Science.gov

Sample records for oxysulfides

  1. Kinetics and Mechanisms of Nanosilver Oxysulfidation

    PubMed Central

    Liu, Jingyu; Pennell, Kelly G.; Hurt, Robert H.

    2011-01-01

    Among the many new engineered nanomaterials, nanosilver is one of the highest priority cases for environmental risk assessment. Recent analysis of field samples from water treatment facilities suggests that silver is converted to silver sulfide, whose very low solubility may limit the bioavailability and adverse impact of silver in the environment. The present study demonstrates that silver nanoparticles react with dissolved sulfide species (HS−, S2−) under relevant but controlled laboratory conditions to produce silver sulfide nanostructures similar to those observed in the field. The reaction is tracked by time-resolved sulfide depletion measurements to yield quantitative reaction rates and stoichiometries. The reaction requires dissolved oxygen, and it is sensitive to pH and natural organic matter. Focusedion-beam analysis of surface films reveals an irregular coarse-grained sulfide phase that allows deep (> 1 μm) conversion of silver surfaces without passivation. At high sulfide concentrations, nanosilver oxysulfidation occurs by a direct particle-fluid reaction. At low sulfide concentration, quantitative kinetic analysis suggests a mechanistic switch to an oxidative dissolution/precipitation mechanism, in which the biologically active Ag+ ion is generated as an intermediate. The environmental transformation pathways for nanosilver will vary depending on the media-specific competing rates of oxidative dissolution and direct oxysulfidation. PMID:21770469

  2. Zinc oxysulfide ternary alloy nanocrystals: A bandgap modulated photocatalyst

    SciTech Connect

    Pandey, Shiv K.; Pandey, Shipra; Pandey, Avinash C.; Mehrotra, G. K.

    2013-06-10

    Herein, we report a green economic route for the synthesis of a series of Zinc Oxysulfide (ZOS) (ZnO{sub 1-x}S{sub x}; 0 {<=} x {>=} 1; x = Sulfur) alloys nanoparticles. The crystallographic features of ZnO, ZOS, and ZnS confirmed by X-Ray Diffraction and validated by Transmission Electron Microscopy reveal the variation of lattice spacing in binary and ternary compositions with homogenous elemental distribution. The photocatalytic analysis of ZOS (0.4) is performed and compared with Degussa P25 to ascertain its photocatalytic activity against methyl orange under irradiation of 365 nm UV-Vis light. A bandgap of 2.7 eV for ZOS (0.4) aptly establishes its prospects for sunlight driven photocatalysis.

  3. Molten iron oxysulfide as a superior sulfur sorbent

    SciTech Connect

    Hepworth, M.T.

    1991-01-01

    Slagging combustors with injected lime or limestone are being considered as replacements for conventional coal burners. They have advantages in that they can be staged to reduce NO{sub x} and So{sub x} emissions. Iron oxide, as an alternative to lime or limestone may be effective not only as a desulfurizing agent, but under the right conditions of oxygen potential and after combination with sulfur, the reaction products of coal gases with iron oxide can act as a flux to produce a fluid phase. The thermodynamic conditions for optimum removal of sulfur from the first stage of a coal combustor are being determined by experiment and by use of existing data. Contour plots in which the pounds Of S0{sub 2} per million Btu of calorific power are plotted on isothermal ternary phase diagrams of the iron-oxygen-sulfur system. These contour plots determine the most favorable conditions for coal combustion in the presence of added iron oxide. Lowest S0{sub 2} pressures are close to the phase boundary limit between iron saturation and the oxysulfide liquid phase. Experimental studies in which ceramic containers (99% alumina) were used to contain the liquid were hampered by the tendency for the liquid to flow up and over the walls of containing vessels presumably as a result of surface tension effects. These effects, which make equilibration measurements difficult, may be favorable with respect to producing a high degree of reactivity of the oxysulfide with coal gases and resultant rapid reaction kinetics. As result of this problem, platinum containment vessels containers appear to avoid these surface tension effects. Thermodynamic and kinetic measurements are now being explored by thermogravimetric analysis.

  4. The BiCu1-xOS oxysulfide: Copper deficiency and electronic properties

    NASA Astrophysics Data System (ADS)

    Berthebaud, D.; Guilmeau, E.; Lebedev, O. I.; Maignan, A.; Gamon, J.; Barboux, P.

    2016-05-01

    An oxysulfide series of nominal compositions BiCu1-xOS with x<0.20 has been prepared and its structural properties characterized by combining powder X-ray diffraction and transmission electron microscopy techniques. It is found that this oxysulfide, crystallizing in the P4/nmm space group, tends to adopt a constant amount of copper vacancy corresponding to x=0.05 in the BiCu1-xOS formula. The presence of Cu vacancies is confirmed by HAADF-STEM analysis showing, in the Cu atomic columns, alternating peaks of different intensities in some very localized regions. For larger Cu deficiencies (x>0.05 in the nominal composition), other types of structural nanodefects are evidenced such as bismuth oxysulfides of the "BiOS" ternary system which might explain the report of superconductivity for the BiCu1-xOS oxysulfide. Local epitaxial growth of the BiCuOS oxysulfide on top of CuO is also observed. In marked contrast to the BiCu1-xOSe oxyselenide, these results give an explanation to the limited impact of Cu deficiency on the Seebeck coefficient in BiCu1-xOS compounds.

  5. Quantitative study on the chemical solution deposition of zinc oxysulfide

    DOE PAGES

    Reinisch, Michael; Perkins, Craig L.; Steirer, K. Xerxes

    2015-11-21

    Zinc Oxysulfide (ZnOS) has demonstrated potential in the last decade to replace CdS as a buffer layer material since it is a wide-band-gap semiconductor with performance advantages over CdS (Eg = 2.4 eV) in the near UV-range for solar energy conversion. However, questions remain on the growth mechanisms of chemical bath deposited ZnOS. In this study, a detailed model is employed to calculate solubility diagrams that describe simple conditions for complex speciation control using only ammonium hydroxide without additional base. For these conditions, ZnOS is deposited via aqueous solution deposition on a quartz crystal microbalance in a continuous flow cell.more » Data is used to analyze the growth rate dependence on temperature and also to elucidate the effects of dimethylsulfoxide (DMSO) when used as a co-solvent. Activation energies (EA) of ZnOS are calculated for different flow rates and solution compositions. As a result, the measured EA relationships are affected by changes in the primary growth mechanism when DMSO is included.« less

  6. Quantitative study on the chemical solution deposition of zinc oxysulfide

    SciTech Connect

    Reinisch, Michael; Perkins, Craig L.; Steirer, K. Xerxes

    2015-11-21

    Zinc Oxysulfide (ZnOS) has demonstrated potential in the last decade to replace CdS as a buffer layer material since it is a wide-band-gap semiconductor with performance advantages over CdS (Eg = 2.4 eV) in the near UV-range for solar energy conversion. However, questions remain on the growth mechanisms of chemical bath deposited ZnOS. In this study, a detailed model is employed to calculate solubility diagrams that describe simple conditions for complex speciation control using only ammonium hydroxide without additional base. For these conditions, ZnOS is deposited via aqueous solution deposition on a quartz crystal microbalance in a continuous flow cell. Data is used to analyze the growth rate dependence on temperature and also to elucidate the effects of dimethylsulfoxide (DMSO) when used as a co-solvent. Activation energies (EA) of ZnOS are calculated for different flow rates and solution compositions. As a result, the measured EA relationships are affected by changes in the primary growth mechanism when DMSO is included.

  7. Comparison with industrial oxysulfide phosphors for solid state lighting

    NASA Astrophysics Data System (ADS)

    Pote, S. S.

    2016-05-01

    Y2O2S:Eu3+ was prepared by the flux method which is different from conventional solid state reaction and has many advantages over the conventional method in terms of ease of preparation and yield also. In this paper we have reported the crystal structure, XRD and method of preparation of Y2O2S:Eu3+ along with Eu3+ mechanism of emission and excitation with reference to solid state lighting. In the emission spectra, the strongest red-emission lines at 626 and 616 nm are due to transition from 5D0 → 7F2 level. The stronger emission at λem=626 nm confirms the formation of the oxysulfide host. We also made a comparison of our prepared sample with commercial sample from NICHIA Corporation Japan in terms of PL intensity which results that our sample is equally intense as that of NICHIA's sample. It is suggested that these characteristics can be useful for obtaining a low cost, red phosphor for the solid state lighting using near UV LED.

  8. Molten metal containment vessel with rare earth oxysulfide protective coating thereon and method of making same

    DOEpatents

    Krikorian, Oscar H.; Curtis, Paul G.

    1992-01-01

    An improved molten metal containment vessel is disclosed in which wetting of the vessel's inner wall surfaces by molten metal is inhibited by coating at least the inner surfaces of the containment vessel with one or more rare earth oxysulfide or rare earth sulfide compounds to inhibit wetting and or adherence by the molten metal to the surfaces of the containment vessel.

  9. Geometric magnetic frustration in RE{sub 2}O{sub 2}S oxysulfides (RE = Sm, Eu and Gd)

    SciTech Connect

    Biondo, V.; Sarvezuk, P.W.C.; Ivashita, F.F.; Silva, K.L.; Paesano, A.; Isnard, O.

    2014-06-01

    Graphical abstract: Stacked planes in the <001> direction of an oxysulfide structure, showing the triangular nets formed by rare earth cations, which moments present geometric magnetic frustration. - Highlights: • We prepared monophasic RE{sub 2}O{sub 2}S Oxysulfides (RE = Sm, Eu and Gd). • RE{sub 2}O{sub 2}S compounds were characterized regarding structural and magnetic properties. • Mössbauer spectra were obtained for Eu{sub 2}O{sub 2}S and Gd{sub 2}O{sub 2}S at different temperatures. • Oxysulfides present geometric magnetic frustration of the rare-earth sublattice. - Abstract: RE{sub 2}O{sub 2}S oxysulfides (with RE = Sm, Eu and Gd) were prepared and characterized regarding their structural and magnetic properties. The compounds crystallized in the trigonal symmetry (space group P-3m/D{sub 3}{sup 3}d), with the lattice parameter varying linearly with the ionic radius of the RE cation. All these oxysulfides are magnetically frustrated and only the gadolinium sample showed magnetic order down to 3 K. The magnetic frustration is attributed to the spatial distribution of cations over the lattice, where the RE’s magnetic moments occupy the sites forming a triangular plane lattice, perpendicular to the direction. This geometric magnetic frustration was firstly recognized for these oxysulfides.

  10. Molten iron oxysulfide as a superior sulfur sorbent. Final report, [September 1989--1993

    SciTech Connect

    Hepworth, M.T.

    1993-03-31

    The studies had as original objective the analysis of conditions for using liquid iron oxysulfide as a desulfuring agent during coal gasification. Ancillary was a comparison of iron oxysulfide with lime as sorbents under conditions where lime reacts with S-bearing gases to form Ca sulfate or sulfide. Primary thrust is to determine the thermodynamic requirements for desulfurization by iron additions (e.g., taconite concentrate) during combustion in gasifiers operating at high equivalence ratios. Thermodynamic analysis of lime-oxygen-sulfur system shows why lime is injected into burners under oxidizing conditions; reducing conditions forms CaS, requiring its removal, otherwise oxidation and release of S would occur. Iron as the oxysulfide liquid has a range of stability and can be used as a desulfurizing agent, if the burner/gasifier operates in a sufficiently reducing regime (high equivalence ratio); this operating range is given and is calculable for a coal composition, temperature, stoichiometry. High moisture or hydrogen contents of the coal yield a poorer degree of desulfurization. Kinetic tests on individual iron oxide particles on substrates or Pt cups with a TGA apparatus fail to predict reaction rates within a burner. Preliminary tests on the Dynamic Containment Burner with acetylene give some promise that this system can produce the proper conditions of coal gasification for use of added iron as a sulfur sorbent.

  11. Preparation of Highly Crystallized Yttrium Oxysulfide Suspension via a Novel Colloidal Processing.

    PubMed

    Wang, Hong; Jiang, Tao; Xing, Ming-Ming; Fu, Yao; Peng, Yong; Luo, Xi-Xian

    2016-04-01

    High-crystallized Y2O2S suspension was synthesized by a novel two-step method of high temperature solid-state reaction and subsequent colloidal processing. The synthesis method proposed in this study retains all advantages of the high temperature solid-state reaction method. The obtained data agrees with that of the PDF card, which indicates the product is pure Y2O2S crystals. The results show that the prepared Y2O2S particles are highly crystallized without any significant defects. The fine smooth particles were almost regular, exhibiting an approximately subspherical shape. Quantitative image analysis of particles suggests a mean particle size of 120±34 nm. That is to say, the yttrium oxysulfide colloid prepared by this method have a very narrow size distribution. The obtained ethanol suspension shows Tyndall effect when irradiated with laser of wavelength 532 nm. In addition, the particles exhibit excellent dispersibility in ethanol solution. This is rarely observed for the covalent compounds, which generally present poor dispersibility in solution. As is known to all, the state of the dispersion depends on the acid leaching process. The acid leaching process facilitates the adsorption of ethanol molecules on the surface of the particles. The electrostatic repulsive force among colloidal particles will improve their rheological properties and dispersibility in solution. In this study, the particles can be dispersed well in ethanol after acid leaching. The method'proposed in this study can be extended for the preparation of mono-dispersed oxysulfide nanophosphors and may provide an efficient way for the preparation of stable covalent compound dispersions. PMID:27451744

  12. Solution preparation of the amorphous molybdenum oxysulfide MoOS{sub 2} and its use for catalysis

    SciTech Connect

    Genuit, Daisy; Bezverkhyy, Igor; Afanasiev, Pavel . E-mail: afanas@catalyse.univ-lyon1.fr

    2005-09-15

    Acid condensation of aqueous MoO{sub 2}S{sub 2} {sup 2-} anion yields amorphous MoOS{sub 2} oxysulfide. This compound possesses tubular morphology and when freshly precipitated is soluble in polar organics such as acetone and ethanol. The ensemble of characterizations (IR, UV-visible, EXAFS spectroscopy) suggests that it contains cyclic or short linear oligomers of neutral molybdenum (V) oxysulfide MoOS{sub 2} core. Thermal decomposition of MoOS{sub 2} under inert atmosphere leads to the formation of a mixture of MoO{sub 2} and MoS{sub 2} phases. Promotion of MoOS{sub 2} with cobalt followed by sulfidation leads to highly active HDS catalysts.

  13. Silicon Oxysulfide, OSiS: Rotational Spectrum, Quantum-Chemical Calculations, and Equilibrium Structure.

    PubMed

    Thorwirth, Sven; Mück, Leonie Anna; Gauss, Jürgen; Tamassia, Filippo; Lattanzi, Valerio; McCarthy, Michael C

    2011-06-01

    Silicon oxysulfide, OSiS, and seven of its minor isotopic species have been characterized for the first time in the gas phase at high spectral resolution by means of Fourier transform microwave spectroscopy. The equilibrium structure of OSiS has been determined from the experimental data using calculated vibration-rotation interaction constants. The structural parameters (rO-Si = 1.5064 Å and rSi-S = 1.9133 Å) are in very good agreement with values from high-level quantum chemical calculations using coupled-cluster techniques together with sophisticated additivity and extrapolation schemes. The bond distances in OSiS are very short in comparison with those in SiO and SiS. This unexpected finding is explained by the partial charges calculated for OSiS via a natural population analysis. The results suggest that electrostatic effects rather than multiple bonding are the key factors in determining bonding in this triatomic molecule. The data presented provide the spectroscopic information needed for radio astronomical searches for OSiS.

  14. Thermodynamics of MnO-SiO2-Al2O3-MnS Liquid Oxysulfide: Experimental and Thermodynamic Modeling

    NASA Astrophysics Data System (ADS)

    Kim, Ye-Jin; Woo, Dae-Hee; Gaye, Henri; Lee, Hae-Geon; Kang, Youn-Bae

    2011-06-01

    The activities of MnO and MnS in a MnO-SiO2-Al2O3(or AlO1.5)-MnS liquid oxysulfide solution were investigated by employing the gas/liquid/Pt-Mn alloy chemical equilibration technique under a controlled atmosphere at 1773 K (1500 °C). Also, the sulfide capacity, defined as C S = (wt pct S)( pO2/ pS2)1/2, in MnO-SiO2-Al2O3 slag with a dilute MnS concentration was obtained from the measured experimental data. As X SiO2/( X MnO + X SiO2) in liquid oxysulfide increases, the activity coefficient of MnO decreases, while that of MnS first increases and then decreases. As X(AlO1.5) in liquid oxysulfide increases, the activity coefficient of MnS increases, while no remarkable change is observed for the activity coefficient of MnO. The behavior of the activity coefficient of MnS was qualitatively analyzed by considering MnO + A x S y (SiS2 or Al2S3) = MnS + A x O y (SiO2 or Al2O3) reciprocal exchange reactions in the oxysulfide solution. The behavior was shown to be consistent with phase diagram data, namely, the MnS saturation boundary. Quantitative analysis of the activity coefficient of the oxysulfide solution was also carried out by employing the modified quasichemical model in the quadruplet approximation.

  15. Molten iron oxysulfide as a superior sulfur sorbent. Technical progress report, June 1, 1991--August 31, 1991

    SciTech Connect

    Hepworth, M.T.

    1991-12-31

    Slagging combustors with injected lime or limestone are being considered as replacements for conventional coal burners. They have advantages in that they can be staged to reduce NO{sub x} and So{sub x} emissions. Iron oxide, as an alternative to lime or limestone may be effective not only as a desulfurizing agent, but under the right conditions of oxygen potential and after combination with sulfur, the reaction products of coal gases with iron oxide can act as a flux to produce a fluid phase. The thermodynamic conditions for optimum removal of sulfur from the first stage of a coal combustor are being determined by experiment and by use of existing data. Contour plots in which the pounds Of S0{sub 2} per million Btu of calorific power are plotted on isothermal ternary phase diagrams of the iron-oxygen-sulfur system. These contour plots determine the most favorable conditions for coal combustion in the presence of added iron oxide. Lowest S0{sub 2} pressures are close to the phase boundary limit between iron saturation and the oxysulfide liquid phase. Experimental studies in which ceramic containers (99% alumina) were used to contain the liquid were hampered by the tendency for the liquid to flow up and over the walls of containing vessels presumably as a result of surface tension effects. These effects, which make equilibration measurements difficult, may be favorable with respect to producing a high degree of reactivity of the oxysulfide with coal gases and resultant rapid reaction kinetics. As result of this problem, platinum containment vessels containers appear to avoid these surface tension effects. Thermodynamic and kinetic measurements are now being explored by thermogravimetric analysis.

  16. A new continuous two-step molecular precursor route to rare-earth oxysulfides Ln{sub 2}O{sub 2}S

    SciTech Connect

    De Crom, N.

    2012-07-15

    A continuous two-step molecular precursor pathway is designed for the preparation of rare-earth oxysulfides Ln{sub 2}O{sub 2}S (Ln=Y, La, Pr, Nd, Sm-Lu). This new route involves a first oxidation step leading to the rare-earth oxysulfate Ln{sub 2}O{sub 2}SO{sub 4} which is subsequently reduced to the rare-earth oxysulfide Ln{sub 2}O{sub 2}S by switching to a H{sub 2}-Ar atmosphere. The whole process occurs at a temperature significantly lower than usual solid state synthesis (T{<=}650 Degree-Sign C) and avoids the use of dangerous sulfur-based gases, providing a convenient route to the synthesis of the entire series of Ln{sub 2}O{sub 2}S. The molecular precursors consist in heteroleptic dithiocarbamate complexes [Ln(Et{sub 2}dtc){sub 3}(phen)] and [Ln(Et{sub 2}dtc){sub 3}(bipy)] (Et{sub 2}dtc=N,N-diethyldithiocarbamate; phen=1,10-phenanthroline; bipy=2,2 Prime -bipyridine) and were synthesized by a new high yield and high purity synthesis route. The nature of the molecular precursor determines the minimum synthesis temperature and influences therefore the purity of the final Ln{sub 2}O{sub 2}S crystalline phase. - Graphical abstract: A continuous two-step molecular precursor pathway was designed for the preparation of rare-earth oxysulfides Ln{sub 2}O{sub 2}S (Ln=Y, La, Pr, Nd, Sm-Lu), starting from heteroleptic dithiocarbamate complexes. The influence of the nature of the molecular precursor on the minimum synthesis temperature and on the purity of the final Ln{sub 2}O{sub 2}S crystalline phase is discussed. Highlights: Black-Right-Pointing-Pointer A new high yield and high purity synthesis route of rare earth dithiocarbamates is described. Black-Right-Pointing-Pointer These compounds are used as precursors in a continuous process leading to rare-earth oxysulfides. Black-Right-Pointing-Pointer The oxysulfides are obtained under much more moderate conditions than previously described.

  17. Molten iron oxysulfide as a superior sulfur sorbent. Technical progress report, September 1, 1991--November 30, 1991

    SciTech Connect

    Hepworth, M.T.

    1991-12-31

    Slagging combustors with injected lime or limestone are being considered as replacements for conventional coal burners. They have advantages in that they can be staged to reduce NO{sub x} and So{sub x} emissions. Iron oxide, as an alternative to lime or limestone may be effective not only as a desulfurizing agent, but under the right conditions of oxygen potential and after combination with sulfur, the reaction products of coal gases with iron oxide can act as a flux to produce a fluid phase. The thermodynamic conditions for optimum removal of sulfur from the first stage of a coal combustor are being determined by experiment and by use of existing data. Analysis of the phase equilibria indicates that optimum conditions for deployment of the reducing stage of a multi-stage burner operating with iron injection are close to the boundary of the liquid iron oxysulfide phase with iron-saturation. Two prior investigations differ with respect to the location of this phase boundary at temperatures over 1400{degree}C, with reference 1, showing the phase boundary nearer the iron-rich corner than reference 2 which gives the boundary further into the liquid region. Effort has been directed during this quarter to showing that this phase boundary is sufficiently close to the iron-rich liquid region, at higher temperatures, in order to allow for smooth operation of a multistage burner without the problem of iron deposition.

  18. Terbium-doped gadolinium oxysulfide (Gd2O2S:Tb) scintillation-based polymer optical fibre sensor for real time monitoring of radiation dose in oncology

    NASA Astrophysics Data System (ADS)

    Lewis, E.; O'Keeffe, S.; Grattan, M.; Hounsell, A.; McCarthy, D.; Woulfe, P.; Cronin, J.; Mihai, L.; Sporea, D.; Santhanam, A.; Agazaryan, N.

    2014-05-01

    A PMMA based plastic optical fibre sensor for use in real time radiotherapy dosimetry is presented. The optical fibre tip is coated with a scintillation material, terbium-doped gadolinium oxysulfide (Gd2O2S:Tb), which fluoresces when exposed to ionising radiation (X-Ray). The emitted visible light signal penetrates the sensor optical fibre and propagates along the transmitting fibre at the end of which it is remotely monitored using a fluorescence spectrometer. The results demonstrate good repeatability, with a maximum percentage error of 0.5% and the response is independent of dose rate.

  19. Molten iron oxysulfide as a superior sulfur sorbent. Technical progress report, December 1, 1991--February 29, 1992

    SciTech Connect

    Hepworth, M.T.

    1992-02-28

    Slagging combustors with injected lime or limestone are being considered as replacements for conventional coal burners. They have advantages in that they can be staged to reduce NO{sub x} and SO{sub x} emissions. Iron oxide, as an alternative to lime or limestone may be effective not only as a desulfurizing agent, but under the right conditions of oxygen potential and after combination with sulfur, the reaction products of coal gases with iron oxide can act as a flux to produce a fluid phase. The thermodynamic conditions for optimum removal of sulfur from the first stage of a coal combustor are being determined by experiment and by use of existing data. Analysis of the phase equilibria indicates that optimum conditions for deployment of the reducing stage of a multi-stage, burner operating with iron injection are close to the boundary of the liquid iron oxysulfide phase with iron-saturation. Two prior investigations differ with respect to the location of this phase boundary at temperatures over 1400{degree}C: with reference 1, showing the phase boundary nearer the iron-rich corner than reference 2 which gives the boundary further into the liquid region. In this quarter experimental studies were conducted on equilibrium compositions which are the most effective in achieving desulfurization. These conditions were studied by thermogravimetric analysis (TGA). They serve to check the data reported by the two above-reference investigations for their experimental conditions of 1200{degree}C, and also to check extend the data given in the literature to a temperature of 1300{degree}C. The model used for this interpolation was reported upon in the prior quarterly report (9/1/91-11/30/92 Appendix A).

  20. Recycling of the anode from spent Ni-MH batteries for synthesis of the lanthanide oxysulfide/oxysulfate compounds used in an oxygen storage and release system

    NASA Astrophysics Data System (ADS)

    Dixini, P. V. M.; Celante, V. G.; Lelis, M. F. F.; Freitas, M. B. J. G.

    2014-08-01

    In this work, lanthanide oxysulfide/oxysulfate compounds, denominated as an oxygen storage and release system, have been synthesized from the anode electrodes of spent Ni-MH batteries. The rare earth metals have recovered by means of chemical precipitation as a mixture of La2(SO4)3, Ce2(SO4)3, and Nd2(SO4)3. The synthesis of (La·Nd)O2S·CeO2 have been carried out by subjecting a mixture of La2(SO4)3, Ce2(SO4)3, and Nd2(SO4)3 to a heat treatment in a reducing atmosphere up to 1000 °C. The (La·Nd)O2SO4·CeO2 compounds have been obtained after thermal treatment of (La·Nd)O2S·CeO2 in a synthetic air atmosphere. The oxysulfide/oxysulfate compounds have been subjected to thermal cycles, respectively, in synthetic air as well as in an N2-CO atmosphere. The thermogravimetric plot (TG) for (La·Nd)2O2S·CeO2 shows a mass gain of 14.98% w/w in a temperature range of 300-550 °C, which is due to the oxidation of (La·Nd)2O2S·CeO2 to (La·Nd)2O2SO4CeO2, where 2 mol of O2 are added. Likewise, in the (La·Nd)2O2SO4CeO2 thermogravimetric plot, a mass loss of 17.16% w/w is observed in the range of 500-750 °C. This loss of mass can be associated with output of 2 mol of O2 forming again the (La·Nd)2O2S·CeO2. The transformation of the (La·Nd)2·O2S·CeO2 to (La·Nd)2O2SO4CeO2 causes an increase in the macropores.

  1. Effects of the Cu off-stoichiometry on transport properties of wide gap p-type semiconductor, layered oxysulfide LaCuSO

    SciTech Connect

    Goto, Yosuke Tanaki, Mai; Okusa, Yuki; Matoba, Masanori; Kamihara, Yoichi; Shibuya, Taizo; Yasuoka, Kenji

    2014-07-14

    Layered oxysulfide LaCu{sub 1−x}SO (x = 0–0.03) was prepared to elucidate the effect of Cu off-stoichiometry on their electrical and thermal transport properties. Electrical resistivity drastically decreases down from ∼10{sup 5} Ω·cm to ∼10{sup −1} Ω·cm as a result of Cu deficiency (x = 0.01) at 300 K. Thermal conductivity of the samples at 300 K, which is dominated by lattice components, is estimated to be 2.3(3) Wm{sup −1}K{sup −1}. Stoichiometric LaCuSO has an optical band gap of 3.1 eV, while broad optical absorption at photon energies of approximately 2.1 eV was observed for Cu-deficient samples. Density functional theory calculation suggests that these broad absorption structures probably originate from the in-gap states generated by the sulfur vacancies created to compensate the charge imbalance due to Cu off-stoichiometry. These results clearly demonstrate that Cu deficiency plays a crucial role in determining the electrical transport properties of Cu-based p-type transparent semiconductors.

  2. Influence of Partial Pressure of Sulfur and Oxygen on Distribution of Fe and Mn between Liquid Fe-Mn Oxysulfide and Molten Slag

    NASA Astrophysics Data System (ADS)

    Kim, Sun-Joong; Shibata, Hiroyuki; Takekawa, Jun; Kitamura, Shin-Ya; Yamaguchi, Katsunori; Kang, Youn-Bae

    2012-10-01

    The authors proposed an innovative process for recovering Mn from steelmaking slag. The process starts with the sulfurization of steelmaking slag to separate P from Mn by the formation of a liquid sulfide phase (matte). Then, the obtained matte is weakly oxidized to make a Mn-rich oxide phase without P. High-purity Fe-Mn alloys can therefore be produced by the reduction of the Mn-rich oxide phase. However, to the authors' knowledge, the sulfurization of molten slag containing P and Mn has not been sufficiently investigated. It was recently found that P was not distributed to the matte in equilibrium with the molten slag. To gain knowledge of the process's development, it is important to investigate the influence of the partial pressures of sulfur and oxygen on the equilibrium distribution of Mn and Fe between the matte and the molten slag. In the current work, a mineralogical microstructure analysis of the matte revealed that the existence of the oxysulfide and metal phases was dependent on the partial pressure of sulfur and oxygen. The Mn content of the matte increased with partial pressure of sulfur while the O content of the matte decreased. In contrast, the ratio of Mn/Fe in the matte was constant when the metal phase of the matte was observed at a log P_{{{{O}}2 }} below -11. These results also corresponded to the relationship between the activity coefficient ratio of MnS/FeS and the mole fraction of MnS/FeS in the matte. The γ MnS/ γ FeS value decreased exponentially as the mole fraction of MnS/FeS increased.

  3. Framework to predict optimal buffer layer pairing for thin film solar cell absorbers: A case study for tin sulfide/zinc oxysulfide

    SciTech Connect

    Mangan, Niall M.; Brandt, Riley E.; Steinmann, Vera; Jaramillo, R.; Poindexter, Jeremy R.; Chakraborty, Rupak; Buonassisi, Tonio; Yang, Chuanxi; Park, Helen Hejin; Zhao, Xizhu; Gordon, Roy G.

    2015-09-21

    An outstanding challenge in the development of novel functional materials for optoelectronic devices is identifying suitable charge-carrier contact layers. Herein, we simulate the photovoltaic device performance of various n-type contact material pairings with tin(II) sulfide (SnS), a p-type absorber. The performance of the contacting material, and resulting device efficiency, depend most strongly on two variables: conduction band offset between absorber and contact layer, and doping concentration within the contact layer. By generating a 2D contour plot of device efficiency as a function of these two variables, we create a performance-space plot for contacting layers on a given absorber material. For a simulated high-lifetime SnS absorber, this 2D performance-space illustrates two maxima, one local and one global. The local maximum occurs over a wide range of contact-layer doping concentrations (below 10{sup 16 }cm{sup −3}), but only a narrow range of conduction band offsets (0 to −0.1 eV), and is highly sensitive to interface recombination. This first maximum is ideal for early-stage absorber research because it is more robust to low bulk-minority-carrier lifetime and pinholes (shunts), enabling device efficiencies approaching half the Shockley-Queisser limit, greater than 16%. The global maximum is achieved with contact-layer doping concentrations greater than 10{sup 18 }cm{sup −3}, but for a wider range of band offsets (−0.1 to 0.2 eV), and is insensitive to interface recombination. This second maximum is ideal for high-quality films because it is more robust to interface recombination, enabling device efficiencies approaching the Shockley-Queisser limit, greater than 20%. Band offset measurements using X-ray photoelectron spectroscopy and carrier concentration approximated from resistivity measurements are used to characterize the zinc oxysulfide contacting layers in recent record-efficiency SnS devices. Simulations representative of these

  4. Crystal Structure, Electronic Structure, and Photocatalytic Activity of Oxysulfides: La2Ta2ZrS2O8, La2Ta2TiS2O8, and La2Nb2TiS2O8.

    PubMed

    Goto, Yosuke; Seo, Jeongsuk; Kumamoto, Kazunori; Hisatomi, Takashi; Mizuguchi, Yoshikazu; Kamihara, Yoichi; Katayama, Masao; Minegishi, Tsutomu; Domen, Kazunari

    2016-04-01

    The novel oxysulfides La2Ta2ZrS2O8 (LTZSO), La2Ta2TiS2O8 (LTTSO), and La2Nb2TiS2O8 (LNTSO) were synthesized, and their crystal structures, electronic structures, and photocatalytic activities for water splitting under visible light were investigated. Density functional theory calculations showed that these compounds are direct-band-gap semiconductors. Close to the conduction band minimum, the main contribution to the band structure comes from the d orbitals of Zr or Ti ions, while the region near the valence band maximum is associated with the 3p orbitals of S ions. The absorption-edge wavelength was determined to be 540 nm for LTZSO and 700 nm for LTTSO and LNTSO. An analysis of the crystal structure using synchrotron X-ray diffraction revealed that these compounds contained antisite defects at transition metal ion sites, and these were considered to be the origin of the broad absorption at wavelengths longer than that corresponding to band-gap excitation. LTZSO was revealed to be active in the oxygen evolution reaction from aqueous solution containing a sacrificial electron acceptor under visible-light illumination. This result was supported by the band alignment and flat-band potential determined by photoelectron spectroscopy and Mott-Schottky plots.

  5. Molten iron oxysulfide as a superior sulfur sorbent

    SciTech Connect

    Hepworth, M.T.

    1990-01-01

    Slagging combustors with injected lime or limestone are being considered as replacements for conventional coal burners. They have advantages in that they can be staged to reduce NO{sub x} and SO{sub x} emissions. Iron oxide, as an alternative to lime or limestone may be effective not only as a desulfurizing agent, but, under the right conditions of oxygen potential, it can act as a flux to produce a glassy slag. This glassy slag should be dense and environmentally inert. In this reporting period, the thermodynamic conditions are determined for the operation of the first stage of a combustor which would have as its feed six types of coals. The calculations are made for the four phase equilibrium: FeO(wustite)/Fe/Liquid/Gas over the temperature range 950{degrees} to 1300{degrees}C. The minimum dosage of iron oxide required at equilibrium an the calculated maximum percent sulfur removal are reported. Also given are the expected pounds of S0{sub 2} per million Btu of heat evolution calculated for complete combustion. These preliminary results indicate in the Fe-O-S system that higher temperatures give better results approaching 96 percent sulfur removal from a coal containing (on a dry basis) 3.29% by weight sulfur. In the prior reporting period, a comparison is made between iron oxide and lime as a desulfurizing agent. With lime, the thermodynamic conditions were chosen: a set of conditions where the compound calcium sulfide is the product and a set of conditions where calcium sulfate is the product. The temperature limits of the sulfate forming and sulfide forming reactions were defined.

  6. Molten iron oxysulfide as a superior sulfur sorbent

    SciTech Connect

    Hepworth, M.T.

    1990-01-01

    Slagging combustors with injected lime or limestone are being considered as replacements for conventional coal burners. They have advantages in that they can be staged to reduce NO{sub x} and SO{sub x} emissions. Iron oxide, as an alternative to lime or limestone may be effective not only as a desulfurizing agent, but under the right conditions of oxygen potential and after combination with sulfur, the reaction products of coal gases with iron oxide can act as a flux to produce a fluid phase. The thermodynamic conditions for determining the most effective operating conditions of the first stage of a combustor are calculated for several Illinois coals. These conditions include contact of the gas with the phase combinations: CaO/CaSO{sub 4}, CaO/CaS, and Fe/FeO/liquid for the temperature range 950{degree} to 1300{degree}C. In the latter system, the minimum dosage of iron required at equilibrium and the calculated maximum percent sulfur removal are reported. Also given are the expected pounds of SO{sub 2} per million Btu of heat evolution calculated for complete combustion. The calculations indicate that for the Fe-O-S system, higher temperatures give better results approaching 96 percent sulfur removal from a coal containing 4.2% sulfur. For this example, the stack gas emerging from the second stage of combustion under stoichiometric conditions would contain 0.36 pounds of SO{sub 2} per million BTU's of heat generated. The temperature limits of the sulfate and sulfide forming reactions are defined.

  7. Bulk superconductivity in bismuth oxysulfide Bi4O4S3.

    PubMed

    Singh, Shiva Kumar; Kumar, Anuj; Gahtori, Bhasker; Shruti; Sharma, Gyaneshwar; Patnaik, Satyabrata; Awana, Veer P S

    2012-10-10

    A very recent report on the observation of superconductivity in Bi(4)O(4)S(3) [Mizuguchi, Y.; http://arxiv.org/abs/1207.3145] could potentially reignite the search for superconductivity in a broad range of layered sulfides. We report here the synthesis of Bi(4)O(4)S(3) at 500 °C by a vacuum encapsulation technique and its basic characterizations. The as-synthesized Bi(4)O(4)S(3) was contaminated with small amounts of Bi(2)S(3) and Bi impurities. The majority phase was found to be tetragonal (space group I4/mmm) with lattice parameters a = 3.9697(2) Å and c = 41.3520(1) Å. Both AC and DC magnetization measurements confirmed that Bi(4)O(4)S(3) is a bulk superconductor with a superconducting transition temperature (T(c)) of 4.4 K. Isothermal magnetization (M-H) measurements indicated closed loops with clear signatures of flux pinning and irreversible behavior. The lower critical field (H(c1)) at 2 K for the new superconductor was found to be ~15 Oe. Magnetotransport measurements showed a broadening of the resistivity (ρ) and a decrease in T(c) (ρ = 0) with increasing magnetic field. The extrapolated upper critical field H(c2)(0) was ~31 kOe with a corresponding Ginzburg-Landau coherence length of ~100 Å . In the normal state, the ρ ~ T(2) dependence was not indicated. Hall resistivity data showed a nonlinear magnetic field dependence. Our magnetization and electrical transport measurements substantiate the appearance of bulk superconductivity in as-synthesized Bi(4)O(4)S(3). On the other hand, Bi heat-treated at the same temperature is not superconducting, thus excluding the possibility of impurity-driven superconductivity in the newly discovered superconductor Bi(4)O(4)S(3).

  8. Co-solvent enhanced zinc oxysulfide buffer layers in Kesterite copper zinc tin selenide solar cells.

    PubMed

    Steirer, K Xerxes; Garris, Rebekah L; Li, Jian V; Dzara, Michael J; Ndione, Paul F; Ramanathan, Kannan; Repins, Ingrid; Teeter, Glenn; Perkins, Craig L

    2015-06-21

    A co-solvent, dimethylsulfoxide (DMSO), is added to the aqueous chemical "bath" deposition (CBD) process used to grow ZnOS buffer layers for thin film Cu2ZnSnSe4 (CZTSe) solar cells. Device performance improves markedly as fill factors increase from 0.17 to 0.51 upon the co-solvent addition. X-ray photoelectron spectroscopy (XPS) analyses are presented for quasi-in situ CZTSe/CBD-ZnOS interfaces prepared under an inert atmosphere and yield valence band offsets equal to -1.0 eV for both ZnOS preparations. When combined with optical band gap data, conduction band offsets exceed 1 eV for the water and the water/DMSO solutions. XPS measurements show increased downward band bending in the CZTSe absorber layer when the ZnOS buffer layer is deposited from water only. Admittance spectroscopy data shows that the ZnOS deposited from water increases the built-in potential (Vbi) yet these solar cells perform poorly compared to those made with DMSO added. The band energy offsets imply an alternate form of transport through this junction. Possible mechanisms are discussed, which circumvent the otherwise large conduction band spike between CZTSe and ZnOS, and improve functionality with the low-band gap absorber, CZTSe (Eg = 0.96 eV). PMID:26000570

  9. Nanoparticles of lanthanide oxysulfate/oxysulfide for improved oxygen storage/release.

    PubMed

    Zhang, Wuyuan; Arends, Isabel W C E; Djanashvili, Kristina

    2016-09-28

    Lanthanide oxysulfates have the ability to store and release large volumes of oxygen under oxidizing/reducing conditions, rendering them interesting as automotive catalysts. Herein we demonstrate a remarkable improvement of both processes by utilization of nanoparticles compared to the bulk materials. A further improvement of the catalytic activity was achieved by cost-effective doping with 1.9 wt% of Ni. PMID:27515224

  10. Co-solvent enhanced zinc oxysulfide buffer layers in Kesterite copper zinc tin selenide solar cells.

    PubMed

    Steirer, K Xerxes; Garris, Rebekah L; Li, Jian V; Dzara, Michael J; Ndione, Paul F; Ramanathan, Kannan; Repins, Ingrid; Teeter, Glenn; Perkins, Craig L

    2015-06-21

    A co-solvent, dimethylsulfoxide (DMSO), is added to the aqueous chemical "bath" deposition (CBD) process used to grow ZnOS buffer layers for thin film Cu2ZnSnSe4 (CZTSe) solar cells. Device performance improves markedly as fill factors increase from 0.17 to 0.51 upon the co-solvent addition. X-ray photoelectron spectroscopy (XPS) analyses are presented for quasi-in situ CZTSe/CBD-ZnOS interfaces prepared under an inert atmosphere and yield valence band offsets equal to -1.0 eV for both ZnOS preparations. When combined with optical band gap data, conduction band offsets exceed 1 eV for the water and the water/DMSO solutions. XPS measurements show increased downward band bending in the CZTSe absorber layer when the ZnOS buffer layer is deposited from water only. Admittance spectroscopy data shows that the ZnOS deposited from water increases the built-in potential (Vbi) yet these solar cells perform poorly compared to those made with DMSO added. The band energy offsets imply an alternate form of transport through this junction. Possible mechanisms are discussed, which circumvent the otherwise large conduction band spike between CZTSe and ZnOS, and improve functionality with the low-band gap absorber, CZTSe (Eg = 0.96 eV).

  11. Nanoparticles of lanthanide oxysulfate/oxysulfide for improved oxygen storage/release.

    PubMed

    Zhang, Wuyuan; Arends, Isabel W C E; Djanashvili, Kristina

    2016-09-28

    Lanthanide oxysulfates have the ability to store and release large volumes of oxygen under oxidizing/reducing conditions, rendering them interesting as automotive catalysts. Herein we demonstrate a remarkable improvement of both processes by utilization of nanoparticles compared to the bulk materials. A further improvement of the catalytic activity was achieved by cost-effective doping with 1.9 wt% of Ni.

  12. Molten iron oxysulfide as a superior sulfur sorbent. Third quarter technical progress report, June 1--August 31, 1990

    SciTech Connect

    Hepworth, M.T.

    1990-12-31

    Slagging combustors with injected lime or limestone are being considered as replacements for conventional coal burners. They have advantages in that they can be staged to reduce NO{sub x} and SO{sub x} emissions. Iron oxide, as an alternative to lime or limestone may be effective not only as a desulfurizing agent, but under the right conditions of oxygen potential and after combination with sulfur, the reaction products of coal gases with iron oxide can act as a flux to produce a fluid phase. The thermodynamic conditions for determining the most effective operating conditions of the first stage of a combustor are calculated for several Illinois coals. These conditions include contact of the gas with the phase combinations: CaO/CaSO{sub 4}, CaO/CaS, and Fe/FeO/liquid for the temperature range 950{degree} to 1300{degree}C. In the latter system, the minimum dosage of iron required at equilibrium and the calculated maximum percent sulfur removal are reported. Also given are the expected pounds of SO{sub 2} per million Btu of heat evolution calculated for complete combustion. The calculations indicate that for the Fe-O-S system, higher temperatures give better results approaching 96 percent sulfur removal from a coal containing 4.2% sulfur. For this example, the stack gas emerging from the second stage of combustion under stoichiometric conditions would contain 0.36 pounds of SO{sub 2} per million BTU`s of heat generated. The temperature limits of the sulfate and sulfide forming reactions are defined.

  13. Molten iron oxysulfide as a superior sulfur sorbent. Third quarter technical progress report, March 1, 1990--June 1, 1990

    SciTech Connect

    Hepworth, M.T.

    1990-12-31

    Slagging combustors with injected lime or limestone are being considered as replacements for conventional coal burners. They have advantages in that they can be staged to reduce NO{sub x} and SO{sub x} emissions. Iron oxide, as an alternative to lime or limestone may be effective not only as a desulfurizing agent, but, under the right conditions of oxygen potential, it can act as a flux to produce a glassy slag. This glassy slag should be dense and environmentally inert. In this reporting period, the thermodynamic conditions are determined for the operation of the first stage of a combustor which would have as its feed six types of coals. The calculations are made for the four phase equilibrium: FeO(wustite)/Fe/Liquid/Gas over the temperature range 950{degrees} to 1300{degrees}C. The minimum dosage of iron oxide required at equilibrium an the calculated maximum percent sulfur removal are reported. Also given are the expected pounds of S0{sub 2} per million Btu of heat evolution calculated for complete combustion. These preliminary results indicate in the Fe-O-S system that higher temperatures give better results approaching 96 percent sulfur removal from a coal containing (on a dry basis) 3.29% by weight sulfur. In the prior reporting period, a comparison is made between iron oxide and lime as a desulfurizing agent. With lime, the thermodynamic conditions were chosen: a set of conditions where the compound calcium sulfide is the product and a set of conditions where calcium sulfate is the product. The temperature limits of the sulfate forming and sulfide forming reactions were defined.

  14. Molten iron oxysulfide as a superior sulfur sorbent. Technical progress report, September 1, 1989--March 1, 1990

    SciTech Connect

    Hepworth, M.T.

    1990-03-06

    Slagging combustors with injected lime or limestone are being considered as replacements for conventional coal burners. They have advantages in that they can be stages to reduce NO{sub x} and SO{sub x} emissions. Iron oxide, as an alternative to lime or-limestone may be effective not only as a desulfurizing agent, but, under the right conditions of oxygen potential, it can act as a flux to produce a glassy slag This glassy slag should be dense and environmentally inert. In this reporting period, the thermodynamic conditions for the operation of the first stage of a combustor operating on a Illinois No. 2 Coal have been examined with respect to the formation of the four phase equilibrium:FeO(wustite)/Fe/liquid/gas over the temperature 950{degree} to 1300{degree}C. The minimum dosages of iron oxide which are required at equilibrium and the calculated maximum percent sulfur removal are reported. Also given are the expected pounds of S per million Btu of heat SO{sub 2} evolution calculated for complete combustion. These preliminary results indicate that higher temperatures, in the range studied, give better results approaching 96 percent sulfur removal from a coal containing (on a dry basis) 3.29% by weight sulfur. A comparison is made between iron oxide and lime as a desulfurizing agent. With lime, the thermodynamic conditions were chosen: a set of conditions where the compound calcium sulfide is the product and a set of conditions where calcium sulfate is the product. The temperature limits of the sulfate forming and sulfide forming reactions are defined.

  15. Crystal structure and electrical properties of the mixed valent titanium oxysulfide Sm 2Ti 2S 2O 4.5

    NASA Astrophysics Data System (ADS)

    Guillot-Deudon, C.; Meignen, V.; Cario, L.; Lafond, A.; Meerschaut, A.

    2004-07-01

    A new phase Sm 2Ti 2S 2O 4.5 was synthesized and its crystal structure was solved by single-crystal X-ray diffraction. This compound crystallizes in the monoclinic system ( C2 /m) with lattice constants a=17.9987(11) Å, b=3.71607(14) Å, c=12.6172(8) Å and β=133.645(4)°. The structure is built up from double chains of Ti-centered octahedra between which Sm-polyhedra develop. In spite of very close formulations, the structure of Sm 2Ti 2S 2O 4.5 differs completely from that of the defect Ruddelsden-Popper phase Sm 2Ti 2S 2O 5 previously reported. The title compound presents a mixed valence for titanium with Ti(III) ( d1) and Ti(IV) ( d0) located in different crystallographic sites. However, conductivity measurements show that this compound is non-metallic.

  16. Bandgap narrowing in the layered oxysulfide semiconductor Ba3Fe2O5Cu2S2: Role of FeO2 layer

    NASA Astrophysics Data System (ADS)

    Han, Zhang; Shifeng, Jin; Liwei, Guo; Shijie, Shen; Zhiping, Lin; Xiaolong, Chen

    2016-02-01

    A new layered Cu-based oxychalcogenide Ba3Fe2O5Cu2S2 has been synthesized and its magnetic and electronic properties were revealed. Ba3Fe2O5Cu2S2 is built up by alternatively stacking [Cu2S2]2- layers and iron perovskite oxide [(FeO2)(BaO)(FeO2)]2- layers along the c axis that are separated by barium ions with Fe3+ fivefold coordinated by a square-pyramidal arrangement of oxygen. From the bond valence arguments, we inferred that in layered CuCh-based (Ch = S, Se, Te) compounds the +3 cation in perovskite oxide sheet prefers a square pyramidal site, while the lower valence cation prefers the square planar sites. The studies on susceptibility, transport, and optical reflectivity indicate that Ba3Fe2O5Cu2S2 is an antiferromagnetic semiconductor with a Néel temperature of 121 K and an optical bandgap of 1.03 eV. The measurement of heat capacity from 10 K to room temperature shows no anomaly at 121 K. The Debye temperature is determined to be 113 K. Theoretical calculations indicate that the conduction band minimum is predominantly contributed by O 2p and 3d states of Fe ions that antiferromagnetically arranged in FeO2 layers. The Fe 3d states are located at lower energy and result in a narrow bandgap in comparison with that of the isostructural Sr3Sc2O5Cu2S2. Project supported by the National Natural Science Foundation of China (Grant Nos. 51472266, 51202286, and 91422303), the Strategic Priority Research Program (B) of the Chinese Academy of Sciences (Grant No. XDB07020100) and the ICDD.

  17. Photoluminescence properties and energy levels of RE (RE = Pr, Sm, Er, Tm) in layered-CaZnOS oxysulfide

    SciTech Connect

    Zhang, Zhi-Jun; Feng, Ang; Chen, Xiang-Yang; Zhao, Jing-Tai

    2013-12-07

    RE{sup 3+} (RE = Pr, Sm, Er, Tm)-activated CaZnOS samples were prepared by a solid-state reaction method at high temperature, and their photoluminescence properties were investigated. Doping with RE{sup 3+} (RE = Pr, Sm, Er, Tm) into layered-CaZnOS resulted in typical RE{sup 3+} (RE = Pr, Sm, Er, Tm) f-f line absorptions and emissions, as well as the charge transfer band of Sm{sup 3+} at about 3.3 eV. The energy level scheme containing the position of the 4f and 5d levels of all divalent and trivalent lanthanide ions with respect to the valence and conduction bands of CaZnOS has been constructed based on the new data presented in this work, together with the data from literature on Ce{sup 3+} and Eu{sup 2+} doping in CaZnOS. The detailed energy level scheme provides a platform for interpreting the optical spectra and could be used to comment on the valence stability of the lanthanide ions in CaZnOS.

  18. Comparison of high-MTF and reduced-noise radiographic imaging systems

    NASA Astrophysics Data System (ADS)

    Bunch, Phillip C.

    1995-05-01

    The objective imaging characteristics of a wide range of gandolinium oxysulfide-based, zero- crossover, screen-film combinations are presented and compared. It is shown that complex high-spatial frequency versus low-spatial frequency performance tradeoffs are found among these systems, when these systems are examined in terms of sensitometric response, modulation transfer function, noise equivalent quanta, and detective quantum efficiency.

  19. Thermodynamics and phase relations of the Fe-O-S-Si2(sat) system at 1200 °C and the effect of copper

    NASA Astrophysics Data System (ADS)

    Li, H.; Rankin, W. J.

    1994-01-01

    A laboratory investigation was carried out in which iron was reacted in silica crucibles with an atmosphere of controlled oxygen and sulfur partial pressures. The equilibrium compositions of the melts were determined over the range 10-12 to 10-9 atm oxygen and 10-2.75 to 10-1 atm sulfur and it was found that the Fe-O-S-SiO2 system can exist as either a slag or oxysulfide. The oxysulfide contained appreciable quantities of dissolved oxygen and silica, although the levels decreased as the sulfur content was increased. Sulfur also had the effect of reducing the solubility of silica in the slag. When copper was added to the system, the solubility of oxygen and silica in the oxysulfide phase decreased dramatically. The results are examined in terms of the thermodynamics of the relevant reactions, and the predominance area diagram for the copper-free system was established by combining the present results with those of earlier investigations.

  20. Spencer-Attix water/medium stopping-power ratios for the dosimetry of proton pencil beams.

    PubMed

    Gomà, C; Andreo, P; Sempau, J

    2013-04-21

    This paper uses Monte Carlo simulations to calculate the Spencer-Attix water/medium stopping-power ratios (sw, med) for the dosimetry of scanned proton pencil beams. It includes proton energies from 30 to 350 MeV and typical detection materials such as air (ionization chambers), radiochromic film, gadolinium oxysulfide (scintillating screens), silicon and lithium fluoride. Track-ends and particles heavier than protons were found to have a negligible effect on the water/air stopping-power ratios (sw, air), whereas the mean excitation energy values were found to carry the largest source of uncertainty. The initial energy spread of the beam was found to have a minor influence on the sw, air values in depth. The water/medium stopping-power ratios as a function of depth in water were found to be quite constant for air and radiochromic film-within 2.5%. Also, the sw, med values were found to have no clinically relevant dependence on the radial distance-except for the case of gadolinium oxysulfide and proton radiography beams. In conclusion, the most suitable detection materials for depth-dose measurements in water were found to be air and radiochromic film active layer, although a small correction is still needed to compensate for the different sw, med values between the plateau and the Bragg peak region. Also, all the detection materials studied in this work-except for gadolinium oxysulfide-were found to be suitable for lateral dose profiles and field-specific dose distribution measurements in water.

  1. Thermodynamic Modeling of Sulfide Capacity of Na2O-Containing Oxide Melts

    NASA Astrophysics Data System (ADS)

    Moosavi-Khoonsari, Elmira; Jung, In-Ho

    2016-07-01

    Thermodynamic modeling of the sulfide dissolution in the Na2O-FetO-CaO-MgO-MnO-Al2O3-SiO2 multicomponent slags was performed to investigate the desulfurization of hot metal using Na2O-containing fluxes. The dissolution behavior of sulfur in the melts was modeled using the modified quasi-chemical model in the quadruplet approximation. This model can take into account the short-range ordering and the reciprocal exchange reaction of cations and anions in oxy-sulfide slags. Experimental sulfide capacity data were well predicted from the model with only three model parameters.

  2. Thermodynamic Modeling of Sulfide Capacity of Na2O-Containing Oxide Melts

    NASA Astrophysics Data System (ADS)

    Moosavi-Khoonsari, Elmira; Jung, In-Ho

    2016-10-01

    Thermodynamic modeling of the sulfide dissolution in the Na2O-FetO-CaO-MgO-MnO-Al2O3-SiO2 multicomponent slags was performed to investigate the desulfurization of hot metal using Na2O-containing fluxes. The dissolution behavior of sulfur in the melts was modeled using the modified quasi-chemical model in the quadruplet approximation. This model can take into account the short-range ordering and the reciprocal exchange reaction of cations and anions in oxy-sulfide slags. Experimental sulfide capacity data were well predicted from the model with only three model parameters.

  3. Towards the design of novel cuprate-based superconductors

    NASA Astrophysics Data System (ADS)

    Yee, Chuck-Hou

    The rapid maturation of materials databases combined with recent development of theories seeking to quantitatively link chemical properties to superconductivity in the cuprates provide the context to design novel superconductors. In this talk, we describe a framework designed to search for new superconductors, which combines chemical rules-of-thumb, insights of transition temperatures from dynamical mean-field theory, first-principles electronic structure tools, materials databases and structure prediction via evolutionary algorithms. We apply the framework to design a family of copper oxysulfides and evaluate the prospects of superconductivity.

  4. Proton-conducting cerate ceramics

    SciTech Connect

    Pederson, L.R.; Coffey, G.W.; Bates, J.L.; Weber, W.J.

    1996-08-01

    Single-cell solid oxide fuel cells were constructed using strontium cerate as the electrolyte and their performance tested. Like certain zirconates, hafnates, and tantalates, the cerate perovskites are among a class of solid electrolytes that conduct protons at elevated temperatures. Depending on the temperature and chemical environment, these ceramics also support electronic and oxygen ion currents. A maximum power output of {approx}100 mW per cm{sup 2} electrolyte surface area was obtained at 900{degrees}C using 4% hydrogen as the fuel and air as the oxidant. A series of rare earth/ceria/zirconia were prepared and their electrical properties characterized. Rare earth dopants included ytterbia, yttria, terbia, and europia. Ionic conductivities were highest for rare earth/ceria and rare earth zirconia compositions; a minimum in ionic conductivity for all series were found for equimolar mixtures of ceria and zirconia. Cerium oxysulfide is of interest in fossil energy applications because of its high chemical stability and refractory nature. An alternative synthesis route to preparing cerium oxysulfide powders has been developed using combustion techniques.

  5. Synthesis and characterization Bi2O2S thin film via chemical bath deposition at low pH

    NASA Astrophysics Data System (ADS)

    KARİPER, İ. Afşin

    2016-06-01

    Bismuth oxysulfide thin film was prepared using Bi(NO3)3 and Na2S as reactive. Since bismuth in the form of bismuth oxide is dissolved into water, bismuth and sulfide concentration of the chemical bath is very important. Bismuth oxysulfide (Bi2O2S) thin films were produced below pH 2. Tested bismuth and sulfide concentrations are as follows: 2 × 10- 1 M, 2 × 10- 2 M, 2 × 10- 3 M, 2 × 10- 4 M bismuth and 1 × 10- 1 M, 1 × 10- 2 M, 1 × 10- 3 M, 1 × 10- 4 M sulfide. The structure of the films was examined via X-ray diffraction (XRD). Optical properties, such as transmission and absorbance were measured with Ultra violet-visible spectrum, and then refractive index and reflectivity were calculated. The pH of chemical bath was stabilized below pH of 2 using 13.85 mL concentrated nitric acid. Deposition time and temperature of the baths were 4 h and 30 °C. It has been found that bismuth and sulfide concentrations affected the structure and thickness of the film. Also, optical band gap of the films varied with concentration, parallel to the change of the structure and film thickness.

  6. Synthesis and characterization Bi2O2S thin film via chemical bath deposition at low pH.

    PubMed

    Kariper, I Afşin

    2016-06-15

    Bismuth oxysulfide thin film was prepared using Bi(NO3)3 and Na2S as reactive. Since bismuth in the form of bismuth oxide is dissolved into water, bismuth and sulfide concentration of the chemical bath is very important. Bismuth oxysulfide (Bi2O2S) thin films were produced below pH2. Tested bismuth and sulfide concentrations are as follows: 2×10(-1)M, 2×10(-2)M, 2×10(-3)M, 2×10(-4)M bismuth and 1×10(-1)M, 1×10(-2)M, 1×10(-3)M, 1×10(-4)M sulfide. The structure of the films was examined via X-ray diffraction (XRD). Optical properties, such as transmission and absorbance were measured with Ultra violet-visible spectrum, and then refractive index and reflectivity were calculated. The pH of chemical bath was stabilized below pH of 2 using 13.85mL concentrated nitric acid. Deposition time and temperature of the baths were 4h and 30°C. It has been found that bismuth and sulfide concentrations affected the structure and thickness of the film. Also, optical band gap of the films varied with concentration, parallel to the change of the structure and film thickness. PMID:27043873

  7. Synthesis and characterization of physical properties of Gd2O2S:Pr3+ semi-nanoflower phosphor

    NASA Astrophysics Data System (ADS)

    Bagheri, A.; Rezaee Ebrahim Saraee, Kh.; Shakur, H. R.; Zamani Zeinali, H.

    2016-05-01

    Pure gadolinium oxysulfide phosphor (Gd2O2S) and trivalent praseodymium-doped gadolinium oxysulfide phosphor (Gd2O2S:Pr3+) scintillators with semi-nanoflower crystalline structures were successfully synthesized through a precipitation method and subsequent calcination treatment as a converter for X-ray imaging detectors. The characterization such as the crystal structures and nanostructure of Gd2O2S:Pr3+ scintillator measured by XRD and FeE-SEM experiment. The optical properties of Gd2O2S:Pr3+ scintillator were studied. Luminescence spectra of Gd2O2S:Pr3+ under 320 nm UV excitation show a green emission at near 511 nm corresponding to the 3P0-3H4 of Pr ions. After scintillation properties of synthesized Gd2O2S:Pr3+ scintillator investigated, Gd2O2S:Pr3+ scintillating film fabricated on a glass substrate by a sedimentation method. X-ray imaging of the fabricated scintillators confirmed that the Gd2O2S:Pr3+ scintillator could be used for radiography applications in which good spatial resolution is needed.

  8. Characterizing energy dependence and count rate performance of a dual scintillator fiber-optic detector for computed tomography

    SciTech Connect

    Hoerner, Matthew R. Stepusin, Elliott J.; Hyer, Daniel E.; Hintenlang, David E.

    2015-03-15

    Purpose: Kilovoltage (kV) x-rays pose a significant challenge for radiation dosimetry. In the kV energy range, even small differences in material composition can result in significant variations in the absorbed energy between soft tissue and the detector. In addition, the use of electronic systems in light detection has demonstrated measurement losses at high photon fluence rates incident to the detector. This study investigated the feasibility of using a novel dual scintillator detector and whether its response to changes in beam energy from scatter and hardening is readily quantified. The detector incorporates a tissue-equivalent plastic scintillator and a gadolinium oxysulfide scintillator, which has a higher sensitivity to scatter x-rays. Methods: The detector was constructed by coupling two scintillators: (1) small cylindrical plastic scintillator, 500 μm in diameter and 2 mm in length, and (2) 100 micron sheet of gadolinium oxysulfide 500 μm in diameter, each to a 2 m long optical fiber, which acts as a light guide to transmit scintillation photons from the sensitive element to a photomultiplier tube. Count rate linearity data were obtained from a wide range of exposure rates delivered from a radiological x-ray tube by adjusting the tube current. The data were fitted to a nonparalyzable dead time model to characterize the time response. The true counting rate was related to the reference free air dose air rate measured with a 0.6 cm{sup 3} Radcal{sup ®} thimble chamber as described in AAPM Report No. 111. Secondary electron and photon spectra were evaluated using Monte Carlo techniques to analyze ionization quenching and photon energy-absorption characteristics from free-in-air and in phantom measurements. The depth/energy dependence of the detector was characterized using a computed tomography dose index QA phantom consisting of nested adult head and body segments. The phantom provided up to 32 cm of acrylic with a compatible 0.6 cm{sup 3} calibrated

  9. Improving the Spatial Resolution of Neutron Imaging at Paul Scherrer Institut - The Neutron Microscope Project

    NASA Astrophysics Data System (ADS)

    Trtik, Pavel; Hovind, Jan; Grünzweig, Christian; Bollhalder, Alex; Thominet, Vincent; David, Christian; Kaestner, Anders; Lehmann, Eberhard H.

    Here we present results stemming from the first prototype of the Neutron Microscope instrument at Paul ScherrerInstitut (PSI). The instrument is based on a very thin gadolinium oxysulfide (Gd2O2S:Tb+) scintillator screen and a magnifying optics. The Neutron Microscope prototype has been tested at the ICON and the BOA beamlines at PSI and sub-10 μm features can be clearly resolved on a focussed ion beam (FIB) enhance test object - a gadolinium-based Siemens star. The spatial resolution of the images of the gadolinium-based Siemensstar assessed by Fourier ring correlation was about 7.6 μm. The outlook for future improvement of the Neutron Microscope system is presented.

  10. Optical fiber sensor for low dose gamma irradiation monitoring

    NASA Astrophysics Data System (ADS)

    de Andrés, Ana I.; Esteban, Ã.`scar; Embid, Miguel

    2016-05-01

    An optical fiber gamma ray detector is presented in this work. It is based on a Terbium doped Gadolinium Oxysulfide (Gd2O2S:Tb) scintillating powder which cover a chemically etched polymer fiber tip. This etching improves the fluorescence gathering by the optical fiber. The final diameter has been selected to fulfill the trade-off between light gathering and mechanical strength. Powder has been encapsulated inside a microtube where the fiber tip is immersed. The sensor has been irradiated with different air Kerma doses up to 2 Gy/h with a 137Cs source, and the spectral distribution of the fluorescence intensity has been recorded in a commercial grade CCD spectrometer. The obtained signal-to-noise ratio is good enough even for low doses, which has allowed to reduce the integration time in the spectrometer. The presented results show the feasibility for using low cost equipment to detect/measure ionizing radiation as gamma rays are.

  11. In situ microscopic studies on the structural and chemical behaviors of lithium-ion battery materials

    NASA Astrophysics Data System (ADS)

    Shao, Minhua

    2014-12-01

    The direct observation of the microstructural evolution and state-of-charge (SOC) distribution in active materials is crucial to understand the lithiation/delithiation mechanisms during electrochemical cycling of lithium-ion batteries (LIBs). Owing to their high spatial resolutions and capability to map chemical states by combining other spectroscopic techniques, microscopic techniques including X-ray fluorescence (XRF) microscopy, Raman microscopy, transmission X-ray microscopy (TXM), scanning electron microscopy (SEM), and transmission electron microscopy (TEM) play significant roles in real time monitoring the dynamic changes in the LIB electrodes and materials. This paper reviews the recent progress of using in situ microscopic techniques to study LIB materials, including Si-, Sn-, Ge-, C- and metal oxides-based anode materials, and layered oxysulfide, metal fluorides, LiCoO2, LiNi0.8Co0.15Al0.05O2, LiMn2O4, LiFePO4 cathode materials.

  12. Laser-induced fluorescence of phosphors for remote cryogenic thermometry

    NASA Technical Reports Server (NTRS)

    Beshears, D. L.; Capps, G. J.; Cates, M. R.; Simmons, C. M.; Schwenterly, S. W.

    1990-01-01

    Remote cryogenic temperature measurements can be made by inducing fluorescence in phosphors with temperature-dependent emissions and measuring the emission lifetimes. The thermographic phosphor technique can be used for making precision, noncontact, cryogenic-temperature measurements in electrically hostile environments, such as high dc electric or magnetic fields. The National Aeronautics and Space Administration is interested in using these thermographic phosphors for mapping hot spots on cryogenic tank walls. Europium-doped lanthanum oxysulfide (La2O2S:Eu) and magnesium fluorogermanate doped with manganese (Mg4FGeO6:Mn) are suitable for low-temperature surface thermometry. Several emission lines, excited by a 337-nm ultraviolet laser, provide fluorescence lifetimes having logarithmic dependence with temperature from 4 to above 125 K. A calibration curve for both La2O2S:Eu and Mg4FGeO6:Mn is presented, as well as emission spectra taken at room temperature and 11 K.

  13. Catalytic oxidation of aqueous hydrogen sulfide in the presence of sulfite

    SciTech Connect

    Weres, O.; Tsao, L.; Chhatre, R.M.

    1985-06-01

    Nickel sulfate catalyzes the reaction of hydrogen sulfide with oxygen in aqueous solution. This reaction was studied, and an empirical rate expression and a reaction mechanism were deduced. The rate of oxidation is independent of oxygen concentration and pH over the range investigated. The reaction rate is one half order in nickel, and it changes from second to first order in sulfide with increasing concentration. The oxidation reaction is an autocatalytic, free radical chain reaction. Nickel catalyzes the chain initiation step, and polysulfido radical ions propagate the chains. Colloidal sulfur is a major, frequently undesirable reaction product. Sodium sulfite suppresses formation of colloidal sulfur by converting it to thiosulfate. Cobalt is an equally potent catalyst, but a colloidal dispersion of cobalt oxysulfide is produced. Iron compounds are much weaker catalysts; iron citrate and iron HEDTA (n-hydroxyethylenediaminetriacetic acid) were among those tested. 24 references, 15 figures, 3 tables.

  14. Electroluminescence in Tb-doped Gd2O2S phosphor

    NASA Astrophysics Data System (ADS)

    Shanker, V.; Chatterjee, S.; Ghosh, P. K.

    1992-12-01

    We report a strong ac green electroluminescence (EL) in powder layers of terbium doped gadolinium oxysulfide (Gd2O2S:Tb) with methyl methacrylate as binder. An intensity of the order of 30 nits (Cd/sq m) has been achieved. The EL emission spectra shows line emissions corresponding to 5D3 and 5D4 fluorescing levels of Tb(3+) ions. A very sharply rising B-V curve normally related to insulator-phosphor interface properties of a thin film electroluminescent device has been observed in these cells. This indicates the possibilities of barrier formation due to the localized space charge region in the absence of any prominent interfaces leading to impact excitation of Tb(3+) ions. This has further been confirmed by the excitation spectrum of Gd2O2S:Tb phosphor, which reveals Tb(3+) impurity absorption bands related to 4f8 shell transitions.

  15. Performance characteristics of high-MTF screen-film systems

    NASA Astrophysics Data System (ADS)

    Bunch, Phillip C.

    1994-05-01

    The development of specialized dyes that essentially prevent light from crossing the film base in double-coated gadolinium oxysulfide (GOS) phosphor-based radiographic systems has made it possible to design screen-film combinations with significantly improved MTF characteristics. Specifically, by using GOS-based screens with reduced light diffusion properties in combination with near-zero-crossover radiographic films, significantly improved MTF can be obtained at competitive speed and effective x-ray attenuation levels. The basic performance characteristics of such screen-film systems are described in some detail, including x-ray attenuation properties, sensitivity to scattered x-radiation, sensitometric data, contrast transfer functions, noise equivalent quanta, and detective quantum efficiency. It is also shown that high-MTF GOS screens are available that meet or exceed the performance characteristics of comparable UV-emitting yttrium tantalate phosphor-based materials.

  16. Atomic layer deposition of Al-incorporated Zn(O,S) thin films with tunable electrical properties

    SciTech Connect

    Park, Helen Hejin; Jayaraman, Ashwin; Heasley, Rachel; Yang, Chuanxi; Hartle, Lauren; Gordon, Roy G.; Mankad, Ravin; Haight, Richard; Gunawan, Oki; Mitzi, David B.

    2014-11-17

    Zinc oxysulfide, Zn(O,S), films grown by atomic layer deposition were incorporated with aluminum to adjust the carrier concentration. The electron carrier concentration increased up to one order of magnitude from 10{sup 19} to 10{sup 20} cm{sup −3} with aluminum incorporation and sulfur content in the range of 0 ≤ S/(Zn+Al) ≤ 0.16. However, the carrier concentration decreased by five orders of magnitude from 10{sup 19} to 10{sup 14} cm{sup −3} for S/(Zn+Al) = 0.34 and decreased even further when S/(Zn+Al) > 0.34. Such tunable electrical properties are potentially useful for graded buffer layers in thin-film photovoltaic applications.

  17. The reaction of ceria coatings on mica with H{sub 2}S An in-situ X-ray diffraction study

    SciTech Connect

    Bertaux, S.; Reynders, P.; Schweda, E

    2004-05-05

    Thin layers of ceria were deposited on the surface of mica platelets in solution. The reaction of such particles with hydrogen sulfide yields a red colored special effect pigment. The ceria layer reacts with H{sub 2}S to produce a variety of sulfide and oxysulfide phases. The reaction path discovered in situ by time and temperature resolved X-ray diffraction is CeO{sub 2}{yields}CeS{sub 2}{yields}C-Ce{sub 2}S{sub 3}{yields}Ce{sub 10}S{sub 14}O. The reaction itself is extremely variable depending on gas flow, heating rates and decomposition atmospheres. Effects on the thin film are recorded by scanning electron microscopy (SEM) and revealed a destruction of the layer once red Ce{sub 10}S{sub 14}O was formed. The product layer then reveals the typical nonwetting behaviour of a liquid on a surface.

  18. Temperature driven reactant solubilization synthesis of BiCuOSe.

    PubMed

    Stampler, Evan S; Sheets, William C; Bertoni, Mariana I; Prellier, Wilfrid; Mason, Thomas O; Poeppelmeier, Kenneth R

    2008-11-01

    Phase-pure BiCuOSe, which is isostructural to the layered p-type transparent conductor LaCuOS, has been synthesized in high yield by a single-step hydrothermal reaction at low temperature (250 degrees C) and pressure (<20 atm). A moderate reaction temperature of 250 degrees C was sufficiently high to solubilize both Bi2O3 and Cu2O and stabilize monovalent copper and low enough to impede the oxidation of dianionic selenium. BiCuOSe exhibits a relatively high electrical conductivity (sigma approximately 3.3 S cm(-1)) and a reduced band gap (E(g) = 0.75 eV), which compare favorably with the optoelectronic properties of BiCuOS and the cerium-based oxysulfides, CeAgOS and CeCuOS. PMID:18831580

  19. Spencer-Attix water/medium stopping-power ratios for the dosimetry of proton pencil beams

    NASA Astrophysics Data System (ADS)

    Gomà, C.; Andreo, P.; Sempau, J.

    2013-04-01

    This paper uses Monte Carlo simulations to calculate the Spencer-Attix water/medium stopping-power ratios (sw, med) for the dosimetry of scanned proton pencil beams. It includes proton energies from 30 to 350 MeV and typical detection materials such as air (ionization chambers), radiochromic film, gadolinium oxysulfide (scintillating screens), silicon and lithium fluoride. Track-ends and particles heavier than protons were found to have a negligible effect on the water/air stopping-power ratios (sw, air), whereas the mean excitation energy values were found to carry the largest source of uncertainty. The initial energy spread of the beam was found to have a minor influence on the sw, air values in depth. The water/medium stopping-power ratios as a function of depth in water were found to be quite constant for air and radiochromic film—within 2.5%. Also, the sw, med values were found to have no clinically relevant dependence on the radial distance—except for the case of gadolinium oxysulfide and proton radiography beams. In conclusion, the most suitable detection materials for depth-dose measurements in water were found to be air and radiochromic film active layer, although a small correction is still needed to compensate for the different sw, med values between the plateau and the Bragg peak region. Also, all the detection materials studied in this work—except for gadolinium oxysulfide—were found to be suitable for lateral dose profiles and field-specific dose distribution measurements in water.

  20. Structural and kinetic study of CoMo/. gamma. Al/sub 2/O/sub 3/ hydrodesulfurization catalyst using EXAFS and XANES

    SciTech Connect

    Parham, T.G.

    1983-01-01

    In situ Extended X-ray Absorption Fine Structure (EXAFS) and X-ray Absorption Near Edge (XANES) spectroscopies were combined in a study designed to elucidate the molecular structure of molybdenum in CoMo/..gamma..Al/sub 2/O/sub 3/ hydrodesulfurization catalysts. This structure was related to catalytic activity using a model thiophene hydrodesulfurization reaction. Oxide CoMo/..gamma..Al/sub 2/O/sub 3/ was found to consist of tetrahedrally coordinated molybdenum with two or three short Mo = O bonds and one or two oxide ligands with longer Mo-O distances. The catalyst reacts with H/sub 2/S at 25 C with terminal Mo = O species being replaced by sulfur ligands. As the sulfiding temperature is increased, oxysulfides are replaced with a MoS/sub 2/-like phase. No evidence was found of oxysulfides at sulfiding temperatures in excess of 200 C. The first shell sulfur and second shell molybdenum coordination numbers were observed to increase linearly with sulfiding temperature, as was the present MoS/sub 2/-like phase. The MoS/sub 2/-like phase is remarkably similar to MoS/sub 2/, but has a Mo-S coordination number of only four. The second shell coordination is also lower, with only three molybdenum neighbors at 3.16 A. Sulfiding is about 90% complete after two hours at 400 C, with only minor change after 24 hours of sulfiding. This information is consistent with a structural model consisting of small MoS/sub 2/ crystallites of c.a. 10 A if the perimeter molybdenums are considered to have lost labile sulfur. Kinetic EXAFS, XANES and sulfur uptake measurements were made in situ during catalyst sulfiding and HDS. These measurements showed that at high temperature (400 C) the rate of sulfur adsorption onto the catalyst limits the rate of reaction between surface sulfur and molybdenum.

  1. Dynamics of near-alpha titanium welding

    NASA Astrophysics Data System (ADS)

    Neuberger, Brett William

    Typically, when gas tungsten arc welding (GTAW) is employed to join near-alpha titanium alloys, the resulting weld fusion zone (FZ) is much harder than that of the base metal (BM), thereby leading to lost ductility. The aim of this investigation was to improve FZ ductility of Ti-5Al-1Sn-1V-1Zr-0.8Mo by modifying filler metal chemistry. In this regard, metallic yttrium was added to the filler metal and aluminum concentration reduced. It was believed that additions of yttrium would lead to formation of yttria in the weld melt, thereby promoting heterogeneous nucleation. Since oxygen and aluminum both act as alpha-stabilizers, expected pickup of oxygen during the welding process will be offset by the aluminum reduction. Tensile testing indicated that modified filler metal welds showed a dramatic increase in ductility of the FZ. Fracture toughness testing showed that while JIC values decreased in all welds, the tearing modulus, T, in modified filler metal welds was significantly higher than that of matching filler metal welds. Microhardness mapping of the weld zones illustrated that modified filler metal welds were significantly softer than matching filler metal welds. Microstructural examinations were completed through the use of optical, SEM and TEM studies, indicating that there was a presence of nano-particles in the weld FZ. XPS analysis identified these particles as yttrium oxysulfate. WDS analysis across the welds' heat affected zones demonstrated that there is an internal diffusion of oxygen from the BM into the FZ. Research results indicate yttrium oxysulfide particles form in the weld pool, act as a drag force on the solidification front and limit growth of prior-beta grain boundaries. The reduced prior-beta grain size and removal of interstitial oxygen from the matrix in modified filler metal welds, further enhanced by oxidation of yttrium oxysulfide to yttrium oxysulfate, leads to increased ductility in the weld's FZ. Addition of yttrium to the weld also

  2. Effect of the CaO-Al2O3-Based Top Slag on the Cleanliness of Stainless Steel During Secondary Metallurgy

    NASA Astrophysics Data System (ADS)

    Yan, Pengcheng; Huang, Shuigen; Pandelaers, Lieven; Van Dyck, Joris; Guo, Muxing; Blanpain, Bart

    2013-10-01

    The ladle treatment of a 18 pct Cr-9 pct Ni stainless steel, with desulfurization as its main purpose, was simulated on a laboratory scale. The influence of the top slag chemistry on the steel cleanliness was evaluated. A higher steel cleanliness was obtained with an optimized lime-alumina-based slag than with a lime-fluorspar-based slag. The inclusions were found to be mainly in the form of oxysulfide; the alumina content in the inclusions first increased and subsequently showed a slow drop, while the sulfide content decreased during the treatment. The equilibrium between steel and inclusions was found to be more easily reached than that between slag and steel. A slag-steel kinetic model was used to predict the steel chemistry evolution during the treatment. Furthermore, a slag-steel-inclusions interaction kinetic model was developed to calculate the change of alumina content in the inclusions during the ladle treatment. The sulfide content of inclusions was also calculated and compared with the measured values.

  3. Resistive switching characteristics of Cu/ZnO0.4S0.6/Al devices constructed on plastic substrates.

    PubMed

    Han, Yong; Cho, