Tunneling-recombination luminescence between Ag0 and Ag2+ in KCl:AgCl

International Nuclear Information System (INIS)

Delbecq, C.J.; Dexter, D.L.; Yuster, P.H.

1978-01-01

Appropriate treatment of a KCl:AgCl crystal results in the trapping of electrons as silver atoms, Ag 0 , and positive holes as AgCl 4 2- , Ag 2+ , centers. Optical excitation of Ag 0 in such a crystal at T 0 and Ag 2+ pairs, similar to the Ag 0 -Cl 2 - tunneling-recombination studies we previously reported. We have shown that Ag 2+ centers are involved in the emission process by preferentially orienting the anisotropic Ag 2+ at 6 K by excitation with polarized light and observing that the afterglow is polarized. Upon warming to 50 K, where the preferentially oriented Ag 2+ can change orientation, a strong reversal in the degree of polarization occurs which finally decays to zero. The characteristics of this luminescence can be understood if we assume: (i) a tunneling-recombination mechanism in which the orientation of the electric vector of the emitted radiation depends on the position of the Ag 0 relative to the Ag 2+ and (ii) the tunneling is anisotropic and depends on the location of the Ag 0 relative to the anisotropic Ag 2+ . The latter assumption is based on the tetragonal (d-like) symmetry of the Ag 2+ complex. Good quantitative agreement between theory and experiment has been obtained on the decay kinetics, the degree of polarization, and the polarization reversal

Glass formation in AgI:Ag2O:V2O5 and AgI:Ag2O:(V2O5+B2O3) systems

International Nuclear Information System (INIS)

Kaushik, R.; Hariharan, K.

1988-01-01

Transport properties of glasses in the system AgI:Ag 2 O: V 2 O 5 and AgI:Ag 2 O: (V 2 O 5 +B 2 O 3 ) have ben investigated. It was found that, at high AgI concentrations, the addition of another glass former (B 2 O 3 ) did not improve the conduction characteristics of the pure vanadate glasses, the best conducting composition of which had ambient temperature, ionic conductivity comparable to that of conventional liquid electrolytes. The highest conducting composition was used as an electrolyte in the study of silver solid state cells. The discharge characteristics of different cells fabricated with the glassy electrolyte, have been compared with those having the best conducting polycrystalline ompositions as electrolytes. 11 refs.; 4 figs.; 1 table

Thermodynamic properties of solid solutions in the system Ag2S–Ag2Se

International Nuclear Information System (INIS)

Pal’yanova, G.A.; Chudnenko, K.V.; Zhuravkova, T.V.

2014-01-01

We have summarized experimental data on the phase diagram of the system Ag 2 S–Ag 2 Se. Standard thermodynamic functions of four solid solutions in this system have been calculated using the model of regular and subregular solutions: a restricted fcc solid solution γ-Ag 2 S-Ag 2 S 1−x Se x (x 2 S–Ag 2 Se, monoclinic solid solution (α) from Ag 2 S to Ag 2 S 0.4 Se 0.6 , and orthorhombic solid solution (α) from Ag 2 S 0.3 Se 0.7 to the Ag 2 Se. G mix and S mix have been evaluated using the subregular model for asymmetric solution for the region Ag 2 S 0.4 Se 0.6 –Ag 2 S 0.3 Se 0.7 . The thermodynamic data can be used for modeling in complex natural systems and in matters of semiconductor materials

A further insight into the mechanism of Ag + biosorption by Lactobacillus sp. strain A09

Science.gov (United States)

Lin, Zhongyu; Zhou, Chaohui; Wu, Jianming; Zhou, Jianzhang; Wang, Lin

2005-04-01

The mechanism of Ag + biosorption by resting cell of Lactobacillus sp. strain A09 has been further investigated at the molecular level using spectroscopic techniques. The values of estimated equilibrium constants, rate constants, half-life periods and apparent enthalpies of the binding reaction were calculated via the determination of Ag + adsorbed by the biomass using atomic absorption spectrophotometry (AAS). The reductive ratio of the Ag + to Ag 0 by the A09 biomass was examined by X-ray photoelectron spectroscopy (XPS). Analysis for sulfur and nitrogen atomic contents in dry powder of the biomass with EA-1110 elemental analysis (EA) showed that amino acid residues retaining the reductive property of Ag + to Ag 0 are very small quantity, whereas glucose content in the hydrolysates of the biomass analyzed by ultraviolet-visible spectrophotometry (UV-vis) indicated that the amount of reducing sugars in the biomass is much larger than 2.71%. The fourier transform infrared (FTIR) spectrophotometry on blank and silver-loaded biomass demonstrated that the chemical functional group such as the free aldehyde group of the hemiacetalic hydroxyl group from reducing sugars, i.e. the hydrolysates of the polysaccharides from the cell wall plays a leading role in serving as the electron donor for reducing the Ag + to Ag 0. This result was further supported by characterizations on the interaction of the Ag + with glucose using X-ray powder diffractometry (XRD) and FTIR spectroscopy.

Compatibilidad de Trichoderma harzianum Rifai con fungicidas del arroz y su efecto sobre tres fitopatógenos fúngicos

OpenAIRE

Manuel Francisco Rodríguez Saldaña; Pausides Milanés Virelles; Ernesto Juniors Pérez Torres; Yurisandra Sierra Reyes

2016-01-01

Resumen La investigación se realizó en el Laboratorio Provincial de Sanidad Vegetal en Camagüey, en la etapa comprendida de septiembre de 2013 a septiembre de 2015, en condiciones in vitro donde se determinó la compatibilidad y capacidad antagónica frente a pesticidas usados en el arroz, de Trichoderma harzianum Rifai cepa A-34 sobre los patógenos del arroz (Bipolaris oryzae Breda de Haan, Saracladium oryzae (Sawada) w. Gams & D.Hawksworth y Magnaporthe grisea (Hebert) Barr). Las ev...

One-pot synthesis of Ag-SiO2-Ag sandwich nanostructures

International Nuclear Information System (INIS)

Li Chaorong; Mei Jie; Li Shuwen; Lu Nianpeng; Wang Lina; Chen Benyong; Dong Wenjun

2010-01-01

Ag-SiO 2 -Ag sandwich nanostructures were prepared by a facile one-pot synthesis method. The Ag core, SiO 2 shell and Ag nanoparticle shell were all synthesized with polyvinylpyrrolidone, catalysed by ammonia, in the one-pot reaction. The polyvinylpyrrolidone, acting as a smart reducing agent, reduced the Ag + to Ag cores and Ag shells separately. Furthermore, the polyvinylpyrrolidone served as a protective agent to prevent the silver cores from aggregating. The SiO 2 shell and outer layer Ag nanoparticles were obtained when tetraethyl orthosilicate and ammonia were added to the silver core solution. Ammonia, acting as the catalyst, accelerated the hydrolysis of the tetraethyl orthosilicate to SiO 2 , which coated the silver cores. Furthermore, Ag(NH 3 ) 2 + ions were formed when aqueous ammonia was added to the solution, which increased the reduction capability. Then the polyvinylpyrrolidone reduced the Ag(NH 3 ) 2 + ions to small Ag nanoparticles on the surface of the Ag-SiO 2 and formed Ag-SiO 2 -Ag sandwich structures with a standard deviation of less than 4%. This structure effectively prevented the Ag nanoparticles on the silica surface from aggregating. Furthermore, the Ag-SiO 2 -Ag sandwich structures showed good catalysis properties due to the large surface area/volume value and activity of surface atoms of Ag particles.

Effect of nutrition, vitamin, grains, and temperature on the mycelium growth and antioxidant capacity of Cordyceps militaris (strains AG-1 and PSJ-1

Directory of Open Access Journals (Sweden)

Hung-Ngoc Dang

2018-04-01

Full Text Available Effects of subculture conditions on the mycelium growth and antioxidant capacity assessment of Cordyceps militaris trains AG-1 and PSJ-1 were carried out in laboratory during the autumn-winter season of 2015. Different temperature regimes and nutrition, vitamins levels, grain in substrate were evaluated for optimization on mycelium growth. The results showed that two strains AG-1 and PSJ-1 can grow the maximum mycelium radial at the temperature of 24 °C. The mycelium growth was improved by carbon sources such as glucose, dextrose, fructose, and maltose at 30 g/L concentration. Whereas glucose achieved the highest value of mycelium colony diameter in strains AG-1 and PSJ-1. Vitamins B1 concentrations at 0.03 g/L also gave the great values in mycelium colony diameter of both strains AG-1 and PSJ-1. The studies depicted that a substrate mixed with various grains sources (brown rice, white rice, and wheat, black glutinous rice Vietnam, and corn cultured at 24 °C, for 12 days supported maximum mycelia growth of the two strains AG-1 and PSJ-1 of C. militaris. The effect of liquid culture medium (MYPS and PD with mycelium on the anti-oxidation capacity was assessed. The results showed that the increasing of DPPH radical scavenging capacity with the extract concentration exist a proportional relation and Fe2+-chelating capacity as well. The cultured Cordyceps mycelium of two strains AG-1 and PSJ-1had the equally strong antioxidant capacity. Keywords: Cordyceps militaris, Mycelium growth, Nutritional condition, Temperature, Vitamins, Anti-oxidation activity

Precipitation of Ag2Te in the thermoelectric material AgSbTe2

International Nuclear Information System (INIS)

Sugar, Joshua D.; Medlin, Douglas L.

2009-01-01

The microstructure of AgSbTe 2 , prepared by solidification, is investigated using electron microscopy. During solidification and thermal treatment, the material separates into a two-phase mixture of a rocksalt phase, which is Ag 22 Sb 28 Te 50 , and silver telluride, Ag 2 Te. Ag 2 Te formation results either from eutectic solidification (large lamellar structures), or by solid-state precipitation (fine-scale particles). The crystal structure of the AgSbTe 2 phase determined by electron diffraction is consistent with a rocksalt structure that has a disordered cation sublattice. A preferred crystallographic orientation relationship at the interface between the matrix and the low-temperature monoclinic Ag 2 Te phase is defined and discussed. This orientation relationship is observed for both second-phase morphologies. In both cases, the orientation relationship originates from a topotactic (cube-on-cube) alignment of the Te sublattices in the initially cubic Ag 2 Te and the matrix at elevated temperature. This Te sublattice alignment is retained as the Ag 2 Te undergoes a cubic-to-monoclinic transformation during cooling. This orientation relationship is observed for both second-phase morphologies.

Comparative Study of Antimicrobial Activity of AgBr and Ag Nanoparticles (NPs)

Science.gov (United States)

Suchomel, Petr; Kvitek, Libor; Panacek, Ales; Prucek, Robert; Hrbac, Jan; Vecerova, Renata; Zboril, Radek

2015-01-01

The diverse mechanism of antimicrobial activity of Ag and AgBr nanoparticles against gram-positive and gram-negative bacteria and also against several strains of candida was explored in this study. The AgBr nanoparticles (NPs) were prepared by simple precipitation of silver nitrate by potassium bromide in the presence of stabilizing polymers. The used polymers (PEG, PVP, PVA, and HEC) influence significantly the size of the prepared AgBr NPs dependently on the mode of interaction of polymer with Ag+ ions. Small NPs (diameter of about 60–70 nm) were formed in the presence of the polymer with low interaction as are PEG and HEC, the polymers which interact with Ag+ strongly produce nearly two times bigger NPs (120–130 nm). The prepared AgBr NPs were transformed to Ag NPs by the reduction using NaBH4. The sizes of the produced Ag NPs followed the same trends – the smallest NPs were produced in the presence of PEG and HEC polymers. Prepared AgBr and Ag NPs dispersions were tested for their biological activity. The obtained results of antimicrobial activity of AgBr and Ag NPs are discussed in terms of possible mechanism of the action of these NPs against tested microbial strains. The AgBr NPs are more effective against gram-negative bacteria and tested yeast strains while Ag NPs show the best antibacterial action against gram-positive bacteria strains. PMID:25781988

[Ag(NH3)2]Ag(OsO3N)2: a new nitridoosmate(VIII)

International Nuclear Information System (INIS)

Wickleder, M.S.; Pley, Martin

2004-01-01

Dark brown single crystals of [Ag(NH 3 ) 2 ]Ag(OsO 3 N) 2 were obtained from the reaction of Ag 2 CO 3 , OsO 4 , and NH 3 in aqueous solution. The crystal structure was solved in the monoclinic space group C2/m, with the following unit-cell dimensions: a=1962.5(3), b=633.1(1), c=812.6(1) pm, β=96.71(1) deg. The final reliability factor was R=0.0256 for 1034 reflections with I>2σ(I). Linear [Ag(NH 3 ) 2 ] + ions are present oriented perpendicular to the [010] direction, leading to short Ag + -Ag + distances of 316 pm. A second type of Ag + ions in the crystal structure present coordination number '6+1' and are surrounded by oxygen and nitrogen atoms of the nitridoosmate groups. Within the first of the two crystallographically distinguishable anions one can clearly differentiate between oxygen and nitrogen atoms while the second one exhibits a N/O disorder over two positions. The infrared spectrum of [Ag(NH 3 ) 2 ]Ag(OsO 3 N) 2 shows the typical absorptions which can be attributed to the complex anions and the NH 3 ligands

Preparation and Characterization of γ-AgI in Superionic Composite Glasses (AgIx(AgPO31-x

Directory of Open Access Journals (Sweden)

S. Suminta

2007-07-01

Full Text Available The γ-AgI phase was stabilized at room temperature in the composites glasses (AgIx(AgPO31-x with x = 0.6 and 0.7 via rapid quenching of their molten mixture. The measurement of the crystal structure has been carried out using an X-ray Difractometer at the Physics Departement of Ibaraki University, Japan. The micro strain and crystal size are derived from Hall’s equation. The X-ray diffraction pattern shows some Bragg peaks that correspond to the crystalline γ-AgI. By increasing the concentration of AgI, the peak width becomes more narrow and the position shifts to the higher angle. This indicates that the crystalline size and microstrain are increasing. The increase of micro strain (η, and particle size (D will increase the ionic mobility, thus increasing the ionic conductivity. It is concluded that solidification process on melt AgI into glass matrix AgPO3 not only decreases the micro strain and the particle size, but it also increases the ionic conductivity.

Facile synthesis, structure, and properties of Ag{sub 2}S/Ag heteronanostructure

Energy Technology Data Exchange (ETDEWEB)

Sadovnikov, S. I., E-mail: sadovnikov@ihim.uran.ru; Gusev, A. I. [Ural Branch of the Russian Academy of Sciences, Institute of Solid State Chemistry (Russian Federation)

2016-09-15

Ag{sub 2}S/Ag heteronanostructure has been produced by a simple one-stage chemical deposition from aqueous solutions of silver nitrate, sodium sulfide, and sodium citrate with the use of monochromatic light irradiation. For simultaneous synthesis of Ag{sub 2}S and Ag nanoparticles, deposition has been performed from reaction mixtures with reduced sodium sulfide concentration. The size of Ag{sub 2}S and Ag nanoparticles is 45–50 and 15–20 nm, respectively. It is established that in the contact layer between silver sulfide and silver, nonconducting α-Ag{sub 2}S acanthite transforms into superionic β-Ag{sub 2}S argentite under the action of external electric field. The scheme of the operation of a resistive switch based on an Ag{sub 2}S/Ag heteronanostructure is proposed. The UV–Vis optical absorption spectra of colloidal solutions of Ag{sub 2}S/Ag heteronanostructures have been studied.Graphical Abstract.

Room temperature synthesis and photocatalytic property of AgO/Ag2Mo2O7 heterojunction nanowires

International Nuclear Information System (INIS)

Hashim, Muhammad; Hu, Chenguo; Wang, Xue; Wan, Buyong; Xu, Jing

2012-01-01

Graphical abstract: The AgO nanoparticles are attached on the surface of the Ag 2 Mo 2 O 7 nanowires to form a heterojunction structure. The AgO nanoparticles start embedding into the nanowires with increasing reaction temperature or time. Highlights: ► AgO/Ag 2 Mo 2 O 7 heterojunction NWs were synthesized at room temperature for the first time. ► AgO particles embed into the Ag 2 Mo 2 O 7 NWs with increase in reaction time and temperature. ► The heterojunction NWs display much better photocatalytic activity than the none-heterojunction NWs. ► The catalytic mechanism was proposed. -- Abstract: AgO/Ag 2 Mo 2 O 7 heterojunction nanowires were synthesized at temperatures of 25 °C, 50 °C, 80 °C, and 110 °C, under magnetic stirring in solution reaction. The catalytic activity of AgO/Ag 2 Mo 2 O 7 nanowires was evaluated by the degradation of Rhodmine B dye under the irradiation of the simulated sunlight. The synthesized samples were characterized by X-ray diffractometer, energy dispersive spectrometry, X-ray photoelectron spectrometer, scanning electron microscopy, and transmission electron microscopy. The results show that the AgO nanoparticles are attached on the surface of the Ag 2 Mo 2 O 7 nanowires to form a heterojunction structure. The length of the nanowires is up to 10 μm and the size of the AgO nanoparticles is 10–20 nm. The length of nanowires increases with increasing reaction time and temperature while the AgO particles are gradually embedded into the nanowires. The photocatalytic activity is greatly improved for the AgO/Ag 2 Mo 2 O 7 heterojunction nanowires compared with that of the pure Ag 2 Mo 2 O 7 nanowires, indicating a remarkable role of AgO particles on the Ag 2 Mo 2 O 7 nanowires in the photodegradation.

Ag K- and L3-edge XAFS study on Ag species in Ag/Ga2O3 photocatalysts

International Nuclear Information System (INIS)

Yamamoto, M; Yamamoto, N; Yoshida, T; Nomoto, T; Yamamoto, A; Yoshida, H; Yagi, S

2016-01-01

Ag loaded Ga 2 O 3 (Ag/Ga 2 O 3 ) shows photocatalytic activity for reduction of CO 2 with water. Ag L 3 -edge XANES and K-edge EXAFS spectra were measured for various Ag/Ga 2 O 3 samples, which suggested that structural and chemical states of Ag species varied with the loading amount of Ag and the preparation method. The Ag species were metallic Ag particles with an AgGaO 2 -like interface structure in the sample with high loading amount of Ag while predominantly Ag metal clusters in the sample with low loading amount of Ag. The XANES feature just above the edge represented the interaction between the Ag species and the Ga 2 O 3 surface, showing that the Ag metal clusters had more electrons in the d -orbitals by interacting with the Ga 2 O 3 surface, which would contribute the high photocatalytic activity. (paper)

Plasmonic Ag{sub 2}MoO{sub 4}/AgBr/Ag composite: Excellent photocatalytic performance and possible photocatalytic mechanism

Energy Technology Data Exchange (ETDEWEB)

Wang, Zhongliao [College of Physics and Electronic Information, Anhui Key Laboratory of Energetic Materials, Huaibei Normal University, Huaibei, 235000 (China); Zhang, Jinfeng, E-mail: zjf_y2004@126.com [College of Physics and Electronic Information, Anhui Key Laboratory of Energetic Materials, Huaibei Normal University, Huaibei, 235000 (China); Lv, Jiali [College of Physics and Electronic Information, Anhui Key Laboratory of Energetic Materials, Huaibei Normal University, Huaibei, 235000 (China); Dai, Kai, E-mail: daikai940@chnu.edu.cn [College of Physics and Electronic Information, Anhui Key Laboratory of Energetic Materials, Huaibei Normal University, Huaibei, 235000 (China); Liang, Changhao [College of Physics and Electronic Information, Anhui Key Laboratory of Energetic Materials, Huaibei Normal University, Huaibei, 235000 (China); Key Laboratory of Materials Physics and Anhui Key Laboratory of Nanomaterials and Nanotechnology, Institute of Solid State Physics, Chinese Academy of Sciences, Hefei, 230031 (China)

2017-02-28

Highlights: • Novel Ag{sub 2}MoO{sub 4}/AgBr/Ag photocatalyst was prepared. • Ag{sub 2}MoO{sub 4}/AgBr/Ag showed high photocatalytic activity. • Ag{sub 2}MoO{sub 4}/AgBr/Ag showed long reusable life. - Abstract: Plasmonic Ag{sub 2}MoO{sub 4}/AgBr/Ag composite is fabricated by in-situ ion exchange and reduction methods at room temperature. The samples are characterized by X-ray diffraction (XRD), UV–vis diffuse reflectance (DRS), energy-dispersive X-ray spectroscopy (EDS), scanning electron microscope (SEM) and photoluminescence (PL) measurements. The results show that butterfly-like Ag{sub 2}MoO{sub 4} nanosheets served as the precursor, and Ag{sub 2}MoO{sub 4}/AgBr/Ag is formed in phase transformation with MoO{sub 4}{sup 2−} displaced by Br{sup −}. The ternary Ag{sub 2}MoO{sub 4}/AgBr/Ag composite photocatalysts show greatly enhanced photocatalytic activity in photodegrading methylene blue (MB) under visible light irradiation compared with AgBr and Ag{sub 2}MoO{sub 4}. The pseudo-first-order rate constant k{sub app} of Ag{sub 2}MoO{sub 4}/AgBr/Ag is 0.602 min{sup −1}, which is 11.6 and 18.3 times as high as that of AgBr and Ag{sub 2}MoO{sub 4}, respectively. Meanwhile, the efficiency of degradation still kept 90% after ten times cyclic experiments. Eventually, possible photocatalytic mechanism was proposed.

AgSbSe2 and AgSb(S,Se)2 thin films for photovoltaic applications

International Nuclear Information System (INIS)

Garza, J.G.; Shaji, S.; Rodriguez, A.C.; Das Roy, T.K.; Krishnan, B.

2011-01-01

Silver antimony selenide (AgSbSe 2 ) thin films were prepared by heating sequentially deposited multilayers of antimony sulphide (Sb 2 S 3 ), silver selenide (Ag 2 Se), selenium (Se) and silver (Ag). Sb 2 S 3 thin film was prepared from a chemical bath containing SbCl 3 and Na 2 S 2 O 3 , Ag 2 Se from a solution containing AgNO 3 and Na 2 SeSO 3 and Se thin films from an acidified solution of Na 2 SeSO 3 , at room temperature on glass substrates. Ag thin film was deposited by thermal evaporation. The annealing temperature was 350 deg. C in vacuum (10 -3 Torr) for 1 h. X-ray diffraction analysis showed that the thin films formed were polycrystalline AgSbSe 2 or AgSb(S,Se) 2 depending on selenium content in the precursor films. Morphology and elemental analysis of these films were done using scanning electron microscopy and energy dispersive X-ray spectroscopy. Optical band gap was evaluated from the UV-visible absorption spectra of these films. Electrical characterizations were done using Hall effect and photocurrent measurements. A photovoltaic structure: glass/ITO/CdS/AgSbSe 2 /Al was formed, in which CdS was deposited by chemical bath deposition. J-V characteristics of this structure showed V oc = 435 mV and J sc = 0.08 mA/cm 2 under illumination using a tungsten halogen lamp. Preparation of a photovoltaic structure using AgSbSe 2 as an absorber material by a non-toxic selenization process is achieved.

The negative temperature coefficient resistivities of Ag2S-Ag core–shell structures

International Nuclear Information System (INIS)

Yu, Mingming; Liu, Dongzhi; Li, Wei; Zhou, Xueqin

2014-01-01

In this paper, the conductivity of silver nanoparticle films protected by 3-mercaptopropionic acid (Ag/MPA) has been investigated. When the nanoparticles were annealed in air at 200 °C, they converted to stable Ag 2 S-Ag core–shell structures. The mechanism for the formation of the Ag 2 S-Ag core–shell structures along with the compositional changes and the microstructural evolution of the Ag/MPA nanoparticles during the annealing process are discussed. It is proposed that the Ag 2 S-Ag core–shell structure was formed through a solid-state reduction reaction, in which the Ag + ions coming from Ag 2 S were reduced by sulfonate species and sulfur ions. The final Ag 2 S-Ag films display an exponentially decreased resistivity with increasing temperature from 25 to 170 °C. The negative temperature coefficient resistivity of Ag 2 S-Ag films can be adjusted by changing the S/Ag molar ratio used for the synthesis of the Ag/MPA nanoparticles, paving the way for the preparation of negative temperature-coefficient thermistors via printing technology for use in the electronics.

Precipitation of Ag{sub 2}Te in the thermoelectric material AgSbTe{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Sugar, Joshua D. [Materials Physics Department, Sandia National Laboratories, Livermore, CA (United States)], E-mail: jdsugar@sandia.gov; Medlin, Douglas L. [Materials Physics Department, Sandia National Laboratories, Livermore, CA (United States)

2009-06-10

The microstructure of AgSbTe{sub 2}, prepared by solidification, is investigated using electron microscopy. During solidification and thermal treatment, the material separates into a two-phase mixture of a rocksalt phase, which is Ag{sub 22}Sb{sub 28}Te{sub 50}, and silver telluride, Ag{sub 2}Te. Ag{sub 2}Te formation results either from eutectic solidification (large lamellar structures), or by solid-state precipitation (fine-scale particles). The crystal structure of the AgSbTe{sub 2} phase determined by electron diffraction is consistent with a rocksalt structure that has a disordered cation sublattice. A preferred crystallographic orientation relationship at the interface between the matrix and the low-temperature monoclinic Ag{sub 2}Te phase is defined and discussed. This orientation relationship is observed for both second-phase morphologies. In both cases, the orientation relationship originates from a topotactic (cube-on-cube) alignment of the Te sublattices in the initially cubic Ag{sub 2}Te and the matrix at elevated temperature. This Te sublattice alignment is retained as the Ag{sub 2}Te undergoes a cubic-to-monoclinic transformation during cooling. This orientation relationship is observed for both second-phase morphologies.

Using Ag/Ag2O/SnO2 Nanocomposites to Remove Malachite Green by a Photocatalytic Process

Science.gov (United States)

Taufik, A.; Paramarta, V.; Prakoso, S. P.; Saleh, R.

2017-03-01

Silver/silver oxide/tin oxide nanocomposites of various weight ratios were synthesized using a microwave-assisted method. The Ag/Ag2O:SnO2 nanoparticle weight ratios used were 25:75, 50:50, and 75:25. All samples were characterized using X-ray diffraction, UV-Vis spectroscopy, Differential Scanning Calorimetry and Thermogravimetric Analysis (TGA). The Ag/Ag2O/SnO2 nanocomposites contained cubic structures provided by the Ag and Ag2O and tetragonal structures provided by the SnO2. The silver resulted in surface plasmon resonance (SPR) at a wavelength of about 435 nm. The silver oxide material was transformed into pure Ag at a temperature of about 370 °C The photocatalytic activity was tested on the degradation of malachite green (MG) from an aqueous solution. The results showed that Ag/Ag2O/SnO2 at a ratio of 50:50 exhibited the best photocatalytic performance for degrading MG under visible-light irradiation. The degradation of MG using Ag/Ag2O/SnO2 nanocomposites followed pseudo first-order kinetic reactions, and electron holes were found to be the main species acting on the degradation process.

Photoreduction of Ag{sup +} in Ag/Ag{sub 2}S/Au memristor

Energy Technology Data Exchange (ETDEWEB)

Mou, N.I.; Tabib-Azar, M., E-mail: azar.m@utah.edu

2015-06-15

Highlights: • The effect of illumination on the operating voltages and switching speed of Ag/Ag{sub 2}S/Au memristors is studied • Illumination decreased the average switching time from high to low resistance states by ∼19% and decreased the turn-off voltages dramatically from −0.8 V to −0.25 V. • Photo-induced reduction of silver in Ag{sub 2}S may be used in three dimensional optical memories that can be electronically read and reset. • Illumination changed sulfur's valency and modified its oxidation/reduction potential. - Abstract: Silver halides and chalcogenides are excellent memristor materials that have been extensively used in the past as photosensitive layers in photography. Here we examine the effect of illumination on the operating voltages and switching speed of Ag/Ag{sub 2}S/Au memristors using a green laser (473–523 nm). Our results indicate that illumination decreases the average switching time from high to low resistance states by ∼19% and decreases the turn-off voltages dramatically from −0.8 V to −0.25 V that we attribute to the change in sulfur valency and a photo-induced change in its oxidation/reduction potential. Photo-induced reduction of silver in Ag{sub 2}S may be used in three dimensional optical memories that can be electronically read and reset.

Synthesis, morphological control, and antibacterial properties of hollow/solid Ag2S/Ag heterodimers

KAUST Repository

Pang, Maolin

2010-08-11

Ag2S and Ag are important functional materials that have received considerable research interest in recent years. In this work, we develop a solution-based synthetic method to combine these two materials into hollow/solid Ag2S/Ag heterodimers at room temperature. Starting from monodisperse Cu2O solid spheres, CuS hollow spheres can be converted from Cu2O through a modified Kirkendall process, and the obtained CuS can then be used as a solid precursor for preparation of the Ag2S/Ag heterodimers through ion exchange and photo-assisted reduction. We have found that formation of the Ag2S/Ag heterodimers is instantaneous, and the size of Ag nanocrystals on the hollow spheres of Ag2S can be controlled by changing the concentration and power of reducing agents in the synthesis. The growth of Ag nanoparticles on hollow spheres of Ag2S in the dimers is along the [111] direction of the silver crystal; the light absorption properties have also been investigated. Furthermore, coupling or tripling of Ag2S/Ag heterodimers into dumbbell-like trimers ((Ag 2S)2/Ag, linear) and triangular tetramers ((Ag 2S)3/Ag, coplanar) can also be attained at 60°C by adding the bidentate ligand ethylenediamine as a cross-linking agent. To test the applicability of this highly asymmetric dipolar composite, photocatalytic inactivation of Escherichia coli K-12 in the presence of the as-prepared Ag 2S/Ag heterodimers has been carried out under UV irradiation. The added Ag2S/Ag heterodimers show good chemical stability under prolonged UV irradiation, and no appreciable solid dissolution is found. Possible mechanisms regarding the enhanced antibacterial activity have also been addressed. © 2010 American Chemical Society.

High Resolution Transmission Electron Microscope Observation of Zero-Strain Deformation Twinning Mechanisms in Ag

Science.gov (United States)

Liu, L.; Wang, J.; Gong, S. K.; Mao, S. X.

2011-04-01

We have observed a new deformation-twinning mechanism using the high resolution transmission electron microscope in polycrystalline Ag films, zero-strain twinning via nucleation, and the migration of a Σ3{112} incoherent twin boundary (ITB). This twinning mechanism produces a near zero macroscopic strain because the net Burgers vectors either equal zero or are equivalent to a Shockley partial dislocation. This observation provides new insight into the understanding of deformation twinning and confirms a previous hypothesis: detwinning could be accomplished via the nucleation and migration of Σ3{112} ITBs. The zero-strain twinning mechanism may be unique to low staking fault energy metals with implications for their deformation behavior.

High-temperature deformation of YBa2Cu3O7-δ with Ag additions

International Nuclear Information System (INIS)

Routbort, J.L.; Goretta, K.C.; Singh, J.P.

1990-01-01

The steady-state flow stress of YBa 2 Cu 3 O 7-δ containing 15 to 30 vol.% Ag has been measured in air at nearly constant compressive strain rates between 5 x 10 -6 and 1 x 10 -4 s -1 from 830 to 900 degrees C. Addition of Ag dramatically decreases the flow stress compared to that of the pure superconductor, but the stress exponents and the activation energy for deformation remain unchanged

Strain buildup in GaAs due to 100 MeV Ag ion irradiation

Energy Technology Data Exchange (ETDEWEB)

Mishra, Shramana; Bhaumik, Sudipta; Panda, Jaya Kumar [Department of Physics and Meteorology, Indian Institute of Technology, Kharagpur 721 302 (India); Ojha, Sunil [Inter-University Accelerator Center, Aruna Asaf Ali Marg, New Delhi 110 067 (India); Dhar, Achintya [Department of Physics and Meteorology, Indian Institute of Technology, Kharagpur 721 302 (India); Kabiraj, D. [Inter-University Accelerator Center, Aruna Asaf Ali Marg, New Delhi 110 067 (India); Roy, Anushree, E-mail: anushree@phy.iitkgp.ernet.in [Department of Physics and Meteorology, Indian Institute of Technology, Kharagpur 721 302 (India)

2013-12-01

The formation of strained layers and a non-monotonic evolution of strain in high energy (100 MeV) silver ion (Ag{sup 7+}) irradiated undoped semi-insulating GaAs are observed and analyzed using Raman scattering and high resolution X-ray diffraction (HRXRD) measurements. At low fluence, compressively strained layers are formed, whereas, with increase in fluence both compressive and tensile strains appear as observed from HRXRD measurements. Further, at low fluence, the change in compressive strain with increase in fluence is found to be sharper than what is observed at higher fluence, thereby suggesting a critical fluence value, beyond which there is a simultaneous generation and annihilation of vacancy type defects. The initial blue shift and subsequent relative red shift beyond above critical fluence in the Raman peak also qualitatively reveal non-monotonic evolution of strain in this case. Finally, we demonstrate the sensitivity of Raman spectroscopy in detecting the decrease in lattice ordering in the crystal in the low fluence regime, below the detection limit of Rutherford back-scattering channeling (c-RBS) measurements.

AgSbSe{sub 2} and AgSb(S,Se){sub 2} thin films for photovoltaic applications

Energy Technology Data Exchange (ETDEWEB)

Garza, J.G. [Facultad de Ingenieria Mecanica y Electrica, Universidad Autonoma de Nuevo Leon, San Nicolas de los Garza, Nuevo Leon (Mexico); Shaji, S. [Facultad de Ingenieria Mecanica y Electrica, Universidad Autonoma de Nuevo Leon, San Nicolas de los Garza, Nuevo Leon (Mexico); Facultad de Ingenieria Mecanica y Electrica, CIIDIT - Universidad Autonoma de Nuevo Leon, Apodaca, Nuevo Leon (Mexico); Rodriguez, A.C.; Das Roy, T.K. [Facultad de Ingenieria Mecanica y Electrica, Universidad Autonoma de Nuevo Leon, San Nicolas de los Garza, Nuevo Leon (Mexico); Krishnan, B., E-mail: kbindu_k@yahoo.com [Facultad de Ingenieria Mecanica y Electrica, Universidad Autonoma de Nuevo Leon, San Nicolas de los Garza, Nuevo Leon (Mexico); Facultad de Ingenieria Mecanica y Electrica, CIIDIT - Universidad Autonoma de Nuevo Leon, Apodaca, Nuevo Leon (Mexico)

2011-10-01

Silver antimony selenide (AgSbSe{sub 2}) thin films were prepared by heating sequentially deposited multilayers of antimony sulphide (Sb{sub 2}S{sub 3}), silver selenide (Ag{sub 2}Se), selenium (Se) and silver (Ag). Sb{sub 2}S{sub 3} thin film was prepared from a chemical bath containing SbCl{sub 3} and Na{sub 2}S{sub 2}O{sub 3}, Ag{sub 2}Se from a solution containing AgNO{sub 3} and Na{sub 2}SeSO{sub 3} and Se thin films from an acidified solution of Na{sub 2}SeSO{sub 3}, at room temperature on glass substrates. Ag thin film was deposited by thermal evaporation. The annealing temperature was 350 deg. C in vacuum (10{sup -3} Torr) for 1 h. X-ray diffraction analysis showed that the thin films formed were polycrystalline AgSbSe{sub 2} or AgSb(S,Se){sub 2} depending on selenium content in the precursor films. Morphology and elemental analysis of these films were done using scanning electron microscopy and energy dispersive X-ray spectroscopy. Optical band gap was evaluated from the UV-visible absorption spectra of these films. Electrical characterizations were done using Hall effect and photocurrent measurements. A photovoltaic structure: glass/ITO/CdS/AgSbSe{sub 2}/Al was formed, in which CdS was deposited by chemical bath deposition. J-V characteristics of this structure showed V{sub oc} = 435 mV and J{sub sc} = 0.08 mA/cm{sup 2} under illumination using a tungsten halogen lamp. Preparation of a photovoltaic structure using AgSbSe{sub 2} as an absorber material by a non-toxic selenization process is achieved.

Evaluation of the Components Released by Wine Yeast Strains on Protein Haze Formation in White Wine

Directory of Open Access Journals (Sweden)

Ellen Cristine Giese

2016-12-01

Full Text Available Cultures of 23 indigenous yeast strains (22 Saccharomyces cerevisiae and a non-Saccharomyces, Torulaspora delbrueckii, isolated from fermentation tanks at wineries in Castilla-La Mancha (Spain, and were performed under winemaking conditions using a synthetic must. Polysaccharide analysis and turbidity assays were conducted so as to observe the capacity of the released mannoproteins against protein haze formation in white wine, and 3 strains (2 Saccharomyces cerevisiae and T. delbrueckii were chosen for further experiments. The action of a commercial b-glucanolytic enzyme preparation (Lallzyme BETA®, and a β-(1→3-glucanase preparation from Trichoderma harzianum Rifai were evaluated to release polysaccharides from the different yeast strains’ cell walls. Protection against protein haze formation was strain dependent, and only two strains (Sc2 and Sc4 presented >50% stabilization in comparison to controls. Addition of β-glucanases did not increase the concentrations of polysaccharides in the fermentation musts; however, a significant increase of polymeric mannose (mannoproteins was detected using an enzymatic assay following total acid hydrolysis of the soluble polysaccharides. Enzymatic treatment presented positive effects and decreased protein haze formation in white wine. DOI http://dx.doi.org/10.17807/orbital.v8i6.869

Antimicrobial activity of TiO{sub 2}:Ag nanocrystalline heterostructures: Experimental and theoretical insights

Energy Technology Data Exchange (ETDEWEB)

André, Rafaela S. [UFSCar – Universidade Federal de São Carlos, Department of Chemistry, 13565-905 São Carlos, SP (Brazil); Zamperini, Camila A. [UNESP – Universidade Estadual Paulista, Instituto de Química, 14801-907 Araraquara, SP (Brazil); Mima, Ewerton G. [UNESP – Universidade Estadual Paulista, Escola de Odontologia de Araraquara, Departamento de Materias Odontológicos e Próteses Dentárias, 14801-903 Araraquara, SP (Brazil); Longo, Valéria M., E-mail: valeria.longo@liec.ufscar.br [USP – Universidade de São Paulo, Instituto de Física de São Carlos, 13560-970 São Carlos, SP (Brazil); Albuquerque, Anderson R. [UNESP – Universidade Estadual Paulista, Grupo de Modelagem e Simulação Molecular, P.O. Box 477, CEP 17033-360 Bauru, SP (Brazil); Instituto Federal de Educação, Ciência e Tecnologia do Sertão Pernambucano, IFSetão-PE, 56400-000 Floresta, PE (Brazil); Sambrano, Júlio R. [UNESP – Universidade Estadual Paulista, Grupo de Modelagem e Simulação Molecular, P.O. Box 477, CEP 17033-360 Bauru, SP (Brazil); and others

2015-09-28

Highlights: • Greener hydrothermal process to obtain nanocrystalline TiO{sub 2} anatase with Ag nanoparticles. • Antifungal effect against planktonic cells of C. albicans and Staphylococcus aureus. • DFT calculations of anatase TiO{sub 2} and metallic Ag. • Mechanism for the formation of reactive species at surface. - Abstract: We report the synthesis and characterization of silver-decorated titanium dioxide (TiO{sub 2}:Ag) nanoparticles, as well as a discussion of their antimicrobial activity. This material was synthesized by microwave-assisted hydrothermal treatment and characterized by complementary techniques. The minimum inhibitory concentration and minimum bactericidal/fungicidal concentration of TiO{sub 2}:Ag nanoparticles against planktonic and biofilm-forming strains of methicillin-resistant Staphylococcus aureus, Candida species (spp.) and the total biofilm mass were determined. The basis of the biological activity of TiO{sub 2}:Ag was investigated by electronic analysis of the material using theoretical quantum chemical calculations. In the proposed mechanism of action, the impregnated semiconductor donates electrons to the forbidden band gaps in the metal, generating point defects, with partially located electrons and holes at the surface, initiating a radical process involving the solvent and biological target. Our results suggest that this TiO{sub 2}:Ag nanomaterial has potential for use in the development of new therapeutic agents.

Preparation of Ag{sub 2}O/Ag{sub 2}CO{sub 3}/MWNTs composite photocatalysts for enhancement of ciprofloxacin degradation

Energy Technology Data Exchange (ETDEWEB)

Wang, Huiqin [School of Materials Science & Engineering, Jiangsu University, Zhenjiang 212013 (China); Li, Jinze [School of Chemistry & Chemical Engineering, Jiangsu University, Zhenjiang 212013 (China); Huo, Pengwei, E-mail: huopw1@163.com [School of Chemistry & Chemical Engineering, Jiangsu University, Zhenjiang 212013 (China); Institute of Green Chemistry and Chemical Technology, Jiangsu University, Zhenjiang 212013 (China); Yan, Yongsheng [School of Chemistry & Chemical Engineering, Jiangsu University, Zhenjiang 212013 (China); Institute of Green Chemistry and Chemical Technology, Jiangsu University, Zhenjiang 212013 (China); Guan, Qingfeng [School of Materials Science & Engineering, Jiangsu University, Zhenjiang 212013 (China)

2016-03-15

Graphical abstract: - Highlights: • Ag{sub 2}O/Ag{sub 2}CO{sub 3}/MWNTs were prepared by calcination of the obtained precipitate. • The holes were main contributor for the degradation processes of ciprofloxacin. • The synergistic effect enhanced the activity and stability of composites. - Abstract: The Ag{sub 2}O/Ag{sub 2}CO{sub 3}/multi-walled carbon nanotube (MWNTs) composite photocatalysts were prepared by calcination of the obtained precipitate. The structures and morphology of as-prepared composite photocatalysts were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), diffuse reflectance spectroscopy (DRS), photoluminescence (PL) spectroscopy, X-ray photoelectron spectroscopy (XPS). The Ag{sub 2}O/Ag{sub 2}CO{sub 3}/MWNTs composite photocatalysts exhibit higher degradation rate of ciprofloxacin (CIP) than the pure Ag{sub 2}CO{sub 3}, Ag{sub 2}O/Ag{sub 2}CO{sub 3} and Ag{sub 2}CO{sub 3}/MWNTs under visible light irradiation. The amount of loaded Ag{sub 2}CO{sub 3} onto MWNTs and calcined time for Ag{sub 2}CO{sub 3}/MWNTs were systematically investigated, and the optimal amount of loaded Ag{sub 2}CO{sub 3} and calcined time of Ag{sub 2}CO{sub 3}/MWNTs are 150 wt% and 10 min, respectively. The highest photocatalytic degradation rate of CIP could reach 76% under optimal conditions. The active species trapping experiments were also analyzed, the results show that the holes are main contributor for the degradation processes of CIP, furthermore the electrons, ·O{sub 2}{sup −} and ·OH are also crucially influenced the photocatalytic degradation processes of CIP. The possible photocatalytic processes of CIP with Ag{sub 2}O/Ag{sub 2}CO{sub 3}/MWNTs composite photocatalyst are also proposed.

Synthesis and Characterization of Ag-Ag2O/TiO2@polypyrrole Heterojunction for Enhanced Photocatalytic Degradation of Methylene Blue

Directory of Open Access Journals (Sweden)

Rajeev Kumar

2016-05-01

Full Text Available Hybrid multi-functional nanomaterials comprising two or more disparate materials have become a powerful approach to obtain advanced materials for environmental remediation applications. In this work, an Ag-Ag2O/TiO2@polypyrrole (Ag/TiO2@PPy heterojunction has been synthesized by assembling a self-stabilized Ag-Ag2O (p type semiconductor (denoted as Ag and polypyrrole (π-conjugated polymer on the surface of rutile TiO2 (n type. Ag/TiO2@PPy was synthesized through simultaneous oxidation of pyrrole monomers and reduction of AgNO3 in an aqueous solution containing well-dispersed TiO2 particles. Thus synthesized Ag/TiO2@PPy was characterized using X-ray diffraction (XRD, X-ray photoelectron spectroscopy (XPS, field emission scanning electron microscopy (FE-SEM, transmission electron microscopy (TEM, and UV-Vis diffuse reflectance spectroscopy (UV-vis DSR. The photocatalytic activity of synthesized heterojunction was investigated for the decomposition of methylene blue (MB dye under UV and visible light irradiation. The results revealed that π-conjugated p-n heterojunction formed in the case of Ag/TiO2@PPy significantly enhanced the photodecomposition of MB compared to the p-n type Ag/TiO2 and TiO2@PPy (n-π heterojunctions. A synergistic effect between Ag-Ag2O and PPy leads to higher photostability and a better electron/hole separation leads to an enhanced photocatalytic activity of Ag/TiO2@PPy under both UV and visible light irradiations.

Silver(I) complexes of the weakly coordinating solvents SO(2) and CH(2)Cl(2): crystal structures, bonding, and energetics of [Ag(OSO)][Al{OC(CF(3))(3)}(4)], [Ag(OSO)(2/2)][SbF(6)], and [Ag(CH(2)Cl(2))(2)][SbF(6)].

Science.gov (United States)

Decken, Andreas; Knapp, Carsten; Nikiforov, Grigori B; Passmore, Jack; Rautiainen, J Mikko; Wang, Xinping; Zeng, Xiaoqing

2009-06-22

Pushing the limits of coordination chemistry: The most weakly coordinated silver complexes of the very weakly coordinating solvents dichloromethane and liquid sulfur dioxide were prepared. Special techniques at low temperatures and the use of weakly coordinating anions allowed structural characterization of [Ag(OSO)][Al{OC(CF(3))(3)}(4)], [Ag(OSO)(2/2)][SbF(6)], and [Ag(Cl(2)CH(2))(2)][SbF(6)] (see figure). An investigation of the bonding shows that these complexes are mainly stabilized by electrostatic monopole-dipole interactions.The synthetically useful solvent-free silver(I) salt Ag[Al(pftb)(4)] (pftb=--OC(CF(3))(3)) was prepared by metathesis reaction of Li[Al(pftb)(4)] with Ag[SbF(6)] in liquid SO(2). The solvated complexes [Ag(OSO)][Al(pftb)(4)], [Ag(OSO)(2/2)][SbF(6)], and [Ag(CH(2)Cl(2))(2)][SbF(6)] were prepared and isolated by special techniques at low temperatures and structurally characterized by single-crystal X-ray diffraction. The SO(2) complexes provide the first examples of coordination of the very weak Lewis base SO(2) to silver(I). The SO(2) molecule in [Ag(OSO)][Al(pftb)(4)] is eta(1)-O coordinated to Ag(+), while the SO(2) ligands in [Ag(OSO)(2/2)][SbF(6)] bridge two Ag(+) ions in an eta(2)-O,O' (trans,trans) manner. [Ag(CH(2)Cl(2))(2)][SbF(6)] contains [Ag(CH(2)Cl(2))(2)](+) ions linked through [SbF(6)](-) ions to give a polymeric structure. The solid-state silver(I) ion affinities (SIA) of SO(2) and CH(2)Cl(2), based on bond lengths and corresponding valence units in the corresponding complexes and tensimetric titrations of Ag[Al(pftb)(4)] and Ag[SbF(6)] with SO(2) vapor, show that SO(2) is a weaker ligand to Ag(+) than the commonly used weakly coordinating solvent CH(2)Cl(2) and indicated that binding strength of SO(2) to silver(I) in the silver(I) salts increases with increasing size of the corresponding counteranion ([Al(pftb)(4)](-)>[SbF(6)](-)). The experimental findings are in good agreement with theoretical gas-phase ligand

AC loss characteristics of Bi2223/Ag sheathed tape wires subjected to mechanical strains and stresses

International Nuclear Information System (INIS)

Tsukamoto, Osami; Li, Z

2007-01-01

The influence of uniaxial tensile stress-strain on the AC loss characteristics of multifilamentary Bi2223/Ag sheathed tape wires was investigated. The uniaxial tensile stress-strain was applied to the sample wire in liquid nitrogen at atmospheric pressure, and the AC losses (transport, magnetization and total losses) were measured by an electric method. Two kinds of wire, oxide-dispersion strengthened Ag-alloy sheathed and Ag-alloy sheathed wires, were tested. The stress-strain curves of the tested wires were divided in three regions, i.e. elastic deformation, continuous plastic deformation and serrated-like plastic deformation regions, though the ranges of those regions were different for different kinds of wire. In the elastic and continuous plastic regions, the stress-strain curve was smooth and continuous, and in the serrated-like plastic region, the curve was rough. In the serrated-like plastic region, the wires kept elongating, while increase of the tensile stress was suspended. Dependences of the critical currents on the stress-strain were generally as follows. While decreases of the wire critical currents were in the range of less than 4% of the original values of the no-stress condition, the critical currents of the wires were reversible, that is, the critical currents recovered the original values at zero stress when the stress were released, regardless of whether the wires were in the elastic or continuous plastic region. In the continuous plastic region, the critical currents decreased up to 10%-15% of the original values and the critical currents were irreversible when the degradations of the critical currents exceeded about 4%. In the serrated-like plastic regions, the critical currents were more severely degraded. The AC loss characteristics of the wires are different in those regions. In the elastic and continuous plastic regions, the absolute values of AC losses were dependent on the stress-strain. However, the dependences of those normalized

Experimental and theoretical investigation on photocatalytic activities of 1D Ag/Ag2WO4 nanostructures

Science.gov (United States)

Liu, Danqing; Huang, Weicheng; Li, Long; Liu, Lu; Sun, Xiaojun; Liu, Bo; Yang, Bin; Guo, Chongshen

2017-09-01

Ag2WO4 is a significant photocatalyst that responds to UV light irradiation only, which greatly hinders it for further practical application for solar light. To address this problem, herein, 1D plasmonic Ag/Ag2WO4 photocatalysts have been fabricated by a successive process including hydrothermal synthesis to obtain Ag2WO4 followed by an additional in situ chemical-reduction process for Ag decoration. Then, the structural features, optical properties, and electronic structures of Ag2WO4 and Ag/Ag2WO4 nanowires were systematically investigated via a combination of theoretical calculations and experimental evidence. The plasmon-enhanced Ag/Ag2WO4 nanowires exhibited higher visible-light-driven photocatalytic activity, which performed a desired photodestruction ratio of 91.2% on methylene blue within 60 min and good stability in five cycles. The Ag decoration greatly facilitates visible-light harvesting and thus promotes photogenerated radical oxidation to dye, which is evidenced by the higher hydroxyl radical level of Ag/Ag2WO4 detected in the ESR test during the photocatalytic process. The theoretical calculation based on density functional theory indicates that Ag nanoparticles formed on the surface of Ag2WO4 could narrow the band gap of Ag2WO4. In addition, the surface plasmon resonance absorption effect and fast charge transfer effect in the metal-semiconductor system contribute to the photocatalytic performance of Ag/Ag2WO4.

