single crystals were implanted with multiple-energy N{sup +} ions ranging from 50 to 380 keV with doses from 10{sup 12} to 10{sup 14} cm{sup -2}. Positron annihilation measurements show that vacancy defects are introduced in the implanted layers. The concentration of the vacancy defects increases with increasing ion dose. The annealing behaviour of the defects can be divided into four stages, which correspond to the formation and recovery of large vacancy clusters and the formation and disappearance of vacancy-impurity complexes, respectively. All the implantation-induced defects are removed by annealing at 1200 deg. C. Cathodoluminescence measurements show that the ion-implantation-induced defects act as nonradiative recombination centres to suppress the ultraviolet (UV) emission. After annealing, these defects disappear gradually and the UV emission reappears, which coincides with positron annihilation measurements. Hall measurements reveal that after N{sup +} implantation, the ZnO layer still shows n-type conductivity.

  14. Zinc-sensitive MRI contrast agent detects differential release of Zn(II) ions from the healthy vs. malignant mouse prostate.

    Science.gov (United States)

    Clavijo Jordan, M Veronica; Lo, Su-Tang; Chen, Shiuhwei; Preihs, Christian; Chirayil, Sara; Zhang, Shanrong; Kapur, Payal; Li, Wen-Hong; De Leon-Rodriguez, Luis M; Lubag, Angelo J M; Rofsky, Neil M; Sherry, A Dean

    2016-09-13

    Many secretory tissues release Zn(II) ions along with other molecules in response to external stimuli. Here we demonstrate that secretion of Zn(II) ions from normal, healthy prostate tissue is stimulated by glucose in fasted mice and that release of Zn(II) can be monitored by MRI. An ∼50% increase in water proton signal enhancement is observed in T1-weighted images of the healthy mouse prostate after infusion of a Gd-based Zn(II) sensor and an i.p. bolus of glucose. Release of Zn(II) from intracellular stores was validated in human epithelial prostate cells in vitro and in surgically exposed prostate tissue in vivo using a Zn(II)-sensitive fluorescent probe known to bind to the extracellular surface of cells. Given the known differences in intracellular Zn(II) stores in healthy versus malignant prostate tissues, the Zn(II) sensor was then evaluated in a transgenic adenocarcinoma of the mouse prostate (TRAMP) model in vivo. The agent proved successful in detecting small malignant lesions as early as 11 wk of age, making this noninvasive MR imaging method potentially useful for identifying prostate cancer in situations where it may be difficult to detect using current multiparametric MRI protocols.

  15. Quantum Chemical Benchmarking, Validation, and Prediction of Acidity Constants for Substituted Pyridinium Ions and Pyridinyl Radicals.

    Science.gov (United States)

    Keith, John A; Carter, Emily A

    2012-09-11

    Sensibly modeling (photo)electrocatalytic reactions involving proton and electron transfer with computational quantum chemistry requires accurate descriptions of protonated, deprotonated, and radical species in solution. Procedures to do this are generally nontrivial, especially in cases that involve radical anions that are unstable in the gas phase. Recently, pyridinium and the corresponding reduced neutral radical have been postulated as key catalysts in the reduction of CO2 to methanol. To assess practical methodologies to describe the acid/base chemistry of these species, we employed density functional theory (DFT) in tandem with implicit solvation models to calculate acidity constants for 22 substituted pyridinium cations and their corresponding pyridinyl radicals in water solvent. We first benchmarked our calculations against experimental pyridinium deprotonation energies in both gas and aqueous phases. DFT with hybrid exchange-correlation functionals provide chemical accuracy for gas-phase data and allow absolute prediction of experimental pKas with unsigned errors under 1 pKa unit. The accuracy of this economical pKa calculation approach was further verified by benchmarking against highly accurate (but very expensive) CCSD(T)-F12 calculations. We compare the relative importance and sensitivity of these energies to selection of solvation model, solvation energy definitions, implicit solvation cavity definition, basis sets, electron densities, model geometries, and mixed implicit/explicit models. After determining the most accurate model to reproduce experimentally-known pKas from first principles, we apply the same approach to predict pKas for radical pyridinyl species that have been proposed relevant under electrochemical conditions. This work provides considerable insight into the pitfalls using continuum solvation models, particularly when used for radical species.

  16. APLIKASI PENGOLAHAN POLUTAN ANION KHROM(VI DENGAN MENGGUNAKAN AGEN PENUKAR ION HYDROTALCIT ZN-AI-SO4 (Synthesis of and its Application to Treat Chrom(VI Pollutant Using Hydrotalcite Zn-Al_SO4 as Anion Exchanger

    Directory of Open Access Journals (Sweden)

    Roto Roto

    2009-03-01

    Full Text Available ABSTRAK Keberadaan logam khrom di dalam sistem perairan bersifat polutan yang harus ditangani dengan baik, dan untuk khrom (Vl yang sering dijumpai dalam bentuk anion dapat diolah dengan menggunakan mekanisme pertukaran ion. Suatu agen penukar anion telah dibuat berupa senyawa hidrotalsit Zn-Al-SOa melalui proses sintesis, karakterisasi serta dilakukan pula pengujian aplikasinya untuk pengurangan polutant anion khrom (VI dalam bentuk ion dikromat. Sintesis hidrotalsit Zn-Al-SOa dilakukan dengan metode stoikiometri pada pH 8 dan perlakuan hidrotermal. Aplikasi pertukaran dikromat dengan anion sulfat dalam antar lapis hidrotalsit serta uji regenerasi bahan diamati dengan bantuan analisis struktur dan analisis kinetika reaksi pertukaran. Produk pertukaran ion dikarakterisasi dengan XRD, spektrofotometri IR dan spektrometri serapan atom. Rumus kimia hidrotalsit produk diketahui adalah Zn0,74Al0,26(OH1,74(SO40,13.0,52H2O. Anion dikromat dapat menukar sulfat dalam antarlapis hidrotalsit yang ditunjukkan dalam spektra IR dan pola XRD. Kapasitas pertukaran anion untuk dikromat diketahui 216,84 mek/100 g, sedangkan kinetika reaksi pertukaran ion mengikuti orde dua dengan k = 3 x 10-8 ppm-1.detik-1. Hasil menunjukkan Zn-Al-Cr2O7 dapat mudah diregenerasi.    ABSTRACT  Chrom as pollutant in aquatics system usually establishes as crom (VI and should be worked with special treatment and as an example is ion exchanger. Material Zn-Al-SO4 hydrotalcite product have been synthesized and its application as anion exchanger for dichromate have been studied. Synthesis of Zn-Al-SO4 hydrotalcite was carried out by stoichiometric method at pH 8 and hydrothermal treatment. Sulphate in hydrotalcite interlayer was exchanged by dichromate. Kinetics of ion exchange was also investigated. The product of ion exchange was characterized by XRD, IR spectrophotometry and atomic adsorption  spectrometry. The chemical formula of the  hydrotalcite is Zn0.74Al0.26(OH1.74(SO4 0

  17. Structural, photoluminescence and XPS properties of Tm3þ ions in ZnO nanostructures

    CSIR Research Space (South Africa)

    Kabongo, GL

    2017-07-01

    Full Text Available of photoluminescence (PL) spectroscopy. Finally, Tm 4d core level was detected in ZnO: 0.5 mol% Tm(sup3+) sample from high resolution X-Ray Photoelectron Spectroscopy (XPS) scan....

  18. Enhancing the effective energy barrier of a Dy(III) SMM using a bridged diamagnetic Zn(II) ion.

    Science.gov (United States)

    Upadhyay, Apoorva; Singh, Saurabh Kumar; Das, Chinmoy; Mondol, Ranajit; Langley, Stuart K; Murray, Keith S; Rajaraman, Gopalan; Shanmugam, Maheswaran

    2014-08-18

    Field induced single-molecule-magnet behaviour is observed for both a heterodinuclear [ZnDy(L(-))2](3+) complex (1) and a mononuclear [Dy(HL)2](3+) complex (2), with effective energy barriers of 83 cm(-1) and 16 cm(-1), respectively. Insights into the relaxation mechanism(s) and barrier heights are provided via ab initio and DFT calculations. Our findings reveal an interesting observation that the U(eff) of SMMs can be enhanced by incorporating diamagnetic metal ions.

  19. Measurements of Si, Ti, V, Cu, Zn, Zr and Pd stopping power using 14N and 16O ions

    International Nuclear Information System (INIS)

    Vilela, M.M.

    1986-01-01

    The energy losses of 14 N and 16 O ions in solids (Si, Ti, V, Cu, Zn, Zr and Pd) at energy range from 1 MeV/amu to 4 MeV/amu were measured. The technique consists in the energy measurement of scattered projectiles at 25 0 by a thin target of Au, before and after to across the foil of breaker element. The experimental results are compared with semi empirical calculations of Northcliffe and Schilling (N and S), Ziegler and a new version of N and S done by Hubert et all, observing a reasonable agreement between the measured values and semi empirical curves. (M.C.K.) [pt

  20. Defects in N{sup +} ion-implanted ZnO single crystals studied by positron annihilation and Hall effect

    Energy Technology Data Exchange (ETDEWEB)

    Brauer, G.; Anwand, W.; Skorupa, W. [Institut fuer Ionenstrahlphysik und Materialforschung, Forschungszentrum Rossendorf, Dresden (Germany); Kuriplach, J.; Melikhova, O.; Cizek, J.; Prochazka, I. [Department of Low Temperature Physics, Faculty of Mathematics and Physics, Charles Univ., Prague (Czech Republic); Wenckstern, H. von; Brandt, M.; Lorenz, M.; Grundmann, M. [Institut fuer Experimentelle Physik II, Universitaet Leipzig (Germany)

    2007-07-01

    High quality ZnO single crystals of dimensions 10 x 10 x 0.5 mm{sup 3}, grown by a hydrothermal approach, have been implanted by 40 keV N{sup +} ions to a fluence of 1 x 10{sup 15} cm{sup -2} at room temperature. Their properties revealed by positron annihilation and Hall effect measurements are given in the as-grown and as-irradiated states, and after post-implantation annealing in an oxygen ambient at 200 C and 500 C. (copyright 2007 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  1. Irradiation route to aqueous synthesis of highly luminescent ZnSe quantum dots and its function as a copper ion fluorescence sensor

    Energy Technology Data Exchange (ETDEWEB)

    Rao, Yeluri Narayana; Datta, Aparna [UGC-DAE Consortium for Scientific Research, Kolkata Centre, III/LB-8 Bidhannagar, Kolkata 700 098 (India); Das, Satyendra K. [Radiochemistry Division, Variable Energy Cyclotron Centre, 1/AF Bidhannagar, Kolkata 700 064 (India); Saha, Abhijit, E-mail: abhijit@alpha.iuc.res.in [UGC-DAE Consortium for Scientific Research, Kolkata Centre, III/LB-8 Bidhannagar, Kolkata 700 098 (India)

    2016-08-15

    Highlights: • Radiation chemical technique can provide a useful route for synthesis of ZnSe QDs. • Chelating nature of ethylene diamine is exploited for capping nanoparticles. • ZnSe QDs can be a suitable sensitive alternative to toxic cadmium-based system. • Cu(II) ion is probed by QDs in the presence of other physiologically relevant ions. - Abstract: Size-controlled synthesis of stable ZnSe QDs with narrow distribution in aqueous environment through conventional soft chemical method still poses a challenge. The proposed radiation assisted strategy demonstrates aqueous synthesis of stable, monodisperse and luminescent ZnSe QDs capped with chelating ethylene diamine under ambient conditions and at room temperature. Radiation chemical method facilitates in slow and in-situ release of selenium ion from sodium selenosulfate. The concentrations of precursors, such as zinc salt, selenium source, ethylene diamine and absorbed radiation (7–90 kGy) dose were optimized for obtaining good quality particles. Selective quenching of luminescence of as-synthesized quantum dots (QDs) by Cu{sup 2+} ions vis-à-vis other physiologically important cations provide evidence for use of ZnSe quantum dots as alternative to toxic Cd-based quantum dots to probe Cu{sup 2+} ions. The linear relation of ratio of loss in emission intensity as a function of concentration of Cu(II) indicates detection limit in nano-molar range.

  2. Adsorbents/ion exchangers-PVA blend membranes: Preparation, characterization and performance for the removal of Zn2+ by electrodialysis

    Science.gov (United States)

    Caprarescu, Simona; Radu, Anita-Laura; Purcar, Violeta; Ianchis, Raluca; Sarbu, Andrei; Ghiurea, Marius; Nicolae, Cristian; Modrogan, Cristina; Vaireanu, Danut-Ionel; Périchaud, Alain; Ebrasu, Daniela-Ion

    2015-02-01

    The present paper was aimed at studying the possibility of zinc (Zn) removal from the wastewater discharged from zinc electroplating processes. In order to save industrial and environmental resources, the concentrated solution could be reused after electrodialysis process. A mini-electrodialysis system with three cylindrical compartments and different membranes containing various resins (Purolite A500 and Hypersol-Macronet MN500) was employed, which can be further applied for the treatment of synthetic effluent which contained zinc ions. The electrodialysis system was operated at constant voltage using different concentrations of synthetic solutions of zinc ions, without and with electrolyte recirculation for 1.5 h. The pH and conductivity of solutions were measured before and after the electrodialysis process occurs. Also the removal ratio (Rr) and mass flow (J) of zinc ions, energy consumption (EC) and current efficiency (CE) were determined. It was found that electrodialysis treatment generated a very low conductivity solution, enabling its reuse as rinse water. According to the obtained results when using a membrane pair with higher ion exchange capacity (IEC) the removal ratio is improved (over 80%). The physico-chemical, structural and mechanical properties of prepared membranes were registered, before and after electrodialysis process takes place, by means of complementary analytical techniques, namely, ion-exchange capacity, water content and thickness measurements. Furthermore analysis were also carried out by Fourier transform infrared spectroscopy (FT-IR), environmental scanning electron microscopy (ESEM), thermal gravimetric analysis (TGA) and electrochemical impedance spectroscopy (EIS).

  3. Anchoring ZnO Nanoparticles in Nitrogen-Doped Graphene Sheets as a High-Performance Anode Material for Lithium-Ion Batteries

    Directory of Open Access Journals (Sweden)

    Guanghui Yuan

    2018-01-01

    Full Text Available A novel binary nanocomposite, ZnO/nitrogen-doped graphene (ZnO/NG, is synthesized via a facile solution method. In this prepared ZnO/NG composite, highly-crystalline ZnO nanoparticles with a size of about 10 nm are anchored uniformly on the N-doped graphene nanosheets. Electrochemical properties of the ZnO/NG composite as anode materials are systematically investigated in lithium-ion batteries. Specifically, the ZnO/NG composite can maintain the reversible specific discharge capacity at 870 mAh g−1 after 200 cycles at 100 mA g−1. Besides the enhanced electronic conductivity provided by interlaced N-doped graphene nanosheets, the excellent lithium storage properties of the ZnO/NG composite can be due to nanosized structure of ZnO particles, shortening the Li+ diffusion distance, increasing reaction sites, and buffering the ZnO volume change during the charge/discharge process.

  4. Magnetic properties of Sn-substituted Ni-Zn ferrites synthesized from nano-sized powders of NiO, ZnO, Fe2O3, and SnO2

    Science.gov (United States)

    Ali, MA; Uddin, MM; Khan, MNI; Chowdhury, FUZ; Hoque, SM; Liba, SI

    2017-06-01

    A series of Ni0.6-x/2Zn0.4-x/2Sn x Fe2O4 (x = 0.0, 0.05, 0.1, 0.15, 0.2, and 0.3) (NZSFO) ferrite composities have been synthesized from nano powders using a standard solid state reaction technique. The spinel cubic structure of the investigated samples has been confirmed by x-ray diffraction (XRD). The magnetic properties such as saturation magnetization ({M}{{s}}), remanent magnetization ({M}{{r}}), coercive field ({H}{{c}}), and Bohr magneton (μ) are calculated from the hysteresis loops. The value of {M}{{s}} is found to decrease with increasing Sn content in the samples. This change is successfully explained by the variation of A-B interaction strength due to Sn substitution in different sites. The compositional stability and quality of the prepared ferrite composites have also been endorsed by the fairly constant initial permeability ({μ }^{\\prime }) over a wide range of frequency. The decreasing trend of {μ }^{\\prime } with increasing Sn content has been observed. Curie temperature {T}{{C}} has been found to increase with the increase in Sn content. A wide spread frequency utility zone indicates that the NZSFO can be considered as a good candidate for use in broadband pulse transformers and wide band read-write heads for video recording. The composition of x = 0.05 shows unusual results and the possible reason is also mentioned with the established formalism.

  5. Characteristics of ZnO Wafers Implanted with 60 keV Sn+ Ions at Room Temperature and at 110 K

    International Nuclear Information System (INIS)

    Dang, Giang T.; Taniwaki, Masafumi; Kawaharamura, Toshiyuki; Hirao, Takashi; Nitta, Noriko

    2011-01-01

    ZnO wafers implanted with 60 keV Sn + ions at room temperature (RT) and at 110 K are investigated by means of X-ray diffraction (XRD) and photoluminescence (PL) techniques. The effect of implantation temperature is evident in the XRD and PL data. A yellow-orange (YO) band near 600 nm appears in the PL spectra of the ZnO wafers implanted to the doses of 4x10 14 and 8x10 14 ions/cm 2 at RT. The intensity of this band increases and the peak position blue-shifts after illumination of the samples with the 325 nm line of a He-Cd laser. The PL data suggests that the CB (conduction band)→V O + and Zn i + →V Zn - transitions contribute to the photoemission of the YO band.

  6. Formation mechanism and yield of molecules ejected from ZnS, CdS, and FeS2 during ion bombardment

    International Nuclear Information System (INIS)

    Nikzad, S.; Calaway, W.F.; Pellin, M.J.; Young, C.E.; Gruen, D.M.; Tombrello, T.A.

    1994-01-01

    Neutral species ejected from single crystals of ZnS, CdS, and FeS 2 during ion bombardment by 3 keV Ar + were detected by laser post-ionization followed by time-of-flight mass spectrometry. While metal atoms (Fe, Zn, Cd) and S 2 were the dominant species observed, substantial amounts of S, FeS, Zn 2 , ZnS, Cd 2 , and CdS were also detected. The experimental results demonstrate that molecules represent a larger fraction of the sputtered yield than was previously believed from secondary ion mass spectrometry experiments. In addition, the data suggest that the molecules are not necessarily formed from adjacent atoms in the solid and that a modified form of the recombination model could provide a mechanism for their formation

  7. Vibrational frequencies and structural investigation of (M(CN)4)2- (M Cd, Hg and Zn) ions

    International Nuclear Information System (INIS)

    Gurkan, Keshan; Tomas, Polivka; Cemal, Parlak; Mustafa, Shenyel

    2011-01-01

    The normal mode frequencies and corresponding vibrational assignments of tetracyanometallate (II) ions ([M(CN) 4 ] 2 -, M = Cd, Hg and Zn) have been theoretically examined by means of standard quantum chemical techniques. All normalmodes have been successfully assigned to one of six types of motion utilizing the T d symmetry of M(CN) 4 2 -. Calculations have been performed at the Becke-3-Lee-Yang-Parr (B3LYP) density functional method using the Lanl2dz effective core basis set. Furthermore, reliable vibrational assignments have been made on the basis of potential energy distribution (PED) calculated and the thermodynamics functions, highest occupied and lowest unoccupied molecular orbitals (HOMO and LUMO) of the title ions have been predicted together with their infrared intensities and Raman activities. Theoretical results have been successfully compared against available experimental data

  8. Low-temperature growth of (2 1-bar 1-bar 0) ZnO nanofilm on NaCl (0 0 1) surface by ion beam sputtering

    International Nuclear Information System (INIS)

    Shen, Jung-Hsiung; Yeh, Sung-Wei; Huang, Hsing-Lu; Gan, Dershin

    2009-01-01

    ZnO nanofilm of the (2 1 -bar 1 -bar 0) surface was prepared by ion beam sputtering deposition. The nanofilm was prepared on NaCl (0 0 1) surface at 200 o C to produce nearly pure (2 1 -bar 1 -bar 0) ZnO texture and the orientation relationship was determined and the interface discussed. Transmission electron microscopy lattice images were used to find the interface formed between ZnO nanocrystals. The ZnO nanocrystals coalesced to form a straight (0 1 -bar 1 -bar 2) interface. The photoluminescence spectrum from the (2 1 -bar 1 -bar 0) ZnO surface showed only a near-band-edge UV emission peak.

  9. Embedding ultrafine ZnSnO3 nanoparticles into reduced graphene oxide composites as high-performance electrodes for lithium ion batteries

    Science.gov (United States)

    Ma, Yuhang; Jiang, Ranran; Li, Dan; Dong, Yutao; Liu, Yushan; Zhang, Jianmin

    2018-05-01

    Ultrafine ZnSnO3 nanoparticles, with an average diameter of 45 nm, homogeneously grown on reduced graphene oxide (rGO) have been successfully fabricated via methods of low temperature coprecipitation, colloid electrostatic self-assembly, and hydrothermal treatment. The uniformly distributed ZnSnO3 nanocrystals could inhibit the restacking of rGO sheets. In turn, the existence of rGO could hinder the growth and aggregation of ZnSnO3 nanoparticles in the synthesis process, increase the conductivity of the composite, and buffer the volume expansion of the ZnSnO3 nanocrystals upon lithium ion insertion and extraction. The obtained ZnSnO3/rGO exhibited superior cycling stability with a discharge/charge capacity of 718/696 mA h g-1 after 100 cycles at a current density of 0.1 A g-1.

  10. Calculations of kinetic isotope effects in the Hofmann eliminations of substituted (2-phenylethyl)trimethylammonium ions

    International Nuclear Information System (INIS)

    Lewis, D.E.; Sims, L.B.; Yamataka, H.; McKenna, J.

    1980-01-01

    Theoretical calculations of kinetic isotope effects (KIE) for the Hofmann elimination of the (2-phenylethyl)trimethylammonium ion (I,Z = H) have been carried out for an extensive series of transition-state models encompassing the Elcb-like region of the E2 mechanistic spectrum. The reaction coordinate employed corresponded to the irreversible fragmentation of the base-H'-C/sub β/-C/sub α/-N system, with proton transfer being the dominant contributor. Structural parameters (bond distances and angles) were related to the independent bond orders n/sub α-N/ and n/sub β-H'/ by empirical and semiempirical relationships. The most probable transition-state structure for the reaction was determined by interpolation of the experimental values for the β-D 2 and 15 N KIE into plots of the trends of the calculated KIE. The nonsolvated models obtained in this manner gave only poor agreement between calculated and experimental secondary deuterium (α-D 2 ) and leaving group deuterium [N(CD 3 )/sub x/(CH 3 )/sub 3-x/, x = 1 to 3) KIE; explicit consideration of differential solvation of the reactant and transition state afforded the most chemically reasonable resolution of these discrepancies. Using solvated models, transition-state structures were also determined for the Hofmann elimination of parasubstituted derivatives of I (Z = OCH 3 , Cl, CF 3 ). These transition states are related by a shift parallel to the central E2 diagogonal of an O'Ferrall-Jencks reaction diagram, as predicted by Thorton, indicating that, in the absence of other factors (differing solvent or base, etc.), the extent to which negative charge is accumulated at Cβ in the transition state is solely a factor of the leaving group. Both independent bond orders (n/sub α-N/ and n/sub β-H'/) exhibit a linear dependence on the sigma value of the substituent, allowing for the first time prediction of transition states

  11. High-energy lithium-ion battery using substituted LiCoPO4: From coin type to 1 Ah cell

    Science.gov (United States)

    Liu, D.; Zhu, W.; Kim, C.; Cho, M.; Guerfi, A.; Delp, S. A.; Allen, J. L.; Jow, T. R.; Zaghib, K.

    2018-06-01

    Cr, Fe and Si were added to improve the performance of olivine LiCoPO4 in cathodes for lithium-ion batteries. A substituted-LiCoPO4 in a half cell delivered a reversible capacity of 125 mAh/g at C/3 rate, with no capacity loss after over 100 cycles at 25 °C. The well-known capacity fade of LiCoPO4-based cathodes was almost completely eliminated by substituting Cr, Fe and Si.

  12. ABILITY OF Phanerochaete chrysosporium AND Trametes versicolor TO REMOVE Zn2+, Cr3+, Pb2+ METAL IONS

    Directory of Open Access Journals (Sweden)

    Josué Solís Pacheco

    2015-07-01

    Full Text Available The use of fungal biomass as an alternative for removing heavy metals has become increasingly important in recent years, replacing conventional methods based on chemical physical processes. In this study, we evaluated the biosorption of Zn2+, Cr3+ and Pb2+, which were analyzed to determine their effect on growth kinetic parameters of Phanerochaete chrysosporium strain ATCC 32629 and Trametes versicolor ATCC 1267. Growth kinetics were performed in four liquid culture media: 1 Yeast Nitrogen Base (YNB used as control, 2 YNB medium plus Pb2+ (0.25, 1 and 2 mg L-1, 3 YNB medium plus Zn2+ (5, 10 and 20 mg L-1 and 4 YNB medium plus Cr3+ (0.5, 1 and 2 mg L-1. The flasks were incubated at 25 °C with shaking at 150 rpm. Metal concentrations were determined by inductively coupled plasma atomic emission spectroscopy (ICP-AES with prior acid digestion of the sample. The results demonstrated that Phanerochaete chrysosporium ATCC 32629 and Trametes versicolor ATCC 12679 are able to grow in the culture medium with Pb2+, Zn2+ and Cr3+ ions at different concentrations. However, P. chrysosporium ATCC 32629 showed greater adaptability and ability to adsorb Cr3+ in the culture medium at concentrations of 0.5 and 1 mg L-1, whereas T. versicolor ATCC 12679 was capable of Pb2+ biosorption at concentrations of 0.25, 1 and 2 mg L-1.

  13. Magnesium- and strontium-co-substituted hydroxyapatite: the effects of doped-ions on the structure and chemico-physical properties.

    Science.gov (United States)

    Aina, Valentina; Lusvardi, Gigliola; Annaz, Basil; Gibson, Iain R; Imrie, Flora E; Malavasi, Gianluca; Menabue, Ledi; Cerrato, Giuseppina; Martra, Gianmario

    2012-12-01

    The present study is aimed at investigating the contribution of two biologically important cations, Mg(2+) and Sr(2+), when substituted into the structure of hydroxyapatite (Ca(10)(PO(4))(6)(OH)(2),HA). The substituted samples were synthesized by an aqueous precipitation method that involved the addition of Mg(2+)- and Sr(2+)-containing precursors to partially replace Ca(2+) ions in the apatite structure. Eight substituted HA samples with different concentrations of single (only Mg(2+)) or combined (Mg(2+) and Sr(2+)) substitution of cations have been investigated and the results compared with those of pure HA. The obtained materials were characterized by X-ray powder diffraction, specific surface area and porosity measurements (N(2) adsorption at 77 K), FT-IR and Raman spectroscopies and scanning electron microscopy. The results indicate that the co-substitution gives rise to the formation of HA and β-TCP structure types, with a variation of their cell parameters and of the crystallinity degree of HA with varying levels of substitution. An evaluation of the amount of substituents allows us to design and prepare BCP composite materials with a desired HA/β-TCP ratio.

  14. Effect of Mg(2+), Ca(2+), Sr(2+) and Ba(2+) metal ions on the antifungal activity of ZnO nanoparticles tested against Candida albicans.

    Science.gov (United States)

    Haja Hameed, Abdulrahman Syedahamed; Karthikeyan, Chandrasekaran; Senthil Kumar, Venugopal; Kumaresan, Subramanian; Sasikumar, Seemaisamy

    2015-01-01

    The antifungal ability of pure and alkaline metal ion (Mg(2+), Ca(2+), Sr(2+) and Ba(2+)) doped ZnO nanoparticles (NPs) prepared by the co-precipitation method was tested against the pathogenic yeast, Candida albicans (C. albicans), and the results showed that the Mg-doped ZnO NPs possessed greater effect than the other alkaline metal ion doped ZnO NPs. The impact of the concentration of Mg doped ZnO sample on the growth of C. albicans was also studied. The Minimal Fungicidal Concentration (MFC) of the Mg doped ZnO NPs was found to be 2000 μg/ml for which the growth of C. albicans was completely inhibited. The ZnO:Mg sample (1.5mg/ml) with various concentrations of histidine reduced the fungicidal effect of the nanoparticles against C. albicans, which was deliberately explained by the role of ROS. The ZnO:Mg sample added with 5mM of histidine scavenged the ample amount of generated ROS effectively. The binding of the NPs with fungi was observed by their FESEM images and their electrostatic attraction is confirmed by the zeta potential measurement. Copyright © 2015. Published by Elsevier B.V.

  15. Comparative study of as-implanted and pre-damaged ion-beam-synthesized ZnS nanocrystallites in SiO sub 2

    CERN Document Server

    Gao, K Y; Grosshans, I; Hipp, W; Stritzker, B

    2002-01-01

    The semiconducting ZnS nanocrystallites were synthesized by sequential high dose ion implantation of Zn and S in thermally grown SiO sub 2 on Si(1 0 0) and subsequent rapid thermal annealing (RTA). Some samples were pre-implanted with Ar ions in order to investigate the influence of radiation induced damage on the formation of ZnS nanocrystallites. The crystal structure of the ZnS crystallites, their size distribution and the concentration depth profile were analyzed by X-ray diffraction (XRD), Rutherford backscattering spectroscopy (RBS) and cross-sectional transmission-electron-microscopy (XTEM). The XRD results indicate, that the phase transition from cubic zinc blende to hexagonal wurtzite structure of ZnS nanocrystallites begins at temperatures below 1000 degree sign C. The RBS results show a clear redistribution of Zn and S after RTA annealing. The concentration of Zn is seriously reduced due to strong diffusion towards deeper regions and the surface, while Ar pre-implantation partially suppressed the c...

  16. Nuclear reaction analysis of Ge ion-implanted ZnO bulk single crystals: The evaluation of the displacement in oxygen lattices

    Energy Technology Data Exchange (ETDEWEB)

    Kamioka, K.; Oga, T.; Izawa, Y. [College of Engineering and Research Center of Ion Beam Technology, Hosei University, Koganei, Tokyo 184-8584 (Japan); Kuriyama, K., E-mail: kuri@ionbeam.hosei.ac.jp [College of Engineering and Research Center of Ion Beam Technology, Hosei University, Koganei, Tokyo 184-8584 (Japan); Kushida, K. [Department of Arts and Science, Osaka Kyouiku University, Kashiwara, Osaka 582-8582 (Japan); Kinomura, A. [National Institute of Advanced Industrial Science and Technology, Tsukuba, Ibaraki 305-8568 (Japan)

    2014-08-01

    The displacement of oxygen lattices in Ge ion-implanted ZnO bulk single crystals is studied by nuclear reaction analysis (NAR), photoluminescence (PL), and Van der Pauw methods. The Ge ion-implantation (net concentration: 2.6 × 10{sup 20} cm{sup −3}) into ZnO is performed using a multiple-step energy. The high resistivity of ∼10{sup 3} Ω cm in un-implanted samples remarkably decreased to ∼10{sup −2} Ω cm after implanting Ge-ion and annealing subsequently. NRA measurements of as-implanted and annealed samples suggest the existence of the lattice displacement of O atoms acting as acceptor defects. As O related defects still remain after annealing, these defects are not attributed to the origin of the low resistivity in 800 and 1000 °C annealed ZnO.

  17. Nuclear reaction analysis of Ge ion-implanted ZnO bulk single crystals: The evaluation of the displacement in oxygen lattices

    Science.gov (United States)

    Kamioka, K.; Oga, T.; Izawa, Y.; Kuriyama, K.; Kushida, K.; Kinomura, A.

    2014-08-01

    The displacement of oxygen lattices in Ge ion-implanted ZnO bulk single crystals is studied by nuclear reaction analysis (NAR), photoluminescence (PL), and Van der Pauw methods. The Ge ion-implantation (net concentration: 2.6 × 1020 cm-3) into ZnO is performed using a multiple-step energy. The high resistivity of ∼103 Ω cm in un-implanted samples remarkably decreased to ∼10-2 Ω cm after implanting Ge-ion and annealing subsequently. NRA measurements of as-implanted and annealed samples suggest the existence of the lattice displacement of O atoms acting as acceptor defects. As O related defects still remain after annealing, these defects are not attributed to the origin of the low resistivity in 800 and 1000 °C annealed ZnO.

  18. Solution-combustion synthesized nickel-substituted spinel cathode materials (LiNixMn2-xO4; 0≤x≤0.2) for lithium ion battery: enhancing energy storage, capacity retention, and lithium ion transport

    CSIR Research Space (South Africa)

    Kebede, MA

    2014-01-01

    Full Text Available Spherically shaped Ni-substituted LiNi(subx)Mn(sub2-x)O(sub4) (x=0, 0.1, 0.2) spinel cathode materials for lithium ion battery with high first cycle discharge capacity and remarkable cycling performance were synthesized using the solution...

  19. Effect of Co2+ and Y3+ ions insertion on the microstructure development and magnetic properties of Ni0.5Zn0.5Fe2O4 powders synthesized using Co-precipitation method

    Science.gov (United States)

    Rashad, M. M.; Rayan, D. A.; Turky, A. O.; Hessien, M. M.

    2015-01-01

    Nanocrystalline Ni0.5Zn0.5-xCoxFe2-zYzO4 powders (x=0-0.3 and z from 0 to 0.3) have been synthesized via a facile co-precipitation technique. X-ray diffraction (XRD), scanning electron microscopy (SEM) and vibrating sample magnetometer (VSM) are utilized in order to study the effect of variation of cobalt and yttrium substitutions and its impact on crystalline size, lattice parameter, X-ray density, microstructure and magnetic properties of the formed powders. X-ray diffraction data indicated that, after doping, all samples consisted of the main spinel phase for the formed precursors precipitated at pH 10 annealed at 1000 oC for 2 h. The lattice parameter and the unit cell were decreased linearly with increasing Co content whereas they were increased with increasing the Y incorporation. Additionally, the porosity was increased with increasing Co concentration while it was decreased with increasing the Y insertion. The mean ionic radii and hopping and bond lengths was decreased with the value of Co2+ and they were increased with the value of Y3+ ion as well as both of Y3+ and Co2+ ions. The microstructures of the produced powders were found to be cubic like structure. The addition of Y3+ ion suppressed the grain size whereas addition of Co2+ ion enhanced the grain growth availably. An examination of the magnetic properties revealed an increase in saturation magnetization with increasing Co and Y concentrations incorporation up to x=0.3. Meanwhile, the formed powders exhibited superparamagnetic characteristics. A high saturation magnetization (77.0 emu/g) was achieved for Ni0.5Zn0.2Co0.3Fe2O4 sample annealed at 1000 oC for 2 h.

  20. Solid-solution-like ZnO/C composites as excellent anode materials for lithium ion batteries

    International Nuclear Information System (INIS)

    Zhang, Guanhua; Zhang, Hang; Zhang, Xiang; Zeng, Wei; Su, Qingmei; Du, Gaohui; Duan, Huigao

    2015-01-01

    Exploring advanced anode materials to maximize the capacity of lithium ion batteries has been an active research area for decades. Constructing composites materials has been proved to be one of the most effective methods to achieve higher capacity due to the synergistic effect. In this work, we proposed and demonstrated a concept of solid-solution-like ZnO/C composites to approach the largest possible synergistic effect by introducing the most interfaces and minimizing the pulverization. The solid-solution-like ZnO/C electrode could achieve a high reversible capacity of 813.3 mAh g −1 at a current density of 100 mA g −1 after 100 cycles with a decrease rate of only 0.4% per cycle. Moreover, the discharge capacity still maintained 53.5% of the original value even when the current density increased to 40 times as much as the original, showing a distinguished rate performance. In addition, such solid-solution-like nanofibers can be easily prepared because of their compatibility with the existing industrial PAN-based spinning process. This may pave the way to mass produce lithium ion batteries with significantly enhanced performance using existing low-cost commercial facilities and recipes.

  1. Photoluminescence of rare-earth ion (Eu3+, Tm3+, and Er3+)-doped and co-doped ZnNb2O6 for solar cells

    Science.gov (United States)

    Gao, Sen-Pei; Qian, Yan-Nan; Wang, Biao

    2015-08-01

    Visible converted emissions produced at an excitation of 286 nm in ZnNb2O6 ceramics doped with rare-earth ions (RE = Eu3+, Tm3+, Er3+ or a combination of these ions) were investigated with the aim of increasing the photovoltaic efficiency of solar cells. The structure of RE:ZnNb2O6 ceramics was confirmed by x-ray diffraction patterns. The undoped ZnNb2O6 could emit a blue emission under 286-nm excitation, which is attributed to the self-trapped excitons’ recombination of the efficient luminescence centers of edge-shared NbO6 groups. Upon 286-nm excitation, Eu:ZnNb2O6, Tm:ZnNb2O6, and Er:ZnNb2O6 ceramics showed blue, green, and red emissions, which correspond to the transitions of 5D0 → 7FJ (J = 1-4) (Eu3+), 1G4 → 3H6 (Tm3+), and 2H11/2/4S3/2 → 4I15/2 (Er3+), respectively. The calculated CIE chromaticity coordinates of Eu:ZnNb2O6, Tm:ZnNb2O6, and Er:ZnNb2O6 are (0.50, 0.31), (0.14, 0.19), and (0.29, 0.56), respectively. RE ion-co-doped ZnNb2O6 showed a combination of characteristic emissions. The chromaticity coordinates of Eu/Tm:ZnNb2O6, Eu/Er:ZnNb2O6, and Tm/Er:ZnNb2O6 were calculated to be (0.29, 0.24), (0.45, 0.37), and (0.17, 0.25). Project supported by the National Natural Science Foundation of China (Grant Nos. 10572155 and 10732100) and the Research Fund for the Doctoral Program of Ministry of Education, China (Grant No. 20130171130003).

  2. An open-framework bimetallic chalcogenide structure K3Rb3Zn4Sn3Se13 built on a unique [Zn4Sn3Se16]12- cluster: synthesis, crystal structure, ion exchange and optical properties

    International Nuclear Information System (INIS)

    Wu Min; Su Weiping; Jasutkar, Niren; Huang, Xiaoying; Li Jing

    2005-01-01

    Single crystals of K 3 Rb 3 Zn 4 Sn 3 Se 13 were synthesized by solvothermal method. The building block in this structure is a [Zn 4 Sn 3 Se 16 ] 12- cluster which consists of four ZnSe 4 and three SnSe 4 tetrahedra connected through corner-sharing of Se atoms. The 3D network contains intersecting channels running parallel to the crystallographic [2 1 1], [1-1-1] and [12-1] directions. The disordered K + and Rb + cations reside in these channels. Ion exchange of Cs + with disordered Rb + /K + ions in the structure showed a partial replacement of 15.8%. Optical diffuse reflectance experiments were carried out and gave a sharp absorption edge at 2.6 eV

  3. Raman study of alloy potential fluctuations in MgxZn1-xO nanopowders

    International Nuclear Information System (INIS)

    Pan, C-J; Lin, K-F; Hsu, W-T; Hsieh, W-F

    2007-01-01

    The blueshift of near-band-edge emission and excitonic absorption indicate that Zn 2+ ions are successfully substituted by Mg 2+ ions in Mg x Zn 1-x O nanopowders for 0≤x≤0.14. The changes in Raman spectral linewidth and the asymmetry of the E 2 (high) mode for various Mg contents can be well described by a modified spatial correlation model that considers the grain size distribution. With increasing Mg concentration, the alloy potential fluctuations lead to a decrease in the grain size, which is induced by the surplus Mg 2+ that could form MgO clusters surrounding the crystalline MgZnO

  4. Ion species dependence of the implantation-induced defects in ZnO studied by a slow positron beam

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Z.Q. [Department of Physics, Wuhan University (China); Maekawa, M.; Kawasuso, A.; Naramoto, H. [Advanced Science Research Center, Japan Atomic Energy Agency, Takasaki, Gunma (Japan)

    2007-07-01

    In this work, we implanted B{sup +}, O{sup +}, Al{sup +}, and P{sup +} ions into ZnO with energy of 50-380 keV and total doses of 4 x 10{sup 15} cm{sup -2} for each ion. The implantation-induced defects and their thermal recovery were studied using a slow positron beam. Vacancy clusters are produced in all the implanted samples. It is found that the thermal recovery of these vacancies induced by different ions shows much difference. In case of B{sup +} and Al{sup +}-implantation, the vacancy clusters agglomerate to much larger size and might evolve to microvoids during annealing. However, for O{sup +} and P{sup +} ions, which are heavier than B{sup +} and Al{sup +}, the vacancies show a much weaker agglomeration process. The mechanism of such difference is discussed. (copyright 2007 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  5. Structural and optical characterization of Mn doped ZnS nanocrystals elaborated by ion implantation in SiO{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Bonafos, C. E-mail: bonafos@el.ub.es; Garrido, B.; Lopez, M.; Romano-Rodriguez, A.; Gonzalez-Varona, O.; Perez-Rodriguez, A.; Morante, J.R.; Rodriguez, R

    1999-01-01

    Mn doped ZnS nanocrystals have been formed in SiO{sub 2} layers by ion implantation and thermal annealing. The structural analysis of the processed samples has been performed mainly by Secondary Ion Mass Spectroscopy (SIMS) and Transmission Electron Microscopy (TEM). The data show the precipitation of ZnS nanocrystals self-organized into two layers parallel to the free surface. First results of the optical analysis of samples co-implanted with Mn show the presence of a yellow-green photoluminescence depending on the Mn concentration and the size of the nanocrystals, suggesting the doping with Mn of some precipitates.

  6. Ammonia sensing properties of V-doped ZnO:Ca nanopowders prepared by sol–gel synthesis

    International Nuclear Information System (INIS)

    Fazio, E.; Hjiri, M.; Dhahri, R.; El Mir, L.; Sabatino, G.; Barreca, F.; Neri, F.; Leonardi, S.G.; Pistone, A.; Neri, G.

    2015-01-01

    V-doped ZnO:Ca nanopowders with different V loading were prepared by sol–gel synthesis and successive drying in ethanol under supercritical conditions. Characterization data of nanopowders annealed at 700 °C in air, revealed that they have the wurtzite structure. Raman features of V-doped ZnO:Ca samples were found to be substantially modified with respect to pure ZnO or binary ZnO:Ca samples, which indicate the substitution of vanadium ions in the ZnO lattice. The ammonia sensing properties of V-doped ZnO:Ca thick films were also investigated. The results obtained demonstrate the possibility of a fine tuning of the sensing characteristics of ZnO-based sensors by Ca and V doping. In particular, their combined effect has brought to an enhanced response towards NH 3 compared to bare ZnO and binary V-ZnO and Ca-ZnO samples. Raman investigation suggested that the presence of Ca play a key role in enhancing the sensor response in these ternary composite nanomaterials. - Graphical abstract: V-doped ZnO:Ca nanopowders prepared by sol–gel synthesis possess enhanced sensing characteristics towards NH 3 compared to bare ZnO. - Highlights: • V-doped ZnO:Ca nanopowders with different V loading were prepared by sol–gel synthesis. • Raman features of V-doped ZnO:Ca samples indicate the substitution of V ions in the ZnO lattice. • Combined effects of dopants have brought to an enhanced response to NH 3 compared to ZnO. • Ca play a key role in enhancing the sensor response of ternary V-doped ZnO:Ca composites

  7. Recent Progress in the Development of Supercritical Carbon Dioxide-Soluble Metal Ion Extractants: Aggregation, Extraction, and Solubility Properties of Silicon-Substituted Alkylenediphosphonic Acids

    Energy Technology Data Exchange (ETDEWEB)

    Dietz, Mark L.; McAlister, Daniel R.; Stepinski, Dominique C.; Zalupski, Peter R.; Dzilawa, Julie A.; Barrans, Richard E.; Hess, J.N.; Rubas, Audris V.; Chiarizia, Renato; Lubbers, Christopher M.; Scurto, Aaron M.; Brennecke, Joan F.; Herlinger, Albert W.

    2003-09-11

    Partially esterified alkylenediphosphonic acids (DPAs) have been shown to be effective reagents for the extraction of actinide ions from acidic aqueous solution into conventional organic solvents. Efforts to employ these compounds in supercritical fluid extraction have been hampered by their modest solubility in unmodified supercritical carbon dioxide (SC-CO2). In an effort to design DPAs that are soluble in SC-CO2, a variety of silicon-substituted alkylenediphosphonic acids have been prepared and characterized, and their behavior compared with that of conventional alkyl-substituted reagents. Silicon substitution is shown to enhance the CO2-philicity of the reagents, while other structural features, in particular, the number of methylene groups bridging the phosphorus atoms of the extractant, are shown to exert a significant influence on their aggregation and extraction properties. The identification of DPAs combining desirable extraction properties with adequate solubility in SC-CO2 is shown to be facilitated by the application of molecular connectivity indices.

  8. Synthesis and electrochemical performances of ZnO/MnO2 sea urchin-like sleeve array as anode materials for lithium-ion batteries

    International Nuclear Information System (INIS)

    Fang, J.; Yuan, Y.F.; Wang, L.K.; Ni, H.L.; Zhu, H.L.; Yang, J.L.; Gui, J.S.; Chen, Y.B.; Guo, S.Y.

    2013-01-01

    MnO 2 is electrodeposited onto ZnO nanorod array grown on Ni foil, forming a binder-free ZnO/MnO 2 composited electrode. XRD, EDS, SEM and TEM are used to analyze the phase and microstructure of this composite. Burr-like MnO 2 nanoflakes grows on ZnO nanorod array, the top of the composite is hollow and at the bottom exists ZnO large block core as an internal support, forming ZnO/MnO 2 sea urchin-like sleeve array. As anode material for lithium ion batteries, ZnO/MnO 2 sleeve array exhibits higher discharge capacity and coulombic efficiency, better rate performance and cycling stability than single ZnO nanorod array or directly electrodepsited MnO 2 , and the composite effect is very remarkable. After 100 cycles, the discharge capacity of ZnO/MnO 2 still reaches 1259 mA h g −1 , and coulombic efficiency surpasses 98%, higher than those of ZnO nanorod array (111 mA h g −1 ) and directly electrodeposited MnO 2 (507 mA h g −1 ). The improvement of the electrochemical performances is due to the unique sea urchin-like sleeve array architecture. MnO 2 burr tube shell structure leads to high electrochemical activity while the internal ZnO core support ensures good structure stability. The gradually opening of sea urchin-like sleeve during the cycling further enhances the electrochemical activity of MnO 2 , stabilizing and increasing electrochemical performances of the ZnO/MnO 2 composite

  9. Preparation and characterization of Ce-doped ZnO nanofibers by an electrospinning method

    Directory of Open Access Journals (Sweden)

    Jong-Pil Kim

    2011-02-01

    Full Text Available ZnO and Ce-doped ZnO Nanofibers on (111 Pt/SiO2/Si substrates were produced using an electrospinning technique. The as-prepared composite fibres were subjected to high-temperature calcination to produce inorganic fibers. After calcining at a temperature of 500 °C, the average diameter of the ZnO and Ce-doped ZnO nanofibers were determined to be 170 nm and 225 nm, respectively. The average grain size of the ZnO and Ce-doped ZnO nanofibers were about 50 nm and 57 nm, respectively. The microstructure, chemical bonding state and photoluminescence of the produced ZnO and Ce-doped ZnO nanofibers were investigated. The Ce-doped ZnO nanofiber can be assigned to the presence of Ce ions on substitutional sites of Zn ions and the Ce3+ state from X-ray photoelectron spectra. Compared with PL spectra of ZnO nanofibers, the peak position of the UV emission of the Ce-doped ZnO nanofibers is sharply suppressed while the green emission band is highly enhanced.

  10. Bias-dependent photo-detection of dual-ion beam sputtered MgZnO ...

    Indian Academy of Sciences (India)

    Discipline of Electrical Engineering, Indian Institute of Technology, Indore 452003, India. MS received .... crystallite size and stress generation on MgZnO thin films for different growth temperatures. ..... This work was partially supported by Department of Sci- ... [24] American Standard for Testing of Materials—ASTM 36-1451.

  11. Sorption behavior of Zn(II) ions on synthetic apatitic calcium phosphates

    Science.gov (United States)

    Sebei, Haroun; Pham Minh, Doan; Nzihou, Ange; Sharrock, Patrick

    2015-12-01

    The synthesis, characterization and the reactivity of apatitic calcium phosphates (Ca-HA, chemical formula Ca10(PO4)6(OH)2) is reported. Calcium carbonate (CaCO3) and potassium dihydrogen orthophosphate (KH2PO4) were selected as economical starting materials for the synthesis of Ca-HA under atmospheric conditions. Monocalcium phosphate monohydrate (MCPM), dicalcium phosphate dihydrate (DCPD), and octacalcium phosphate pentahydrate (OCP) were identified as the main intermediates of the synthesis reaction. The product obtained after 48 h of reaction contains mainly low-crystalline Ca-HA and small amounts of other calcium phosphates such as octacalcium phosphate (OCP), B-type carbonate apatite (CAP), as well as unreacted calcium carbonate. This Ca-HA was found to be active for the removal of Zn2+ from an aqueous solution. Its sorption capacity reached up to 120 mg of Zn2+ per g of Ca-HA powder after 24 h of reaction. The monitoring of soluble Zn, Ca and P during the sorption experiment allowed characterizing the mechanism of Zn uptake. Dissolution-precipitation, ionic exchange and surface complexation are the three main mechanisms involved in the sorption processes. The contribution of these mechanisms is discussed in detail.

  12. Influence of Ni substitution at B-site for Fe{sup 3+} ions on morphological, optical, and magnetic properties of HoFeO{sub 3} ceramics

    Energy Technology Data Exchange (ETDEWEB)

    Habib, Zubida; Majid, Kowsar [National Institute of Technology, Department of Chemistry, Srinagar (India); Ikram, Mohd; Sultan, Khalid; Mir, Sajad Ahmad [National Institute of Technology, Department of Physics, Srinagar (India); Asokan, K. [Inter University Accelerator Centre, New Delhi (India)

    2016-05-15

    Present study reports the effect of Ni substitution at B-site in HoFeO{sub 3} on the morphological, optical and magnetic properties. These compounds were prepared by solid-state reaction method. Scanning electron microscope reveals an increase in average grain sizes with Ni concentration. Absorption and emission spectra show redshift in band gap with increase in Ni ion concentrations. The Tauc plots show direct allowed transitions. Temperature-dependent magnetization studies on these compounds revealed the transition from ferromagnetism to paramagnetism. There is separation between temperature at which zero-field-cooled and field-cooled occurs at varied temperature with Ni substitution. The separation effect is related to the impact of the paramagnetic Ho{sup 3+} ions, whose magnitude becomes more prominent at higher temperature. The value of squareness ratio in these materials is below 0.5 indicating presence of multidomain structures. (orig.)

  13. Lattice location of the group V elements Sb, As, and P in ZnO

    CERN Document Server

    Wahl, Ulrich; Mendonça, Tânia; Decoster, Stefan

    2010-01-01

    Modifying the properties of ZnO by means of incorporating antimony, arsenic or phosphorus impurities is of interest since these group V elements have been reported in the literature among the few successful p-type dopants in this technologically promising II-VI compound. The lattice location of ion-implanted Sb, As, and P in ZnO single crystals was investigated by means of the electron emission channeling technique using the radioactive isotopes $^{124}$Sb, $^{73}$As and $^{33}$P and it is found that they preferentially occupy substitutional Zn sites while the possible fractions on substitutional O sites are a few percent at maximum. The lattice site preference is understandable from the relatively large ionic size of the heavy mass group V elements. Unfortunately the presented results cannot finally settle the interesting issue whether substitutional Sb, As or P on oxygen sites or Sb$_{Zn}$−2V$_{Zn}$, As$_{Zn}$−2V$_{Zn}$ or P$_{Zn}$−2V$_{Zn}$ complexes (as suggested in the literature) are responsible f...

  14. Inverse spinel ZnFe2O4 nanoparticles synthesized by ion implantation and post-annealing: An investigation using X-ray spectroscopy and magneto-transport

    International Nuclear Information System (INIS)

    Zhou Shengqiang; Potzger, K.; Buerger, D.; Kuepper, K.; Helm, M.; Fassbender, J.; Schmidt, H.

    2009-01-01

    Noncrystalline ZnFe 2 O 4 has been investigated intensively due to the drastic difference in cation distribution compared with bulk materials. We previously synthesized ZnFe 2 O 4 nanoparticles by ion implantation and post-annealing [S. Zhou, K. Potzger, H. Reuther, G. Talut, F. Eichhorn, J. von Borany, W. Skorupa, M. Helm, J. Fassbender, J. Phys. D - Appl. Phys. 40 (2007) 964]. These ZnFe 2 O 4 nanocrystals are crystallographically oriented inside the ZnO matrix and show a hysteretic behavior upon magnetization reversal at 5 K. Their magnetic properties are explained by assuming that Fe 3+ ions partially occupy tetrahedral sites. In this paper an X-ray spectroscopic and magneto-transport investigation on ZnFe 2 O 4 nanocrystals in a ZnO matrix will be presented. The occupation of Fe 3+ at tetrahedral sites has been directly proved. A positive magnetoresistance (MR) effect is observed and is attributed to ordinary MR.

  15. Cu and Zn substituted silicon clathrates with the cubic type-II structure. Synthesis and characterization of Cs{sub 8}Na{sub 16}Cu{sub 3.8}Si{sub 132.2} and Cs{sub 8}Na{sub 16}Zn{sub 6.9}Si{sub 129.1}

    Energy Technology Data Exchange (ETDEWEB)

    Schaefer, Marion C.; Bobev, Svilen [Department of Chemistry and Biochemistry, University of Delaware, Newark, DE (United States)

    2017-12-13

    Studies in the systems Cs-Na-Cu-Si and Cs-Na-Zn-Si yielded the novel clathrates Cs{sub 8}Na{sub 16}(Cu,Si){sub 136} and Cs{sub 8}Na{sub 16}(Zn,Si){sub 136}, both with the cubic type-II structure [space group Fd anti 3m (no. 227), Pearson symbol cF160]. The structures of the title compounds were established from single-crystal X-ray diffraction methods, confirming the complete ordering of the Cs and Na guest atoms. The framework-building Si atoms are found to be randomly substituted by Cu atoms on framework site 96g, exclusively. In the structure of Cs{sub 8}Na{sub 16}(Zn,Si){sub 136}, the refinements indicate that the Zn and Si atoms co-occupy two of the three framework sites with notable preference for site 96g over site 32e. The corresponding refined compositions and unit cell parameters are as follows: Cs{sub 8}Na{sub 16}Cu{sub 3.8}Si{sub 132.2(1)} [a = 14.7583(15) Aa]; Cs{sub 8}Na{sub 16}Zn{sub 6.9}Si{sub 129.1(1)} [a = 14.7682(5) Aa], respectively. The type-II clathrates can be obtained only from experiments employing both Na and Cs, whereas work in the ternary Cs-Cu-Si, Cs-Zn-Si, Na-Cu-Si, and Na-Zn-Si systems failed to yield any clathrate phases. At the same conditions, exploratory studies in the K-Zn-Si and Rb-Zn-Si systems provided evidence that type-I clathrates are favored. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  16. Zn/V2O5 Aqueous Hybrid-Ion Battery with High Voltage Platform and Long Cycle Life.

    Science.gov (United States)

    Hu, Ping; Yan, Mengyu; Zhu, Ting; Wang, Xuanpeng; Wei, Xiujuan; Li, Jiantao; Zhou, Liang; Li, Zhaohuai; Chen, Lineng; Mai, Liqiang

    2017-12-13

    Aqueous zinc-ion batteries attract increasing attention due to their low cost, high safety, and potential application in stationary energy storage. However, the simultaneous realization of high cycling stability and high energy density remains a major challenge. To tackle the above-mentioned challenge, we develop a novel Zn/V 2 O 5 rechargeable aqueous hybrid-ion battery system by using porous V 2 O 5 as the cathode and metallic zinc as the anode. The V 2 O 5 cathode delivers a high discharge capacity of 238 mAh g -1 at 50 mA g -1 . 80% of the initial discharge capacity can be retained after 2000 cycles at a high current density of 2000 mA g -1 . Meanwhile, the application of a "water-in-salt" electrolyte results in the increase of discharge platform from 0.6 to 1.0 V. This work provides an effective strategy to simultaneously enhance the energy density and cycling stability of aqueous zinc ion-based batteries.

  17. Porous carbon-coated ZnO nanoparticles derived from low carbon content formic acid-based Zn(II) metal-organic frameworks towards long cycle lithium-ion anode material

    International Nuclear Information System (INIS)

    Gao, Song; Fan, Ruiqing; Li, Bingjiang; Qiang, Liangsheng; Yang, Yulin

    2016-01-01

    Graphical abstract: The nanocomposites constructed from Zn-based MOFs exhibit low carbon content with super-high rate capability and long cycling life. - Highlights: • Novel ZnO@porous carbon matrix nanocomposites are constructed by pyrolysis of Zn-based MOFs. • The nanocomposites constructed with Zn-based MOFs show low carbon content. • The constructed nanocomposites exhibit high energy density, super-high rate capability and long cycling life. - Abstract: Single-C formic acid-based metal-organic frameworks (MOFs) are used to construct novel ZnO@porous carbon matrix nanocomposites by controlled pyrolysis. In the constructed nanocomposites, the porous carbon matrices act as a confined support to prevent agglomeration of the ZnO nanoparticles and create a rapid electron conductive network. Meanwhile, the well-defined, continuous porous structured MOFs provide a large specific surface area, which increases the contact of electrolyte-electrode and improves the penetration of electrolyte. Especially, the reasonable choice of formic acid-based MOFs construct the low carbon content composite, which contribute to the high energy density and long cycle life. The constructed nanocomposites show stable, ultrahigh rate lithium ion storage properties of 650 mAh g −1 at charge/discharge rate of 1 C even after 200 cycles.

  18. Upconversion in rare earth ions doped TeO2-ZnO glass

    International Nuclear Information System (INIS)

    Mohanty, Deepak Kumar; Rai, Vineet Kumar

    2012-01-01

    The Er 3+ /Yb 3+ doped/codoped TeO 2 -ZnO glasses have been fabricated by conventional melt and quenching technique. The absorption spectra of the doped/codoped glasses have been performed. The visible upconversion emissions of both doped and codoped glasses have been observed using 808 nm diode laser excitation. The process involved in upconversion emissions has been discussed in detail. (author)

  19. Cr-substituted LiCoPO4 core with a conductive carbon layer towards high-voltage lithium-ion batteries

    Science.gov (United States)

    Wang, Yue; Chen, Junhong; Qiu, Jingyi; Yu, Zhongbao; Ming, Hai; Li, Meng; Zhang, Songtong; Yang, Yusheng

    2018-02-01

    Electrical and ionic conductivity are two major limiting factors for LiCoPO4 cathode material. To overcome these shortcomings, a Cr-substituted LiCoPO4 core with a conductive carbon layer cathode material is synthesized using the sol-gel method. The physical chemistry properties of these materials are systematically investigated by using various characterization methods. For instance, the XRD and Rietveld refinement results reveal that Cr successfully substitutes the Co within the LiCoPO4 core to form LiCo1-1.5xCrxPO4/C (x = 0, 0.02, 0.04, 0.06) without changing the olivine structure but exhibits a decrease in the unit cell volume with increasing Cr substitution. SEM and TEM images indicate that Cr substitution does not lead to changes in the basic morphology of LiCo1-1.5xCrxPO4/C (x = 0, 0.02, 0.04, 0.06) material, which is composed of agglomerated nanoparticles with an 8 nm carbon layer on the surface. The EDS and XPS results confirm that Cr is uniformly distributed on the surface and that the oxidation state of Cr is +3. FTIR spectra indicate that the antisite defect concentration decreases with increasing Cr substitution. Furthermore, Cr substitution significantly improves the electrochemical performances of LiCo1-1.5xCrxPO4/C (x = 0.02, 0.04, 0.06) cathode. Notably, the LiCo0.94Cr0.04PO4/C delivers an initial discharge capacity of 144 mA h g-1 at 0.1 C and shows a capacity retention of 71% after 100 cycles between 3.0 and 5.0 V. The CV and EIS results indicate that the polarization is reduced and that the electronic and ionic conductivities are improved by Cr substitution. The good electrochemical performances for Cr-substituted LiCoPO4/C electrodes are attributed to the lower antisite defect concentration, as the reduction of polarization, the improvement of electronic and ion conductivity and the uniform carbon layer. These features will accelerate the commercial application of LiCoPO4 towards the start-art of the high voltage lithium-ion batteries.

  20. Using fluorescence measurement of zinc ions liberated from ZnS nanoparticle labels in bioassay for Escherichia coli O157:H7

    International Nuclear Information System (INIS)

    Cowles, Chad L.; Zhu Xiaoshan; Pai, Chi-Yun

    2011-01-01

    In this study, an alternative approach using ZnS nanoparticle biolabels as fluorescence signal transducers is reported for the immunoassay of E. coli O157:H7 in tap water samples. Instead of measuring the fluorescence of ZnS nanoparticles in the assay, the fluorescence signal is generated through the binding of zinc ions released from nanoparticle labels with zinc-ion sensitive fluorescence indicator Fluozin-3. In the assay, ZnS nanoparticles around 50 nm in diameter were synthesized, bioconjugated, and applied for the detection of E. coli O157:H7. The assay shows a detection range over two orders of magnitude and a detection limit around 1000 colony-forming units (cfu) of E. coli O157:H7.

  1. Hierarchical porous ZnMn{sub 2}O{sub 4} microspheres architectured with sub-nanoparticles as a high performance anode for lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Rong, Haibo; Xie, Guiting; Cheng, Si; Zhen, Zihao [New Energy Research Institute, College of Environment and Energy, South China University of Technology, Guangzhou 510006, Guangdong (China); Jiang, Zhongqing [Department of Chemical Engineering, Ningbo University of Technology, Ningbo 315016, Zhejiang (China); Huang, Jianlin; Jiang, Yu; Chen, Bohong [New Energy Research Institute, College of Environment and Energy, South China University of Technology, Guangzhou 510006, Guangdong (China); Jiang, Zhong-Jie, E-mail: zhongjiejiang1978@hotmail.com [New Energy Research Institute, College of Environment and Energy, South China University of Technology, Guangzhou 510006, Guangdong (China)

    2016-09-15

    A simple two-step procedure, which involves the synthesis of the Zn{sub 0.33}Mn{sub 0.67}CO{sub 3} microspheres through a hydrothermal process and the subsequent calcination, has been used to synthesize the ZnMn{sub 2}O{sub 4} microspheres with a hierarchical porous morphology consisting of the ZnMn{sub 2}O{sub 4} sub-nanoparticles. When evaluated as anode materials for lithium ion batteries (LIBs), these hierarchical porous ZnMn{sub 2}O{sub 4} microspheres could exhibit a stable reversible capability of ∼723.7 mAh g{sup −1} at the current density of 400 mA g{sup −1}, which is much higher than those of the ZnMn{sub 2}O{sub 4} based materials reported previously, indicating the great potential of using them as the anode for the LIBs. This is further supported by their better rate capability and higher cycling stability. Careful analysis has shown that the unique porous structure of the hierarchical porous ZnMn{sub 2}O{sub 4} microspheres which consists of the ZnMn{sub 2}O{sub 4} sub-nanoparticles plays an important role in their higher electrochemical performance, since it allows the accommodation of the volume expansion during the repeated discharge–charge cycles, preventing them from the structural destruction, and increase the accessibility of the electrode material to the Li{sup +} storage, making a better utilization of active materials and an easy diffusion of electrolytes in and out of the electrode material. - Graphical abstract: The ZnMn{sub 2}O{sub 4} microspheres with a hierarchical porous morphology consisting of the ZnMn{sub 2}O{sub 4} sub-nanoparticles have been synthesized by the calcination of the Zn{sub 0.33}Mn{sub 0.67}CO{sub 3} microspheres and could exhibit superior electrochemical performance when used as anode materials for lithium ion batteries. - Highlights: • A simple procedure has been used to synthesize the ZnMn{sub 2}O{sub 4} microspheres. • The ZnMn{sub 2}O{sub 4} microspheres exhibit excellent performance when used in LIBs

  2. Hierarchical porous ZnMn_2O_4 microspheres architectured with sub-nanoparticles as a high performance anode for lithium ion batteries

    International Nuclear Information System (INIS)

    Rong, Haibo; Xie, Guiting; Cheng, Si; Zhen, Zihao; Jiang, Zhongqing; Huang, Jianlin; Jiang, Yu; Chen, Bohong; Jiang, Zhong-Jie

    2016-01-01

    A simple two-step procedure, which involves the synthesis of the Zn_0_._3_3Mn_0_._6_7CO_3 microspheres through a hydrothermal process and the subsequent calcination, has been used to synthesize the ZnMn_2O_4 microspheres with a hierarchical porous morphology consisting of the ZnMn_2O_4 sub-nanoparticles. When evaluated as anode materials for lithium ion batteries (LIBs), these hierarchical porous ZnMn_2O_4 microspheres could exhibit a stable reversible capability of ∼723.7 mAh g"−"1 at the current density of 400 mA g"−"1, which is much higher than those of the ZnMn_2O_4 based materials reported previously, indicating the great potential of using them as the anode for the LIBs. This is further supported by their better rate capability and higher cycling stability. Careful analysis has shown that the unique porous structure of the hierarchical porous ZnMn_2O_4 microspheres which consists of the ZnMn_2O_4 sub-nanoparticles plays an important role in their higher electrochemical performance, since it allows the accommodation of the volume expansion during the repeated discharge–charge cycles, preventing them from the structural destruction, and increase the accessibility of the electrode material to the Li"+ storage, making a better utilization of active materials and an easy diffusion of electrolytes in and out of the electrode material. - Graphical abstract: The ZnMn_2O_4 microspheres with a hierarchical porous morphology consisting of the ZnMn_2O_4 sub-nanoparticles have been synthesized by the calcination of the Zn_0_._3_3Mn_0_._6_7CO_3 microspheres and could exhibit superior electrochemical performance when used as anode materials for lithium ion batteries. - Highlights: • A simple procedure has been used to synthesize the ZnMn_2O_4 microspheres. • The ZnMn_2O_4 microspheres exhibit excellent performance when used in LIBs. • The porous structure plays a crucial role in their high performance. • These spheres exhibit a good morphology retention

  3. Synthesis and electrochemical properties of Li{sub 2}ZnTi{sub 3}O{sub 8} fibers as an anode material for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Wang Li; Wu Lijuan; Li Zhaohui; Lei Gangtie [Key Laboratory of Environmentally Friendly Chemistry and Applications of Ministry of Education, College of Chemistry, Xiangtan University, Hunan 411105 (China); Xiao Qizhen, E-mail: qizhenxiao2004@yahoo.com.cn [Key Laboratory of Environmentally Friendly Chemistry and Applications of Ministry of Education, College of Chemistry, Xiangtan University, Hunan 411105 (China); College of Civil Engineering and Mechanics, Xiangtan University, Hunan 411105 (China); Zhang Ping [College of Civil Engineering and Mechanics, Xiangtan University, Hunan 411105 (China)

    2011-06-01

    Highlights: > A simple electrospinning method has been developed to fabricate Li{sub 2}ZnTi{sub 3}O{sub 8} fibers. > Li{sub 2}ZnTi{sub 3}O{sub 8} fibers as anode material for lithium-ion batteries. > A stable and reversible capacity of over 227 mAh g{sup -1} is achieved at a rate of 0.1 C. > Li{sub 2}ZnTi{sub 3}O{sub 8} anode exhibits good cycle performance and high rate capability. - Abstract: Li{sub 2}ZnTi{sub 3}O{sub 8} fibers are synthesized by thermally treating electrospun Zn(CH{sub 3}COO){sub 2}/LiOAc/TBT/PVP fibers and utilized as an energy storage material for rechargeable lithium-ion batteries. The material is characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and thermal analysis. Scanning electron microscopy results show that the Li{sub 2}ZnTi{sub 3}O{sub 8} fibers have an average diameter of 200 nm. Electrochemical properties of the material are evaluated using cyclic voltammetry, galvanostatic cycling and electrochemical impedance spectroscopy. The results show that as-prepared Li{sub 2}ZnTi{sub 3}O{sub 8} has a high specific discharge capacity of 227.6 mAh g{sup -1} at the 2nd cycle. Its electrochemical performance at subsequent cycles shows good cycling capacity and rate capability. The obtained results thus strongly support that the electrospinning method is an effective method to prepare Li{sub 2}ZnTi{sub 3}O{sub 8} anode material with higher capacity and rate capability.

  4. Concentration of Co2+, Fe3+ and Zn2+ ions with microbiological collectors

    International Nuclear Information System (INIS)

    Fisel, S.; Dulman, V.; Cecal, A.

    1975-01-01

    By means of the Spicaria Biolacea Abbott fungus a satisfactory microbiological concentration of 60 Co 2+ , sup(55+59)Fe 3+ and 65 Zn 2+ can be obtained under optimum experimental conditions. By repeating the cultures on the media obtained after filtration, multistage processes, and by adding the necessary nutritive substances, practically quantitative concentration of these three elements can be produced. The experimental results plead in favour of a concentration mechanism of the isotopes inside the cell with no surface adsorption. The influence of the experimental conditions i.e. pH, time and concentration have been investigated. (T.G.)

  5. Effect of B-site substitution of complex ions on dielectric and piezoelectric properties in (Bi1/2Na1/2)TiO3 piezoelectric ceramics

    International Nuclear Information System (INIS)

    Zhou Changrong; Liu Xinyu

    2008-01-01

    The effect of B-site substitution of complex ions on dielectric and piezoelectric properties in (Bi 1/2 Na 1/2 )Ti 1-x (Zn 1/3 Nb 2/3 ) x O 3 (BNTZN-100x) lead-free piezoelectric ceramics was investigated. X-ray diffraction analysis shows that the materials are mono-perovskite phase. The morphotropic phase boundary (MPB) of BNTZN-100x ceramics between rhombohedral and tetragonal locates in the range of 0.5% ≤ x ≤ 2.0%. Temperature dependence of dielectric constant shows that these compounds are relaxor ferroelectrics. The compositions near the MPB exhibit relatively high piezoelectric properties. The piezoelectric constant (d 33 ) and the electromechanical coupling factor (k t ) show the maximum values of d 33 = 97 pC N -1 and k t = 0.46 at x = 2.0% and x = 1.0%, respectively. The BNTZN-100x ceramics are good candidate for use as ultrasonic transducer ceramics for high anisotropic with high k t value and low k p value

  6. Effects of Al substitution and thermal annealing on magnetoelectric Ba0.5Sr1.5Zn2Fe12O22 investigated by the enhancement factor of 57Fe nuclear magnetic resonance.

    Science.gov (United States)

    Kwon, Sangil; Kang, Byeongki; Kim, Changsoo; Jo, Euna; Lee, Soonchil; Chai, Yi Sheng; Chun, Sae Hwan; Kim, Kee Hoon

    2014-04-09

    The magnetoelectric properties of hexaferrite Ba0.5Sr1.5Zn2Fe12O22 are significantly improved by Al substitution and thermal annealing. Measuring the enhancement factor of 57Fe NMR, we found direct microscopic evidence that the magnetic moments of the L and S blocks are rotated by a magnetic field in such a way as to increase the net magnetic moment of a magnetic unit, even after the field is removed. Al substitution makes magnetoelectric property arise easily by suppressing the easy-plane anisotropy. The effect of thermal annealing is to stabilize the multiferroic state by reducing the number of pinning sites and the electron spin fluctuation. The transverse conic structure gradually changes to the alternating longitudinal conic structure where spins fluctuate more severely.

  7. Tuning the Origin of Magnetic Relaxation by Substituting the 3d or Rare-Earth Ions into Three Isostructural Cyano-Bridged 3d-4f Heterodinuclear Compounds.

    Science.gov (United States)

    Zhang, Yan; Guo, Zhen; Xie, Shuang; Li, Hui-Li; Zhu, Wen-Hua; Liu, Li; Dong, Xun-Qing; He, Wei-Xun; Ren, Jin-Chao; Liu, Ling-Zhi; Powell, Annie K

    2015-11-02

    Three isostructural cyano-bridged 3d-4f compounds, [YFe(CN)6(hep)2(H2O)4] (1), [DyFe(CN)6(hep)2(H2O)4] (2), and [DyCo(CN)6(hep)2(H2O)4] (3), were successfully assembled by site-targeted substitution of the 3d or rare-earth ions. All compounds have been structurally characterized to display slightly distorted pentagonal-bipyramidal local coordination geometry around the rare-earth ions. Magnetic analyses revealed negligible magnetic coupling in compound 1, antiferromagnetic intradimer interaction in 2, and weak ferromagnetic coupling through dipolar-dipolar interaction in 3. Under an applied direct-current (dc) field, 1 (Hdc = 2.5 kOe, τ0 = 1.3 × 10(-7) s, and Ueff/kB = 23 K) and 3 (Hdc = 2.0 kOe, τ0 = 7.1 × 10(-11) s, and Ueff/kB = 63 K) respectively indicated magnetic relaxation behavior based on a single [Fe(III)]LS ion and a Dy(III) ion; nevertheless, 2 (Hdc = 2.0 kOe, τ0 = 9.7 × 10(-8) s, and Ueff/kB = 23 K) appeared to be a single-molecule magnet based on a cyano-bridged DyFe dimer. Compound 1, which can be regarded as a single-ion magnet of the [Fe(III)]LS ion linked to a diamagnetic Y(III) ion in a cyano-bridged heterodimer, represents one of the rarely investigated examples based on a single Fe(III) ion explored in magnetic relaxation behavior. It demonstrated that the introduction of intradimer magnetic interaction of 2 through a cyano bridge between Dy(III) and [Fe(III)]LS ions negatively affects the energy barrier and χ″(T) peak temperature compared to 3.

  8. Kinetic study on alkaline hydrolysis of Y-substituted phenyl X-substituted benzenesulfonates: Effects of changing nucleophile from azide to hydroxide ion on reactivity and transition-state structure

    International Nuclear Information System (INIS)

    Moon, Ji Hyun; Kim, Min Young; Han, So Yeop; Um, Ik Hwan

    2015-01-01

    Second-order rate constants (math formula) for alkaline hydrolysis of 2,4-dinitrophenyl X-substituted benzenesulfonates (1a–1f) and Y-substituted phenyl 4-nitrobezenesulfonates (2a–2g) have been measured spectrophotometrically. Comparison of math formula with the math formula values reported previously for the corresponding reactions with math formula has revealed that OH [BOND] is only 10"3-fold more reactive than math formula, although the former is 11 pK _a units more basic than the latter. The Yukawa–Tsuno plot for the reactions of 1a–1f results in an excellent linear correlation with ρ_X = 2.09 and r = 0.41. The Brønsted-type plot for the reactions of 2a–2g is linear with β_l_g = −0.51, which is typical for reactions reported to proceed through a concerted mechanism. The Yukawa–Tsuno plot for the reactions of 2a–2g exhibits excellent linearity with ρ_Y = 1.85 and r = 0.25, indicating that a partial negative charge develops on the O atom of the leaving group in the transition state. Thus, the alkaline hydrolysis of 1a–1f and 2a–2g has been concluded to proceed through a concerted mechanism. Comparison of the ρ_X and β_l_g values for the reactions with math formula ions suggests that the reactions with hydroxide ion proceed through a tighter transition-state structure than those with azide ion

  9. Anti-inflammatory drugs interacting with Zn(II), Cd(II) and Pt(II) metal ions.

    Science.gov (United States)

    Dendrinou-Samara, C; Tsotsou, G; Ekateriniadou, L V; Kortsaris, A H; Raptopoulou, C P; Terzis, A; Kyriakidis, D A; Kessissoglou, D P

    1998-09-01

    Complexes of Zn(II), Cd(II) and Pt(II) metal ions with the anti-inflammatory drugs, 1-methyl-5-(p-toluoyl)-1H-pyrrole-2-acetic acid (Tolmetin), alpha-methyl-4-(2-methylpropyl)benzeneacetic acid (Ibuprofen), 6-methoxy-alpha-methylnaphthalene-2-acetic acid (Naproxen) and 1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indole-3-acetic acid (indomethacin) have been synthesized and characterized. In the structurally characterized Cd(naproxen)2 complex the anti-inflammatory drugs acts as bidentate chelate ligand coordinatively bound to metal ions through the deprotonated carboxylate group. Crystal data for 1: [C32H26O8Cd], orthorhombic, space group P22(1)2(1), a = 5.693(2) (A), b = 8.760(3) (A), c = 30.74(1) (A), V = 1533(1) A3, Z = 2. Antibacterial and growth inhibitory activity is higher than that of the parent ligands or the platinum(II) diamine compounds.

  10. Adsorption of Pb(II) ions from aqueous solutions by date bead carbon activated with ZnCl{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Danish, Mohammed; Hashim, Rokiah; Rafatullah, Mohd; Sulaiman, Othman [Division of Bioresource, Paper and Coatings Technology, School of Industrial Technology, Universiti Sains Malaysia, Penang (Malaysia); Ahmad, Anees [Division of Environmental Technology, School of Industrial Technology, Universiti Sains Malaysia, Penang (Malaysia); Govind [Surface Physics and Nanostructures Group, National Physical Laboratory, New Delhi (India)

    2011-04-15

    This study reports on the adsorption characteristics of Pb(II) ions from aqueous solutions using ZnCl{sub 2}-activated date (Phoenix dactylifera) bead (ADB) carbon with respect to change in adsorbent dosage, initial pH, contact time, initial concentration, and temperature of the solution. Kinetic studies of the data showed that the adsorption follows the pseudo-second-order kinetic model. Thermodynamic parameters, enthalpy change ({Delta}H = 55.11 kJ/mol), entropy change ({Delta}S = - 0.193 kJ/mol/K), and Gibbs free energy change ({Delta}G ) were also calculated for the uptake of Pb(II) ions. These parameters show that adsorption on the surface of ADB was feasible, spontaneous in nature, and endothermic between temperatures of 298.2 and 318.2 K. The equilibrium data better fitted the Langmuir and Freundlich isotherm models than the D-R adsorption isotherm model for studying the adsorption behavior of Pb(II) onto the ADB carbon. It could be observed that the maximum adsorption capacity of ADB was 76.92 mg/g at 318.2 K and pH 6.5. (Copyright copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  11. Mechanistic insights into the interaction between energetic oxygen ions and nanosized ZnFe2O4: XAS-XMCD investigations.

    Science.gov (United States)

    Singh, Jitendra Pal; Kaur, Baljeet; Sharma, Aditya; Kim, So Hee; Gautam, Sanjeev; Srivastava, Ramesh Chandra; Goyal, Navdeep; Lim, Weol Cheol; Lin, H-J; Chen, J M; Asokan, K; Kanjilal, D; Won, Sung Ok; Lee, Ik-Jae; Chae, Keun Hwa

    2018-04-20

    The interactions of energetic ions with multi-cation compounds and their consequences in terms of changes in the local electronic structure, which may facilitate intriguing hybridization between O 2p and metal d orbitals and magnetic ordering, are the subject of debate and require a deep understanding of energy transfer processes and magnetic exchange mechanisms. In this study, nanocrystals of ZnFe2O4 were exposed to O7+ ions with an energy of 100 MeV to understand, qualitatively and quantitatively, the metal-ligand field interactions, cation migration and magnetic exchange interactions by employing X-ray absorption fine structure measurements and X-ray magnetic circular dichroism to get deeper mechanistic insights. Nanosized zinc ferrite nanoparticles (NPs) with a size of ∼16 nm synthesized in the cubic spinel phase exhibited deterioration of the crystalline phase when 100 MeV O7+ ions passed through them. However, the size of these NPs remained almost the same. The behaviour of crystal deterioration is associated with the confinement of heat in this interaction. The energy confined inside the nanoparticles promotes cation redistribution as well as the modification of the local electronic structure. Prior to this interaction, almost 42% of Zn2+ ions occupied AO4 tetrahedra; however, this value increased to 63% after the interaction. An inverse effect was observed for metal ion occupancies in BO6 octahedra. The L-edge spectra of Fe and Zn reveal that the spin and valence states of the metal ions were not affected by this interaction. This effect is also supported by K-edge measurements for Fe and Zn. The t2g/eg intensity ratio in the O K-edge spectra decreased after this interaction, which is associated with detachment of Zn2+ ions from the lattice. The extent of hybridization, as estimated from the ratio of the post-edge to the pre-edge region of the O K-edge spectra, decreased after this interaction. The metal-oxygen and metal-metal bond lengths were modified

  12. The Design of Dual-Emissive Composite Material [Zn2(HL)3]+@MOF-5 as Self-Calibrating Luminescent Sensors of Al3+ Ions and Monoethanolamine.

    Science.gov (United States)

    Wu, Meng-Meng; Wang, Jiao-Yang; Sun, Rui; Zhao, Cui; Zhao, Jiong-Peng; Che, Guang-Bo; Liu, Fu-Chen

    2017-08-21

    Introducing another chromophore into a luminescent MOF is a potential way to assembling novel dual-emissive luminescent materials. Putting the chromophore, for which luminescence can be enhanced by Zn 2+ ion, into MOF-5 by the "bottle around ship" strategy is a simple but efficient synthesis method to realize such dual-emissive materials. According to this strategy, a novel dual-emissive luminescent composite material [Zn 2 (HL) 3 ] + @MOF-5 was constructed by loading the [La 3 (HL) 2 L 2 (NO 3 ) 3 H 2 O] (1) (H 2 L = 7,7'-(ethane-1,1'-diyl)8-hydro-quinoline) into MOF-5, in which the [Zn 2 (HL) 3 ] + anions were transformed from 1 with the existence of Zn 2+ . The dual-emissive composite materials show excellent luminescence with two emissions of MOF-5 at 410 nm and [Zn 2 (HL) 3 ] + at 524 nm. Furthermore, by combining characteristics of MOF-5 and the guest chromophore, the composite material is highly selectively sensitive toward Al 3+ and monoethanolamine, which makes [Zn 2 (HL) 3 ] + @MOF-5 a potential self-calibrated fluorescence sensor.

  13. Application of Carrier Element-Free Co-precipitation Method for Ni(II), Cu(II) and Zn(II) Ions Determination in Water Samples Using Chrysin

    International Nuclear Information System (INIS)

    Layth Imad Abd Ali; Wan Aini Wan Ibrahim; Azli Sulaiman; Mohd Marsin Sanagi

    2015-01-01

    A co-precipitation method was developed to separate and pre-concentrate Ni(II), Cu(II) and Zn(II) ions using an organic co precipitant, chrysin without adding any carrier element termed as carrier element-free co-precipitation (CEFC). Analytes were determined using flame atomic absorption spectrometry (FAAS). The influence of analytical conditions, such as pH of the solution, quantity of co-precipitant, standing time, centrifugation rate and time, sample volume, and interference of concomitant ions were investigated over the recovery yields of the trace metals. The limit of detection, the limit of quantification and linearity range obtained from the FAAS measurements were found to be in the range of 0.64 to 0.86 μg L -1 , 2.13 to 2.86 μg L -1 and 0.9972 to 0.9989 for Ni(II), Cu(III) and Zn(II) ions, respectively. The precision of the method, evaluated as the relative standard deviation (RSD) obtained after analyzing a series of 10 replicates, was between 2.6 % to 3.9 % for the trace metal ions. The proposed procedure was applied and validated by analyzing river water reference material for trace metals (SLRS-5) and spiking trace metal ions in some water samples. The recoveries of the analyte metal ions were between 94.7-101.2 %. (author)

  14. Effective removal of heavy metal ions Cd2+, Zn2+, Pb2+, Cu2+ from aqueous solution by polymer-modified magnetic nanoparticles

    International Nuclear Information System (INIS)

    Ge, Fei; Li, Meng-Meng; Ye, Hui; Zhao, Bao-Xiang

    2012-01-01

    We prepared novel Fe 3 O 4 magnetic nanoparticles (MNPs) modified with 3-aminopropyltriethoxysilane (APS) and copolymers of acrylic acid (AA) and crotonic acid (CA). The MNPs were characterized by transmission electron microscopy, X-ray diffraction, infra-red spectra and thermogravimetric analysis. We explored the ability of the MNPs for removing heavy metal ions (Cd 2+ , Zn 2+ , Pb 2+ and Cu 2+ ) from aqueous solution. We investigated the adsorption capacity of Fe 3 O 4 -APS-AA-co-CA at different pH in solution and metal ion uptake capacity as a function of contact time and metal ion concentration. Moreover, adsorption isotherms, kinetics and thermodynamics were studied to understand the mechanism of the synthesized MNPs adsorbing metal ions. In addition, we evaluated the effect of background electrolytes on the adsorption. Furthermore, we explored desorption and reuse of MNPs. Fe 3 O 4 -APS-AA-co-CA MNPs are excellent for removal of heavy metal ions such as Cd 2+ , Zn 2+ , Pb 2+ and Cu 2+ from aqueous solution. Furthermore, the MNPs could efficiently remove the metal ions with high maximum adsorption capacity at pH 5.5 and could be used as a reusable adsorbent with convenient conditions.

  15. Improving soft magnetic properties of Mn-Zn ferrite by rare earth ions doping

    Science.gov (United States)

    Zhong, X. C.; Guo, X. J.; Zou, S. Y.; Yu, H. Y.; Liu, Z. W.; Zhang, Y. F.; Wang, K. X.

    2018-04-01

    Mn-Zn ferrites doped with different Sm2O3, Gd2O3, Ce2O3 or Y2O3 were prepared by traditional ceramic technology using industrial pre-sintered powders. A small amount of Sm2O3, Gd2O3, Ce2O3 or Y2O3 can significantly improve the microstructure and magnetic properties. The single spinel phase structure can be maintained with the doping amount up to 0.07 wt.%. A refined grain structure and uniform grain size distribution can be obtained by doping. For all rare earth oxides, a small amount of doping can significantly increase the permeability and reduce the coercivity and magnetic core loss. The optimized doping amount for Sm2O3 or Gd2O3 is 0.01 wt.%, while for Ce2O3 or Y2O3 is 0.03 wt.%. A further increase of the doping content will lead to reduced soft magnetic properties. The ferrite sample with 0.01 wt.% Sm2O3 exhibits the good magnetic properties with permeability, loss, and coercivity of 2586, 316 W/kg, and 24A/m, respectively, at 200 mT and 100 kHz. The present results indicate that rare earth doping can be suggested to be one of the effective ways to improve the performance of soft ferrites.

  16. Optical spectroscopy of lanthanide ions in ZnO-TeO2 glasses.

    Science.gov (United States)

    Rolli, R; Wachtler, K; Wachtler, M; Bettinelli, M; Speghini, A; Ajò, D

    2001-09-01

    Zinc tellurite glasses of compositions 19ZnO-80TeO2-1Ln2O3 with Ln = Eu, Er, Nd and Tm were prepared by melt quenching. The absorption spectra were measured and from the experimental oscillator strengths of the f-->f transitions the Judd-Ofelt parameters ohm(lambda) were obtained. The values of the ohm(lambda) parameters are in the range usually observed for oxide glasses. For Nd3+ and Er3+, luminescence spectra in the near infrared were measured and the stimulated emission cross sections sigma(p) were evaluated for some laser transitions. The high values of sigma(p), especially for Nd3+, make them possible candidates for optical applications. Fluorescence line narrowing (FLN) spectra of the Eu3+ doped glass were measured at 20 K, and the energies of the Stark components of the 7F1 and 7F2 states were obtained. A crystal field analysis was carried out assuming a C2v site symmetry. The behaviour of the crystal field ratios B22/B20 and B44/B40 agrees reasonably well with the values calculated using the geometric model proposed by Brecher and Riseberg. The crystal field strength at the Eu3+ sites appears to be very low compared to other oxide glasses.

  17. Improving soft magnetic properties of Mn-Zn ferrite by rare earth ions doping

    Directory of Open Access Journals (Sweden)

    X. C. Zhong

    2018-04-01

    Full Text Available Mn-Zn ferrites doped with different Sm2O3, Gd2O3, Ce2O3 or Y2O3 were prepared by traditional ceramic technology using industrial pre-sintered powders. A small amount of Sm2O3, Gd2O3, Ce2O3 or Y2O3 can significantly improve the microstructure and magnetic properties. The single spinel phase structure can be maintained with the doping amount up to 0.07 wt.%. A refined grain structure and uniform grain size distribution can be obtained by doping. For all rare earth oxides, a small amount of doping can significantly increase the permeability and reduce the coercivity and magnetic core loss. The optimized doping amount for Sm2O3 or Gd2O3 is 0.01 wt.%, while for Ce2O3 or Y2O3 is 0.03 wt.%. A further increase of the doping content will lead to reduced soft magnetic properties. The ferrite sample with 0.01 wt.% Sm2O3 exhibits the good magnetic properties with permeability, loss, and coercivity of 2586, 316 W/kg, and 24A/m, respectively, at 200 mT and 100 kHz. The present results indicate that rare earth doping can be suggested to be one of the effective ways to improve the performance of soft ferrites.

  18. Composition-structure-property (Zn{sup 2+} and Ca{sup 2+} ion release) evaluation of Si-Na-Ca-Zn-Ce glasses: Potential components for nerve guidance conduits

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, X.F.; Kehoe, S. [Cork Institute of Technology, Cork (Ireland); Adhi, S.K. [Department of Instrumentation Science, University of Pune, Pune 411007 (India); Ajithkumar, T.G. [Central NMR Facility, National Chemical Laboratory, Pune 411008 (India); Moane, S. [Shannon ABC Research Group, Limerick Institute of Technology, Limerick (Ireland); O' Shea, H. [Cork Institute of Technology, Cork (Ireland); Boyd, D., E-mail: d.boyd@dal.ca [Department of Applied Oral Sciences, Biomaterials, and Oral Biology, Dalhousie University, Halifax, NS, B3H 3J5 (Canada)

    2011-04-08

    Bioactive glasses have demonstrated tailored therapeutic ion release, primarily with respect to the augmentation of hard tissues. However, controlled degradation and release of therapeutic ions from biomaterials may also play an important role in soft tissue regeneration such as repair of peripheral nerve discontinuities. In this study, three silica based glasses (0.5SiO{sub 2}-0.2CaO-0.13ZnO-XNa{sub 2}O-(0.17-X) CeO{sub 2}) where, (0.04 < X < 0.14) were synthesised and characterised. The local environment of the {sup 29}Si isotope was probed for each glass using {sup 29}Si MAS-NMR, whilst the thermal characteristics of each glass were examined using DTA. Following these analyses, ion release profiles for Ca{sup 2+} and Zn{sup 2+} were evaluated; an equivalent specific surface area of 1 m{sup 2} of each glass powder was incubated (37 deg. C) in 10 ml of citric acid buffer and TRIS-HCI buffer solution (pH 3.0 and pH 7.4 respectively) for incubation periods of up to 30 days. The Zn{sup 2+} concentration of each filtrate was analysed using flame Atomic Absorption Spectroscopy (Varian AA240FS Fast Sequential AAS) and the Ca{sup 2+} concentration of each filtrate was determined using Inductively Coupled Plasma-Mass Spectrometer (Varian 820 ICP-MS). Results obtained from the {sup 29}Si MAS-NMR spectra indicated Q{sup 2} structures pervading the network. An analytical model was proposed to analyse the ion release profiles for each glass, and indicated heterogeneous dissolution of glass networks. The ion release data demonstrates that ion release in the range (19.26-3130 ppm) for Ca{sup 2+} and in the range (5.97-4904 ppm) for Zn{sup 2+} occurred. Release of such elements, at appropriate levels, from peripheral nerve guidance conduits may be advantageous with respect to the repair of peripheral nerve discontinuities.

  19. One-Step Thermolysis Synthesis of Divalent Transition Metal Ions Monodoped and Tridoped CdS and ZnS Luminescent Nanomaterials

    Directory of Open Access Journals (Sweden)

    S. E. Saeed

    2014-01-01

    Full Text Available Mn2+, Co2+, or Ni2+ monodoped CdS (or ZnS and Mn2+-Co2+-Ni2+ tridoped CdS (or ZnS have been successfully synthesized by novel one-step thermolysis method using thiourea as a sulphur source. The synthesized nanomaterials were characterized by X-ray diffraction (XRD, transmission electron microscopy (TEM, and scanning electron microscopy (SEM. It is found that the average diameter and morphology of the synthesized samples varied with the nature of dopant ion. The successful doping of Mn2+-Co2+-Ni2+ tridoped ions into the host CdS (or ZnS was proved by the EDX spectra. The luminescence of CdS is only enhanced when monodoped with Mn2+ whereas it is enhanced when ZnS is either monodoped with Mn2+, Co2+, or Ni2+ or tridoped with Mn2+-Co2+-Ni2+. The synthesized samples could therefore offer opportunities for further fundamental research and technological applications.

  20. Self-assembled 3D ZnSnO3 hollow cubes@reduced graphene oxide aerogels as high capacity anode materials for lithium-ion batteries

    International Nuclear Information System (INIS)

    Wang, Yankun; Li, Dan; Liu, Yushan; Zhang, Jianmin

    2016-01-01

    Highlights: • 3D ZnSnO 3 hollow cubes@reducedgrapheneoxideaerogels(ZGAs) were fabricated. • The electrochemical properties of ZGAs were investigated for LIBs. • ZGAs demonstrated superior lithium storage performance. - Abstract: 3D ZnSnO 3 hollow cubes@reduced graphene oxide aerogels (ZGAs) were fabricated via a colloid electrostatic self-assembly method between the graphene oxide (GO) nanosheets and poly(diallyldimethylammonium chloride) (PDDA) modified ZnSnO 3 hollow cubes colloid, followed by hydrothermal and freeze-drying treatments. The unique porous architecture of ZnSnO 3 hollow cubes encapsulated by flexible reduced graphene oxide (rGO) sheets not only effectively retarded the huge volume expansion during repeated charge-discharge cycles, but also facilitated fast lithium ion and electron transport through 3D networks. The ZGAs exhibited significantly enhanced cycling stability (745.4 mAh g −1 after 100 cycles at a current of 100 mA g −1 ) and superior rate capability (as high as 552.6 mAh g −1 at 1200 mA g −1 ). The results indicate that the ZGAs are promising anode materials for high-performance lithium-ion batteries.

  1. A general approach for MFe2O4 (M = Zn, Co, Ni) nanorods and their high performance as anode materials for lithium ion batteries

    Science.gov (United States)

    Wang, Nana; Xu, Huayun; Chen, Liang; Gu, Xin; Yang, Jian; Qian, Yitai

    2014-02-01

    MFe2O4 (M = Zn, Co, Ni) nanorods are synthesized by a template-engaged reaction, with β-FeOOH nanorods as precursors which are prepared by a hydrothermal method. The final products are characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and high-resolution transmission electron microscopy (HRTEM). The electrochemical properties of the MFe2O4 (M = Zn, Co, Ni) nanorods are tested as the anode materials for lithium ion batteries. The reversible capacities of 800, 625 and 520 mAh g-1 are obtained for CoFe2O4, ZnFe2O4 and NiFe2O4, respectively, at the high current density of 1000 mA g-1 even after 300 cycles. The superior lithium-storage performances of MFe2O4 (M = Zn, Co, Ni) nanorods can be attributed to the one-dimensional (1D) nanostructure, which can shorten the diffusion paths of lithium ions and relax the strain generated during electrochemical cycling. These results indicate that this method is an effective, simple and general way to prepare good electrochemical properties of 1D spinel Fe-based binary transition metal oxides. In addition, the impact of different reaction temperatures on the electrochemical properties of MFe2O4 nanorods is also investigated.

  2. The fabrication of highly uniform ZnO/CdS core/shell structures using a spin-coating-based successive ion layer adsorption and reaction method

    International Nuclear Information System (INIS)

    Joo, Jinmyoung; Kim, Darae; Yun, Dong-Jin; Jun, Hwichan; Rhee, Shi-Woo; Lee, Jae Sung; Yong, Kijung; Jeon, Sangmin; Kim, Sungjee

    2010-01-01

    We developed a successive ion layer adsorption and reaction method based on spin-coating (spin-SILAR) and applied the method to the fabrication of highly uniform ZnO/CdS core/shell nanowire arrays. Because the adsorption, reaction, and rinsing steps occur simultaneously during spin-coating, the spin-SILAR method does not require rinsing steps between the alternating ion adsorption steps, making the growth process simpler and faster than conventional SILAR methods based on dip-coating (dip-SILAR). The ZnO/CdS core/shell nanowire arrays prepared by spin-SILAR had a denser and more uniform structure than those prepared by dip-SILAR, resulting in the higher power efficiency for use in photoelectrochemical cells.

  3. The fabrication of highly uniform ZnO/CdS core/shell structures using a spin-coating-based successive ion layer adsorption and reaction method

    Energy Technology Data Exchange (ETDEWEB)

    Joo, Jinmyoung; Kim, Darae; Yun, Dong-Jin; Jun, Hwichan; Rhee, Shi-Woo; Lee, Jae Sung; Yong, Kijung; Jeon, Sangmin [System on Chip Chemical Process Research, Department of Chemical Engineering, Pohang University of Science and Technology (POSTECH), Pohang (Korea, Republic of); Kim, Sungjee, E-mail: jeons@postech.ac.kr [Department of Chemistry, Pohang University of Science and Technology (POSTECH), Pohang (Korea, Republic of)

    2010-08-13

    We developed a successive ion layer adsorption and reaction method based on spin-coating (spin-SILAR) and applied the method to the fabrication of highly uniform ZnO/CdS core/shell nanowire arrays. Because the adsorption, reaction, and rinsing steps occur simultaneously during spin-coating, the spin-SILAR method does not require rinsing steps between the alternating ion adsorption steps, making the growth process simpler and faster than conventional SILAR methods based on dip-coating (dip-SILAR). The ZnO/CdS core/shell nanowire arrays prepared by spin-SILAR had a denser and more uniform structure than those prepared by dip-SILAR, resulting in the higher power efficiency for use in photoelectrochemical cells.

  4. Kinetics and exchange mechanism of Zn2+and Eu3+ ions on tin and zirconium silicates as a cation exchange materials

    International Nuclear Information System (INIS)

    Zakaria, E.S.; Ali, I.M.; Aly, H.F.

    2005-01-01

    Tin and zirconium silicates have been prepared with Sn/Si and Zr/Si molar ratios of 1 and 0.75, respectively. Kinetics and exchange studies of Zn 2+ and Eu 3+ ions on the prepared stannous and zirconium silicates have been carried out as a function of reaction temperature, particle diameters, solution concentration of the exchanging cations from water and alcohol-water mixture. The capacity of the exchangers for the studied cations from alcohol-water mixture was found higher than in pure aqueous solutions. The rate of exchange was dependent on particle diameters and independent on concentration of metal ions. The kinetic and thermodynamic parameters, vis. effective diffusion coefficients, activation energies and entropies of activation have been evaluated. Negative values of entropy, enthalpy and free energy of activation for Zn 2+ /M + and Eu 3+ /H + on both exchangers have been recorded at different conditions

  5. Chemical substitution of Cd ions by Hg in CdSe nanorods and nanodots: Spectroscopic and structural examination

    International Nuclear Information System (INIS)

    Prudnikau, Anatol; Artemyev, Mikhail; Molinari, Michael; Troyon, Michel; Sukhanova, Alyona; Nabiev, Igor; Baranov, Alexandr V.; Cherevkov, Sergey A.; Fedorov, Anatoly V.

    2012-01-01

    Highlights: ► We studied cadmium-by-mercury chemical substitution in CdSe nanocrystals. ► Zinc blende CdSe quantum dots can be easily converted to isostructural Cd x Hg 1−x Se. ► Wurtzite CdSe QDs require longer time to convert to a zinc blende Cd x Hg 1−x Se. ► Wurtzite CdSe nanorods transform to nanoheterogeneous luminescent Cd x Hg 1−x Se rods. - Abstract: The chemical substitution of cadmium by mercury in colloidal CdSe quantum dots (QDs) and nanorods has been examined by absorption, photoluminescence and Raman spectroscopy. The crystalline structure of original CdSe QDs used for Cd/Hg substitution (zinc blende versus wurtzite) shows a strong impact on the optical and structural properties of resultant Cd x Hg 1−x Se nanocrystals. Substitution of Cd by Hg in isostructural zinc blende CdSe QDs converts them to ternary Cd x Hg 1−x Se zinc blende nanocrystals with significant NIR emission. Whereas, the wurtzite CdSe QDs transformed first to ternary nanocrystals with almost no emission followed by slow structural reorganization to a NIR-emitting zinc blende Cd x Hg 1−x Se QDs. CdSe nanorods with intrinsic wurtzite structure show unexpectedly intense NIR emission even at early Cd/Hg substitution stage with PL active zinc blende Cd x Hg 1−x Se regions.

  6. Kinetic Study of Zn2+ and Cd2+ Ions Sorption by Ceric Oxide Powder

    International Nuclear Information System (INIS)

    Hassan, H.S.; Abd El-Rahman, K.M.; El Sayed, A.A.

    2008-01-01

    Ceric Oxide powder was chemically synthesized and characterized using infrared spectra and x-ray diffraction. The sorptive removal of Zinc and Cadmium ions from aqueous waste solution using synthetic ceric oxide powder was investigated using batch technique. Experiments were carried out as a function of ph, particle size, solute concentration and temperature. The uptake of zinc was found to be greater than that of cadmium. A comparison of kinetic models applied to the sorption process of each ion was evaluated for the pseudo first order, the pseudo second order, and homogeneous particle diffusion kinetic models, respectively. The results showed that both the pseudo second order and the homogeneous particle diffusion model (HPDM) were found to best correlate the experimental rate data. The numerical values of the rate constants and particle diffusion coefficients were determined from the graphical representation of the proposed models. Activation energy (Ε a ) and entropy (δ S * ) of activation for each sorption process were also calculated from the linearized form of Arrhenius equation

  7. Swift heavy ion irradiation of Cu-Zn-Al and Cu-Al-Ni alloys.

    Science.gov (United States)

    Zelaya, E; Tolley, A; Condo, A M; Schumacher, G

    2009-05-06

    The effects produced by swift heavy ions in the martensitic (18R) and austenitic phase (β) of Cu based shape memory alloys were characterized. Single crystal samples with a surface normal close to [210](18R) and [001](β) were irradiated with 200 MeV of Kr(15+), 230 MeV of Xe(15+), 350 and 600 MeV of Au(26+) and Au(29+). Changes in the microstructure were studied with transmission electron microscopy (TEM) and high resolution transmission electron microscopy (HRTEM). It was found that swift heavy ion irradiation induced nanometer sized defects in the 18R martensitic phase. In contrast, a hexagonal close-packed phase formed on the irradiated surface of β phase samples. HRTEM images of the nanometer sized defects observed in the 18R martensitic phase were compared with computer simulated images in order to interpret the origin of the observed contrast. The best agreement was obtained when the defects were assumed to consist of local composition modulations.

  8. On the interplay of point defects and Cd in non-polar ZnCdO films

    International Nuclear Information System (INIS)

    Zubiaga, A.; Reurings, F.; Tuomisto, F.; Plazaola, F.; García, J. A.; Kuznetsov, A. Yu.; Egger, W.; Zúñiga-Pérez, J.; Muñoz-Sanjosé, V.

    2013-01-01

    Non-polar ZnCdO films, grown over m- and r-sapphire with a Cd concentration ranging between 0.8% and 5%, have been studied by means of slow positron annihilation spectroscopy (PAS) combined with chemical depth profiling by secondary ion mass spectroscopy and Rutherford back-scattering. Vacancy clusters and Zn vacancies with concentrations up to 10 17 cm −3 and 10 18 cm −3 , respectively, have been measured inside the films. Secondary ion mass spectroscopy results show that most Cd stays inside the ZnCdO film but the diffused atoms can penetrate up to 1.3 μm inside the ZnO buffer. PAS results give an insight to the structure of the meta-stable ZnCdO above the thermodynamical solubility limit of 2%. A correlation between the concentration of vacancy clusters and Cd has been measured. The concentration of Zn vacancies is one order of magnitude larger than in as-grown non-polar ZnO films and the vacancy cluster are, at least partly, created by the aggregation of smaller Zn vacancy related defects. The Zn vacancy related defects and the vacancy clusters accumulate around the Cd atoms as a way to release the strain induced by the substitutional Cd Zn in the ZnO crystal.

  9. On the interplay of point defects and Cd in non-polar ZnCdO films

    Energy Technology Data Exchange (ETDEWEB)

    Zubiaga, A.; Reurings, F.; Tuomisto, F. [Department of Applied Physics, Aalto University, P.O. Box 11100, 00076 Aalto, Espoo (Finland); Plazaola, F. [Elektrizitatea eta Elektronika/Fisika Aplikatua II Sailak, Euskal Herriko Unibertsitatea, Posta Kutxatila 644, 48080 Bilbao (Spain); Garcia, J. A. [Fisika Aplikatua II Saila, Euskal Herriko Unibertsitatea, Posta Kutxatila 644, 48080 Bilbao (Spain); Kuznetsov, A. Yu. [Department of Physics, University of Oslo, P.O. Box 1048 Blindern, NO-0316 Oslo (Norway); Egger, W. [Inst. fuer Angewandte Physik und Messtechnik, Univ. der Bundeswehr Muenchen, 87755 Neubiberg (Germany); Zuniga-Perez, J. [CRHEA CNRS, F-06560 Valbonne (France); Munoz-Sanjose, V. [Dept. de Fisica Aplicada i Electromagnetisme, c/ Doctor Moliner 50, E-46100 Burjassot (Valencia) (Spain)

    2013-01-14

    Non-polar ZnCdO films, grown over m- and r-sapphire with a Cd concentration ranging between 0.8% and 5%, have been studied by means of slow positron annihilation spectroscopy (PAS) combined with chemical depth profiling by secondary ion mass spectroscopy and Rutherford back-scattering. Vacancy clusters and Zn vacancies with concentrations up to 10{sup 17} cm{sup -3} and 10{sup 18} cm{sup -3}, respectively, have been measured inside the films. Secondary ion mass spectroscopy results show that most Cd stays inside the ZnCdO film but the diffused atoms can penetrate up to 1.3 {mu}m inside the ZnO buffer. PAS results give an insight to the structure of the meta-stable ZnCdO above the thermodynamical solubility limit of 2%. A correlation between the concentration of vacancy clusters and Cd has been measured. The concentration of Zn vacancies is one order of magnitude larger than in as-grown non-polar ZnO films and the vacancy cluster are, at least partly, created by the aggregation of smaller Zn vacancy related defects. The Zn vacancy related defects and the vacancy clusters accumulate around the Cd atoms as a way to release the strain induced by the substitutional Cd{sub Zn} in the ZnO crystal.

  10. On the interplay of point defects and Cd in non-polar ZnCdO films

    Science.gov (United States)

    Zubiaga, A.; Reurings, F.; Tuomisto, F.; Plazaola, F.; García, J. A.; Kuznetsov, A. Yu.; Egger, W.; Zúñiga-Pérez, J.; Muñoz-Sanjosé, V.

    2013-01-01

    Non-polar ZnCdO films, grown over m- and r-sapphire with a Cd concentration ranging between 0.8% and 5%, have been studied by means of slow positron annihilation spectroscopy (PAS) combined with chemical depth profiling by secondary ion mass spectroscopy and Rutherford back-scattering. Vacancy clusters and Zn vacancies with concentrations up to 1017 cm-3 and 1018 cm-3, respectively, have been measured inside the films. Secondary ion mass spectroscopy results show that most Cd stays inside the ZnCdO film but the diffused atoms can penetrate up to 1.3 μm inside the ZnO buffer. PAS results give an insight to the structure of the meta-stable ZnCdO above the thermodynamical solubility limit of 2%. A correlation between the concentration of vacancy clusters and Cd has been measured. The concentration of Zn vacancies is one order of magnitude larger than in as-grown non-polar ZnO films and the vacancy cluster are, at least partly, created by the aggregation of smaller Zn vacancy related defects. The Zn vacancy related defects and the vacancy clusters accumulate around the Cd atoms as a way to release the strain induced by the substitutional CdZn in the ZnO crystal.

  11. Enhanced photoluminescence and thermal stability of divalent ions (Zn2+, Mg2+) assisted CaTiO3:Eu3+ perovskite phosphors for lighting applications

    Science.gov (United States)

    Singh, Dhananjay Kumar; Manam, J.

    2018-03-01

    Current study proposes the improved red emission of Zn2+ and Mg2+ ions incorporated CaTiO3:Eu3+ phosphors synthesized via the well-known solid-state reaction method. Under the 397 nm UV excitation, the Zn2+- and Mg2+-incorporated CaTiO3:0.15Eu3+ phosphor having orthorhombic structure with space group Pbnm exhibited an intense red emission at 619 nm. This can be credited to the hypersensitive 5D0 → 7F2 transition of Eu3+ ions, which is also indicative of the fact that the Eu3+ ions populated the non-inversion symmetry sites in the CaTiO3 lattices. The optimized composition CaTiO3:0.15Eu3+, 0.20Zn2+ and CaTiO3:0.15Eu3+, 0.10Mg2+ phosphors, pronounces in a magnificent enhancement of PL intensity by 5.5 and 2.5 times, respectively, as compared to CaTiO3:0.15 Eu3+ phosphor. From the temperature-dependent emission spectra, ΔEa were enunciated to be 0.101 and 0.086 eV for CaTiO3:0.15Eu3+, 0.20Zn2+ and CaTiO3:0.15Eu3+, 0.10Mg2+ phosphors, respectively, for thermal quenching. In addition, it can be better understood as related to the adequate thermal stability of 60% even at 450 and 420 K, respectively. Furthermore, the Judd-Ofelt theory was used to study the radiative intensity parameters of Eu3+ ions in the CaTiO3 lattices. The experimental results incited the bright prospects of synthesized ceramics as a promising candidate for lighting applications.

  12. Identification and precise measurements of the wavelengths of high-n transitions in N-, O-, and F-like Zn ions

    International Nuclear Information System (INIS)

    Fournier, K B; Faenov, A Ya; Pikuz, T A; Magunov, A I; Skobelev, I Yu; Belyaev, V S; Vinogradov, V I; Kyrilov, A S; Matafonov, A P; Flora, F; Bollanti, S; Lazzaro, P Di; Murra, D; Reale, A; Reale, L; Tomassetti, G; Ritucci, A; Francucci, M; Martellucci, S; Petrocelli, G

    2003-01-01

    We have observed spectra of highly charged zinc ions from a variety of laser-produced plasmas. High-precision measurements of transition wavelengths have been made in the range 6.7-8.6 A, with accuracies of ∼1 mA. Line identifications for high-n transitions (n ≤ 7) in the N-, O-, and F-like spectra of Zn XXIV, XXIII, XXII, respectively, are made by comparison with steady-state collisional-radiative models

  13. Green Template-Free Synthesis of Hierarchical Shuttle-Shaped Mesoporous ZnFe2 O4 Microrods with Enhanced Lithium Storage for Advanced Li-Ion Batteries.

    Science.gov (United States)

    Hou, Linrui; Hua, Hui; Lian, Lin; Cao, Hui; Zhu, Siqi; Yuan, Changzhou

    2015-09-07

    Invited for the cover of this issue is Changzhou Yuan and co-workers at the Anhui University of Technology. The image depicts hierarchical shuttle-shaped mesoporous ZnFe2 O4 micro-rods, as a low-cost yet high-performance anode, for advanced next-generation Li-ion batteries. Read the full text of the article at 10.1002/chem.201501876. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  14. Identification and precise measurements of the wavelengths of high-n transitions in N-, O-, and F-like Zn ions

    Energy Technology Data Exchange (ETDEWEB)

    Fournier, K B [Lawrence Livermore National Laboratory, PO Box 808, L-41, Livermore, CA 94550 (United States); Faenov, A Ya [Multicharged Ions Spectra Data Centre of VNIIFTRI, Moscow, 141570 (Russian Federation); Pikuz, T A [Multicharged Ions Spectra Data Centre of VNIIFTRI, Moscow, 141570 (Russian Federation); Magunov, A I [Multicharged Ions Spectra Data Centre of VNIIFTRI, Moscow, 141570 (Russian Federation); Skobelev, I Yu [Multicharged Ions Spectra Data Centre of VNIIFTRI, Moscow, 141570 (Russian Federation); Belyaev, V S [Central Research Institute of Machine Building, 4, Pionerskaya Street, Korolev, Moscow Region, 141070 (Russian Federation); Vinogradov, V I [Central Research Institute of Machine Building, 4, Pionerskaya Street, Korolev, Moscow Region, 141070 (Russian Federation); Kyrilov, A S [Central Research Institute of Machine Building, 4, Pionerskaya Street, Korolev, Moscow Region, 141070 (Russian Federation); Matafonov, A P [Central Research Institute of Machine Building, 4, Pionerskaya Street, Korolev, Moscow Region, 141070 (Russian Federation); Flora, F [ENEA, Dipartimento Innovazione, Settore Fisica Applicata, 00044 Frascati, Rome (Italy); Bollanti, S [ENEA, Dipartimento Innovazione, Settore Fisica Applicata, 00044 Frascati, Rome (Italy); Lazzaro, P Di [ENEA, Dipartimento Innovazione, Settore Fisica Applicata, 00044 Frascati, Rome (Italy); Murra, D [ENEA, Dipartimento Innovazione, Settore Fisica Applicata, 00044 Frascati, Rome (Italy); Reale, A [Dipartimento di Fisica e INFM, INFN g.c. LNGS, Universita dell' Aquila, 67010 L' Aquila (Italy); Reale, L [Dipartimento di Fisica e INFM, INFN g.c. LNGS, Universita dell' Aquila, 67010 L' Aquila (Italy); Tomassetti, G [Dipartimento di Fisica e INFM, INFN g.c. LNGS, Universita dell' Aquila, 67010 L' Aquila (Italy); Ritucci, A [Dipartimento di Fisica e INFM, INFN g.c. LNGS, Universita dell' Aquila, 67010 L' Aquila (Italy)] [and others

    2003-09-28

    We have observed spectra of highly charged zinc ions from a variety of laser-produced plasmas. High-precision measurements of transition wavelengths have been made in the range 6.7-8.6 A, with accuracies of {approx}1 mA. Line identifications for high-n transitions (n {<=} 7) in the N-, O-, and F-like spectra of Zn XXIV, XXIII, XXII, respectively, are made by comparison with steady-state collisional-radiative models.

  15. The role of annealing temperature and bio template (egg white) on the structural, morphological and magnetic properties of manganese substituted MFe2O4 (M=Zn, Cu, Ni, Co) nanoparticles

    Science.gov (United States)

    Ranjith Kumar, E.; Jayaprakash, R.; Kumar, Sanjay

    2014-02-01

    Manganese substituted ferrites (ZnFe2O4, CuFe2O4, NiFe2O4 and CoFe2O4) have been prepared in the bio template medium by using a simple evaporation method. The annealing temperature plays an important position on changing particle size and morphology of the mixed ferrite nanoparticles were found out by X-ray diffraction, transmission electron microscopy and scanning electron microscopy methods. The role of manganese substitution in the mixed ferrite nanoparticles were also analyzed for different annealing temperature. The substitution of Mn also creates a vital change in magnetic properties which is studied by using vibrating sample magnetometer (VSM). These spinel ferrites are decomposed to α-Fe2O3 after annealing above 550 °C in air. However, α-Fe2O3 phase was slowly vanished after ferrites annealing above 900 °C. The effect of this secondary phase on the structural change and magnetic properties of the mixed ferrite nanoparticles is discussed.

  16. A newly developed highly selective Zn2+-AcO- ion-pair sensor through partner preference: equal efficiency under solitary and colonial situation.

    Science.gov (United States)

    Karar, Monaj; Paul, Suvendu; Biswas, Bhaskar; Majumdar, Tapas; Mallick, Arabinda

    2018-05-10

    Unusual self-sorting of an ion-pair under highly crowded conditions driven by a synthesized intelligent molecule 2-((E)-(3-((E)-2-hydroxy-3-methoxybenzylideneamino)-2-hydroxypropyl imino)methyl)-6-methoxyphenol, hereafter HBP, is described. When a mixture of various metal salts was allowed to react with HBP, only a specific ion-pair ZnII/AcO- in the solution simultaneously reacted, resulting in high-fidelity ion-pair recognition of HBP. This phenomenon was evidenced by significant changes in the absorption spectra and huge enhancement in emission intensity of HBP. The property that one molecule preferring one particular cation-anion pair over others is a rare but interesting phenomenon. Thus, the potential to interact selectively with the targeted ion-pair resulting in the formation of a specific complex recognized HBP as a new class of molecule that might find future applications in real time and on-site monitoring and separation of new molecules.

  17. Influence of ZnO/MgO substitution on sintering, crystallisation, and bio-activity of alkali-free glass-ceramics

    Energy Technology Data Exchange (ETDEWEB)

    Kapoor, Saurabh [Department of Materials and Ceramics Engineering, University of Aveiro, CICECO, 3810-193 Aveiro (Portugal); Goel, Ashutosh [Department of Materials Science and Engineering, Rutgers, The State University of New Jersey, Piscataway, NJ 08854-8065 (United States); Correia, Ana Filipa [Department of Materials and Ceramics Engineering, University of Aveiro, CICECO, 3810-193 Aveiro (Portugal); Pascual, Maria J. [Instituto de Cerámica y Vidrio (CSIC), Kelsen 5, Campus de Cantoblanco, 28049 Madrid (Spain); Lee, Hye-Young; Kim, Hae-Won [Institute of Tissue Regeneration Engineering (ITREN) & College of Dentistry, Dankook University, Cheonan 330714 (Korea, Republic of); Department of Nanobiomedical Science & BK21 PLUS NBM Global Research Centre for Regenerative Medicine, Dankook University, Cheonan 330714 (Korea, Republic of); Ferreira, José M.F., E-mail: jmf@ua.pt [Department of Materials and Ceramics Engineering, University of Aveiro, CICECO, 3810-193 Aveiro (Portugal)

    2015-08-01

    The present study reports on the influence of partial replacement of MgO by ZnO on the structure, crystallisation behaviour and bioactivity of alkali-free bioactive glass-ceramics (GCs). A series of glass compositions (mol%): 36.07 CaO–(19.24 − x) MgO–x ZnO–5.61 P{sub 2}O{sub 5}–38.49 SiO{sub 2}–0.59 CaF{sub 2} (x = 2–10) have been synthesised by melt–quench technique. The structural changes were investigated by solid-state magic angle spinning nuclear magnetic resonance (MAS-NMR), X-ray diffraction and differential thermal analysis. The sintering and crystallisation behaviours of glass powders were studied by hot-stage microscopy and differential thermal analysis, respectively. All the glass compositions exhibited good densification ability resulting in well sintered and mechanically strong GCs. The crystallisation and mechanical behaviour were studied under non-isothermal heating conditions at 850 °C for 1 h. Diopside was the primary crystalline phase in all the GCs followed by fluorapatite and rankinite as secondary phases. Another phase named petedunnite was identified in GCs with ZnO content > 4 mol. The proliferation of mesenchymal stem cells (MSCs) and their alkaline phosphatase activity (ALP) on GCs was revealed to be Zn-dose dependent with the highest performance being observed for 4 mol% ZnO. - Highlights: • The addition of zinc to glasses decreased T{sub g} and promoted crystallisation. • Zinc enhanced the sintering ability and increased mechanical strength by 36%. • The apatite formation ability decreased with increasing Zn contents. • Zinc stimulated mesenchymal stem cell proliferation in a dose dependent manner.

  18. Influence of ZnO/MgO substitution on sintering, crystallisation, and bio-activity of alkali-free glass-ceramics

    International Nuclear Information System (INIS)

    Kapoor, Saurabh; Goel, Ashutosh; Correia, Ana Filipa; Pascual, Maria J.; Lee, Hye-Young; Kim, Hae-Won; Ferreira, José M.F.

    2015-01-01

    The present study reports on the influence of partial replacement of MgO by ZnO on the structure, crystallisation behaviour and bioactivity of alkali-free bioactive glass-ceramics (GCs). A series of glass compositions (mol%): 36.07 CaO–(19.24 − x) MgO–x ZnO–5.61 P 2 O 5 –38.49 SiO 2 –0.59 CaF 2 (x = 2–10) have been synthesised by melt–quench technique. The structural changes were investigated by solid-state magic angle spinning nuclear magnetic resonance (MAS-NMR), X-ray diffraction and differential thermal analysis. The sintering and crystallisation behaviours of glass powders were studied by hot-stage microscopy and differential thermal analysis, respectively. All the glass compositions exhibited good densification ability resulting in well sintered and mechanically strong GCs. The crystallisation and mechanical behaviour were studied under non-isothermal heating conditions at 850 °C for 1 h. Diopside was the primary crystalline phase in all the GCs followed by fluorapatite and rankinite as secondary phases. Another phase named petedunnite was identified in GCs with ZnO content > 4 mol. The proliferation of mesenchymal stem cells (MSCs) and their alkaline phosphatase activity (ALP) on GCs was revealed to be Zn-dose dependent with the highest performance being observed for 4 mol% ZnO. - Highlights: • The addition of zinc to glasses decreased T g and promoted crystallisation. • Zinc enhanced the sintering ability and increased mechanical strength by 36%. • The apatite formation ability decreased with increasing Zn contents. • Zinc stimulated mesenchymal stem cell proliferation in a dose dependent manner

  19. Comparative acid-base properties of the surface of components of the CdTe-ZnS system in series of substitutional solid solutions and their analogs

    Science.gov (United States)

    Kirovskaya, I. A.; Kasatova, I. Yu.

    2011-07-01

    The acid-base properties of the surface of solid solutions and binary components of the CdTe-ZnS system are studied by hydrolytic adsorption, nonaqueous conductometric titration, mechanochemistry, IR spectroscopy, and Raman scattering spectroscopy. The strength, nature, and concentration of acid centers on the original surface and that exposed to CO are determined. The changes in acid-base properties in dependence on the composition of the system under investigation in the series of CdB6, ZnB6 analogs are studied.

  20. Structure and optical properties of [In{sub 1−2x}Sn{sub x}Zn{sub x}]GaO{sub 3}(ZnO){sub m}

    Energy Technology Data Exchange (ETDEWEB)

    Eichhorn, Simon; Mader, Werner, E-mail: mader@uni-bonn.de

    2016-01-15

    Compounds of [In{sub 1−2x}Sn{sub x}Zn{sub x}]GaO{sub 3}(ZnO){sub 1} (x≤0.22) and [In{sub 1−2x}Sn{sub x}Zn{sub x}]GaO{sub 3}(ZnO){sub 2} (x≤0.42) were prepared by solid state processing proving a substantial solid solution of Sn in the layered compounds InGaO{sub 3}(ZnO){sub m} (m=1, 2). Single crystal X-ray diffraction of the compounds reveals two In{sup 3+} ions to be substituted by one Sn{sup 4+} and one Zn{sup 2+} at the octahedral layer preserving the average charge of +3 at these sites. The substitution does not lead to an ordering of the ions but proves for the first time that the octahedral site can be occupied by different ions while all characteristics of the layered structures remain unchanged. Consequences of indium substitution are (i) decrease of the a axis compared to InGaO{sub 3}(ZnO){sub m} according to smaller ionic radii of Sn{sup 4+} and Zn{sup 2+} compared to In{sup 3+} and (ii) shift of the optical band gap to higher energies shown by UV–vis measurements. - Graphical abstract: Substitution limits of indium in InGaO{sub 3}(ZnO){sub m} (IGZO) by Sn and Zn are studied for m=1, 2 by single crystal X-ray diffraction and micro-chemical analysis. - Highlights: • New Oxides [In{sub 1−2x}Sn{sub x}Zn{sub x}]GaO{sub 3}(ZnO){sub m} (m=1, 2) with IGZO type structure. • Sn and Zn substitute for In at octahedral sites. • Crystal structures were characterized by single crystal X-ray diffraction. • Optical band gap energies were determined by UV–vis spectroscopy.

  1. Removal of Ni(II), Zn(II) and Pb(II) ions from single metal aqueous solution using rice husk-based activated carbon

    Energy Technology Data Exchange (ETDEWEB)

    Taha, Mohd F., E-mail: faisalt@petronas.com.my; Shaharun, Maizatul S. [Fundamental and Applied Sciences Department, Universiti Teknologi PETRONAS, Bandar Seri Iskandar, 31750, Perak Darul Ridzuan (Malaysia); Shuib, Anis Suhaila, E-mail: anisuha@petronas.com.my; Borhan, Azry [Chemical Engineering Department, Universiti Teknologi PETRONAS, Bandar Seri Iskandar, 31750, Perak Darul Ridzuan (Malaysia)

    2014-10-24

    An attempt was made to investigate the potential of rice husk-based activated carbon as an alternative low-cost adsorbent for the removal of Ni(II), Zn(II) and Pb(II) ions from single aqueous solution. Rice husk-based activated carbon was prepared via treatment of rice husk with NaOH followed by the carbonization process at 400°C for 2 hours. Three samples, i.e. raw rice husk, rice husk treated with NaOH and rice husk-based activated carbon, were analyzed for their morphological characteristics using field-emission scanning electron microscope/energy dispersive X-ray (FESEM/EDX). These samples were also analyzed for their carbon, hydrogen, nitrogen, oxygen and silica contents using CHN elemental analyzer and FESEM/EDX. The porous properties of rice husk-based activated carbon were determined by Brunauer-Emmett-Teller (BET) surface area analyzer, and its surface area and pore volume were 255 m{sup 2}/g and 0.17 cm{sup 2}/g, respectively. The adsorption studies for the removal of Ni(II), Zn(II) and Pb(II) ions from single metal aqueous solution were carried out at a fixed initial concentration of metal ion (150 ppm) with variation amount of adsorbent (rice husk-based activated carbon) as a function of varied contact time at room temperature. The concentration of each metal ion was analyzed using atomic absorption spectrophotometer (AAS). The results obtained from adsorption studies indicate the potential of rice husk as an economically promising precursor for the preparation of activated carbon for removal of Ni(II), Zn(II) and Pb(II) ions from single aqueous solution. Isotherm and kinetic model analyses suggested that the experimental data of adsorption studies fitted well with Langmuir, Freundlich and second-order kinetic models.

  2. Usage of X-ray absorption spectroscopy and extractive fractionation in studies of the Cu (II and Zn (II ions in soils

    Directory of Open Access Journals (Sweden)

    Dina Nevidomskaya

    2014-12-01

    Full Text Available XANES spectroscopy is an effective method for the study of bonds between metals and soil components. The study of structural organization in different soil samples and soil phases saturated with Cu2+ and Zn2+ ions by using XANES allowed determining the mechanism of their interaction with soil phases and all the chemical bindings taken place in the course of this process. Changes in the structure of the metal ion, in particular breakdown of the symmetry of electron orbits of atoms, take place due to interaction with soil components. Application of this method demonstrated that the state of copper and zinc introduced in chernozem as oxides did not change after one year of incubation. Copper is absorbed after being introduced as soluble salts, and copper ions are incorporated in the octahedral and tetrahedral sites of minerals and bonded with humic materials at the expense of covalent bond and the formation of coordination humate copper complexes. Zinc included into octahedric structures of layered minerals and hydro(oxides can be inner-and outer-sphere adsorbed. It is shown that the action of the metal bound to soil components becomes weakened in case of increasing the Cu and Zn load (from 2000 to 10000 mg/kg especially applied in the form of soluble salts. Extractive fractionation of metal compounds in chernozem samples, artificially contaminated with copper and zinc salts serves as evidence of absorbing the applied Cu2+ ions by the soil organic matter and Zn2+ ions – by silicates, carbonates, and Fe-Mn oxides.

  3. Adhesion profile and differentiation capacity of human adipose tissue derived mesenchymal stem cells grown on metal ion (Zn, Ag and Cu) doped hydroxyapatite nano-coated surfaces.

    Science.gov (United States)

    Bostancioglu, R Beklem; Gurbuz, Mevlut; Akyurekli, Ayse Gul; Dogan, Aydin; Koparal, A Savas; Koparal, A Tansu

    2017-07-01

    Accelerated Mesenchymal Stem Cells (MSCs) condensation and robust MSC-matrix and MSC-MSC interactions on nano-surfaces may provide critical factors contributing to such events, likely through the orchestrated signal cascades and cellular events modulated by the extracellular matrix. In this study, human adipose tissue derived mesenchymal stem cells (hMSC)', were grown on metal ion (Zn, Ag and Cu) doped hydroxyapatite (HAP) nano-coated surfaces. These metal ions are known to have different chemical and surface properties; therefore we investigated their respective contributions to cell viability, cellular behavior, osteogenic differentiation capacity and substrate-cell interaction. Nano-powders were produced using a wet chemical process. Air spray deposition was used to accumulate the metal ion doped HAP films on a glass substrate. Cell viability was determined by MTT, LDH and DNA quantitation methods Osteogenic differentiation capacity of hMSCs was analyzed with Alizarin Red Staining and Alkaline Phosphatase Specific Activity. Adhesion of the hMSCs and the effect of cell adhesion on biomaterial biocompatibility were explored through cell adhesion assay, immunofluorescence staining for vinculin and f-actin cytoskeleton components, SEM and microarray including 84 known extracellular matrix proteins and cell adhesion pathway genes, since, adhesion is the first step for good biocompability. The results demonstrate that the viability and osteogenic differentiation of the hMSCs (in growth media without osteogenic stimulation) and cell adhesion capability are higher on nanocoated surfaces that include Zn, Ag and/or Cu metal ions than commercial HAP. These results reveal that Zn, Ag and Cu metal ions contribute to the biocompatibility of exogenous material. Copyright © 2017 Elsevier B.V. All rights reserved.

  4. Effect of chromium substitution on the dielectric properties of mixed Ni-Zn ferrite prepared by WOWS sol–gel technique

    International Nuclear Information System (INIS)

    Ashtar, M.; Munir, A.; Anis-ur-Rehman, M.; Maqsood, A.

    2016-01-01

    Graphical abstract: Variation of AC conductivity (σ AC ) as a function of natural log of angular frequency (lnω) for Ni 0.5 Zn 0.5 Fe 2-x Cr x O 4 nanoferrites at room temperature. - Highlights: • Cr doped mixed Ni-Zn ferrites were successfully synthesized by a newly developed WOWS sol gel technique. • The specific surface area and specific surface area to volume ratio increased with decrease in particle size. • The resonance peaks appeared in dielectric loss graphs, shifting towards low frequency with the increase in Cr concentration. • The prepared samples have the lowest values of the dielectric constant. • The dielectric constant were observed to be inversely proportional to square root of the AC resistivity. - Abstract: Cr +3 doped Ni-Zn nanoferrite samples with composition Ni 0.5 Zn 0.5 Fe 2-x Cr x O 4 (x = 0.1, 0.2, 0.3, 0.4) were synthesized With Out Water and Surfactant (WOWS) sol-gel technique. The structural, morphological and dielectric properties of the samples were investigated. The lattice constant, crystallite size, theoretical density and porosity of each sample were obtained from X-ray diffraction (XRD) data. The specific surface area and specific surface area to volume ratio increased with the decrease in the size of Cr +3 doped Ni-Zn ferrite nanoparticles, as the concentration of Cr +3 increased. The SEM analysis revealed that the particles were of nano size and of spherical shape. The dielectric parameters such as dielectric constant (ε′) and dielectric loss (tanδ) of all the samples as a function of frequency at room temperature were measured. The AC conductivity (σ AC ) was determined from the dielectric parameters, which showed increasing trend with the rise in frequency.

  5. Influence of helium-ion bombardment on the optical properties of ZnO nanorods/p-GaN light-emitting diodes

    Science.gov (United States)

    Alvi, Naveed Ul Hassan; Hussain, Sajjad; Jensen, Jen; Nur, Omer; Willander, Magnus

    2011-12-01

    Light-emitting diodes (LEDs) based on zinc oxide (ZnO) nanorods grown by vapor-liquid-solid catalytic growth method were irradiated with 2-MeV helium (He+) ions. The fabricated LEDs were irradiated with fluencies of approximately 2 × 1013 ions/cm2 and approximately 4 × 1013 ions/cm2. Scanning electron microscopy images showed that the morphology of the irradiated samples is not changed. The as-grown and He+-irradiated LEDs showed rectifying behavior with the same I-V characteristics. Photoluminescence (PL) measurements showed that there is a blue shift of approximately 0.0347 and 0.082 eV in the near-band emission (free exciton) and green emission of the irradiated ZnO nanorods, respectively. It was also observed that the PL intensity of the near-band emission was decreased after irradiation of the samples. The electroluminescence (EL) measurements of the fabricated LEDs showed that there is a blue shift of 0.125 eV in the broad green emission after irradiation and the EL intensity of violet emission approximately centered at 398 nm nearly disappeared after irradiations. The color-rendering properties show a small decrease in the color-rendering indices of 3% after 2 MeV He+ ions irradiation.

  6. Influence of N-octanoyl-N-methylglucamine and N-decanoyl-N-methylglucamine on the kinetics and mechanism of Zn2+ ions electroreduction

    International Nuclear Information System (INIS)

    Nieszporek, Jolanta; Dagci, Kader

    2014-01-01

    Graphical abstract: - Highlights: • The inhibiting influence of two neutral surfactants OMG and DMG on Zn 2+ electroreduction was shown. • Larger inhibiting effect is observed in the presence of N-decanoyl-N-methylglucamine (DMG). • The first step is slower thus determining the rate of the whole process. • Different mechanistic schemes assuming a two-step character of Zn 2+ electroreduction were discussed. • At a certain surfactant concentration the change of electroreduction mechanism is observed. - Abstract: We examined the electroreduction of Zn 2+ in NaClO 4 as a supporting electrolyte in the presence of neutral surfactants of various molecular sizes on a mercury electrode. The studies were carried out at different temperatures. The inhibiting effect of N-decanoyl-N-methylglucamine (DMG) on the kinetics of the investigated electrode process was stronger compared to that of N-octanoyl-N-methylglucamine (OMG). In order to describe the Zn 2+ reduction in the studied systems, four mechanisms were taken into consideration: EE, CE, IA, and IE. Ion transfer was considered as the most probable first step, whereas electron transfer or reagent adsorption were postulated to be the second step of the electrode process

  7. Chemical effect of Si+ ions on the implantation-induced defects in ZnO studied by a slow positron beam

    Science.gov (United States)

    Jiang, M.; Wang, D. D.; Chen, Z. Q.; Kimura, S.; Yamashita, Y.; Mori, A.; Uedono, A.

    2013-01-01

    Undoped ZnO single crystals were implanted with 300 keV Si+ ions to a dose of 6 × 1016 cm-2. A combination of X-ray diffraction (XRD), positron annihilation, Raman scattering, high resolution transmission electron microscopy (HRTEM), and photoluminescence (PL) was used to study the microstructure evolution after implantation and subsequent annealing. A very large increase of Doppler broadening S parameters in Si+-implanted region was detected by using a slow positron beam, indicating that vacancy clusters or microvoids are induced by implantation. The S parameters increase further after annealing up to 700 °C, suggesting agglomeration of these vacancies or microvoids to larger size. Most of these defects are removed after annealing up to 1100 °C. The other measurements such as XRD, Raman scattering, and PL all indicate severe damage and even disordered structure induced by Si+ implantation. The damage and disordered lattice shows recovery after annealing above 700 °C. Amorphous regions are observed by HRTEM measurement, directly testifies that amorphous phase is induced by Si+ implantation in ZnO. Analysis of the S - W correlation and the coincidence Doppler broadening spectra gives direct evidence of SiO2 precipitates in the sample annealed at 700 °C, which strongly supports the chemical effect of Si ions on the amorphization of ZnO lattice.

  8. In vitro metal ion release and biocompatibility of amorphous Mg67Zn28Ca5 alloy with/without gelatin coating

    International Nuclear Information System (INIS)

    Chan, W.Y.; Chian, K.S.; Tan, M.J.

    2013-01-01

    Amorphous zinc-rich Mg–Zn–Ca alloys have exhibited good tissue compatibility and low hydrogen evolution in vivo. However, suboptimal cell–surface interaction on magnesium alloy surface observed in vitro could lead to reduced integration with host tissue for regenerative purpose. This study aims to improve cell–surface interaction of amorphous Mg 67 Zn 28 Ca 5 alloy by coating a gelatin layer by electrospinning. Coated/uncoated alloys were immersed and extracted for 3 days under different CO 2 . The immersion results showed that pH and metal ion release in the alloy extracts were affected by gelatin coating and CO 2 , suggesting their roles in alloy biocorrosion and a mechanism has been proposed for the alloy–CO 2 system with/without coating. Cytotoxicity results are evident that gelatin-coated alloy with 2-day crosslinking not only exhibited no indirect cytotoxicity, but also supported attachment of L929 and MG63 cell lines around/on the alloy with high viability. Therefore, amorphous Mg 67 Zn 28 Ca 5 alloy coated with gelatin by electrospinning technique provides a useful method to improve alloy biocompatibility. - Highlights: • Electrospinning is a new method to coat amorphous Mg 67 Zn 28 Ca 5 alloy with gelatin. • Gelatin-coated alloy has differential effect on pH and ion release at various CO 2 . • L929 cell proliferation correlates with Mg 2+ level in alloy extracts. • Biomimetic gelatin coating significantly improves cell–surface interaction

  9. MOF-Derived ZnO Nanoparticles Covered by N-Doped Carbon Layers and Hybridized on Carbon Nanotubes for Lithium-Ion Battery Anodes.

    Science.gov (United States)

    Zhang, Hui; Wang, Yunsong; Zhao, Wenqi; Zou, Mingchu; Chen, Yijun; Yang, Liusi; Xu, Lu; Wu, Huaisheng; Cao, Anyuan

    2017-11-01

    Metal-organic frameworks (MOFs) have many promising applications in energy and environmental areas such as gas separation, catalysis, supercapacitors, and batteries; the key toward those applications is controlled pyrolysis which can tailor the porous structure, improve electrical conductivity, and expose metal ions in MOFs. Here, we present a systematic study on the structural evolution of zeolitic imidazolate frameworks hybridized on carbon nanotubes (CNTs) during the carbonization process. We show that a number of typical products can be obtained, depending on the annealing time, including (1) CNTs wrapped by relatively thick carbon layers, (2) CNTs grafted by ZnO nanoparticles which are covered by thin nitrogen-doped carbon layers, and (3) CNTs grafted by aggregated ZnO nanoparticles. We also investigated the electrochemical properties of those hybrid structures as freestanding membrane electrodes for lithium ion batteries, and the second one (CNT-supported ZnO covered by N-doped carbon) shows the best performance with a high specific capacity (850 mA h/g at a current density of 100 mA/g) and excellent cycling stability. Our results indicate that tailoring and optimizing the MOF-CNT hybrid structure is essential for developing high-performance energy storage systems.

  10. Pyro-Synthesis of Nanostructured Spinel ZnMn2O4/C as Negative Electrode for Rechargeable Lithium-Ion Batteries

    International Nuclear Information System (INIS)

    Alfaruqi, Muhammad Hilmy; Rai, Alok Kumar; Mathew, Vinod; Jo, Jeonggeun; Kim, Jaekook

    2015-01-01

    ZnMn 2 O 4 /C nanoparticles are synthesized by one step polyol assisted pyro-synthesis for use as the anode in rechargeable lithium ion batteries without any post heat treatment. The as-prepared ZnMn 2 O 4 /C is tetragonal with a spherical particle size in the range of 10–30 nm. Electrochemical measurements were performed using the as-prepared powders as the active material for a lithium-ion cell. The nanoparticle electrode delivered an initial charge capacity of 666.1 mAh g −1 and exhibited a capacity retention of ∼81% (539.4 mAh g −1 ) after 50 cycles. The capacity enhancement in the as-prepared ZnMn 2 O 4 /C may be explained on the basis of the polyol medium that enables to develop a sufficient carbon network that can act as electrical conduits during electrochemical reactions. The carbon network appears to enhance the particle-connectivity and hence improve the electronic conductivities

  11. Irregular distribution of metal ions in ferrites prepared by co-precipitation technique structure analysis of Mn-Zn ferrite using extended X-ray absorption fine structure

    International Nuclear Information System (INIS)

    Jeyadevan, B.; Tohji, K.; Nakatsuka, K.; Narayanasamy, A.

    2000-01-01

    The tetrahedral/octahedral site occupancy of non-magnetic zinc ion, added to maximize the net magnetic moment of mixed ferrites has been found to depend on the method of preparation. In this paper, we qualitatively analyze the metal ion distribution in Mn-Zn ferrite particles prepared by co-precipitation and ceramic methods using extended X-ray absorption fine structure (EXAFS) technique. The results suggest that the differences observed in the magnetic properties of the samples prepared by different methods are not only due to the difference in particle size but also due to the difference in cation distribution. The difference in cation distributions between ferrites of similar composition prepared differently has been found to depend on the crystal field stability energies of the metal ion of interest and associated cations

  12. Facile fabrication of high-performance InGaZnO thin film transistor using hydrogen ion irradiation at room temperature

    Energy Technology Data Exchange (ETDEWEB)

    Ahn, Byung Du [School of Electrical and Electronic Engineering, 50, Yonsei University, Seoul 120-749 (Korea, Republic of); Park, Jin-Seong [Division of Materials Science and Engineering, Hanyang University, Seoul 133-791 (Korea, Republic of); Chung, K. B., E-mail: kbchung@dongguk.edu [Division of Physics and Semiconductor Science, Dongguk University, Seoul 100-715 (Korea, Republic of)

    2014-10-20

    Device performance of InGaZnO (IGZO) thin film transistors (TFTs) are investigated as a function of hydrogen ion irradiation dose at room temperature. Field effect mobility is enhanced, and subthreshold gate swing is improved with the increase of hydrogen ion irradiation dose, and there is no thermal annealing. The electrical device performance is correlated with the electronic structure of IGZO films, such as chemical bonding states, features of the conduction band, and band edge states below the conduction band. The decrease of oxygen deficient bonding and the changes in electronic structure of the conduction band leads to the improvement of device performance in IGZO TFT with an increase of the hydrogen ion irradiation dose.

  13. Enhanced electrochemical performance of a ZnO-MnO composite as an anode material for lithium ion batteries.

    Science.gov (United States)

    Song, Min Seob; Nahm, Sahn; Cho, Won Il; Lee, Chongmok

    2015-09-28

    A ZnO-MnO composite was synthesized using a simple solvothermal method combined with a high-temperature treatment. To observe the phase change during the heating process, in situ high-temperature XRD analysis was performed under vacuum conditions. The results indicated that ZnMn2O4 transformed into the ZnO-MnO composite phase starting from 500 °C and that this composite structure was retained until 700 °C. The electrochemical performances of the ZnO-MnO composite electrode were evaluated through galvanostatic discharge-charge tests and cyclic voltammetry analysis. Its initial coulombic efficiency was significantly improved to 68.3% compared to that of ZnMn2O4 at 54.7%. Furthermore, the ZnO-MnO composite exhibited improved cycling performance and enhanced rate capability compared with untreated ZnMn2O4. To clarify the discharge-charge mechanism of the ZnO-MnO composite electrode, the structural changes during the charge and discharge processes were also investigated using ex situ XRD and TEM.

  14. Development of surface functionalized ZnO-doped LiFePO{sub 4}/C composites as alternative cathode material for lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Saroha, Rakesh [Department of Applied Physics, Delhi Technological University, Delhi 110042 (India); Panwar, Amrish K., E-mail: amrish.phy@dce.edu [Department of Applied Physics, Delhi Technological University, Delhi 110042 (India); Sharma, Yogesh [Department of Physics, IIT Roorkee, Roorkee, Uttarakhand 247667 (India); Tyagi, Pawan K. [Department of Applied Physics, Delhi Technological University, Delhi 110042 (India); Ghosh, Sudipto [Department of Metallurgical & Materials Engineering, IIT Kharagpur, West Bengal 721302 (India)

    2017-02-01

    Highlights: • Pristine LFP and ZnO-doped LFP/C samples have been synthesized using sol-gel assisted ball milling route. • Electronic conductivity of pristine LFP increases to 10{sup 2}-10{sup 3} orders of magnitude for ZnO doped LFP/C samples. • AFM results indicate the presence of more volumetric charge density at the surface for ZnO-doped LFP/C sample. • LFPZ2.5 shows best cycling and rate performances among all the prepared samples. • Lithium ion diffusion coefficient increases significantly. - Abstract: Surface modified olivine-type LiFePO{sub 4}/C-ZnO doped samples were synthesized using sol-gel assisted ball-milling route. In this work, the influence of ZnO-doping on the physiochemical, electrochemical and surface properties such as charge separation at solid-liquid interphase, surface force gradient, surface/ionic conductivity of pristine LiFePO{sub 4}/C (LFP) has been investigated thoroughly. Synthesized samples were characterized using X-ray diffraction, scanning electron microscopy, atomic force microscopy, and transmission electron microscopy. All the synthesized samples were indexed to the orthorhombic phase with Pnma space group. Pristine LiFePO{sub 4} retain its structure for higher ZnO concentrations (i.e. 2.5 and 5.0 wt.% of LFP). Surface topography and surface force gradient measurements by EFM revealed that the kinetics of charge carriers, e{sup −}/Li{sup +} is more in ZnO-doped LFP samples, which may be attributed to diffusion or conduction process of the charges present at the surface. Among all the synthesized samples LFP/C with 2.5 wt.% of ZnO (LFPZ2.5) displays the highest discharge capacity at all C-rates and exhibit excellent rate performance. LFPZ2.5 delivers a specific discharge capacity of 164 (±3) mAh g{sup −1} at 0.1C rate. LFPZ2.5 shows best cycling performance as it provides a discharge capacity of 135 (±3) mAh g{sup −1} at 1C rate and shows almost 95% capacity retention after 50 charge/discharge cycles. Energy

  15. Modulating the electronic properties of asymmetric push–pull and symmetric Zn(II)-diarylporphyrinates with para substituted phenylethynyl moieties in 5,15 meso positions: A combined electrochemical and spectroscopic investigation

    International Nuclear Information System (INIS)

    Mussini, Patrizia Romana; Orbelli Biroli, Alessio; Tessore, Francesca; Pizzotti, Maddalena; Biaggi, Cinzia; Di Carlo, Gabriele; Lobello, Maria Grazia; De Angelis, Filippo

    2012-01-01

    Graphical abstract: - Abstract: Push–pull Zn(II)-porphyrinates have recently shown attracting performances as light harvesting systems in dye-sensitized solar cells (DSSCs). To fully exploit their intrinsically high efficiency it is important to finely tune their HOMO and LUMO levels, which can be achieved by proper choice of the push and pull substituents. Of course such target-oriented molecular design requires the availability of reliable relationships between molecular structure and electronic properties; therefore we have carried out a combined electrochemical, spectroscopic and computational investigation on a wide, systematic range of Zn(II)-porphyrinates 5,15 meso substituted with phenylethynyl linkers, including a first symmetric series carrying on the opposite terminals the same substituent (-N(CH 3 ) 2 , -OCH 3 , -COOCH 3 , -COOH, -NO 2 ); and a second push–pull one, with the terminal positions carrying one donor and one acceptor group belonging to the series above. Moreover, two suitably modified porphyrins allowed evaluation of the effects of (i) the presence or absence of the phenyl group in the linker between the porphyrin core and the acceptor group, and (ii) the effect of perfluorination on the same phenyl group. A rationalization scheme is proposed encompassing the whole porphyrin set, affording inter alia interesting clues on the different localization of the redox centres and effective conjugation between the porphyrin core and the side chains as a function of the molecular design.

  16. Suppression of Na interstitials in Na-F codoped ZnO

    Science.gov (United States)

    Huo, Wenxing; Mei, Zengxia; Tang, Aihua; Liang, Huili; Du, Xiaolong

    2018-04-01

    Controlling the formation of interstitial Na (Nai) self-compensating defects has been a long-term physics problem for effective Na doping in ZnO. Herein, we present an experimental approach to the suppression of Nai defects in ZnO via Na and F codoping under an oxygen-rich condition during the molecular beam epitaxy growth process. It is found that the incorporation of such large numbers of Na and F dopants (˜1020 cm-3) does not cause an obvious influence on the lattice parameters. Hall-effect measurements demonstrate that F doping efficiently raises the Fermi level (EF) of ZnO films, which is expected to make the formation energy of Nai and NaZn increase and decrease, respectively. Most of the Na atoms occupy the substitutional Zn sites, and the formation of Nai is suppressed consequently. Secondary ion mass spectrometry measurements reveal that F and Na atoms are tightly bonded together due to their strong Coulomb interaction. The enhanced deep level emission (DLE) in ZnO:Na-F is ascribed to the considerable amount of isolated Zn vacancy (VZn) defects induced by the elevated EF and the formation of neutral (" separators="| FO + - Na Zn - ) 0 complexes. On the other hand, formation of (" separators="| FO + - VZn 2 - ) - complexes in ZnO:F exhausts most of the isolated Zn vacancies, leading to the disappearance of the DLE band.

  17. Influence of ligand coordination of cobalt ions on structural properties of ZnO-ZnF{sub 2}-B{sub 2}O{sub 3} glass system by means of spectroscopic studies

    Energy Technology Data Exchange (ETDEWEB)

    Naresh, P.; Naga Raju, G. [Department of Physics, Acharya Nagarjuna University-Nuzvid Campus, Nuzvid 521201, A.P. (India); Srinivasa Rao, Ch. [Department of Physics, Andhra Loyola College, Vijayawada 520008, A.P. (India); Prasad, S.V.G.V.A. [Department of Physics, Andhra Jateeya Kalasala, Machilipatnam 520001, A.P. (India); Ravi Kumar, V. [Department of Physics, Acharya Nagarjuna University-Nuzvid Campus, Nuzvid 521201, A.P. (India); Veeraiah, N., E-mail: nvr8@rediffmail.com [Department of Physics, Acharya Nagarjuna University-Nuzvid Campus, Nuzvid 521201, A.P. (India)

    2012-02-15

    The glasses of the composition 10ZnO-30ZnF{sub 2}-60B{sub 2}O{sub 3} doped with different concentrations of CoO were prepared. Differential scanning calorimetric (DSC) studies, optical absorption, photoluminescence and infrared spectra of these glasses have been carried out. DSC studies have indicated that the resistance of the glass against devitrification increases with the increase in the concentration of CoO. Optical absorption spectra have exhibited one octahedral band due to {sup 4}T{sub 1g}(F){yields}{sup 2}T{sub 1g}(H) and two tetrahedral bands due to {sup 4}A{sub 2}({sup 4}F){yields}{sup 4}T{sub 1}({sup 4}P) {sup 4}A{sub 2}({sup 4}F){yields}{sup 4}T{sub 1}({sup 4}F) transitions of Co{sup 2+} ions at about 525, 570 and 1400 nm, respectively. As the concentration of CoO is increased the tetrahedral bands are observed to grow at the expense of octahedral band. The luminescence spectra have exhibited two emission bands in the spectral regions of 600-700 nm and 800-900 nm due to {sup 4}T{sub 1}({sup 4}P){yields}{sup 4}A{sub 2}({sup 4}F) and {sup 4}T{sub 1}({sup 4}P){yields}{sup 4}T{sub 2}({sup 4}F) tetrahedral transitions of Co{sup 2+} ions, respectively. With the increasing content of cobalt ions in the glass matrix, the half width and intensity of these bands are observed to increase. The analysis of the results of these two spectra coupled with IR spectra has indicated that as the concentration of CoO is increased in the glass matrix, the tetrahedral occupancy of cobalt ions dominates over the octahedral occupancy and increase the rigidity of the glass network.

  18. Narrowing the gap: from semiconductor to semimetal in the homologous series of rare-earth zinc arsenides RE(2-y)Zn4As4·n(REAs) and Mn-substituted derivatives RE(2-y)Mn(x)Zn(4-x)As4·n(REAs) (RE = La-Nd, Sm, Gd).

    Science.gov (United States)

    Lin, Xinsong; Tabassum, Danisa; Mar, Arthur

    2015-12-14

    A homologous series of ternary rare-earth zinc arsenides, prepared by reactions of the elements at 750 °C, has been identified with the formula RE(2-y)Zn4As4·n(REAs) (n = 2, 3, 4) for various RE members. They adopt trigonal structures: RE(4-y)Zn4As6 (RE = La-Nd), space group R3̄m1, Z = 3; RE(5-y)Zn4As7 (RE = Pr, Nd, Sm, Gd), space group P3̄m1, Z = 1; RE(6-y)Zn4As8 (RE = La-Nd, Sm, Gd), space group R3̄m1, Z = 3. The Zn atoms can be partially substituted by Mn atoms, resulting in quaternary derivatives RE(2-y)Mn(x)Zn(4-x)As4·n(REAs). Single-crystal structures were determined for nine ternary and quaternary arsenides RE(2-y)M4As4·n(REAs) (M = Mn, Zn) as representative examples of these series. The structures are built by stacking close-packed nets of As atoms, sometimes in very long sequences, with RE atoms occupying octahedral sites and M atoms occupying tetrahedral sites, resulting in an intergrowth of [REAs] and [M2As2] slabs. The recurring feature of all members of the homologous series is a sandwich of [M2As2]-[REAs]-[M2As2] slabs, while rocksalt-type blocks of [REAs] increase in thickness between these sandwiches with higher n. Similar to the previously known related homologous series REM(2-x)As2·n(REAs) which is deficient in M, this new series RE(2-y)M4As4·n(REAs) exhibits deficiencies in RE to reduce the electron excess that would be present in the fully stoichiometric formulas. Enthalpic and entropic factors are considered to account for the differences in site deficiencies in these two homologous series. Band structure calculations indicate that the semiconducting behaviour of the parent n = 0 member (with CaAl2Si2-type structure) gradually evolves, through a narrowing of the gap between valence and conduction bands, to semimetallic behaviour as the number of [REAs] blocks increases, to the limit of n = ∞ for rocksalt-type REAs.

  19. Effect on the structural, DC resistivity and magnetic properties of Zr and Cu co-SubstitutedNi0.5Zn0.5Fe2O4using sol-gel auto-combustion method

    Science.gov (United States)

    Jalaiah, K.; Vijaya Babu, K.; Chandra mouli, K.; Subba Rao, P. S. V.

    2018-04-01

    The Zr and Cu co-substituted Ni0.5Zn0.5Fe2O4 ferrite nanoparticles have been synthesized by the sol-gel auto combustion method. The XRD patterns confirmed single phase cubic spinel structure for present ferrite systems. The substitution of co-dopants in the spinel structure initially decreases the lattice parameter from x = 0.00 to 0.08 and thereafter increases and the same tendency reflecting in cell volume. The DC resistivity was initially increased later followed the decreasing trend; however the drift mobility of all ferrite samples appears to be in opposite phenomenon to DC resistivity. The saturation magnetization and net magnetic moments of all ferrite samples are decreasing with increasing dopant concentration. The coercive field and Y-K angles are increased with dopant concentration. The initial permeability of all samples is decreased with increasing dopant concentration. The Q-Factor for all samples shows the narrow frequency band with increasing frequency.

  20. Three-dimensional carbon cloth-supported ZnO nanorod arrays as a binder-free anode for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Lanyan; Wang, Xin, E-mail: wangxin@scnu.edu.cn [South China Normal University, Institute of Electronic Paper Displays, South China Academy of Advanced Optoelectronics (China); Yin, Fuxing [Synergy Innovation Institute of GDUT (China); Zhang, Chengwei [Hebei University of Technology, Research Institute for Energy Equipment Materials, Tianjin Key Laboratory of Materials Laminating Fabrication and Interface Control Technology (China); Gao, Jinwei; Liu, Junming [South China Normal University, Institute of Advanced Materials, South China Academy of Advanced Optoelectronics (China); Zhou, Guofu [South China Normal University, Institute of Electronic Paper Displays, South China Academy of Advanced Optoelectronics (China); Zhang, Yongguang, E-mail: yongguangzhang@hebut.edu.cn; Bakenov, Zhumabay [Synergy Innovation Institute of GDUT (China)

    2017-02-15

    Three-dimensional ZnO nanorod arrays on flexible high surface area carbon cloth were successfully synthesized and directly used as negative electrodes for lithium-ion batteries without using any binder additive. The structure and morphology of the as-prepared hybrid ZnO electrode were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and high-resolution transmission electron microscopy (HRTEM). When tested as anodes in a lithium cell, the hybrid electrode demonstrated a high discharge capacity along with excellent rate capability and good cycling stability, delivering a reversible capacity of 891 mAh g{sup −1} at the second cycle and retaining a capacity of 469 mAh g{sup −1} after 100 cycles.

  1. Efficiency in the avail (by Com) of zinc (65ZnCl2) and phosphorus (Na H2 PO4) ions

    International Nuclear Information System (INIS)

    Calvache, Marcelo.

    1994-01-01

    The efficiency of corn to use phosphorus and zinc ions at different growing periods was determined in two soils Udic Eutrandept and Andic Haplustoll of Pichincha Province, after adding 10 ppm zinc labelled with 65Zn (gamma emisor, 1.115 meV), 50 and 100 ppm phosphorus, and a complementary fertilization. Root, stem and leaf samples were analyzed at 15 days intervals during the growing period. Zinc efficiency use was determined by isotopic method, and phosphorus by the non-isotopic. Significant differences were found for sampling period and soil types. The efficiency of use of zinc and phosphorus fertilizer increased with the age of the crop, being higher for the soil originally containing less Zn and P. Dry matter content increased linearly with phosphorus fertilizer addition

  2. Thioglycolic acid-capped CuInS{sub 2}/ZnS quantum dots as fluorescent probe for cobalt ion detection

    Energy Technology Data Exchange (ETDEWEB)

    Zi, Lili; Huang, Yu [Key Laboratory of Drug Quality Control and Pharmacovigilance, Ministry of Education, 4 Tongjia Lane, Gulou District, Nanjing 210009 (China); Department of Analytical Chemistry, China Pharmaceutical University, 24 Tongjia Lane, Gulou District, Nanjing 210009 (China); Yan, Zhengyu, E-mail: yanzhengyujiang@126.com [Key Laboratory of Drug Quality Control and Pharmacovigilance, Ministry of Education, 4 Tongjia Lane, Gulou District, Nanjing 210009 (China); Department of Analytical Chemistry, China Pharmaceutical University, 24 Tongjia Lane, Gulou District, Nanjing 210009 (China); Liao, Shenghua, E-mail: liaoshenghuacpu@hotmail.com [Key Laboratory of Drug Quality Control and Pharmacovigilance, Ministry of Education, 4 Tongjia Lane, Gulou District, Nanjing 210009 (China); Department of Analytical Chemistry, China Pharmaceutical University, 24 Tongjia Lane, Gulou District, Nanjing 210009 (China)

    2014-04-15

    A novel sensing fluorescent probe based on the fluorescence quenching of the thioglycolic acid-capped CuInS{sub 2}/ZnS quantum dots (CuInS{sub 2}/ZnS/TGA QDs) was established for cobalt ions detection. The fluorescence quenching of CuInS{sub 2}/ZnS/TGA QDs was due to the increasing surface deficiency and the inner-filter effect, which were attributed to the reaction between Co{sup 2+} and sulfur bonds on the surface of QDs. The quenching curve could be fitted by a typical Stern–Volmer-type equation, with a linear relationship between the quenching efficiency and the concentration of cobalt ions in the range of 0.3012–90.36 μmol L{sup −1}. And the detection limit (S/N=3) for Co{sup 2+} was 0.16 μmol L{sup −1}. Therefore, the established probe provided a simple, rapid, cheap and sensitive method for Co{sup 2+} detection. In a word, this method can be used to detect Co{sup 2+} in the environment. -- Highlights: • The CuInS2/ZnS QDs were used for the first time as a fluorescent probe for Co{sup 2+} detection. • The dramatic color change could be observed when Co{sup 2+} was added into the QDs solution. • The quenching of QDs was due to the increasing surface deficiency and the inner-filter effect. • This rapid, cheap and sensitive method was applied to the detection of Co{sup 2+} in simulated water.

  3. Thioglycolic acid-capped CuInS2/ZnS quantum dots as fluorescent probe for cobalt ion detection

    International Nuclear Information System (INIS)

    Zi, Lili; Huang, Yu; Yan, Zhengyu; Liao, Shenghua

    2014-01-01

    A novel sensing fluorescent probe based on the fluorescence quenching of the thioglycolic acid-capped CuInS 2 /ZnS quantum dots (CuInS 2 /ZnS/TGA QDs) was established for cobalt ions detection. The fluorescence quenching of CuInS 2 /ZnS/TGA QDs was due to the increasing surface deficiency and the inner-filter effect, which were attributed to the reaction between Co 2+ and sulfur bonds on the surface of QDs. The quenching curve could be fitted by a typical Stern–Volmer-type equation, with a linear relationship between the quenching efficiency and the concentration of cobalt ions in the range of 0.3012–90.36 μmol L −1 . And the detection limit (S/N=3) for Co 2+ was 0.16 μmol L −1 . Therefore, the established probe provided a simple, rapid, cheap and sensitive method for Co 2+ detection. In a word, this method can be used to detect Co 2+ in the environment. -- Highlights: • The CuInS2/ZnS QDs were used for the first time as a fluorescent probe for Co 2+ detection. • The dramatic color change could be observed when Co 2+ was added into the QDs solution. • The quenching of QDs was due to the increasing surface deficiency and the inner-filter effect. • This rapid, cheap and sensitive method was applied to the detection of Co 2+ in simulated water

  4. Water soluble and efficient amino acid Schiff base receptor for reversible fluorescence turn-on detection of Zn²⁺ ions: Quantum chemical calculations and detection of bacteria.

    Science.gov (United States)

    Subha, L; Balakrishnan, C; Natarajan, Satheesh; Theetharappan, M; Subramanian, Balanehru; Neelakantan, M A

    2016-01-15

    An amino acid Schiff base (R) capable of recognizing Zn(2+) ions selectively and sensitively in an aqueous medium was prepared and characterized. Upon addition of Zn(2+) ions, the receptor exhibits fluorescence intensity enhancements (~40 fold) at 460 nm (quantum yield, Φ=0.05 for R and Φ=0.18 for R-Zn(2+)) and can be detected by naked eye under UV light. The receptor can recognize the Zn(2+) (1.04×10(-8) M) selectively for other metal ions in the pH range of 7.5-11. The Zn(2+) chelation with R decreases the loss of energy through non-radiative transition and leads to fluorescence enhancement. The binding mode of the receptor with Zn(2+) was investigated by (1)H NMR titration and further validated by ESI-MS. The elemental color mapping and SEM/EDS analysis were also used to study the binding of R with Zn(2+). Density functional theory calculations were carried out to understand the binding mechanism. The receptor was applied as a microbial sensor for Escherichia coli and Staphylococcus aureus. Copyright © 2015 Elsevier B.V. All rights reserved.

  5. Formation of p-type ZnO thin film through co-implantation

    Science.gov (United States)

    Chuang, Yao-Teng; Liou, Jhe-Wei; Woon, Wei-Yen

    2017-01-01

    We present a study on the formation of p-type ZnO thin film through ion implantation. Group V dopants (N, P) with different ionic radii are implanted into chemical vapor deposition grown ZnO thin film on GaN/sapphire substrates prior to thermal activation. It is found that mono-doped ZnO by N+ implantation results in n-type conductivity under thermal activation. Dual-doped ZnO film with a N:P ion implantation dose ratio of 4:1 is found to be p-type under certain thermal activation conditions. Higher p-type activation levels (1019 cm-3) under a wider thermal activation range are found for the N/P dual-doped ZnO film co-implanted by additional oxygen ions. From high resolution x-ray diffraction and x-ray photoelectron spectroscopy it is concluded that the observed p-type conductivities are a result of the promoted formation of PZn-4NO complex defects via the concurrent substitution of nitrogen at oxygen sites and phosphorus at zinc sites. The enhanced solubility and stability of acceptor defects in oxygen co-implanted dual-doped ZnO film are related to the reduction of oxygen vacancy defects at the surface. Our study demonstrates the prospect of the formation of stable p-type ZnO film through co-implantation.

  6. Computational study of cation substitutions in apatites

    International Nuclear Information System (INIS)

    Tamm, Toomas; Peld, Merike

    2006-01-01

    Density-functional theory plane-wave modeling of fluor- and hydroxyapatites has been performed, where one or two calcium ions per unit cell were replaced with cadmium or zinc cations. It was found that cadmium ions favor Ca(1) positions in fluorapatites and Ca(2) positions in hydroxyapatites, in agreement with experiment. A similar pattern is predicted for zinc substitutions. In the doubly substituted cases, where only hydroxyapatites were modeled, a preference for the substituting ions to be located in Ca(2) position was also observed. Displacement of the hydroxide ions from their symmetrical positions on the hexagonal axis can be used to explain the preferred configurations of substituting ions around the axis. -- Deformation of the hydroxide ion chain due to substitutions around the ion channel in substituted hydroxyapatites

  7. Substitution effect of pentavalent bismuth ions on the electronic structure and physicochemical properties of perovskite-structured Ba(In0.5Ta0.5-xBix)O3 semiconductors

    International Nuclear Information System (INIS)

    Kim, Tae Woo; Hur, Su Gil; Hwang, Seong-Ju; Park, Hyunwoong; Park, Yiseul; Choi, Wonyong; Choy, Jin-Ho

    2007-01-01

    We have investigated the substitution effect of pentavalent bismuth ions on the electronic structure and physicochemical properties of barium indium tantalate. X-ray diffraction, X-ray absorption spectroscopic, and energy dispersive spectroscopic microprobe analyses reveal that, under oxygen atmosphere of 1 atm, pentavalent Bi ions are successfully stabilized in the octahedral site of the perovskite tantalate lattice. According to diffuse reflectance UV-vis spectroscopic analysis, the Bi substitution gives rise to the significant narrowing of band gap of barium indium tantalate even at a low Bi content of ∼5%, underscoring a high efficiency of Bi substitution in the band gap engineering. Such an effective narrowing of the band gap upon the Bi substitution would be attributable to the lowering of conduction band position due to the high electronegativity of Bi V substituent. As a result of band gap engineering, the Ba(In 0.5 Ta 0.5-x Bi x )O 3 compounds with x ≥ 0.03 can generate photocurrents under visible light irradiation (λ > 420 nm). Based on the present experimental findings, it becomes clear that the substitution of highly electronegative p-block element like Bi V ion can provide a very powerful tool for tailoring the electronic structure and physicochemical properties of wide band gap semiconductors

  8. Convenient and high-yielding strategy for preparing nano-ZnMn_2O_4 as anode material in lithium-ion batteries

    International Nuclear Information System (INIS)

    Zhang, Tong; Gao, Yu; Yue, Huijuan; Qiu, Hailong; Guo, Zhendong; Wei, Yingjin; Wang, Chunzhong; Chen, Gang; Zhang, Dong

    2016-01-01

    Graphical abstract: A convenient combustion assist coprecipitation approach to synthesis nano-ZnMn2O4 anode material with excellent electrochemical performance. - Highlights: • ZnMn_2O_4 material has been gained from a novel combustion approach. • The ZnMn_2O_4 generated at 800 °C exhibits the best electrochemical performance. • This convenient method enables scale-up production of transition metal oxides. - Abstract: Time and energy saving synthesis method is crucial to the scale up applications of energy conversion and storage materials. In this report, we demonstrate a convenient and novel approach to fabricate the highly crystalline ZnMn_2O_4 nanoparticles as anode materials for Li rechargeable batteries. Pure phase ZnMn_2O_4 samples can be feasibly obtained under different calcination temperature from the precursor via combustion assisted coprecipitation method. Various techniques are used to characterize the structure and morphology of the products. Sample gained at 800 °C exhibits the best electrochemical property for lithium ion batteries. A reversible specific capacity of 716 mAh g"−"1 can be retained under a current density of 100 mA g"−"1 after 90 circles. Even the current density elevated up to 1000 mA g"−"1, the reversible capacity of the material still can be kept as high as 500 mAh g"−"1 after 1200 cycles. The outstanding performance compared to the other samples benefits from its good crystallinity and uniform dispersion with appropriate particle size.

  9. Spatial atomic layer deposition on flexible porous substrates: ZnO on anodic aluminum oxide films and Al2O3 on Li ion battery electrodes

    International Nuclear Information System (INIS)

    Sharma, Kashish; Routkevitch, Dmitri; Varaksa, Natalia; George, Steven M.

    2016-01-01

    Spatial atomic layer deposition (S-ALD) was examined on flexible porous substrates utilizing a rotating cylinder reactor to perform the S-ALD. S-ALD was first explored on flexible polyethylene terephthalate polymer substrates to obtain S-ALD growth rates on flat surfaces. ZnO ALD with diethylzinc and ozone as the reactants at 50 °C was the model S-ALD system. ZnO S-ALD was then performed on nanoporous flexible anodic aluminum oxide (AAO) films. ZnO S-ALD in porous substrates depends on the pore diameter, pore aspect ratio, and reactant exposure time that define the gas transport. To evaluate these parameters, the Zn coverage profiles in the pores of the AAO films were measured using energy dispersive spectroscopy (EDS). EDS measurements were conducted for different reaction conditions and AAO pore geometries. Substrate speeds and reactant pulse durations were defined by rotating cylinder rates of 10, 100, and 200 revolutions per minute (RPM). AAO pore diameters of 10, 25, 50, and 100 nm were utilized with a pore length of 25 μm. Uniform Zn coverage profiles were obtained at 10 RPM and pore diameters of 100 nm. The Zn coverage was less uniform at higher RPM values and smaller pore diameters. These results indicate that S-ALD into porous substrates is feasible under certain reaction conditions. S-ALD was then performed on porous Li ion battery electrodes to test S-ALD on a technologically important porous substrate. Li 0.20 Mn 0.54 Ni 0.13 Co 0.13 O 2 electrodes on flexible metal foil were coated with Al 2 O 3 using 2–5 Al 2 O 3 ALD cycles. The Al 2 O 3 ALD was performed in the S-ALD reactor at a rotating cylinder rate of 10 RPM using trimethylaluminum and ozone as the reactants at 50 °C. The capacity of the electrodes was then tested versus number of charge–discharge cycles. These measurements revealed that the Al 2 O 3 S-ALD coating on the electrodes enhanced the capacity stability. This S-ALD process could be extended to roll-to-roll operation for

  10. The formation of [M-H]+ ions in N-alkyl-substituted thieno[3,4-c]-pyrrole-4,6-dione derivatives during atmospheric pressure photoionization mass spectrometry

    KAUST Repository

    Sioud, Salim

    2014-10-09

    RESULTS [M-H]+ ions were observed under APPI conditions. The type of dopant and the length of the alkyl chain affected the formation of these ions. MS/MS fragmentation of [M-H]+ and [M + H]+ ions exhibited completely different patterns. Theoretical calculations revealed that the loss of hydrogen molecules from the [M + H]+ ions is the most favourable condition under which to form [M-H]+ ions.CONCLUSIONS [M-H]+ ions were detected in all the TPD derivatives studied here under the special experimental conditions during APPI, using a halogenated benzene dopant, and TPD containing substituted N-alkyl side chains with a minimum of four carbon atoms. Density functional theory calculations showed that for [M-H]+ ions to be formed under these conditions, the loss of hydrogen molecules from the [M + H]+ ions is proposed to be necessary.RATIONALE The formation of ions during atmospheric pressure photoionization (APPI) mass spectrometry in the positive mode usually provides radical cations and/or protonated species. Intriguingly, during the analysis of some N-alkyl-substituted thieno[3,4-c]pyrrole-4,6-dione (TPD) derivatives synthesized in our laboratory, unusual [M-H]+ ion peaks were observed. In this work we investigate the formation of [M-H]+ ions observed under APPI conditions.METHODS Multiple experimental parameters, including the type of ionization source, the composition of the solvent, the type of dopant, the infusion flow rate, and the length of the alkyl side chain were investigated to determine their effects on the formation of [M-H]+ ions. In addition, a comparison study of the gas-phase tandem mass spectrometric (MS/MS) fragmentation of [M + H]+ vs [M-H]+ ions and computational approaches were used.

  11. Adsorbents/ion exchangers-PVA blend membranes: Preparation, characterization and performance for the removal of Zn{sup 2+} by electrodialysis

    Energy Technology Data Exchange (ETDEWEB)

    Caprarescu, Simona [Politehnica University of Bucharest, Faculty of Applied Chemistry and Materials Science, Inorganic Chemistry, Physical Chemistry and Electrochemistry Department, 1-7 Polizu Street, 011061 Bucharest (Romania); Radu, Anita-Laura, E-mail: raduanita@gmail.com [Polymer Department, National Research and Development Institute for Chemistry and Petrochemistry – ICECHIM, Splaiul Independentei, No. 202, 060021 Bucharest (Romania); Purcar, Violeta; Ianchis, Raluca; Sarbu, Andrei; Ghiurea, Marius; Nicolae, Cristian [Polymer Department, National Research and Development Institute for Chemistry and Petrochemistry – ICECHIM, Splaiul Independentei, No. 202, 060021 Bucharest (Romania); Modrogan, Cristina [Politehnica University of Bucharest, Faculty of Applied Chemistry and Materials Science, Inorganic Substances and Environmental Protection Department, 1-7 Polizu Street, 011061 Bucharest (Romania); Vaireanu, Danut-Ionel [Politehnica University of Bucharest, Faculty of Applied Chemistry and Materials Science, Inorganic Chemistry, Physical Chemistry and Electrochemistry Department, 1-7 Polizu Street, 011061 Bucharest (Romania); Périchaud, Alain [Catalyse, lot 25, Master Park – 116, Bd de la Pomme, 13011 Marseille (France); Ebrasu, Daniela-Ion [National Research & Development Institute for Cryogenics and Isotopic Technologies-ICSI-Rm. Valcea, P.O. Box Raureni 7, 240050 Ramnicu Valcea (Romania)

    2015-02-28

    Highlights: • Removal of Zn{sup 2+} from the wastewater discharged from electroplating processes was studied. • A mini-electrodialysis system and different resin membranes were used. • The electrodialysis experiments were carried out at 25 °C, with and without recirculation. • The EIS measurements were carried out using new stainless steel disk electrodes. • The efficiency of the electrodialysis cell, mass flow, energy consumption was investigated. - Abstract: The present paper was aimed at studying the possibility of zinc (Zn) removal from the wastewater discharged from zinc electroplating processes. In order to save industrial and environmental resources, the concentrated solution could be reused after electrodialysis process. A mini-electrodialysis system with three cylindrical compartments and different membranes containing various resins (Purolite A500 and Hypersol-Macronet MN500) was employed, which can be further applied for the treatment of synthetic effluent which contained zinc ions. The electrodialysis system was operated at constant voltage using different concentrations of synthetic solutions of zinc ions, without and with electrolyte recirculation for 1.5 h. The pH and conductivity of solutions were measured before and after the electrodialysis process occurs. Also the removal ratio (R{sub r}) and mass flow (J) of zinc ions, energy consumption (EC) and current efficiency (CE) were determined. It was found that electrodialysis treatment generated a very low conductivity solution, enabling its reuse as rinse water. According to the obtained results when using a membrane pair with higher ion exchange capacity (IEC) the removal ratio is improved (over 80%). The physico-chemical, structural and mechanical properties of prepared membranes were registered, before and after electrodialysis process takes place, by means of complementary analytical techniques, namely, ion-exchange capacity, water content and thickness measurements. Furthermore

  12. Stable synthetic bacteriochlorins for photodynamic therapy: role of dicyano peripheral groups, central metal substitution (2H, Zn, Pd), and Cremophor EL delivery.

    Science.gov (United States)

    Huang, Ying-Ying; Balasubramanian, Thiagarajan; Yang, Eunkyung; Luo, Dianzhong; Diers, James R; Bocian, David F; Lindsey, Jonathan S; Holten, Dewey; Hamblin, Michael R

    2012-12-01

    A series of four stable synthetic bacteriochlorins was tested in vitro in HeLa cells for their potential in photodynamic therapy (PDT). The parent bacteriochlorin (BC), dicyano derivative (NC)(2)BC and corresponding zinc chelate (NC)(2)BC-Zn and palladium chelate (NC)(2)BC-Pd were studied. Direct dilution of a solution of bacteriochlorin in an organic solvent (N,N-dimethylacetamide) into serum-containing medium was compared with the dilution of bacteriochlorin in Cremophor EL (CrEL; polyoxyethylene glycerol triricinoleate) micelles into the same medium. CrEL generally reduced aggregation (as indicated by absorption and fluorescence) and increased activity up to tenfold (depending on bacteriochlorin), although it decreased cellular uptake. The order of PDT activity against HeLa human cancer cells after 24 h incubation and illumination with 10 J cm(-2) of near-infrared (NIR) light is (NC)(2)BC-Pd (LD(50)=25 nM) > (NC)(2)BC > (NC)(2)BC-Zn ≈ BC. Subcellular localization was determined to be in the endoplasmic reticulum, mitochondria and lysosomes, depending on the bacteriochlorin. (NC)(2)BC-Pd showed PDT-mediated damage to mitochondria and lysosomes, and the greatest production of hydroxyl radicals as determined using a hydroxyphenylfluorescein probe. The incorporation of cyano substituents provides an excellent motif for the enhancement of the photoactivity and photostability of bacteriochlorins as PDT photosensitizers. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  13. Investigation on structural aspects of ZnO nano-crystal using radio-active ion beam and PAC

    Energy Technology Data Exchange (ETDEWEB)

    Ganguly, Bichitra Nandi, E-mail: bichitra.ganguly@saha.ac.in [Saha Institute of Nuclear Physics, Kolkata 700064 (India); Dutta, Sreetama; Roy, Soma [Saha Institute of Nuclear Physics, Kolkata 700064 (India); Röder, Jens [Physics Department, ISOLDE/CERN, Geneva (Switzerland); Physical Chemistry, RWTH-Aachen, Aachen (Germany); Johnston, Karl [Physics Department, ISOLDE/CERN, Geneva (Switzerland); Experimental Physics, University of the Saarland, Saarbrücken (Germany); Martin, Manfred [Physical Chemistry, RWTH-Aachen, Aachen (Germany)

    2015-11-01

    Nano-crystalline ZnO has been studied with perturbed angular correlation using {sup 111m}Cd, implanted at ISOLDE/CERN and X-ray diffraction using Rietveld analysis. The data show a gradual increase in the crystal size and stress for a sample annealed at 600 °C, and reaching nearly properties of standard ZnO with tempering at 1000 °C. The perturbed angular correlation data show a broad frequency distribution at low annealing temperatures and small particle sizes, whereas at high annealing temperature and larger crystal sizes, results similar to bulk ZnO have been obtained. The ZnO nano-crystalline samples were initially prepared through a wet chemical route, have been examined by Fourier Transform Infrared Spectroscopy (FT-IR) and chemical purity has been confirmed with Energy Dispersive X-ray (EDAX) analysis as well as Transmission Electron Microscopy (TEM).

  14. Effect of excitation-autoionization processes on the line emission of Zn I-- and GaI--like rare-earth ions in hot coronal plasmas

    International Nuclear Information System (INIS)

    Mandelbaum, P.; Finkenthal, M.; Meroz, E.; Schwob, J.L.; Oreg, J.; Goldstein, W.H.; Klapisch, M.; Osterheld, L.; Bar Shalom, A.; Lippman, S.; Huang, L.K.; Moos, H.W.

    1990-01-01

    A systematic variation in the line-intensity ratios of GaI-- and ZnI--like Pr (Z=59) to Dy (Z=66) ions has been observed in spectra emitted by atoms injected in a low-density high-temperature tokamak plasma. This variation is shown to be correlated with the progressive closing of the autoionizing channels through the excited 3d 9 4s 2 4p4f configuration in the GaI--like ionization state as Z increases

  15. Single-color, in situ photolithography marking of individual CdTe/ZnTe quantum dots containing a single Mn{sup 2+} ion

    Energy Technology Data Exchange (ETDEWEB)

    Sawicki, K.; Malinowski, F. K.; Gałkowski, K.; Jakubczyk, T.; Kossacki, P.; Pacuski, W.; Suffczyński, J., E-mail: Jan.Suffczynski@fuw.edu.pl [Institute of Experimental Physics, Faculty of Physics, University of Warsaw, Pasteura 5 St., PL-02-093 Warsaw (Poland)

    2015-01-05

    A simple, single-color method for permanent marking of the position of individual self-assembled semiconductor Quantum Dots (QDs) at cryogenic temperatures is reported. The method combines in situ photolithography with standard micro-photoluminescence spectroscopy. Its utility is proven by a systematic magnetooptical study of a single CdTe/ZnTe QD containing a Mn{sup 2+} ion, where a magnetic field of up to 10 T in two orthogonal, Faraday and Voigt, configurations is applied to the same QD. The presented approach can be applied to a wide range of solid state nanoemitters.

  16. Hydrothermal synthesis of ZnSe:Cu quantum dots and their luminescent mechanism study by first-principles

    Energy Technology Data Exchange (ETDEWEB)

    Liang, Qingshuang; Bai, Yijia; Han, Lin; Deng, Xiaolong [State Key Laboratory of Rare Earth Resources Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China); Graduate School, Chinese Academy of Sciences, Beijing 10049 (China); Wu, Xiaojie [State Key Laboratory of Rare Earth Resources Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China); Wang, Zhongchang [WPI Research Center, Advanced Institute for Materials Research, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai 980-8577 (Japan); Liu, Xiaojuan, E-mail: lxjuan@ciac.jl.cn [State Key Laboratory of Rare Earth Resources Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China); Meng, Jian, E-mail: jmeng@ciac.jl.cn [State Key Laboratory of Rare Earth Resources Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China)

    2013-11-15

    An one-pot synthesis of aqueous ZnSe:Cu nanocrystals (NCs) is realized in aqueous solution by a facile yet efficient hydrothermal technique. The dopant emission spectrum of the NCs is tunable, spanning a wide range from 438 to 543 nm. Room-temperature quantum yield for the NCs prepared at the optimal conditions reaches as high as 20% without any post-treatment. The ZnSe:Cu NCs prepared in a neutral aqueous solution (pH=8) are remarkably stable and exhibit comparatively high photoluminescent quantum yield (PL QY) as high as 17%. First-principles pseudopotential calculations using plane-wave basis functions have been performed. The formation energies of copper ions occupied in the interstitial octahedron and substitutional tetrahedral Zn{sup 2+} sites have been calculated. The occupation of copper ions in the interstitial octahedral site is found to be more thermodynamics-facilitated by −0.98 eV. The density of state analysis indicates that the Cu-related emission is primary dominated by the substitutional tetrahedral Cu ions, and the large dopant related emission width of ZnSe:Cu NCs originated from the corresponding Cu 3d impurity band. Highlights: • One-pot synthesis of aqueous ZnSe:Cu nanocrystals with tunable emission and high QY%. • ZnSe:Cu NCs exhibit high QY% at neutral pH suitable for biological application. • The microscopic mechanism underlying Cu-related emission has been provided.

  17. High impact of uranyl ions on carrying-releasing oxygen capability of hemoglobin-based blood substitutes

    Energy Technology Data Exchange (ETDEWEB)

    Duan, Li; Du, Lili; Liu, Wenyuan; Liu, Zhichao [Northwest Institute of Nuclear Technology, Xi' an, Shaanxi (China); Jia, Yi; Li, Junbai [Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Colloid Interface and Chemical Thermodynamics, Institute of Chemistry, Chinese Academy of Sciences, Beijing (China)

    2015-01-07

    The effect of radioactive UO{sub 2}{sup 2+} on the oxygen-transporting capability of hemoglobin-based oxygen carriers has been investigated in vitro. The hemoglobin (Hb) microspheres fabricated by the porous template covalent layer-by-layer (LbL) assembly were utilized as artificial oxygen carriers and blood substitutes. Magnetic nanoparticles of iron oxide (Fe{sub 3}O{sub 4}) were loaded in porous CaCO{sub 3} particles for magnetically assisted chemical separation (MACS). Through the adsorption spectrum of magnetic Hb microspheres after adsorbing UO{sub 2}{sup 2+}, it was found that UO{sub 2}{sup 2+} was highly loaded in the magnetic Hb microspheres, and it shows that the presence of UO{sub 2}{sup 2+} in vivo destroys the structure and oxygen-transporting capability of Hb microspheres. In view of the high adsorption capacity of UO{sub 2}{sup 2+}, the as-assembled magnetic Hb microspheres can be considered as a novel, highly effective adsorbent for removing metal toxins from radiation-contaminated bodies, or from nuclear-power reactor effluent before discharge into the environment. (copyright 2015 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  18. Subsurface hydrogen bonds at the polar Zn-terminated ZnO(0001) surface

    DEFF Research Database (Denmark)

    Hellström, Matti; Beinik, Igor; Broqvist, Peter

    2016-01-01

    techniques, we find that the polar Zn-terminated ZnO(0001) surface becomes excessively Zn deficient during high-temperature annealing (780 K) in ultrahigh vacuum (UHV). The Zn vacancies align themselves into rows parallel to the [10-10] direction, and the remaining surface Zn ions alternately occupy wurtzite...

  19. Ratiometric fluorescent receptors for both Zn2+ and H2PO4(-) ions based on a pyrenyl-linked triazole-modified homooxacalix[3]arene: a potential molecular traffic signal with an R-S latch logic circuit.

    Science.gov (United States)

    Ni, Xin-long; Zeng, Xi; Redshaw, Carl; Yamato, Takehiko

    2011-07-15

    A ratiometric fluorescent receptor with a C(3) symmetric structure based on a pyrene-linked triazole-modified homooxacalix[3]arene (L) was synthesized and characterized. This system exhibited an interesting ratiometric detection signal output for targeting cations and anions through switching the excimer emission of pyrene from the "on-off" to the "off-on" type in neutral solution. (1)H NMR titration results suggested that the Zn(2+) center of receptor L·Zn(2+) provided an excellent pathway of organizing anion binding groups for optimal host-guest interactions. It is thus believed that this receptor has potential application in sensing, detection, and recognition of both Zn(2+) and H(2)PO(4)(-) ions with different optical signals. In addition, the fluorescence emission changes by the inputs of Zn(2+) and H(2)PO(4)(-) ions can be viewed as a combinational R-S latch logic circuit at the molecular level.

  20. Paramagnetism and antiferromagnetic interactions in single-phase Fe-implanted ZnO

    CERN Document Server

    Pereira, Lino Miguel da Costa; Correia, João Guilherme; Van Bael, M J; Temst, Kristiaan; Vantomme, André; Araújo, João Pedro

    2013-01-01

    As the intrinsic origin of the high temperature ferromagnetism often observed in wide-gap dilute magnetic semiconductors becomes increasingly debated, there is a growing need for comprehensive studies on the single-phase region of the phase diagram of these materials. Here we report on the magnetic and structural properties of Fe-doped ZnO prepared by ion implantation of ZnO single crystals. A detailed structural characterization shows that the Fe impurities substitute for Zn in ZnO in a wurtzite Zn$_{1−x}$Fe$_{x}$O phase which is coherent with the ZnO host. In addition, the density of beam-induced defects is progressively decreased by thermal annealing up to 900$^{\\circ}$C, from highly disordered after implantation to highly crystalline upon subsequent annealing. Based on a detailed analysis of the magnetometry data, we demonstrate that isolated Fe impurities occupying Zn substitutional sites behave as localized paramagnetic moments down to 2$^{\\circ}$K, irrespective of the Fe concentration and the density...

  1. Single and couple doping ZnO nanocrystals characterized by positron techniques

    International Nuclear Information System (INIS)

    Pasang, Tenzin; Namratha, Keerthiraj; Byrappa, Kullaiah; Guagliardo, Paul; Ranganathaiah, Chikkakuntappa; Samarin, S; Williams, J F

    2015-01-01

    Zinc oxide (ZnO) nanocrystals have been synthesized using a mild hydrothermal process using low temperatures and pressures with the advantages of free growth catalyst, low cost and alternative technology. Positron annihilation lifetime spectroscopy and coincidence Doppler broadening (CDB) spectroscopic methods have been used to investigate the roles of single- and co-dopants and native defects of the ZnO nanocrystals controlled by the synthesis process. It is shown that single Ag 1+ and Pd 2+ dopants occupy interstitial sites of the ZnO lattice and single Ru 3+ doping replaces Zn vacancies substitutionally with a significant effect on the CDB momentum ratio curves when compared using ZnO as the reference spectrum. The co-doping of the ZnO lattice with (Sn 4+ + Co 2+ ) shows similar CDB ratios as Ru 3+ single-doping. Also co-doping with (Ag 1+ + Pd 2+ ) or (Ag 1+ + W 6+ ) shows significant decreases in the band gap energy up to about 12.6% compared to single doping. The momentum ratio curves, referenced to undoped ZnO, indicate dopants in interstitial and substitutional sites. The presence of transition metal ions interstitially will trap electrons which resist the recombination of electrons and in turn affect the conductivity of the material. (paper)

  2. Single and couple doping ZnO nanocrystals characterized by positron techniques

    Science.gov (United States)

    Pasang, Tenzin; Namratha, Keerthiraj; Guagliardo, Paul; Byrappa, Kullaiah; Ranganathaiah, Chikkakuntappa; Samarin, S.; Williams, J. F.

    2015-04-01

    Zinc oxide (ZnO) nanocrystals have been synthesized using a mild hydrothermal process using low temperatures and pressures with the advantages of free growth catalyst, low cost and alternative technology. Positron annihilation lifetime spectroscopy and coincidence Doppler broadening (CDB) spectroscopic methods have been used to investigate the roles of single- and co-dopants and native defects of the ZnO nanocrystals controlled by the synthesis process. It is shown that single Ag1+ and Pd2+ dopants occupy interstitial sites of the ZnO lattice and single Ru3+ doping replaces Zn vacancies substitutionally with a significant effect on the CDB momentum ratio curves when compared using ZnO as the reference spectrum. The co-doping of the ZnO lattice with (Sn4+ + Co2+) shows similar CDB ratios as Ru3+ single-doping. Also co-doping with (Ag1+ + Pd2+) or (Ag1+ + W6+) shows significant decreases in the band gap energy up to about 12.6% compared to single doping. The momentum ratio curves, referenced to undoped ZnO, indicate dopants in interstitial and substitutional sites. The presence of transition metal ions interstitially will trap electrons which resist the recombination of electrons and in turn affect the conductivity of the material.

  3. Fine structure of an exciton coupled to a single Fe2 + ion in a CdSe/ZnSe quantum dot

    Science.gov (United States)

    Smoleński, T.; Kazimierczuk, T.; Goryca, M.; Pacuski, W.; Kossacki, P.

    2017-10-01

    We present a polarization-resolved photoluminescence study of the exchange interaction effects in a prototype system consisting of an individual Fe2 + ion and a single neutral exciton confined in a CdSe/ZnSe quantum dot. A maximal possible number of eight fully linearly polarized lines in the bright exciton emission spectrum is observed, evidencing complete degeneracy lifting in the investigated system. We discuss the conditions required for such a scenario to take place: anisotropy of the electron-hole interaction and the zero-field splitting of the Fe2 + ion spin states. Neglecting either of these components is shown to restore partial degeneracy of the transitions, making the excitonic spectrum similar to those previously reported for all other systems of quantum dots with single magnetic dopants.

  4. SnO{sub 2}/ZnO composite structure for the lithium-ion battery electrode

    Energy Technology Data Exchange (ETDEWEB)

    Ahmad, Mashkoor, E-mail: mashkoorahmad2003@yahoo.com [Beijing National Center for Electron Microscopy, The State Key Laboratory of New Ceramics and Fine Processing, Laboratory of Advanced Material, China Iron and Steel Research Institute Group, Department of Material Science and Engineering, Tsinghua University, Beijing 100084 (China); Nanomaterial Research Group, Physics Division, PINSTECH, P.O. Nilore, Islamabad (Pakistan); Yingying, Shi [Laboratory of Advanced Materials, Department of Materials Science and Engineering, Tsinghua University, Beijing 100084 (China); Sun, Hongyu [Beijing National Center for Electron Microscopy, The State Key Laboratory of New Ceramics and Fine Processing, Laboratory of Advanced Material, China Iron and Steel Research Institute Group, Department of Material Science and Engineering, Tsinghua University, Beijing 100084 (China); Shen, Wanci [Laboratory of Advanced Materials, Department of Materials Science and Engineering, Tsinghua University, Beijing 100084 (China); Zhu, Jing, E-mail: jzhu@mail.tsinghua.edu.cn [Beijing National Center for Electron Microscopy, The State Key Laboratory of New Ceramics and Fine Processing, Laboratory of Advanced Material, China Iron and Steel Research Institute Group, Department of Material Science and Engineering, Tsinghua University, Beijing 100084 (China)

    2012-12-15

    In this article, SnO{sub 2}/ZnO composite structures have been synthesized by two steps hydrothermal method and investigated their lithium storage capacity as compared with pure ZnO. It has been found that these composite structures combining the large specific surface area, stability and catalytic activity of SnO{sub 2} micro-crystals, demonstrate the higher initial discharge capacity of 1540 mA h g{sup -1} with a Coulombic efficiency of 68% at a rate of 120 mA h g{sup -1} between 0.02 and 2 V and found much better than that of any previously reported ZnO based composite anodes. In addition, a significantly enhanced cycling performance, i.e., a reversible capacity of 497 mA h g{sup -1} is retained after 40 cycles. The improved lithium storage capacity and cycle life is attributed to the addition of SnO{sub 2} structure, which act as good electronic conductors and better accommodation of the large volume change during lithiation/delithiation process. - Graphical abstract: SnO{sub 2}/ZnO composite structures demonstrate the improved lithium storage capacity and cycle life as compared with pure ZnO nanostructure. Highlights: Black-Right-Pointing-Pointer Synthesis of SnO{sub 2}/ZnO composite structures by two steps hydrothermal approach. Black-Right-Pointing-Pointer Investigation of lithium storage capacity. Black-Right-Pointing-Pointer Excellent lithium storage capacity and cycle life of SnO{sub 2}/ZnO composite structures.

  5. In Situ Tracking Kinetic Pathways of Li+/Na+ Substitution during Ion-Exchange Synthesis of LixNa1.5-xVOPO4F0.5.

    Science.gov (United States)

    Park, Young-Uk; Bai, Jianming; Wang, Liping; Yoon, Gabin; Zhang, Wei; Kim, Hyungsub; Lee, Seongsu; Kim, Sung-Wook; Looney, J Patrick; Kang, Kisuk; Wang, Feng

    2017-09-13

    Ion exchange is a ubiquitous phenomenon central to wide industrial applications, ranging from traditional (bio)chemical separation to the emerging chimie douce synthesis of materials with metastable structure for batteries and other energy applications. The exchange process is complex, involving substitution and transport of different ions under non-equilibrium conditions, and thus difficult to probe, leaving a gap in mechanistic understanding of kinetic exchange pathways toward final products. Herein, we report in situ tracking kinetic pathways of Li + /Na + substitution during solvothermal ion-exchange synthesis of Li x Na 1.5-x VOPO 4 F 0.5 (0 ≤ x ≤ 1.5), a promising multi-Li polyanionic cathode for batteries. The real-time observation, corroborated by first-principles calculations, reveals a selective replacement of Na + by Li + , leading to peculiar Na + /Li + /vacancy orderings in the intermediates. Contradicting the traditional belief of facile topotactic substitution via solid solution reaction, an abrupt two-phase transformation occurs and predominantly governs the kinetics of ion exchange and transport in the 1D polyanionic framework, consequently leading to significant difference of Li stoichiometry and electrochemical properties in the exchanged products. The findings may help to pave the way for rational design of ion exchange synthesis for making new materials.

  6. Synthesis of highly conductive thin-walled Al-doped ZnO single-crystal microtubes by a solid state method

    Science.gov (United States)

    Hu, Shuopeng; Wang, Yue; Wang, Qiang; Xing, Cheng; Yan, Yinzhou; Jiang, Yijian

    2018-06-01

    ZnO has attracted considerable attention in fundamental studies and practical applications for the past decade due to its outstanding performance in gas sensing, photocatalytic degradation, light harvesting, UV-light emitting/lasing, etc. The large-sized thin-walled ZnO (TW-ZnO) microtube with stable and rich VZn-related acceptors grown by optical vapor supersaturated precipitation (OVSP) is a novel multifunctional optoelectronic material. Unfortunately, the OVSP cannot achieve doping due to the vapor growth process. To obtain doped TW-ZnO microtubes, a solid state method is introduced in this work to achieve thin-walled Al-doping ZnO (TW-ZnO:Al) microtubes with high electrical conductivity. The morphology and microstructures of ZnO:Al microtubes are similar to undoped ones. The Al3+ ions are confirmed to substitute Zn2+ sites and Zn(0/-1) vacancies in the lattice of ZnO by EDS, XRD, Raman and temperature-dependent photoluminescence analyses. The Al dopant acting as a donor level offers massive free electrons to increase the carrier concentrations. The resistivity of the ZnO:Al microtube is reduced down to ∼10-3 Ω·cm, which is one order of magnitude lower than that of the undoped microtube. The present work provides a simple way to achieve doped ZnO tubular components for potential device applications in optoelectronics.

  7. The influence of Zn-dopant on the precipitation of α-FeOOH in highly alkaline media

    International Nuclear Information System (INIS)

    Krehula, Stjepko; Music, Svetozar; Skoko, Zeljko; Popovic, Stanko

    2006-01-01

    The influence of Zn-dopant on the precipitation of α-FeOOH in highly alkaline media was monitored by X-ray diffraction (XRD), 57 Fe Moessbauer and Fourier transform infrared (FT-IR) spectroscopies and field emission scanning electron microscopy (FE SEM). Acicular and monodisperse α-FeOOH particles were precipitated at a very high pH by adding a tetramethylammonium hydroxide solution to an aqueous solution of FeCl 3 . The XRD analysis of the samples precipitated in the presence of Zn 2+ ions showed the formation of solid solutions of α-(Fe, Zn)OOH up to a concentration ratio r = [Zn]/([Zn] + [Fe]) = 0.0909. ZnFe 2 O 4 was additionally formed in the precipitate for r = 0.1111, whereas the three phases α-FeOOH, α-Fe 2 O 3 and ZnFe 2 O 4 were formed for r 0.1304. In the corresponding FT-IR spectra, the Fe-OH and Fe-O stretching bands were sensitive to the Zn 2+ substitution, whereas the Fe-OH bending bands of α-FeOOH at 892 and 796 cm -1 were almost insensitive. The Moessbauer spectra showed a high sensitivity to the formation of α-(Fe, Zn)OOH solid solutions which were monitored on the basis of a decrease in B hf values in dependence on Zn-doping. A strictly linear decrease in B hf for α-FeOOH doped with Zn 2+ ions was measured up to r = 0.0291, whereas for r = 0.0476 and higher there was a deviation from linearity. The presence of α-(Fe, Zn)OOH, α-Fe 2 O 3 and ZnFe 2 O 4 phases in the samples was determined quantitatively by Moessbauer spectroscopy. Likewise, Moessbauer spectroscopy did not show any formation of the solid solutions of α-Fe 2 O 3 with Zn 2+ ions. FE SEM showed a strong effect of Zn-doping on the elongation of acicular α-FeOOH particles (∼500-700 nm in length) up to r = 0.1111. For r = 0.1304 the sizes of ZnFe 2 O 4 particles were around 30-50 nm, and those of α-Fe 2 O 3 particles were around 500 nm, whereas a relatively small number of very elongated α-(Fe, Zn)OOH particles was observed. A possible mechanism of the formation of

  8. Drug delivery system for an anticancer agent, chlorogenate-Zn/Al-layered double hydroxide nanohybrid synthesised using direct co-precipitation and ion exchange methods

    Energy Technology Data Exchange (ETDEWEB)

    Barahuie, Farahnaz [Materials Synthesis and Characterization Laboratory, Institute of Advanced Technology (ITMA), Universiti Putra Malaysia, 43400 UPM Serdang, Selangor (Malaysia); Hussein, Mohd Zobir, E-mail: mzobir@putra.upm.edu.my [Materials Synthesis and Characterization Laboratory, Institute of Advanced Technology (ITMA), Universiti Putra Malaysia, 43400 UPM Serdang, Selangor (Malaysia); Arulselvan, Palanisamy [Laboratory of Vaccines and Immunotherapeutics, Institute of Bioscience, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor (Malaysia); Fakurazi, Sharida [Laboratory of Vaccines and Immunotherapeutics, Institute of Bioscience, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor (Malaysia); Department of Human Anatomy, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor (Malaysia); Zainal, Zulkarnain [Materials Synthesis and Characterization Laboratory, Institute of Advanced Technology (ITMA), Universiti Putra Malaysia, 43400 UPM Serdang, Selangor (Malaysia)

    2014-09-15

    A nano-structured drug-inorganic clay hybrid involving an active anticancer compound, which is chlorogenic acid (CA) intercalated into Zn/Al-layered double hydroxide, has been assembled via ion-exchange and co-precipitation methods to form a nanohybrid CZAE (a chlorogenic acid-Zn/Al nanohybrid synthesised using an ion-exchange method) and CZAC (a chlorogenic acid-Zn/Al nanohybrid synthesised using a direct method), respectively. The X-ray diffraction (XRD) results confirmed that the CA-LDH had a hybrid structure in which the anionic chlorogenate is arranged between the interlayers as a horizontal monolayer at 90 and 20° angles from the x axis for CZAE and CZAC, respectively. Both nanohybrids have the properties of mesoporous materials. The high loading percentage of chlorogenic acid (approximately 43.2% for CZAE and 45.3% for CZAC) with basal spacings of 11.7 and 12.6 Å for CZAE and CZAC, respectively, corroborates the successful intercalation of chlorogenic acid into the interlayer gallery of layered double hydroxides. Free chlorogenic acid and the synthesised nanocomposites (CZAE, CZAC) were assessed for their cytotoxicity against various cancer cells. The Fourier transform infrared data supported the formation of both nanohybrids, and a thermal analysis showed that the nanohybrids are more thermally stable than their counterparts. The chlorogenate shows a sustained release, and the release rate of chlorogenate from CZAE and CZAC nanohybrids at pH 7.4 is remarkably lower than that at pH 4.8 due to their different release mechanisms. The release rate of chlorogenate from both nanohybrids can be described as pseudo-second order. The present investigation revealed the potential of the nanohybrids to enhance the in vitro anti-tumour effect of chlorogenic acid in liver and lung cancer cells in vitro. - Highlights: • We intercalated chlorogenic into Zn/Al-layered double hydroxide by ion-exchange and coprecipitation methods. • The two methods gave nanocomposites

  9. Competitive adsorption of Pb(II), Cu(II), and Zn(II) ions onto hydroxyapatite-biochar nanocomposite in aqueous solutions

    Science.gov (United States)

    Wang, Yu-Ying; Liu, Yu-Xue; Lu, Hao-Hao; Yang, Rui-Qin; Yang, Sheng-Mao

    2018-05-01

    A hydroxyapatite-biochar nanocomposite (HAP-BC) was successfully fabricated and its physicochemical properties characterized. The analyses showed that HAP nanoparticles were successfully loaded on the biochar surface. The adsorption of Pb(II), Cu(II), and Zn(II) by HAP-BC was systematically studied in single and ternary metal systems. The results demonstrated that pH affects the adsorption of heavy metals onto HAP-BC. Regarding the adsorption kinetics, the pseudo-second-order model showed the best fit for all three heavy metal ions on HAP-BC. In both single and ternary metal ion systems, the adsorption isotherm of Pb(II) by HAP-BC followed Langmuir model, while those of Cu(II) and Zn(II) fitted well with Freundlich model. The maximum adsorption capacity for each tested metal by HAP-BC was higher than that of pristine rice straw biochar (especially for Pb(II)) or those of other reported adsorbents. Therefore, HAP-BC could explore as a new material for future application in heavy metal removal.

  10. Time-Resolved Transient Optical Absorption Study of Bis(terpyridyl)oligothiophenes and Their Metallo-Supramolecular Polymers with Zn(II) Ion Couplers.

    Science.gov (United States)

    Rais, David; Menšík, Miroslav; Štenclová-Bláhová, Pavla; Svoboda, Jan; Vohlídal, Jiří; Pfleger, Jiří

    2015-06-18

    α,ω-Bis(terpyridyl)oligothiophenes spontaneously assemble with Zn(II) ions giving conjugated constitutional dynamic polymers (dynamers) of the metallo-supramolecular class, which potentially might be utilized in optoelectronics. Their photophysical properties, which are of great importance in this field of application, are strongly influenced by the dynamic morphology. It was assessed in this study by using ultrafast pump-probe optical absorption spectroscopy. We identified and characterized relaxation processes running in photoexcited molecules of these oligomers and dynamers and show impacts of disturbed coplanarity of adjacent rings (twisting the thiophene-thiophene and thiophene-terpyridyl bonds by attached hexyl side groups) and Zn(II) ion couplers on these processes. Major effects are seen in the time constants of rotational relaxation, intersystem crossing, and de-excitation lifetimes. The photoexcited states formed on different repeating units within the same dynamer chain do not interact with each other even at very high excitation density. The method is presented that allows determining the equilibrium fraction of unbound oligothiophene species in a dynamer solution, from which otherwise hardly accessible values of the average degree of polymerization of constitutionally dynamic chains in solution can be estimated.

  11. Structure Interlacing and Pore Engineering of Zn2GeO4 Nanofibers for Achieving High Capacity and Rate Capability as an Anode Material of Lithium Ion Batteries.

    Science.gov (United States)

    Wang, Wei; Qin, Jinwen; Cao, Minhua

    2016-01-20

    An interlaced Zn2GeO4 nanofiber network with continuous and interpenetrated mesoporous structure was prepared using a facile electrospinning method followed by a thermal treatment. The mesoporous structure in Zn2GeO4 nanofibers is directly in situ constructed by the decomposition of polyvinylpyrolidone (PVP), while the interlaced nanofiber network is achieved by the mutual fusion of the junctions between nanofibers in higher calcination temperatures. When used as an anode material in lithium ion batteries (LIBs), it exhibits superior lithium storage performance in terms of specific capacity, cycling stability, and rate capability. The pore engineering and the interlaced network structure are believed to be responsible for the excellent lithium storage performance. The pore structure allows for easy diffusion of electrolyte, shortens the pathway of Li(+) transport, and alleviates large volume variation during repeated Li(+) extraction/insertion. Moreover, the interlaced network structure can provide continuous electron/ion pathways and effectively accommodate the strain induced by the volume change during the electrochemical reaction, thus maintaining structural stability and mechanical integrity of electrode materials during lithiation/delithiation process. This strategy in current work offers a new perspective in designing high-performance electrodes for LIBs.

  12. In vitro metal ion release and biocompatibility of amorphous Mg{sub 67}Zn{sub 28}Ca{sub 5} alloy with/without gelatin coating

    Energy Technology Data Exchange (ETDEWEB)

    Chan, W.Y., E-mail: chan.wing.yue@sgh.com.sg [School of Mechanical and Aerospace Engineering, Nanyang Technological University (Singapore); Department of Plastic, Reconstructive and Aesthetic Surgery, Singapore General Hospital (Singapore); Chian, K.S.; Tan, M.J. [School of Mechanical and Aerospace Engineering, Nanyang Technological University (Singapore)

    2013-12-01

    Amorphous zinc-rich Mg–Zn–Ca alloys have exhibited good tissue compatibility and low hydrogen evolution in vivo. However, suboptimal cell–surface interaction on magnesium alloy surface observed in vitro could lead to reduced integration with host tissue for regenerative purpose. This study aims to improve cell–surface interaction of amorphous Mg{sub 67}Zn{sub 28}Ca{sub 5} alloy by coating a gelatin layer by electrospinning. Coated/uncoated alloys were immersed and extracted for 3 days under different CO{sub 2}. The immersion results showed that pH and metal ion release in the alloy extracts were affected by gelatin coating and CO{sub 2}, suggesting their roles in alloy biocorrosion and a mechanism has been proposed for the alloy–CO{sub 2} system with/without coating. Cytotoxicity results are evident that gelatin-coated alloy with 2-day crosslinking not only exhibited no indirect cytotoxicity, but also supported attachment of L929 and MG63 cell lines around/on the alloy with high viability. Therefore, amorphous Mg{sub 67}Zn{sub 28}Ca{sub 5} alloy coated with gelatin by electrospinning technique provides a useful method to improve alloy biocompatibility. - Highlights: • Electrospinning is a new method to coat amorphous Mg{sub 67}Zn{sub 28}Ca{sub 5} alloy with gelatin. • Gelatin-coated alloy has differential effect on pH and ion release at various CO{sub 2}. • L929 cell proliferation correlates with Mg{sup 2+} level in alloy extracts. • Biomimetic gelatin coating significantly improves cell–surface interaction.

  13. Hydrogen interstitial in H-ion implanted ZnO bulk single crystals: Evaluation by elastic recoil detection analysis and electron paramagnetic resonance

    Energy Technology Data Exchange (ETDEWEB)

    Kaida, T.; Kamioka, K.; Nishimura, T. [College of Engineering and Research Center of Ion Beam Technology, Hosei University, Koganei, Tokyo 184-8584 (Japan); Kuriyama, K., E-mail: kuri@ionbeam.hosei.ac.jp [College of Engineering and Research Center of Ion Beam Technology, Hosei University, Koganei, Tokyo 184-8584 (Japan); Kushida, K. [Department of Arts and Sciences, Osaka Kyoiku University, Kashiwara, Osaka 582-8582 (Japan); Kinomura, A. [National Institute of Advanced Industrial Science and Technology, Tsukuba, Ibaraki 305-8568 (Japan)

    2015-12-15

    The origins of low resistivity in H ion-implanted ZnO bulk single crystals are evaluated by elastic recoil detection analysis (ERDA), electron paramagnetic resonance (EPR), and Van der Pauw methods. The H-ion implantation (peak concentration: 5.0 × 10{sup 15} cm{sup −2}) into ZnO is performed using a 500 keV implanter. The maximum of the concentration of the implanted H estimated by a TRIM simulation is at 3600 nm in depth. The resistivity decreases from ∼10{sup 3} Ω cm for un implanted ZnO to 6.5 Ω cm for as-implanted, 2.3 × 10{sup −1} Ω cm for 200 °C annealed, and 3.2 × 10{sup −1} Ω cm for 400 °C annealed samples. The ERDA measurements can evaluate the concentration of hydrogens which move to the vicinity of the surface (surface to 300 nm or 100 nm) because of the diffusion by the annealing at 200 °C and 400 °C. The hydrogen concentration near the surface estimated using the 2.0 MeV helium beam is ∼3.8 × 10{sup 13} cm{sup −2} for annealed samples. From EPR measurements, the oxygen vacancy of +charge state (V{sub o}{sup +}) is observed in as-implanted samples. The V{sub o}{sup +} related signal (g = 1.96) observed under no illumination disappears after successive illumination with a red LED and appears again with a blue light illumination. The activation energy of as-implanted, 200 °C annealed, and 400 °C annealed samples estimated from the temperature dependence of carrier concentration lies between 29 meV and 23 meV, suggesting the existence of H interstitial as a shallow donor level.

  14. Effect of 120 MeV 28Si9+ ion irradiation on structural and magnetic properties of NiFe2O4 and Ni0.5Zn0.5Fe2O4

    Science.gov (United States)

    Sharma, R.; Raghuvanshi, S.; Satalkar, M.; Kane, S. N.; Tatarchuk, T. R.; Mazaleyrat, F.

    2018-05-01

    NiFe2O4, Ni0.5Zn0.5Fe2O4 samples were synthesized using sol-gel auto combustion method, and irradiated by using 120 MeV 28Si9+ ion with ion fluence of 1×1012 ions/cm2. Characterization of pristine, irradiated samples were done using X-Ray Diffraction (XRD), Field Emission Scanning Microscopy (FE-SEM), Energy Dispersive X-ray Analysis (EDAX) and Vibrating Sample Magnetometer (VSM). XRD validates the single phase nature of pristine, irradiated Ni- Zn nano ferrite except for Ni ferrite (pristine, irradiated) where secondary phases of α-Fe2O3 and Ni is observed. FE- SEM images of pristine Ni, Ni-Zn ferrite show inhomogeneous nano-range particle size distribution. Presence of diamagnetic ion (Zn2+) in NiFe2O4 increases oxygen positional parameter (u 4¯3m ), experimental, theoretical saturation magnetization (Msexp., Msth.), while decreases the grain size (Ds) and coercivity (Hc). With irradiation Msexp., Msth. increases but not much change are observed in Hc. New antistructure modeling for the pristine, irradiated Ni and Ni-Zn ferrite samples was used for describing the surface active centers.

  15. Two different mechanisms on UV emission enhancement in Ag-doped ZnO thin films

    International Nuclear Information System (INIS)

    Xu, Linhua; Zheng, Gaige; Zhao, Lilong; Pei, Shixin

    2015-01-01

    Ag-doped ZnO thin films were prepared by a sol–gel method. The structural, morphological and optical properties of the samples were analyzed by X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), UV–vis and photoluminescence spectra. The results show that the Ag in the ZnO thin films annealed at 500 °C for 1 h substitutes for Zn and exists in the form of Ag + ion (Ag Zn ) while the Ag in the ZnO thin films without a post-annealing mainly exists in the form of simple substance (Ag 0 ). The incorporation of Ag indeed can improve the ultraviolet emission of ZnO thin films and suppress the visible emissions at the same time. However, the mechanisms on the ultraviolet emission enhancement in the annealed and unannealed Ag-doped ZnO thin films are very different. As for the post-annealed Ag-doped ZnO thin films, the UV emission enhancement maybe mainly results from more electron–hole pairs (excitons) due to Ag-doping while for the unannealed Ag-doped ZnO thin films; the UV emission enhancement is attributed to the resonant coupling between exciton emission in ZnO and localized surface plasmon in Ag nanoparticles. - Highlights: • Ag-doped ZnO thin films have been prepared by the sol–gel method. • Ag-doping can enhance ultraviolet emission of ZnO thin films and depress the visible emissions at the same time. • There are two different mechanisms on UV emission enhancement in Ag-doped ZnO thin films. • The UV emission enhancement from the resonant coupling between excitonic emissions and localized surface plasmon in Ag nanoparticle is very attractive

  16. Kinetical Analysis of the Mechanism of the Ligand Substitution Reaction between the Ethylenediamine-N,N{sup `}-bis[2-(2-hydroxyphenyl) acetato] cadmate (2) Ion and the Ethylenediaminetetraacetatoferrate (3) Ion; Echienjiami-N,N`-bisu[2-(2-hidorokishifueniru)asetato] kadomiume (2) san eion to echirenjiamintetoraasetato tetsu (3) san ion tono aida no haiishi okikae hanno no hanno sokudoron ni yoru kiko kaiseki

    Energy Technology Data Exchange (ETDEWEB)

    Katsuyama, Tetsuo.; Orihara, Katsuo.; Takahata, Yasuyuki.; Yokota, Toshiyuki. [Yamagata University, Yamagata (Japan). Department of Materials Science and Enginering

    1998-12-10

    The kinetics of the ligand substitution reaction between the ethylenediamine-N,N`- bis[2-(2-hydroxyphenyl) acetato] cadmate (2) ion and the ethylenediaminetetraacetatoferrate (3) ion were carried out at 25 degreeC and ionic strength=0.1 mol dm{sup -3}. The substitution reaction was shown to proceed by a chain reaction mechanism where the chain propageting steps are the reactions of metal complexes with metal ions. The properties of the metal chain reaction mechanism are discussed. The metal-substitution of [Fe (edta)]{sup -} with cadmium ion was studied by the use of the chain reactins. The observed rae constants of the reaction were separated into two rate constants. The mechamism of the reactions is discussed. (author)

  17. Kinetical Analysis of the Mechanism of the Ligand Substitution Reaction between the Ethylenediamine-N,N[sup ']-bis[2-(2-hydroxyphenyl) acetato] cadmate (2) Ion and the Ethylenediaminetetraacetatoferrate (3) Ion. Echienjiami-N,N'-bisu[2-(2-hidorokishifueniru)asetato] kadomiume (2) san eion to echirenjiamintetoraasetato tetsu (3) san ion tono aida no haiishi okikae hanno no hanno sokudoron ni yoru kiko kaiseki

    Energy Technology Data Exchange (ETDEWEB)

    Katsuyama, Tetsuo.; Orihara, Katsuo.; Takahata, Yasuyuki.; Yokota, Toshiyuki. (Yamagata University, Yamagata (Japan). Department of Materials Science and Enginering)

    1998-12-10

    The kinetics of the ligand substitution reaction between the ethylenediamine-N,N'- bis[2-(2-hydroxyphenyl) acetato] cadmate (2) ion and the ethylenediaminetetraacetatoferrate (3) ion were carried out at 25 degreeC and ionic strength=0.1 mol dm[sup -3]. The substitution reaction was shown to proceed by a chain reaction mechanism where the chain propageting steps are the reactions of metal complexes with metal ions. The properties of the metal chain reaction mechanism are discussed. The metal-substitution of [Fe (edta)][sup -] with cadmium ion was studied by the use of the chain reactins. The observed rae constants of the reaction were separated into two rate constants. The mechamism of the reactions is discussed. (author)

  18. Spectroscopic properties of Fe2+ ions at tetragonal sites-Crystal field effects and microscopic modeling of spin Hamiltonian parameters for Fe2+ (S=2) ions in K2FeF4 and K2ZnF4

    International Nuclear Information System (INIS)

    Rudowicz, C.; Piwowarska, D.

    2011-01-01

    Magnetic and spectroscopic properties of the planar antiferromagnet K 2 FeF 4 are determined by the Fe 2+ ions at tetragonal sites. The two-dimensional easy-plane anisotropy exhibited by K 2 FeF 4 is due to the zero field splitting (ZFS) terms arising from the orbital singlet ground state of Fe 2+ ions with the spin S=2. To provide insight into the single-ion magnetic anisotropy of K 2 FeF 4 , the crystal field theory and the microscopic spin Hamiltonian (MSH) approach based on the tensor method is adopted. Survey of available experimental data on the crystal field energy levels and free-ion parameters for Fe 2+ ions in K 2 FeF 4 and related compounds is carried out to provide input for microscopic modeling of the ZFS parameters and the Zeeman electronic ones. The ZFS parameters are expressed in the extended Stevens notation and include contributions up to the fourth-order using as perturbation the spin-orbit and electronic spin-spin couplings within the tetragonal crystal field states of the ground 5 D multiplet. Modeling of the ZFS parameters and the Zeeman electronic ones is carried out. Variation of these parameters is studied taking into account reasonable ranges of the microscopic ones, i.e. the spin-orbit and spin-spin coupling constants, and the energy level splittings, suitable for Fe 2+ ions in K 2 FeF 4 and Fe 2+ :K 2 ZnF 4 . Conversions between the ZFS parameters in the extended Stevens notation and the conventional ones are considered to enable comparison with the data of others. Comparative analysis of the MSH formulas derived earlier and our more complete ones indicates the importance of terms omitted earlier as well as the fourth-order ZFS parameters and the spin-spin coupling related contributions. The results may be useful also for Fe 2+ ions at axial symmetry sites in related systems, i.e. Fe:K 2 MnF 4 , Rb 2 Co 1-x Fe x F 4 , Fe 2+ :Rb 2 CrCl 4 , and Fe 2+ :Rb 2 ZnCl 4 . - Highlights: → Truncated zero field splitting (ZFS) terms for Fe 2+ in K

  19. Effect of chelate ring sizes and their substitution on intensities of hypersensitive transitions of lanthanoids (Ln(III)) ions and j (total quantum number profiles)

    International Nuclear Information System (INIS)

    Dubey, J.; Pandey, P.; Yadav, A.; Limaye, S.N.

    1998-01-01

    Full text: Electronic spectral studies of Pr(III), Nd(III), Sm(III) Dy(III), Eu(III) and Tm(III) complexes with some aliphatic and aromatic O-O donor ligands viz., Glycolic (gly), Malonic (main) Succinic (suc), Glutaric (glut), Salicylic (sal), Phthalic acids and Catechol (cat) having varied chelate ring sizes and different substitutions as side chains have been carried out with a view to study the effect of chelate ring sizes on the intensities of hypersensitive and pseudo-hypersensitive transitions in lanthanoids. The intensities of these HST transitions have also been correlated with the total quantum number (J) of the lanthanoid metal ions in order to seek a probable mechanism for the phenomenon hypersensitivity. A comparison of the spectral and nephelauxetic parameters for Pr(III), Nd(III), Sm(III) with Dy(III) Er(III) and Tm(III) exhibit a variation in the bonding pattern from electrostatic to covalo-electrostatic from pre-Gd elements to post-Gd elements. The J-(total) quantum number profiles of the oscillator strength values for the specific HST transitions have also been examined

  20. Evaluation of CNTs/MnO{sub 2} composite for adsorption of {sup 60}Co(II), {sup 65}Zn(II) and Cd(II) ions from aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Sharaf El-Deen, Sahar E.A.; Moussa, Saber I.; Mekawy, Zakaria A.; Shehata, Mohamed K.K.; Someda, Hanan H. [Atomic Energy Authority, Inshas (Egypt). Dept. of Nuclear Chemistry; Sadeek, Sadeek A. [Zagazig Univ. (Egypt). Dept. of Chemistry

    2017-03-01

    CNTs/MnO{sub 2} composite was synthesized by a co-precipitation method after preparation of carbon nanotubes (CNTs) using a chemical oxidation method and was characterized using Fourier transformer infrared (FT-IR), X-ray diffraction (XRD) and scanning electron microscope (SEM). The synthesized CNTs/MnO{sub 2} composite was used as a sorbent for the removal of some radionuclides ({sup 60}Co and {sup 65}Zn-radioisotopes) and Cd (II) ions from aqueous solutions. Different parameters affecting the removal process including pH, contact time and metal ion concentration were investigated. Isotherm and kinetic models were studied. Adsorption data was interpreted in terms of both Freundlich and Langmuir isotherms and indicated that the CNTs/MnO{sub 2} composite complied well with both Langmuir and Freundlich models for {sup 60}Co and Cd(II) ions and with the Freundlich model only for the {sup 65}Zn radioisotope. A pseudo-second-order model was effectively employed to describe the adsorption behavior of {sup 60}Co, {sup 65}Zn and Cd(II) ions. Desorption of {sup 60}Co and {sup 65}Zn and Cd(II) ions from loaded samples was studied using different eluents.

  1. Coupling of the orthorhombic distortion to the depression of the Tc's due to Zn2+ doping in the ''RE-123'' HTSC's: A (d + s)-wave picture

    International Nuclear Information System (INIS)

    Tang, I.M.; Thongruang, R.; Charoenthai, N.

    1999-01-01

    The depressions of the T c 's of the 123 REBa 2 Cu 3 O 7 HTSC's due to the substitution of Zn 2+ ions into the Cu(2) layer are studied. The orthorhombic distortion which occurs in the 123 ceramics is assumed to induce a modification to the spin-fluctuation (SF) mediated pairing interaction which in turn causes the order parameters of these HTSC's to be of mixed (d + s)-wave symmetry. It is shown that part of the rapid depression of the T c 's caused by Zn 2+ substitution into the CuO 2 is due to a reduction of the SF-mediated pairing interaction. The differences in the rates of suppression of T c due to Zn 2+ doping in the different RE-123 HTSC's are shown to be due to the changes in the orthorhombicity which depend on the size of the rare earth ions

  2. Coupling of the Orthorhombic Distortion to the Depression of the Tc'S due to Zn2+ Doping in the "RE-123" Htsc's:. a (d+s)-WAVE Picture

    Science.gov (United States)

    Tang, I. M.; Charoenthai, N.; Thongruang, R.

    The depressions of the Tc's of the "123" REBa2Cu3O7 HTSC's due to the substitution of Zn2+ ions into the Cu(2) layer are studied. The orthorhombic distortion which occurs in the "123" ceramics is assumed to induce a modification to the spin-fluctuation (SF) mediated pairing interaction which inturn causes the order parameters of these HTSC's to be of mixed (d+s)-wave symmetry. It is shown that part of the rapid depression of the Tc's caused by Zn2+ substitution into the CuO2 is due to a reduction of the SF-mediated pairing interaction. The differences in the rates of suppression of Tc due to Zn2+ doping in the different "RE-123" HTSC's are shown to be due to the changes in the orthorhombicity which depend on the size of the rare earth ions.

  3. Mechanically induced strong red emission in samarium ions doped piezoelectric semiconductor CaZnOS for dynamic pressure sensing and imaging

    Science.gov (United States)

    Wang, Wei; Peng, Dengfeng; Zhang, Hanlu; Yang, Xiaohong; Pan, Caofeng

    2017-07-01

    Piezoelectric semiconductor with optical, electrical and mechanical multifunctions has great potential applications in future optoelectronic devices. The rich properties and applications mainly encompass the intrinsic structures and their coupling effects. Here, we report that lanthanide ions doped piezoelectric semiconductor CaZnOS:Sm3+ showing strong red emission induced by dynamic mechanical stress. Under moderate mechanical load, the doped piezoelectric semiconductor exhibits strong visible red emission to the naked eyes even under the day light. A flexible dynamic pressure sensor device is fabricated based on the prepared CaZnOS:Sm3+ powders. The mechanical-induced emission properties of the device are investigated by the optical fiber spectrometer. The linear characteristic emissions are attributed to the 4G5/2→6H5/2 (566 nm), 4G5/2→6H7/2 (580-632 nm), 4G5/2→6H9/2 (653-673 nm) and 4G5/2→6H11/2 (712-735 nm) f-f transitions of Sm3+ ions. The integral emission intensity is proportional to the value of applied pressure. By using the linear relationship between integrated emission intensity and the dynamic pressure, the real-time pressure distribution is visualized and recorded. Our results highlight that the incorporation of lanthanide luminescent ions into piezoelectric semiconductors as smart materials could be applied into the flexible mechanical-optical sensor device without additional auxiliary power, which has great potential for promising applications such as mapping of personalized handwriting, smart display, and human machine interface.

  4. Batch adsorptive removal of Fe(III), Cu(II) and Zn(II) ions in aqueous and aqueous organic–HCl media by Dowex HYRW2-Na Polisher resin as adsorbents

    OpenAIRE

    Aboul-Magd, Abdul-Aleem Soliman; Al-Husain, Salwa Al-Rashed; Al-Zahrani, Salma Ahmed

    2016-01-01

    Of the metal ions in tap, Nile, waste and sea water samples and some ores were carried out. Removal of heavy metal ions such as Fe(III), Cd(II), Zn(II), Cu(II), Mn(II), Mg(II), and Pb(II) from water and wastewater is obligatory in order to avoid water pollution. Batch shaking adsorption experiments to evaluate the performance of nitric and hydrochloric acid solutions in the removal of metal ions by cation exchange resin at the same conditions for both, such as the effect of initial metal ion ...

  5. Study of substitution in the systems UNi5sub(-)sub(x)Msub(x) and ZrNi5sub(-)sub(x)Msub(x) (M = In, Sn, Zn)

    International Nuclear Information System (INIS)

    Blazina, Z.; Drasner, A.; Ban, Z.; Zagreb Univ.

    1981-01-01

    X-ray powder diffraction studies and metallographic examinations in the systems UNi 5 sub(-)sub(x)Msub(x) and ZrNi 5 sub(-)sub(x)Msub(x) (M = In, Sn, Zn) revealed the existence of single phase regions up to the composition 1 : 4 : 1, i.e. up to UNi 4 M and ZrNi 4 M, respectively. Comparison between calculated and observed intensity values showed that nickel atoms, in the crystallographic positions 4(c) of the isostructural binary compounds UNi 5 or ZrNi 5 (UNi 5 -type, S.G. F43m), are substituted by M atoms. Vegard's rule is obeyed in the single phase regions of all investigated systems. The crystal structures of UNi 4 M and ZrNi 4 M are superlattice structures of the MgSnCu 4 -type (S.G. F43m). Structural correlations of these phases with corresponding binary prototypes are made in terms of stacking sequences. (orig.)

  6. Preparation of hollow Zn2SnO4 boxes@C/graphene ternary composites with a triple buffering structure and their electrochemical performance for lithium-ion batteries

    International Nuclear Information System (INIS)

    Huang, Haijian; Huang, Ying; Wang, Mingyue; Chen, Xuefang; Zhao, Yang; Wang, Ke; Wu, Haiwei

    2014-01-01

    Highlights: • A new hollow Zn 2 SnO 4 boxes@C/graphene ternary composites were synthesized through two hydrothermal processes followed by a calcined process for the first time. • The structure, morphology and electrochemical properties of the ternary composites were investigated by means of XRD, FTIR, Raman, BET, BJH, SEM, TEM, and electrochemical measurements. • The hollow Zn 2 SnO 4 boxes@C/graphene ternary composites were proved to have a triple buffering nanostructure. The hollow interior of the Zn 2 SnO 4 boxes, the carbon coating layer on the surface of the boxes and the 3D carbon network constructed by the graphene sheets can work together to effectively improve the electrochemical performance of the material. • The hollow Zn 2 SnO 4 boxes@C/graphene ternary composites show an enhanced electrochemical performance (726.9 mAh g −1 at a current density of 300 mA g −1 after 50 cycles) and high rate capability compared with the hollow Zn 2 SnO 4 boxes@graphene binary composites, the hollow Zn 2 SnO 4 boxes@C binary composites, the hollow Zn 2 SnO 4 boxes and the solid Zn 2 SnO 4 cubes. - Abstract: Hollow Zn 2 SnO 4 boxes@C/graphene ternary composites with a three-dimensional triple buffering structure are prepared by two hydrothermal processes followed by a calcined process. The structure, morphology and electrochemical properties of the ternary composites were investigated by means of XRD, FTIR, Raman, BET, BJH, SEM, TEM, and electrochemical measurements. The hollow Zn 2 SnO 4 boxes are coated with carbon layer and then supported by graphene sheets to form a 3D carbon conductive network. Compared with the hollow Zn 2 SnO 4 boxes@graphene binary composites, the hollow Zn 2 SnO 4 boxes@C binary composites, the hollow Zn 2 SnO 4 boxes and the solid Zn 2 SnO 4 cubes, the hollow Zn 2 SnO 4 boxes@C/graphene ternary composites show an enhanced electrochemical performance (726.9 mAh g −1 at a current density of 300 mA g −1 after 50 cycles) and high rate

  7. Improving the SMM and luminescence properties of lanthanide complexes with LnO9 cores in the presence of ZnII: an emissive Zn2Dy single ion magnet.

    Science.gov (United States)

    Fondo, Matilde; Corredoira-Vázquez, Julio; Herrera-Lanzós, Antía; García-Deibe, Ana M; Sanmartín-Matalobos, Jesús; Herrera, Juan Manuel; Colacio, Enrique; Nuñez, Cristina

    2017-12-12

    Mononuclear complexes of stoichiometry [Ln(H 3 L)(H 2 O)(NO 3 )](NO 3 ) 2 (Ln = Tb, 1; Dy, 2, Er, 3), which crystallise with different solvates, and the heterotrinuclear compound [Zn 2 Dy(L)(NO 3 ) 3 (OH)] (4) can be obtained with the same H 3 L compartmental ligand. The single X-ray crystal structure of the mononuclear complexes shows a LnO 9 core with a muffin-like disposition while the geometry of the DyO 9 core in 4 seems to be closer to spherical capped square antiprism. The analysis of the magnetic properties of all the complexes demonstrates that the mononuclear lanthanide compounds do not show slow relaxation of the magnetization, even when the samples are diluted with a diamagnetic matrix and subjected to a dc applied field of 1000 Oe. Nevertheless, the heterotrinuclear dysprosium complex 4·3H 2 O is a field-induced single ion magnet, with an estimated U eff barrier of 59 K. The luminescence characterisation of all the metal complexes in methanol solution at 298 K also shows a notable increase in the fluorescence emission of the heterotrinuclear complex with respect to the mononuclear ones, in such a way that 4 can be defined as a fluorescent single ion magnet.

  8. Zinc and Carbonate Co-Substituted Nano-Hydroxyapatite

    Science.gov (United States)

    Girija, E. K.; Kumar, G. Suresh; Thamizhavel, A.

    2011-07-01

    Synthesis of Zn or CO32- substituted nano-hydroxyapatite (HA) and its physico-chemical properties have been well documented. However, the effects of the simultaneous substitution of Zn and CO32- in nano-HA have not been reported. In the present study, Zn and CO32- substitutions in nano HA independently and concurrently have been done by wet precipitation method and characterized by XRD and FT-IR for its phase purity and chemical homogeneity. Further modulations of the bioactivity and thermal stability of HA due to the substitutions have been studied.

  9. Hydrothermal synthesis and magnetic properties of Mn doped ZnS nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Rashad, M M; Rayan, D A; El-Barawy, K [Central Metallurgical Research and Development Institute PO Box: 87 Helwan, Cairo (Egypt)

    2010-01-01

    Nanocrystallite Mn doped Zn{sub 1-X}S (X = 0 to 0.4) powders have been synthesized through a hydrothermal route. The effect of the hydrothermal temperature and Mn{sup 2+} ions substitution on the crystal structure, crystallite size, microstructure and magnetic properties were investigated using (XRD), (SEM) and (VSM). The results revealed that wurtzite zinc sulfide phase was formed using thiourea as a sulfur source at temperature 150- 200{sup o}C for 24 h. The crystallite size was (7.9-15.1 nm) was obtained at the same conditions. The doping of Mn{sup 2+} ions decreased the crystallite size of the formed ZnS wurtzite phase was in the range between 7.9 and 3.8 nm. SEM micrographs showed that the produced ZnS and Mn doped ZnS particles were appeared as spherical shape. The magnetic properties were improved by substitution of Mn{sup 2+} ions up to 0.2.

  10. Lattice location of implanted As in ZnO

    CERN Document Server

    Wahl, U; Correia, J G; Marques, A C; Alves, E; Soares, J C

    2007-01-01

    Radioactive 73As ions were implanted into a ZnO single crystal at room temperature with 60 keV up to a fluence of 2×1013 cm−2. Subsequently, the angular emission channeling patterns of emitted conversion electrons were recorded by means of a position-sensitive detector in the as-implanted state and following annealing up to 900 C, and were compared to simulated emission yields for a variety of different lattice sites. We find that As does not occupy substitutional O sites, but mainly occupies the substitutional Zn sites. The fraction of As on O sites was at most a few per cent. Arsenic in ZnO is thus an interesting example of an impurity in a semiconductor where the major impurity lattice site is determined by atomic size and electronegativity rather than its position in the periodic system. Possible consequences with respect to the role of arsenic as a p-type dopant in ZnO are being discussed.

  11. An equilibrium model for ligand-modified micellar-enhanced ultrafiltration. Selective separation of metal ions using iminoacetic substituted polyamines and a theoretical model for the titration behavior of polyamines

    Energy Technology Data Exchange (ETDEWEB)

    Dharmawardana, Udeni Rajaratna [Univ. of Oklahoma, Norman, OK (United States)

    1992-01-01

    This thesis consists of three chapters. Chapter 1, An equilibrium model for ligand-modified micellar-enhanced ultrafiltration, describes a theoretical model and experimental investigations which used the semi-equilibrium-dialysis method with N-n-dodecyl iminodiacetic acid as the ligand. In Chapter 2, Selective separation of metal ions using iminoacetic substituted polyamines, polyamines with a substituted ligand group are synthesized and used in investigating selective separation of copper ions from aqueous solution. In Chapter 3, A theoretical model for the titration behavior of polyamines, a novel approach to explain the titration behavior of polymeric amines based on the binding behavior of counterions is described. The application of this study is to the investigation of inexpensive and efficient methods of industrial waste water treatment.

  12. A novel highly sensitive and selective optical sensor based on a symmetric tetradentate Schiff-base embedded in PVC polymeric film for determination of Zn{sup 2+} ion in real samples

    Energy Technology Data Exchange (ETDEWEB)

    Abdel Aziz, Ayman A., E-mail: aymanaziz31@gmail.com [Chemistry Department, Faculty of Science, Ain Shams University, 11566 Cairo (Egypt); Chemistry Department, Faculty of Science, University of Tabuk, 71421, Tabuk (Saudi Arabia)

    2013-11-15

    A novel prepared Zn{sup 2+} ion PVC membrane sensor based on a novel Schiff base; N,N′bis(salicylaldehyde)2,3-diaminonaphthalene (SDN) for the determination of Zn{sup 2+} ion was described. The chemosensor was synthesized under microwave irradiation via condensation of 2,3-diaminonaphthalene and salicylaldehyde. Photoluminescence characteristics of the novel Schiff base ligand were investigated in different solvents including dicholoromethane (DCM), tetrahydrofuran (THF) and ethanol (EtOH). SDN was found to have higher emission intensity and Stoke’s shift value (Δλ{sub ST}) in EtOH solution. The sensor exhibited a specific fluorescent on response to Zn{sup 2+}. The response of the sensor is based on the fluorescence enhancement of SDN (LH{sub 2}) by Zn{sup 2+} ion as a result of formation the rigid structure L-Zn complex. The experiment results also show that the response behavior of SDN to Zn{sup 2+} is pH independent in the range of pH 6.0–8.0. At pH 7.0, the proposed sensor displays a calibration response for Zn{sup 2+} over a wide concentration range of 1.0×10{sup −9}–2.0×10{sup −3} mol L{sup −1} with a limit of detection (LOD) 8.1×10{sup −10} mol L{sup −1} (0.0529659 μg L{sup −1}). The sensor shows excellent selectivity toward Zn{sup 2+} with respect to common coexisting cations. The proposed fluorescence optode was successfully applied to detect Zn{sup 2+} in human hair samples, different brands of powdered milk and some pharmaceuticals. -- Highlights: • A novel Zn(II) chemosensor has been developed. • Wide linear concentration range of 1.0×10{sup −9}–2.0×10{sup −3} mol L{sup −1}. • Application for determination of Zn(II) in real samples.

  13. Structural refinement, photoluminescence and Raman spectroscopy of wurtzite Mn-doped Zn O pellets

    Energy Technology Data Exchange (ETDEWEB)

    Marquina, J.; Martin, J.; Luengo, J.; Vera, F.; Roa, L. [Centro de Estudios Avanzados en Optica, Universidad de los Andes, Merida 5101 (Venezuela, Bolivarian Republic of); Gonzalez, J. [Centro de Estudios de Semiconductores, Universidad de los Andes, Merida 5101 (Venezuela, Bolivarian Republic of); Rodriguez, F.; Renero L, C.; Valiente, R. [Malta-Consolider Team, CITIMAC, Facultad de Ciencias, Universidad de Cantabria, Santander 69005 (Spain); Delgado, G. E., E-mail: marquinajesus@gmail.com [Laboratorio de Cristalografia, Facultad de Ciencias, Universidad de los Andes, Merida 5101 (Venezuela, Bolivarian Republic of)

    2017-11-01

    We report the results of the Rietveld refinement, photoluminescence and Raman spectroscopy of Mn-doped Zn O ceramic pellets. Rietveld refinement shows that samples crystallize in the wurtzite structure and for the Mn-doped sample indicated that the Mn atoms substitute the Zn tetrahedral crystallographic sites in the Zn O host lattice. The emission and absorption spectra of Mn-doped Zn O have been investigated in the visible-UV region and the data have been interpreted in terms of the wurtzite Zn O electronic structure. Two broad bands, one due to superposition between donor bound excitons (DX) and free excitons (FX) and other due free-to bond excitonic recombination (FB) dominates the low-temperature photoluminescence spectra of Mn-doped Zn O bulk. In the Raman spectrum, an extra mode at ∼520 cm{sup -1} has been observed in agreement with earlier works, and it is an indicator for the incorporation of Mn{sup +2} ions into the Zn O host matrix since it is not is observed in Zn O pristine. Rietveld refinement of the X-ray diffraction patterns, energy-dispersive X-ray spectroscopy (EDS) technique, and Raman spectroscopies were performed to study these effects. (Author)

  14. Thermodynamic assessment of the Pr-Zn binary system

    International Nuclear Information System (INIS)

    Huang, X.M.; Liu, L.B.; Zhang, L.G.; Jia, B.R.; Jin, Z.P.; Zheng, F.

    2008-01-01

    On the basis of available experimental data of phase diagram and thermodynamic properties, the Pr-Zn binary system has been optimized using the CALPHAD approach. The phases, including liquid and bcc A 2(βPr) were treated as substitutional solutions, while the intermetallic compounds, including PrZn, PrZn 2 , PrZn 3 , Pr 3 Zn 11 , Pr 13 Zn 58 , Pr 3 Zn 22 , Pr 2 Zn 17 and PrZn 11 were modeled as stoichiometric compounds. As the result of optimization, a set of self-consistent thermodynamic parameters has been obtained, which can be used to reproduce the reported experimental data

  15. Effect of Precursors on Key Opto-electrical Properties of Successive Ion Layer Adsorption and Reaction-Prepared Al:ZnO Thin Films

    Science.gov (United States)

    Kumar, K. Deva Arun; Valanarasu, S.; Ganesh, V.; Shkir, Mohd.; Kathalingam, A.; AlFaify, S.

    2018-02-01

    Aluminum-doped zinc oxide (Al:ZnO) thin films were deposited on glass substrates by successive ion layer adsorption and reaction (SILAR) method using different precursors. This inexpensive SILAR method involves dipping of substrate sequentially in zinc solution, de-ionized water and ethylene glycol in multiple cycles. Prepared films were investigated by x-ray diffraction (XRD), scanning electron microscope (SEM), atomic force microscope (AFM), optical absorption, photoluminescence (PL), Raman spectroscopy and electrical studies. XRD study confirmed incorporation of aluminum in ZnO lattice with a polycrystalline hexagonal wurtzite structure of the films. The crystallite size determined by the Scherrer equation showed an increase from 28 nm to 35 nm for samples S1 to S4, respectively. SEM study showed smooth morphology with homogeneous distribution of particles. From the AFM images, the surface roughness was found to change according to precursors. For the optical analysis, the zinc chloride precursor showed high optical transmittance of about 90% in the visible range with a band gap value 3.15 eV. The room-temperature PL spectra exhibited a stronger violet emission peak at 420 nm for all the prepared samples. The Raman spectra showed a peak around 435 cm-1 which could be assigned to non-polar optical phonons (E2-high) mode AZO films of a ZnO wurtzite structure. Hall effect measurements showed n-type conductivity with low resistivity ( ρ) and high carrier concentrations ( n) of 2.39 × 10-3 Ω-cm and 8.96 × 1020 cm-3, respectively, for the film deposited using zinc chloride as precursor. The above properties make the prepared AZO film to be regarded as a very promising electrode material for fabrication of optoelectronic devices.

  16. Origin of Blue-Green Emission in α-Zn2P2O7 and Local Structure of Ln3+ Ion in α-Zn2P2O7:Ln3+ (Ln = Sm, Eu): Time-Resolved Photoluminescence, EXAFS, and DFT Measurements.

    Science.gov (United States)

    Gupta, Santosh Kumar; Ghosh, Partha Sarathi; Yadav, Ashok Kumar; Jha, Shambhu Nath; Bhattacharyya, Dibyendu; Kadam, Ramakant Mahadeo

    2017-01-03

    Considering the fact that pyrophosphate-based hosts are in high demand for making highly efficient luminescence materials, we doped two visible lanthanide ions, viz. Sm 3+ and Eu 3+ , in Zn 2 P 2 O 7 . Interestingly, it was oberved that pure Zn 2 P 2 O 7 displayed blue-green dual emission on irradiation with ultraviolet light. Emission and lifetime spectroscopy shows the presence of defects in pyrophosphate samples which are responsible for such emission. DFT calculations clearly pinpointed that the electronic transitions between defect states located at just below the conduction band minimum (arises due to V O 1+ and V O 2+ defects) and valence band maximum, as well as impurity states situated in the band gap, can lead to dual emission in the blue-green region, as is also indicated by emission and lifetime spectra. X-ray absorption near edge spectroscopy (XANES) shows the stabilization of europium as well as samarium ion in the +3 oxidation state in α-Zn 2 P 2 O 7 . The fact that α-Zn 2 P 2 O 7 has two different coordination numbers for zinc ions, i.e. five- and six-coordinate, the study of dopant ion distribution in this particular matrix will be an important step in realizing a highly efficient europium- and samarium-based red-emitting phosphor. Time resolved photoluminescence (TRPL) shows that both of these ions are heterogeneously distributed between five- and six-coordinated Zn 2+ sites and it is the six-coordinated Zn 2+ site which is the most favorable for lanthanide ion doping. Extended X-ray absorption fine structure (EXAFS) measurements also suggested that a six-coordinated zinc ion is the preferred site occupied by trivalent lanthanide ions, which is in complete agreement with TRPL results. It was observed that there is almost complete transfer of photon energy from Zn 2 P 2 O 7 to Eu 3+ , whereas this transfer is inefficient and almost incomplete in case of Sm 3+ , which is indeed important information for the realization of pyrophosphate

  17. Oxygen vacancy induced by La and Fe into ZnO nanoparticles to modify ferromagnetic ordering

    International Nuclear Information System (INIS)

    Verma, Kuldeep Chand; Kotnala, R.K.

    2016-01-01

    into ZnO nanoparticles induce defects in terms of oxygen vacancy. • The La ions in Fe substituted ZnO formed nanoparticles than nanorods. • Antiferromagnetic interactions are observed at room temperature magnetic measurement. • Rietveld analysis evaluated structural deformation in the Wurtzite ZnO lattice.

  18. Spectroscopic investigation of an intrinsic room temperature ferromagnetism in Co doped ZnO nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    N, Srinatha [Department of Physics, JB Campus, Bangalore University, Bangalore 560056 (India); Angadi, Basavaraj, E-mail: brangadi@gmail.com [Department of Physics, JB Campus, Bangalore University, Bangalore 560056 (India); Nair, K.G.M. [UGC-DAE-CSR, Kalpakkam Node, Kalpakkam, Kokilamedu 603 102 (India); Deshpande, Nishad G.; Shao, Y.C.; Pong, Way-Faung [Department of Physics, Tamkang University, Tamsui, Taipei 251, Taiwan (China)

    2014-08-15

    Highlights: • For the first time L-Valine was used as a fuel to synthesize Co:ZnO nanoparticles by solution combustion method. • Single phase and ferromagnetic nature were confirmed through XRD, SQUID, NEXAFS and XMCD. • Through NEXAFS and XMCD, the effect of ‘Co’ substitution at O K-edge, Co L{sub 3,2} edge, Zn L{sub 3,2} edge have been investigated. • Spectral features of NEXAFS and XMCD confirms an intrinsic RTFM by substitution of ‘Co{sup 2+}’ at ‘Zn{sup 2+}’ site and rules out the presence of secondary phases. - Abstract: Pure and Co substituted ZnO nano crystalline particles were prepared by solution combustion technique using L-Valine as a fuel. As synthesized powder samples were characterized by X-ray diffractometer and SQUID magnetometer to confirm the formation of single phase wurtzite structure and to study the bulk magnetic response of the sample, respectively. Magnetic studies show that Co doped ZnO nanoparticles exhibit ferromagnetism (FM) at room temperature (RT). Furthermore, the electronic structure and element specific magnetic properties were investigated by near-edge X-ray absorption fine structure (NEXAFS) and X-ray magnetic circular dichroism (XMCD) measurements, respectively. The effect of Co substitution on the spectral features of Co–ZnO at O K-edge, Co L{sub 3,2} edge, Zn L{sub 3,2} edge have been investigated. The spectral features of NEXAFS at Co L{sub 3,2} edge is entirely different from the spectral features of metallic clusters and other impurity phases, which rules out the presence of impurity phases. The valence state of ‘Co’ ion is found to be in +2 state. The FM nature of the sample was confirmed through XMCD spectra, which is due to the incorporation of divalent ‘Co’ ions. Hence the presented results confirm the substitution of ‘Co’ ions at ‘Zn’ site in the host lattice, which is responsible for the RTFM.

  19. Precursor polymers for the carbon coating of Au@ZnO multipods for application as active material in lithium-ion batteries.

    Science.gov (United States)

    Oschmann, Bernd; Tahir, Muhammad Nawaz; Mueller, Franziska; Bresser, Dominic; Lieberwirth, Ingo; Tremel, Wolfgang; Passerini, Stefano; Zentel, Rudolf

    2015-06-01

    The synthesis of statistical and block copolymers based on polyacrylonitrile, as a source for carbonaceous materials, and thiol-containing repeating units as inorganic nanoparticle anchoring groups is reported. These polymers are used to coat Au@ZnO multipod heteroparticles with polymer brushes. IR spectroscopy and transmission electron microscopy prove the successful binding of the polymer onto the inorganic nanostructures. Thermogravimetric analysis is applied to compare the binding ability of the block and statistical copolymers. Subsequently, the polymer coating is transformed into a carbonaceous (partially graphitic) coating by pyrolysis. The obtained carbon coating is characterized by Raman spectroscopy and energy-dispersive X-ray (EDX) spectroscopy. The benefit of the conformal carbon coating of the Au@ZnO multipods regarding its application as lithium-ion anode material is revealed by performing galvanostatic cycling, showing a highly enhanced and stabilized electrochemical performance of the carbon-coated particles (still 831 mAh g(-1) after 150 cycles) with respect to the uncoated ones (only 353 mAh g(-1) after 10 cycles). © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  20. Effects of phosphorus doping by plasma immersion ion implantation on the structural and optical characteristics of Zn0.85Mg0.15O thin films

    International Nuclear Information System (INIS)

    Saha, S.; Nagar, S.; Chakrabarti, S.

    2014-01-01

    ZnMgO thin films deposited on 〈100〉 Si substrates by RF sputtering were annealed at 800, 900, and 1000 °C after phosphorus plasma immersion ion implantation. X-ray diffraction spectra confirmed the presence of 〈101 ¯ 0〉 and 〈101 ¯ 3〉 peaks for all the samples. However, in case of the annealed samples, the 〈0002〉 peak was also observed. Scanning electron microscopy images revealed the variation in surface morphology caused by phosphorus implantation. Implanted and non-implanted samples were compared to examine the effects of phosphorus implantation on the optical properties of ZnMgO. Optical characteristics were investigated by low-temperature (15 K) photoluminescence experiments. Inelastic exciton–exciton scattering and localized, and delocalized excitonic peaks appeared at 3.377, 3.42, and 3.45 eV, respectively, revealing the excitonic effect resulting from phosphorus implantation. This result is important because inelastic exciton–exciton scattering leads to nonlinear emission, which can improve the performance of many optoelectronic devices

  1. Spectroscopic and optical properties of the VO2+ ion doped TeO2-TiO2-ZnO-Nb2O5 glass system

    Science.gov (United States)

    Swapna; Upender, G.; Sreenivasulu, V.; Prasad, M.

    2016-04-01

    Studies such as optical absorption, Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, Electron paramagnetic resonance (EPR) spectroscopy and Differential scanning calorimetry (DSC) were carried out on VO2+ ion doped TeO2-TiO2-ZnO-Nb2O5 glass system. Raman and FTIR spectra of the glasses revealed the presence of [TeO3], [TeO4] and [NbO6] structural units in the glass network. The Urbach energy (Δ E), cut-off wavelength (λ c ), optical band gap ( E opt ), optical basicity (Λ) and electron polarizability ( α) of the glasses were determined from optical absorption studies. The density ( ρ), molar volume ( V m ), oxygen molar volume ( V o ) and refractive index ( n) were also measured. Spin-Hamiltonian parameters were calculated from the EPR studies. When Nb2O5 was increased at the expense of ZnO, the density, optical band gap and Urbach energy of the glasses increased, and the electronic polarizability and optical basicity decreased. The EPR spectra clearly showed that vanadium was in the glass as VO2+ and occupied octahedral sites with tetrahedral compression. Spin-Hamiltonian parameters g‖ and g⊥ decreased as Nb2O5 content increased in the glass. The glass transition temperature ( T g ) also increased with increasing Nb2O5 content in the glass.

  2. Effect on the Inhibitory Activity of Potential Microbes on the Complexation of Methyl Anthranilate Derived Hydrazide with Cu, Ni and Zn (II) Metal Ions

    International Nuclear Information System (INIS)

    Ikram, M.; Rehman, S.; Khan, K.

    2013-01-01

    The hydrazide ligand 2-amino-(N-aminobezoyl)benzohydrazide (ABH) have been synthesized and characterized by 1H-NMR, 13C-NMR, ES+-MS, elemental analyses and infrared studies. The ligand was complexed with Ni(II), Cu(II) and Zn(II) metal ions and were characterized by analytical and spectroscopic methods including elemental analyses, ES+-MS, conductance, infrared, UV-Visible and magnetic susceptibilities studies. Infrared spectra show that the ligand form complexes through -NH2 and carbonyl moieties, the elemental studies suggested the M(ABH)X2 composition of the coordination compounds. The synthesized complexes were studied for their biological activities against gram negative bacteria including Escherichia coli, Salmonella typhi, Enterobacter aerogenes, Proteus vulgaris, Pseudomonas aeruginosa, Gram positive bacterial strains like Staphylococcus aureus and fungus like Candida albican. These activities show that the metal complexes are more active to the tested microbes as compared to neat ligand. (author)

  3. UV N{sub 2} laser ablation of a Cu-Sn-Zn-Pb alloy: Microstructure and topography studied by focused ion beam

    Energy Technology Data Exchange (ETDEWEB)

    Zupanic, Franc [University of Maribor, Faculty of Mechanical Engineering, University Centre for Electron Microscopy, Smetanova 17, SI-2000 Maribor (Slovenia)], E-mail: franc.zupanic@uni-mb.si; Boncina, Tonica [University of Maribor, Faculty of Mechanical Engineering, University Centre for Electron Microscopy, Smetanova 17, SI-2000 Maribor (Slovenia); Pipic, Davor; Henc-Bartolic, Visnja [University of Zagreb, Faculty of Electrical Engineering and Computing, Department of Applied Physics, Unska 3, 10000 Zagreb (Croatia)

    2008-10-06

    A Cu-Sn-Zn-Pb alloy was irradiated by ultraviolet nitrogen laser pulses (N{sub 2} laser, wavelength 337 nm, pulse duration 6 ns, frequency 1 Hz, power 0.5 MW and average power density 0.67 GW/m{sup 2}). The surface topography and microstructure were mainly studied by scanning electron microscopy, and a focused ion beam. The non-homogenized spatial beam profile resulted in the activation of several ablative mechanisms, the main being phase explosion and hydrodynamic instability. They caused a crater to be formed, surrounded by a raised rim and wavelike structure in a halo. FIB cross-sectioning and imaging showed a shallow (few micrometers) molten and resolidified surface layer. Streaks were observed in the heat-affected zone beneath the molten layer, indicating partial recrystallization of initially cold-worked material.

  4. Microwave annealing effect for highly reliable biosensor: dual-gate ion-sensitive field-effect transistor using amorphous InGaZnO thin-film transistor.

    Science.gov (United States)

    Lee, In-Kyu; Lee, Kwan Hyi; Lee, Seok; Cho, Won-Ju

    2014-12-24

    We used a microwave annealing process to fabricate a highly reliable biosensor using amorphous-InGaZnO (a-IGZO) thin-film transistors (TFTs), which usually experience threshold voltage instability. Compared with furnace-annealed a-IGZO TFTs, the microwave-annealed devices showed superior threshold voltage stability and performance, including a high field-effect mobility of 9.51 cm(2)/V·s, a low threshold voltage of 0.99 V, a good subthreshold slope of 135 mV/dec, and an outstanding on/off current ratio of 1.18 × 10(8). In conclusion, by using the microwave-annealed a-IGZO TFT as the transducer in an extended-gate ion-sensitive field-effect transistor biosensor, we developed a high-performance biosensor with excellent sensing properties in terms of pH sensitivity, reliability, and chemical stability.

  5. The effect of Li2CO3 substitution on synthesis of LiBOB compounds as salt of electrolyte battery lithium ion

    Science.gov (United States)

    Lestariningsih, Titik; Wigayati, Etty Marty; Sabrina, Qolby; Prihandoko, Bambang; Priyono, Slamet

    2018-04-01

    Development of the synthesis of LiB(C2O4)2 compounds continues to evolve along with the need for electrolyte salts to support the research of the manufacture of lithium ion batteries. A study had been conducted on the effect of Li2CO3 substitution on the synthesis of LiB(C2O4)2 or LiBOB compounds. LiBOB was a major candidate to replace LiPF6 as a highly toxic lithium battery electrolyte and harmful to human health. Synthesis of Lithium bis(oxalato) borate used powder metallurgy method. The raw materials used are H2C2O4.2H2O, Li2CO3 or LiOH and H2BO3 from Merck Germany products. The materials are mixed with 2: 1: 1 mol ratio until homogeneous. The synthesis of LiBOB refers to previous research, where the heating process was done gradually. The first stage heating is carried out at 120°C for 4 hours, then the next stage heating is carried out at 240°C for 7 hours. The sample variation in this study was to distinguish the lithium source from Li2CO3 and LiOH. Characterization was done by XRD to know the phase formed, FTIR to confirm that functional group of LiB(C2O4)2 compound, SEM to know the morphological structure, and TG/DTA to know the thermal properties. The results of the analysis shows that LiBOB synthesis using Lithium source from Li2CO3 has succeeded to form LiBOB compound with more LiBOB phase composition is 59.1% and 40.9% LiBOB hydrate phase, SEM morphology shows powder consist of elongated round particle porous and similar to LiBOB commercial and show higher thermal stability.

  6. Synthesis and characterization of organic–inorganic core–shell structure nanocomposite and application for Zn ions removal from aqueous solution in a fixed-bed column

    Energy Technology Data Exchange (ETDEWEB)

    Ghasemi, Shokoofeh [Faculty of Chemical, Gas and Petroleum Engineering, Semnan University, Semnan 35131-19111 (Iran, Islamic Republic of); Ghorbani, Mohsen, E-mail: M.ghorbani@nit.ac.ir [Faculty of Chemical Engineering, Babol University of Technology, P.O. Box 484, Babol (Iran, Islamic Republic of); Ghazi, Mohsen Mehdipour [Faculty of Chemical, Gas and Petroleum Engineering, Semnan University, Semnan 35131-19111 (Iran, Islamic Republic of)

    2015-12-30

    Graphical abstract: - Highlights: • The γ-Fe{sub 2}O{sub 3} nanoparticles were prepared in one step using ultrasonic radiation and coated by polyrhodanine. • Nanocomposite synthesized with core average diameter of 15 nm and polyrhodanine as shell with thickness of 1.5 nm • Application of products was investigated to separate zinc ions from aqueous solution in a fixed-bed column. • The Adams–Bohart, BDST, Thomas and Yoon–Nelson models used to predict model parameters. • The models were nearly in good agreement with the experimental data. - Abstract: An organic–inorganic core/shell structure, γ-Fe{sub 2}O{sub 3}/polyrhodanine nanocomposite with γ-Fe{sub 2}O{sub 3} nanoparticle as core with average diameter of 15 nm and polyrhodanine as shell with thickness of 1.5 nm, has been synthesized via chemical oxidation polymerization and applied for adsorption of Zn ions from aqueous solution in a fixed-bed column. The properties of nanocomposite were characterized with transmission electron microscope (TEM), Fourier transform infrared (FT-IR) spectroscopy and vibrating sample magnetometer (VSM). The performance of the column was assessed under variable bed heights (10, 15 and 20 cm) and influent Zn concentrations (50, 100 and 150 ppm) at a constant flow rate (0.5 mL/min). The results demonstrated that the breakthrough curves are S-shaped and the breakthrough time increases with increasing bed height and decreases with increasing influent concentration. Moreover, the dynamics of the adsorption process were evaluated by using Adams–Bohart, bed depth service time (BDST), Thomas and Yoon–Nelson kinetic models. The models were nearly in good agreement with the experimental data.

  7. Structural and magnetic properties of two branches of the tripod-kagome-lattice family A2R3Sb3O14 (A = Mg, Zn; R = Pr, Nd, Gd, Tb, Dy, Ho, Er, Yb)

    Science.gov (United States)

    Dun, Z. L.; Trinh, J.; Lee, M.; Choi, E. S.; Li, K.; Hu, Y. F.; Wang, Y. X.; Blanc, N.; Ramirez, A. P.; Zhou, H. D.

    2017-03-01

    We present a systematic study of the structural and magnetic properties of two branches of the rare-earth tripod-kagome-lattice (TKL) family A2R3Sb3O14 (A = Mg, Zn; R = Pr, Nd, Gd, Tb, Dy, Ho, Er, Yb; here, we use abbreviation A-R, as in MgPr for Mg2Pr3Sb3O14 ), which complements our previously reported work on MgDy, MgGd, and MgEr [Z. L. Dun et al., Phys. Rev. Lett. 116, 157201 (2016), 10.1103/PhysRevLett.116.157201]. The present susceptibility (χdc, χac) and specific-heat measurements reveal various magnetic ground states, including the nonmagnetic singlet state for MgPr, ZnPr; long-range orderings (LROs) for MgGd, ZnGd, MgNd, ZnNd, and MgYb; a long-range magnetic charge ordered state for MgDy, ZnDy, and potentially for MgHo; possible spin-glass states for ZnEr, ZnHo; the absence of spin ordering down to 80 mK for MgEr, MgTb, ZnTb, and ZnYb compounds. The ground states observed here bear both similarities as well as striking differences from the states found in the parent pyrochlore systems. In particular, while the TKLs display a greater tendency towards LRO, the lack of LRO in MgHo, MgTb, and ZnTb can be viewed from the standpoint of a balance among spin-spin interactions, anisotropies, and non-Kramers nature of single-ion state. While substituting Zn for Mg changes the chemical pressure, and subtly modifies the interaction energies for compounds with larger R ions, this substitution introduces structural disorder and modifies the ground states for compounds with smaller R ions (Ho, Er, Yb).

  8. Substitutional analysis

    CERN Document Server

    Rutherford, Daniel Edwin

    2013-01-01

    Classic monograph, suitable for advanced undergraduates and graduate students. Topics include calculus of permutations and tableaux, semi-normal representation, orthogonal and natural representations, group characters, and substitutional equations. 1968 edition.

  9. Enhanced electrochemical performance of Ti substituted P2-Na2/3Ni1/4Mn3/4O2 cathode material for sodium ion batteries

    International Nuclear Information System (INIS)

    Zhao, Wenwen; Tanaka, Akinobu; Momosaki, Kyoko; Yamamoto, Shinji; Zhang, Fabi; Guo, Qixin; Noguchi, Hideyuki

    2015-01-01

    Highlights: • Ti substituted P2-Na 2/3 Ni 1/4 Mn 3/4 O 2 cathode was synthesized. • Structural and electrochemical properties of Na 2/3 Ni 1/4 Ti x Mn 3/4-x O 2 were studied. • Ti substituted cathodes exhibit enhanced cycleability and rate performance. • Ti substitution has impact on stabilizing the P2 structure during cycling. -- Abstract: Ti substituted P2-Na 2/3 Ni 1/4 Mn 3/4 O 2 cathode material with the composition of Na 2/3 Ni 1/4 Ti x Mn 3/4-x O 2 has been synthesized by solid state method. The influence of Ti substitution for Mn on the structure, morphology and electrochemical performances of P2-Na 2/3 Ni 1/4 Mn 3/4 O 2 has been investigated. X-ray diffraction (XRD) results of Ti substituted sample show that they exhibit same diffraction patterns as those of pristine P2-Na 2/3 Ni 1/4 Mn 3/4 O 2 . Progressive change in the lattice parameters of Ti substituted samples suggests that Mn was successfully substituted by Ti. In contrast to P2-Na 2/3 Ni 1/4 Mn 3/4 O 2 which shows step-type voltage profiles, Ti substituted samples show sloping voltage profiles. Drastic capacity fade occurred for P2-Na 2/3 Ni 1/4 Mn 3/4 O 2 cathode, while Ti substituted cathodes still show high capacity retention over 92% after 25 cycles at the voltage range of 2.0-4.3 V. Even cycled at high upper cut-off voltage of 4.5 V, Ti=0.20 sample can deliver a reversible capacity of 140 mAhg −1 with the capacity retention over 92% after 25 cycles. Furthermore, Ti substituted cathodes exhibit enhanced rate capability over pristine P2-Na 2/3 Ni 1/4 Mn 3/4 O 2 cathode. Comparison of the Ex-situ XRD results of the cycled P2-Na 2/3 Ni 1/4 Mn 3/4 O 2 and its substituted samples provides evidence that the improved electrochemical performance of Ti substituted cathodes would be attributed to the stabilization of the structure with Ti substitution

  10. Investigation of the negative ions in Ar/O.sub.2./sub. plasma of magnetron sputtering discharge with Al:Zn target by ion mass spectrometry

    Czech Academy of Sciences Publication Activity Database

    Pokorný, Petr; Mišina, Martin; Bulíř, Jiří; Lančok, Ján; Fitl, Přemysl; Musil, Jindřich; Novotný, Michal

    2011-01-01

    Roč. 8, č. 5 (2011), s. 459-464 ISSN 1612-8850 R&D Projects: GA AV ČR IAA100100718; GA AV ČR KAN400100653; GA ČR GP202/09/P324 Institutional research plan: CEZ:AV0Z10100522 Keywords : energy-resolved ion mass spectrometry * formation of negative ions * magnetron sputtering * mass spectrometry * transparent conductive oxide Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 2.468, year: 2011

  11. Structural and dielectric studies of Zr and Co co-substituted Ni0.5Zn0.5Fe2O4 using sol-gel auto combustion method

    Science.gov (United States)

    Jalaiah, K.; Vijaya Babu, K.; Rajashekhar Babu, K.; Chandra Mouli, K.

    2018-06-01

    Zr and Co substituted Ni0.5Zn0.5 ZrxCuxFe2-2xO4 with x values varies from the 0.0 to 0.4 in steps of 0.08 wt% ferrites synthesized by using sol-gel auto combustion method. The XRD patterns give evidence for formation of the single phase cubic spinel. The lattice constant was initially decreased from 8.3995 Å to 8.3941 Å with dopant concentration for x = 0.00-0.08 thereafter the lattice parameter steeply increased up to 8.4129 Å fox x = 0.4 with increasing dopant concentration. The estimated crystallite size and measured particle sizes are in comparable nano size. The grain size initially increased 2.3137-3.0430 μm, later it decreased to 2.2952 μm with increasing dopant concentration. The prepared samples porosity shows the opposite trend to grain size. The FT-IR spectrum for prepared samples shows the Fd3m (O7h). The wavenumber for tetrahedral site increased from 579 cm-1 to 593 cm-1 with increasing dopant concentration and the wavenumber of octahedral site are initially decreased from 414 cm-1 to 400 cm-1 for x = 0.00 to x = 0.08 later increased to 422 cm-1 with increasing dopant concentration. The dielectric constant increased from 8.85 to 34.5127 with dopant increasing concentration. The corresponding loss factor was fallows the similar trend as dielectric constant. The AC conductivity increased with increasing dopant concentration from 3.0261 × 10-7 S/m to 4.4169 × 10-6 S/m.

  12. Defects induced luminescence and tuning of bandgap energy narrowing in ZnO nanoparticles doped with Li ions

    KAUST Repository

    Awan, Saif Ullah; Hasanain, S. K.; Hassnain Jaffari, G.; Anjum, Dalaver H.; Qurashi, Umar S.

    2014-01-01

    Microstructural and optical properties of Zn1-yLiyO (0.00 ≤y ≤0.10) nanoparticles are investigated. Li incorporation leads to substantial changes in the structural characterization. From micro-structural analysis, no secondary phases or clustering of Li was detected. Elemental maps confirmed homogeneous distribution of Li in ZnO. Sharp UV peak due to the recombination of free exciton and defects based luminescence broad visible band was observed. The transition from the conduction band to Zinc vacancy defect level in photoluminescence spectra is found at 518±2.5nm. The yellow luminescence was observed and attributed to Li related defects in doped samples. With increasing Li doping, a decrease in energy bandgap was observed in the range 3.26±0.014 to 3.17±0.018eV. The bandgap narrowing behavior is explained in terms of the band tailing effect due to structural disorder, carrier-impurities, carrier-carrier, and carrier-phonon interactions. Tuning of the bandgap energy in this class of wide bandgap semiconductor is very important for room temperature spintronics applications and optical devices. © 2014 AIP Publishing LLC.

  13. Defects induced luminescence and tuning of bandgap energy narrowing in ZnO nanoparticles doped with Li ions

    KAUST Repository

    Awan, Saif Ullah

    2014-08-28

    Microstructural and optical properties of Zn1-yLiyO (0.00 ≤y ≤0.10) nanoparticles are investigated. Li incorporation leads to substantial changes in the structural characterization. From micro-structural analysis, no secondary phases or clustering of Li was detected. Elemental maps confirmed homogeneous distribution of Li in ZnO. Sharp UV peak due to the recombination of free exciton and defects based luminescence broad visible band was observed. The transition from the conduction band to Zinc vacancy defect level in photoluminescence spectra is found at 518±2.5nm. The yellow luminescence was observed and attributed to Li related defects in doped samples. With increasing Li doping, a decrease in energy bandgap was observed in the range 3.26±0.014 to 3.17±0.018eV. The bandgap narrowing behavior is explained in terms of the band tailing effect due to structural disorder, carrier-impurities, carrier-carrier, and carrier-phonon interactions. Tuning of the bandgap energy in this class of wide bandgap semiconductor is very important for room temperature spintronics applications and optical devices. © 2014 AIP Publishing LLC.

  14. The Influence of Doping with Transition Metal Ions on the Structure and Magnetic Properties of Zinc Oxide Thin Films

    Directory of Open Access Journals (Sweden)

    Jenica Neamtu

    2014-01-01

    Full Text Available Zn1−xNixO (x=0.03÷0.10 and Zn1−xFexO (x=0.03÷0.15 thin films were synthesized by sol-gel method. The structure and the surface morphology of zinc oxide thin films doped with transition metal (TM ions have been investigated by X-ray diffraction (XRD and atomic force microscopy (AFM. The magnetic studies were done using vibrating sample magnetometer (VSM at room temperature. Experimental results revealed that the substitution of Ni ions in ZnO wurtzite lattice for the contents x=0.03÷0.10 (Ni2+ leads to weak ferromagnetism of thin films. For Zn1-xFexO with x=0.03÷0.05, the Fe3+ ions are magnetic coupling by superexchange interaction via oxygen ions in wurtzite structure. For x=0.10÷0.15 (Fe3+ one can observe the increasing of secondary phase of ZnFe2O4 spinel. The Zn0.9Fe0.1O film shows a superparamagnetic behavior due to small crystallite sizes and the net spin magnetic moments arisen from the interaction between the iron ions through an oxygen ion in the spinel structure.

  15. Influences of Ti4+ and Mg2+ substitutions on the properties of lithium ferrites

    International Nuclear Information System (INIS)

    Su Hua; Zhang Huaiwu; Tang Xiaoli; Liu Baoyuan

    2009-01-01

    The Ti 4+ and Mg 2+ co-substituted lithium ferrites with different compositions of Zn 0.1 Li 0.45 Mn 0.1 Fe 2.35-2x (TiMg) x O 4 (x=0.0-0.5) were prepared by the ceramic standard processing. The magnetic properties and microstructure of the samples were investigated. A single phase spinel structure was confirmed by XRD in substituting range. Sintering densities continuously decreased with the increase at x value, which was attributed to the fact that the heavier Fe 3+ ions were replaced by the relatively lighter Ti 4+ and Mg 2+ ions. However, relative density of the samples had no obvious relationship with the substituting value. Saturation magnetization continuously decreased with x value, which was attributed to the decrease of resultant magnetic moment between A and B sub-lattice. Remanence decreased monotonously with x value due to the decrease of saturation magnetization and magnetocrystalline anisotropy constant. But the effect of Ti 4+ and Mg 2+ substitutions on the Br/Bs ratio values was not obvious. Coercive force was mainly determined by the microstructure and magnetocrystalline anisotropy constant of the ferrites. In this research, with the increase of Ti 4+ and Mg 2+ substitutions, the advantageous influence by the decrease of magnetocrystalline anisotropy constant was more significant than the disadvantageous influence caused by the increase of closed pores. As a result, coercive force of the ferrites also decreased monotonously with the increase at x value.

  16. Magnetic and structural properties of Zn-doped yttrium iron garnet nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Pena-Garcia, R.; Delgado, A.; Guerra, Y.; Farias, B.V.M.; Martinez, D. [Pos Graduacao em Ciencia de Materiais, Universidade Federal de Pernambuco, Recife, PE (Brazil); Skovroinski, E. [Departamento de Quimica Fundamental, Universidade Federal de Pernambuco, Recife, PE (Brazil); Galembeck, A. [Pos Graduacao em Ciencia de Materiais, Universidade Federal de Pernambuco, Recife, PE (Brazil); Departamento de Quimica Fundamental, Universidade Federal de Pernambuco, Recife, PE (Brazil); Padron-Hernandez, E. [Pos Graduacao em Ciencia de Materiais, Universidade Federal de Pernambuco, Recife, PE (Brazil); Departamento de Fisica, Universidade Federal de Pernambuco, Recife, PE (Brazil)

    2016-09-15

    Zn-doped YIG was prepared using the sol-gel method with TGA measurements showing the phase formation between 900 and 1000 C. XRD analysis showed close to 1100 C the formation of Franklinite phase, coexisting with the cubic YIG. Y{sub 3}(Fe{sub 1-x}Zn{sub x}){sub 5}O{sub 12} samples with different Zn concentrations (x = 0, 0.01, 0.03, and 0.05) were prepared and analyzed for a magnetic study. A decrease in magnetic moment of the samples was confirmed on increasing the concentration of Zn ions. This decrease is due to the substitution of Fe ions by Zn. This also confirmed the results of XRD showing the linear increase in the lattice parameter. Fittings by Bloch's law shows results compared with those already reported in the literature. The exponent and constant for the Bloch law presented similar values to those reported for YIG doped with other ions. We obtained the parameter α ∝10{sup -6} K{sup -n} with n close to 1.9 for all samples. (copyright 2016 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  17. Solution NMR characterization of Sgf73(1-104) indicates that Zn ion is required to stabilize zinc finger motif

    International Nuclear Information System (INIS)

    Lai, Chaohua; Wu, Minhao; Li, Pan; Shi, Chaowei; Tian, Changlin; Zang, Jianye

    2010-01-01

    Zinc finger motif contains a zinc ion coordinated by several conserved amino acid residues. Yeast Sgf73 protein was identified as a component of SAGA (Spt/Ada/Gcn5 acetyltransferase) multi-subunit complex and Sgf73 protein was known to contain two zinc finger motifs. Sgf73(1-104), containing the first zinc finger motif, was necessary to modulate the deubiquitinase activity of SAGA complex. Here, Sgf73(1-104) was over-expressed using bacterial expression system and purified for solution NMR (nuclear magnetic resonance) structural studies. Secondary structure and site-specific relaxation analysis of Sgf73(1-104) were achieved after solution NMR backbone assignment. Solution NMR and circular dichroism analysis of Sgf73(1-104) after zinc ion removal using chelation reagent EDTA (ethylene-diamine-tetraacetic acid) demonstrated that zinc ion was required to maintain stable conformation of the zinc finger motif.

  18. Effects of high-dose hydrogen implantation on defect formation and dopant diffusion in silver implanted ZnO crystals

    Energy Technology Data Exchange (ETDEWEB)

    Yaqoob, Faisal [Department of Physics, State University of New York at Albany, Albany, New York 12222 (United States); Huang, Mengbing, E-mail: mhuang@sunypoly.edu [College of Nanoscale Science and Engineering, State University of New York Polytechnic Institute, Albany, New York 12203 (United States)

    2016-07-28

    This work reports on the effects of a deep high-dose hydrogen ion implant on damage accumulation, defect retention, and silver diffusion in silver implanted ZnO crystals. Single-crystal ZnO samples were implanted with Ag ions in a region ∼150 nm within the surface, and some of these samples were additionally implanted with hydrogen ions to a dose of 2 × 10{sup 16 }cm{sup −2}, close to the depth ∼250 nm. Rutherford backscattering/ion channeling measurements show that crystal damage caused by Ag ion implantation and the amount of defects retained in the near surface region following post-implantation annealing were found to diminish in the case with the H implantation. On the other hand, the additional H ion implantation resulted in a reduction of substitutional Ag atoms upon post-implantation annealing. Furthermore, the presence of H also modified the diffusion properties of Ag atoms in ZnO. We discuss these findings in the context of the effects of nano-cavities on formation and annihilation of point defects as well as on impurity diffusion and trapping in ZnO crystals.

  19. Solubility limit of Mn{sup 2+} ions in Zn{sub 1−x}Mn{sub x}Te nanocrystals grown within an ultraviolet-transparent glass template

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Alessandra dos Santos, E-mail: alemestrado@gmail.com [Universidade Federal de Uberlândia, Laboratório de Novos Materiais Isolantes e Semicondutores (LNMIS), Instituto de Física (Brazil); Silva, Sebastião William da; Morais, Paulo Cesar de [Universidade de Brasília, Núcleo de Física Aplicada, Instituto de Física (Brazil); Dantas, Noelio Oliveira [Universidade Federal de Uberlândia, Laboratório de Novos Materiais Isolantes e Semicondutores (LNMIS), Instituto de Física (Brazil)

    2016-05-15

    This paper reports on the synthesis of Zn{sub 1−x}Mn{sub x}Te nanocrystals (NCs) (with 0 ≤ x ≤ 0.800) within a PZABP glass system (P{sub 2}O{sub 5}–ZnO–Al{sub 2}O{sub 3}–BaO–PbO) using the fusion method. The as-grown samples were investigated by optical absorption measurements, atomic force microscopy, X-ray diffraction, and Raman spectroscopy. The mean radius of the as-produced NCs (around R ≈ 2.2 nm) was well below the exciton Bohr radius of the bulk ZnTe (5.2 nm). All the characterization techniques employed in this report confirmed the successful inclusion of Mn{sup 2+} ions in the ZnTe-based NCs (Zn{sub 1−x}Mn{sub x}Te NCs) up to the nominal solubility limit of x = 0.100. Above this solubility limit (around x = 0.100), one can observe the formation of MnO and α-MnO{sub 2} NCs, since the nucleation rate for the formation of these NCs is greater than that of Zn{sub 1−x}Mn{sub x}Te NCs, at high x concentrations.Graphical abstract.

  20. Optical and structural properties of individual Co-doped ZnO microwires

    Science.gov (United States)

    Kolomys, O. F.; Strelchuk, V. V.; Rarata, S. V.; Hayn, R.; Savoyant, A.; Giovannelli, F.; Delorme, F.; Tkach, V.

    2018-06-01

    The Co-doped ZnO microwires (MWs) were grown using the optical furnace method. We used Scanning electron microscopy (SEM), polarized micro-Raman spectroscopy, photoluminescence (PL) and optical absorption spectroscopy to systematic investigation of the optical and structural properties of Co-doped ZnO MWs. The SEM analysis reveals that Co-doped ZnO MWs has hexagonal facets and cavity inside. The EDS results confirmed the presence and non-uniform distribution of Co impurities in the samples. Co doping of ZnO MWs leads to the decreased intensity, drastically broadening and high-energy shift of the NBE PL band. The red emission band at 1.85 eV originates from 2E(2G) → 4A2 (4F) intra-3d-transition of Co2+ in the ZnO lattice has been observed. The intense structured absorption bands within the near infrared ranges 3800-4800 and 5500-9000 cm-1 are caused by electronic spin-allowed transitions 4T2(F) ← 4A2(F) and 4T1(F) ← 4A2(F) of the tetrahedrally coordinated Co2+ (3 d7) ions substituting Zn2+ ions in Co-doped ZnO MWs. Micro-Raman studies of Co doped ZnO MWs show doping/disorder induced additional modes as compared to the undoped sample. The resonant enhancement of the additional local Co-related A1-symmetry Raman mode is observed in the parallel polarization geometry y(z , z) ybar . For the Co doped ZnO MWs, the enhancement of the additional Co-related local vibration mode with an increase in the excitation photon energy is also observed in the Raman spectra.

  1. Structural and magnetic properties in Mn-doped ZnO films prepared by pulsed-laser deposition

    International Nuclear Information System (INIS)

    Li, Qiang; Wang, Yuyin; Liu, Jiandang; Kong, Wei; Ye, Bangjiao

    2014-01-01

    We investigated the structural and magnetic properties of Zn 0.95 Mn 0.05 O films prepared on sapphire substrates by pulsed-laser deposition. Only low temperature ferromagnetism (Curie temperature lower than 50 K) was observed in Mn-doped samples, while pure ZnO film shows a typical paramagnetic behavior. Structural analyses indicate that the substitutional Mn 2+ ions play a significant role for the low temperature ferromagnetism. Lattice defects such as V O and V Zn were not proven to be effective factors for the origin of ferromagnetism in the films. The low temperature ferromagnetism might be interpreted as p–d hybridization from indirect coupling of Mn ions (Mn–O–Mn).

  2. Hierarchical 3D ZnIn2S4/graphene nano-heterostructures: their in situ fabrication with dual functionality in solar hydrogen production and as anodes for lithium ion batteries.

    Science.gov (United States)

    Kale, Sayali B; Kalubarme, Ramchandra S; Mahadadalkar, Manjiri A; Jadhav, Harsharaj S; Bhirud, Ashwini P; Ambekar, Jalinder D; Park, Chan-Jin; Kale, Bharat B

    2015-12-21

    Hierarchical 3D ZnIn2S4/graphene (ZnIn2S4/Gr) nano-heterostructures were successfully synthesized using an in-situ hydrothermal method. The dual functionality of these nano-heterostructures i.e. for solar hydrogen production and lithium ion batteries has been demonstrated for the first time. The ZnIn2S4/Gr nano-heterostructures were optimized by varying the concentrations of graphene for utmost hydrogen production. An inspection of the structure shows the existence of layered hexagonal ZnIn2S4 wrapped in graphene. The reduction of graphene oxide (GO) to graphene was confirmed by Raman and XPS analyses. The morphological analysis demonstrated that ultrathin ZnIn2S4 nanopetals are dispersed on graphene sheets. The optical study reveals the extended absorption edge to the visible region due to the presence of graphene and hence is used as a photocatalyst to transform H2S into eco-friendly hydrogen using solar light. The ZnIn2S4/Gr nano-heterostructure that is comprised of graphene and ZnIn2S4 in a weight ratio of 1 : 99 exhibits enhanced photocatalytically stable hydrogen production i.e. ∼6365 μmole h(-1) under visible light irradiation using just 0.2 g of nano-heterostructure, which is much higher as compared to bare hierarchical 3D ZnIn2S4. The heightened photocatalytic activity is attributed to the enhanced charge carrier separation due to graphene which acts as an excellent electron collector and transporter. Furthermore, the usage of nano-heterostructures and pristine ZnIn2S4 as anodes in lithium ion batteries confers the charge capacities of 590 and 320 mA h g(-1) after 220 cycles as compared to their initial reversible capacities of 645 and 523 mA h g(-1), respectively. These nano-heterostructures show high reversible capacity, excellent cycling stability, and high-rate capability indicating their potential as promising anode materials for LIBs. The excellent performance is due to the nanostructuring of ZnIn2S4 and the presence of a graphene layer, which

  3. Luminescence mechanisms of organic/inorganic hybrid organic light-emitting devices fabricated utilizing a Zn2SiO4:Mn color-conversion layer

    International Nuclear Information System (INIS)

    Choo, D.C.; Ahn, S.D.; Jung, H.S.; Kim, T.W.; Lee, J.Y.; Park, J.H.; Kwon, M.S.

    2010-01-01

    Zn 2 SiO 4 :Mn phosphor layers used in this study were synthesized by using the sol-gel method and printed on the glass substrates by using a vehicle solution and a heating process. Organic/inorganic hybrid organic light-emitting devices (OLEDs) utilizing a Zn 2 SiO 4 :Mn color-conversion layer were fabricated. X-ray diffraction data for the synthesized Zn 2 SiO 4 :Mn phosphor films showed that the Zn ions in the phosphor were substituted into Mn ions. The electroluminescence (EL) spectrum of the deep blue OLEDs showed that a dominant peak at 461 nm appeared. The photoluminescence spectrum for the Zn 2 SiO 4 :Mn phosphor layer by using a 470 nm excitation source showed that a dominant peak at 527 nm appeared, which originated from the 4 T 1 - 6 A 1 transitions of Mn ions. The appearance of the peak around 527 nm of the EL spectra for the OLEDs fabricated utilizing a Zn 2 SiO 4 :Mn phosphor layer demonstrated that the emitted blue color from the deep blue OLEDs was converted into a green color due to the existence of the color-conversion layer. The luminescence mechanisms of organic/inorganic hybrid OLEDs fabricated utilizing a Zn 2 SiO 4 :Mn color-conversion layer are described on the basis of the EL and PL spectra.

  4. Batch adsorptive removal of Fe(III, Cu(II and Zn(II ions in aqueous and aqueous organic–HCl media by Dowex HYRW2-Na Polisher resin as adsorbents

    Directory of Open Access Journals (Sweden)

    Abdul-Aleem Soliman Aboul-Magd

    2016-09-01

    Full Text Available Of the metal ions in tap, Nile, waste and sea water samples and some ores were carried out. Removal of heavy metal ions such as Fe(III, Cd(II, Zn(II, Cu(II, Mn(II, Mg(II, and Pb(II from water and wastewater is obligatory in order to avoid water pollution. Batch shaking adsorption experiments to evaluate the performance of nitric and hydrochloric acid solutions in the removal of metal ions by cation exchange resin at the same conditions for both, such as the effect of initial metal ion concentration, different proportions of some organic solvents, H+-ion concentrations and reaction temperature on the partition coefficients. The metal adsorption for the cation exchanger was found to be significant in different media for both nitric and hydrochloric acids, i.e., the adsorption up take of metal ions presented in this work is very significant depending on the characteristics of ions and on the external concentrations of solute. The presence of low ionic strength or low concentration of acids does have a significant adsorption of metal ions on ion-exchange resin. The results show that the ion exchanger could be employed for the preconcentration, separation and the determination.

  5. Interaction of Zn2+ Ions with Single-Stranded PolyU and PolyC in Neutral Solutions

    Czech Academy of Sciences Publication Activity Database

    Sorokin, V. A.; Usenko, E. L.; Valeev, V. A.; Berezniak, E. G.; Andrushchenko, Valery

    2015-01-01

    Roč. 119, č. 12 (2015), s. 4409-4416 ISSN 1520-6106 R&D Projects: GA ČR GAP208/11/0105; GA ČR GA15-09072S Institutional support: RVO:61388963 Keywords : metal ions * polyU * polyC * metallized DNA * differential UV spectroscopy * thermal denaturation * phase diagram Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 3.187, year: 2015