Enhanced Visible Light Photocatalytic Degradation of Organic Pollutants over Flower-Like Bi2O2CO3 Dotted with Ag@AgBr

Directory of Open Access Journals (Sweden)

Shuanglong Lin

2016-10-01

Full Text Available A facile and feasible oil-in-water self-assembly approach was developed to synthesize flower-like Ag@AgBr/Bi2O2CO3 micro-composites. The photocatalytic activities of the samples were evaluated through methylene blue degradation under visible light irradiation. Compared to Bi2O2CO3, flower-like Ag@AgBr/Bi2O2CO3 micro-composites show enhanced photocatalytic activities. In addition, results indicate that both the physicochemical properties and associated photocatalytic activities of Ag@AgBr/Bi2O2CO3 composites are shown to be dependent on the loading quantity of Ag@AgBr. The highest photocatalytic performance was achieved at 7 wt % Ag@AgBr, degrading 95.18% methylene blue (MB after 20 min of irradiation, which is over 1.52 and 3.56 times more efficient than that of pure Ag@AgBr and pure Bi2O2CO3, respectively. Bisphenol A (BPA was also degraded to further demonstrate the degradation ability of Ag@AgBr/Bi2O2CO3. A photocatalytic mechanism for the degradation of organic compounds over Ag@AgBr/Bi2O2CO3 was proposed. Results from this study illustrate an entirely new approach to fabricate semiconductor composites containing Ag@AgX/bismuth (X = a halogen.

Measurement of the energetics of metal film growth on a semiconductor: Ag/ Si(100)-2x1

DEFF Research Database (Denmark)

Starr, D.E.; Ranney, J.T.; Larsen, Jane Hvolbæk

2001-01-01

The first direct calorimetric measurements of the energetics of metal film growth on a semiconductor surface are presented. The heat of adsorption of Ag on Si(100)-(2 x 1) at 300 K decreases from similar to 347 to 246 kJ/mol with coverage in the first monolayer (ML) due to overlap of substrate...... strain from nearby Ag islands. It then rises quickly toward the bulk sublimation enthalpy (285 kJ/mol) as 3D particles grow. A wetting layer grows to 1.0 ML, but is metastable above similar to0.55 ML and dewets when kinetics permit. This may be common when adsorbate islands induce a large strain...

Photocatalytic oxidation removal of Hg"0 using ternary Ag/AgI-Ag_2CO_3 hybrids in wet scrubbing process under fluorescent light

International Nuclear Information System (INIS)

Zhang, Anchao; Zhang, Lixiang; Chen, Xiaozhuan; Zhu, Qifeng; Liu, Zhichao; Xiang, Jun

2017-01-01

Highlights: • Ag/AgI-Ag_2CO_3 hybrids were employed for Hg"0 removal under fluorescent light. • Superoxide radical (·O_2"−) played a key role in Hg"0 removal. • NO exhibited a significant effect on Hg"0 removal in comparison to SO_2. • The mechanism for enhanced Hg"0 removal over Ag/AgI-Ag_2CO_3 was proposed. - Abstract: A series of ternary Ag/AgI-Ag_2CO_3 photocatalysts synthesized using a facile coprecipitation method were employed to investigate their performances of Hg"0 removal in a wet scrubbing reactor. The hybrids were characterized by N_2 adsorption-desorption, XRD, SEM-EDS, HRTEM, XPS, DRS and ESR. The photocatalytic activities of Hg"0 removal were evaluated under fluorescent light. The results showed that AgI content, fluorescent light irradiation, reaction temperature all showed significant influences on Hg"0 removal. NO exhibited significant effect on Hg"0 removal in comparison to SO_2. Among these ternary Ag/AgI-Ag_2CO_3 hybrids, Ag/AgI(0.1)-Ag_2CO_3 showed the highest Hg"0 removal efficiency, which could be ascribed to the effective separation of photogenerated electron-hole pairs between AgI and Ag_2CO_3 and the surface plasmon resonance (SPR) effect in the visible region by metallic silver nanoparticles (Ag"0 NPs). The trapping studies of reactive radicals showed that the superoxide radicals (·O_2"−) may play a key role in Hg"0 removal under fluorescent light. According to the experimental and characterization results, a possible photocatalytic oxidation mechanism for enhanced Hg"0 removal over Ag/AgI(0.1)-Ag_2CO_3 hybrid under fluorescent light was proposed.

RRR and thermal conductivity of Ag and Ag0.2wt%Mg alloy in Ag/Bi-2212 wires

Energy Technology Data Exchange (ETDEWEB)

Li, Pei [Fermilab; Ye, L. [North Carolina State U.; Jiang. J., Jiang. J. [Natl. High Mag. Field Lab.; Shen, T. [Fermilab

2015-08-19

The residual resistivity ratio (RRR) and thermal conductivity of metal matrix in metal/superconductor composite wires are important parameters for designing superconducting magnets. However, the resistivity of silver in reacted Ag/Bi-2212 wires has yet to be determined over temperature range from 4.2 K to 80 K because Bi-2212 filaments have a critical transition temperature Tc of ~ 80 K, and because it is unknown whether the RRR of Ag/Bi-2212 degrades with Cu diffusing from Bi-2212 filaments into silver sheathes at elevated temperatures and to what degree it varies with heat treatment. We measured the resistivity of stand-alone Ag and AgMg (Ag-0.2wt%Mg) wires as well as the resistivity of Ag and Ag- 0.2wt%Mg in the state-of-the-art Ag/Bi-2212 round wires reacted in 1 bar oxygen at 890 °C for 1, 8, 24 and 48 hours and quickly cooled to room temperature. The heat treatment was designed to reduce the critical current Ic of Bi-2212 wires to nearly zero while allowing Cu loss to fully manifest itself. We determined that pure silver exhibits a RRR of ~ 220 while the oxide-dispersion strengthened AgMg exhibits a RRR of ~ 5 in stand-alone samples. A surprising result is that the RRR of silver in the composite round wires doesn’t degrade with extended time at 890 °C for up to 48 hours. This surprising result may be explained by our observation that the Cu that diffuses into the silver tends to form Cu2O precipitates in oxidizing atmosphere, instead of forming Ag-Cu solution alloy. We also measured the thermal conductivity and the magneto-resistivity of pure Ag and Ag-0.2 wt%Mg from 4.2 K to 300 K in magnetic fields up to 14.8 T and summarized them using a Kohler plot.

Reversible conversion between AgCl and Ag in AgCl-doped RSiO{sub 3/2}-TiO{sub 2} films prepared by a sol-gel technique

Energy Technology Data Exchange (ETDEWEB)

Kawamura, Go, E-mail: gokawamura@ee.tut.ac.jp [Department of Electrical and Electronic Information Engineering, Toyohashi University of Technology, Toyohashi, Aichi 441-8580 (Japan); Tsurumi, Yuuki [Department of Environmental and Life Sciences, Toyohashi University of Technology, Toyohashi, Aichi 441-8580 (Japan); Muto, Hiroyuki [Department of Electrical and Electronic Information Engineering, Toyohashi University of Technology, Toyohashi, Aichi 441-8580 (Japan); Department of Environmental and Life Sciences, Toyohashi University of Technology, Toyohashi, Aichi 441-8580 (Japan); Sakai, Mototsugu; Inoue, Mitsuteru [Department of Electrical and Electronic Information Engineering, Toyohashi University of Technology, Toyohashi, Aichi 441-8580 (Japan); Matsuda, Atsunori [Department of Electrical and Electronic Information Engineering, Toyohashi University of Technology, Toyohashi, Aichi 441-8580 (Japan); Department of Environmental and Life Sciences, Toyohashi University of Technology, Toyohashi, Aichi 441-8580 (Japan)

2011-10-17

Highlights: {center_dot} The reversible redox behavior between AgCl and Ag in RSiO{sub 3/2}-TiO{sub 2} film is studied. {center_dot} TiO{sub 2} component induces Cl to remain in the film after conversion of AgCl to Ag. {center_dot} The survival of Cl is essential for reconversion of Ag to AgCl. {center_dot} The film shows potential to be applied as rewritable holographic material. - Abstract: The reversible redox behavior exhibited by AgCl-doped organosilsesquioxane-titania gel films is studied. Films prepared by the sol-gel method show reversible color changes with blue laser irradiation and subsequent heat treatment, which is based on the formation of Ag and AgCl nanoparticles, respectively. Two-beam interference exposure experiments reveal that the films have potential to be applied as rewritable holographic materials. A large titania content is essential for the conversion of Ag to AgCl because it induces the Cl to remain near the Ag nanoparticles during blue laser irradiation, allowing the Cl to react with neighboring Ag nanoparticles to reform AgCl upon subsequent heat treatment.

Synthesis, morphological control, and antibacterial properties of hollow/solid Ag2S/Ag heterodimers

KAUST Repository

Pang, Maolin; Hu, Jiangyong; Zeng, Huachun

2010-01-01

of this highly asymmetric dipolar composite, photocatalytic inactivation of Escherichia coli K-12 in the presence of the as-prepared Ag 2S/Ag heterodimers has been carried out under UV irradiation. The added Ag2S/Ag heterodimers show good chemical stability under

Cytotoxicity of serum protein-adsorbed visible-light photocatalytic Ag/AgBr/TiO2 nanoparticles

International Nuclear Information System (INIS)

Seo, Ji Hye; Jeon, Won Il; Dembereldorj, Uuriintuya; Lee, So Yeong; Joo, Sang-Woo

2011-01-01

Highlights: ► Photocytotoxicity of visible-light catalytic NPs was examined in vitro. ► Ag/AgBr/TiO 2 NPs were well internalized in cells after adsorption of serum proteins. ► Cell viability was decreased by 40–60% using ∼8 ppm NPs and 60 W/cm 2 visible light within 5 h. ► Mitochondria activity test indicated the reactive oxygen species for photo-destruction of cells. ► Ag/AgBr/TiO 2 NPs were found to eliminate xenograft tumors significantly in vivo. - Abstract: Photocytotoxicity of visible-light catalytic Ag/AgBr/TiO 2 nanoparticles (NPs) was examined both in vitro and in vivo. The Ag/AgBr/TiO 2 NPs were prepared by the deposition–precipitation method. Their crystalline structures, atomic compositions, and light absorption property were examined by X-ray diffraction (XRD) patterns, X-ray photoelectron (XPS) intensities, and ultraviolet-visible (UV–vis) diffuse reflectance spectroscopic tools. The Ag/AgBr/TiO 2 NPs appeared to be well internalized in human carcinoma cells as evidenced by transmission electron microscopy (TEM). The cytotoxicity of cetylmethylammonium bromide (CTAB) appeared to be significantly reduced by adsorption of serum proteins in the cellular medium on the NP surfaces. Two types of human cervical HeLa and skin A431 cancer cells were tested to check their viability after the cellular uptake of the Ag/AgBr/TiO 2 NPs and subsequent exposure to an illumination of visible light from a 60 W/cm 2 halogen lamp. Fluorescence images taken to label mitochondria activity suggest that the reactive oxygen species should trigger the photo-destruction of cancer cells. After applying the halogen light illumination for 50–250 min and ∼8 ppm (μg/mL) of photocatalytic Ag/AgBr/TiO 2 NPs, we observed a 40–60% selective decrease of cell viability. Ag/AgBr/TiO 2 NPs were found to eliminate xenograft tumors significantly by irradiating visible light in vivo for 10 min.

DFT calculations of strain and interface effects on electronic structures and magnetic properties of L10-FePt/Ag heterojunction of GMR applications

Science.gov (United States)

Pramchu, Sittichain; Jaroenjittichai, Atchara Punya; Laosiritaworn, Yongyut

2018-03-01

In this work, density functional theory (DFT) was employed to investigate the effect of strain and interface on electronic structures and magnetic properties of L10-FePt/Ag heterojunction. Two possible interface structures of L10-FePt(001)/Ag(001), that is, interface between Fe and Ag layers (Fe/Ag) and between Pt and Ag layers (Pt/Ag), were inspected. It was found that Pt/Ag interface is more stable than Fe/Ag interface due to its lower formation energy. Further, under the lattice mismatch induced tensile strain, the enhancement of magnetism for both Fe/Ag and Pt/Ag interface structures has been found to have progressed, though the magnetic moments of "interfacial" Fe and Pt atoms have been found to have decreased. To explain this further, the local density of states (LDOS) analysis suggests that interaction between Fe (Pt) and Ag near Fe/Ag (Pt/Ag) interface leads to spin symmetry breaking of the Ag atom and hence induces magnetism magnitude. In contrast, the magnetic moments of interfacial Fe and Pt atoms reduce because of the increase in the electronic states near the Fermi level of the minority-spin electrons. In addition, the significant enhancements of the LDOS near the Fermi levels of the minority-spin electrons signify the boosting of the transport properties of the minority-spin electrons and hence the spin-dependent electron transport at this ferromagnet/metal interface. From this work, it is expected that this clarification of the interfacial magnetism may inspire new innovation on how to improve spin-dependent electron transport for enhancing the giant magnetoresistance (GMR) ratio of potential GMR-based spintronic devices.

DFT calculations of strain and interface effects on electronic structures and magnetic properties of L10-FePt/Ag heterojunction of GMR applications

Directory of Open Access Journals (Sweden)

Sittichain Pramchu

2018-03-01

Full Text Available In this work, density functional theory (DFT was employed to investigate the effect of strain and interface on electronic structures and magnetic properties of L10-FePt/Ag heterojunction. Two possible interface structures of L10-FePt(001/Ag(001, that is, interface between Fe and Ag layers (Fe/Ag and between Pt and Ag layers (Pt/Ag, were inspected. It was found that Pt/Ag interface is more stable than Fe/Ag interface due to its lower formation energy. Further, under the lattice mismatch induced tensile strain, the enhancement of magnetism for both Fe/Ag and Pt/Ag interface structures has been found to have progressed, though the magnetic moments of “interfacial” Fe and Pt atoms have been found to have decreased. To explain this further, the local density of states (LDOS analysis suggests that interaction between Fe (Pt and Ag near Fe/Ag (Pt/Ag interface leads to spin symmetry breaking of the Ag atom and hence induces magnetism magnitude. In contrast, the magnetic moments of interfacial Fe and Pt atoms reduce because of the increase in the electronic states near the Fermi level of the minority-spin electrons. In addition, the significant enhancements of the LDOS near the Fermi levels of the minority-spin electrons signify the boosting of the transport properties of the minority-spin electrons and hence the spin-dependent electron transport at this ferromagnet/metal interface. From this work, it is expected that this clarification of the interfacial magnetism may inspire new innovation on how to improve spin-dependent electron transport for enhancing the giant magnetoresistance (GMR ratio of potential GMR-based spintronic devices.

Chemically deposited In2S3–Ag2S layers to obtain AgInS2 thin films by thermal annealing

International Nuclear Information System (INIS)

Lugo, S.; Peña, Y.; Calixto-Rodriguez, M.; López-Mata, C.; Ramón, M.L.; Gómez, I.; Acosta, A.

2012-01-01

Highlights: ► We obtained polycrystalline silver indium sulfide thin films through the annealing of chemically deposited In 2 S 3 –Ag 2 S films. ► According to XRD chalcopyrite structure of AgInS 2 was obtained. ► AgInS 2 thin film has a band gap of 1.86 eV and a conductivity value of 1.2 × 10 −3 (Ω cm) −1 . - Abstract: AgInS 2 thin films were obtained by the annealing of chemical bath deposited In 2 S 3 –Ag 2 S layers at 400 °C in N 2 for 1 h. According to the XRD and EDX results the chalcopyrite structure of AgInS 2 has been obtained. These films have an optical band gap, E g , of 1.86 eV and an electrical conductivity value of 1.2 × 10 −3 (Ω cm) −1 .

Stable and metastable phases in reciprocal systems PbSe + Ag2I2 Ag2Se + PbI2 and PbSe + CdI2 = CdSe + PbI2

International Nuclear Information System (INIS)

Odin, I.N.; Grin'ko, V.V.; Kozlovskij, V.F.; Safronov, E.V.

2005-01-01

Mutual system PbSe + Ag 2 I 2 = Ag 2 Se + PbI 2 is investigated. It is shown that diagonal Ag 2 Se-PbI 2 is stable. Liquidus surface and isothermal section at 633 K of phase diagram of PbSe-Ag 2 Se-PbI 2 system are built. Transformations directing to crystallization metastable ternary compound forming in PbSe-PbI 2 system and metastable polytype modifications of lead iodide in PbSe-Ag 2 Se-PbI 2 system at 620-685 K are studied. By hardening from molten state (1150-1220 K) new interstitial metastable phases crystallizing in CdCl 2 structural type are obtained in PbSe-Ag 2 Se-PbI 2 and PbSe + CdI 2 = CdSe + PbI 2 systems [ru

High Ms Fe16N2 thin film with Ag under layer on GaAs substrate

Energy Technology Data Exchange (ETDEWEB)

Allard Jr, Lawrence Frederick [ORNL

2016-01-01

(001) textured Fe16N2 thin film with Ag under layer is successfully grown on GaAs substrate using a facing target sputtering (FTS) system. After post annealing, chemically ordered Fe16N2 phase is formed and detected by X-ray diffraction (XRD). High saturation magnetization (Ms) is measured by a vibrating sample magnetometer (VSM). In comparison with Fe16N2 with Ag under layer on MgO substrate and Fe16N2 with Fe under layer on GaAs substrate, the current layer structure shows a higher Ms value, with a magnetically softer feature in contrast to the above cases. In addition, X-ray photoelectron spectroscopy (XPS) is performed to characterize the binding energy of N atoms. To verify the role of strain that the FeN layer experiences in the above three structures, Grazing Incidence X-ray Diffraction (GIXRD) is conducted to reveal a large in-plane lattice constant due to the in-plane biaxial tensile strain. INTRODUCTION

Novel Flexible Transparent Conductive Films with Enhanced Chemical and Electromechanical Sustainability: TiO2 Nanosheet-Ag Nanowire Hybrid.

Science.gov (United States)

Sohn, Hiesang; Kim, Seyun; Shin, Weonho; Lee, Jong Min; Lee, Hyangsook; Yun, Dong-Jin; Moon, Kyoung-Seok; Han, In Taek; Kwak, Chan; Hwang, Seong-Ju

2018-01-24

Flexible transparent conductive films (TCFs) of TiO 2 nanosheet (TiO 2 NS) and silver nanowire (Ag NW) network hybrid were prepared through a simple and scalable solution-based process. The as-formed TiO 2 NS-Ag NW hybrid TCF shows a high optical transmittance (TT: 97% (90.2% including plastic substrate)) and low sheet resistance (R s : 40 Ω/sq). In addition, the TiO 2 NS-Ag NW hybrid TCF exhibits a long-time chemical/aging and electromechanical stability. As for the chemical/aging stability, the hybrid TCF of Ag NW and TiO 2 NS reveals a retained initial conductivity (ΔR s /R s 4000%) or RuO 2 NS-Ag NW hybrid (ΔR s /R s > 200%). As corroborated by the density functional theory simulation, the superb chemical stability of TiO 2 NS-Ag NW hybrid is attributable to the unique role of TiO 2 NS as a barrier, which prevents Ag NW's chemical corrosion via the attenuated adsorption of sulfidation molecules (H 2 S) on TiO 2 NS. With respect to the electromechanical stability, in contrast to Ag NWs (ΔR/R 0 ∼ 152.9%), our hybrid TCF shows a limited increment of fractional resistivity (ΔR/R 0 ∼ 14.4%) after 200 000 cycles of the 1R bending test (strain: 6.7%) owing to mechanically welded Ag NW networks by TiO 2 NS. Overall, our unique hybrid of TiO 2 NS and Ag NW exhibits excellent electrical/optical properties and reliable chemical/electromechanical stabilities.

Enhanced photocatalysts based on Ag-TiO2 and Ag-N-TiO2 nanoparticles for multifunctional leather surface coating

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Gaidau Carmen

2016-01-01

Full Text Available The Ag deposition on TiO2 nanoparticles (Ag-TiO2 NPs and N-TiO2 nanoparticles (Ag-N-TiO2 NPs has been made by electrochemical methodology in view of improved antibacterial properties and enhanced photocatalytic activity under visible light irradiation. The particle size in powder and in dispersion showed similar values and good stability in aqueous medium which made them suitable for use in leather surface covering for new multifunctional properties development. The diffuse reflectance spectra of Ag-TiO2 NPs, Ag-N-TiO2 NPs and TiO2 NPs have been investigated and correlated with their photocatalytic performances under UV and visible light against different silver concentrations. The leather surfaces treated with Ag-N-TiO2 NPs showed advanced self-cleaning properties under visible light exposure through the hydrophilic mechanism of organic soil decomposition. Moreover the bacterial sensitivity and proven fungitoxic properties of Ag-N-TiO2 NPs leads to the possibility of designing new multifunctional additives to extend the advanced applications for more durable and useable materials.

Development of a multiplex Q-PCR to detect Trichoderma harzianum Rifai strain T22 in plant roots.

Science.gov (United States)

Horn, Ivo R; van Rijn, Menno; Zwetsloot, Tom J J; Basmagi, Said; Dirks-Mulder, Anita; van Leeuwen, Willem B; Ravensberg, Willem J; Gravendeel, Barbara

2016-02-01

The fungal species Trichoderma harzianum is widely used as a biological agent in crop protection. To verify the continued presence of this fungus on plant roots manually inoculated with T. harzianum strain T22, a Q-PCR was designed using specific probes for this particular strain. To develop these molecular diagnostic tools, genome mining was first carried out to retrieve putative new regions by which different strains of T. harzianum could be distinguished. Subsequently, Sanger sequencing of the L-aminoacid oxidase gene (aox1) in T. harzianum was applied to determine the mutations differing between various strains isolated from the Trichoderma collection of Koppert Biological Systems. Based on the sequence information obtained, a set of hydrolysis probes was subsequently developed which discriminated T. harzianum T22 strains varying in only a single nucleotide. Probes designed for two strains uniquely recognized the respective strains in Q-PCR with a detection limit of 12,5ng DNA. Titration assays in which T. harzianum DNA from distinct strains was varied further underscored the specificity of the probes. Lastly, fungal DNA extracted from roots of greenhouse cultured tomato plants was analyzed using the probe-based assay. DNA from T. harzianum strain T22 could readily be identified on roots of greenhouse reared tomato plants inoculated with varying concentrations up to one week after treatment with a detection limit of 3e6 colony forming units of T. harzianum T22. We conclude that the Q-PCR method is a reliable and robust method for assessing the presence and quantity of T. harzianum strain T22 in manually inoculated plant material. Our method provides scope for the development of DNA based strain specific identification of additional strains of Trichoderma and other fungal biological control agents. Copyright © 2015 Elsevier B.V. All rights reserved.

Hierarchical Ag/AgCl-TiO{sub 2} hollow spheres with enhanced visible-light photocatalytic activity

Energy Technology Data Exchange (ETDEWEB)

Wang, Xu Long; Yin, Hao Yong [College of Materials Environment Engineering, Hangzhou Dianzi University, Hangzhou 310018 (China); Nie, Qiu Lin, E-mail: nieqiulin@hdu.edu.cn [College of Materials Environment Engineering, Hangzhou Dianzi University, Hangzhou 310018 (China); Wu, Wei Wei [College of Materials Environment Engineering, Hangzhou Dianzi University, Hangzhou 310018 (China); Zhang, Yang; LiYuan, Qiu [College of Science, Hangzhou Dianzi University, Hangzhou 310018 (China)

2017-01-01

The hierarchical Ag/AgCl-TiO{sub 2} hollow spheres were synthesized by depositing Ag/AgCl nanoparticles on TiO{sub 2} hollow spheres via a precipitation photoreduction method, and they were further characterized using TGA, SEM, TEM, XRD, XPS, UV–vis DRS and photoelectric chemical analysis. The analysis showed that the hierarchical Ag/AgCl-TiO{sub 2} hollow spheres exhibited the highest photocatalytic activity, which was approximately 13 times higher than that of TiO{sub 2} hollow spheres. The high photocatalytic activity of the composites is due to efficient electron-hole pairs separation at the photocatalyst interfaces, and localized surface plasmon resonance of Ag nanoparticles formed on AgCl particles in the degradation reaction. - Highlights: • TiO{sub 2} hollow spheres were prepared by a sacrificial template method. • The hollow spheres were modified with Ag/AgCl to form the heterojunctions. • The modification may produce synergistic effect of LSPR and hollow structure. • Visible light photocatalytic activity was enhanced on this hollow catalyst. • The mechanism of the improved photocatalytic performance was discussed.

Coherent-Interface-Assembled Ag2O-Anchored Nanofibrillated Cellulose Porous Aerogels for Radioactive Iodine Capture.

Science.gov (United States)

Lu, Yun; Liu, Hongwei; Gao, Runan; Xiao, Shaoliang; Zhang, Ming; Yin, Yafang; Wang, Siqun; Li, Jian; Yang, Dongjiang

2016-10-26

Nanofibrillated cellulose (NFC) has received increasing attention in science and technology because of not only the availability of large amounts of cellulose in nature but also its unique structural and physical features. These high-aspect-ratio nanofibers have potential applications in water remediation and as a reinforcing scaffold in composites, coatings, and porous materials because of their fascinating properties. In this work, highly porous NFC aerogels were prepared based on tert-butanol freeze-drying of ultrasonically isolated bamboo NFC with 20-80 nm diameters. Then nonagglomerated 2-20-nm-diameter silver oxide (Ag 2 O) nanoparticles (NPs) were grown firmly onto the NFC scaffold with a high loading content of ∼500 wt % to fabricate Ag 2 O@NFC organic-inorganic composite aerogels (Ag 2 O@NFC). For the first time, the coherent interface and interaction mechanism between the cellulose I β nanofiber and Ag 2 O NPs are explored by high-resolution transmission electron microscopy and 3D electron tomography. Specifically, a strong hydrogen between Ag 2 O and NFC makes them grow together firmly along a coherent interface, where good lattice matching between specific crystal planes of Ag 2 O and NFC results in very small interfacial straining. The resulting Ag 2 O@NFC aerogels take full advantage of the properties of the 3D organic aerogel framework and inorganic NPs, such as large surface area, interconnected porous structures, and supreme mechanical properties. They open up a wide horizon for functional practical usage, for example, as a flexible superefficient adsorbent to capture I - ions from contaminated water and trap I 2 vapor for safe disposal, as presented in this work. The viable binding mode between many types of inorganic NPs and organic NFC established here highlights new ways to investigate cellulose-based functional nanocomposites.

Ag/AgCl Loaded Bi2WO6 Composite: A Plasmonic Z-Scheme Visible Light-Responsive Photocatalyst

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Xiangchao Meng

2016-01-01

Full Text Available Hierarchical flower-like Bi2WO6 was successfully synthesized by facile hydrothermal method at low pH. And Ag/AgCl was loaded by photoreduction on its surface. As-prepared photocatalysts were characterized by various techniques. Bi2WO6 was successfully synthesized at a size of 2-3 μm. Depositing Ag/AgCl did not destroy the crystal structure, and both Ag+ and metallic Ag0 were found. The band gap of the composite was 2.57 eV, which indicates that visible light could be the activating irradiation. In the photocatalytic activity test, the composite with 10 wt% Ag/AgCl boasted the highest removal efficiency (almost 100% in 45 min. The significant enhancement can be attributed to the surface plasmon resonance (SPR effect and the establishment of heterostructures between Ag/AgCl and Bi2WO6. A possible mechanism of photocatalytic oxidation in the presence of Ag/AgCl-Bi2WO6 was proposed. This work sheds light on the potential applications of plasmonic metals in photocatalysis to enhance their activities.

Pressure-sensitive strain sensor based on a single percolated Ag nanowire layer embedded in colorless polyimide

Energy Technology Data Exchange (ETDEWEB)

Lee, Chan-Jae [Display Materials & Components Research Center, Korea Electronics Technology Institute, 68 Yatap-dong, Bundang-gu, Seongnam 463-816 (Korea, Republic of); Jun, Sungwoo [Display Materials & Components Research Center, Korea Electronics Technology Institute, 68 Yatap-dong, Bundang-gu, Seongnam 463-816 (Korea, Republic of); Display and Nanosystem Laboratory, College of Engineering, Korea University, Seoul 136-713 (Korea, Republic of); Ju, Byeong-Kwon [Display and Nanosystem Laboratory, College of Engineering, Korea University, Seoul 136-713 (Korea, Republic of); Kim, Jong-Woong, E-mail: wyjd@keti.re.kr [Display Materials & Components Research Center, Korea Electronics Technology Institute, 68 Yatap-dong, Bundang-gu, Seongnam 463-816 (Korea, Republic of)

2017-06-01

This paper presents the fabrication of an elastomer-free, transparent, pressure-sensitive strain sensor consisting of a specially designed silver nanowire (AgNW) pattern and colorless polyimide (cPI). A percolated AgNW network was patterned with a simple tandem compound circuit, which was then embedded in the surface of the cPI via inverted layer processing. The resulting film-type sensor was highly transparent (~93.5% transmittance at 550 nm) and mechanically stable (capable of resisting 10000 cycles of bending to a 500 µm radius of curvature). We demonstrated that a thin, transparent, and mechanically stable electrode can be produced using a combination of AgNWs and cPI, and used to produce a system sensitive to pressure-induced bending. The capacitance of the AgNW tandem compound electrode pattern grew via fringing, which increased with the pressure-induced bending applied to the surface of the sensor. The sensitivity was four times higher than that of an elastomeric pressure sensor made with the same design. Finally, we demonstrated a skin-like pressure sensor attached to the inside wrist of a human arm. - Highlights: • A thin, transparent pressure sensor was fabricated from AgNWs and cPI. • An AgNW network was patterned with a simple circuit, and then embedded into cPI. • The resulting film-type sensor was highly transparent and mechanically stable. • The sensor sensitivity was 4x higher than that of an elastomeric pressure sensor.

Plasma-induced formation of flower-like Ag2O nanostructures

International Nuclear Information System (INIS)

Yang, Zen-Hung; Ho, Chun-Hsien; Lee, Szetsen

2015-01-01

Graphical abstract: Flower-like Ag 2 O nanostructures. - Highlights: • Flower-like Ag 2 O nanostructures were synthesized from Ag colloids using plasma. • XPS was used to monitor plasma treatment effect on Ag colloids. • SERS of methyl orange was used to monitor the plasma oxidation–reduction processes. • Photocatalytic degradation of methylene blue was performed using Ag 2 O. • Ag 2 O is a more efficient visible light photocatalyst than Ag colloids. - Abstract: Plasma treatment effect on Ag colloids was investigated using X-ray photoelectron spectroscopy (XPS) and surface-enhanced Raman scattering (SERS) techniques. XPS showed that O 2 plasma was critical in removing organic residues in Ag colloids synthesized using citric acid as a reducing agent. With O 2 plasma treatment, Ag colloids were also oxidized to form flower-like Ag 2 O nanostructures. The formation mechanism is proposed. The SERS spectral intensity of methyl orange (MO) adsorbed on Ag surface became deteriorated with O 2 plasma treatment. Followed by H 2 plasma treatment, the SERS intensity of MO on Ag regained, which indicated that Ag 2 O has been reduced to Ag. Nonetheless, the reduction by H 2 plasma could not bring Ag back to the original as-synthesized nanoparticle morphology. The flower-like nanostructure morphology still remained. The photocatalytic degradation reactions of methylene blue (MB) aqueous solutions were carried out using Ag colloids and Ag 2 O nanostructures. The results show that Ag 2 O is more efficient than Ag colloids and many other metal oxides for the photocatalytic degradation of MB in solution when utilizing visible light

Ozone decomposition on Ag/SiO2 and Ag/clinoptilolite catalysts at ambient temperature

International Nuclear Information System (INIS)

Nikolov, Penko; Genov, Krassimir; Konova, Petya; Milenova, Katya; Batakliev, Todor; Georgiev, Vladimir; Kumar, Narendra; Sarker, Dipak K.; Pishev, Dimitar; Rakovsky, Slavcho

2010-01-01

Silver modified zeolite (Bulgarian natural clinoptilolite) and Ag/silica catalysts were synthesized by ion exchange and incipient wet impregnation method respectively and characterized by different techniques. DC arc-AES was used for Ag detection. XRD spectra show that Ag is loaded over the surface of the SiO 2 sample and that after the ion-exchange process the HEU type structure of clinoptilolite is retained. UV-VIS (specific reflection at 310 nm) and IR (band at 695 cm -1 ) spectroscopy analysis proved that silver is loaded as a T-atom into zeolite channels as Ag + , instead of Na + , Ca 2+ , or K + ions, existing in the natural clinoptilolite form. The samples Ag/SiO 2 and Ag-clinoptilolite were tested as catalysts for decomposition of gas phase ozone. Very high catalytic activity (up to 99%) was observed and at the same time the catalysts remained active over time at room temperature.

Salivary sIg-A response against the recombinant Ag38 antigen of Mycobacterium tuberculosis Indonesian strain.

Science.gov (United States)

Raras, Tri Yudani Mardining; Sholeh, Gamal; Lyrawati, Diana

2014-01-01

An evaluation of the humoral response based on secretory immunoglobulin A levels in the saliva of pulmonary tuberculosis (TB) acid-fast bacillus-positive (TB-AFB+) patients against a recombinant 38 kDa antigen (Ag38-rec) is reported. A total of 60 saliva samples consist of 30 TB-AFB+ patients and 30 healthy controls were tested against 500 ng of semi-purified antigen using the dot blot method. Results showed that the protein antigen could differentiate between healthy individuals and TB-AFB(+) patients. Whole saliva demonstrated better reactivity than centrifuged saliva. The Ag38-rec protein indicated statistically comparable sensitivity (80% versus 90%), but lower specificity (36.6% versus 70%) compared with purified protein derivative (PPD). Surprisingly, both antigens similarly recognized secretory immunoglobulin A in the saliva of the healthy group (50% versus 50%, respectively). These findings suggest that the Ag38-rec protein originating from a local strain of Mycobacterium tuberculosis may be used for TB screening, however require purity improvement.

Development of a Rhizoctonia solani AG1-IB Specific Gene Model Enables Comparative Genome Analyses between Phytopathogenic R. solani AG1-IA, AG1-IB, AG3 and AG8 Isolates.

Directory of Open Access Journals (Sweden)

Daniel Wibberg

Full Text Available Rhizoctonia solani, a soil-born plant pathogenic basidiomycetous fungus, affects various economically important agricultural and horticultural crops. The draft genome sequence for the R. solani AG1-IB isolate 7/3/14 as well as a corresponding transcriptome dataset (Expressed Sequence Tags--ESTs were established previously. Development of a specific R. solani AG1-IB gene model based on GMAP transcript mapping within the eukaryotic gene prediction platform AUGUSTUS allowed detection of new genes and provided insights into the gene structure of this fungus. In total, 12,616 genes were recognized in the genome of the AG1-IB isolate. Analysis of predicted genes by means of different bioinformatics tools revealed new genes whose products potentially are involved in degradation of plant cell wall components, melanin formation and synthesis of secondary metabolites. Comparative genome analyses between members of different R. solani anastomosis groups, namely AG1-IA, AG3 and AG8 and the newly annotated R. solani AG1-IB genome were performed within the comparative genomics platform EDGAR. It appeared that only 21 to 28% of all genes encoded in the draft genomes of the different strains were identified as core genes. Based on Average Nucleotide Identity (ANI and Average Amino-acid Identity (AAI analyses, considerable sequence differences between isolates representing different anastomosis groups were identified. However, R. solani isolates form a distinct cluster in relation to other fungi of the phylum Basidiomycota. The isolate representing AG1-IB encodes significant more genes featuring predictable functions in secondary metabolite production compared to other completely sequenced R. solani strains. The newly established R. solani AG1-IB 7/3/14 gene layout now provides a reliable basis for post-genomics studies.

Green Synthesis Methods of CoFe_2O_4 and Ag-CoFe_2O_4 Nanoparticles Using Hibiscus Extracts and Their Antimicrobial Potential

International Nuclear Information System (INIS)

Gingasu, D.; Mindru, I.; Patron, L.; Caleron-Moreno, J.M.; Mocioiu, O.C.; Preda, S.; Stanica, N.; Nita, S.; Dobre, N.; Popa, M.; Gradisteanu, G.; Chifiriuc, M. C.

2016-01-01

The cobalt ferrite (CoFe_2O_4) and silver-cobalt ferrite (Ag-CoFe_2O_4) nanoparticles were obtained through self-combustion and wet ferritization methods using aqueous extracts of Hibiscus rosa-sinensis flower and leaf. X-ray diffraction, scanning electron microscopy, Fourier transform infrared spectroscopy, and magnetic measurements were used for the characterization of the obtained oxide powders. The antimicrobial activity of the cobalt ferrite and silver-cobalt ferrite nanoparticles against Gram-positive and Gram-negative bacteria, as well as fungal strains, was investigated by qualitative and quantitative assays. The most active proved to be the Ag-CoFe_2O_4 nanoparticles, particularly those obtained through self-combustion using hibiscus leaf extract, which exhibited very low minimal inhibitory concentration values (0.031-0.062 mg/ml) against all tested microbial strains, suggesting their potential for the development of novel antimicrobial agents.

Green Synthesis Methods of CoFe2O4 and Ag-CoFe2O4 Nanoparticles Using Hibiscus Extracts and Their Antimicrobial Potential

Directory of Open Access Journals (Sweden)

Dana Gingasu

2016-01-01

Full Text Available The cobalt ferrite (CoFe2O4 and silver-cobalt ferrite (Ag-CoFe2O4 nanoparticles were obtained through self-combustion and wet ferritization methods using aqueous extracts of Hibiscus rosa-sinensis flower and leaf. X-ray diffraction, scanning electron microscopy, Fourier transform infrared spectroscopy, and magnetic measurements were used for the characterization of the obtained oxide powders. The antimicrobial activity of the cobalt ferrite and silver-cobalt ferrite nanoparticles against Gram-positive and Gram-negative bacteria, as well as fungal strains, was investigated by qualitative and quantitative assays. The most active proved to be the Ag-CoFe2O4 nanoparticles, particularly those obtained through self-combustion using hibiscus leaf extract, which exhibited very low minimal inhibitory concentration values (0.031–0.062 mg/mL against all tested microbial strains, suggesting their potential for the development of novel antimicrobial agents.

Preparation of Ag deposited TiO2 (Ag/TiO2) composites and investigation on visible-light photocatalytic degradation activity in magnetic field

Science.gov (United States)

Zhang, L.; Ma, C. H.; Wang, J.; Li, S. G.; Li, Y.

2014-12-01

In this study, Ag deposited TiO2 (Ag/TiO2) composites were prepared by three different methods (Ultraviolet Irradiation Deposition (UID), Vitamin C Reduction (VCR) and Sodium Borohydride Reduction (SBR)) for the visible-light photocatalytic degradation of organic dyes in magnetic field. And then the prepared Ag deposited TiO2 (Ag/TiO2) composites were characterized physically by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The visible-light photocatalytic activities of these three kinds of Ag deposited TiO2 (Ag/TiO2) composites were examined and compared through the degradation of several organic dyes under visible-light irradiation in magnetic field. In addition, some influence factors such as visible-light irradiation time, organic dye concentration, revolution speed, magnetic field intensity and organic dye kind on the visible-light photocatalytic activity of Ag deposited TiO2 (Ag/TiO2) composite were reviewed. The research results showed that the presence of magnetic field significantly enhanced the visible-light photocatalytic activity of Ag deposited TiO2 (Ag/TiO2) composites and then contributed to the degradation of organic dyes.

Photocatalytic oxidation removal of Hg{sup 0} using ternary Ag/AgI-Ag{sub 2}CO{sub 3} hybrids in wet scrubbing process under fluorescent light

Energy Technology Data Exchange (ETDEWEB)

Zhang, Anchao, E-mail: aczhang@qq.com [School of Mechanical and Power Engineering, Henan Polytechnic University, Jiaozuo, 454000 (China); Zhang, Lixiang; Chen, Xiaozhuan; Zhu, Qifeng; Liu, Zhichao [School of Mechanical and Power Engineering, Henan Polytechnic University, Jiaozuo, 454000 (China); Xiang, Jun, E-mail: xiangjun@mail.hust.edu.cn [State Key Laboratory of Coal Combustion, Huazhong University of Science and Technology, Wuhan, 430074 (China)

2017-01-15

Highlights: • Ag/AgI-Ag{sub 2}CO{sub 3} hybrids were employed for Hg{sup 0} removal under fluorescent light. • Superoxide radical (·O{sub 2}{sup −}) played a key role in Hg{sup 0} removal. • NO exhibited a significant effect on Hg{sup 0} removal in comparison to SO{sub 2}. • The mechanism for enhanced Hg{sup 0} removal over Ag/AgI-Ag{sub 2}CO{sub 3} was proposed. - Abstract: A series of ternary Ag/AgI-Ag{sub 2}CO{sub 3} photocatalysts synthesized using a facile coprecipitation method were employed to investigate their performances of Hg{sup 0} removal in a wet scrubbing reactor. The hybrids were characterized by N{sub 2} adsorption-desorption, XRD, SEM-EDS, HRTEM, XPS, DRS and ESR. The photocatalytic activities of Hg{sup 0} removal were evaluated under fluorescent light. The results showed that AgI content, fluorescent light irradiation, reaction temperature all showed significant influences on Hg{sup 0} removal. NO exhibited significant effect on Hg{sup 0} removal in comparison to SO{sub 2}. Among these ternary Ag/AgI-Ag{sub 2}CO{sub 3} hybrids, Ag/AgI(0.1)-Ag{sub 2}CO{sub 3} showed the highest Hg{sup 0} removal efficiency, which could be ascribed to the effective separation of photogenerated electron-hole pairs between AgI and Ag{sub 2}CO{sub 3} and the surface plasmon resonance (SPR) effect in the visible region by metallic silver nanoparticles (Ag{sup 0} NPs). The trapping studies of reactive radicals showed that the superoxide radicals (·O{sub 2}{sup −}) may play a key role in Hg{sup 0} removal under fluorescent light. According to the experimental and characterization results, a possible photocatalytic oxidation mechanism for enhanced Hg{sup 0} removal over Ag/AgI(0.1)-Ag{sub 2}CO{sub 3} hybrid under fluorescent light was proposed.

Efecto bioestimulante de Trichoderma harzianum Rifai en posturas de Leucaena, Cedro y Samán

Directory of Open Access Journals (Sweden)

Leonides Castellanos González

2018-01-01

Full Text Available El presente artículo evaluó el efecto bioestimulante de Trichoderma harzianum Rifai en la producción de postura de Leucaena leucocephala (Lam de Wit., Cedrela odorata L. y Albizia saman (Jacq. Merr. Se desarrollaron tres experimentos en condiciones de vivero, uno para cada especie. Se empleó un diseño completamente aleatorio con cuatro parcelas por tratamiento. En cada experimento los tratamientos fueron: Trichoderma harzianum a razón de 20 g.L-1, 40 g.L-1 y un testigo. Se evaluó el porcentaje de germinación y las variables morfométricas diámetro y altura del tallo, así como biomasa seca en raíz y parte aérea de la planta. Los tratamientos con Trichoderma no incrementaron el porcentaje de germinación en cedro, samán y leucaena. T. harzianum incrementó la altura, el número de hojas y la biomasa seca del área foliar en las plántulas de cedro, mientras que en leucaena y samán solo provocó incrementos del diámetro basal de las plántulas.

The potential application of fungus Trichoderma harzianum Rifai in biodegradation of detergent and industry

Directory of Open Access Journals (Sweden)

Jakovljević Violeta D.

2015-01-01

Full Text Available The potential application of fungus Trichoderma harzianum Rifai in biodegradation of commercial detergent (MERIX, Henkel, Serbia was in the focus of this study. The fungus was isolated from wastewater samples of the Rasina River, downstream where the industrial wastewaters of factory Henkel (Krusevac, Serbia discharge into river. The fungus was cultivated in liquid growth medium by Czapek with addition of detergent at a concentration of 0.3% during 16 days. Analysis of fermentation broth evaluated the chemical and biochemical changes of pH, redox potential, activity of alkaline and acid invertase as well as activity of alkaline protease. In addition, the influence of detergent on fungal growth and total dry weight biomass was determined. At the same time, detergent disappearance in terms of methylene blue active substances in the medium was measured. The detergent at a concentration of 0.3% influenced significant decrease of pH value and increase of redox potential. The detergent showed inhibitory effect on acid invertase activity and stimulatory effect on alkaline invertase and protease activity. The fungus decomposed about 74.24% of tested detergent during 16 days, but total dry weight biomass reduced about 20% in relation to control. [Projekat Ministarstva nauke Republike Srbije, br. III 43004

Transformation from Ag@Ag{sub 3}PO{sub 4} to Ag@Ag{sub 2}SO{sub 4} hybrid at room temperature: preparation and its visible light photocatalytic activity

Energy Technology Data Exchange (ETDEWEB)

Wei, Ting; Gao, Shanmin, E-mail: gaosm@ustc.edu; Wang, Qingyao; Xu, Hui [Ludong University, College of Chemistry and Materials Science (China); Wang, Zeyan; Huang, Baibiao, E-mail: bbhuang@sdu.edu.cn; Dai, Ying [Shandong University, State Key Laboratory of Crystal Materials (China)

2017-02-15

In the present study, Ag/Ag{sub 2}SO{sub 4} hybrid photocatalysts were obtained via a facile redox–precipitation reaction approach by using Ag@Ag{sub 3}PO{sub 4} nanocomposite as the precursor and KMnO{sub 4} as the oxidant. Multiple techniques, such as X-ray diffraction pattern (XRD), transmission electron microscope (TEM), high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), UV–vis diffuse reflectance spectroscopy (DRS) and Brunauer–Emmett–Teller (BET), photocurrent and electrochemical impedance spectroscopy (EIS), were applied to investigate the structures, morphologies, optical, and electronic properties of as-prepared samples. The photocatalytic activities were evaluated by photodegradation of organic rhodamine B (RhB) and methyl orange (MO) under visible light irradiation. It was found that pure Ag{sub 2}SO{sub 4} can partially transform into metallic Ag during the photocatalytic degradation of organic pollutants, but the Ag/Ag{sub 2}SO{sub 4} hybrids can maintain its structure stability and show enhanced visible light photocatalytic activity because of the surface plasma resonance effect of the metallic Ag.

Low-voltage, large-strain soft electrothermal actuators based on laser-reduced graphene oxide/Ag particle composites

Science.gov (United States)

Wang, Qian; Li, Yu-Tao; Zhang, Tian-Yu; Wang, Dan-Yang; Tian, Ye; Yan, Jun-Chao; Tian, He; Yang, Yi; Yang, Fan; Ren, Tian-Ling

2018-03-01

In this paper, low-voltage, large-strain flexible electrothermal actuators (ETAs) based on laser-reduced graphene oxide (LRGO)/Ag particle composites were fabricated in a simple and cost-efficient process. By adding Ag particles to the LRGO, the sheet resistance decreased effectively. Under a driving voltage of 28 V, the actuator obtained a bending angle of 192° within 6 s. Besides, the bending deformation could be precisely controlled by the driving voltage ranging from 10° to 192°. Finally, a gripper composed of two actuators was demonstrated to manipulate a piece of polydimethylsiloxane block. With the advantages of low-voltage, fast-response, and easy-to-manufacture, the graphene based ETAs have a promising application in soft robotics and soft machines.

Structural and electric properties of AgGaTe{sub 2} layers prepared using mixed source of Ag{sub 2}Te and Ga{sub 2}Te{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Uruno, Aya [Department of Electrical Engineering and Bioscience, Waseda University, Tokyo (Japan); Kobayashi, Masakazu [Department of Electrical Engineering and Bioscience, Waseda University, Tokyo (Japan); Kagami Memorial Research Institute for Materials Science and Technology, Waseda University, Tokyo (Japan)

2017-01-15

AgGaTe{sub 2} layers were prepared on Si substrates by a closed space sublimation method using a mixed powder source of Ag{sub 2}Te and Ga{sub 2}Te{sub 3}. Ag{sub 2}Te buffer layer deposition was introduced to eliminate melt-back etching. The effect of the molar ratio of Ag{sub 2}Te and Ga{sub 2}Te{sub 3} in the mixed source on the crystallinity of the AgGaTe{sub 2} layer was investigated. The composition and the phase of the layer was found to change depending on the molar ratio in the deposits, which could be controlled by the source molar ratio along with the Ag{sub 2}Te buffer layer thickness. It was confirmed that (112) oriented uniform AgGaTe{sub 2} layer with an abrupt interface between AgGaTe{sub 2} and Si was formed after those parameters were tuned. The obtained layer exhibited the acceptor concentration of around 2.5 x 10{sup 16} cm{sup -3}. A solar cell was fabricated using the p-AgGaTe{sub 2}/n-Si heterojunction, and exhibited a conversion efficiency of 1.15%. (copyright 2016 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Reducing strength prevailing at root surface of plants promotes reduction of Ag+ and generation of Ag(0/Ag2O nanoparticles exogenously in aqueous phase.

Directory of Open Access Journals (Sweden)

Peddisetty Pardha-Saradhi

Full Text Available Potential of root system of plants from wide range of families to effectively reduce membrane impermeable ferricyanide to ferrocyanide and blue coloured 2,6-dichlorophenol indophenol (DCPIP to colourless DCPIPH2 both under non-sterile and sterile conditions, revealed prevalence of immense reducing strength at root surface. As generation of silver nanoparticles (NPs from Ag+ involves reduction, present investigations were carried to evaluate if reducing strength prevailing at surface of root system can be exploited for reduction of Ag+ and exogenous generation of silver-NPs. Root system of intact plants of 16 species from 11 diverse families of angiosperms turned clear colorless AgNO3 solutions, turbid brown. Absorption spectra of these turbid brown solutions showed silver-NPs specific surface plasmon resonance peak. Transmission electron microscope coupled with energy dispersive X-ray confirmed the presence of distinct NPs in the range of 5-50 nm containing Ag. Selected area electron diffraction and powder X-ray diffraction patterns of the silver NPs showed Bragg reflections, characteristic of crystalline face-centered cubic structure of Ag(0 and cubic structure of Ag2O. Root system of intact plants raised under sterile conditions also generated Ag(0/Ag2O-NPs under strict sterile conditions in a manner similar to that recorded under non-sterile conditions. This revealed the inbuilt potential of root system to generate Ag(0/Ag2O-NPs independent of any microorganism. Roots of intact plants reduced triphenyltetrazolium to triphenylformazon and impermeable ferricyanide to ferrocyanide, suggesting involvement of plasma membrane bound dehydrogenases in reduction of Ag+ and formation of Ag(0/Ag2O-NPs. Root enzyme extract reduced triphenyltetrazolium to triphenylformazon and Ag+ to Ag(0 in presence of NADH, clearly establishing potential of dehydrogenases to reduce Ag+ to Ag(0, which generate Ag(0/Ag2O-NPs. Findings presented in this manuscript put

Chemically deposited In{sub 2}S{sub 3}-Ag{sub 2}S layers to obtain AgInS{sub 2} thin films by thermal annealing

Energy Technology Data Exchange (ETDEWEB)

Lugo, S. [Universidad Autonoma de Nuevo Leon, UANL, Fac. de Ciencias Quimicas, Av. Universidad S/N Ciudad Universitaria San Nicolas de Los Garza Nuevo Leon, C.P. 66451 (Mexico); Pena, Y., E-mail: yolapm@gmail.com [Universidad Autonoma de Nuevo Leon, UANL, Fac. de Ciencias Quimicas, Av. Universidad S/N Ciudad Universitaria San Nicolas de Los Garza Nuevo Leon, C.P. 66451 (Mexico); Calixto-Rodriguez, M. [Centro de Investigacion en Energia-Universidad Nacional Autonoma de Mexico, 62580, Temixco, Morelos (Mexico); Lopez-Mata, C. [Instituto Tecnologico de Chetumal, Av. Insurgentes No. 330, C.P. 77013, Col. David Gustavo Gtz., Chetumal, Quintana Roo (Mexico); Ramon, M.L. [Centro de Investigacion en Energia-Universidad Nacional Autonoma de Mexico, 62580, Temixco, Morelos (Mexico); Gomez, I.; Acosta, A. [Universidad Autonoma de Nuevo Leon, UANL, Fac. de Ciencias Quimicas, Av. Universidad S/N Ciudad Universitaria San Nicolas de Los Garza Nuevo Leon, C.P. 66451 (Mexico)

2012-12-15

Highlights: Black-Right-Pointing-Pointer We obtained polycrystalline silver indium sulfide thin films through the annealing of chemically deposited In{sub 2}S{sub 3}-Ag{sub 2}S films. Black-Right-Pointing-Pointer According to XRD chalcopyrite structure of AgInS{sub 2} was obtained. Black-Right-Pointing-Pointer AgInS{sub 2} thin film has a band gap of 1.86 eV and a conductivity value of 1.2 Multiplication-Sign 10{sup -3} ({Omega} cm){sup -1}. - Abstract: AgInS{sub 2} thin films were obtained by the annealing of chemical bath deposited In{sub 2}S{sub 3}-Ag{sub 2}S layers at 400 Degree-Sign C in N{sub 2} for 1 h. According to the XRD and EDX results the chalcopyrite structure of AgInS{sub 2} has been obtained. These films have an optical band gap, E{sub g}, of 1.86 eV and an electrical conductivity value of 1.2 Multiplication-Sign 10{sup -3} ({Omega} cm){sup -1}.

Synthesis of biocompatible AuAgS/Ag2S nanoclusters and their applications in photocatalysis and mercury detection

International Nuclear Information System (INIS)

Zhao, Qian; Chen, Shenna; Zhang, Lingyang; Huang, Haowen; Liu, Fengping; Liu, Xuanyong

2014-01-01

In this paper, a facile approach for preparation of AuAgS/Ag 2 S nanoclusters was developed. The unique AuAgS/Ag 2 S nanoclusters capped with biomolecules exhibit interesting excellent optical and catalytic properties. The fluorescent AuAgS/Ag 2 S nanoclusters show tunable luminescence depending on the nanocluster size. The apoptosis assay demonstrated that the AuAgS/Ag 2 S nanoclusters showed low cytotoxicity and good biocompatibility. Therefore, the nanoclusters can be used not only as a probe for labeling cells but also for their photocatalytic activity for photodegradation of organic dye. Moreover, a highly selective and sensitive assay for detection of mercury including Hg 2+ and undissociated mercury complexes was developed based on the quenching fluorescent AuAgS/Ag 2 S nanoclusters, which provides a promising approach for determining various forms of Hg in the mercury-based compounds in environment. These unique nanoclusters may have potential applications in biological labeling, sensing mercury, and photodegradation of various organic pollutants in waste water.Graphical Abstract

Medium-range correlation of Ag ions in superionic melts of Ag{sub 2}Se and AgI by reverse Monte Carlo structural modelling-connectivity and void distribution

Energy Technology Data Exchange (ETDEWEB)

Tahara, Shuta; Ohno, Satoru [Faculty of Pharmacy, Niigata University of Pharmacy and Applied Life Sciences, 265-1 Higashijima, Akiha-ku, Niigata 956-8603 (Japan); Ueno, Hiroki; Takeda, Shin' ichi [Department of Physics, Faculty of Sciences, Kyushu University 6-10-1 Hakozaki, Higashi-ku, Fukuoka 812-8581 (Japan); Ohara, Koji; Kohara, Shinji [Research and Utilization Division, Japan Synchrotron Radiation Research Institute (JASRI, SPring-8), 1-1-1 Kouto, Sayo-cho, Sayo-gun, Hyogo 679-5198 (Japan); Kawakita, Yukinobu [J-PARC Center, Japan Atomic Energy Agency, 2-4 Shirakata Shirane, Tokai-mura, Naka-gun, Ibaraki 319-1195 (Japan)

2011-06-15

High-energy x-ray diffraction measurements on molten Ag{sub 2}Se were performed. Partial structure factors and radial distribution functions were deduced by reverse Monte Carlo (RMC) structural modelling on the basis of our new x-ray and earlier published neutron diffraction data. These partial functions were compared with those of molten AgI. Both AgI and Ag{sub 2}Se have a superionic solid phase prior to melting. New RMC structural modelling for molten AgI was performed to revise our previous model with a bond-angle restriction to reduce the number of unphysical Ag triangles. The refined model of molten AgI revealed that isolated unbranched chains formed by Ag ions are the cause of the medium-range order of Ag. In contrast with molten AgI, molten Ag{sub 2}Se has 'cage-like' structures with approximately seven Ag ions surrounding a Se ion. Connectivity analysis revealed that most of the Ag ions in molten Ag{sub 2}Se are located within 2.9 A of each other and only small voids are found, which is in contrast to the wide distribution of Ag-void radii in molten AgI. It is conjectured that the collective motion of Ag ions through small voids is required to realize the well-known fast diffusion of Ag ions in molten Ag{sub 2}Se, which is comparable to that in molten AgI.

Ag-bridged Ag{sub 2}O nanowire network/TiO{sub 2} nanotube array p–n heterojunction as a highly efficient and stable visible light photocatalyst

Energy Technology Data Exchange (ETDEWEB)

Liu, Chengbin, E-mail: chem_cbliu@hnu.edu.cn [Key Laboratory of Jiangxi Province for Persistent Pollutants Control and Resources Recycle, Nanchang Hangkong University, Nanchang 330063 (China); State Key Laboratory of Chemo/Biosensing and Chemometrics, Hunan University, Changsha 410082 (China); Cao, Chenghao [State Key Laboratory of Chemo/Biosensing and Chemometrics, Hunan University, Changsha 410082 (China); Luo, Xubiao [Key Laboratory of Jiangxi Province for Persistent Pollutants Control and Resources Recycle, Nanchang Hangkong University, Nanchang 330063 (China); Luo, Shenglian [Key Laboratory of Jiangxi Province for Persistent Pollutants Control and Resources Recycle, Nanchang Hangkong University, Nanchang 330063 (China); State Key Laboratory of Chemo/Biosensing and Chemometrics, Hunan University, Changsha 410082 (China)

2015-03-21

Graphical abstract: A unique Ag-bridged Ag{sub 2}O nanowire network/TiO{sub 2} nanotube array p–n heterojunction was fabricated by simple electrochemical method. The heterostructures exhibit high photocatalytic activity and excellent recycling performance. - Highlights: • Ag-bridged Ag{sub 2}O nanowire network self-stability structure. • Ag{sub 2}O nanowire network/TiO{sub 2} nanotube p–n heterojunction. • High visible light photocatalytic activity. • Highly stable recycling performance. - Abstract: A unique Ag-bridged Ag{sub 2}O nanowire network/TiO{sub 2} nanotube array p–n heterojunction (Ag–Ag{sub 2}O/TiO{sub 2} NT) was fabricated by simple electrochemical method. Ag nanoparticles were firstly electrochemically deposited onto the surface of TiO{sub 2} NT and then were partly oxidized to Ag{sub 2}O nanowires while the rest of Ag mother nanoparticles were located at the junctions of Ag{sub 2}O nanowire network. The Ag–Ag{sub 2}O/TiO{sub 2} NT heterostructure exhibited strong visible-light response, effective separation of photogenerated carriers, and high adsorption capacity. The integration of Ag–Ag{sub 2}O self-stability structure and p–n heterojunction permitted high and stable photocatalytic activity of Ag–Ag{sub 2}O/TiO{sub 2} NT heterostructure photocatalyst. Under 140-min visible light irradiation, the photocatalytic removal efficiency of both dye acid orange 7 (AO7) and industrial chemical p-nitrophenol (PNP) over Ag–Ag{sub 2}O/TiO{sub 2} NT reached nearly 100% much higher than 17% for AO7 or 13% for PNP over bare TiO{sub 2} NT. After 5 successive cycles under 600-min simulated solar light irradiation, Ag–Ag{sub 2}O/TiO{sub 2} NT remained highly stable photocatalytic activity.

Photoinduced formation of Ag nanoparticles on the surface of As2S3/Ag thin bilayer

International Nuclear Information System (INIS)

Binu, S; Khan, Pritam; Barik, A R; Sharma, Rituraj; Adarsh, K V; Golovchak, R; Jain, H

2014-01-01

In this article, we demonstrate the combined effect of photodoping and photoinduced-surface deposition in a bilayer of chalcogenide glass (ChG) and Ag as an alternative method to optically synthesize Ag nanoparticles (AgNP) on the surface of ChG. In our experiment, AgNP formation occurs through two distinct stages: In the first stage, Ag is transported through the As 2 S 3 layer as Ag + ions, and in the second stage Ag + ions are photo-deposited as AgNP. The ex situ x-ray photoelectron spectroscopy measurements and AFM observations show photoinduced Ag mass transport and the formation of AgNP. (paper)

Strain reduced critical current in Bi-2223/Ag superconductors under axial tension and compression

International Nuclear Information System (INIS)

Haken, B. ten; Godeke, A.; Kate, H.H.J. ten

1997-01-01

The critical current of Ag sheathed Bi(Pb)SrCaCuO-2223 tape conductors is investigated as a function of various strain components. A reduction of the critical current occurs due to both tensile or a compressive strain. The critical current reduction is qualitatively similar with the results as observed in Bi-2212 conductors. An axial compression leads to an immediate critical current reduction. The critical current in an axially elongated sample remains nearly constant up to a certain limit typically close to 0.3% strain. For a larger elongation the critical current reduces rapidly. A transverse pressure acting on the tape surface leads also to an irreversible critical current reduction. This behavior is compared with the influence of an axial compression with an effective Young's modulus. The deformation induced critical current reductions in Bi-2223 conductors can be described by a model that is already proposed for Bi-2212 conductors. This model is based on the irreversible nature of the critical current reduction due to a certain deformation

Ozone decomposition on Ag/SiO{sub 2} and Ag/clinoptilolite catalysts at ambient temperature

Energy Technology Data Exchange (ETDEWEB)

Nikolov, Penko, E-mail: penmail@mail.bg [Institute of Catalysis, Bulgarian Academy of Sciences, 1113 Sofia (Bulgaria); Genov, Krassimir; Konova, Petya [Institute of General and Inorganic Chemistry, Bulgarian Academy of Sciences, 1113 Sofia (Bulgaria); Milenova, Katya; Batakliev, Todor; Georgiev, Vladimir [Institute of Catalysis, Bulgarian Academy of Sciences, 1113 Sofia (Bulgaria); Kumar, Narendra [Laboratory of Industrial Chemistry, Process Chemistry Centre, Abo Akademi University, Biskopsgatan 8, 20500 Abo/Turku (Finland); Sarker, Dipak K. [School of Pharmacy and Biomolecular Sciences, University of Brighton, Lewes Road, Brighton BN2 4GJ (United Kingdom); Pishev, Dimitar [University of Chemical Technology and Metallurgy, 1756 Sofia (Bulgaria); Rakovsky, Slavcho [Institute of Catalysis, Bulgarian Academy of Sciences, 1113 Sofia (Bulgaria)

2010-12-15

Silver modified zeolite (Bulgarian natural clinoptilolite) and Ag/silica catalysts were synthesized by ion exchange and incipient wet impregnation method respectively and characterized by different techniques. DC arc-AES was used for Ag detection. XRD spectra show that Ag is loaded over the surface of the SiO{sub 2} sample and that after the ion-exchange process the HEU type structure of clinoptilolite is retained. UV-VIS (specific reflection at 310 nm) and IR (band at 695 cm{sup -1}) spectroscopy analysis proved that silver is loaded as a T-atom into zeolite channels as Ag{sup +}, instead of Na{sup +}, Ca{sup 2+}, or K{sup +} ions, existing in the natural clinoptilolite form. The samples Ag/SiO{sub 2} and Ag-clinoptilolite were tested as catalysts for decomposition of gas phase ozone. Very high catalytic activity (up to 99%) was observed and at the same time the catalysts remained active over time at room temperature.

Plasma-induced formation of flower-like Ag{sub 2}O nanostructures

Energy Technology Data Exchange (ETDEWEB)

Yang, Zen-Hung; Ho, Chun-Hsien; Lee, Szetsen, E-mail: slee@cycu.edu.tw

2015-09-15

Graphical abstract: Flower-like Ag{sub 2}O nanostructures. - Highlights: • Flower-like Ag{sub 2}O nanostructures were synthesized from Ag colloids using plasma. • XPS was used to monitor plasma treatment effect on Ag colloids. • SERS of methyl orange was used to monitor the plasma oxidation–reduction processes. • Photocatalytic degradation of methylene blue was performed using Ag{sub 2}O. • Ag{sub 2}O is a more efficient visible light photocatalyst than Ag colloids. - Abstract: Plasma treatment effect on Ag colloids was investigated using X-ray photoelectron spectroscopy (XPS) and surface-enhanced Raman scattering (SERS) techniques. XPS showed that O{sub 2} plasma was critical in removing organic residues in Ag colloids synthesized using citric acid as a reducing agent. With O{sub 2} plasma treatment, Ag colloids were also oxidized to form flower-like Ag{sub 2}O nanostructures. The formation mechanism is proposed. The SERS spectral intensity of methyl orange (MO) adsorbed on Ag surface became deteriorated with O{sub 2} plasma treatment. Followed by H{sub 2} plasma treatment, the SERS intensity of MO on Ag regained, which indicated that Ag{sub 2}O has been reduced to Ag. Nonetheless, the reduction by H{sub 2} plasma could not bring Ag back to the original as-synthesized nanoparticle morphology. The flower-like nanostructure morphology still remained. The photocatalytic degradation reactions of methylene blue (MB) aqueous solutions were carried out using Ag colloids and Ag{sub 2}O nanostructures. The results show that Ag{sub 2}O is more efficient than Ag colloids and many other metal oxides for the photocatalytic degradation of MB in solution when utilizing visible light.

Progress report on the analytical determination of Ag2+

International Nuclear Information System (INIS)

Van Alsenoy, V.

1997-01-01

The strong oxidising properties of Ag 2+ have been used in the chemical and nuclear industry to destroy organic waste. We aim to apply the process on radioactive graphite, organic resins and effluents. The reaction mechanisms have been studied, taking into account the thermodynamic and kinetic properties of the different reactions involved. For the experimental analysis of these reactions, the accurate analytical determination of all species involved, including Ag 2+ , is needed. The results of a systematic study of the volumetric quantification of Ag 2+ using Tl + and BrO 3 - , and of the spectrophotometric and polarographic quantification of Ag + and Ag 2+ are described. The influence of the nitric acid during the quantification of Tl + by titration with KBrO 3 is investigated and the optimal analytical conditions for our purposes were determined. The best analytical results were obtained when the titration was carried out with maximum 3 M HNO 3 and 0.5 M NaCl. When those conditions are used, the determination is accurate and reproducible. The prepared Ag 2+ solutions were analysed for Ag + using polarography with a platinum electrode. The benefits and the limitation of the polarographic measurement of Ag + using a platinum electrode are described. An indirect measurement was performed by the determination of Ce 4+ after reaction with Ce 3+ . The produced Ce 4+ was measured by direct spectrophotometry. In the future, the quantification of Ag 2+ by measuring the Ce 4+ concentration produced by the reaction with Ce 3+ , will also be verified using potentiometric titration with Fe 2+ . Ag 2+ can also be determined by the direct spectrophotometry. There is a region in which the absorbance of Ag 2+ changes linearly with the concentration. Further evaluation of the titrimetric, spectrophotometric and polarographic methods will continue, until two methods give comparable Ag 2+ concentrations, beginning with the potentiometric titration of Ce 4+ with Fe 2+

Nano Ag@AgBr surface-sensitized Bi{sub 2}WO{sub 6} photocatalyst: oil-in-water synthesis and enhanced photocatalytic degradation

Energy Technology Data Exchange (ETDEWEB)

Lin, Shuanglong; Liu, Li; Hu, Jinshan; Liang, Yinghua, E-mail: liangyh@heuu.edu.cn; Cui, Wenquan, E-mail: wkcui@163.com

2015-01-01

Graphical abstract: - Highlights: • The plasmatic Ag@AgBr surface-sensitized Bi{sub 2}WO{sub 6} composite photocatalysts. • Ag@AgBr greatly increased visible-light absorption for Bi{sub 2}WO{sub 6}. • The plasmonic photocatalysts exhibited enhanced activity for the degradation of MB, phenol and salicylic acid. - Abstract: Nano Ag@AgBr decorated on the surface of flower-like Bi{sub 2}WO{sub 6} (hereafter designated Ag@AgBr/Bi{sub 2}WO{sub 6}) were prepared via a facile oil-in-water self-assembly method. The photocatalysts were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV–vis diffuse reflectance spectroscopy (DRS), etc. The characterization results indicated that nano Ag@AgBr was observed to be evenly dispersed on the surface of Bi{sub 2}WO{sub 6}, and was approximately 20 nm in size. Ag@AgBr/Bi{sub 2}WO{sub 6} composites exhibited excellent UV–vis absorption, due to quantum dimension effect of Ag@AgBr, the surface plasmonic resonance (SPR) of Ag nanoparticles and the special flower-like structure of Bi{sub 2}WO{sub 6}. The photoelectrochemical measurement verified that the suitable band potential of Ag@AgBr and Bi{sub 2}WO{sub 6} and the existence of metal Ag resulted in the high efficiency in charge separation of the composite. The photocatalytic activities of the Ag@AgBr/Bi{sub 2}WO{sub 6} samples were examined under visible-light irradiation for the degradation of methylene blue (MB). The composite presented excellent photocatalytic activity due to the synergetic effect of Bi{sub 2}WO{sub 6}, AgBr, and Ag nanoparticles. The Ag@AgBr(20 wt.%)/Bi{sub 2}WO{sub 6} sample exhibited the best photocatalytic activity, degrading 95.03% MB after irradiation for 2 h, which was respectively 1.29 times and 1.28 times higher than that of Ag@AgBr and Bi{sub 2}WO{sub 6} photocatalyst. Meanwhile, phenol and salicylic acid were degraded to further prove the degradation ability of Ag@AgBr/Bi{sub 2

Preparation, characterization and photocatalytic activity of visible-light-driven plasmonic Ag/AgBr/ZnFe2O4 nanocomposites

International Nuclear Information System (INIS)

Li, Xiaojuan; Tang, Duanlian; Tang, Fan; Zhu, Yunyan; He, Changfa; Liu, Minghua; Lin, Chunxiang; Liu, Yifan

2014-01-01

Highlights: • A plasmonic Ag/AgBr/ZnFe 2 O 4 photocatalyst has been successfully synthesized. • Ag/AgBr/ZnFe 2 O 4 nanocomposites exhibit high visible light photocatalytic activity. • Ag/AgBr/ZnFe 2 O 4 photocatalyst is stable and magnetically separable. - Abstract: A visible-light-driven plasmonic Ag/AgBr/ZnFe 2 O 4 nanocomposite has been successfully synthesized via a deposition–precipitation and photoreduction through a novel one-pot process. X-ray diffraction spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy, transmission electron microscopy and UV–vis diffuse reflectance spectroscopy were employed to investigate the crystal structure, chemical composition, morphology, and optical properties of the as-prepared nanocomposites. The photocatalytic activities of the nanocomposites were evaluated by photodegradation of Rhodamine B (RhB) and phenol under visible light. The results demonstrated that the obtained Ag/AgBr/ZnFe 2 O 4 nanocomposites exhibited higher photocatalytic activity as compared to pure ZnFe 2 O 4 . In addition, the sample photoreduced for 20 min and calcined at 500 °C achieved the highest photocatalytic activity. Furthermore, the Ag/AgBr/ZnFe 2 O 4 nanocomposite has high stability under visible light irradiation and could be conveniently separated by using an external magnetic field

Vancomycin-functionalised Ag-TiO{sub 2} phototoxicity for bacteria

Energy Technology Data Exchange (ETDEWEB)

Wan Yi [Chinese Academy of Sciences, Key Lab of Corrosion Science, Shandong Province, Institute of Oceanology, 7 Nanhai Road, Qingdao 266071 (China); Zhang Dun, E-mail: zhangdun@ms.qdio.ac.cn [Chinese Academy of Sciences, Key Lab of Corrosion Science, Shandong Province, Institute of Oceanology, 7 Nanhai Road, Qingdao 266071 (China); Wang Yi; Qi Peng; Wu Jiajia; Hou Baorong [Chinese Academy of Sciences, Key Lab of Corrosion Science, Shandong Province, Institute of Oceanology, 7 Nanhai Road, Qingdao 266071 (China)

2011-02-15

Research highlights: {yields} A multivalent interaction between Van-Ag-TiO{sub 2} and SRB. {yields} Van-Ag-TiO{sub 2} allow for selective photokilling of pathogen. {yields} Van-Ag-TiO{sub 2} show certain bactericidal property in dark. - Abstract: This study reports on the synthesis of vancomycin (Van)-functionalised Ag-TiO{sub 2} nanoparticles and their enhanced bactericidal activities. Van-Ag-TiO{sub 2} nanoparticles were prepared by nanoparticle deposition and chemical cross-linking reactions. The catalysts showed high efficiency for the degradation of methylene blue under ultraviolet (UV) illumination. The photocatalytic inactivation of the sulphate-reducing bacteria, Desulfotomaculum, was also studied under UV light irradiation and in the dark using aqueous mixtures of Ag, Ag-SiO{sub 2}, Ag-TiO{sub 2}, and Van-Ag-TiO{sub 2}. The Van-Ag-TiO{sub 2} nanoparticles showed a capacity to target Van-sensitive bacteria. They also effectively prevented bacterial cell growth through the functionalised nanoparticles under UV irradiation for 1 h. To investigate the specificity of the catalyst phototoxicity, a Van-resistant bacteria, Vibrio anguillarum, was used as the negative control. The results indicated that Van-Ag-TiO{sub 2} nanoparticles had a higher selective phototoxicity for Van-sensitive bacteria. Therefore, the antibiotic molecule-functionalised core-shell nanoparticles allow for selective photokilling of pathogenic bacteria.

Fabrication of AgX-loaded Ag2CO3 (X = Cl, I) composites and their efficient visible-light-driven photocatalytic activity

International Nuclear Information System (INIS)

Xu, Hui; Zhu, Jiaxiang; Song, Yongxiu; Zhu, Tingting; Zhao, Wenkai; Song, Yanhua; Da, Zulin; Liu, Chengbao; Li, Huaming

2015-01-01

Highlights: • The novel AgX/Ag 2 CO 3 composites have been synthesized by ion exchange reaction. • AgX/Ag 2 CO 3 exhibit higher photoactivity and stability than that of Ag 2 CO 3 . • The band structure of AgX/Ag 2 CO 3 is beneficial to improve the photoactivity. - Abstract: The novel visible-light-driven AgX/Ag 2 CO 3 (X = Cl, I) hybrid materials were synthesized by ion exchange reaction. The physical and chemical properties of the catalysts were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM), energy dispersive spectrometer (EDS), transmission electron microscopy (TEM), diffuse-reflection spectra (DRS) and photocurrent techniques. The as-prepared AgX/Ag 2 CO 3 (X = Cl, I) composites showed higher photocatalytic activity than that of the pure Ag 2 CO 3 photocatalyst under visible light irradiation (λ ⩾ 400 nm) in the process of methylene blue (MB) degradation. The optimal mass percentage of AgCl and AgI in the AgX/Ag 2 CO 3 (X = Cl, I) composite was 20.54 wt% and 40 wt%, respectively. The enhancement of photocatalytic activity was attributed to the suitable band potential between AgX and Ag 2 CO 3 , which was beneficial to increase the separation efficiency of electrons and holes. Besides, the photocatalytic mechanism of AgX/Ag 2 CO 3 (X = Cl, I) composites was also proposed

Strain effects in oxide superconductors

International Nuclear Information System (INIS)

Wada, H.; Kuroda, T.; Sekine, H.; Yuyama, M.; Itoh, K.

1991-01-01

Strain sensitivities of superconducting properties are critical to high magnetic field applications of superconductors, since critical temperature, T c , upper critical field, H c2 , and critical current (density), I c (J c ), are all degraded under strains. Oxide superconductors so far known are all very fragile, thus requiring to be fabricated in the form of composite. In the case of practical metallic superconductors, such as Nb 3 Sn and V 3 Ga, the so-called bronze method has been developed where these superconducting intermetallics are enveloped in a ductile metallic sheath. Recently, a fabrication method similar to the bronze method has been developed for the Bi 2 Sr 2 Ca 2 Cu 3 O x superconductors using Ag tubes as sheath. In the present study mono- and multicore BiPbSrCaCuO tape conductors were prepared by means of this Ag-sheath composite method, and examined in terms of strain sensitivity by measuring their T c and I c (J c ) under bending or tensile strains. (orig.)

Electrochemical depositions of fluorohydroxyapatite doped by Cu2+, Zn2+, Ag+ on stainless steel substrates

International Nuclear Information System (INIS)

Bir, F.; Khireddine, H.; Touati, A.; Sidane, D.; Yala, S.; Oudadesse, H.

2012-01-01

Fluoridated hydroxyapatite (FHA, Ca 10 (PO 4 ) 6 (OH) 2-x F x where 0 2+ , Cu 2+ , Ag + ) substituted fluoridated hydroxyapatite coatings (M-FHA) were deposited on the surface of medical grade 316L stainless steel samples by electrochemical deposition technique. The FHA coatings were co-substituted with antibacterial ions (Zn 2+ , Cu 2+ or Ag + ) by co-precipitation and ion-exchange methods. Characterization studies of coatings from X-ray diffraction (XRD), Scanning electron microscopy (SEM) and Energy dispersive X-ray spectroscopy (EDX) showed that the obtained layers are monophase crystals FHA and did not contain any discernible crystalline impurity. The particles of all samples are of nano size that gives thin layers. The surface morphology, microstructure and Ca/P atomic ratio of the FHA coatings can be regulated by varying electrolyte temperature. This later affects the porosity of the coating surface and the chemical compositions of the deposits. Quantitative elemental analysis indicates that the copper, zinc and silver ions are incorporated into the Fluorohydroxyapatite. The antimicrobial effects of doped fluorohydroxyapatite coatings against pathogen bacterial strains Staphylococcus aureus were tested in liquid media. The results are promising and demonstrated that all doped FHA samples exhibit excellent antimicrobial activity “in vitro” against the microorganism, so the antimicrobial properties of the coatings developed are improved.

Structure and decomposition of the silver formate Ag(HCO2)

International Nuclear Information System (INIS)

Puzan, Anna N.; Baumer, Vyacheslav N.; Mateychenko, Pavel V.

2017-01-01

Crystal structure of the silver formate Ag(HCO 2 ) has been determined (orthorhombic, sp.gr. Pccn, a=7.1199(5), b=10.3737(4), c=6.4701(3)Å, V=477.88(4) Å 3 , Z=8). The structure contains isolated formate ions and the pairs Ag 2 2+ which form the layers in (001) planes (the shortest Ag–Ag distances is 2.919 in the pair and 3.421 and 3.716 Å between the nearest Ag atoms of adjacent pairs). Silver formate is unstable compound which decompose spontaneously vs time. Decomposition was studied using Rietveld analysis of the powder diffraction patterns. It was concluded that the diffusion of Ag atoms leads to the formation of plate-like metal particles as nuclei in the (100) planes which settle parallel to (001) planes of the silver formate matrix. - Highlights: • Silver formate Ag(HCO 2 ) was synthesized and characterized. • Layered packing of Ag-Ag pairs in the structure was found. • Decomposition of Ag(HCO 2 ) and formation of metal phase were studied. • Rietveld-refined micro-structural characteristics during decomposition reveal the space relationship between the matrix structure and forming Ag phase REPLACE with: Space relationship between the matrix structure and forming Ag phase.

Crystal Structure of AgBi2I7 Thin Films.

Science.gov (United States)

Xiao, Zewen; Meng, Weiwei; Mitzi, David B; Yan, Yanfa

2016-10-06

Synthesis of cubic-phase AgBi 2 I 7 iodobismuthate thin films and fabrication of air-stable Pb-free solar cells using the AgBi 2 I 7 absorber have recently been reported. On the basis of X-ray diffraction (XRD) analysis and nominal composition, it was suggested that the synthesized films have a cubic ThZr 2 H 7 crystal structure with AgBi 2 I 7 stoichiometry. Through careful examination of the proposed structure and computational evaluation of the phase stability and bandgap, we find that the reported "AgBi 2 I 7 " films cannot be forming with the ThZr 2 H 7 -type structure, but rather more likely adopt an Ag-deficient AgBiI 4 type. Both the experimental X-ray diffraction pattern and bandgap can be better explained by the AgBiI 4 structure. Additionally, the proposed AgBiI 4 structure, with octahedral bismuth coordination, removes unphysically short Bi-I bonding within the [BiI 8 ] hexahedra of the ThZr 2 I 7 model. Our results provide critical insights for assessing the photovoltaic properties of AgBi 2 I 7 iodobismuthate materials.

Synthesis of β-AgVO3 nanowires decorated with Ag2CrO4, with improved visible light photocatalytic performance

Science.gov (United States)

Ouyang, Qi; Li, Zhonghua; Liu, Jiawen

2018-05-01

Silver chromate‑silver vanadate (Ag2CrO4/β-AgVO3) heterojunction composites are synthesized through a facile precipitation process. The Ag2CrO4/β-AgVO3 hybrids obtained exhibit better photocatalytic activity in degradation of RhB than both pure Ag2CrO4 and β-AgVO3 under visible light irradiation. The 20 wt% Ag2CrO4/β-AgVO3 heterojunction possesses the best photocatalytic ability for degrading RhB: 24.4 times that of pristine β-AgVO3 nanowires and 3.2 times that of individual Ag2CrO4 particles. The phase of the nanocomposites was analyzed using x-ray diffraction as well as x-ray photoelectron spectroscopy. Their morphology was observed via scanning electron microscopy and transmission electron microscopy. The improvement in photocatalytic performance is chiefly ascribed to the synergies between Ag2CrO4/β-AgVO3 heterostructure, which can enhance the light absorbance ability and also accelerate the separation and transfer of photoinduced electrons and holes under visible light irradiation; this is also confirmed by UV–vis diffuse reflection spectrometry and fluorescence emission spectra.

Characterization and Comparison of Photocatalytic Activity Silver Ion doped on TiO2(TiO2/Ag+) and Silver Ion doped on Black TiO2(Black TiO2/Ag+)

Science.gov (United States)

Kim, Jin Yi; Sim, Ho Hyung; Song, Sinae; Noh, Yeoung Ah; Lee, Hong Woon; Taik Kim, Hee

2018-03-01

Titanium dioxide (TiO2) is one of the representative ceramic materials containing photocatalyst, optic and antibacterial activity. The hydroxyl radical in TiO2 applies to the intensive oxidizing agent, hence TiO2 is suitable to use photocatalytic materials. Black TiO2was prepared through reduction of amorphous TiO2 conducting under H2 which leads to color changes. Its black color is proven that absorbs 100% light across the whole-visible light, drawing enhancement of photocatalytic property. In this study, we aimed to compare the photocatalytic activity of silver ion doped on TiO2(TiO2/Ag+) and silver ion doped on black TiO2(black TiO2/Ag+) under visible light range. TiO2/Ag+ was fabricated following steps. 1) TiO2 was synthesized by a sol-gel method from Titanium tetraisopropoxide (TTIP). 2) Then AgNO3 was added during an aging process step for silver ion doping on the surface of TiO2. Moreover, Black TiO2/Ag+ was obtained same as TiO2/Ag+ except for calcination under H2. The samples were characterized X-ray diffraction (XRD), UV-visible reflectance (UV-vis DRS), and Methylene Blue degradation test. XRD analysis confirmed morphology of TiO2. The band gap of black TiO2/Ag+ was confirmed (2.6 eV) through UV-vis DRS, which was lower than TiO2/Ag+ (2.9 eV). The photocatalytic effect was conducted by methylene blue degradation test. It demonstrated that black TiO2/Ag+ had a photocatalytic effect under UV light also visible light.

Structural and optical properties of AgCl-sensitized TiO2 (TiO2 @AgCl prepared by a reflux technique under alkaline condition

Directory of Open Access Journals (Sweden)

V. A. Mu’izayanti

Full Text Available Abstract The AgCl-sensitized TiO2 (TiO2@AgCl has been prepared from the precursor of TiO2-rutile type which on its surface adsorb chloride anion (Cl- and various amounts of silver using AgNO3 as starting material: AgNO3/(AgNO3+TiO2 mass ratio of 0.00, 1.14, 3.25, 6.38 and 10.32%. Reflux under alkaline condition was the employed technique. All samples were characterized by X-ray diffraction (XRD and diffuse reflectance UV-vis spectroscopy. The sample without the addition of AgNO3 was analyzed by scanning electron microscope and surface area analyzer. The morphology of the sample showed a distribution of microspheres of approximately 0.5 to 1.0 µm and the specific surface area was 68 m2/g. XRD patterns indicated that the sample without the addition of AgNO3 contained two types of TiO2: rutile (major and anatase (minor, whereas the samples with the addition of AgNO3 consisted of one phase of AgCl and two types of TiO2: rutile and anatase. The bandgaps of the samples were in the range of 2.97 to 3.24 eV, which were very close to the bandgap of intrinsic TiO2 powder. The presence of 0.8, 2.6 and 4.4 wt% of AgCl in each sample resulted in an additional bandgap in visible light region of 1.90, 1.94 and 2.26 eV, respectively, whereas the presence of 9.4 wt% of AgCl in the sample resulted in two bandgaps in visible light region of 1.98 and 1.88 eV.

Hydrothermal Synthesis and Mechanism of Unusual Zigzag Ag2Te and Ag2Te/C Core-Shell Nanostructures

Directory of Open Access Journals (Sweden)

Saima Manzoor

2014-01-01

Full Text Available A single step surfactant-assisted hydrothermal route has been developed for the synthesis of zigzag silver telluride nanowires with diameter of 50–60 nm and length of several tens of micrometers. Silver nitrate (AgNO3 and sodium tellurite (Na2TeO3, are the precursors and polyvinylpyrrolidone (PVP is used as surfactant in the presence of the reducing agent, that is, hydrazine hydrate (N2H4·H2O. In addition to the zigzag nanowires a facile hydrothermal reduction-carbonization route is proposed for the preparation of uniform core-shell Ag2Te/C nanowires. In case of Ag2Te/C synthesis process the same precursors are employed for Ag and Te along with the ethylene glycol used as reducing agent and glucose as the carbonizing agent. Morphological and compositional properties of the prepared products are analyzed with the help of scanning electron microscopy, transmission electron microscopy, and energy dispersive X-ray spectroscopy, respectively. The detailed formation mechanism of the zigzag morphology and reduction-carbonization growth mechanism for core-shell nanowires are illustrated on the bases of experimental results.

Understanding the Composition Dependence of the Fragility of AgI-Ag2O-MxOy Glassy Systems

International Nuclear Information System (INIS)

Aniya, M

2011-01-01

It has been reported that the fragility in the AgI-Ag 2 O-M x O y (M = B, Ge, P, Mo) system is determined by Ag 2 O-M x O y and does not depend on the amount of AgI. This is an interesting result and provides a hint to understand the nature of the glassy state of these materials. However, the origin of such behavior has not been sufficiently discussed. In the present report a model for the above behavior is presented. According to the model, the behavior arises from the solid like nature of the network formed by Ag 2 O-M x O y and the liquid like AgI which flow between the networks. The model is consistent with the structural model of superionic glasses proposed previously.

细粒棘球绦虫AgB8/1-AgB8/2重组嵌合抗原表达系统的构建%Establishment of Echinococcus granulosus AgB8/1-AgB8/2 chimeric recombinant protein expression system

Institute of Scientific and Technical Information of China (English)

古力帕丽·麦曼提依明; 马海梅; 吾拉木·马木提; 陈洁; 陈璐; 丁剑冰; 马秀敏; 温浩

2011-01-01

目的 构建pET32a-AgB8/1-AgB8/2原核表达载体,并对其重组蛋白进行原核细胞表达.方法 从细粒棘球绦虫原头蚴中提取总RNA,反转录生成cDNA,以此cDNA为模板,用基因特异性引物分别扩增EgAgB8/1和EgAgB8/2基因编码其分泌型多肽的片段,经测序后,以此两条基因片段为依据,人工合成EgAgB8/1-EgAgB8/2嵌合抗原编码核酸序列,将其克隆至pUCm-T载体,测序鉴定其正确性.通过对pUCm-T/AgB8/1-AgB8/2重组质粒进行双酶切,将获得的AgB8/1-AgB8/2嵌合抗原编码核酸序列用定向克隆技术克隆至原核表达质粒pET32a上,测序鉴定插入片段正确后,转化至E.coli BL21(DE3)Lys S,IPTG初步诱导表达pET32a-AgB8/1-AgB8/2重组嵌合蛋白.用SDS-PAGE电泳分析鉴定重组蛋白的表达水平.结果 测序表明,AgB8/1-AgB8/2嵌合抗原编码核酸序列正方向插入至pET32a质粒.SDS-PAGE电泳分析显示,IPTG诱导后重组嵌合蛋白得到成功表达,在相对分子量约38 kD处有表达条带.结论 成功构建了pET32a-AgB8/1-AgB8/2原核表达质粒,并初步诱导表达出AgB8/1-AgB8/2嵌合重组蛋白,为进一步研究其免疫学特性奠定了基础.%In order to construct the pET32a-AgB8/1-AgB8/2 chimeric antigen prokaryotic expression recombinant plasmid and the expression of its recombinant protein, the total RNA was extracted from protoscoleces of Echinococcus granulosus,and reverse transcribed into cDNA, the cDNA encoding mature form of EgAgB8/land EgAgB8/2 antigen were amplified by PCR using gene specific primers.Based on the both gene fragments, a nucleotide sequence encoding EgAgB8/1-EgAgB8/2 chimeric antigen were artificially synthesized after sequence confirmation.The synthesized nucleotide sequence encoding EgAgB8/1-EgAgB8/2 chimeric antigen were conformed by sequencing after cloning into pUCm-T vector, then the target sequence was directionally ligated into pET32a plasmid after double digestion with restriction enzymes for prokaryotic

Optical properties of Ag nanoclusters formed by irradiation and annealing of SiO{sub 2}/SiO{sub 2}:Ag thin films

Energy Technology Data Exchange (ETDEWEB)

Güner, S., E-mail: sguner@fatih.edu.tr [Department of Physics, Fatih University, 34500 Büyükçekmece, İstanbul (Turkey); Budak, S. [Department of Electrical Engineering and Computer Science, Alabama A and M University, Huntsville, AL 35810 (United States); Gibson, B. [Department of Physics, UAH, Huntsville, AL 35899 (United States); Ila, D. [Department of Chemistry and Physics, Fayetteville St. University, Fayetteville, NC 28301 (United States)

2014-08-15

Highlights: • Fabrication of films through the Reactive Electron Beam deposition technique. • Perfect and reproducible Ag nanoclustered host matrix. • Potential technological applicability in thermoelectric devices. - Abstract: We have deposited five periodic SiO{sub 2}/SiO{sub 2} + Ag multi-nano-layered films on fused silica substrates using physical vapor deposition technique. The co-deposited SiO{sub 2}:Ag layers were 2.7–5 nm and SiO{sub 2} buffer layers were 1–15 nm thick. Total thickness was between 30 and 105 nm. Different concentrations of Ag, ranging from 1.5 to 50 molecular% with respect to SiO{sub 2} were deposited to determine relevant rates of nanocluster formation and occurrence of interaction between nanoclusters. Using interferometry as well as in situ thickness monitoring, we measured the thickness of the layers. The concentration of Ag in SiO{sub 2} was measured with Rutherford Backscattering Spectrometry (RBS). To nucleate Ag nanoclusters, 5 MeV cross plane Si ion bombardments were performed with fluence varying between 5 × 10{sup 14} and 1 × 10{sup 16} ions/cm{sup 2} values. Optical absorption spectra were recorded in the range of 200–900 nm in order to monitor the Ag nanocluster formation in the thin films. Thermal annealing treatment at different temperatures was applied as second method to form varying size of nanoclusters. The physical properties of formed super lattice were criticized for thermoelectric applications.

Glycosylation of the self-recognizing Escherichia coli Ag43 autotransporter protein

DEFF Research Database (Denmark)

Sherlock, O.; Dobrindt, U.; Jensen, J.B.

2006-01-01

a novel member to this exclusive group, namely, antigen 43 (Ag43), a self-recognizing autotransporter protein. By mass spectrometry Ag43 was demonstrated to be glycosylated by addition of heptose residues at several positions in the passenger domain. Glycosylation of Ag43 by the action of the Aah and Tib......C glycosyltransferases was observed in laboratory strains. Importantly, Ag43 was also found to be glycosylated in a wild-type strain, suggesting that Ag43-glycosylation may be a widespread phenomenon. Glycosylation of Ag43 does not seem to interfere with its self-associating properties. However, the glycosylated form...

A Simple Method for the Preparation of TiO2 /Ag-AgCl@Polypyrrole Composite and Its Enhanced Visible-Light Photocatalytic Activity.

Science.gov (United States)

Yao, Tongjie; Shi, Lei; Wang, Hao; Wang, Fangxiao; Wu, Jie; Zhang, Xiao; Sun, Jianmin; Cui, Tieyu

2016-01-01

A novel and facile method was developed to prepare a visible-light driven TiO2 /Ag-AgCl@polypyrrole (PPy) photocatalyst with Ag-AgCl nanoparticles supported on TiO2 nanofibers and covered by a thin PPy shell. During the synthesis, the PPy shell and Ag-AgCl nanoparticles were prepared simultaneously onto TiO2 nanofibers, which simplified the preparation procedure. In addition, because Ag-AgCl aggregates were fabricated via partly etching the Ag nanoparticles, their size was well controlled at the nanoscale, which was beneficial for improvement of the contact surface area. Compared with reference photocatalysts, the TiO2 /Ag-AgCl@PPy composite exhibited an enhanced photodegradation activity towards rhodamine B under visible-light irradiation. The superior photocatalytic property originated from synergistic effects between TiO2 nanofibers, Ag-AgCl nanoparticles and the PPy shell. Furthermore, the TiO2 /Ag-AgCl@PPy composite could be easily separated and recycled without obvious reduction in activity. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Fabrication of graphene oxide enwrapped Z-scheme Ag{sub 2}SO{sub 3}/AgBr nanoparticles with enhanced visible-light photocatalysis

Energy Technology Data Exchange (ETDEWEB)

Wan, Yujuan; Liang, Chunyan; Xia, Yue, E-mail: xiayue_chem@126.com; Huang, Wei; Li, Zelin

2017-02-28

Highlights: • A novel GO/Ag{sub 2}SO{sub 3}/AgBr composite was prepared via a solution method. • It showed enhanced photocatalytic performance to degrade dyes under visible light irradiation. • Its photocatalytic ability was effectively maintained for 4 cycles without sacrificial reagents. - Abstract: A novel graphene oxide (GO) enwrapped Ag{sub 2}SO{sub 3}/AgBr (GO/Ag{sub 2}SO{sub 3}/AgBr) composite was fabricated through a facile solution approach via electrostatic interaction and precipitation transformation reaction for the first time. The results of XRD, Raman, SEM, TEM and XPS confirmed the structure, morphology and composition of the GO/Ag{sub 2}SO{sub 3}/AgBr composite very well. The Ag{sub 2}SO{sub 3}/AgBr nanoparticles were found to be encapsulated by GO sheets. The photocatalytic activity of the composite was investigated by the degradation of methyl orange (MO), rhodamine B (RhB) and methylene blue (MB) in water under visible light. The incorporation of GO sheets not only significantly enhanced the photocatalytic activity but also improved the reusability of Ag{sub 2}SO{sub 3}/AgBr nanoparticles. The photocatalytic ability of GO/Ag{sub 2}SO{sub 3}/AgBr can be maintained at a high level for 4 times cycle experiments. The trapping experiments confirmed that holes and superoxide ion radicals were the main active species responsible for the degradation reaction. A plasmonic Z-scheme photocatalytic mechanism was proposed to illustrate the possible transferred and separated behavior of electron-hole pairs among Ag, Ag{sub 2}SO{sub 3}, AgBr and GO quaternary system under visible light irradiation.

Physical properties of glasses in the Ag2GeS3-AgBr system

Science.gov (United States)

Moroz, M. V.; Demchenko, P. Yu.; Prokhorenko, S. V.; Moroz, V. M.

2013-08-01

Glasses have been prepared by quenching melts in the Ag2GeS3-AgBr system in a range of 0-53 mol % AgBr. The concentration dependences of density, microhardness, glass transition temperatures, and crystallization of alloys have been established. The conductivity of glasses has been investigated by the dc probe method in a range of 240-420 K. The models of the drift motion of silver and halogen ions have been proposed.

Direct in situ activation of Ag0 nanoparticles in synthesis of Ag/TiO2 and its photoactivity

International Nuclear Information System (INIS)

Jaafar, N.F.; Jalil, A.A.; Triwahyono, S.; Efendi, J.; Mukti, R.R.; Jusoh, R.; Jusoh, N.W.C.; Karim, A.H.; Salleh, N.F.M.; Suendo, V.

2015-01-01

Graphical abstract: - Highlights: • Ag 0 loaded on TiO 2 was prepared by a direct in situ electrochemical method. • 5 wt% Ag–TiO 2 demonstrated the best photocatalytic degradation of 2-CP. • Isomorphous substitution of Ag with Ti occurred to form Ti−O−Ag bonds. • Ag 0 and oxygen vacancies trapped electrons to enhance e–H + separation. • Substitution of Ag in the TiO 2 structure decreased the number of oxygen vacancies. - Abstract: Metallic Ag nanoparticles (Ag 0 ) were successfully activated using a direct in situ electrochemical method before being supported on TiO 2 . Catalytic testing showed that 5 wt% Ag–TiO 2 gave the highest photodegradation (94%) of 50 mg L −1 2-chlorophenol (2-CP) at pH 5 using 0.375 g L −1 catalyst within 6 h, while under similar conditions, 1 wt% and 10 wt% Ag–TiO 2 only gave 75% and 78% degradation, respectively. Characterization results illustrated that the photoactivity was affected by the amount of Ag 0 and oxygen vacancies which act as an electrons trap to enhance the electron–hole separation. While, the Ag−O−Ti bonds formation reduced the photoactivity. The degradation followed a pseudo-first order Langmuir–Hinshelwood model where adsorption was the controlling step. Study on the effect of scavengers showed that the hole (H + ) and hydroxyl radical (OH·) play important roles in the photodegradation. The regenerated photocatalyst was still stable after five cycling runs

Effect of Mixed Glass Former on Ionic Conductivity of Silver Boron Tungstate glass system x[0.75AgI:0.25AgCl]: (1-x) [Ag2O-(B2O3:WO3)

International Nuclear Information System (INIS)

Dehariya, Harsha; Kumar, R; Polu, A R

2012-01-01

The idea to explore new 'Superionic Electrolytes', 'Fast ionic conductors' is due to their tremendous potential applications in solid state electrochemical devices viz. solid state batteries, fuel cells, sensors, super capacitors. Superionic glasses have attracted great deal of attention due to their several advantageous over their crystalline counterparts such as high ionic conductivity, easy preparation, wide selection of compositions, isotropic properties and high stability etc [4-7]. Large numbers of silver ion based glasses have been reported in the literature for the glassy system of AgI:Ag2O: MxOy (MxOy = B2O3, SiO2, P2O5, GeO2, V2O5, As2O5, CrO3, SeO2, MoO3 and TeO3 etc many of them shows high silver ion conductivity [8]. Ion transport behavior of Silver Boro Tungstate glass system x[0.75AgI:0.25AgCl]: (1-x) [Ag2O(B2O3:WO3)], where 0 ≤ x ≤ 1 in molar wt% prepared by melt quench technique were reported. The new host [0.75AgI:0.25AgCl] was used as a better alternate in place of conventional host salt AgI. Conductivity measurement were carried out on this glass system as a function of frequency from 50 Hz to 5 MHz, over a temperature range of 27 C to 200 C, for different compositions by Impedance spectroscopy. The composition 0.7[0.75AgI:0.25AgCl]: 0.3[Ag2O(B2O3:WO3)] shows the highest conductivity of the order of σrt ∼ 2.76x10-2 S/cm, referred to as the Optimum Conducting Composition (OCC). The enhancement in the conductivity has been obtained by mixed former effect. XRD result shows that the system is completely amorphous. Temperature dependence of conductivity of all compositions were studied and reported. Activation energies (Ea) were also evaluated from the slope of .Log(σ) vs 1000/T, Arrhenius plots.

Effect of Mixed Glass Former on Ionic Conductivity of Silver Boro Tungstate glass system x[0.75AgI:0.25AgCl]: (1-x) [Ag2O-{B2O3:WO3}

Science.gov (United States)

Dehariya, Harsha; Kumar, R.; Polu, A. R.

2012-05-01

The idea to explore new 'Superionic Electrolytes', "Fast ionic conductors" is due to their tremendous potential applications in solid state electrochemical devices viz. solid state batteries, fuel cells, sensors, super capacitors. Superionic glasses have attracted great deal of attention due to their several advantageous over their crystalline counterparts such as high ionic conductivity, easy preparation, wide selection of compositions, isotropic properties and high stability etc [4-7]. Large numbers of silver ion based glasses have been reported in the literature for the glassy system of AgI:Ag2O: MxOy (MxOy = B2O3, SiO2, P2O5, GeO2, V2O5, As2O5, CrO3, SeO2, MoO3 & TeO3 etc many of them shows high silver ion conductivity [8]. Ion transport behavior of Silver Boro Tungstate glass system x[0.75AgI:0.25AgCl]: (1-x) [Ag2O{B2O3:WO3}], where 0 <= x <= 1 in molar wt% prepared by melt quench technique were reported. The new host [0.75AgI:0.25AgCl] was used as a better alternate in place of conventional host salt AgI. Conductivity measurement were carried out on this glass system as a function of frequency from 50 Hz to 5 MHz, over a temperature range of 27°C to 200°C, for different compositions by Impedance spectroscopy. The composition 0.7[0.75AgI:0.25AgCl]: 0.3[Ag2O{B2O3:WO3}] shows the highest conductivity of the order of σrt ~ 2.76 × 10-2 S/cm, referred to as the Optimum Conducting Composition (OCC). The enhancement in the conductivity has been obtained by mixed former effect. XRD result shows that the system is completely amorphous. Temperature dependence of conductivity of all compositions were studied & reported. Activation energies (Ea) were also evaluated from the slope of .Log(σ) vs 1000/T, Arrhenius plots.

Sn-In-Ag phase equilibria and Sn-In-(Ag)/Ag interfacial reactions

International Nuclear Information System (INIS)

Chen Sinnwen; Lee Wanyu; Hsu Chiaming; Yang Chingfeng; Hsu Hsinyun; Wu Hsinjay

2011-01-01

Research highlights: → Thermodynamic models of Sn-In and Sn-In-Ag are developed using the CALPHAD approach. → Reaction layer in the Sn-In-(Ag)/Ag couples at 100 deg. C is thinner than those at 25 deg. C, 50 deg. C, and 75 deg. C. → Reactions in the Sn-20 wt%In-2.8 wt%Ag/Ag couples are faster than those in the Sn-20 wt%In/Ag couples. - Abstract: Experimental verifications of the Sn-In and Sn-In-Ag phase equilibria have been conducted. The experimental measurements of phase equilibria and thermodynamic properties are used for thermodynamic modeling by the CALPHAD approach. The calculated results are in good agreement with experimental results. Interfacial reactions in the Sn-In-(Ag)/Ag couples have been examined. Both Ag 2 In and AgIn 2 phases are formed in the Sn-51.0 wt%In/Ag couples reacted at 100 and 150 deg. C, and only the Ag 2 In phase is formed when reacted at 25, 50 and 75 deg. C. Due to the different growth rates of different reaction phases, the reaction layer at 100 deg. C is thinner than those at 25 deg. C, 50 deg. C, and 75 deg. C. In the Sn-20.0 wt%In/Ag couples, the ζ phase is formed at 250 deg. C and ζ/AgIn 2 phases are formed at 125 deg. C. Compared with the Sn-20 wt%In/Ag couples, faster interfacial reactions are observed in the Sn-20.0 wt%In-2.8 wt%Ag/Ag couples, and minor Ag addition to Sn-20 wt%In solder increases the growth rates of the reaction phases.

An experimental investigation of ionic transport properties in CuI-Ag2WO4 and CuI-Ag2CrO4 mixed systems

International Nuclear Information System (INIS)

Suthanthiraraj, S. Austin; Premchand, Y. Daniel

2004-01-01

The phenomenon of ionic transport in the case of two different mixed systems (CuI) (1-x) -(Ag 2 WO 4 ) x (0.15= (1-y) -(Ag 2 CrO 4 ) y (0.15= -3 Scm -1 for the composition (CuI) 0.45 -(Ag 2 WO 4 ) 0.55 and 1.1x10 -4 Scm -1 in the case of (CuI) 0.55 -(Ag 2 CrO 4 ) 0.45 at room temperature has been discussed in terms of the observed characteristics

Misfit dislocations in (001) Cu/(111) Ag epitaxial bilayers

Energy Technology Data Exchange (ETDEWEB)

Vook, R W; Chao, S S

1979-01-01

Two sets of elongated epitaxial (111) Ag islands rotated by 90/sup 0/ with respect to each other were observed to grow on (001) Cu substrates. In addition, two sets of edge misfit dislocations lay parallel to (110) Cu and (110) Cu or equivalently along (110) Ag and (112) Ag. Their Burgers vectors were determined, together with the elastic strains in these two directions. The island elongation was interpreted as arising from a lower strain energy in the preferred direction of growth.

Structure and decomposition of the silver formate Ag(HCO{sub 2})

Energy Technology Data Exchange (ETDEWEB)

Puzan, Anna N., E-mail: anna_puzan@mail.ru; Baumer, Vyacheslav N.; Mateychenko, Pavel V.

2017-02-15

Crystal structure of the silver formate Ag(HCO{sub 2}) has been determined (orthorhombic, sp.gr. Pccn, a=7.1199(5), b=10.3737(4), c=6.4701(3)Å, V=477.88(4) Å{sup 3}, Z=8). The structure contains isolated formate ions and the pairs Ag{sub 2}{sup 2+} which form the layers in (001) planes (the shortest Ag–Ag distances is 2.919 in the pair and 3.421 and 3.716 Å between the nearest Ag atoms of adjacent pairs). Silver formate is unstable compound which decompose spontaneously vs time. Decomposition was studied using Rietveld analysis of the powder diffraction patterns. It was concluded that the diffusion of Ag atoms leads to the formation of plate-like metal particles as nuclei in the (100) planes which settle parallel to (001) planes of the silver formate matrix. - Highlights: • Silver formate Ag(HCO{sub 2}) was synthesized and characterized. • Layered packing of Ag-Ag pairs in the structure was found. • Decomposition of Ag(HCO{sub 2}) and formation of metal phase were studied. • Rietveld-refined micro-structural characteristics during decomposition reveal the space relationship between the matrix structure and forming Ag phase REPLACE with: Space relationship between the matrix structure and forming Ag phase.

Synthesis of Ag or Pt Nanoparticles by Hydrolysis of Either Ag2Na or PtNa

Directory of Open Access Journals (Sweden)

Huabin Wang

2008-01-01

Full Text Available Ag and Pt nanoparticles have successfully been synthesized by hydrolysis of either Ag2Na or PtNa at room temperature. The oxidation of sodium in the Pt-Na pellets was much faster than that in the Ag-Na pellets since Pt is a catalyst for H2O formation reaction from hydrogen and oxygen at room temperature. The hydrolysis byproduct, NaOH, has a high solubility and easily is removed. This method offers a simple method of preparing transition metal nanoparticles. The Ag and Pt nanoparticles prepared by this method were crystalline in nature, and spherical in shape with a mean size of around 10 nm.

Effect of Ag film thickness on the optical and the electrical properties in CuAlO2/Ag/CuAlO2 multilayer films grown on glass substrates

International Nuclear Information System (INIS)

Oh, Dohyun; No, Young Soo; Kim, Su Youn; Cho, Woon Jo; Kwack, Kae Dal; Kim, Tae Whan

2011-01-01

Research highlights: The CuAlO 2 /Ag/CuAlO 2 multilayer films were grown on glass substrates using radio-frequency magnetron sputtering at room temperature. Effects of Ag film thickness on the optical and the electrical properties in CuAlO 2 /Ag/CuAlO 2 multilayer films grown on glass substrates were investigated. X-ray diffraction patterns showed that the phase of the CuAlO 2 layer was amorphous. Atomic force microscopy images showed that Ag films with a thickness of a few nanometers had island structures. The morphology Ag films with a thickness of 8 nm was uniform. The morphology of the Ag films inserted in the CuAlO 2 films significantly affected the optical transmittance and the resistivity of the CuAlO 2 films deposited on glass substrates. The maximum transmittance of the CuAlO 2 /Ag/CuAlO 2 multilayer films with a thickness of 8 nm was 89.16%. The resistivity of the CuAlO 2 /Ag/CuAlO 2 multilayer films with an Ag film thickness of 18 nm was as small as about 2.8 x 10 -5 Ω cm. The resistivity of the CuAlO 2 /Ag/CuAlO 2 multilayer films was decreased as a result of the thermal annealing treatment. These results indicate that CuAlO 2 /Ag/CuAlO 2 multilayer films grown on glass substrates hold promise for potential applications as TCO films in solar cells. - Abstract: Effects of Ag film thickness on the optical and the electrical properties in CuAlO 2 /Ag/CuAlO 2 multilayer films grown on glass substrates were investigated. Atomic force microscopy images showed that Ag films with a thickness of a few nanometers had island structures. X-ray diffraction patterns showed that the phase of the CuAlO 2 layer was amorphous. The resistivity of the 40 nm-CuAlO 2 /18 nm-Ag/40 nm-CuAlO 2 multilayer films was 2.8 x 10 -5 Ω cm, and the transmittance of the multilayer films with an Ag film thickness of 8 nm was approximately 89.16%. These results indicate that CuAlO 2 /Ag/CuAlO 2 multilayer films grown on glass substrates hold promise for potential applications as

A novel metal-to-metal bonding process through in-situ formation of Ag nanoparticles using Ag2O microparticles

International Nuclear Information System (INIS)

Hirose, Akio; Tatsumi, Hiroaki; Takeda, Naoya; Akada, Yusuke; Ogura, Tomo; Ide, Eiichi; Morita, Toshiaki

2009-01-01

The metal-to-metal bonding has been successfully achieved via the bonding process using Ag metallo-organic nanoparticles at a bonding temperature of around 300-, which can be alternative to the current microsoldering in electronics assembly using high-temperature solders. However, further reduction of bonding temperature and/or bonding pressure is needed. In the present research, a novel bonding process through in-situ formation of Ag nanoparticles instead of the filler material of the Ag metallo-organic nanoparticles has been developed. The Ag nanoparticles can form by the reduction of Ag 2 O particles. In this study, the Ag 2 O particles were mixed with triethylene glycol as a reducing agent to form a paste for bonding. The Au coated cylindrical specimens were bonded using the paste. The Ag nanoparticles formed at around 130 to 160 through the reduction process of Ag2O particles with triethylene glycol. The Ag nanoparticles were immediately sintered each other due to a great surface energy per volume. A transmission electron microscope observation revealed that the sintered Ag metallurgically bonded to the Au substrate at around 160 and a dense Ag layer formed after further heating. The tensile strength of the joint bonded at 250 under a bonding pressure of 5MPa was around 60MPa

Synthesis and Characterization of the Rubidium Thiophosphate Rb 6 (PS 5 )(P 2 S 10 ) and the Rubidium Silver Thiophosphates Rb 2 AgPS 4 , RbAg 5 (PS 4 ) 2 and Rb 3 Ag 9 (PS 4 ) 4

KAUST Repository

Alahmary, Fatimah S.; Davaasuren, Bambar; Khanderi, Jayaprakash; Rothenberger, Alexander

2016-01-01

The metal thiophosphates Rb2AgPS4 (2), RbAg5(PS4)2 (3), and Rb3Ag9(PS4)4 (4) were synthesized by stoichiometric reactions, whereas Rb6(PS5)(P2S10) (1) was prepared with excess amount of sulfur. The compounds crystallize as follows: 1 monoclinic, P21

Visible-light photoactivity of plasmonic silver supported on mesoporous TiO2 nanoparticles (Ag-MTN) for enhanced degradation of 2-chlorophenol: Limitation of Ag-Ti interaction

International Nuclear Information System (INIS)

Jaafar, N.F.; Jalil, A.A.; Triwahyono, S.

2017-01-01

Highlights: • Ag 0 loaded on MTN was prepared by a direct in-situ electrochemical method. • The introduction of Ag 0 lowers the band gap and increases the number of OV and TSD. • Ag 0 acted as an electrons trapper and also a plasmonic sensitizer. • The formation of Ti-O-Ag in 10 wt% Ag-MTN decreased the amount of Ag 0 , TSD and OV. • 5 wt% Ag-MTN gave the highest percentage of photodegradation of 2-CP. - Abstract: Various weight loadings of Ag (1–10 wt.%) were introduced to mesoporous titania nanoparticles (MTN) via a direct in-situ electrochemical method. The catalysts were characterized by XRD, surface area analysis, FTIR, ESR, FESEM-EDX and TEM. Characterization results indicated that the introduction of Ag onto MTN decreased the particles size and band gap of the MTN while increasing the number of oxygen vacancies (OV) and Ti 3+ site defects (TSD). The activity performance of Ag-MTN on photodegradation of 2-chlorophenol (2-CP) under visible light irradiation was in the following order: 5 wt% Ag-MTN> 1 wt% Ag-MTN > MTN > 10 wt% Ag-MTN, with degradation percentages of 97, 88, 80 and 63%, respectively. The synergistic effect between Ag 0 and MTN seemed to play an important role in the system. The Ag0 acted as both an electron trap and a plasmonic sensitizer which suppressed the electron-hole recombination, while OV and TSD in the MTN accelerated the production of hydroxyl radicals for enhanced degradation of 2-CP. However, the formation of Ti-O-Ag in 10 wt% Ag-MTN was found to decrease the photoactivity due to the decrease in the formation of Ag 0 , TSD and OV as well as the increase in band gap energy. The photodegradation of 5 wt% Ag-MTN followed a pseudo-first-order Langmuir- Hinshelwood model and the catalyst was still stable after five cycles.

Coating stainless steel plates with Ag/TiO2 for chlorpyrifos decontamination

Science.gov (United States)

Abdel Fattah, Wafa I.; Gobara, Mohammed M.; El-Hotaby, Walid; Mostafa, Sherif F. M.; Ali, Ghareib W.

2016-05-01

Spray coatings of either nanosilver (Ag), titanium (TiO2) or nanosilver titanium (Ag/TiO2) on stainless steel substrates prepared by sol-gel process were successfully achieved. The efficiency of the Ag/TiO2 coat onto 316 stainless steel surface towards cloropyrifos degradation as a chemical warfare agent (CWA) was proved. The crystalline structure and morphological characterization, as well as surface roughness measurements, were assessed. X-ray diffraction results proved the crystalline TiO2 anatase phase. The uniform distribution of Ag along with TiO2 nanoparticles was evidenced through transmission electron microscopy and scanning electron microscopy mapping. The hydrophilic nature of individual Ag, TiO2 and Ag/TiO2 coats was proved by contact angle measurements. The loading of Ag nanoparticles influenced positively the Ag/TiO2 coats surface roughness. The photocatalytic cloropyrifos degradation achieved about 50% within one-hour post UV treatment proving, therefore, the promising Ag/TiO2 continued decontamination efficiency. In conclusion, tuning the physical and morphological properties of TiO2 coated on stainless steel surface could be significantly enhanced by Ag nanoparticles incorporation. The developed Ag/TiO2 coat could be conveniently applied as CWA decontaminant.

Observation of a Ag protrusion on a Ag2S island using a scanning tunneling microscope

Directory of Open Access Journals (Sweden)

Takeo Ohno

2015-01-01

Full Text Available A silver sulfide (Ag2S island as an ionic conductor in resistive switching memories was formed and a protrusion of silver from the Ag2S formed by an electrochemical reaction was observed using a scanning tunneling microscope.

Controllable Charge Transfer in Ag-TiO2 Composite Structure for SERS Application

Directory of Open Access Journals (Sweden)

Yaxin Wang

2017-06-01

Full Text Available The nanocaps array of TiO2/Ag bilayer with different Ag thicknesses and co-sputtering TiO2-Ag monolayer with different TiO2 contents were fabricated on a two-dimensional colloidal array substrate for the investigation of Surface enhanced Raman scattering (SERS properties. For the TiO2/Ag bilayer, when the Ag thickness increased, SERS intensity decreased. Meanwhile, a significant enhancement was observed when the sublayer Ag was 10 nm compared to the pure Ag monolayer, which was ascribed to the metal-semiconductor synergistic effect that electromagnetic mechanism (EM provided by roughness surface and charge-transfer (CT enhancement mechanism from TiO2-Ag composite components. In comparison to the TiO2/Ag bilayer, the co-sputtered TiO2-Ag monolayer decreased the aggregation of Ag particles and led to the formation of small Ag particles, which showed that TiO2 could effectively inhibit the aggregation and growth of Ag nanoparticles.

Syntheses, structures, and properties of Ag4(Mo2O5)(SeO4)2(SeO3) and Ag2(MoO3)3SeO3

International Nuclear Information System (INIS)

Ling Jie; Albrecht-Schmitt, Thomas E.

2007-01-01

Ag 4 (Mo 2 O 5 )(SeO 4 ) 2 (SeO 3 ) has been synthesized by reacting AgNO 3 , MoO 3 , and selenic acid under mild hydrothermal conditions. The structure of this compound consists of cis-MoO 2 2+ molybdenyl units that are bridged to neighboring molybdenyl moieties by selenate anions and by a bridging oxo anion. These dimeric units are joined by selenite anions to yield zigzag one-dimensional chains that extended down the c-axis. Individual chains are polar with the C 2 distortion of the Mo(VI) octahedra aligning on one side of each chain. However, the overall structure is centrosymmetric because neighboring chains have opposite alignment of the C 2 distortion. Upon heating Ag 4 (Mo 2 O 5 )(SeO 4 ) 2 (SeO 3 ) looses SeO 2 in two distinct steps to yield Ag 2 MoO 4 . Crystallographic data: (193 K; MoKα, λ=0.71073 A): orthorhombic, space group Pbcm, a=5.6557(3), b=15.8904(7), c=15.7938(7) A, V=1419.41(12), Z=4, R(F)=2.72% for 121 parameters with 1829 reflections with I>2σ(I). Ag 2 (MoO 3 ) 3 SeO 3 was synthesized by reacting AgNO 3 with MoO 3 , SeO 2 , and HF under hydrothermal conditions. The structure of Ag 2 (MoO 3 ) 3 SeO 3 consists of three crystallographically unique Mo(VI) centers that are in 2+2+2 coordination environments with two long, two intermediate, and two short bonds. These MoO 6 units are connected to form a molybdenyl ribbon that extends along the c-axis. These ribbons are further connected together through tridentate selenite anions to form two-dimensional layers in the [bc] plane. Crystallographic data: (193 K; MoKα, λ=0.71073 A): monoclinic, space group P2 1 /n, a=7.7034(5), b=11.1485(8), c=12.7500(9) A, β=105.018(1) V=1002.7(2), Z=4, R(F)=3.45% for 164 parameters with 2454 reflections with I>2σ(I). Ag 2 (MoO 3 ) 3 SeO 3 decomposes to Ag 2 Mo 3 O 10 on heating above 550 deg. C. - Graphical abstract: A view of the one-dimensional [(Mo 2 O 5 )(SeO 4 ) 2 (SeO 3 )] 4- chains that extend down the c-axis in the structure of Ag 4 (Mo 2 O 5 )(SeO 4

Changes in the microbiological and chemical characteristics of white bread during storage in paper packages modified with Ag/TiO2-SiO2, Ag/N-TiO2 or Au/TiO2.

Science.gov (United States)

Peter, Anca; Mihaly-Cozmuta, Leonard; Mihaly-Cozmuta, Anca; Nicula, Camelia; Ziemkowska, Wanda; Basiak, Dariusz; Danciu, Virginia; Vulpoi, Adriana; Baia, Lucian; Falup, Anca; Craciun, Grigore; Ciric, Alexandru; Begea, Mihaela; Kiss, Claudia; Vatuiu, Daniela

2016-04-15

Microbiological and chemical characteristics of white bread during storage in paper-packages modified with Ag/TiO2-SiO2, Ag/N-TiO2 or Au/TiO2 were investigated. The whiteness and the water retention of the modified packages were slightly superior to those exhibited by the reference sample, as the color of the composite was lighter. The water retention was very good especially for the Ag/TiO2-SiO2-paper. These improvements can be associated with the high specific surface area and with the low agglomeration tendency of Ag nanoparticles in comparison with the Au ones. The preservation activity of the composites for the bread storage is positively influenced by photoactivity and presence of nano-Ag. Packages Ag/TiO2-SiO2-paper and Ag/N-TiO2-paper can find their applicability for extending the shelf life of bread by 2 days as compared with the unmodified paper-package. No influence of the Au/TiO2 on the extending the shelf life of bread was observed. Copyright © 2015 Elsevier Ltd. All rights reserved.

Tyrphostin AG-related compounds attenuate H2O2-induced TRPM2-dependent and -independent cellular responses.

Science.gov (United States)

Yamamoto, Shinichiro; Toda, Takahiro; Yonezawa, Ryo; Negoro, Takaharu; Shimizu, Shunichi

2017-05-01

TRPM2 is a Ca 2+ -permeable channel that is activated by H 2 O 2 . TRPM2-mediated Ca 2+ signaling has been implicated in the aggravation of inflammatory diseases. Therefore, the development of TRPM2 inhibitors to prevent the aggravation of these diseases is expected. We recently reported that some Tyrphostin AG-related compounds inhibited the H 2 O 2 -induced activation of TRPM2 by scavenging the intracellular hydroxyl radical. In the present study, we examined the effects of AG-related compounds on H 2 O 2 -induced cellular responses in human monocytic U937 cells, which functionally express TRPM2. The effects of AG-related compounds on H 2 O 2 -induced changes in intracellular Ca 2+ concentrations, extracellular signal-regulated kinase (ERK) activation, and CXCL8 secretion were assessed using U937 cells. Ca 2+ influxes via TRPM2 in response to H 2 O 2 were blocked by AG-related compounds. AG-related compounds also inhibited the H 2 O 2 -induced activation of ERK, and subsequent secretion of CXCL8 mediated by TRPM2-dependent and -independent mechanisms. Our results show that AG-related compounds inhibit H 2 O 2 -induced CXCL8 secretion following ERK activation, which is mediated by TRPM2-dependent and -independent mechanisms in U937 cells. We previously reported that AG-related compounds blocked H 2 O 2 -induced TRPM2 activation by scavenging the hydroxyl radical. The inhibitory effects of AG-related compounds on TRPM2-independent responses may be due to scavenging of the hydroxyl radical. Copyright © 2017 The Authors. Production and hosting by Elsevier B.V. All rights reserved.

Preparation and Use of Photocatalytically Active Segmented Ag|ZnO and Coaxial TiO2-Ag Nanowires Made by Templated Electrodeposition

Science.gov (United States)

Maijenburg, A. Wouter; Rodijk, Eddy J.B.; Maas, Michiel G.; ten Elshof, Johan E.

2014-01-01

Photocatalytically active nanostructures require a large specific surface area with the presence of many catalytically active sites for the oxidation and reduction half reactions, and fast electron (hole) diffusion and charge separation. Nanowires present suitable architectures to meet these requirements. Axially segmented Ag|ZnO and radially segmented (coaxial) TiO2-Ag nanowires with a diameter of 200 nm and a length of 6-20 µm were made by templated electrodeposition within the pores of polycarbonate track-etched (PCTE) or anodized aluminum oxide (AAO) membranes, respectively. In the photocatalytic experiments, the ZnO and TiO2 phases acted as photoanodes, and Ag as cathode. No external circuit is needed to connect both electrodes, which is a key advantage over conventional photo-electrochemical cells. For making segmented Ag|ZnO nanowires, the Ag salt electrolyte was replaced after formation of the Ag segment to form a ZnO segment attached to the Ag segment. For making coaxial TiO2-Ag nanowires, a TiO2 gel was first formed by the electrochemically induced sol-gel method. Drying and thermal annealing of the as-formed TiO2 gel resulted in the formation of crystalline TiO2 nanotubes. A subsequent Ag electrodeposition step inside the TiO2 nanotubes resulted in formation of coaxial TiO2-Ag nanowires. Due to the combination of an n-type semiconductor (ZnO or TiO2) and a metal (Ag) within the same nanowire, a Schottky barrier was created at the interface between the phases. To demonstrate the photocatalytic activity of these nanowires, the Ag|ZnO nanowires were used in a photocatalytic experiment in which H2 gas was detected upon UV illumination of the nanowires dispersed in a methanol/water mixture. After 17 min of illumination, approximately 0.2 vol% H2 gas was detected from a suspension of ~0.1 g of Ag|ZnO nanowires in a 50 ml 80 vol% aqueous methanol solution. PMID:24837535

Visible-light photoactivity of plasmonic silver supported on mesoporous TiO{sub 2} nanoparticles (Ag-MTN) for enhanced degradation of 2-chlorophenol: Limitation of Ag-Ti interaction

Energy Technology Data Exchange (ETDEWEB)

Jaafar, N.F. [Department of Chemistry, Faculty of Science, Universiti Teknologi Malaysia, UTM, 81310 Johor Bahru, Johor (Malaysia); Jalil, A.A., E-mail: aishahaj@utm.my [Centre of Hydrogen Energy, Institute of Future Energy, Universiti Teknologi Malaysia, UTM, 81310 Johor Bahru, Johor (Malaysia); Department of Chemical Engineering, Faculty of Chemical and Energy Engineering, Universiti Teknologi Malaysia, UTM, 81310 Johor Bahru, Johor (Malaysia); Triwahyono, S. [Department of Chemistry, Faculty of Science, Universiti Teknologi Malaysia, UTM, 81310 Johor Bahru, Johor (Malaysia); Centre for Sustainable Nanomaterials, Ibnu Sina Institute for Scientific and Industrial Research, Universiti Teknologi Malaysia, UTM, 81310 Johor Bahru, Johor (Malaysia)

2017-01-15

Highlights: • Ag{sup 0} loaded on MTN was prepared by a direct in-situ electrochemical method. • The introduction of Ag{sup 0} lowers the band gap and increases the number of OV and TSD. • Ag{sup 0} acted as an electrons trapper and also a plasmonic sensitizer. • The formation of Ti-O-Ag in 10 wt% Ag-MTN decreased the amount of Ag{sup 0}, TSD and OV. • 5 wt% Ag-MTN gave the highest percentage of photodegradation of 2-CP. - Abstract: Various weight loadings of Ag (1–10 wt.%) were introduced to mesoporous titania nanoparticles (MTN) via a direct in-situ electrochemical method. The catalysts were characterized by XRD, surface area analysis, FTIR, ESR, FESEM-EDX and TEM. Characterization results indicated that the introduction of Ag onto MTN decreased the particles size and band gap of the MTN while increasing the number of oxygen vacancies (OV) and Ti{sup 3+} site defects (TSD). The activity performance of Ag-MTN on photodegradation of 2-chlorophenol (2-CP) under visible light irradiation was in the following order: 5 wt% Ag-MTN> 1 wt% Ag-MTN > MTN > 10 wt% Ag-MTN, with degradation percentages of 97, 88, 80 and 63%, respectively. The synergistic effect between Ag{sup 0} and MTN seemed to play an important role in the system. The Ag0 acted as both an electron trap and a plasmonic sensitizer which suppressed the electron-hole recombination, while OV and TSD in the MTN accelerated the production of hydroxyl radicals for enhanced degradation of 2-CP. However, the formation of Ti-O-Ag in 10 wt% Ag-MTN was found to decrease the photoactivity due to the decrease in the formation of Ag{sup 0}, TSD and OV as well as the increase in band gap energy. The photodegradation of 5 wt% Ag-MTN followed a pseudo-first-order Langmuir- Hinshelwood model and the catalyst was still stable after five cycles.

An oil-in-water self-assembly synthesis, characterization and photocatalytic properties of nano Ag@AgCl surface-sensitized K2Ti4O9

International Nuclear Information System (INIS)

Liang, Yinghua; Lin, Shuanglong; Liu, Li; Hu, Jinshan; Cui, Wenquan

2014-01-01

Highlights: • The plasmatic Ag@AgCl surface-sensitized K 2 Ti 4 O 9 composite photocatalysts. • Ag@AgCl greatly increased visible light absorption for K 2 Ti 4 O 9 . • The photocatalysts exhibited enhanced photocatalytic dye degradation. - Abstract: Nano-sized plasmonic Ag@AgCl surface-sensitized K 2 Ti 4 O 9 composite photocatalysts (hereafter designated as Ag@AgCl/K 2 Ti 4 O 9 ) was synthesized via a facile oil-in-water self-assembly method. The photocatalytic activity of the prepared materials for RhB (Rhodamine B) degradation was examined under visible light irradiation. The results reveal that the size of Ag@AgCl, which evenly dispersed on the surface of K 2 Ti 4 O 9 , distributes about 20–50 nm. The UV–vis diffuse reflectance spectra indicate that Ag@AgCl/K 2 Ti 4 O 9 samples have a significantly enhanced optical absorption in 380–700 nm. The photocatalytic activities of the Ag@AgCl/K 2 Ti 4 O 9 samples increase first and then decrease with increasing amount of loading Ag@AgCl and the Ag@AgCl(20 wt.%)/K 2 Ti 4 O 9 sample exhibits the best photocatalytic activity and 94.47% RhB was degraded after irradiation for 2 h. Additionally, studies performed using radical scavengers indicated that O 2 · − and Cl 0 acted as the main reactive species. The electronic interaction was systematically studied and confirmed by the photo-electrochemical measurements

Phase formation in the Ag2O - MgO - MoO3 system and the crystal structure of new double molybdate Ag2Mg2(MoO4)3

International Nuclear Information System (INIS)

Tsyrenova, G.D.; Khajkina, E.G.; Khobrakova, Eh.T.; Solodovnikov, S.F.

2001-01-01

The phase correlations in subsolidus area of the Ag 2 O - MgO - MoO 3 system were studied, the Ag 2 MoO 4 - MgMoO 4 polythermal cross-section was investigated and its T-x diagram was constructed. X-ray diffraction and thermal analytic researches were conducted. The formation of the new double Ag 2 Mg 2 (MoO 4 ) 3 molybdates relating to the structural group Na 2 Mg 5 (MoO 4 ) 6 was established, and its structure (a=6.978(1), b=8.715(2), c=10.294(2) A, α=107.56(3) Deg, β=105.11(3) Deg, γ=103.68(3) Deg, Z=2, sp. gr. P 1-bar, R=0.038) was determined. The mixed carcass from the twin MgO 6 -octahedrons and MoO 4 -tetrahedrons, in which blankness the Ag atoms are arranged, stand out in the structure.The character of disordering in the part of Ag + is analogous to previously found one in the Ag 2 Zn 2 (MoO 4 ) 3 structure. The possible limits in the fields of homogeneity of silver-magnesium molybdate and its analogs, as well as the differences their structure from the structure of isotopic sodium-containing phases, are discussed [ru

Ag2WO4 nanorods decorated with AgI nanoparticles: Novel and efficient visible-light-driven photocatalysts for the degradation of water pollutants

Directory of Open Access Journals (Sweden)

Shijie Li

2018-04-01

Full Text Available To develop efficient and stable visible-light-driven (VLD photocatalysts for pollutant degradation, we synthesized novel heterojunction photocatalysts comprised of AgI nanoparticle-decorated Ag2WO4 nanorods via a facile method. Various characterization techniques, including XRD, SEM, TEM, EDX, and UV–vis DRS were used to investigate the morphology and optical properties of the as-prepared AgI/Ag2WO4 catalyst. With AgI acting as the cocatalyst, the resulting AgI/Ag2WO4 heterostructure shows excellent performance in degrading toxic, stable pollutants such as rhodamine B (RhB, methyl orange (MO and para-chlorophenol (4-CP. The high performance is attributed to the enhanced visible-light absorption properties and the promoted separation efficiency of charge carriers through the formation of the heterojunction between AgI and Ag2WO4. Additionally, AgI/Ag2WO4 exhibits durable stability. The active species trapping experiment reveals that active species (O2•− and h+ dominantly contribute to RhB degradation. The AgI/Ag2WO4 heterojunction photocatalyst characterized in this work holds great potential for remedying environmental issues due to its simple preparation method and excellent photocatalytic performance.

Enhanced photocatalytic performances and magnetic recovery capacity of visible-light-driven Z-scheme ZnFe2O4/AgBr/Ag photocatalyst

Science.gov (United States)

He, Jie; Cheng, Yahui; Wang, Tianzhao; Feng, Deqiang; Zheng, Lingcheng; Shao, Dawei; Wang, Weichao; Wang, Weihua; Lu, Feng; Dong, Hong; Zheng, Rongkun; Liu, Hui

2018-05-01

High efficiency, high stability and easy recovery are three key factors for practical photocatalysts. Z-scheme heterostructure is one of the most promising photocatalytic systems to meet all above requirements. However, efficient Z-scheme photocatalysts which could absorb visible light are still few and difficult to implement at present. In this work, the composite photocatalysts ZnFe2O4/AgBr/Ag were prepared through a two-step method. A ∼92% photodegradation rate on methyl orange was observed within 30 min under visible light, which is much better than that of individual ZnFe2O4 or AgBr/Ag. The stability was also greatly improved compared with AgBr/Ag. The increased performance is resulted from the suitable band alignment of ZnFe2O4 and AgBr, and it is defined as Z-scheme mechanism which was demonstrated by detecting active species and electrochemical impedance spectroscopy. Besides, ZnFe2O4/AgBr/Ag is ferromagnetic and can be recycled by magnet. These results show that ZnFe2O4/AgBr/Ag is a potential magnetically recyclable photocatalyst which can be driven by visible light.

Visible-light photoactivity of plasmonic silver supported on mesoporous TiO2 nanoparticles (Ag-MTN) for enhanced degradation of 2-chlorophenol: Limitation of Ag-Ti interaction

Science.gov (United States)

Jaafar, N. F.; Jalil, A. A.; Triwahyono, S.

2017-01-01

Various weight loadings of Ag (1-10 wt.%) were introduced to mesoporous titania nanoparticles (MTN) via a direct in-situ electrochemical method. The catalysts were characterized by XRD, surface area analysis, FTIR, ESR, FESEM-EDX and TEM. Characterization results indicated that the introduction of Ag onto MTN decreased the particles size and band gap of the MTN while increasing the number of oxygen vacancies (OV) and Ti3+ site defects (TSD). The activity performance of Ag-MTN on photodegradation of 2-chlorophenol (2-CP) under visible light irradiation was in the following order: 5 wt% Ag-MTN> 1 wt% Ag-MTN > MTN > 10 wt% Ag-MTN, with degradation percentages of 97, 88, 80 and 63%, respectively. The synergistic effect between Ag0 and MTN seemed to play an important role in the system. The Ag0 acted as both an electron trap and a plasmonic sensitizer which suppressed the electron-hole recombination, while OV and TSD in the MTN accelerated the production of hydroxyl radicals for enhanced degradation of 2-CP. However, the formation of Ti-O-Ag in 10 wt% Ag-MTN was found to decrease the photoactivity due to the decrease in the formation of Ag0, TSD and OV as well as the increase in band gap energy. The photodegradation of 5 wt% Ag-MTN followed a pseudo-first-order Langmuir- Hinshelwood model and the catalyst was still stable after five cycles.

In situ growth of Ag nanoparticles on α-Ag2WO4 under electron irradiation: probing the physical principles

Science.gov (United States)

San-Miguel, Miguel A.; da Silva, Edison Z.; Zannetti, Sonia M.; Cilense, Mario; Fabbro, Maria T.; Gracia, Lourdes; Andrés, Juan; Longo, Elson

2016-06-01

Exploiting the plasmonic behavior of Ag nanoparticles grown on α-Ag2WO4 is a widely employed strategy to produce efficient photocatalysts, ozone sensors, and bactericides. However, a description of the atomic and electronic structure of the semiconductor sites irradiated by electrons is still not available. Such a description is of great importance to understand the mechanisms underlying these physical processes and to improve the design of silver nanoparticles to enhance their activities. Motivated by this, we studied the growth of silver nanoparticles to investigate this novel class of phenomena using both transmission electron microscopy and field emission scanning electron microscopy. A theoretical framework based on density functional theory calculations (DFT), together with experimental analysis and measurements, were developed to examine the changes in the local geometrical and electronic structure of the materials. The physical principles for the formation of Ag nanoparticles on α-Ag2WO4 by electron beam irradiation are described. Quantum mechanical calculations based on DFT show that the (001) of α-Ag2WO4 displays Ag atoms with different coordination numbers. Some of them are able to diffuse out of the surface with a very low energy barrier (less than 0.1 eV), thus, initiating the growth of metallic Ag nanostructures and leaving Ag vacancies in the bulk material. These processes increase the structural disorder of α-Ag2WO4 as well as its electrical resistance as observed in the experimental measurements.

Highly sensitive wearable strain sensor based on silver nanowires and nanoparticles

Science.gov (United States)

Shengbo, Sang; Lihua, Liu; Aoqun, Jian; Qianqian, Duan; Jianlong, Ji; Qiang, Zhang; Wendong, Zhang

2018-06-01

Here, we propose a highly sensitive and stretchable strain sensor based on silver nanoparticles and nanowires (Ag NPs and NWs), advancing the rapid development of electronic skin. To improve the sensitivity of strain sensors based on silver nanowires (Ag NWs), Ag NPs and NWs were added to polydimethylsiloxane (PDMS) as an aid filler. Silver nanoparticles (Ag NPs) increase the conductive paths for electrons, leading to the low resistance of the resulting sensor (14.9 Ω). The strain sensor based on Ag NPs and NWs showed strong piezoresistivity with a tunable gauge factor (GF) at 3766, and a change in resistance as the strain linearly increased from 0% to 28.1%. The high GF demonstrates the irreplaceable role of Ag NPs in the sensor. Moreover, the applicability of our high-performance strain sensor has been demonstrated by its ability to sense movements caused by human talking, finger bending, wrist raising and walking.

The Ag2Se-HgSe-GeSe2 system and crystal structures of the compounds

International Nuclear Information System (INIS)

Parasyuk, O.V.; Gulay, L.D.; Romanyuk, Ya.E.; Olekseyuk, I.D.; Piskach, L.V.

2003-01-01

The phase diagram of the quasi-ternary Ag 2 Se-HgSe-GeSe 2 system at 298 K was investigated using X-ray phase analysis and metallography. The formation of five intermediate quaternary phases β (Ag ∼7.12-∼6.32 Hg ∼0.44-∼0.82 GeSe 6 ), γ (Ag ∼6.08-∼4.00 Hg ∼0.96-∼2.00 GeSe 6 ), δ (Ag 3.4 Hg 2.3 GeSe 6 ), ε (Ag ∼2.24-∼2.00 Hg ∼2.88-∼3.00 GeSe 6 ) and ∼Ag 1.4 Hg 1.3 GeSe 6 was established. The crystal structure of the β-phase (for the Ag 6.504 Hg 0.912 GeSe 6 composition) was determined using X-ray single crystal diffraction. It crystallizes in a cubic structure (space group F4-bar 3m) with the lattice parameter a=1.09026(4) nm. The crystal structure of the δ-phase (Ag 3.4 Hg 2.3 GeSe 6 ) was determined using X-ray powder diffraction (space group F4-bar 3m, a=1.07767(8) nm). The crystal structure determination of the γ-phase (space group Pmn2 1 ) was performed for the compositions Ag 5.6 Hg 1.2 GeSe 6 , Ag 4.8 Hg 1.6 GeSe 6 and Ag 4 Hg 2 GeSe 6 using X-ray powder diffraction. The crystal structure of the LT-Hg 2 GeSe 4 compound (space group I4-bar , a=0.56786(2), c=1.12579(5) nm) was confirmed by powder diffraction also.

Photodegradation properties and optics of Ag/TiO{sub 2} films; Propiedades de fotodegradacion y opticas de peliculas Ag/TiO{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Tirado G, S. [IPN, Escuela Superior de Fisica y Matematicas, San Pedro Zacatenco, 07738 Ciudad de Mexico (Mexico); Valenzuela Z, M. A., E-mail: tirado@esfm.ipn.mx [IPN, Escuela Superior de Ingenieria Quimica e Industrias Extractivas, Laboratorio de Catalisis y Materiales, San Pedro Zacatenco, 07738 Ciudad de Mexico (Mexico)

2016-10-15

In the thin semiconductor films of Ag/TiO{sub 2} the topographic properties were recorded by atomic force microscopy and the main parameters of roughness were determined; the optical properties were also recorded when determining their transmittance degree, their refractive indexes, their thickness and the bandwidth of the semiconductor Eg, both for pure TiO{sub 2} films and the modified Ag/TiO{sub 2} films with various layers of the Ag catalyst. The Ag/TiO{sub 2} films that were grown by sol-gel and repeated immersion, chemical technique that has been used in the development of thin film technology, were carried out in photo catalysis, when are used in photo degradation of methyl orange at an aqueous concentration of 14 ppm, once they are characterized with several techniques required to be able to explain the possible photo catalytic reactions at the solid-aqueous interface, when irradiated with UV; with the possible application in water treatment. The photoluminescence spectra of the prepared Ag/TiO{sub 2} samples are reported, which resulted in a green emission, characteristic of the visible, in addition to emissions in the UV range. (Author)

A facile fabrication of plasmonic g-C{sub 3}N{sub 4}/Ag{sub 2}WO{sub 4}/Ag ternary heterojunction visible-light photocatalyst

Energy Technology Data Exchange (ETDEWEB)

Dai, Kai, E-mail: daikai940@chnu.edu.cn [College of Physics and Electronic Information, Huaibei Normal University, Huaibei, 235000 (China); Lv, Jiali [College of Physics and Electronic Information, Huaibei Normal University, Huaibei, 235000 (China); Lu, Luhua, E-mail: lhlu@cug.edu.cn [Faculty of Material Science and Chemical Engineering, China University of Geosciences, Wuhan, 430074 (China); Liang, Changhao [College of Physics and Electronic Information, Huaibei Normal University, Huaibei, 235000 (China); Key Laboratory of Materials Physics and Anhui Key Laboratory of Nanomaterials and Nanotechnology, Institute of Solid State Physics, Hefei Institutes of Physical Science, Chinese Academy of Sciences, Hefei, 230031 (China); Geng, Lei; Zhu, Guangping [College of Physics and Electronic Information, Huaibei Normal University, Huaibei, 235000 (China)

2016-07-01

It's important to reduce recombination of electrons and holes and enhance charge transfer through fine controlled interfacial structure. In this work, novel graphitic-C{sub 3}N{sub 4} (g-C{sub 3}N{sub 4})/Ag{sub 2}WO{sub 4}/Ag ternary photocatalyst has been synthesized by deposition of Ag{sub 2}WO{sub 4} onto g-C{sub 3}N{sub 4} template and followed by sun light reduction of Ag{sub 2}WO{sub 4} into Ag{sub 2}WO{sub 4}/Ag. As-prepared g-C{sub 3}N{sub 4}/Ag{sub 2}WO{sub 4}/Ag presented significantly enhanced photocatalytic performance in degrading methylene blue (MB) under 410 nm LED light irradiation. Metallic Ag{sup 0} is used as plasmonic hot spots to generate high energy charge carriers. Optimal g-C{sub 3}N{sub 4} content has been confirmed to be 40 wt%, corresponding to apparent pseudo-first-order rate constant kapp of 0.0298 min{sup −1}, which is 3.3 times and 37.3 times more than that of pure g-C{sub 3}N{sub 4} and Ag{sub 2}WO{sub 4}, respectively. This novel ternary g-C{sub 3}N{sub 4}/Ag{sub 2}WO{sub 4}/Ag structure material is an ideal candidate in environmental treatment and purifying applications. - Graphical abstract: A high efficient plasmonic graphitic-C{sub 3}N{sub 4}/Ag{sub 2}WO{sub 4}/Ag ternary nanocomposite photocatalyst was synthesized. - Highlights: • g-C{sub 3}N{sub 4}/Ag{sub 2}WO{sub 4}/Ag ternary nanocomposite photocatalyst was prepared. • g-C{sub 3}N{sub 4}/Ag{sub 2}WO{sub 4}/Ag showed high photocatalytic activity. • g-C{sub 3}N{sub 4}/Ag{sub 2}WO{sub 4}/Ag showed long reusable life.

Structural features of AgCaCdMg2(PO4)3 and AgCd2Mg2(PO4)3, two new compounds with the alluaudite-type structure, and their catalytic activity in butan-2-ol conversion

International Nuclear Information System (INIS)

Kacimi, Mohammed; Ziyad, Mahfoud; Hatert, Frederic

2005-01-01

AgCaCdMg 2 (PO 4 ) 3 and AgCd 2 Mg 2 (PO 4 ) 3 , two new compounds with the alluaudite-type structure, were synthesized by a solid state reaction in air at 750 deg. C. The X-ray powder diffraction pattern of AgCaCdMg 2 (PO 4 ) 3 indicates the presence of small amounts of (Ca, Mg) 3 (PO 4 ) 2 with the whitlockite structure, as impurity, whereas AgCd 2 Mg 2 (PO 4 ) 3 is constituted by pure alluaudite. The Rietveld refinements of the X-ray powder diffraction patterns indicate an ordered cationic distribution for AgCd 2 Mg 2 (PO 4 ) 3 , with Ag on A(2)', Cd on A(1) and M(1), and Mg on M(2), whereas a disordered distribution of Cd and Ca between the A(1) and M(1) sites is observed for AgCaCdMg 2 (PO 4 ) 3 . The catalytic properties of these compounds has been measured in reaction of butan-2-ol dehydrogenation. In the absence of oxygen, both samples exhibit poor dehydrogenation activity. All samples displayed no dehydration activity. Introduction of oxygen into the feed changed totally the catalytic behavior of the catalysts. The production of methyl ethyl ketone increases with time on stream and the reaction temperature. AgCaCdMg 2 (PO 4 ) 3 is more efficient than AgCd 2 Mg 2 (PO 4 ) 3

In situ controllable synthesis of novel surface plasmon resonance-enhanced Ag{sub 2}WO{sub 4}/Ag/Bi{sub 2}MoO{sub 6} composite for enhanced and stable visible light photocatalyst

Energy Technology Data Exchange (ETDEWEB)

Lv, Jiali [College of Physics and Electronic Information, Huaibei Normal University, Huaibei 235000 (China); Dai, Kai, E-mail: daikai940@chnu.edu.cn [College of Physics and Electronic Information, Huaibei Normal University, Huaibei 235000 (China); Zhang, Jinfeng [College of Physics and Electronic Information, Huaibei Normal University, Huaibei 235000 (China); Lu, Luhua, E-mail: lhlu@cug.edu.cn [Engineering Research Center of Nano-Geomaterials of Ministry of Education, China University of Geosciences, Wuhan 430074 (China); Liang, Changhao, E-mail: chliang@issp.ac.cn [College of Physics and Electronic Information, Huaibei Normal University, Huaibei 235000 (China); Key Laboratory of Materials Physics and Anhui Key Laboratory of Nanomaterials and Nanotechnology, Institute of Solid State Physics, Chinese Academy of Sciences, Hefei 23003 (China); Geng, Lei; Wang, Zhongliao; Yuan, Guangyu; Zhu, Guangping [College of Physics and Electronic Information, Huaibei Normal University, Huaibei 235000 (China)

2017-01-01

Highlights: • Novel Ag{sub 2}WO{sub 4}/Ag/Bi{sub 2}MoO{sub 6} ternary photocatalyst was prepared. • Ag{sub 2}WO{sub 4}/Ag/Bi{sub 2}MoO{sub 6} showed enhanced catalytic activity. • Ag{sub 2}WO{sub 4}/Ag/Bi{sub 2}MoO{sub 6} showed long reusable life. - Abstract: A novel hierarchical Ag{sub 2}WO{sub 4}/Ag/Bi{sub 2}MoO{sub 6} ternary visible-light-driven photocatalyst was successfully synthesized by in situ doping Ag{sub 2}WO{sub 4} with Bi{sub 2}MoO{sub 6} nanosheets through a facile hydrothermal and photochemical process. The morphology, structure, optical performance and crystallinity of the products were measured by field emission scanning electron microscope (FESEM), energy dispersive spectrometer (EDS), UV–vis diffuse reflectance spectroscopy (DRS) and X-ray diffraction (XRD). The results showed that Ag{sub 2}WO{sub 4}/Ag was uniformly dispersed on the surface of Bi{sub 2}MoO{sub 6} nanosheets. The photocatalytic performance of Ag{sub 2}WO{sub 4}/Ag/Bi{sub 2}MoO{sub 6} heterostructures was evaluated by the degradation of methylene blue (MB) under 410 nm LED arrays. The ternary Ag{sub 2}WO{sub 4}/Ag/Bi{sub 2}MoO{sub 6} nanocomposite exhibits higher photocatalytic activity than Bi{sub 2}MoO{sub 6} and Ag{sub 2}WO{sub 4}. The synergistic effect of Ag{sub 2}WO{sub 4} and Bi{sub 2}MoO{sub 6} could generated more heterojunctions which promoted photoelectrons transfer from Ag{sub 2}WO{sub 4} to Bi{sub 2}MoO{sub 6}, leading to the improvement of photocatalytic performance by photoelectrons-holes recombination suppression. At the same time, the surface plasmon resonance of Ag{sub 2}WO{sub 4}/Ag/Bi{sub 2}MoO{sub 6} is another crucial reason for the high photocatalytic performance of organic pollutants degradation. And the 20 wt% Ag{sub 2}WO{sub 4}-loaded Bi{sub 2}MoO{sub 6} shows the optimal photocatalytic performance in the degradation of MB. In addition, the ternary composites can be easily reclaimed by precipitation and exhibits high stability of photocatalytic

Synthesis and photoactivity of the highly efficient Ag species/TiO2 nanoflakes photocatalysts

International Nuclear Information System (INIS)

Liu Yong; Hu Juncheng; Li Jinlin

2011-01-01

Research highlights: → Highly efficient Ag species-TiO 2 nanoflakes catalyst was prepared. → The variety and relative amount of Ag species in TiO 2 can be well tuned. → The enhanced photocatalytic activity can be attributed to the Ag species. - Abstract: Ag species/TiO 2 nanoflakes photocatalysts with different relative contents (Ag + , Ag 2+ , Ag 0 ) have been successfully synthesized by a simple template-free synthetic strategy. X-ray photoelectron spectroscopy, X-ray diffraction, and UV-vis diffuse reflectance spectra indicated that the dopant ions (Ag + or Ag 2+ ) were partly incorporated into the titanium dioxide nanoflakes. Meanwhile, part of the silver ions migrated to the surface after the subsequent calcination and aggregated into ultra-small metallic Ag nanoclusters (NCs) (1-2 nm), which are well dispersed on the surface of TiO 2 nanoflakes. The photocatalytic activities of the Ag species/TiO 2 materials obtained were evaluated by testing the photodegradation of the azo dye reactive brilliant X-3B (X-3B) under near UV irradiation. Interestingly, it was found that the maximum photocatalytic efficiency was observed when Ag species coexisted in three valence states (Ag + , Ag 2+ , Ag 0 NCs), which was higher than that of Degussa P25. The high photocatalytic activity of the Ag species/TiO 2 can be attributed to the synergy effect of the three Ag species.

Direct in situ activation of Ag{sup 0} nanoparticles in synthesis of Ag/TiO{sub 2} and its photoactivity

Energy Technology Data Exchange (ETDEWEB)

Jaafar, N.F. [Department of Chemistry, Faculty of Science, Universiti Teknologi Malaysia, 81310 UTM Johor Bahru, Johor (Malaysia); Jalil, A.A., E-mail: aishah@cheme.utm.my [Institute of Hydrogen Economy, Universiti Teknologi Malaysia, 81310 UTM Johor Bahru, Johor (Malaysia); Department of Chemical Engineering, Faculty of Chemical Engineering, Universiti Teknologi Malaysia, 81310 UTM Johor Bahru, Johor (Malaysia); Triwahyono, S. [Department of Chemistry, Faculty of Science, Universiti Teknologi Malaysia, 81310 UTM Johor Bahru, Johor (Malaysia); Ibnu Sina Institute for Fundamental Science Studies, Universiti Teknologi Malaysia, 81310 UTM Johor Bahru, Johor (Malaysia); Efendi, J. [Department of Chemistry, Universitas Negeri Padang, Jl. Prof. Hamka, Air Tawar, Padang, West Sumatera (Indonesia); Mukti, R.R. [Division of Inorganic and Physical Chemistry, Faculty of Mathematics and Natural Science, Institut Teknologi Bandung, Jl Ganesha No. 10, Bandung 40132 (Indonesia); Jusoh, R.; Jusoh, N.W.C. [Department of Chemical Engineering, Faculty of Chemical Engineering, Universiti Teknologi Malaysia, 81310 UTM Johor Bahru, Johor (Malaysia); Karim, A.H. [Department of Chemistry, Faculty of Science, Universiti Teknologi Malaysia, 81310 UTM Johor Bahru, Johor (Malaysia); Salleh, N.F.M. [Department of Chemical Engineering, Faculty of Chemical Engineering, Universiti Teknologi Malaysia, 81310 UTM Johor Bahru, Johor (Malaysia); Suendo, V. [Division of Inorganic and Physical Chemistry, Faculty of Mathematics and Natural Science, Institut Teknologi Bandung, Jl Ganesha No. 10, Bandung 40132 (Indonesia)

2015-05-30

Graphical abstract: - Highlights: • Ag{sup 0} loaded on TiO{sub 2} was prepared by a direct in situ electrochemical method. • 5 wt% Ag–TiO{sub 2} demonstrated the best photocatalytic degradation of 2-CP. • Isomorphous substitution of Ag with Ti occurred to form Ti−O−Ag bonds. • Ag{sup 0} and oxygen vacancies trapped electrons to enhance e–H{sup +} separation. • Substitution of Ag in the TiO{sub 2} structure decreased the number of oxygen vacancies. - Abstract: Metallic Ag nanoparticles (Ag{sup 0}) were successfully activated using a direct in situ electrochemical method before being supported on TiO{sub 2}. Catalytic testing showed that 5 wt% Ag–TiO{sub 2} gave the highest photodegradation (94%) of 50 mg L{sup −1} 2-chlorophenol (2-CP) at pH 5 using 0.375 g L{sup −1} catalyst within 6 h, while under similar conditions, 1 wt% and 10 wt% Ag–TiO{sub 2} only gave 75% and 78% degradation, respectively. Characterization results illustrated that the photoactivity was affected by the amount of Ag{sup 0} and oxygen vacancies which act as an electrons trap to enhance the electron–hole separation. While, the Ag−O−Ti bonds formation reduced the photoactivity. The degradation followed a pseudo-first order Langmuir–Hinshelwood model where adsorption was the controlling step. Study on the effect of scavengers showed that the hole (H{sup +}) and hydroxyl radical (OH·) play important roles in the photodegradation. The regenerated photocatalyst was still stable after five cycling runs.

Building novel Ag/CeO2 heterostructure for enhancing photocatalytic activity

International Nuclear Information System (INIS)

Leng, Qiang; Yang, Dezhi; Yang, Qi; Hu, Chenguo; Kang, Yue; Wang, Mingjun; Hashim, Muhammad

2015-01-01

Highlights: • Ag nanoparticle is designed to building Schottky heterojunction on CeO 2 nanocube. • The photocatalytic activity of Ag/CeO 2 heterostructure is much enhanced. • 95.33% of MB can be effectively degraded within half an hour. • Ag as acceptor of photoelectrons blocks the recombination of electron–hole pairs. - Abstract: Stable and recyclable photocatalysts with high efficiency to degrade organic contamination are important and widely demanded under the threat of the environment pollution. Ag/CeO 2 heterostructure is designed as a photocatalyst to degrade organic dye under the simulated sunlight. The catalytic activity of CeO 2 nanocubes (NCs) to degrade methylene blue (MB) is obviously enhanced when Ag nanoparticles (NPs) are deposited on the surface of them. The weight ratio of Ag and CeO 2 in forming high efficiency catalyst, the amount of Ag/CeO 2 catalyst used in degradation process, and the dye concentration and pH value of the initial MB solution are examined systematically. 95.33% of MB can be effectively degraded within half an hour when 50 mg of Ag/CeO 2 catalyst in an optimal weight ratio of 1:3, is added to the 100 mL of MB solution (c 0 = 1 × 10 −5 mol L −1 , pH 6.2). The mechanism of the enhanced catalytic activity of Ag/CeO 2 heterostructure is discussed. The photocatalytic degradation rate is found to obey pseudo-first-order kinetics equations according to Langmuir–Hinshelwood model. The intermediate products in different stages during the degradation of MB are analyzed

Elucidating the real-time Ag nanoparticle growth on α-Ag2WO4 during electron beam irradiation: experimental evidence and theoretical insights.

Science.gov (United States)

Pereira, Wyllamanney da Silva; Andrés, Juan; Gracia, Lourdes; San-Miguel, Miguel A; da Silva, Edison Z; Longo, Elson; Longo, Valeria M

2015-02-21

Why and how Ag is formed when electron beam irradiation takes place on α-Ag2WO4 in a vacuum transmission electron microscopy chamber? To find an answer, the atomic-scale mechanisms underlying the formation and growth of Ag on α-Ag2WO4 have been investigated by detailed in situ transmission electron microscopy (TEM) and field emission scanning electron microscopy (FE-SEM) studies, density functional theory based calculations and ab initio molecular dynamics simulations. The growth process at different times, chemical composition, size distribution and element distribution were analyzed in depth at the nanoscale level using FE-SEM, operated at different voltages (5, 10, 15, and 20 kV), and TEM with energy dispersive spectroscopy (EDS) characterization. The size of Ag nanoparticles covers a wide range of values. Most of the Ag particles are in the 20-40 nm range. The nucleation and formation of Ag on α-Ag2WO4 is a result of structural and electronic changes in the AgOx (x = 2,4, 6, and 7) clusters used as constituent building blocks of this material, consistent with metallic Ag formation. First principle calculations point out that Ag-3 and Ag-4-fold coordinated centers, located in the sub-surface of the (100) surface, are the most energetically favorable to undergo the diffusion process to form metallic Ag. Ab initio molecular dynamics simulations and the nudged elastic band (NEB) method were used to investigate the minimum energy pathways of these Ag atoms from positions in the first slab layer to outward sites on the (100) surface of α-Ag2WO4. The results point out that the injection of electrons decreases the activation barrier for this diffusion step and this unusual behavior results from the presence of a lower energy barrier process.

Crystal structure and thermal stability of AgIn(MoO4)2

International Nuclear Information System (INIS)

Klevtsov, P.V.; Solodovnikov, S.F.; Perepelitsa, A.P.; Klevtsova, R.F.

1984-01-01

Tetragonal crystals of double molybdate AgIn(MoO 4 ) 2 are prepared bi crystallization from solution in Ag 2 Mo 2 O 7 melt (a=4.998, c=36.725 A, space group I4 1 , Z=6). Its crystal structure is determined (autodaffractometer ''Syntex P2 1 '', MoKsub(α)-radiation, 876 reflections, R=0.054) in which along with Mo-tetrahedrons Mo-octahedrons are present. By mutual edges latter are united into bands forming fragments of wolframite structure alonside with (In, Ag) octahedrons. In the direction of c axis wolframite fragments alternate with scheelite fragments consisting of Mo-tetrahedrons and Ag-octavertices. The crystallochemical formula of the compound is Ag(Insub(0.75)Agsub(0.25))sub(2)Mosub(2)Osub(8) [MoO 4 ]. At a temperature of about 600 deq C AgIn-molybdate transforms into modification with NaIn(MoO 4 ) 2 structure NaIn(MoO 4 ) 2 and melts at 650 deg C decomposing into In 2 (MoO 4 ) 3 solid phase and Ag 2 MoO 4 melt

Photocatalytic properties of porous TiO2/Ag thin films

International Nuclear Information System (INIS)

Chang, C.-C.; Chen, J.-Y.; Hsu, T.-L.; Lin, C.-K.; Chan, C.-C.

2008-01-01

In this study, nanocrystalline TiO 2 /Ag composite thin films were prepared by a sol-gel spin-coating technique. By introducing polystyrene (PS) spheres into the precursor solution, porous TiO 2 /Ag thin films were prepared after calcination at a temperature of 500 deg. C for 4 h. Three different sizes (50, 200, and 400 nm) of PS spheres were used to prepare porous TiO 2 films. The as-prepared TiO 2 and TiO 2 /Ag thin films were characterized by X-ray diffractometry (XRD) and by scanning electron microscopy to reveal structural and morphological differences. In addition, the photocatalytic properties of these films were investigated by degrading methylene blue under UV irradiation. When PS spheres of different sizes were introduced after calcination, the as-prepared TiO 2 films exhibited different porous structures. XRD results showed that all TiO 2 /Ag films exhibited a major anatase phase. The photodegradation of porous TiO 2 thin films prepared with 200 nm PS spheres and doped with 1 mol% Ag exhibited the best photocatalytic efficiency where ∼ 100% methylene blue was decomposed within 8 h under UV exposure

Comparative Compton scattering studies in Cu2O and Ag2O

International Nuclear Information System (INIS)

Bandyopadhyay, S.; Chatterjee, A.K.; Saha, S.K.; Chatterjee, A.

1994-01-01

Compton scattering studies in polycrystalline Cu 2 O and Ag 2 O with 59.54 keV γ radiation are reported. A comparison has been made between the valance Compton profiles of these two components scaled to lattice momentum by normalizing them to equal electron density for outer valence electrons, and this comparison shows some differences between the bonding characters of Cu 2 O and Ag 2 O. (author)

Two crystal structures of Ag sup + -and Tl sup + -exchanged zeolite X, Ag sub 2 sub 7 Tl sub 6 sub 5 -X and Ag sub 2 sub 3 Tl sub 6 sub 9 -X

CERN Document Server

Kim, S Y; Kim, Y

2002-01-01

Two crystal structures of dehydrated Ag sup + -and Tl sup + -exchanged zeolite X (Ag sub 2 sub 7 Tl sub 6 sub 5 -X and Ag sub 2 sub 3 Tl sub 6 sub 9 -X) have been determined by single-crystal X-ray diffraction techniques in the cubic space group Fd3 at 21(1) .deg. C (a = 24.758(4) A, a = 24.947(4) A, respectively). Their structures were refined to the final error indices R sub 1 = 0.055 and wR sub 2 = 0.057 with 375 reflections, and R sub 1 = 0.058 and wR sub 2 = 0.057 with 235 reflections, respectively, for which I> 3 sigma(I). In the structure of Ag sub 2 sub 7 Tl sub 6 sub 5 -X, 27 Ag sup + ions were found at two crystallographic sites: 15 Ag sup + ions at site I at the center of the hexagonal prism and the remaining 12 Ag sup + ions at site II' in the sodalite cavity. Sixty-five Tl sup + ions were located at three crystallographic sites: 20 Tl sup + ions at site II opposite single six-rings in the supercage, 18 Tl sup + ions at site I' in the sodalite cavity opposite the D6Rs, and the remaining 27 Tl sup ...

The irradiation influence on the properties of silver sulfide (Ag2S) colloidal nanoparticles

Science.gov (United States)

Rempel, S. V.; Kuznetsova, Yu. V.; Gerasimov, E. Yu.; Rempel', A. A.

2017-08-01

The aqueous solutions of different stability containing silver sulfide (Ag2S) nanoparticles are studied. The stable, transparent, and turbid solutions have been subjected to daylight for 7 months, to ultraviolet and laser irradiation, as well as to an electron beam. Solar radiation is found to favor the Ag2S reduction to Ag and/or the formation of Ag2S/Ag hybrid nanoparticles in the solution. At a high amount of hybrid nanoparticles, the exciton-plasmon interaction causes asymmetry in the absorption spectra. The exposure of Ag2S particles precipitated from the solution with the electron beam leads to the reversible growth of Ag threads. The possible exciton-plasmon interplay mechanisms in Ag2S/Ag hybrid nanoparticles are considered. The physical mechanisms of the changing Ag2S stoichiometry, the formation of metallic Ag and Ag2S/Ag hybrid nanoparticles are the generation of hot carriers and the energy transfer (exciton-plasmon interaction) in a metal-semiconductor hybrid nanosystem are elucidated, as well.

TEM characterization of plate-shaped L12-(Al,Ag)3Ti precipitates in a Ag-modified TiAl based intermetallics

International Nuclear Information System (INIS)

Yuan, Y.; Liu, H.W.; Zhao, X.N.; Meng, X.K.; Liu, Z.G.

2006-01-01

L1 2 -(Al,Ag) 3 Ti phase in a L1 0 -TiAl(Ag) intermetallic compound with a nominal composition of Ti-54 at.% Al-4 at.% Ag has been studied by transmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM) and energy dispersive X-ray (EDX). TEM observations revealed that the alloy aged at 1273 K consists of L1 0 phase and L1 2 phase. The compositions of L1 2 phase and the matrix have been determined. The habit plane of L1 2 phase was analyzed by trace line method. It was revealed that the habit plane changed to one of {1 1 2) planes compared with our previous result. The semi-coherent interface was formed between L1 0 phase and L1 2 phase. HRTEM characterized the interface structure directly. The dislocation loops and ledges at the interphase boundary were observed. The results were discussed in terms of the competition between elastic strain and interfacial energy, ledge mechanism of phase transformation caused by long-range diffusion of the atoms

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

The optical and mechanical properties of PVA-Ag nanocomposite films

Energy Technology Data Exchange (ETDEWEB)

El-Shamy, A.G.; Attia, W.; Abd El-Kader, K.M., E-mail: kamalmarei@yahoo.com

2014-03-25

Highlights: • We prepared PVA -Ag composite films which used in different filed of applications. • The XRD results showed Ag nanoparticles entering the polymer PVA matrix. • Optical band gap as a result of doping has been found to be reduced significantly. • Young's modulus increases while the strain decreases due to increasing Ag content. -- Abstract: Poly (vinyl alcohol) (PVA) loaded silver (Ag) nanoparticles were successfully prepared by chemical reduction methods. The synthesized nanoparticles are characterized using UV–visible spectrophotometer, X-ray diffractometer (XRD) and Transmission electron microscope (TEM). The contents of the inorganic phase in the nanocomposites were determined by using atomic absorption spectroscopy (AA) for silver, and were found to be 0.2, 0.4, 0.8 and 1.5 wt.%. Optical absorption studies in the wavelength range 190–900 nm showed additional peak at 420 nm for differently doped films, in addition to the peak at 200 nm for undoped PVA film. There is observable change in the absorbed intensity at 420 nm with filling levels. This is due to the link between the Ag metal ion and the polymer OH- groups. The indirect energy gaps were calculated. It was found that Young’s modulus and the strength at the break increase, while the energy gaps and the strain decrease as the concentration of Ag content is increased. The XRD results showed that the Ag nanoparticles entering the polymer PVA matrix and the crystallinity was strongly influenced by the amount of Ag nanoparticles. The electron diffraction image for the highest concentration sample shows the crystalline nature of the silver metal nanoparticles. TEM of the nanocomposite films revealed the presence of Ag particles with average diameter of 12 nm.

Conductance switching in Ag(2)S devices fabricated by in situ sulfurization.

Science.gov (United States)

Morales-Masis, M; van der Molen, S J; Fu, W T; Hesselberth, M B; van Ruitenbeek, J M

2009-03-04

We report a simple and reproducible method to fabricate switchable Ag(2)S devices. The alpha-Ag(2)S thin films are produced by a sulfurization process after silver deposition on an Si substrate. Structure and composition of the Ag(2)S are characterized using XRD and RBS. Our samples show semiconductor behaviour at low bias voltages, whereas they exhibit reproducible bipolar resistance switching at higher bias voltages. The transition between both types of behaviour is observed by hysteresis in the I-V curves, indicating decomposition of the Ag(2)S, increasing the Ag(+) ion mobility. The as-fabricated Ag(2)S samples are a good candidate for future solid state memory devices, as they show reproducible memory resistive properties and they are fabricated by an accessible and reliable method.

Conductance switching in Ag2S devices fabricated by in situ sulfurization

International Nuclear Information System (INIS)

Morales-Masis, M; Molen, S J van der; Hesselberth, M B; Ruitenbeek, J M van; Fu, W T

2009-01-01

We report a simple and reproducible method to fabricate switchable Ag 2 S devices. The α-Ag 2 S thin films are produced by a sulfurization process after silver deposition on an Si substrate. Structure and composition of the Ag 2 S are characterized using XRD and RBS. Our samples show semiconductor behaviour at low bias voltages, whereas they exhibit reproducible bipolar resistance switching at higher bias voltages. The transition between both types of behaviour is observed by hysteresis in the I-V curves, indicating decomposition of the Ag 2 S, increasing the Ag + ion mobility. The as-fabricated Ag 2 S samples are a good candidate for future solid state memory devices, as they show reproducible memory resistive properties and they are fabricated by an accessible and reliable method.

Optical Properties of Plasmon Resonances with Ag/SiO2/Ag Multi-Layer Composite Nanoparticles

International Nuclear Information System (INIS)

Ye-Wan, Ma; Li-Hua, Zhang; Zhao-Wang, Wu; Jie, Zhang

2010-01-01

Optical properties of plasmon resonance with Ag/SiO 2 /Ag multi-layer nanoparticles are studied by numerical simulation based on Green's function theory. The results show that compared with single-layer Ag nanoparticles, the multi-layer nanoparticles exhibit several distinctive optical properties, e.g. with increasing the numbers of the multi-layer nanoparticles, the scattering efficiency red shifts, and the intensity of scattering enhances accordingly. It is interesting to find out that slicing an Ag-layer into multi-layers leads to stronger scattering intensity and more 'hot spots' or regions of stronger field enhancement. This property of plasmon resonance of surface Raman scattering has greatly broadened the application scope of Raman spectroscopy. The study of metal surface plasmon resonance characteristics is critical to the further understanding of surface enhanced Raman scattering as well as its applications. (fundamental areas of phenomenology (including applications))

Synthesis of Ag-Cu and Ag-Cu{sub 2}O alloy nanoparticles using a seed-mediated polyol process, thermodynamic and kinetic aspects

Energy Technology Data Exchange (ETDEWEB)

Niknafs, Yasaman; Amirjani, Amirmostafa; Marashi, Pirooz, E-mail: pmarashi@aut.ac.ir; Fatmehsari, Davoud Haghshenas

2017-03-01

In this paper, Ag, Ag-Cu and Ag-Cu{sub 2}O nanoparticles were synthesized using a modified polyol method. Size, shape and composition of the obtained nanostructures were effectively controlled by adjusting the kinetic and thermodynamic conditions. Response surface methodology was employed to consider the interaction of parameters and to develop a polynomial equation for predicting the size of the silver nanoparticles. The precisely controlled silver nanoaprticles were used as the seeds for the formation of alloyed nanoparticles. By manipulating the involved parameters, both spherical and cubical Ag-Cu and Ag-Cu{sub 2}O nanostructures are obtainable in the size range of 90–100 nm. The morphological, optical and compositional characteristics of the obtained nanostructures were studied using SEM, FE-SEM, UV–Vis, EDS and XRD. - Highlights: • Synthesis of Ag, Ag-Cu and Ag-Cu{sub 2}O alloy nanostructures. • RSM was successfully employed for predicting the size of the AgNPs. • Size and composition tuning by adjusting the kinetic and thermodynamic conditions.

Silver vanadium diphosphate Ag2VP2O8: Electrochemistry and characterization of reduced material providing mechanistic insights

International Nuclear Information System (INIS)

Takeuchi, Esther S.; Lee, Chia-Ying; Cheng, Po-Jen; Menard, Melissa C.; Marschilok, Amy C.; Takeuchi, Kenneth J.

2013-01-01

Silver vanadium phosphorous oxides (Ag w V x P y O z ) are notable battery cathode materials due to their high energy density and demonstrated ability to form in-situ Ag metal nanostructured electrically conductive networks within the cathode. While analogous silver vanadium diphosphate materials have been prepared, electrochemical evaluations of these diphosphate based materials have been limited. We report here the first electrochemical study of a silver vanadium diphosphate, Ag 2 VP 2 O 8 , where the structural differences associated with phosphorous oxides versus diphosphates profoundly affect the associated electrochemistry. Reminiscent of Ag 2 VO 2 PO 4 reduction, in-situ formation of silver metal nanoparticles was observed with reduction of Ag 2 VP 2 O 8 . However, counter to Ag 2 VO 2 PO 4 reduction, Ag 2 VP 2 O 8 demonstrates a significant decrease in conductivity upon continued electrochemical reduction. Structural analysis contrasting the crystallography of the parent Ag 2 VP 2 O 8 with that of the proposed Li 2 VP 2 O 8 reduction product is employed to gain insight into the observed electrochemical reduction behavior, where the structural rigidity associated with the diphosphate anion may be associated with the observed particle fracturing upon deep electrochemical reduction. Further, the diphosphate anion structure may be associated with the high thermal stability of the partially reduced Ag 2 VP 2 O 8 materials, which bodes well for enhanced safety of batteries incorporating this material. - Graphical abstract: Structure and galvanostatic intermittent titration-type test data for silver vanadium diphosphate, Ag 2 VP 2 O 8 . Highlights: ► First electrochemical study of a silver vanadium diphosphate, Ag 2 VP 2 O 8 . ► In-situ formation of Ag 0 nanoparticles was observed upon electrochemical reduction. ► Structural analysis used to provide insight of the electrochemical behavior

Irradiation-induced displacement of Ag atoms from lattice sites in an Al-0.2% Mg-0.1% Ag crystal

International Nuclear Information System (INIS)

Swanson, M.L.; Howe, L.M.; Quenneville, A.F.

1976-01-01

In irradiated alloys of Al containing approximately 0.1 at% Ag, the backscattering - channelling method shows that Al-Ag dumbells are created by the trapping of Al interstitial atoms at Ag solute atoms. The present results demonstrate that the addition of 0.2 at% Mg to such irradiated alloys retards not only the formation of Al-Ag dumbells during annealing from 30 to 100 K but also their annihilation during annealing from 180 to 240 K. Al interstitials are released from Mg traps at 100 to 160 K, causing further trapping at Ag atoms. Approximately 70% of the Ag atoms return to lattice sites at approximately 200 K (stage III) (compared with 100% in the Al-0.1% Ag alloys) and the remainder return to lattice sites at approximately 260 K. These results favour migration of Al-Ag dumbells rather than vacancies during stage III annealing. (author)

Photodegradation properties and optics of Ag/TiO2 films

International Nuclear Information System (INIS)

Tirado G, S.; Valenzuela Z, M. A.

2016-10-01

In the thin semiconductor films of Ag/TiO 2 the topographic properties were recorded by atomic force microscopy and the main parameters of roughness were determined; the optical properties were also recorded when determining their transmittance degree, their refractive indexes, their thickness and the bandwidth of the semiconductor Eg, both for pure TiO 2 films and the modified Ag/TiO 2 films with various layers of the Ag catalyst. The Ag/TiO 2 films that were grown by sol-gel and repeated immersion, chemical technique that has been used in the development of thin film technology, were carried out in photo catalysis, when are used in photo degradation of methyl orange at an aqueous concentration of 14 ppm, once they are characterized with several techniques required to be able to explain the possible photo catalytic reactions at the solid-aqueous interface, when irradiated with UV; with the possible application in water treatment. The photoluminescence spectra of the prepared Ag/TiO 2 samples are reported, which resulted in a green emission, characteristic of the visible, in addition to emissions in the UV range. (Author)

Preparation and optical properties of AgGaS{sub 2} nanofilms

Energy Technology Data Exchange (ETDEWEB)

Zhang, Jianjun [School of Materials Sci. and Engineering, Nanchang Hangkong University, Nanchang 330063 (China); Huang, Yi [School of Electronic and Information Engineering, Southwest University for Nationalities, Chengdu 610041 (China)

2011-05-15

In this paper, AgGaS{sub 2} nanofilms have been prepared by a two-step process involving the successive ionic layer absorption and reaction (SILAR) and annealing method. Using AgNO{sub 3}, GaCl{sub 3} and Na{sub 2}S{sub 2}O{sub 3} as reaction sources, the mixture films were firstly deposited on quartz glass substrates at room temperature, and then annealed in Ar environment at 200-500 C for 4 h, respectively. The effects of annealing temperature on structural and optical properties were investigated by XRD, UV-Vis, EDS and photoluminescence (PL) spectra. It was revealed in XRD results that {alpha}-Ag{sub 9}GaS{sub 6} was contained in the samples annealed at 200 C, and this phase was decreased with increase of the annealing temperatures. When the sample was annealed at above 400 C, the chalcopyrite AgGaS{sub 2} nanofilm was obtained. The preferred orientation was exhibited along the (112) plane. It was shown in atomic force microscopy (AFM) results that the grain sizes in AgGaS{sub 2} nanofilms were 18-24 nm and the thin films were smooth and strongly adherent to the substrates. When the annealing temperature was higher than 400 C, it is an optimum condition to improve the structural and optical properties of the AgGaS{sub 2} thin films. The room temperature PL spectra of AgGaS{sub 2} nanofilms showed prominent band edge emission at 2.72 eV. Based on all results mentioned above, it can be concluded that the SILAR-annealing method is preferable to preparing high-quality AgGaS{sub 2} nanofilms. (copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

Analysis of stress-strain behavior in Bi2223 composite tapes

International Nuclear Information System (INIS)

Sugano, M.; Osamura, K.; Nyilas, A.

2004-01-01

Tensile test was carried out for Bi2223/Ag/Ag alloy composite tapes at RT, 77 and 7 K. Two yielding points are observed in the stress-strain curves. From the stress-strain behavior of the components and critical current (I c ) as a function of tensile strain, it was found that the microscopic reason for these yieldings is attributed to yielding of Ag alloy and fracture of Bi2223, respectively. The strain at the second yielding has temperature dependence and it becomes larger with decreasing measured temperature. From the thermo-mechanical analysis, it can be explained by temperature dependence of compressive residual strain of Bi2223. Reversible recovery of I c was found during loading-unloading test. The relationship between the reversible strain limit and the intrinsic strain of Bi2223 was discussed

Thermochemical properties of silver tellurides including empressite (AgTe) and phase diagrams for Ag-Te and Ag-Te-O

Science.gov (United States)

Voronin, Mikhail V.; Osadchii, Evgeniy G.; Brichkina, Ekaterina A.

2017-10-01

This study compiles original experimental and literature data on the thermodynamic properties (ΔfG°, S°, ΔfH°) of silver tellurides (α-Ag2Te, β-Ag2Te, Ag1.9Te, Ag5Te3, AgTe) obtained by the method of solid-state galvanic cell with the RbAg4I5 and AgI solid electrolytes. The thermodynamic data for empressite (AgTe, pure fraction from Empress Josephine Mine, Colorado USA) have been obtained for the first time by the electrochemical experiment with the virtual reaction Ag + Te = AgTe. The Ag-Te phase diagrams in the T - x and log fTe2 (gas) - 1/ T coordinates have been refined, and the ternary Ag-Te-O diagrams with Ag-Te-TeO2 (paratellurite) composition range have been calculated.

Effect of fluctuations on electron and phonon processes and thermodynamic parameters of Ag2Te and Ag2Se in the region of phase transition

International Nuclear Information System (INIS)

Aliev, S. A.; Aliev, F. F.

2008-01-01

Temperature dependences of electrical conductivity σ, thermoelectric power α, results of differential thermal analysis ΔT y , thermal conductivity χ, temperature conductivity κ, and heat capacity C p were studied in Ag 2 Te and Ag 2 Se semiconductors in the region of the phase transition. Two extrema are observed in the temperature dependence χ(T): a maximum in the region of the α' → β' transition and a minimum in the region of the β' → β transition; these extrema are caused by the similar dependence C p (T). It is shown that the α → α' and β' → β transitions are displacement transitions, while the α' → β' transition is of reconstruction type. It is established that the disorder parameter η in silver chalcogenides is highly smeared in the region of the phase transition; therefore, disordering of phases at the point of the phase transition is incomplete: 73, 62, and 48% in Ag 2 Te, Ag 2 Se, and Ag 2 S, respectively. The minimum volumes V ph for new phases are calculated; it is shown that the value of V ph in displacement transitions is larger than in the reconstruction-type transitions

Fabrication, characterization and photocatalytic properties of Ag nanoparticles modified TiO2 NTs

International Nuclear Information System (INIS)

Wang Qingyao; Yang Xiuchun; Liu Dan; Zhao Jianfu

2012-01-01

Graphical abstract: The TiO 2 NTs were first treated with bi-functional mercaptoacetic acid linkers (HOOC–R–S). The –OH group on the surface of TiO 2 NT provides a strong affinity with the carboxylate group in the linker molecules. The thiol functional group in the linker molecules facilitates the binding with Ag from AgNO 3 solution. After Ag + ions were reduced by NaBH 4 , Ag nanoparticles formed by nucleation and growth. Highlights: ► Ag nanoparticles with an average diameter of 9.2 nm were filled in the TiO 2 nanotubes by a successive ionic layer adsorption and reaction (SILAR) technique. ► Bi-functional mercaptoacetic acid linkers were used to bind TiO 2 nanotubes with Ag nanoparticles. ► Ag nanoparticles modification of TiO 2 NTs largely enhanced the photocatalytic degradation of methyl orange under ultraviolet light irradiation. - Abstract: Ordered anatase TiO 2 nanotubes (TiO 2 NTs) on Ti substrate were synthesized by electrochemical anodization and subsequently vapor-thermal treatment. Ag nanoparticles were decorated on TiO 2 NTs by successive ionic layer adsorption and reaction (SILAR) technique. Raman spectroscopy, X-ray absorption near edge spectroscopy (XANES), X-ray diffraction (XRD), UV–vis diffuse reflectance spectroscopy, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) were used for the characterization of surface morphology, phase composition, and microstructure of the original TiO 2 NTs, the vapor-thermally treated TiO 2 NTs and the Ag nanoparticles decorated TiO 2 NTs. The results indicate that vapor-thermal treatment favors to the transformation of amorphous TiO 2 into anatase phase. Increasing the SILAR cycle times favors to increase the loaded amounts of Ag nanoparticles in TiO 2 NTs. Ag nanoparticles are uniformly distributed in the TiO 2 NTs, and the SILAR process does not damage the ordered tubular structure. A possible formation mechanism of Ag/TiO 2 NTs has also been proposed. The

Spectral properties of hydrothermally-grown Nd:LuAG, Yb:LuAG, and Yb:Lu{sub 2}O{sub 3} laser materials

Energy Technology Data Exchange (ETDEWEB)

Brown, David C., E-mail: DBrown@snakecreeklasers.com [Snake Creek Lasers LLC, Friendsville, PA 18818 (United States); McMillen, Colin D.; Moore, Cheryl; Kolis, Joseph W. [Department of Chemistry and Center for Optical Materials Science and Engineering Technologies, Clemson University, Clemson, SC 29634-0973 (United States); Envid, Victoria [Snake Creek Lasers LLC, Friendsville, PA 18818 (United States)

2014-04-15

We have investigated the hydrothermal growth of, and spectrally characterized, the lutetium based laser materials Nd:LuAG, Yb:LuAG, and Yb:Lu{sub 2}O{sub 3}. Absorption cross-section data are presented for Nd:LuAG at 83, 175, and 295 K. Absorption cross-section data was also obtained for Yb:LuAG at 83, 175, and 295 K; the 295 K data was used to generate emission cross-sections using the method of reciprocity. For Yb:Lu{sub 2}O{sub 3}, we present absorption cross-sections at 295 K as well as emission cross-sections derived using reciprocity. -- Highlights: • We present spectral properties for hydrothermally-grown laser crystals. • Absorption cross-section data are presented for Nd:LuAG and Yb:LuAG at 83, 175, and 295 K. • Emission cross-sections are presented for Yb:LuAG at 295 K derived by reciprocity. • We present absorption cross-sections at 295 K as well as emission cross-sections derived using reciprocity for the laser material Yb:Lu{sub 2}O{sub 3}.

Building novel Ag/CeO{sub 2} heterostructure for enhancing photocatalytic activity

Energy Technology Data Exchange (ETDEWEB)

Leng, Qiang; Yang, Dezhi; Yang, Qi [Department of Applied Physics, Chongqing University, Chongqing 400044 (China); Hu, Chenguo, E-mail: hucg@cqu.edu.cn [Department of Applied Physics, Chongqing University, Chongqing 400044 (China); Kang, Yue; Wang, Mingjun [Department of Applied Physics, Chongqing University, Chongqing 400044 (China); Hashim, Muhammad [Department of Applied Physics, Chongqing University, Chongqing 400044 (China); Applied Physics Department, Federal Urdu University of Arts Science and Technology, Islamabad (Pakistan)

2015-05-15

Highlights: • Ag nanoparticle is designed to building Schottky heterojunction on CeO{sub 2} nanocube. • The photocatalytic activity of Ag/CeO{sub 2} heterostructure is much enhanced. • 95.33% of MB can be effectively degraded within half an hour. • Ag as acceptor of photoelectrons blocks the recombination of electron–hole pairs. - Abstract: Stable and recyclable photocatalysts with high efficiency to degrade organic contamination are important and widely demanded under the threat of the environment pollution. Ag/CeO{sub 2} heterostructure is designed as a photocatalyst to degrade organic dye under the simulated sunlight. The catalytic activity of CeO{sub 2} nanocubes (NCs) to degrade methylene blue (MB) is obviously enhanced when Ag nanoparticles (NPs) are deposited on the surface of them. The weight ratio of Ag and CeO{sub 2} in forming high efficiency catalyst, the amount of Ag/CeO{sub 2} catalyst used in degradation process, and the dye concentration and pH value of the initial MB solution are examined systematically. 95.33% of MB can be effectively degraded within half an hour when 50 mg of Ag/CeO{sub 2} catalyst in an optimal weight ratio of 1:3, is added to the 100 mL of MB solution (c{sub 0} = 1 × 10{sup −5} mol L{sup −1}, pH 6.2). The mechanism of the enhanced catalytic activity of Ag/CeO{sub 2} heterostructure is discussed. The photocatalytic degradation rate is found to obey pseudo-first-order kinetics equations according to Langmuir–Hinshelwood model. The intermediate products in different stages during the degradation of MB are analyzed.

Effects of coating process on the characteristics of Ag-SnO2 contact materials

International Nuclear Information System (INIS)

Liu, X.M.; Wu, S.L.; Chu, Paul K.; Chung, C.Y.; Zheng, J.; Li, S.L.

2006-01-01

Good wettability between the SnO 2 and silver matrix can improve the electrical contact performance of Ag-SnO 2 materials. In this work, Ag was deposited onto the surface of Ti-doped SnO 2 particles using chemical plating to enhance the wettability. X-ray diffraction (XRD) and transmission electron microscopy (TEM) were used to characterize the Ag-coated SnO 2 particles. Scanning electron microscopy (SEM), conductivity tests, differential thermal analysis (DTA), and thermogravimetric analysis (TGA) were performed on the Ag-SnO 2 materials. Our results reveal that the chemical plating process can enhance the wettability between the Ti-doped SnO 2 particles and Ag matrix, and the Ag-coated SnO 2 particles are uniformly distributed in the Ag matrix. Both the thermal and electrical conductivity of the Ag-SnO 2 materials are significantly improved

Ternary ZnO/AgI/Ag2CO3 nanocomposites: Novel visible-light-driven photocatalysts with excellent activity in degradation of different water pollutants

International Nuclear Information System (INIS)

Golzad-Nonakaran, Behrouz; Habibi-Yangjeh, Aziz

2016-01-01

ZnO/AgI/Ag 2 CO 3 nanocomposites with different Ag 2 CO 3 contents were fabricated by a facile ultrasonic-irradiation method. The resultant samples were fairly characterized using XRD, EDX, SEM, TEM, UV–vis DRS, FT-IR, and PL techniques to reveal their microstructure, purity, morphology, and spectroscopic properties. Photocatalytic activity of the prepared samples was investigated by photodegradation of four dye pollutants (rhodamine B, methyl orange, methylene blue, and fuchsine) under visible-light irradiation. The photocatalytic experiments in degradation of rhodamine B showed that the ternary ZnO/AgI/Ag 2 CO 3 (30%) nanocomposite has an enhanced activity nearly 19 and 14 times higher than those of the binary ZnO/Ag 2 CO 3 and ZnO/AgI photocatalysts, respectively. Based on the obtained results, the highly enhanced activity was attributed to generation of more electron-hole pairs under visible-light irradiation and separation of the photogenerated charge carriers due to formation of tandem n-n heterojunctions between counterparts of the nanocomposite. The active species trapping experiments were also examined and it was showed that superoxide ion radicals play a vital role in the photocatalytic degradation reaction. More importantly, the ternary photocatalyst demonstrated good photostability. - Highlights: • ZnO/AgI/Ag 2 CO 3 nanocomposites were fabricated by an ultrasonic-irradiation method. • The activity was investigated by photodegradation of four dyes under visible light. • ZnO/AgI/Ag 2 CO 3 (30%) nanocomposite has the best activity under visible light. • Activity is 19 and 14-folds higher than ZnO/Ag 2 CO 3 and ZnO/AgI in degradation of RhB.

Study of the pseudo-ternary Ag2SAs2S3HgI2 vitreous system

Science.gov (United States)

Boidin, R.; Le Coq, D.; Cuisset, A.; Hindle, F.; Brubach, J.-B.; Michel, K.; Bychkov, E.

2013-03-01

Chalcogenide alloys in the Ag2SAs2S3HgI2 pseudo-ternary system were synthesized and their vitreous nature was verified by X-ray diffraction. The glass transition and crystallization temperatures (Tg and Tc), the density (d), and the total electrical conductivity (σ) were measured for all samples of three series, A, B, and C corresponding to (Ag2S)50-x/2(As2S3)50-x/2(HgI2)x, (Ag2S)y(As2S3)80-y(HgI2)20 and (Ag2S)z(As2S3)50(HgI2)50-z, respectively. The maximum of Tg was approximately 160 °C for glasses with low HgI2 content whereas the maximum of density (5.75 g cm-3) was obtained for the sample in the B-series with the highest Ag2S concentration (z=60 mol%). This composition also possesses the highest conductivity at 298 K (σ298 K≈10-3 S cm-1). Unexpectedly the conductivity of the A-series samples was observed to decrease as a function of the Ag2S content. The far-infrared transmission in the 100-600 cm-1 window range (3.3-18.2 THz, 100-16.6 μm) was also given for a few glass compositions highlighting the strong influence of the HgI2 content.

Synthesis and characterization of the NiFe{sub 2}O{sub 4}@TEOS–TPS@Ag nanocomposite and investigation of its antibacterial activity

Energy Technology Data Exchange (ETDEWEB)

Allafchian, Ali R., E-mail: Allafchian@cc.iut.ac.ir [Nanotechnology and Advanced Materials Institute, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of); Jalali, S.A.H., E-mail: ahjalali2002@gmail.com [Department of Natural Resources, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of); Institute of Biotechnology and Bioengineering, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of); Amiri, R., E-mail: razieh.amiri@gmail.com [Nanotechnology and Advanced Materials Institute, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of); Shahabadi, Sh., E-mail: shirinshahabadi@rocketmail.com [Nanotechnology and Advanced Materials Institute, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of)

2016-11-01

Highlights: • The new NiFe{sub 2}O{sub 4}@TEOS–TPS@Ag nanocomposite was synthesized and characterized. • The VSM technique was applied for investigation of their magnetic properties. • By using magnetic decantation, they can be easily removed from the disinfected media. • These nanocomposites exhibit good antibacterial activity and high reusability. - Abstract: In this study, the NiFe{sub 2}O{sub 4} was embedded in (3–mercaptopropyl) trimethoxysilane (TPS) and tetraethyl orthosilicate (TEOS) using the sol–gel method. These compounds were used as the support of Ag nanoparticles (Ag NPs). The NiFe{sub 2}O{sub 4}@TEOS–TPS@Ag nanocomposites were obtained with the development of bonding between the silver atoms of Ag NPs and the sulfur atoms of TPS molecule. Field emission scanning electron microscopy (FE–SEM), transmission electron microscopy (TEM), X–ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT–IR) were used for the characterization of the Ag nanocomposites. Also, the magnetic properties of these nanocomposites were studied by using a vibrating sample magnetometer (VSM) technique. The disk diffusion, minimum inhibition concentration (MIC) and minimum bactericidal concentrations (MBC) tests were used for the investigation of the antibacterial effect of this nanocomposite against bacterial strains. The synthesized nanocomposite presented high reusability and good antibacterial activity against gram–positive and gram–negative bacteria. Remarkably, this nanocomposite could be easily removed from the disinfected media by magnetic decantation.

Study on Synthesis and Antibacterial Properties of Ag NPs/GO Nanocomposites

Directory of Open Access Journals (Sweden)

Lei Huang

2016-01-01

Full Text Available Using graphene oxide as substrate and stabilizer for the silver nanoparticles, silver nanoparticles-graphene oxide (Ag NPs/GO composites with different Ag loading were synthesized through a facile solution-phase method. During the synthesis process, AgNO3 on GO matrix was directly reduced by NaBH4. The structure characterization was studied through X-ray diffraction (XRD, atomic force microscopy (AFM, high-resolution transmission electron microscope (HRTEM, ultraviolet-visible spectroscopy (UV-Vis, and selected area electron diffraction (SAED. The results show that Ag nanoparticles (Ag NPs with the sizes ranging from 5 to 20 nm are highly dispersed on the surfaces of GO sheets. The shape and size of the Ag NPs are decided by the volume of initial AgNO3 solution added in the GO. The antibacterial activities of Ag NPs/GO nanocomposites were investigated and the result shows that all the produced composites exhibit good antibacterial activities against Gram-negative (G− bacterial strain Escherichia coli (E. coli and Gram-positive (G+ strain Staphylococcus aureus (S. aureus. Moreover, the antibacterial activities of Ag NPs/GO nanocomposites gradually increased with the increasing of volume of initial AgNO3 solution added in the GO and this improvement of the antibacterial activities results from the combined action of size effect and concentration effect of Ag NPs in Ag NPs/GO nanocomposites.

Visible-light photocatalytic activity of Ag2O coated Bi2WO6 hierarchical microspheres assembled by nanosheets

International Nuclear Information System (INIS)

Chen, Lin; Hua, Hao; Yang, Qi; Hu, Chenguo

2015-01-01

Graphical abstract: - Highlights: • Bi 2 WO 6 hierarchical microspheres assembled by nanosheets and dispersed nanosheets are synthesized. • Ag 2 O/Bi 2 WO 6 heterostuctures exhibites an enhanced photocatalytic activity compared with the Bi 2 WO 6 nanostructures. • Photocatalytic activity of the Ag 2 O/Bi 2 WO 6 microspheres is higher than that of the nanosheets. • Bi 2 WO 6 hierarchical structure is an excellent architecture for loading of Ag 2 O nanoparticles. - Abstract: Bi 2 WO 6 hierarchical microspheres assembled by nanosheets and dispersed nanosheets were synthesized by hydrothermal reaction in different conditions. Ag 2 O nanoparticles were deposited on the surface of Bi 2 WO 6 microspheres and nanosheets by the chemical precipitation method. The photocatalytic performance of pure Bi 2 WO 6 nanostructures and Ag 2 O/Bi 2 WO 6 heterostructures were evaluated by the photocatalytic decolorization of RhB solution under visible-light irradiation. Compared with the pure Bi 2 WO 6 nanostructures, the Ag 2 O/Bi 2 WO 6 heterostructures exhibited an obviously enhanced photocatalytic activity. And photocatalytic activity of the Ag 2 O/Bi 2 WO 6 microspheres is higher than that of the Ag 2 O/Bi 2 WO 6 nanosheets. This work demonstrates that the Bi 2 WO 6 hierarchical three-dimensional structure is an excellent architecture for the loading of Ag 2 O nanoparticles to build a highly efficient photocatalyst

α-K2AgF4: Ferromagnetism induced by the weak superexchange of different eg orbitals from the nearest neighbor Ag ions

Science.gov (United States)

Zhang, Xiaoli; Zhang, Guoren; Jia, Ting; Zeng, Zhi; Lin, H. Q.

2016-05-01

We study the abnormal ferromagnetism in α-K2AgF4, which is very similar to high-TC parent material La2CuO4 in structure. We find out that the electron correlation is very important in determining the insulating property of α-K2AgF4. The Ag(II) 4d9 in the octahedron crystal field has the t2 g 6 eg 3 electron occupation with eg x2-y2 orbital fully occupied and 3z2-r2 orbital partially occupied. The two eg orbitals are very extended indicating both of them are active in superexchange. Using the Hubbard model combined with Nth-order muffin-tin orbital (NMTO) downfolding technique, it is concluded that the exchange interaction between eg 3z2-r2 and x2-y2 from the first nearest neighbor Ag ions leads to the anomalous ferromagnetism in α-K2AgF4.

α-K2AgF4: Ferromagnetism induced by the weak superexchange of different eg orbitals from the nearest neighbor Ag ions

Directory of Open Access Journals (Sweden)

Xiaoli Zhang

2016-05-01

Full Text Available We study the abnormal ferromagnetism in α-K2AgF4, which is very similar to high-TC parent material La2CuO4 in structure. We find out that the electron correlation is very important in determining the insulating property of α-K2AgF4. The Ag(II 4d9 in the octahedron crystal field has the t 2 g 6 e g 3 electron occupation with eg x2-y2 orbital fully occupied and 3z2-r2 orbital partially occupied. The two eg orbitals are very extended indicating both of them are active in superexchange. Using the Hubbard model combined with Nth-order muffin-tin orbital (NMTO downfolding technique, it is concluded that the exchange interaction between eg 3z2-r2 and x2-y2 from the first nearest neighbor Ag ions leads to the anomalous ferromagnetism in α-K2AgF4.

Core–shell-typed Ag-SiO2 nanoparticles as solar selective coating materials

International Nuclear Information System (INIS)

Gao, Tao; Jelle, Bjørn Petter; Gustavsen, Arild

2013-01-01

Silver (Ag) nanoparticles with typical diameter of about 50 nm have been prepared via a polyol process. The as-prepared Ag nanoparticles are well crystallized and exhibit a characteristic surface plasmon resonance (SPR) band centered at ∼423 nm. The SPR band shows a strong dependence on the sizes of Ag nanoparticles and the types of the dielectric medium. Core–shell-typed Ag-SiO 2 nanoparticles have also been prepared by depositing a thin layer (∼25 nm) of silica on Ag nanoparticles. The core–shell-typed Ag-SiO 2 nanoparticles show similar optical behaviors (absorption, transmission, and reflection) but enhanced stability compared to those of the Ag nanoparticles, indicating that the core–shell-typed Ag-SiO 2 nanoparticles may be used as solar selective coating materials for architectural window applications.

The high-temperature modification of LuAgSn and high-pressure high-temperature experiments on DyAgSn, HoAgSn, and YbAgSn

Energy Technology Data Exchange (ETDEWEB)

Heying, B.; Rodewald, U.C.; Hermes, W.; Schappacher, F.M.; Riecken, J.F.; Poettgen, R. [Muenster Univ. (Germany). Inst. fuer Anorganische und Analytische Chemie; Heymann, G.; Huppertz, H. [Muenchen Univ. (Germany). Dept. fuer Chemie und Biochemie; Sebastian, C.P. [Max-Planck-Institut fuer Chemische Physik Fester Stoffe, Dresden (Germany)

2008-02-15

The high-temperature modification of LuAgSn was obtained by arc-melting an equiatomic mixture of the elements followed by quenching the melt on a water-cooled copper crucible. HT-LuAgSn crystallizes with the NdPtSb-type structure, space group P6{sub 3}mc: a = 463.5(1), c = 723.2(1) pm, wR2 = 0.0270, 151 F{sup 2}, and 11 variables. The silver and tin atoms build up two-dimensional, puckered [Ag{sub 3}Sn{sub 3}] networks (276 pm Ag-Sn) that are charge-balanced and separated by the lutetium atoms. The Ag-Sn distances between the [Ag{sub 3}Sn{sub 3}] layers of 294 pm are much longer. Single crystals of isotypic DyAgSn (a = 468.3(1), c = 734.4(1) pm, wR2 = 0.0343, 411 F{sup 2}, and 11 variables) and HoAgSn (a = 467.2(1), c = 731.7(2) pm, wR2 = 0.0318, 330 F{sup 2}, and 11 variables) were obtained from arc-melted samples. Under high-pressure (up to 12.2 GPa) and high-temperature (up to 1470 K) conditions, no transitions to a ZrNiAl-related phase have been observed for DyAgSn, HoAgSn, and YbAgSn. HT-TmAgSn shows Curie-Weiss paramagnetism with {mu}{sub eff} = 7.53(1) {mu}{sub B}/Tm atom and {theta}P = -15.0(5) K. No magnetic ordering was evident down to 3 K. HT-LuAgSn is a Pauli paramagnet. Room-temperature {sup 119}Sn Moessbauer spectra of HT-TmAgSn and HT-LuAgSn show singlet resonances with isomer shifts of 1.78(1) and 1.72(1) mm/s, respectively. (orig.)

H2O2 rejuvenation-mediated synthesis of stable mixed-morphology Ag3PO4 photocatalysts

Directory of Open Access Journals (Sweden)

Henry Agbe

2018-04-01

Full Text Available Ag3PO4 photocatalyst has attracted interest of the scientific community in recent times due to its reported high efficiency for water oxidation and dye degradation. However, Ag3PO4 photo-corrodes if electron accepter such as AgNO3 is not used as scavenger. Synthesis of efficient Ag3PO4 followed by a simple protocol for regeneration of the photocatalyst is therefore a prerequisite for practical application. Herein, we present a facile method for the synthesis of a highly efficient Ag3PO4, whose photocatalytic efficiency was demonstrated using 3 different organic dyes: Methylene Blue (MB, Methyl orange (MO and Rhodamine B (RhB organic dyes for degradation tests. Approximately, 19 % of Ag3PO4 is converted to Ag0 after 4.30 hours of continuous UV-Vis irradiation in presence of MB organic dye. We have shown that the Ag/Ag3PO4 composite can be rejuvenated by a simple chemical oxidation step after several cycles of photocatalysis tests. At an optimal pH of 6.5, a mixture of cubic, rhombic dodecahedron, nanosphere and nanocrystals morphologies of the photocatalyst was formed. H2O2 served as the chemical oxidant to re-insert the surface metallic Ag into the Ag3PO4 photocatalyst but also as the agent that can control morphology of the regenerated as-prepared photocatalyst without the need for any other morphology controlling Agent (MCA. Surprisingly, the as- regenerated Ag3PO4 was found to have higher photocatalytic reactivity than the freshly made material and superior at least 17 times in comparison with the conventional Degussa TiO2, and some of TiO2 composites tested in this work. Keywords: Materials chemistry, Materials science, Engineering

Enhanced catalyst activity by decorating of Au on Ag@Cu2O nanoshell

Science.gov (United States)

Chen, Lei; Liu, Maomao; Zhao, Yue; Kou, Qiangwei; Wang, Yaxin; Liu, Yang; Zhang, Yongjun; Yang, Jinghai; Jung, Young Mee

2018-03-01

We successfully synthesized Au-decorated Ag@Cu2O heterostructures via a simple galvanic replacement method. As the Au precursor concentration increased, the density of the Au nanoparticles (NPs) on the Ag@Cu2O surface increased, which changed the catalytic activity of the Ag@Cu2O-Au structure. The combination of Au, Ag, and Cu2O exhibited excellent catalytic properties, which can further effect on the catalyst activity of the Ag@Cu2O-Au structure. In addition, the proposed Ag@Cu2O-Au nanocomposite was used to transform the organic, toxic pollutant, 4-nitrophenol (4-NP), into its nontoxic and medicinally important amino derivative via a catalytic reduction to optimize the material performance. The proposed Au-decorated Ag@Cu2O exhibited excellent catalytic activity, and the catalytic reduction time greatly decreased (5 min). Thus, three novel properties of Ag@Cu2O-Au, i.e., charge redistribution and transfer, adsorption, and catalytic reduction of organic pollutants, were ascertained for water remediation. The proposed catalytic properties have potential applications for photocatalysis and localized surface plasmon resonance (LSPR)- and peroxidase-like catalysis.

Photocatalytic properties of nanocrystalline TiO2 thin film with Ag additions

International Nuclear Information System (INIS)

Chang, C.-C.; Lin, C.-K.; Chan, C.-C.; Hsu, C.-S.; Chen, C.-Y.

2006-01-01

In the present study, nanocrystalline TiO 2 /Ag composite thin films were prepared by a sol-gel spin coating technique. While, by introducing polystyrene (PS) microspheres, porous TiO 2 /Ag films were obtained after calcining at a temperature of 500 o C. The as-prepared TiO 2 and TiO 2 /Ag thin films were characterized by X-ray diffractometry, and scanning electron microscopy to reveal the structural and morphological differences. In addition, the photocatalytic properties of these films were investigated by degrading methylene blue under UV irradiation. After 500 o C calcination, the microstructure of PS-TiO 2 film without Ag addition exhibited a sponge-like microstructure while significant sintering effect was noticed with Ag additions and the films exhibited a porous microstructure. Meanwhile, coalescence of nanocrystalline anatase-phase TiO 2 can be observed with respect to the sharpening of XRD diffraction peaks. The photodegradation of porous TiO 2 doped with 1 mol% Ag exhibited the best photocatalytic efficiency where 72% methylene blue can be decomposed after UV exposure for 12 h

Optical and structural properties of TiO2/Ti/Ag/TiO2 and TiO2/ITO/Ag/ITO/TiO2 metal-dielectric multilayers by RF magnetron sputtering for display application

International Nuclear Information System (INIS)

Lee, Jang-Hoon; Lee, Seung-Hyu; Hwangbo, Chang-Kwon; Lee, Kwang-Su

2004-01-01

Electromagnetic-interference (EMI) shielding and near-infrared (NIR) cutoff filters for plasma display panels, based on fundamental structures (ITO/Ag/ITO), (TiO 2 /Ti/Ag/TiO 2 ) and (TiO 2 /ITO/Ag/ITO/TiO 2 ), were designed and prepared by RF-magnetron sputtering. The optical, structural and electrical properties of the filters were investigated by using spectrophotometry, Auger electron spectroscopy, X-ray photoelectron spectroscopy, Rutherford backscattering spectroscopy, atomic force microscopy and four-point-probe measurements. The results show that ITO films as the barriers and base layers lead to higher transmittance in the visible spectrum and smoother surface roughness than Ti metal barriers, while maintaining high NIR cutoff characteristics and chemical stability, which may be attributed to the lower absorption in the interfacial layers and better protection of the Ag layers by the ITO layers.

Microstructure, Mechanical and Tribological Properties of Ag/Bi2Sr2CaCu2O x Self-lubricating Composites

Science.gov (United States)

Tang, Hua; Zhang, Du; Wang, Yuqi; Zhang, Yi; Ji, Xiaorui; Song, Haojie; Li, Changsheng

2014-01-01

Ag/Bi2Sr2CaCu2O x self-lubricating composites were successfully fabricated by a facile powder metallurgy method. The structure and morphology of the as-synthesized composites and the worn surface after tribometer testing are characterized by using X-ray diffraction and scanning electron microscopy together with energy dispersive spectrometry. The results indicated that self-lubricating composites are composed of superconductor phase and Ag phase. Moreover, the effects of Ag on mechanical and tribological properties of the novel composites were investigated. The friction test results showed that the friction coefficient of the pure Bi2212 against stainless steel is about 0.40 at ambient temperature and abruptly decreases to about 0.17 when the temperature is cooled to 77 K. The friction coefficients of the composites from room temperature to high temperature were lower and more stable than those of pure Bi2Sr2CaCu2O x . When the content of Ag is 10 wt.%, the Ag/Bi2Sr2CaCu2O x composites exhibited excellent tribological performance, the improved tribological properties are attributed to the formation of soft metallic Ag films at the contacted zone of the composites.

Analysis of nanostructuring in high figure-of-merit Ag{sub 1-x}Pb{sub m}SbTe{sub 2+m} thermoelectric materials

Energy Technology Data Exchange (ETDEWEB)

Cook, Bruce A; Harringa, Joel L [Materials and Engineering Physics Program, Ames Laboratory, Iowa State University Ames, IA (United States); Kramer, Matthew J [Materials Science and Engineering, Iowa State University Ames, IA (United States); Han, Mi-Kyung [Department of Chemistry, Northwestern University Evanston, IL (United States); Chung, Duck-Young [Material Science Division, Argonne National Laboratory, IL (United States); Kanatzidis, Mercouri G [Department of Chemistry, Northwestern University Evanston, IL (United States); Material Science Division, Argonne National Laboratory, IL (United States)

2009-04-23

Thermoelectric materials based on quaternary compounds Ag{sub 1-x}Pb{sub m}SbTe{sub 2+m} exhibit high dimensionless figure-of-merit values, ranging from 1.5 to 1.7 at 700 K. The primary factor contributing to the high figure of merit is a low lattice thermal conductivity, achieved through nanostructuring during melt solidification. As a consequence of nucleation and growth of a second phase, coherent nanoscale inclusions form throughout the material, which are believed to result in scattering of acoustic phonons while causing only minimal scattering of charge carriers. Here, characterization of the nanosized inclusions in Ag{sub 0.53}Pb{sub 18}Sb{sub 1.2}Te{sub 20} that shows a strong tendency for crystallographic orientation along the {l_brace}001{r_brace} planes, with a high degree of lattice strain at the interface, consistent with a coherent interfacial boundary is reported. The inclusions are enriched in Ag relative to the matrix, and seem to adopt a cubic, 96 atom per unit cell Ag{sub 2}Te phase based on the Ti{sub 2}Ni type structure. In-situ high-temperature synchrotron radiation diffraction studies indicated that the inclusions remain thermally stable to at least 800 K. (Abstract Copyright [2009], Wiley Periodicals, Inc.)

HBsAg d and y subtypes determined by inhibition radio-immunoassay

Energy Technology Data Exchange (ETDEWEB)

Wilkinson, R [Border Blood Transfusion Service, East London (South Africa)

1981-12-01

An inhibition radioimmunoassay for the detection of HBsAg/d and HBsAg/y antigens is described. A survey of 211 asymptomatic HBsAg positive blood donors showed 190 to be of type HBsAg/d and 3 to be of type HBsAg/y, while the remaining 18 could not be typed. Of 43 patients with acute hepatitis 39 were type HBsAg/d and 4 were type HBsAg/y. The statistically significant (p smaller than 0,01) increase in type HBsAg/y may reflect a changing pattern in offending viral strain with the passage of time.

AgCuO2: Preparationand Electrochemical Behaviors in Alkaline Electrolytes%AgCuO2:制备及其在碱性溶液中的电化学行为

Institute of Scientific and Technical Information of China (English)

张婷锦; 张校刚; 胡风平

2005-01-01

The silver cuprate AgCuO2 powder was prepared by a chemical co-precipitation method and characterized by XRD, SEM and TEM techniques. The electrochemical behaviors of AgCuO2 electrodes and AgCuO2 modified by sulfur were studied by means of galvanostatic discharge and line sweep voltammetry experiments. The resuits indicated that the specific capacity of AgCuO2 could reach 422.32 mAh·g-1 at middle discharge rate and the addition of sulfur could significantly improve the discharge performance of AgCuO2. The mechanism for this modified effect was also discussed.

Synthesis of Ag{sub 2}S nanorods by biomimetic method in the lysozyme matrix

Energy Technology Data Exchange (ETDEWEB)

Qin, Dezhi, E-mail: dezhiqin@163.com; Zhang, Li; He, Guoxu; Zhang, Qiuxia

2013-09-01

Graphical abstract: - Highlights: • Firstly, Ag{sub 2}S nanorods were synthesized by biomimetic method in the lysozyme solutions. • The study of the interaction between Ag{sup +} and the lysozyme. • Discussion of possible formation mechanism of Ag{sub 2}S nanorods. • The synthesis process of lyso-conjugated Ag{sub 2}S nanocrystals is facile, effective and environment friendly. - Abstract: Ag{sub 2}S nanorods were successfully synthesized by biomimetic route in the lysozyme solution at physiological temperature and atmospheric pressure. The transmission electron microscopy (TEM) images revealed that the prepared nanorods are uniform and monodisperse with homogeneous size about 50 nm in diameter and 150 nm in length. The optical property of Ag{sub 2}S nanocrystals was studied by the ultraviolet–visible (UV–vis) and photoluminescence (PL) spectroscopy, the results show that the products exhibit well-defined emission at 471 nm and 496 nm excited by 292 nm. The interaction of Ag{sup +}/Ag{sub 2}S with the lysozyme was investigated through Fourier transform infrared (FT-IR) spectroscopy, which shows that the cooperation effect of the lysozyme and Ag{sup +} could be responsible for the formation of as obtained Ag{sub 2}S nanorods.

Selective hydrodechlorination of 1,2-dichloroethane to ethylene over Pd-Ag/Al_2O_3 catalysts prepared by surface reduction

International Nuclear Information System (INIS)

Han, Yuxiang; Gu, Guangfeng; Sun, Jingya; Wang, Wenjuan; Wan, Haiqin; Xu, Zhaoyi; Zheng, Shourong

2015-01-01

Graphical abstract: - Highlights: • Surface reduction method was used for preparation of Pd-Ag(Cu) bimetallic catalysts. • Hydrodechlorination of 1,2-dichloroethane was investigated for production of ethylene. • Ag(Cu) selectively deposited on Pd surface during surface reduction process. • Ethylene selectivity was enhanced over Pd-Ag(Cu)/Al_2O_3 catalyst prepared by surface reduction. • Isolated Pd site is the key species for ethylene selectivity. - Abstract: Alumina supported Pd-Ag and (Cu) bimetallic catalysts (denoted as sr-Pd-Ag/Al_2O_3 or sr-Pd-Cu/Al_2O_3) with varied Pd/Ag (or Cu) ratios were prepared using the surface reduction method, and the gas-phase catalytic hydrodechlorination of 1,2-dichloroethane over the catalysts were investigated. For comparison, Pd-Ag bimetallic catalysts were prepared by the conventional co-impregnation method (denoted as im-Pd-Ag/Al_2O_3). The catalysts were characterized by N_2 adsorption, X-ray diffraction, transmission electron microscopy, X-ray photoelectron spectroscopy, and CO chemisorption. Characterization results indicated that surface reduction led to selective deposition of metallic Ag on the surface of Pd particles, while Pd and Ag just disorderly mixed in the catalyst prepared by impregnation method. Therefore, sr-Pd-Ag/Al_2O_3 exhibited a higher ethylene selectivity than im-Pd-Ag/Al_2O_3 for hydrodechlorination of 1,2-dichloroethane at a similar Ag loading amount. Moreover, among sr-Pd-Ag/Al_2O_3, sr-Pd-Cu/Al_2O_3 and im-Pd-Ag/Al_2O_3 catalysts, the ethylene selectivity decreased over these catalysts following the order: sr-Pd-Ag/Al_2O_3 > sr-Pd-Cu/Al_2O_3 > im-Pd-Ag/Al_2O_3. The present results indicate that surface reduction can be used as a potential method to synthesize catalyst with enhanced ethylene selectivity in hydrodechlorination of 1,2-dichloroethane.

Prion Strain Characterization of a Novel Subtype of Creutzfeldt-Jakob Disease.

Science.gov (United States)

Galeno, Roberta; Di Bari, Michele Angelo; Nonno, Romolo; Cardone, Franco; Sbriccoli, Marco; Graziano, Silvia; Ingrosso, Loredana; Fiorini, Michele; Valanzano, Angelina; Pasini, Giulia; Poleggi, Anna; Vinci, Ramona; Ladogana, Anna; Puopolo, Maria; Monaco, Salvatore; Agrimi, Umberto; Zanusso, Gianluigi; Pocchiari, Maurizio

2017-06-01

In 2007, we reported a patient with an atypical form of Creutzfeldt-Jakob disease (CJD) heterozygous for methionine-valine (MV) at codon 129 who showed a novel pathological prion protein (PrP TSE ) conformation with an atypical glycoform (AG) profile and intraneuronal PrP deposition. In the present study, we further characterize the conformational properties of this pathological prion protein (PrP TSE MV AG ), showing that PrP TSE MV AG is composed of multiple conformers with biochemical properties distinct from those of PrP TSE type 1 and type 2 of MV sporadic CJD (sCJD). Experimental transmission of CJD-MV AG to bank voles and gene-targeted transgenic mice carrying the human prion protein gene (TgHu mice) showed unique transmission rates, survival times, neuropathological changes, PrP TSE deposition patterns, and PrP TSE glycotypes that are distinct from those of sCJD-MV1 and sCJD-MV2. These biochemical and experimental data suggest the presence of a novel prion strain in CJD-MV AG IMPORTANCE Sporadic Creutzfeldt-Jakob disease is caused by the misfolding of the cellular prion protein, which assumes two different major conformations (type 1 and type 2) and, together with the methionine/valine polymorphic codon 129 of the prion protein gene, contribute to the occurrence of distinct clinical-pathological phenotypes. Inoculation in laboratory rodents of brain tissues from the six possible combinations of pathological prion protein types with codon 129 genotypes results in the identification of 3 or 4 strains of prions. We report on the identification of a novel strain of Creutzfeldt-Jakob disease isolated from a patient who carried an abnormally glycosylated pathological prion protein. This novel strain has unique biochemical characteristics, does not transmit to humanized transgenic mice, and shows exclusive transmission properties in bank voles. The identification of a novel human prion strain improves our understanding of the pathogenesis of the disease and of

A study on the resistance switching of Ag2Se and Ta2O5 heterojunctions using structural engineering

Science.gov (United States)

Lee, Tae Sung; Lee, Nam Joo; Abbas, Haider; Hu, Quanli; Yoon, Tae-Sik; Lee, Hyun Ho; Le Shim, Ee; Kang, Chi Jung

2018-01-01

The resistive random access memory (RRAM) devices with heterostuctures have been investigated due to cycling stability, nonlinear switching, complementary resistive switching and self-compliance. The heterostructured devices can modulate the resistive switching (RS) behavior appropriately by bilayer structure with a variety of materials. In this study, the bipolar resistive switching characteristics of the bilayer structures composed of Ta2O5 and Ag2Se, which are transition-metal oxide (TMO) and silver chalcogenide, were investigated. The bilayer devices of Ta2O5 deposited on Ag2Se (Ta2O5/Ag2Se) and Ag2Se deposited on Ta2O5 (Ag2Se/Ta2O5) were fabricated for investigation of the RS characteristics by stacking sequence of Ta2O5 and Ag2Se. All operating voltages were applied to the Ag top electrode with the Pt bottom electrode grounded. The Ta2O5/Ag2Se device showed that a negative voltage sweep switched the device from high resistance state (HRS) to low resistance state (LRS) and a positive voltage sweep switched the device from LRS to HRS. On the contrary, for the Ag2Se/Ta2O5 device a positive voltage sweep switched the device from HRS to LRS, and a negative voltage sweep switched it from LRS to HRS. The polarity dependence of RS was attributed to the stacking sequence of Ta2O5 and Ag2Se. In addition, the combined heterostructured device of both bilayer stacks, Ta2O5/Ag2Se and Ag2Se/Ta2O5, exhibited the complementary switching characteristics. By using threshold switching devices, sneak path leakage can be reduced without additional selectors. The bilayer heterostructures of Ta2O5 and Ag2Se have various advantages such as self-compliance, reproducibility and forming-free stable RS. It confirms the possible applications of TMO and silver chalcogenide heterostructures in RRAM.

Antimicrobial activity and biocompatibility of Ag+- and Cu2+-doped biphasic hydroxyapatite/α-tricalcium phosphate obtained from hydrothermally synthesized Ag+- and Cu2+-doped hydroxyapatite

International Nuclear Information System (INIS)

Radovanović, Željko; Jokić, Bojan; Veljović, Djordje; Dimitrijević, Suzana; Kojić, Vesna; Petrović, Rada; Janaćković, Djordje

2014-01-01

Hydroxyapatite (HAp) powders doped with Ag + or Cu 2+ were synthesized by a hydrothermal method in order to obtain biomaterial with an antimicrobial effect. The synthesis was performed with two contents of dopant (Ag + or Cu 2+ ) by considering both the antimicrobial activities and biocompatibility of the powders. The doped HAp was annealed at 1200 °C for 2 h with the intention of investigating the influence of doping with Ag + and Cu 2+ on the creation of the biphasic HAp/α-tricalcium phosphate (HAp/α-TCP) and determining the antimicrobial activity and biocompatibility of the obtained biphasic powders. Analyses of all powders, undoped and doped HAp and HAp/α-TCP, were performed by Field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), atomic absorption spectroscopy (AAS) and energy-dispersive X-ray spectroscopy (EDS). The in vitro antibacterial activities of the powders were evaluated against: Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa and Candida albicans. All powders showed good antimicrobial activity but generally the powders of doped HAp/α-TCP had more uniform results against all pathogenic microorganisms than the powders of doped HAp. In vitro biocompatibility tests, MTT and DET, were used to evaluate the biocompatibility of Ag + - and Cu 2+ -doped HAp/α-TCP with MRC-5 human fibroblast cells. These tests confirmed that powders do not have a cytotoxic effect. The HAp/α-TCP powders doped with the lower content of Ag + and Cu 2+ showed especially good biocompatibility. Antimicrobial and biocompatibility tests recommend the Ag + - and Cu 2+ -doped HAp/α-TCP as promising material for use in reconstructive surgery of bone.

Quantum dot sensitized solar cell based on TiO2/CdS/Ag2S heterostructure

Science.gov (United States)

Pawar, Sachin A.; Patil, Dipali S.; Kim, Jin Hyeok; Patil, Pramod S.; Shin, Jae Cheol

2017-04-01

Quantum dot sensitized solar cell (QDSSC) is fabricated based on a stepwise band structure of TiO2/CdS/Ag2S to improve the photoconversion efficiency of TiO2/CdS system by incorporating a low band gap Ag2S QDs. Vertically aligned TiO2 nanorods assembly is prepared by a simple hydrothermal technique. The formation of CdS and Ag2S QDs over TiO2 nanorods assembly as a photoanode is carried out by successive ionic layer adsorption and reaction (SILAR) technique. The synthesized electrode materials are characterized by XRD, XPS, field emission scanning electron microscopy (FE-SEM), Optical, solar cell and electrochemical performances. The results designate that the QDs of CdS and Ag2S have efficiently covered exterior surfaces of TiO2 nanorods assembly. A cautious evaluation between TiO2/CdS and TiO2/CdS/Ag2S sensitized cells tells that CdS and Ag2S synergetically helps to enhance the light harvesting ability. Under AM 1.5G illumination, the photoanodes show an improved power conversion efficiency of 1.87%, in an aqueous polysulfide electrolyte with short-circuit photocurrent density of 7.03 mA cm-2 which is four fold higher than that of a TiO2/CdS system.

H2 assisted NH3-SCR over Ag/Al2O3 for automotive applications

DEFF Research Database (Denmark)

Fogel, Sebastian

-BEA can give a high NOx conversion in a broad temperature window without the need to dose H2 at higher temperatures. The aim of this study has been to investigate the combined Ag/Al2O3 and Fe-BEA catalyst system both at laboratory-scale and in full-scale enginebench testing. The catalysts were combined...... both in a sequential dual-bed layout and a dual-layer layout where the catalysts were coated on top of each other. The Ag/Al2O3 catalyst was also investigated with the aim of improving the sulphur tolerance and low-temperature activity by testing different alumina-supports. A large focus of this study...... the layers allowing diffusion of reaction intermediates between them. Ag/Al2O3 only and the combined Ag/Al2O3 – Fe-BEA systems were active during the transient NEDC. The NOx conversions were not very high which is related to the very low temperature of the NEDC and the lower than expected activity of the Ag...

Exploring the Optical and Morphological Properties of Ag and Ag/TiO2 Nanocomposites Grown by Supersonic Cluster Beam Deposition

Directory of Open Access Journals (Sweden)

Emanuele Cavaliere

2017-12-01

Full Text Available Nanocomposite systems and nanoparticle (NP films are crucial for many applications and research fields. The structure-properties correlation raises complex questions due to the collective structure of these systems, often granular and porous, a crucial factor impacting their effectiveness and performance. In this framework, we investigate the optical and morphological properties of Ag nanoparticles (NPs films and of Ag NPs/TiO2 porous matrix films, one-step grown by supersonic cluster beam deposition. Morphology and structure of the Ag NPs film and of the Ag/TiO2 (Ag/Ti 50-50 nanocomposite are related to the optical properties of the film employing spectroscopic ellipsometry (SE. We employ a simple Bruggeman effective medium approximation model, corrected by finite size effects of the nano-objects in the film structure to gather information on the structure and morphology of the nanocomposites, in particular porosity and average NPs size for the Ag/TiO2 NP film. Our results suggest that SE is a simple, quick and effective method to measure porosity of nanoscale films and systems, where standard methods for measuring pore sizes might not be applicable.

Ag/Pd core-shell nanoparticles by a successive method: Pulsed laser ablation of Ag in water and reduction reaction of PdCl{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Mottaghi, N. [Department of Physics, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of); Ranjbar, M., E-mail: ranjbar@cc.iut.ac.ir [Department of Physics, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of); Farrokhpour, H. [Department of Chemistry, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of); Khoshouei, M. [Max Planck Institute of Biochemistry, Department of Molecular Structural Biology, Am Klopferspitz 18, Martinsried 82152 (Germany); Khoshouei, A.; Kameli, P.; Salamati, H. [Department of Physics, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of); Tabrizchi, M. [Department of Chemistry, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of); Jalilian-Nosrati, M. [Physics department, Central Azad University, Tehran 14676-86831 (Iran, Islamic Republic of)

2014-02-15

In this study Ag/Pd nanoparticles (NPs) have been fabricated by a successive method; first, colloids of Ag nanoparticles (NPs) have been prepared in water by pulsed laser ablation in liquid (PLAL) method. Then PdCl{sub 2} solution (up to 0.2 g/l) were added to the as-prepared or aged colloidal Ag NPs. Characterizations were done using UV–vis spectroscopy, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and transmissions electron microscopy (TEM) techniques. Spectroscopy data showed that surface plasmon resonance (SPR) peaks of as-prepared Ag NPs at about λ = 400 nm were completely extinguished after addition of PdCl{sub 2} solution while this effect was not observed when aged Ag NPs are used. XRD and XPS results revealed that by addition of the PdCl{sub 2} solution into the as-prepared Ag NPs, metallic palladium, and silver chloride composition products are generated. TEM images revealed that as a result of this reaction, single and core-shell nanoparticles are obtained and their average sizes are 2.4 nm (Ag) and 3.2 nm (Ag/Pd). The calculated d-spacing values form XRD data with observations on high magnification TEM images were able to explain the chemical nature of different parts of Ag/Pd NPs.

Photocatalytic activity and interfacial carrier transfer of Ag-TiO2 nanoparticle films

International Nuclear Information System (INIS)

Xin Baifu; Ren Zhiyu; Hu Haiyuan; Zhang Xiangyu; Dong Chunlei; Shi Keying; Jing Liqiang; Fu Honggang

2005-01-01

The electrodes of Ag-TiO 2 with different Ag content are prepared by a modified sol-gel method. The photochemical properties of Ag-TiO 2 with different Ag content are characterized by surface photovoltage spectroscopy (SPS). The results show that the SPS intensity decreased with increasing Ag contents. This demonstrates that the doping Ag plays the roles trapping photoinduced electrons, which inhibiting the recombination of photoinduced electrons and holes. The photoelectrochemical properties of Ag-TiO 2 electrodes with different Ag content are performed by electrochemical impedance spectroscopy (EIS) under high-pressure mercury lamp (160 W) illuminating, and photocatalytic degradation of RhB are studied at the same time. The experimental results indicate that the process of charge transfer is a controlled-step of photocatalytic reaction. The SPS intensity and the electrical impedance values of EIS equivalent circuits are contrary to photocatalytic degradation ratio of RhB

Mechanism and experimental study on the photocatalytic performance of Ag/AgCl @ chiral TiO{sub 2} nanofibers photocatalyst: The impact of wastewater components

Energy Technology Data Exchange (ETDEWEB)

Wang, Dawei [Key Laboratory of Integrated Regulation and Resource Development of Shallow Lakes, Ministry of Education, College of Environment, Hohai University. Xi Kang Road #1, Nanjing 210098 (China); Li, Yi, E-mail: envly@hhu.edu.cn [Key Laboratory of Integrated Regulation and Resource Development of Shallow Lakes, Ministry of Education, College of Environment, Hohai University. Xi Kang Road #1, Nanjing 210098 (China); Li Puma, Gianluca [Environmental Nanocatalysis & Photoreaction Engineering, Department of Chemical Engineering, Loughborough University, Loughborough LE11 3TU (United Kingdom); Wang, Chao; Wang, Peifang; Zhang, Wenlong; Wang, Qing [Key Laboratory of Integrated Regulation and Resource Development of Shallow Lakes, Ministry of Education, College of Environment, Hohai University. Xi Kang Road #1, Nanjing 210098 (China)

2015-03-21

Highlights: • The effect of wastewater matrix on Ag/AgCl based nanomaterials was investigated. • DOM acted as a reactive oxygen species scavenger. • Cl{sup −} could accelerate the transformation from Ag to AgCl. • A relative rate technique was used to quantify these components impacts. - Abstract: The effect of the water matrix components of a secondary effluent of a urban wastewater treatment plant on the photocatalytic activity of Ag/AgCl @ chiral TiO{sub 2} nanofibers and the undergoing reaction mechanisms were investigated. These effects were evaluated through the water components-induced changes on the net rate of hydroxyl radical (·OH) generation and modeled using a relative rate technique. Dissolved organic matter DOM (k = −2.8 × 10{sup 8} M{sup −1} s{sup −1}) scavenged reactive oxygen species, Cl{sup −} (k = −5.3 × 10{sup 8} M{sup −1} s{sup −1}) accelerated the transformation from Ag to AgCl (which is not photocatalytically active under visible-light irradiation), while Ca{sup 2+} at concentrations higher than 50 mM (k = −1.3 × 10{sup 9} M{sup −1} s{sup −1}) induced aggregation of Ag/AgCl and thus all of them revealed inhibitory effects. In contrast, NO{sub 3}{sup −} (k = 6.9 × 10{sup 8} M{sup −1} s{sup −1}) and CO{sub 3}{sup 2−} (k = 3.7 × 10{sup 8} M{sup −1} s{sup −1}) improved the photocatalytic activity of Ag/AgCl slightly by improving the rate of HO· generation. Other ubiquitous secondary effluent components including SO{sub 4}{sup 2−} (k = 3.9 × 10{sup 5} M{sup −1} s{sup −1}), NH{sub 3}{sup +} (k = 3.5 × 10{sup 5} M{sup −1} s{sup −1}) and Na{sup +} (k = 2.6 × 10{sup 4} M{sup −1} s{sup −1}) had negligible effects. 90% of 17-α-ethynylestradiol (EE2) spiked in the secondary effluent was removed within 12 min, while the structure and size of Ag/AgCl @ chiral TiO{sub 2} nanofibers remained stable. This work may be helpful not only to uncover the photocatalytic mechanism of Ag/AgCl based

Effect of rare earth Ce on the fatigue life of SnAgCu solder joints in WLCSP device using FEM and experiments

International Nuclear Information System (INIS)

Zhang, Liang; Han, Ji-guang; Guo, Yong-huan; He, Cheng-wen

2014-01-01

With the addition of 0.03 wt% rare earth Ce, in our previous works, the properties of SnAgCu solder were enhanced obviously. Based on the Garofalo–Arrhenius creep constitutive model, finite element method was used to simulate the stress–strain response during thermal cycle loading, and combined with the fatigue life prediction models, the fatigue life of SnAgCu/SnAgCuCe solder joints was calculated respectively, which can demonstrate the effect of the rare earth Ce on the fatigue life of SnAgCu solder joints. The results indicated that the maximum stress–strain can be found on the top surface of the corner solder joint, and the warpage of the PCB substrate occurred during thermal cycle loading. The trends obtained from modeling results have a good agreement with the experimental data reported in the literature for WLCSP devices. In addition, the stress–strain of SnAgCuCe solder joints is lower than that of SnAgCu solder joints. The thermal fatigue lives of solder joints calculated based on the creep model and creep strain energy density model show that the fatigue life of SnAgCuCe solder joints is higher than the SnAgCu solder joints. The fatigue life of SnAgCuCe solder joints can be enhanced significantly with the addition of Ce, is 30.2% higher than that of SnAgCu solder joints, which can be attributed to the CeSn 3 particles formed resisting the motion of dislocation; moreover, the refinement of microstructure and the IMC sizes also contribute to the enhancement of fatigue life, which elucidates that SnAgCuCe solder can be utilized in electronic industry with high reliability replacing the SnAgCu solder

An approach for scalable production of silver (Ag) decorated WS2 nanosheets

Science.gov (United States)

Sumesh, C. K.; Kapatel, Sanni; Chaudhari, Arti

2018-05-01

In the Present study we report the synthesis of Ag nanoparticles (NPs) decorated WS2 nanosheets by sonochemical exfoliation followed by simple chemical reduction process at room temperature. The morphology and microstructure of the as-synthesized Ag-WS2 nanocomposite were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) and optical absorption (UV-Vis.) spectroscopy. X-ray and TEM analysis shows the presence of Ag with significant peak over 38.08°, 44.22°, 64.37° and 77.33° at 2θ angle for (111), (200), (220) and (311) respectively. The Ag nanoparticles are randomly distributed throughout the surface of the WS2 nanosheets without undergoing further oxidation during the formation of composites. The formation of Ag-WS2 nanocomposites shows a clear blue shift in the absorption as we obtained the characteristics absorption valleys at 456, 536 and 631 nm from the UV Vis spectroscopy analysis compared to pure WS2 nanosheets. Henceforth a facile method for the Ag decoration on WS2 nanosheets was put forward and briefly discussed. The proposed synthesis method is very promising for the low cost and large-scale synthesis of other noble metal incorporation TMDC compounds.

Ag/SiO2 surface-enhanced Raman scattering substrate for plasticizer detection

Science.gov (United States)

Wu, Ming-Chung; Lin, Ming-Pin; Lin, Ting-Han; Su, Wei-Fang

2018-04-01

In this study, we demonstrated a simple method of fabricating a high-performance surface-enhanced Raman scattering (SERS) substrate. Monodispersive SiO2 colloidal spheres were self-assembled on a silicon wafer, and then a silver layer was coated on it to obtain a Ag/SiO2 SERS substrate. The Ag/SiO2 SERS substrates were used to detect three kinds of plasticizer with different concentrations, namely, including bis(2-ethylhexyl)phthalate (DEHP), benzyl butyl phthalate (BBP), and dibutyl phthalate (DBP). The enhancement of Raman scattering intensity caused by surface plasmon resonance can be observed using the Ag/SiO2 SERS substrates. The Ag/SiO2 SERS substrate with a 150-nm-thick silver layer can detect plasticizers, and it satisfies the detection limit of plasticizers at 100 ppm. The developed highly sensitive Ag/SiO2 SERS substrates show a potential for the design and fabrication of functional sensors to identify the harmful plasticizers that plastic products release in daily life.

A simple solution-phase approach to synthesize high quality ternary AgInSe2 and band gap tunable quaternary AgIn(S1-xSe x)2 nanocrystals

KAUST Repository

Bai, Tianyu

2014-01-01

A facile solution-phase route for the preparation of AgInSe2 nanocrystals was developed by using silver nitrate, indium stearate, and oleylamine-selenium (OAm-Se) as precursors. The evolution process of the AgInSe2 nanocrystals is discussed in detail and different reaction conditions all have a great impact on the growth and morphology of the nanocrystals. Alloyed AgIn(S1-xSex)2 nanocrystals with controlled composition across the entire range (0 ≤ x ≤ 1) was also successfully prepared by modulating the S/Se reactant mole ratio. X-ray diffraction (XRD), energy dispersive X-ray (EDX), X-ray photoelectron spectroscopy (XPS) and transmission electron microscopy (TEM) were used to confirm that the alloyed AgIn(S1-xSex)2 nanocrystals are homogeneous. The UV-vis absorption spectra revealed that the band gap energies of the alloyed AgIn(S1-xSex)2 nanocrystals could be continuously tuned by increasing the Se content. © The Royal Society of Chemistry 2014.

Crystal structure of (μ5-decahydro-closo-decaborato) (μ2-O-dimethylformamide)disilver(I) [Ag2(B10H10)(DMF)

International Nuclear Information System (INIS)

Polyakova, I. N.; Malinina, E. A.; Drozdova, V. V.; Kuznetsov, N. T.

2008-01-01

The compound [Ag 2 (B 10 H 10 )(DMF)] is synthesized, and its crystal structure is studied (R = 0.0699 for 2836 observed reflections). The coordination number of each of the four independent Ag atoms is 4 + 2. The nearest environment of the Ag(1) and Ag(4) atoms consists of two O atoms of the DMF molecules and two BH groups, and that of the Ag(2) and Ag(3) atoms consists of four BH groups. All the Ag atoms additionally form weak bonds with two BH groups. The Ag-O and Ag-B bonds lie in the ranges 2.319-2.465(9) and 2.46-2.70(1) A, respectively, and the Ag-B distances are 2.89-3.25(1) A. Due to the binding of each polyhedral anion to five Ag atoms, layers are formed. Bridging DMF molecules link layers into the three-dimensional framework

Conductance switching in Ag{sub 2}S devices fabricated by in situ sulfurization

Energy Technology Data Exchange (ETDEWEB)

Morales-Masis, M; Molen, S J van der; Hesselberth, M B; Ruitenbeek, J M van [Kamerlingh Onnes Laboratorium, Universiteit Leiden, PO Box 9504, 2300 RA Leiden (Netherlands); Fu, W T [Leiden Institute of Chemistry, Gorlaeus Laboratorium, Universiteit Leiden, PO Box 9502, 2300 RA Leiden (Netherlands)], E-mail: ruitenbeek@physics.leidenuniv.nl

2009-03-04

We report a simple and reproducible method to fabricate switchable Ag{sub 2}S devices. The {alpha}-Ag{sub 2}S thin films are produced by a sulfurization process after silver deposition on an Si substrate. Structure and composition of the Ag{sub 2}S are characterized using XRD and RBS. Our samples show semiconductor behaviour at low bias voltages, whereas they exhibit reproducible bipolar resistance switching at higher bias voltages. The transition between both types of behaviour is observed by hysteresis in the I-V curves, indicating decomposition of the Ag{sub 2}S, increasing the Ag{sup +} ion mobility. The as-fabricated Ag{sub 2}S samples are a good candidate for future solid state memory devices, as they show reproducible memory resistive properties and they are fabricated by an accessible and reliable method.

Broadband absorption and enhanced photothermal conversion property of octopod-like Ag@Ag2S core@shell structures with gradually varying shell thickness.

Science.gov (United States)

Jiang, Qian; Zeng, Wenxia; Zhang, Canying; Meng, Zhaoguo; Wu, Jiawei; Zhu, Qunzhi; Wu, Daxiong; Zhu, Haitao

2017-12-19

Photothermal conversion materials have promising applications in many fields and therefore they have attracted tremendous attention. However, the multi-functionalization of a single nanostructure to meet the requirements of multiple photothermal applications is still a challenge. The difficulty is that most nanostructures have specific absoprtion band and are not flexible to different demands. In the current work, we reported the synthesis and multi-band photothermal conversion of Ag@Ag 2 S core@shell structures with gradually varying shell thickness. We synthesized the core@shell structures through the sulfidation of Ag nanocubes by taking the advantage of their spatially different reactivity. The resulting core@shell structures show an octopod-like mopgorlogy with a Ag 2 S bulge sitting at each corner of the Ag nanocubes. The thickness of the Ag 2 S shell gradually increases from the central surface towards the corners of the structure. The synthesized core@shell structures show a broad band absorption spectrum from 300 to 1100 nm. Enhanced photothermal conversion effect is observed under the illuminations of 635, 808, and 1064 nm lasers. The results indicate that the octopod-like Ag@Ag 2 S core@shell structures have characteristics of multi-band photothermal conversion. The current work might provide a guidance for the design and synthesis of multifunctional photothermal conversion materials.

Thermodynamic assessments of the Ag-Gd and Ag-Nd systems

International Nuclear Information System (INIS)

Wang, S.L.; Wang, C.P.; Liu, X.J.; Ishida, K.

2009-01-01

The phase diagrams and thermodynamic properties in the Ag-Re (Re: Gd, Nd) binary systems have been assessed by using the CALPHAD (Calculation of Phase Diagrams) method on the basis of the experimental data including the thermodynamic properties and phase equilibria. The Gibbs free energies of the liquid, bcc, fcc, dhcp and hcp phases were described by the subregular solution model with the Redlich-Kister equation, and those of the intermetallic compounds (Ag 51 Gd 14 , Ag 2 Gd, AgGd, Ag 51 Nd 14 , αAg 2 Nd, βAg 2 Nd and AgNd phases) in these two binary systems were described by the sublattice model. The thermodynamic parameters of each phase in the Ag-Re (Re: Gd, Nd) binary systems were obtained, and an agreement between the calculated results and experimental data was obtained in each binary system.

Effects of low-level Ag doping on Bi2Sr2CaCu2O8+x

International Nuclear Information System (INIS)

Deis, T.A.; Eror, N.G.; Krishnaraj, P.; Prorok, B.C.; Lelovic, M.; Balachandran, U.

1995-07-01

Bi 2 Sr 2 CaCu 2 O 8 has been doped with silver, up to 10,000 ppm, in three ways: excess additions, substitution of Ag for Bi, and substitution of Ag for Sr. Effects of doping on the c-axis lattice parameter and critical temperature (T c ) were measured. Effects from doing were only observed in slow-cooled [10 degree/hr] oxygen equilibrated samples. Doping by excess additions caused a small decrease in T c and an increase in the c-axis length of the lattice. Doping by substitution, compared to excess Ag additions, caused a larger decrease in T c and higher c-axis values for doping levels up to 1,000 ppm. Doping by substitution at higher levels (1,000--10,000 ppm) caused T c to increase and the c-axis to decrease. Samples with similar substitutional doping levels exhibited comparable T c values and samples with Ag substituted for Sr consistently exhibited higher c-axis values than samples that had equivalent amounts of Ag substituted for Bi

Optically stimulated luminescence (OSL) from Ag-doped Li2B4O7 crystals

International Nuclear Information System (INIS)

Kananen, B.E.; Maniego, E.S.; Golden, E.M.; Giles, N.C.; McClory, J.W.; Adamiv, V.T.; Burak, Ya.V.; Halliburton, L.E.

2016-01-01

Optically stimulated luminescence (CW-OSL) is observed from Ag-doped lithium tetraborate (Li 2 B 4 O 7 ) crystals. Photoluminescence, optical absorption, and electron paramagnetic resonance (EPR) are used to identify the defects participating in the OSL process. As-grown crystals have Ag + ions substituting for Li + ions. They also have Ag + ions occupying interstitial sites. During a room-temperature exposure to ionizing radiation, holes are trapped at the Ag + ions that replace Li + ions and electrons are trapped at the interstitial Ag + ions, i.e., the radiation forms Ag 2+ (4d 9 ) ions and Ag 0 (4d 10 5s 1 ) atoms. These Ag 2+ and Ag 0 centers have characteristic EPR spectra. The Ag 0 centers also have a broad optical absorption band peaking near 370 nm. An OSL response is observed when the stimulation wavelength overlaps this absorption band. Specifically, stimulation with 400 nm light produces an intense OSL response when emission is monitored near 270 nm. Electrons optically released from the Ag 0 centers recombine with holes trapped at Ag 2+ ions to produce the ultraviolet emission. The OSL response is progressively smaller as the stimulation light is moved to longer wavelengths (i.e., away from the 370 nm peak of the absorption band of the Ag 0 electron traps). Oxygen vacancies are also present in the Ag-doped Li 2 B 4 O 7 crystals, and their role in the OSL process as a secondary relatively short-lived electron trap is described.

Evolution of local structure in Ag2O-TeO2 glasses with addition of Ag2O analyzed by pulsed neutron diffraction and Raman spectroscopy

International Nuclear Information System (INIS)

Iwadate, Yasuhiko; Suzuki, Mineta; Hattori, Takeo; Fukushima, Kazuko; Nishiyama, Shin; Misawa, Masakatsu; Fukunaga, Toshiharu; Itoh, Keiji

2005-01-01

The local structure of Ag 2 O-TeO 2 glasses was studied by time-of-flight pulsed neutron diffraction (TOF-PND) and Raman spectroscopy. The results of Raman spectroscopy indicated that TeO 4 trigonal bipyramidal units (tbp) were converted to TeO 3 trigonal pyramidal units (tp) by addition of Ag 2 O to TeO 2 . Furthermore in PND, the structural parameters for each atomic pair were optimized in the Q-space, and the distances of the near neighbor Te-O correlations forming tbp units and tp units in the network were estimated with some accuracy

Creep Behavior of a Sn-Ag-Bi Pb-Free Solder

Science.gov (United States)

Vianco, Paul; Rejent, Jerome; Grazier, Mark; Kilgo, Alice

2012-01-01

Compression creep tests were performed on the ternary 91.84Sn-3.33Ag-4.83Bi (wt.%, abbreviated Sn-Ag-Bi) Pb-free alloy. The test temperatures were: −25 °C, 25 °C, 75 °C, 125 °C, and 160 °C (± 0.5 °C). Four loads were used at the two lowest temperatures and five at the higher temperatures. The specimens were tested in the as-fabricated condition or after having been subjected to one of two air aging conditions: 24 hours at either 125 °C or 150 °C. The strain-time curves exhibited frequent occurrences of negative creep and small-scale fluctuations, particularly at the slower strain rates, that were indicative of dynamic recrystallization (DRX) activity. The source of tertiary creep behavior at faster strain rates was likely to also be DRX rather than a damage accumulation mechanism. Overall, the strain-time curves did not display a consistent trend that could be directly attributed to the aging condition. The sinh law equation satisfactorily represented the minimum strain rate as a function of stress and temperature so as to investigate the deformation rate kinetics: dε/dtmin = Asinhn (ασ) exp (−ΔH/RT). The values of α, n, and ΔH were in the following ranges (±95% confidence interval): α, 0.010–0.015 (±0.005 1/MPa); n, 2.2–3.1 (±0.5); and ΔH, 54–66 (±8 kJ/mol). The rate kinetics analysis indicated that short-circuit diffusion was a contributing mechanism to dislocation motion during creep. The rate kinetics analysis also determined that a minimum creep rate trend could not be developed between the as-fabricated versus aged conditions. This study showed that the elevated temperature aging treatments introduced multiple changes to the Sn-Ag-Bi microstructure that did not result in a simple loss (“softening”) of its mechanical strength.

Real-time pcr (qpcr) assay for rhizoctonia solani anastomoses group ag2-2 iiib

International Nuclear Information System (INIS)

Abbas, S.J.; Ahmad, B.

2014-01-01

Rhizoctonia solani anastomosis group AG2-2 IIIB is a severe sugar beet and maize pathogen. It causes crown and root rot disease which leads to yield losses world-wide. The soil-borne pathogen is difficult to detect and quantify by conventional methods. We developed a real-time PCR (qPCR) assay for the quantification of genomic DNA of Rhizoctonia solani AG2-2 IIIB based on the ITS region of rDNA genes. The limit of quantification of the assay is 1.8 pg genomic DNA. The amplification efficiency was 96.4. The assay will be helpful in the diagnoses of Rhizoctonia solani infection of sugar beet and maize roots and in the quantification of R. solani AG2-2 IIIB inoculum in plant debris and soil. (author)

Construction of Ag/AgCl nanostructures from Ag nanoparticles as high-performance visible-light photocatalysts

Energy Technology Data Exchange (ETDEWEB)

Yang, Fan; Liu, Dongzhi; Wang, Tianyang; Li, Wei [Tianjin University, School of Chemical Engineering and Technology (China); Hu, Wenping [Tianjin University, Collaborative Innovation Center of Chemical Science and Engineering (China); Zhou, Xueqin, E-mail: zhouxueqin@tju.edu.cn [Tianjin University, School of Chemical Engineering and Technology (China)

2016-11-15

A combined strategy of in situ oxidation and assembly is developed to prepare Ag/AgCl nanospheres and nanocubes from Ag nanoparticles under room temperature. It is a new facile way to fabricate Ag/AgCl with small sizes and defined morphologies. Ag/AgCl nanospheres with an average size of 80 nm were achieved without any surfactants, while Ag/AgCl nanocubes with a mean edge length of 150 nm were obtained by introduction of N-dodecyl-N,N-dimethyl-2-ammonio-acetate. The possible formation mechanism involves the self-assembly of AgCl nanoparticles, Ostwald ripening and photoreduction of Ag{sup +} into Ag{sup 0} by the room light. The as-prepared Ag/AgCl nanospheres and nanocubes exhibit excellent photocatalytic activity and stability toward degradation of organic pollutants under visible-light irradiation. It is demonstrated that Ag/AgCl nanocubes display enhanced photocatalytic activity in comparison with Ag/AgCl nanospheres due to the more efficient charge transfer. This work may pave an avenue to construct various functional materials via the assembly strategy using nanoparticles as versatile building blocks.

Enhanced photodegradation activity of methyl orange over Ag2CrO4/SnS2 composites under visible light irradiation

International Nuclear Information System (INIS)

Luo, Jin; Zhou, Xiaosong; Ma, Lin; Xu, Xuyao; Wu, Jingxia; Liang, Huiping

2016-01-01

Highlights: • Novel visible-light-driven Ag 2 CrO 4 /SnS 2 composites are synthesized. • Ag 2 CrO 4 /SnS 2 exhibits higher photocatalytic activity than pure Ag 2 CrO 4 and SnS 2 . • Ag 2 CrO 4 /SnS 2 exhibits excellent stability for the photodegradation of MO. • The possible photocatalytic mechanism was discussed in detail. - Abstract: Novel Ag 2 CrO 4 /SnS 2 composites were prepared by a simple chemical precipitation method and characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, UV–vis diffuse reflectance spectroscopy and photoluminescence spectroscopy. The visible light photocatalytic tests showed that the Ag 2 CrO 4 /SnS 2 composites enhanced photocatalytic activities for the photodegradation of methyl orange (MO) under visible light irradiation (λ > 420 nm), and the optimum rate constant of Ag 2 CrO 4 /SnS 2 at a weight content of 1.0% Ag 2 CrO 4 for the degradation of MO was 2.2 and 1.5 times larger than that of pure Ag 2 CrO 4 and SnS 2 , respectively. The improved activity could be attributed to high separation efficiency of photogenerated electrons-hole pairs on the interface of Ag 2 CrO 4 and SnS 2 , which arised from the synergistic effect between Ag 2 CrO 4 and SnS 2 . Moreover, the possible photocatalytic mechanism with superoxide radical anions and holes species as the main reactive species in photocatalysis process was proposed on the basis of experimental results.

AgBr and g-C{sub 3}N{sub 4} co-modified Ag{sub 2}CO{sub 3} photocatalyst: A novel multi-heterostructured photocatalyst with enhanced photocatalytic activity

Energy Technology Data Exchange (ETDEWEB)

Tang, Hua, E-mail: tanghua@mail.ujs.edu.cn [School of Materials Science and Engineering, Jiangsu University, Zhenjiang, Jiangsu Province 212013 (China); Chang, Shufang [School of Materials Science and Engineering, Jiangsu University, Zhenjiang, Jiangsu Province 212013 (China); Tang, Guogang [School of Materials Science and Engineering, Jiangsu University, Zhenjiang, Jiangsu Province 212013 (China); School of Chemistry and Materials Engineering, Zhenjiang College, Zhenjiang, Jiangsu Province 212003 (China); Liang, Wei [School of Materials Science and Engineering, Jiangsu University, Zhenjiang, Jiangsu Province 212013 (China)

2017-01-01

Highlights: • Novel g-C{sub 3}N{sub 4}/Ag{sub 2}CO{sub 3}/AgBr nanocomposites were prepared by a facile method. • g-C{sub 3}N{sub 4}/Ag{sub 2}CO{sub 3}/AgBr-6% has superior activity in degradation of dyes. • The synergetic effect of g-C{sub 3}N{sub 4} and AgBr was the origin of the higher performance. • The photocatalytic mechanism of the g-C{sub 3}N{sub 4}/Ag{sub 2}CO{sub 3}/AgBr was proposed. - Abstract: Novel and highly efficient visible-light-driven g-C{sub 3}N{sub 4}/Ag{sub 2}CO{sub 3}/AgBr multi-heterostructured photocatalysts are achieved from the surface modification of g-C{sub 3}N{sub 4}/Ag{sub 2}CO{sub 3} with AgBr nanoparticles by a facile and efficient ion-exchange method. The as-prepared g-C{sub 3}N{sub 4}/Ag{sub 2}CO{sub 3}/AgBr photocatalysts were characterized by X-ray diffraction (XRD), Fourier transform infrared (FTIR), X-ray photoelectron spectroscopy (XPS), scaning electron microscopy (SEM) and UV–vis diffuse reflectance spectrometry (DRS). Compared with g-C{sub 3}N{sub 4}/Ag{sub 2}CO{sub 3}, g-C{sub 3}N{sub 4}/Ag{sub 2}CO{sub 3}/AgBr hybrids exhibit enhanced the degradation activity for typical RhB, MB, and MO dyes under visible light excitation (>420 nm). Photoluminescence (PL), photo-induced current and electrochemical impedance spectroscopy (EIS) results demonstrate the g-C{sub 3}N{sub 4}/Ag{sub 2}CO{sub 3}/AgBr heterojunctions can effectively suppress the recombination of the generated electron–hole pairs. The higher photocatalytical performance of g-C{sub 3}N{sub 4}/Ag{sub 2}CO{sub 3}/AgBr can be ascribed to the efficient separation of photogenerated electron–hole pairs due to the formation of multi-heterojunctions, in which the Ag nanoparticles acted as the charge transmission bridge. In addition, the possible transferred and separated behavior of electron–hole pairs and photocatalytic mechanisms based on the experimental results are also proposed in detail.

Ag2S/CdS/TiO2 Nanotube Array Films with High Photocurrent Density by Spotting Sample Method.

Science.gov (United States)

Sun, Hong; Zhao, Peini; Zhang, Fanjun; Liu, Yuliang; Hao, Jingcheng

2015-12-01

Ag2S/CdS/TiO2 hybrid nanotube array films (Ag2S/CdS/TNTs) were prepared by selectively depositing a narrow-gap semiconductor-Ag2S (0.9 eV) quantum dots (QDs)-in the local domain of the CdS/TiO2 nanotube array films by spotting sample method (SSM). The improvement of sunlight absorption ability and photocurrent density of titanium dioxide (TiO2) nanotube array films (TNTs) which were obtained by anodic oxidation method was realized because of modifying semiconductor QDs. The CdS/TNTs, Ag2S/TNTs, and Ag2S/CdS/TNTs fabricated by uniformly depositing the QDs into the TNTs via the successive ionic layer adsorption and reaction (SILAR) method were synthesized, respectively. The X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray photoelectron spectrum (XPS) results demonstrated that the Ag2S/CdS/TNTs prepared by SSM and other films were successfully prepared. In comparison with the four films of TNTs, CdS/TNTs, Ag2S/TNTs, and Ag2S/CdS/TNTs by SILAR, the Ag2S/CdS/TNTs prepared by SSM showed much better absorption capability and the highest photocurrent density in UV-vis range (320~800 nm). The cycles of local deposition have great influence on their photoelectric properties. The photocurrent density of Ag2S/CdS/TNTs by SSM with optimum deposition cycles of 6 was about 37 times that of TNTs without modification, demonstrating their great prospective applications in solar energy utilization fields.

Study of energy transfer between riboflavin (vitamin B2) and AgNPs

Science.gov (United States)

Mokashi, Vidya V.; Walekar, Laxman S.; Anbhule, Prashant V.; Lee, Sang Hak; Patil, Shivajirao R.; Kolekar, Govind B.

2014-03-01

Here, we report the studies on the interaction and formation of nanobiocomplex between silver nanoparticle (AgNPs) and vitamin B2, i.e., riboflavin (RF). The binding study of AgNP to RF was studied by fluorescence, UV-Vis, and TEM techniques. AgNPs were prepared by reducing AgNO3 with trisodium citrate. Prepared nanoparticles size obtained at 20 nm having surface Plasmon resonance band at 426 nm. The absorbance band of RF at 264, 374, and 444 nm changes significantly in the presence of AgNPs suggests that there is change in the chemical environment surrounding AgNPs. A fluorescence spectral change for a solution of RF upon the addition of AgNPs and rapid quenching is suggestive of a rapid adsorption of RF on AgNPs.

Fabrication, characterization and photocatalytic properties of Ag nanoparticles modified TiO{sub 2} NTs

Energy Technology Data Exchange (ETDEWEB)

Wang Qingyao [School of Materials Science and Engineering, Tongji University, Shanghai 201804 (China); Yang Xiuchun, E-mail: yangxc@tongji.edu.cn [School of Materials Science and Engineering, Tongji University, Shanghai 201804 (China); Liu Dan; Zhao Jianfu [School of Materials Science and Engineering, Tongji University, Shanghai 201804 (China)

2012-06-25

Graphical abstract: The TiO{sub 2} NTs were first treated with bi-functional mercaptoacetic acid linkers (HOOC-R-S). The -OH group on the surface of TiO{sub 2} NT provides a strong affinity with the carboxylate group in the linker molecules. The thiol functional group in the linker molecules facilitates the binding with Ag from AgNO{sub 3} solution. After Ag{sup +} ions were reduced by NaBH{sub 4}, Ag nanoparticles formed by nucleation and growth. Highlights: Black-Right-Pointing-Pointer Ag nanoparticles with an average diameter of 9.2 nm were filled in the TiO{sub 2} nanotubes by a successive ionic layer adsorption and reaction (SILAR) technique. Black-Right-Pointing-Pointer Bi-functional mercaptoacetic acid linkers were used to bind TiO{sub 2} nanotubes with Ag nanoparticles. Black-Right-Pointing-Pointer Ag nanoparticles modification of TiO{sub 2} NTs largely enhanced the photocatalytic degradation of methyl orange under ultraviolet light irradiation. - Abstract: Ordered anatase TiO{sub 2} nanotubes (TiO{sub 2} NTs) on Ti substrate were synthesized by electrochemical anodization and subsequently vapor-thermal treatment. Ag nanoparticles were decorated on TiO{sub 2} NTs by successive ionic layer adsorption and reaction (SILAR) technique. Raman spectroscopy, X-ray absorption near edge spectroscopy (XANES), X-ray diffraction (XRD), UV-vis diffuse reflectance spectroscopy, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) were used for the characterization of surface morphology, phase composition, and microstructure of the original TiO{sub 2} NTs, the vapor-thermally treated TiO{sub 2} NTs and the Ag nanoparticles decorated TiO{sub 2} NTs. The results indicate that vapor-thermal treatment favors to the transformation of amorphous TiO{sub 2} into anatase phase. Increasing the SILAR cycle times favors to increase the loaded amounts of Ag nanoparticles in TiO{sub 2} NTs. Ag nanoparticles are uniformly distributed in the TiO{sub 2} NTs, and

Quantum Dot Sensitized Solar Cells Based on TiO2/AgInS2

Science.gov (United States)

Pawar, Sachin A.; Jeong, Jae Pil; Patil, Dipali S.; More, Vivek M.; Lee, Rochelle S.; Shin, Jae Cheol; Choi, Won Jun

2018-05-01

Quantum dot heterojunctions with type-II band alignment can efficiently separate photogenerated electron-hole pairs and, hence, are useful for solar cell studies. In this study, a quantum dot sensitized solar cell (QDSSC) made of TiO2/AgInS2 is achieved to boost the photoconversion efficiency for the TiO2-based system by varying the AgInS2 layer's thickness. The TiO2 nanorods array film is prepared by using a simple hydrothermal technique. The formation of a AgInS2 QD-sensitized TiO2-nanorod photoelectrode is carried out by successive ionic layer adsorption and reaction (SILAR) technique. The effect of the QD layer on the performance of the solar cell is studied by varying the SILAR cycles of the QD coating. The synthesized electrode materials are characterized by using X-ray diffraction, X-ray photoelectron spectroscopy, field emission scanning electron microscopy, high resolution transmission electron microscopy and solar cell performances. The results indicate that the nanocrystals have effectively covered the outer surfaces of the TiO2 nanorods. The interfacial structure of quantum dots (QDs)/TiO2 is also investigated, and the growth interface is verified. A careful comparison between TiO2/AgInS2 sensitized cells reveals that the trasfer of electrons and hole proceeds efficiently, the recombination is suppressed for the optimum thickness of the QD layer and light from the entire visible spectrum is utilised. Under AM 1.5G illumination, a high photocurrent of 1.36 mAcm-2 with an improved power conversion efficiency of 0.48% is obtained. The solar cell properties of our photoanodes suggest that the TiO2 nanorod array films co-sensitized by AgInS2 nanoclusters have potential applications in solar cells.

Study on the proliferation of human gastric cancer cell AGS by activation of EGFR in H2O2.

Science.gov (United States)

Wang, Q; Shen, W; Tao, G-Q; Sun, J; Shi, L-P

2017-03-01

This study is to investigate the effect of low concentration hydrogen peroxide (H2O2) on the proliferation of gastric cancer AGS cell line in vitro and the mechanism. AGS cells were treated with different low concentrations of H2O2 (1, 0.1, 0.01, and 0.001 μm) for 48 hours. The effect of H2O2 concentration gradient on the activity of AGS cell activities was detected by methyl thiazolyl tetrazolium (MTT) method. The expression of the epidermal growth factor receptor (EGFR) and its downstream signaling pathway extracellular signal-regulated kinase (ERK) protein in H2O2 was detected by Western blot method; moreover, the effect of H2O2 on intracellular reactive oxygen species (ROS) in AGS cells was observed under the fluorescence microscope and quantitative analysis by flow cytometry. The effect of H2O2 on the level of c-myc mRNA in AGS cells was also detected by reverse transcription polymerase chain reaction (RT-PCR). MTT detection results showed that 1 μm and 0.1 μm H2O2 at 48h can effectively promote the proliferation of AGS cells (pH2O2 treatment of AGS cells, the EGFR protein levels and ERK protein phosphorylation levels increased significantly (pH2O2 increased the intracellular reactive oxygen species (ROS). RT-PCR results showed the levels of c-myc mRNA in AGS cells treated with a low concentration of H2O2 were significantly increased (pH2O2 can significantly promote the proliferation of AGS cells by activating EGFR/ERK signaling pathway.

Optical and photoelectrochemical studies on Ag{sub 2}O/TiO{sub 2} double-layer thin films

Energy Technology Data Exchange (ETDEWEB)

Li, Chuan, E-mail: cli10@yahoo.com [Department of Biomedical Engineering, National Yang Ming University, Taipei, Taiwan 11221 (China); Department of Mechanical Engineering, National Central University, Jhongli, Taoyuan, Taiwan 32001 (China); Hsieh, J.H. [Department of Materials Engineering, Ming Chi University of Technology, Taishan, Taipei, Taiwan 24301 (China); Cheng, J.C. [Department of Electronic Engineering, National Taipei University of Technology, Taipei, Taiwan 10608 (China); Huang, C.C. [Department of Biomedical Engineering, National Yang Ming University, Taipei, Taiwan 11221 (China)

2014-11-03

When two different oxides films stacked together, if the absorption (upper) layer has both its conduction and valence bands more negatively lower than that of the layer underneath, then the photo-excited electrons can be forwarded to the underneath layer to become an effect of energy storage. Recent studies discovered that the double-layers of Cu{sub 2}O/TiO{sub 2} films possess such capacity. In order to investigate this specific phenomenon, we use a DC magnetron reactive sputtering to deposit a double-layer of Ag{sub 2}O/TiO{sub 2} films on glass substrate. The film thicknesses of the double-layer are 300 nm and 200 nm respectively. X-Ray diffraction (XRD), scanning electron microscope (SEM) and UV–VIS–NIR photospectrometer and photoluminance tests were used to study the structure, morphology, optical absorption and band gaps of the stacked films. From XRD and SEM, we can confirm the microstructures of each layer. The UV–VIS–NIR spectrum revealed that the optical absorption of Ag{sub 2}O/TiO{sub 2} fell in between the single film of Ag{sub 2}O and TiO{sub 2}. Further, two band gaps were estimated for Ag{sub 2}O/TiO{sub 2} films based on the Beer-Lambert law and Tauc plot. Photoluminance and photoelectrochemical tests indicated that delayed emission by electron-hole recombination and photoelectrical current was effectively support the mechanism of electrons transfer from Ag{sub 2}O to TiO{sub 2} at Ag{sub 2}O/TiO{sub 2} interface in the double-layer films. - Highlights: • A double-layer of Ag{sub 2}O/TiO{sub 2} films was deposited on glass substrate by sputtering. • XRD confirms the nanocrystalline structures of the stack deposited films. • UV–VIS–NIR spectroscopy shows the enhanced of optical absorption in Ag{sub 2}O/TiO{sub 2}. • Photoluminance and photoelectrochemical tests show electron-hole separation effect.

Synthesis and photocatalytic properties of MgBi2O6 with Ag additions

Science.gov (United States)

Zhong, Liansheng; Hu, Chaohao; Zhu, Binqing; Zhong, Yan; Zhou, Huaiying

2018-02-01

Ag-doped MgBi2O6 photocatalysts were synthesized by the low temperature hydrothermal method in combination with heat treatment reaction using NaBiO3·2H2O, MgCl2·6H2O, and AgNO3 as raw materials. The products were characterized by using power X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), Energy dispersive X-ray detector (EDS), and UV-Vis diffusion reflectance spectra. The photocatalytic activity of MgBi2O6 with Ag additions was evaluated by degrading MB (10 mg/L) under visible light irradiation (λ > 420 nm). The results showed that in comparison with pure MgBi2O6, the photocatalytic activity of MgBi2O6 with about 5% Ag concentration is increased by about 24% after 120 min reaction. The enhancement of catalytic activity of Ag-doped MgBi2O6 photocatalysts should be related to the band structure, morphology and larger specific surface area.

Enhanced photocatalytic performance of sandwiched ZnO@Ag@Cu2O nanorod films: the distinct role of Ag NPs in the visible light and UV region

International Nuclear Information System (INIS)

Ren, Shoutian; Wang, Yingying; Wang, Benyang; Wang, Qiang; Zhao, Guoliang

2015-01-01

Sandwiched ZnO@Ag@Cu 2 O nanorod films were synthesized by successive electrodeposition, magnetron sputtering and the second electrodeposition. The as-synthesized composites were characterized by x-ray diffraction patterns, field emission scanning electron microscopy, low- and high-resolution transmission electron microscopy and a UV–vis spectrophotometer. Their photocatalytic performance was estimated by the degradation of a methyl orange solution under UV or visible-light irradiation, respectively. In the visible region, due to localized surface plasmon resonance absorption of Ag NPs, ZnO@Ag@Cu 2 O showed a significantly enhanced photocatalytic performance. The enhancement factor of Ag NPs on the catalytic performance of ZnO@Ag@Cu 2 O was estimated as a function of the Cu 2 O deposition time, and the corresponding enhancement mechanism was also evaluated by the monochromatic photocatalytic experiment and discrete dipole approximation simulation. In the UV region, due to the formation of a Schottky junction (e.g. Ag/ZnO, Ag/Cu 2 O), a limited enhanced photocatalytic performance was also realized for ZnO@Ag@Cu 2 O photocatalysts. (paper)

Ternary ZnO/AgI/Ag{sub 2}CO{sub 3} nanocomposites: Novel visible-light-driven photocatalysts with excellent activity in degradation of different water pollutants

Energy Technology Data Exchange (ETDEWEB)

Golzad-Nonakaran, Behrouz; Habibi-Yangjeh, Aziz, E-mail: ahabibi@uma.ac.ir

2016-12-01

ZnO/AgI/Ag{sub 2}CO{sub 3} nanocomposites with different Ag{sub 2}CO{sub 3} contents were fabricated by a facile ultrasonic-irradiation method. The resultant samples were fairly characterized using XRD, EDX, SEM, TEM, UV–vis DRS, FT-IR, and PL techniques to reveal their microstructure, purity, morphology, and spectroscopic properties. Photocatalytic activity of the prepared samples was investigated by photodegradation of four dye pollutants (rhodamine B, methyl orange, methylene blue, and fuchsine) under visible-light irradiation. The photocatalytic experiments in degradation of rhodamine B showed that the ternary ZnO/AgI/Ag{sub 2}CO{sub 3} (30%) nanocomposite has an enhanced activity nearly 19 and 14 times higher than those of the binary ZnO/Ag{sub 2}CO{sub 3} and ZnO/AgI photocatalysts, respectively. Based on the obtained results, the highly enhanced activity was attributed to generation of more electron-hole pairs under visible-light irradiation and separation of the photogenerated charge carriers due to formation of tandem n-n heterojunctions between counterparts of the nanocomposite. The active species trapping experiments were also examined and it was showed that superoxide ion radicals play a vital role in the photocatalytic degradation reaction. More importantly, the ternary photocatalyst demonstrated good photostability. - Highlights: • ZnO/AgI/Ag{sub 2}CO{sub 3} nanocomposites were fabricated by an ultrasonic-irradiation method. • The activity was investigated by photodegradation of four dyes under visible light. • ZnO/AgI/Ag{sub 2}CO{sub 3} (30%) nanocomposite has the best activity under visible light. • Activity is 19 and 14-folds higher than ZnO/Ag{sub 2}CO{sub 3} and ZnO/AgI in degradation of RhB.

Excellent selector performance in engineered Ag/ZrO2:Ag/Pt structure for high-density bipolar RRAM applications

Science.gov (United States)

Wang, Chao; Song, Bing; Zeng, Zhongming

2017-12-01

A high-performance selector with bidirectional threshold switching (TS) characteristics of Ag/ZrO2/Pt structure was prepared by incorporating metallic Ag into the ZrO2 matrix. The bidirectional TS device exhibited excellent switching uniformity, forming-free behavior, ultra-low off current of selectivity (from 102 to 107). The experiment results confirmed that metallic Ag clusters were penetrated into the ZrO2 matrix during the annealing process, which would function as an effective active source responsible for the bidirectional TS. The volatile behavior could be explained by the self-dissolution of unstable filaments caused by minimization of the interfacial energy and thermal effect. Furthermore, a bipolar-type one selector-one resistor (1S-1R) memory device was successfully fabricated and exhibited significant suppression of the undesired sneak current, indicating the great potential as selector in a cross-point array.

Photocatalytic degradation of textile dye direct orange 26 by using CoFe2O4/Ag2O

International Nuclear Information System (INIS)

Azhdari, F.; Mehdipour Ghazi, M.

2016-01-01

The magnetic and recyclable nanoparticles of CoFe 2 O 4 were synthesized by a reverse co-precipitation process. Sonication was used to couple the CoFe 2 O 4 surface with Ag 2 O. The characteristics and optical properties of the catalyst were studied by powder X-ray diffraction, UV–visible reflectance spectroscopy and scanning electron microscopy analyses. Pure CoFe 2 O 4 and CoFe 2 O 4 /Ag 2 O were utilized to determine the visible light photo catalytic degradation of Direct Orange 26. The effects of p H, the initial concentration of catalyst and initial dye concentration on the photo catalytic process were investigated. It was found that the presence of Ag 2 O remarkably improved the photo catalytic adsorption capacity and degradation efficiency of CoFe 2 O 4 /Ag 2 O when compared with the pure CoFe 2 O 4 . Moreover, due to the magnetic behavior of CoFe 2 O 4 , these coupled nanoparticles can be easily separated from the aqueous solution by applying an external magnetic field. The prepared Ag 2 O-modified CoFe 2 O 4 exhibited much higher (about 40%) photo catalytic activity than the unmodified one. The results showed that the loading of the Ag 2 O significantly improved the photo catalytic performance of the CoFe 2 O 4 in which the Ag 2 O acted as a charge carrier to capture the delocalized electrons.

The catalytic activity of Ag{sub 2}S-montmorillonites as peroxidase mimetic toward colorimetric detection of H{sub 2}O{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Liu, Qingyun, E-mail: qyliu@sdust.edu.cn [School of Chemistry and Environmental Engineering, Shandong University of Science and Technology, Qingdao 266510 (China); Jiang, Yanling; Zhang, Leyou; Zhou, Xinpei [School of Chemistry and Environmental Engineering, Shandong University of Science and Technology, Qingdao 266510 (China); Lv, Xintian [School of Chemistry and Chemical Engineering, Liaocheng University, Liaocheng 252000 (China); Ding, Yanyuan; Sun, Lifang; Chen, Pengpeng [School of Chemistry and Environmental Engineering, Shandong University of Science and Technology, Qingdao 266510 (China); Yin, Hailiang [Academy of Science & Technology, China University of Petroleum, Dongying 257061 (China)

2016-08-01

Nanocomposites based on silver sulfide (Ag{sub 2}S) and Ca-montmorillonite (Ca{sup 2+}-MMT) were synthesized by a simple hydrothermal method. The nanocomposites were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) and Fourier transform infrared spectra (FTIR). The as-prepared Ag{sub 2}S-MMT nanocomposites were firstly demonstrated to possess intrinsic peroxidase-like activity and could rapidly catalytically oxidize the substrate 3,3′,5,5′-tetramethylbenzidine (TMB) in the presence of H{sub 2}O{sub 2} to produce a blue product which can be seen by the naked eye in only one minute. The experimental results revealed that the Ag{sub 2}S-MMT nanocomposites exhibit higher thermal durance. Based on the TMB–H{sub 2}O{sub 2} catalyzed color reaction, the Ag{sub 2}S-MMT nanocomposites were exploited as a new type of biosensor for detection and estimation of H{sub 2}O{sub 2} through a simple, cheap and selective colorimetric method. - Highlights: • Ag{sub 2}S – montmorillonites (MMT) was synthesized by a facile one step method. • The as-prepared Ag{sub 2}S-MMT nanocomposites firstly demonstrate to possess intrinsic peroxidase-like activity. • Ag{sub 2}S-MMT nanocomposites showed highly catalytic activity. • Ag{sub 2}S-MMT could rapidly catalytically oxidize substrates TMB in the presence of H{sub 2}O{sub 2} in 1 min. • The catalytic mechanism is from the generation of hydroxyl radical (·OH) decomposed from H{sub 2}O{sub 2}.

Strategic flat rolling of Ag/BSCCO-2223 tapes

DEFF Research Database (Denmark)

Nielsen, Morten Storgård; Bech, Jakob Ilsted; Eriksen, Morten

2002-01-01

In the process of single-step flat rolling of multifilament Ag/BSCCO-2223 wire to tape previous work has shown the optimum strategy giving maximum critical current density to be it balance between the length and width strain, so they are of equal size i.e. so, that the logarithmic strain ratio, L...

Interface characteristics in Co2MnSi/Ag/Co2MnSi trilayer

International Nuclear Information System (INIS)

Li, Yang; Chen, Hong; Wang, Guangzhao; Yuan, Hongkuan

2016-01-01

Highlights: • Inferface DO 3 disorder is most favorable in Co 2 MnSi/Ag/Co 2 MnSi trilayer. • Interface itself and inferface DO 3 disorder destroy the half-metallicity of interface layers. • Magnetoresistance is reduced by the interface itself and interface disorder. • Magnetotransport coefficient is largely reduced by the interface itself and interface disorder. - Abstract: Interface characteristics of Co 2 MnSi/Ag/Co 2 MnSi trilayer have been investigated by means of first-principles. The most likely interface is formed by connecting MnSi-termination to the bridge site between two Ag atoms. As annealed at high temperature, the formation of interface DO 3 disorder is most energetically favorable. The spin polarization is reduced by both the interface itself and interface disorder due to the interface state occurs in the minority-spin gap. As a result, the magneto-resistance ratio has a sharp drop based on the estimation of a simplified modeling.

Heterogeneous Ag-TiO2-SiO2 composite materials as novel catalytic systems for selective epoxidation of cyclohexene by H2O2.

Directory of Open Access Journals (Sweden)

Xin Wang

Full Text Available TiO2-SiO2 composites were synthesized using cetyl trimethyl ammonium bromide (CTAB as the structure directing template. Self-assembly hexadecyltrimethyl- ammonium bromide TiO2-SiO2/(CTAB were soaked into silver nitrate (AgNO3 aqueous solution. The Ag-TiO2-SiO2(Ag-TS composite were prepared via a precipitation of AgBr in soaking process and its decomposition at calcination stage. Structural characterization of the materials was carried out by various techniques including X-ray diffraction (XRD, scanning electron microscopy (SEM, transmission electron microscopy (TEM, N2 adsorption-desorption and ultraviolet visible spectroscopy (UV-Vis. Characterization results revealed that Ag particles were incorporated into hierarchical TiO2-SiO2 without significantly affecting the structures of the supports. Further heating-treatment at 723 K was more favorable for enhancing the stability of the Ag-TS composite. The cyclohexene oxide was the major product in the epoxidation using H2O2 as the oxidant over the Ag-TS catalysts. Besides, the optimum catalytic activity and stability of Ag-TS catalysts were obtained under operational conditions of calcined at 723 K for 2 h, reaction time of 120 min, reaction temperature of 353 K, catalyst amount of 80 mg, aqueous H2O2 (30 wt.% as oxidant and chloroform as solvent. High catalytic activity with conversion rate up to 99.2% of cyclohexene oxide could be obtainable in water-bathing. The catalyst was found to be stable and could be reused three times without significant loss of catalytic activity under the optimized reaction conditions.

Synthesis of spindle-shaped AgI/TiO{sub 2} nanoparticles with enhanced photocatalytic performance

Energy Technology Data Exchange (ETDEWEB)

Yang, Liu; Gao, Minggang; Dai, Bin; Guo, Xuhong; Liu, Zhiyong; Peng, Banghua, E-mail: banghuapeng@hotmail.com

2016-11-15

Highlights: • Nanoporous spindle-shaped AgI/TiO{sub 2} was synthesized by the solvothermal approach. • The spindle-shaped TiO{sub 2} was an excellent support for loading nanoparticles, such as AgI, transferring electrons quickly from AgI, which is beneficial for stabilizing the AgI. • AgI/TiO{sub 2} nanoparticles showed enhanced absorption intensity in the visible region and exhibited excellent photocatalytic activity. - Abstract: A novel synthetic route has been developed to prepare silver iodide (AgI) loaded spindle-shaped TiO{sub 2} nanoparticles (NPs). The morphology and crystallinity characterization revealed that small AgI NPs, with an average diameter of 15 nm were dispersed on the surface and interior of nanoporous anatase TiO{sub 2} support. High-resolution transmission electron microscopy (HRTEM), Brunauer-Emmett-Teller (BET) surface area, Raman and X-ray photoelectron spectroscopy (XPS) were used to identify the nanoporous structure of TiO{sub 2} and the existence of AgI NPs. Diffuse reflectance spectra (DRS) showed that AgI/TiO{sub 2} composite exhibited a remarkable enhancement of visible light absorption, which is ascribed to the addition of AgI. For illustrating the superior property of this hybrid as photocatalyst, the degradation experiments were carried out for processing rhodamine B (RhB) solution under visible light irradiation and it was found that the photocatalytic activity was dramatically improved for AgI/TiO{sub 2} compared with nanoporous TiO{sub 2} and commercial P25 TiO{sub 2}. The enhanced photocatalytic properties could be attributed to the large surface area of porous TiO{sub 2}, good stability of AgI particles, and the effective charge separation due to the synergetic effect between AgI and TiO{sub 2} that can facilitate the separation of electron-hole pairs. Our novel composite based on nanoporous spindle-shaped TiO{sub 2} represents a promising new pathway for the design of high-performance photocatalysts for environmental

Thermoelectric transport of Se-rich Ag2Se in normal phases and phase transitions

International Nuclear Information System (INIS)

Mi, Wenlong; Lv, Yanhong; Qiu, Pengfei; Shi, Xun; Chen, Lidong; Zhang, Tiansong

2014-01-01

Small amount of Se atoms are used to tune the carrier concentrations (n H ) and electrical transport in Ag 2 Se. Significant enhancements in power factor and thermoelectric figure of merit (zT) are observed in the compositions of Ag 2 Se 1.06 and Ag 2 Se 1.08 . The excessive Se atoms do not change the intrinsically electron-conducting character in Ag 2 Se. The detailed analysis reveals the experiment optimum carrier concentration in Ag 2 Se is around 5 × 10 18  cm −3 . We also investigate the temperature of maximum zT and the thermoelectric transport during the first order phase transitions using the recently developed measurement system

Auxotrophic recombinant Mycobacterium bovis BCG overexpressing Ag85B enhances cytotoxicity on superficial bladder cancer cells in vitro.

Science.gov (United States)

Begnini, Karine Rech; Rizzi, Caroline; Campos, Vinicius Farias; Borsuk, Sibele; Schultze, Eduarda; Yurgel, Virginia Campello; Nedel, Fernanda; Dellagostin, Odir Antônio; Collares, Tiago; Seixas, Fabiana Kömmling

2013-02-01

BCG therapy remains at the forefront of immunotherapy for treating patients with superficial bladder cancer. The high incidence of local side effects and the presence of non-responder diseases have led to efforts to improve the therapy. Hence, we proposed that an auxotrophic recombinant BCG strain overexpressing Ag85B (BCG ∆leuD/Ag85B), could enhance the cytotoxicity to the human bladder carcinoma cell line 5637. The rBCG was generated using an expression plasmid encoding the mycobacterial antigen Ag85B to transform a BCG ∆leuD strain. The inhibitory effect of BCG ∆leuD/Ag85B on 5637 cells was determined by the MTT method, morphology observation and a LIVE/DEAD assay. Gene expression profiles for apoptotic, cell cycle-related and oxidative stress-related genes were investigated by qRT-PCR. Bax, bcl-2 and p53 induction by BCG ∆leuD/Ag85B treatment was evaluated by Western blotting. BCG ∆leuD/Ag85B revealed a superior cytotoxicity effect compared to the control strains used in this study. The results showed that the expression level of pro-apoptotic and cell cycle-related genes increased after BCG ∆leuD/Ag85B treatment, whereas the mRNA levels of anti-apoptotic genes decreased. Interestingly, BCG ∆leuD/Ag85B also increased the mRNA level of antioxidant enzymes in the bladder cancer cell line. Bax and p53 proteins levels increased following treatment. In conclusion, these results suggest that treatment with BCG ∆leuD/Ag85B enhances cytotoxicity for superficial bladder cancer cells in vitro. Therefore, rBCG therapy may have potential benefits in the treatment of bladder cancer.

OPTOELECTRONIC PROPERTIES OF CdS – AgInS2 SOLAR CELLS

Directory of Open Access Journals (Sweden)

M. A. Abdullaev

2016-01-01

Full Text Available Aim. To conduct experimental studies of optoelectronic properties of CdS - AgInS2 solar cells.Methods. AgInS2 films for solar cell CdS-AgInS2 were obtained by magnetron sputtering of crystalline targets derived from bulk ingots. Cadmium sulfide layers were deposited on the AgInS2 films by an electrochemical method in cadmium salts solution, thiourea and ammonia. AgInS2 bulk crystals were obtained in two stages: a direct fusion of the primary components (99,999 in a stoichiometric ratio, followed by directional solidification in a vertical furnace; re-synthesis has been performed on a staggered basis by heating the obtained ingots at temperatures close to the melting points of elements in the two-zone horizontal furnace.Findings. The paper presents the results of experimental studies of the electrical properties and photosensitivity of CdS-AgInS2 film heterojunction obtained by the magnetron. We measured the current-voltage characteristics and quantum efficiency of photoconversion at temperatures up to 250-356 K. We also identified the short circuit current of up to 25 mA/cm2 and open circuit voltage of 0.38 V.Conclusions. The study of the properties of solar cells in recent years has an important place. The results presented in the work would contribute to more efficient conversion of solar energy into electricity.

Ag nanocrystals anchored CeO2/graphene nanocomposite for enhanced supercapacitor applications

International Nuclear Information System (INIS)

Vanitha, M.; Keerthi; Cao, P.; Balasubramanian, N.

2015-01-01

Highlights: • Quasi spherical Ag and CeO 2 nanoparticles were decorated on rGO matrix. • The Ag/CeO 2 /rGO nanocomposite exhibits specific capacitance of 710 F g −1 . • Ag plays an imperative role in improving the electrochemical performance. - Abstract: A novel ternary Ag decorated CeO 2 /reduced graphene oxide (rGO) nanocomposite was synthesized by a facile hydrothermal method with polyvinylpyrrolidone (PVP) as surface directing agent and was designed as an electrode material for supercapacitors application. The structure and morphology of the nanocomposites were analyzed by X-ray diffraction analysis (XRD), Raman spectroscopy, field emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM). The synergistic effect between the CeO 2 nanoparticles wrapped rGO matrix with Ag nanoparticles gives rise to a nanostructure, empowering the material with enhanced electrochemical performance. The electrochemical characterization was performed using cyclic voltammetry, galvanostatic charge/discharge and electrochemical impedance spectroscopic studies in 3 M KOH aqueous electrolyte. The nanocomposite electrode materials possess a high specific capacitance of 710.42 F g −1 at an applied current density of 0.2 A g −1 , which was nearly two fold higher than CeO 2 /rGO nanocomposite. This work endows a new route for building Ag/CeO 2 /rGO ternary nanocomposite which will have some impact on the exploitation of novel ternary electrode materials for supercapacitor applications

Excellent selector performance in engineered Ag/ZrO2:Ag/Pt structure for high-density bipolar RRAM applications

Directory of Open Access Journals (Sweden)

Chao Wang

2017-12-01

Full Text Available A high-performance selector with bidirectional threshold switching (TS characteristics of Ag/ZrO2/Pt structure was prepared by incorporating metallic Ag into the ZrO2 matrix. The bidirectional TS device exhibited excellent switching uniformity, forming-free behavior, ultra-low off current of <1 nA and adjustable selectivity (from 102 to 107. The experiment results confirmed that metallic Ag clusters were penetrated into the ZrO2 matrix during the annealing process, which would function as an effective active source responsible for the bidirectional TS. The volatile behavior could be explained by the self-dissolution of unstable filaments caused by minimization of the interfacial energy and thermal effect. Furthermore, a bipolar-type one selector-one resistor (1S-1R memory device was successfully fabricated and exhibited significant suppression of the undesired sneak current, indicating the great potential as selector in a cross-point array.

Thermal expansion properties of Bi-2212 in Ag or an Ag-alloy matrix

International Nuclear Information System (INIS)

Tenbrink, J.; Krauth, H.

1994-01-01

The thermal expansion properties of polycrystalline Bi 2 Sr 2 Ca 1 Cu 2 O 8+x melt-processed bulk specimens, and Bi 2 Sr 2 Ca 1 Cu 2 O 8+x monocore as well as multifilamentary round wires in Ag or Ag-alloy matrix have been investigated over the temperature range from -150 to 800 degrees C. Although the thermal expansion of Bi 2 Sr 2 Ca 1 Cu 2 O 8+x is distinctly lower compared with Ag, the thermal expansion properties of the Bi 2 Sr 2 Ca 1 Cu 2 O 8+x -Ag or AgNiMg-alloy composite conductors are essentially governed by the matrix material. The thermal expansion of the encountered oxide-dispersion-strengthened AgNiMg alloys is only slightly lower compared with that of pure Ag. Therefore the thermal expansion of all investigated Bi 2 Sr 2 Ca 1 Cu 2 O 8+x -Ag or Ag-alloy composite wires was found to be close to that of pure Ag. The reason for this striking behaviour is shown to be related to a surprisingly low elastic modulus of the polycrystalline Bi-2212 wire cores of the order of 10 to a maximum 40 GPa. (author)

Sensitive and selective detection of Hg2+ and Cu2+ ions by fluorescent Ag nanoclusters synthesized via a hydrothermal method

Science.gov (United States)

Liu, Jing; Ren, Xiangling; Meng, Xianwei; Fang, Zheng; Tang, Fangqiong

2013-09-01

An easily prepared fluorescent Ag nanoclusters (Ag NCs) probe for the sensitive and selective detection of Hg2+ and Cu2+ ions was developed here. The Ag NCs were synthesized by using polymethacrylic acid sodium salt as a template via a convenient hydrothermal process. The as-prepared fluorescent Ag NCs were monodispersed, uniform and less than 2 nm in diameter, and can be quenched in the presence of mercury (Hg2+) or copper (Cu2+) ions. Excellent linear relationships existed between the quenching degree of the Ag NCs and the concentrations of Hg2+ or Cu2+ ions in the range of 10 nM to 20 μM or 10 nM to 30 μM, respectively. By using ethylenediaminetetraacetate (EDTA) as the masking agent of Cu2+, Hg2+ was exclusively detected in coexistence with Cu2+ with high sensitivity (LOD = 10 nM), which also provided a reusable detection method for Cu2+. Furthermore, the different quenching phenomena caused by the two metals ions such as changes in visible colour, shifts of UV absorbance peaks and changes in size of Ag NCs make it easy to distinguish between them. Therefore the easily synthesized fluorescent Ag NCs may have great potential as Hg2+ and Cu2+ ions sensors.An easily prepared fluorescent Ag nanoclusters (Ag NCs) probe for the sensitive and selective detection of Hg2+ and Cu2+ ions was developed here. The Ag NCs were synthesized by using polymethacrylic acid sodium salt as a template via a convenient hydrothermal process. The as-prepared fluorescent Ag NCs were monodispersed, uniform and less than 2 nm in diameter, and can be quenched in the presence of mercury (Hg2+) or copper (Cu2+) ions. Excellent linear relationships existed between the quenching degree of the Ag NCs and the concentrations of Hg2+ or Cu2+ ions in the range of 10 nM to 20 μM or 10 nM to 30 μM, respectively. By using ethylenediaminetetraacetate (EDTA) as the masking agent of Cu2+, Hg2+ was exclusively detected in coexistence with Cu2+ with high sensitivity (LOD = 10 nM), which also provided a

Optimisation of Ag loading and alumina characteristics to give sulphur-tolerant Ag/Al₂O₃ catalyst for H₂-assisted NH₃-SCR of NO_x

DEFF Research Database (Denmark)

Fogel, Sebastian; Doronkin, Dmitry E.; Gabrielsson, Pär

2012-01-01

A series of Ag/Al2O3 catalysts with different alumina precursors and different Ag loadings were tested for H2 assisted NH3-SCR of NO. The catalysts were characterised (BET, XRD, NH3-TPD, ICP-OES, TEM and UV–vis spectroscopy) and tested as fresh catalyst, during long-term cycling tests with SO2 pr....... A higher Ag loading will affect the state of Ag by increasing the ratio of Ag-clusters and particles to highly dispersed Ag ions. SO2-poisoned Ag-clusters and particles can be regenerated by the high temperature treatment in the deNOx feed, highly dispersed Ag ions cannot....

Synthesis of Ag-TiO2 composite nano thin film for antimicrobial application

Science.gov (United States)

Yu, Binyu; Leung, Kar Man; Guo, Qiuquan; Lau, Woon Ming; Yang, Jun

2011-03-01

TiO2 photocatalysts have been found to kill cancer cells, bacteria and viruses under mild UV illumination, which offers numerous potential applications. On the other hand, Ag has long been proved as a good antibacterial material as well. The advantage of Ag-TiO2 nanocomposite is to expand the nanomaterial's antibacterial function to a broader range of working conditions. In this study neat TiO2 and Ag-TiO2 composite nanofilms were successfully prepared on silicon wafer via the sol-gel method by the spin-coating technique. The as-prepared composite Ag-TiO2 and TiO2 films with different silver content were characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM), x-ray diffraction (XRD) and x-ray photoelectron spectroscopy (XPS) to determine the topologies, microstructures and chemical compositions, respectively. It was found that the silver nanoparticles were uniformly distributed and strongly attached to the mesoporous TiO2 matrix. The morphology of the composite film could be controlled by simply tuning the molar ratio of the silver nitrate aqueous solution. XPS results confirmed that the Ag was in the Ag0 state. The antimicrobial effect of the synthesized nanofilms was carried out against gram-negative bacteria (Escherichia coli ATCC 29425) by using an 8 W UV lamp with a constant relative intensity of 0.6 mW cm - 2 and in the dark respectively. The synthesized Ag-TiO2 thin films showed enhanced bactericidal activities compared to the neat TiO2 nanofilm both in the dark and under UV illumination.

Synthesis of Ag-TiO2 composite nano thin film for antimicrobial application

International Nuclear Information System (INIS)

Yu Binyu; Guo Qiuquan; Yang Jun; Leung, Kar Man; Lau, Woon Ming

2011-01-01

TiO 2 photocatalysts have been found to kill cancer cells, bacteria and viruses under mild UV illumination, which offers numerous potential applications. On the other hand, Ag has long been proved as a good antibacterial material as well. The advantage of Ag-TiO 2 nanocomposite is to expand the nanomaterial's antibacterial function to a broader range of working conditions. In this study neat TiO 2 and Ag-TiO 2 composite nanofilms were successfully prepared on silicon wafer via the sol-gel method by the spin-coating technique. The as-prepared composite Ag-TiO 2 and TiO 2 films with different silver content were characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM), x-ray diffraction (XRD) and x-ray photoelectron spectroscopy (XPS) to determine the topologies, microstructures and chemical compositions, respectively. It was found that the silver nanoparticles were uniformly distributed and strongly attached to the mesoporous TiO 2 matrix. The morphology of the composite film could be controlled by simply tuning the molar ratio of the silver nitrate aqueous solution. XPS results confirmed that the Ag was in the Ag 0 state. The antimicrobial effect of the synthesized nanofilms was carried out against gram-negative bacteria (Escherichia coli ATCC 29425) by using an 8 W UV lamp with a constant relative intensity of 0.6 mW cm -2 and in the dark respectively. The synthesized Ag-TiO 2 thin films showed enhanced bactericidal activities compared to the neat TiO 2 nanofilm both in the dark and under UV illumination.

Controllable synthesis of metal selenide heterostructures mediated by Ag2Se nanocrystals acting as catalysts

Science.gov (United States)

Zhou, Jiangcong; Huang, Feng; Xu, Ju; Wang, Yuansheng

2013-09-01

Ag2Se nanocrystals were demonstrated to be novel semiconductor mediators, or in other word catalysts, for the growth of semiconductor heterostructures in solution. This is a result of the unique feature of Ag2Se as a fast ion conductor, allowing foreign cations to dissolve and then to heterogrow the second phase. Using Ag2Se nanocrystals as catalysts, dimeric metal selenide heterostructures such as Ag2Se-CdSe and Ag2Se-ZnSe, and even multi-segment heterostructures such as Ag2Se-CdSe-ZnSe and Ag2Se-ZnSe-CdSe, were successfully synthesized. Several interesting features were found in the Ag2Se based heterogrowth. At the initial stage of heterogrowth, a layer of the second phase forms on the surface of an Ag2Se nanosphere, with a curved junction interface between the two phases. With further growth of the second phase, the Ag2Se nanosphere tends to flatten the junction surface by modifying its shape from sphere to hemisphere in order to minimize the conjunct area and thus the interfacial energy. Notably, the crystallographic relationship of the two phases in the heterostructure varies with the lattice parameters of the second phase, in order to reduce the lattice mismatch at the interface. Furthermore, a small lattice mismatch at the interface results in a straight rod-like second phase, while a large lattice mismatch would induce a tortuous product. The reported results may provide a new route for developing novel selenide semiconductor heterostructures which are potentially applicable in optoelectronic, biomedical, photovoltaic and catalytic fields.Ag2Se nanocrystals were demonstrated to be novel semiconductor mediators, or in other word catalysts, for the growth of semiconductor heterostructures in solution. This is a result of the unique feature of Ag2Se as a fast ion conductor, allowing foreign cations to dissolve and then to heterogrow the second phase. Using Ag2Se nanocrystals as catalysts, dimeric metal selenide heterostructures such as Ag2Se-CdSe and Ag2Se

Verification of resistance to three mediated microbial strains and cancerous defense against MCF7 compared to HepG2 through microwave synthesized plant-mediated silver nanoparticle

Science.gov (United States)

Abdel-Fattah, W. I.; Eid, M. M.; Hanafy, M. F.; Hussein, M.; Abd El-Moez, Sh I.; El-Hallouty, S. M.; Mohamed, E.

2015-09-01

The antimicrobial and anticancer efficiencies of green synthesized silver nanoparticles (AgNPs) through biogenic extracts were assessed on three bacterial strains and two cancer cell lines. Bio-synthesized AgNPs were achieved through domestic microwave generator for obtaining extracts from Asian nuts and Egyptian blackberry fruits. Surface plasmon resonance (SPR) ˜435 nm demonstrated AgNPs earlier formation by the fruit extract. Capping by triglycerides/almond and phenols/berry extracts were responsible for the reduction proved by FTIR. XRD calculated particle sizes were 18 and 42 nm while TEM sizes are 24.5 and 21.5 nm for AgNPs from almond nut and blackberry fruits extracts (Alm.N.Ext. and BB.F.Ext.), respectively. Ag 3d5/2 was recorded at 368.12 eV for both samples through XPS. The monodispersed AgNPs recorded 0.727 and 0.5 polydispersity indices (PdI) for almond/Ag and berry/Ag, respectively. Zeta potential ˜ -31 and -13.2 for the same sequence confirmed the higher stability of the former. Reaction kinetics confirmed the advantage of fruit extract consuming only six minutes compared to nuts, consuming twice. Bactericidal effect of the extracts seldomly presented remarkable inhibition compared to extracts/Ag against the three species. In addition, Alm.N.Ext. showed the highest inhibition against staphylococcus aureus (S. aureus) at 4 mM. The anti-cancerous effect of Ag/berry against HepG2 is stronger than Ag/almond, and similarly for MCF7.

Verification of resistance to three mediated microbial strains and cancerous defense against MCF7 compared to HepG2 through microwave synthesized plant-mediated silver nanoparticle

International Nuclear Information System (INIS)

Abdel-Fattah, W I; Eid, M M; Hanafy, M F; Hussein, M; Mohamed, E; Abd El-Moez, Sh I; El-Hallouty, S M

2015-01-01

The antimicrobial and anticancer efficiencies of green synthesized silver nanoparticles (AgNPs) through biogenic extracts were assessed on three bacterial strains and two cancer cell lines. Bio-synthesized AgNPs were achieved through domestic microwave generator for obtaining extracts from Asian nuts and Egyptian blackberry fruits. Surface plasmon resonance (SPR) ∼435 nm demonstrated AgNPs earlier formation by the fruit extract. Capping by triglycerides/almond and phenols/berry extracts were responsible for the reduction proved by FTIR. XRD calculated particle sizes were 18 and 42 nm while TEM sizes are 24.5 and 21.5 nm for AgNPs from almond nut and blackberry fruits extracts (Alm.N.Ext. and BB.F.Ext.), respectively. Ag 3d5/2 was recorded at 368.12 eV for both samples through XPS. The monodispersed AgNPs recorded 0.727 and 0.5 polydispersity indices (PdI) for almond/Ag and berry/Ag, respectively. Zeta potential ∼ −31 and −13.2 for the same sequence confirmed the higher stability of the former. Reaction kinetics confirmed the advantage of fruit extract consuming only six minutes compared to nuts, consuming twice. Bactericidal effect of the extracts seldomly presented remarkable inhibition compared to extracts/Ag against the three species. In addition, Alm.N.Ext. showed the highest inhibition against staphylococcus aureus (S. aureus) at 4 mM. The anti-cancerous effect of Ag/berry against HepG2 is stronger than Ag/almond, and similarly for MCF7. (paper)

Microscopic fracture of filaments and its relation to the critical current under bending deformation in (Bi,Pb)2Sr2Ca2Cu3O10 composite superconducting tapes

International Nuclear Information System (INIS)

Hojo, Masaki; Nakamura, Mitsuhiro; Matsuoka, Tomoe; Tanaka, Mototsugu; Ochiai, Shojiro; Sugano, Michinaka; Osamura, Kozo

2003-01-01

The strain dependence of the critical current, I c , of (Bi,Pb) 2 Sr 2 Ca 2 Cu 3 O 10 (Bi2223)/Ag/Ag-Mg composite superconducting tapes has been studied both experimentally and analytically under bending deformation. Tests have been carried out for one type of tape used in the VAMAS bending round-robin programme. The complex stress-strain behaviour of each component was first analysed in tension. This was done by comparing the stress-strain curves of composite tapes with those of Ag and Ag-Mg alloy tapes. Here, the plastic deformation (work hardening) of Ag and Ag-Mg alloy, and the thermal residual strain due to the manufacturing process were taken into account. The fracture strain of Bi2223 filaments was inversely determined as 0.08% to meet the global tensile stress-strain curve of the composite tape. The calculated stress-strain curves finally agreed well with the experimental results when the as-supplied bending strain was taken into account. Then, the analysis was modified to fit the bending deformation. Here, the movement of the neutral axis due to the non-symmetric and elastic-plastic stress-strain curves of the components and their Bauschinger effect were taken into account. The relative decrease of I c with the increase in the Bi2223 tape curvature was calculated from the volume fraction of the broken filaments. The calculated I c agreed well with the experimental results when the movement of the neutral axis and the Bauschinger effect were taken into account. Microscopic observation of the spatial distribution of the filament fracture indicated that the damage occurred at the outermost layer on the tensile side when the curvature was small, and then the damage front shifted to the inside layers. The observed fracture behaviour of the Bi2223 filament agreed well with the estimated location based on the above analysis

Synergetic effect of Ag_2O as co-catalyst for enhanced photocatalytic degradation of phenol on N-TiO_2

International Nuclear Information System (INIS)

Chu, Haipeng; Liu, Xinjuan; Liu, Junying; Li, Jinliang; Wu, Tianyang; Li, Haokun; Lei, Wenyan; Xu, Yan; Pan, Likun

2016-01-01

Graphical abstract: Ag_2O/N-TiO_2 composites were synthesized via a co-precipitation method for visible light photocatalytic degradation of organic pollutions with excellent photocatalytic activity. - Highlights: • Ag_2O/N-TiO_2 composites were synthesized via a facile precipitation method. • Ag_2O/N-TiO_2 composites exhibited enhanced photocatalytic activity. • Ag_2O acts as co-catalyst to separate the photo-generated electron-hole pairs. - Abstract: A facile precipitation method was developed to synthesize the Ag_2O/N-TiO_2 composites. Their morphology, structure and photocatalytic performance in the degradation of methylene blue (MB) and phenol under visible light irradiation were characterized by scanning electron microscopy, transmission electron microscopy, energy dispersive X-ray spectroscopy, X-ray diffraction, photoluminescence spectroscopy and UV–vis absorption spectroscopy, respectively. The results show that the Ag_2O/N-TiO_2 composites exhibit excellent photocatalytic performance. The maximum degradation rates of MB and phenol are about 8.9 and 2.9 times that of pure N-TiO_2, respectively. The excellent photocatalytic performance is mainly ascribed to the synergetic effects of Ag_2O and N-TiO_2 including the increased light absorption and the reduced electron-hole pair recombination in N-TiO_2 with the presence of Ag_2O.

Optical and structural properties of TiO{sub 2}/Ti/Ag/TiO{sub 2} and TiO{sub 2}/ITO/Ag/ITO/TiO{sub 2} metal-dielectric multilayers by RF magnetron sputtering for display application

Energy Technology Data Exchange (ETDEWEB)

Lee, Jang-Hoon; Lee, Seung-Hyu; Hwangbo, Chang-Kwon [Inha University, Incheon (Korea, Republic of); Lee, Kwang-Su [Quantum Photonic Science Research Center, Hanyang University, Seoul (Korea, Republic of)

2004-03-15

Electromagnetic-interference (EMI) shielding and near-infrared (NIR) cutoff filters for plasma display panels, based on fundamental structures (ITO/Ag/ITO), (TiO{sub 2}/Ti/Ag/TiO{sub 2}) and (TiO{sub 2}/ITO/Ag/ITO/TiO{sub 2}), were designed and prepared by RF-magnetron sputtering. The optical, structural and electrical properties of the filters were investigated by using spectrophotometry, Auger electron spectroscopy, X-ray photoelectron spectroscopy, Rutherford backscattering spectroscopy, atomic force microscopy and four-point-probe measurements. The results show that ITO films as the barriers and base layers lead to higher transmittance in the visible spectrum and smoother surface roughness than Ti metal barriers, while maintaining high NIR cutoff characteristics and chemical stability, which may be attributed to the lower absorption in the interfacial layers and better protection of the Ag layers by the ITO layers.

Photoelectric properties of ZnO/Ag2S heterostructure and its photoelectric ethanol sensing characteristics

International Nuclear Information System (INIS)

Zhang Yu; Liu Bingkun; Wang Dejun; Lin Yanhong; Xie Tengfeng; Zhai Jiali

2012-01-01

Highlights: ► The ZnO/Ag 2 S heterostructure shows good photoelectric properties under visible-light irradiation. ► Transient photovoltage results reveal the separation process of photo-generated charges and give further evidence of interfacial effects. ► Photoelectric ethanol sensing characteristics have been found for the ZnO/Ag 2 S heterostructure at room temperature. - Abstract: The photoelectric properties of ZnO microspheres, ZnO/Ag 2 S heterogeneous microspheres and Ag 2 S hollow microspheres were investigated systematically by surface photovoltage, transient photovoltage and surface photocurrent techniques. The ZnO/Ag 2 S heterostructure shows superior photoelectric properties in visible-light region compared with pure Ag 2 S. Transient photovoltage results reveal the separation processes of photo-generated charge carriers in the samples. The photoelectric ethanol sensing property induced by visible light for the ZnO/Ag 2 S heterostructure has been found, which should be valuable for the practical application of semiconductor gas sensors at room temperature.

Preparation and Property Research of Strain Sensor Based on PDMS and Silver Nanomaterials

Directory of Open Access Journals (Sweden)

Lihua Liu

2017-01-01

Full Text Available Based on the advantages and broad applications of stretchable strain sensors, this study reports a simple method to fabricate a highly sensitive strain sensor with Ag nanomaterials-polydimethylsiloxane (AgNMs-PDMS to create a synergic conductive network and a sandwich-structure. Three Ag nanomaterial samples were synthesized by controlling the concentrations of the FeCl3 solution and reaction time via the heat polyols thermal method. The AgNMs network’s elastomer nanocomposite-based strain sensors show strong piezoresistivity with a high gauge factor of 547.8 and stretchability from 0.81% to 7.26%. The application of our high-performance strain sensors was demonstrated by the inducting finger of the motion detection. These highly sensitive sensors conform to the current trends of flexible electronics and have prospects for broad application.

Enhanced Photocatalytic Properties of Ag-Loaded N-Doped Tio2 Nanotube Arrays

Directory of Open Access Journals (Sweden)

Gao Dawei

2018-03-01

Full Text Available Highly ordered TiO2 nanotube (TiO2 NT arrays were prepared by anodic oxidizing method on the surface of the Ti substrate. Nitrogen-doped TiO2 nanotube (N-TiO2 NT arrays were carried out by ammonia solution immersion, and Ag nanoparticles loaded N-doped TiO2 nanotube (Ag/N-TiO2 NT arrays were obtained by successive ionic layer adsorption and reaction (SILAR technique. The samples were characterized by the X-ray diffraction (XRD, X-ray photoelectron spectroscopy (XPS, field emission scanning electron microscopy (FESEM, high-resolution transmission electron microscopy (HRTEM, photoluminescence (PL emission spectra, ultraviolet–visible (UV–vis diffuse reflectance spectroscopy (DRS. The result indicated that the diameter and wall thickness of the TiO2 NT are 100–120 and 20–30 nm, respectively. Moreover, the morphology and structure of the highly ordered TiO2 NTs were not affected by N-doping. Furthermore, Ag nanoparticles were evenly deposited on the surface of TiO2 NTs in the form of elemental silver. Finally, the photocatalytic activity of Ag/N-TiO2 NTs was evaluated by degradation of methyl orange (MO under visible-light irradiation. The Ag/N-TiO2 NTs exhibited enhanced photocatalytic properties, which could reach 95% after 90-min irradiation.

Synthesis and antimicrobial evaluation of nanostructures ZrO2:AG against staphylococcus aureus by hydrothermal method

Energy Technology Data Exchange (ETDEWEB)

Nova, C.V.; Reis, K.H.; Galico, D.A.; Venturini, J.; Pontes, F.M.L.; Pinheiro, A.L. [Universidade Estadual Paulista Julio de Mesquita Filho (UNESP), SP (Brazil); Longo, E. [Universidade Estadual de Campinas (UNICAMP), SP (Brazil)

2016-07-01

Nanostructures of zirconia (ZrO2) has shown great prominence in the area of advanced materials and shows excellent properties such as chemical stability, mechanical strength, electrical and optical properties. When certain metals are supported on the compound, such as Fe, Ag, Au and Al, a potentiation of some properties, such as bactericide and fungicide can occur. Thus, this work deals with the synthesis and characterization of ZrO2 and ZrO2:Ag (1% and 10 % of Ag) nanostructures and the study of the influence of the antimicrobial activity against Staphylococcus aureus. X-ray powder diffractograms of the zirconia and silver with zirconia shown the formation of well defined peaks of tetragonal zirconia in all the samples. Although the ZrO2:Ag (10 % of Ag) shown the characteristics peaks of cubic silver, these peaks do not appear in ZrO2:Ag (1 % of Ag) due to the small amount of silver in comparison with zirconium. The crystal size was estimated by the Scherrer equation and the calculated values for zirconia were 12.84, 12.27 and 12.61 nm for ZrO2, ZrO2 : Ag (1%) and ZrO2 : Ag (10%) respectively and the silver crystal size was 8,09 nm. Diffuse reflectance of the silver particles shown a broad plasmon band at 405 and 424 nm for the ZrO2 : Ag (1%) and ZrO2 : Ag (10%). Antimicrobial assay demonstrated that ZrO2 showed a bacteriostatic effect (61 %) and the inclusion of the silver in the ZrO2 matrix enhanced this effect to 65-72 %. Both particles with different silver content shown similar effect {[ZrO2:Ag 1%] = [ZrO2:Ag 10%]>[ZrO2]}.(author)

The structural and optical constants of Ag2S semiconductor nanostructure in the Far-Infrared.

Science.gov (United States)

Zamiri, Reza; Abbastabar Ahangar, Hossein; Zakaria, Azmi; Zamiri, Golnoosh; Shabani, Mehdi; Singh, Budhendra; Ferreira, J M F

2015-01-01

In this paper a template-free precipitation method was used as an easy and low cost way to synthesize Ag2S semiconductor nanoparticles. The Kramers-Kronig method (K-K) and classical dispersion theory was applied to calculate the optical constants of the prepared samples, such as the reflective index n(ω) and dielectric constant ε(ω) in Far-infrared regime. Nanocrystalline Ag2S was synthesized by a wet chemical precipitation method. Ag2S nanoparticle was characterized by X-ray diffraction, Scanning Electron Microscopy, UV-visible, and FT-IR spectrometry. The refinement of the monoclinic β-Ag2S phase yielded a structure solution similar to the structure reported by Sadanaga and Sueno. The band gap of Ag2S nanoparticles is around 0.96 eV, which is in good agreement with previous reports for the band gap energy of Ag2S nanoparticles (0.9-1.1 eV). The crystallite size of the synthesized particles was obtained by Hall-Williamson plot for the synthesized Ag2S nanoparticles and it was found to be 217 nm. The Far-infrared optical constants of the prepared Ag2S semiconductor nanoparticles were evaluated by means of FTIR transmittance spectra data and K-K method. Graphical abstractThe Far-infrared optical constants of Ag2S semiconductor nanoparticles.

Structural, electronic, elastic and thermal properties of Li{sub 2}AgSb. First-principles calculations

Energy Technology Data Exchange (ETDEWEB)

Li, Ji-Hong [Sichuan Univ., Chengdu (China). Inst. of Atomic and Molecular Physics; Longdong Univ., Qingyang (China). College of Physics and Electronic Engineering; Zhu, Xu-Hui [Sichuan Univ., Chengdu (China). Inst. of Atomic and Molecular Physics; Cheng, Yan [Sichuan Univ., Chengdu (China). Inst. of Atomic and Molecular Physics; Sichuan Univ., Chengdu (China). Key Laboratory of High Energy Density Physics and Technology of Ministry of Education; Ji, Guang-Fu [Chinese Academy of Engineering Physics, Mianyang (China). National Key Laboratory of Shock Wave and Detonation Physics

2015-07-01

Based on the first-principles density functional theory calculations combined with the quasi-harmonic Debye model, the pressure dependencies of the structural, elastic, electronic and thermal properties of Li{sub 2}AgSb were systematically investigated. The calculated lattice parameters and unit cell volume of Li{sub 2}AgSb at the ground state were in good agreement with the available experimental data. The obtained elastic constants, the bulk modulus and the shear modulus revealed that Li{sub 2}AgSb is mechanically stable and behaves in a ductile manner under the applied pressure. The elasticity-relevant properties, the Young's modulus and the Poisson's ratio showed that pressure can enhance the stiffness of Li{sub 2}AgSb and that Li{sub 2}AgSb is mechanically stable up to 20 GPa. The characteristics of the band structure and the partial density of states of Li{sub 2}AgSb were analysed, showing that Li{sub 2}AgSb is a semiconductor with a direct band gap of 217 meV at 0 GPa and that the increasing pressure can make the band structure of Li{sub 2}AgSb become an indirect one. Studies have shown that, unlike temperature, pressure has little effect on the heat capacity and the thermal expansion coefficient of Li{sub 2}AgSb.

Ag2S/CdS/TiO2 Nanotube Array Films with High Photocurrent Density by Spotting Sample Method

OpenAIRE

Sun, Hong; Zhao, Peini; Zhang, Fanjun; Liu, Yuliang; Hao, Jingcheng

2015-01-01

Ag2S/CdS/TiO2 hybrid nanotube array films (Ag2S/CdS/TNTs) were prepared by selectively depositing a narrow-gap semiconductor—Ag2S (0.9 eV) quantum dots (QDs)—in the local domain of the CdS/TiO2 nanotube array films by spotting sample method (SSM). The improvement of sunlight absorption ability and photocurrent density of titanium dioxide (TiO2) nanotube array films (TNTs) which were obtained by anodic oxidation method was realized because of modifying semiconductor QDs. The CdS/TNTs, Ag2S/TNT...

Novel Ag@TiO2 nanocomposite synthesized by electrochemically active biofilm for nonenzymatic hydrogen peroxide sensor

International Nuclear Information System (INIS)

Khan, Mohammad Mansoob; Ansari, Sajid Ali; Lee, Jintae; Cho, Moo Hwan

2013-01-01

A novel nonenzymatic sensor for H 2 O 2 was developed based on an Ag@TiO 2 nanocomposite synthesized using a simple and cost effective approach with an electrochemically active biofilm. The optical, structural, morphological and electrochemical properties of the as-prepared Ag@TiO 2 nanocomposite were examined by UV–vis spectroscopy, X-ray diffraction, transmission electron microscopy and cyclic voltammetry (CV). The Ag@TiO 2 nanocomposite was fabricated on a glassy carbon electrode (GCE) and their electrochemical performance was analyzed by CV, differential pulse voltammetry and electrochemical impedance spectroscopy. The Ag@TiO 2 nanocomposite modified GCE (Ag@TiO 2 /GCE) displayed excellent performance towards H 2 O 2 sensing at − 0.73 V in the linear response range from 0.83 μM to 43.3 μM, within a detection limit and sensitivity of 0.83 μM and ∼ 65.2328 ± 0.01 μAμM −1 cm −2 , respectively. In addition, Ag@TiO 2 /GCE exhibited good operational reproducibility and long term stability. - Graphical abstract: Synthesis of Ag@TiO 2 nanocomposite by electrochemically active biofilm for H 2 O 2 sensing. - Highlights: • Electrochemically active biofilm (EAB) • EAB mediated synthesis of Ag@TiO 2 nanocomposite • Ag@TiO 2 nanocomposite modified glassy carbon electrode • Ag@TiO 2 /GCE for H 2 O 2 sensing • Nonenzymatic sensor for H 2 O 2

Battery Relevant Electrochemistry of Ag7Fe3(P2O7)4 : Contrasting Contributions from the Redox Chemistries of Ag+ and Fe3+

International Nuclear Information System (INIS)

Zhang, Yiman; Marschilok, Amy C.; Stony Brook University, NY; Takeuchi, Esther S.

2016-01-01

Ag 7 Fe 3 (P 2 O 7 ) 4 is an example of an electrochemical displacement material which contains two different electrochemically active metal cations, where one cation (Ag + ) forms metallic silver nanoparticles external to the crystals of Ag 7 Fe 3 (P 2 O 7 ) 4 via an electrochemical reduction displacement reaction, while the other cation (Fe +3 ) is electrochemically reduced with the retention of iron cations within the anion structural framework concomitant with lithium insertion. These contrasting redox chemistries within one pure cathode material enable high rate capability and reversibility when Ag 7 Fe 3 (P 2 O 7 ) 4 is employed as cathode material in a lithium ion battery (LIB). Further, pyrophosphate materials are thermally and electrically stable, desirable attributes for cathode materials in LIBs. In this article, a bimetallic pyrophosphate material Ag 7 Fe 3 (P 2 O 7 ) 4 is synthesized and confirmed to be a single phase by Rietveld refinement. Electrochemistry of Ag 7 Fe 3 (P 2 O 7 ) 4 is reported for the first time in the context of lithium based batteries using cyclic voltammetry and galvanostatic discharge–charge cycling. The reduction displacement reaction and the lithium (de)insertion processes are investigated using ex situ X-ray absorption spectroscopy and X-ray diffraction of electrochemically reduced and oxidized Ag 7 Fe 3 (P 2 O 7 ) 4 . Ag 7 Fe 3 (P 2 O 7 ) 4 exhibits good reversibility at the iron centers indicated by ~80% capacity retention over 100 cycles following the initial formation cycle and excellent rate capability exhibited by ~70% capacity retention upon a 4-fold increase in current.

Ag-loaded TiO2/reduced graphene oxide nanocomposites for enhanced visible-light photocatalytic activity

International Nuclear Information System (INIS)

Vasilaki, E.; Georgaki, I.; Vernardou, D.; Vamvakaki, M.; Katsarakis, N.

2015-01-01

Highlights: • Ag nanoparticles were loaded on TiO 2 by chemical reduction. • TiO 2 /Ag and TiO 2 samples were deposited on reduced graphene oxide (rGO). • Their performance was evaluated via methylene blue removal under visible-light. • TiO 2 /Ag/rGO presented superior activity compared to TiO 2 , TiO 2 /Ag and TiO 2 /rGO. - Abstract: In this work, Ag nanoparticles were loaded by chemical reduction onto TiO 2 P25 under different loadings ranging from 1 up to 4 wt% and hydrothermally deposited on reduced graphene oxide sheets. Chemical reduction was determined to be an effective preparation approach for Ag attachment to titania, leading to the formation of small silver nanoparticles with an average diameter of 4.2 nm. The photocatalytic performance of the hybrid nanocomposite materials was evaluated via methylene blue (MB) dye removal under visible-light irradiation. The rate of dye decolorization was found to depend on the metal loading, showing an increase till a threshold value of 3 wt%, above which the rate drops. Next, the as prepared sample of TiO 2 /Ag of better photocatalytic response, i.e., at a 3 wt% loading value, was hydrothermally deposited on a platform of reduced graphene oxide (rGO) of tunable content (mass ratio). TiO 2 /Ag/rGO coupled nanocomposite presented significantly enhanced photocatalytic activity compared to the TiO 2 /Ag, TiO 2 /rGO composites and bare P25 titania semiconductor photocatalysts. In particular, after 45 min of irradiation almost complete decolorization of the dye was observed for the TiO 2 /Ag/rGO nanocatalyst, while the respective removal efficiency was 92% for TiO 2 /Ag, 93% for TiO 2 /rGO and only 80% for the bare TiO 2 nanoparticles. This simple step by step preparation strategy allows for optimum exploitation of the advanced properties of metal plasmonic effect and reduced graphene oxide as the critical host for boosting the overall photocatalytic activity towards visible-light.

Preparation of mesoporous Ag-containing TiO{sub 2} heterojunction film and its photocatalytic property

Energy Technology Data Exchange (ETDEWEB)

Wang, Q. Y., E-mail: wangqingyao0532@163.com [Ludong University, School of Chemistry and Materials Science (China); Qiao, J. L. [Jilin Agricultural University, College of Horticulture (China); Cui, X. Y. [Mudanjiang Medical University, School of Public Health (China); Zhong, J. S. [Hangzhou Dianzi University, College of Materials and Environmental Engineering (China); Xu, Y. B.; Zhang, S. H.; Zhang, Q. H.; Chang, P.; Li, M.; Zhang, C.; Gao, S. M., E-mail: gaosm@ustc.edu [Ludong University, School of Chemistry and Materials Science (China)

2015-03-15

Mesoporous Ag/TiO{sub 2} heterojunction films (Ag-MTHF) with enhanced photocatalytic activity were synthesized by a three-step approach including an electrochemical anodization technique followed by successive ionic layer adsorption and reaction (SILAR) and solvothermal methods. The distribution of Ag nanoparticles on the inner structure of the mesoporous TiO{sub 2} film was confirmed by field emission scanning electron (FE-SEM) and transmission electron microscopes (TEM). The formation progress of the novel mesoporous Ag/TiO{sub 2} nanojunction film with Ag average diameter of 17 nm was illuminated. The formed nanojunction between Ag and TiO{sub 2} nanoparticles largely enhanced the photocatalytic degradation of methyl orangey (MO), and the corresponding mechanism was proposed.

Preparation and self-sterilizing properties of Ag@TiO2-styrene-acrylic complex coatings.

Science.gov (United States)

Zhou, Xiang-dong; Chen, Feng; Yang, Jin-tao; Yan, Xiao-hui; Zhong, Ming-qiang

2013-04-01

In this study, we report a simple and cost-effective method for self-sterilized complex coatings obtained by Ag@TiO2 particle incorporation into styrene-acrylic latex. The Ag@TiO2 particles were prepared via a coupling agent modification process. The composite latices characterized by transmission electron microscopy (TEM) study were highly homogeneous at the nanometric scale, and the Ag@TiO2 particles were well dispersed and exhibited an intimate contact between both the organic and inorganic components. The Ag@TiO2 nanoparticles significantly enhanced the absorption in the visible region and engendered a good heat-insulating effect of the complex coatings. Moreover, the Ag@TiO2 nanoparticle incorporation into this polymer matrix renders self-sterilized nanocomposite materials upon light excitation, which are tested against Escherichia coli and Staphylococcus aureus. The complex coatings display an impressive performance in the killing of all micro-organisms with a maximum for a Ag@TiO2 loading concentration of 2-5 wt.%. The weathering endurance of the complex coating was also measured. Copyright © 2012 Elsevier B.V. All rights reserved.

Dielectric properties of nanophase Ag2HgI4 and Ag2HgI4–Al2O3 ...

Indian Academy of Sciences (India)

Unknown

ions (Leute and Rusche 1981). Many authors (Neubert ... The particles of Ag2HgI4 were separated from the suspen- sion, washed ... Capacitance (C) and dielectric loss (tan δ) were measured using a .... the energy of formation of lattice defects. Since the ... in fast-ion conductors is interpreted in terms of random hopping of ...

Synthesis, characterization, and thermal stability of SiO2/TiO2/CR-Ag multilayered nanostructures

Science.gov (United States)

Díaz, Gabriela; Chang, Yao-Jen; Philipossian, Ara

2018-06-01

The controllable synthesis and characterization of novel thermally stable silver-based particles are described. The experimental approach involves the design of thermally stable nanostructures by the deposition of an interfacial thick, active titania layer between the primary substrate (SiO2 particles) and the metal nanoparticles (Ag NPs), as well as the doping of Ag nanoparticles with an organic molecule (Congo Red, CR). The nanostructured particles were composed of a 330-nm silica core capped by a granular titania layer (10 to 13 nm in thickness), along with monodisperse 5 to 30 nm CR-Ag NPs deposited on top. The titania-coated support (SiO2/TiO2 particles) was shown to be chemically and thermally stable and promoted the nucleation and anchoring of CR-Ag NPs, which prevented the sintering of CR-Ag NPs when the structure was exposed to high temperatures. The thermal stability of the silver composites was examined by scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HRTEM). Larger than 10 nm CR-Ag NPs were thermally stable up to 300 °C. Such temperature was high enough to destabilize the CR-Ag NPs due to the melting point of the CR. On the other hand, smaller than 10 nm Ag NPs were stable at temperatures up to 500 °C because of the strong metal-metal oxide binding energy. Energy dispersion X-ray spectroscopy (EDS) was carried out to qualitatively analyze the chemical stability of the structure at different temperatures which confirmed the stability of the structure and the existence of silver NPs at temperatures up to 500 °C.

Chalcone dendrimer stabilized core-shell nanoparticles—a comparative study on Co@TiO2, Ag@TiO2 and Co@AgCl nanoparticles for antibacterial and antifungal activity

Science.gov (United States)

Vanathi Vijayalakshmi, R.; Praveen Kumar, P.; Selvarani, S.; Rajakumar, P.; Ravichandran, K.

2017-10-01

A series of core@shell nanoparticles (Co@TiO2, Ag@TiO2 and Co@AgCl) stabilized with zeroth generation triazolylchalcone dendrimer was synthesized using reduction transmetalation method. The coordination of chalcone dendrimer with silver ions was confirmed by UV-vis spectroscopy. The NMR spectrum ensures the number of protons and carbon signals in the chalcone dendrimer. The prepared samples were structurally characterized by XRD, FESEM and HRTEM analysis. The SAED and XRD analyses exhibited the cubic structure with d hkl   =  2.2 Å, 1.9 Å and 1.38 Å. The antibacterial and antifungal activities of the dendrimer stabilized core@shell nanoparticles (DSCSNPs) were tested against the pathogens Bacillus subtilis, Proteus mirabilis, Candida albicans and Aspergillus nigir from which it is identified that the dendrimer stabilized core shell nanoparticles with silver ions at the shell (Co@AgCl) shows effectively high activity against the tested pathogen following the other core@shell nanoparticles viz Ag@TiO2 and Co@TiO2.

Fig .1. X-ray diffraction (XRD) patterns of Ag2Se-G-TiO2 composites.

Indian Academy of Sciences (India)

32

SEM images of Ag2Se-G nanocomposites, (c)TiO2 nanoparticles and (d) SEM images of Ag2Se-. G-TiO2 .... Although photo-catalytic conversion of CO2 using solar energy is the most convenient route for the ..... based structure of graphene, the unpaired π electron merges with the metal nanoparticles, causing a shift in the ...

Research Progress on AgSbTe2-based Thermoelectric Materials

Institute of Scientific and Technical Information of China (English)

CAO Qigao; MA Guang; JIA Zhihua; ZHENG Jing; LI Jin

2012-01-01

Thermoelectric power generation represents a class of energy conversion technology,which has been used in power supply of aeronautic and astronautic exploring missions,now showing notable advantages to harvest the widely distributed waste heat and convert the abundant solar energy into electricity at lower cost than Si-based photovoltaic technology.Thermoelectric dimensionless figure of merit ZT plays a key role in the conversion efficiency from thermal to electrical energy.Low thermal conductivity and large Seebeck coefficient make the AgSbTe2 compound a very promising candidate for high efficiency p-type thermoelectric applications.The AgSbTe2-based thermoelectric system has been repeatedly studied as prospective thermoelectric materials.In this review,we firstly clarify some fundamental tradeoffs dictating the ZT value through the relationship ZT =S2σT/κ.We also pay special attentions to the recent advances in AgSbTe2-based thermoelectric materials.Finally,we provide an outlook of new directions in this filed.

Disruption of crystalline structure of Sn3.5Ag induced by electric current

International Nuclear Information System (INIS)

Huang, Han-Chie; Lin, Kwang-Lung; Wu, Albert T.

2016-01-01

This study presented the disruption of the Sn and Ag_3Sn lattice structures of Sn3.5Ag solder induced by electric current at 5–7 × 10"3 A/cm"2 with a high resolution transmission electron microscope investigation and electron diffraction analysis. The electric current stressing induced a high degree of strain on the alloy, as estimated from the X-ray diffraction (XRD) peak shift of the current stressed specimen. The XRD peak intensity of the Sn matrix and the Ag_3Sn intermetallic compound diminished to nearly undetectable after 2 h of current stressing. The electric current stressing gave rise to a high dislocation density of up to 10"1"7/m"2. The grain morphology of the Sn matrix became invisible after prolonged current stressing as a result of the coalescence of dislocations.

Synthesis and characterization of Ag doped TiO{sub 2} heterojunction films and their photocatalytic performances

Energy Technology Data Exchange (ETDEWEB)

Demirci, Selim, E-mail: selim.demirci@marmara.edu.tr [Marmara University, Department of Metallurgical and Materials Engineering, Kadiköy, 34722 Istanbul (Turkey); Dikici, Tuncay [Izmir Katip Celebi University, Department of Materials Science and Engineering, Cigli, 35620 Izmir (Turkey); Yurddaskal, Metin [Department of Metallurgical and Materials Engineering, Dokuz Eylul University, 35390 Izmir (Turkey); Center for Fabrication and Application of Electronic Materials, Dokuz Eylul University, 35390 Izmir (Turkey); Gultekin, Serdar [Department of Nanoscience and Nanoengineering, Dokuz Eylul University, 35390 İzmir (Turkey); Experimental Science Applications and Research Center, Celal Bayar University, 45140 Manisa (Turkey); Toparli, Mustafa; Celik, Erdal [Department of Metallurgical and Materials Engineering, Dokuz Eylul University, 35390 Izmir (Turkey); Department of Nanoscience and Nanoengineering, Dokuz Eylul University, 35390 İzmir (Turkey); Center for Fabrication and Application of Electronic Materials, Dokuz Eylul University, 35390 Izmir (Turkey)

2016-12-30

Highlights: • Ag doped TiO{sub 2} films were successfully synthesized by sol–gel spin coating method. • Ag in TiO{sub 2} lattice enters in intermediate states to decrease TiO{sub 2} bandgap energy. • Ag dopants increase the photoactivity and superhydrophilicity. • The degradation kinetics of methylene blue was studied. • The 0.7 mol% of Ag was found to be the optimum concentration. - Abstract: In this study, undoped and silver (Ag) doped titanium dioxide (TiO{sub 2}) films were successfully synthesized by sol-gel spin coating technique on the Si substrates. Photocatalytic activities of the TiO{sub 2} films with different Ag content were investigated for the degradation of methylene blue (MB) under UV light irradiation. The crystal phase structure, surface morphology, chemical and optical properties of Ag-doped TiO{sub 2} films were characterized using an X-ray diffractometer (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), UV–vis spectrophotometer, and FTIR spectrophotometer. The results showed that the Ag-doped TiO{sub 2} films calcined at 500 °C had the crystalline anatase phases and the surface morphologies with some cracks. Ag substitution into TiO{sub 2} matrix enhanced the photocatalytic activity of TiO{sub 2} films under UV light irradiation as compared to the undoped TiO{sub 2} film. Furthermore, the results indicated that the 0.7% Ag doped TiO{sub 2} film exhibited a superior photocatalytic activity than that of undoped and other Ag-doped TiO{sub 2} films. This study demonstrated the potential of an application of Ag doped films to efficiently treat dissolved organic contaminants in water.

Effect of Strain Rate on Joint Strength and Failure Mode of Lead-Free Solder Joints

Science.gov (United States)

Lin, Jian; Lei, Yongping; Fu, Hanguang; Guo, Fu

2018-03-01

In surface mount technology, the Sn-3.0Ag-0.5Cu solder joint has a shorter impact lifetime than a traditional lead-tin solder joint. In order to improve the impact property of SnAgCu lead-free solder joints and identify the effect of silver content on tensile strength and impact property, impact experiments were conducted at various strain rates on three selected SnAgCu based solder joints. It was found that joint failure mainly occurred in the solder material with large plastic deformation under low strain rate, while joint failure occurred at the brittle intermetallic compound layer without any plastic deformation at a high strain rate. Joint strength increased with the silver content in SnAgCu alloys in static tensile tests, while the impact property of the solder joint decreased with increasing silver content. When the strain rate was low, plastic deformation occurred with failure and the tensile strength of the Sn-3.0Ag-0.5Cu solder joint was higher than that of Sn-0.3Ag-0.7Cu; when the strain rate was high, joint failure mainly occurred at the brittle interface layer and the Sn-0.3Ag-0.7Cu solder joint had a better impact resistance with a thinner intermetallic compound layer.

Improved solar-driven photocatalytic performance of Ag_2CO_3/(BiO)_2CO_3 prepared in-situ

International Nuclear Information System (INIS)

Zhong, Junbo; Li, Jianzhang; Huang, Shengtian; Cheng, Chaozhu; Yuan, Wei; Li, Minjiao; Ding, Jie

2016-01-01

Highlights: • Ag_2CO_3/(BiO)_2CO_3 photocatalysts were prepared in-situ. • The photo-induced charge separation rate has been greatly increased. • The photocatalytic activity has been greatly promoted. - Abstract: Ag_2CO_3/(BiO)_2CO_3 composites have been fabricated in-situ via a facile parallel flaw co-precipitation method. The specific surface area, structure, morphology, and the separation rate of photo-induced charge pairs of the photocatalysts were characterized by Brunauer–Emmett–Teller (BET) method, X-ray diffraction (XRD), UV–vis diffuse reflectance spectroscopy(DRS), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), and surface photovoltage (SPV) spectroscopy, respectively. XRD patterns and DRS demonstrated that Ag_2CO_3 has no effect on the crystal phase and bandgap of (BiO)_2CO_3. The existence of Ag_2CO_3 in the composites enhances the separation rate of photo-induced charge pairs of the photocatalysts. The photocatalytic performance of Ag_2CO_3/(BiO)_2CO_3 was evaluated by the decolorization of methyl orange (MO) aqueous solution under simulated solar irradiation. It was found that the simulated solar-induced photocatalytic activity of Ag_2CO_3/(BiO)_2CO_3 copmposites was significantly improved, which was mainly attributed to the enhanced surface area and the separation rate of photo-induced charge pairs.

Fabrication of worm-like Ag2S nanocrystals under mediation of protein

Indian Academy of Sciences (India)

1College of Chemistry and Chemical Engineering, Pingdingshan University, Pingdingshan 467000, ... inorganic–organic nanocomposites and there is strong interaction between Ag2S and pepsin. ... applied in the fields of photovoltaics, electroluminescence .... method for fabricating Ag2S nanostructure by using proteins.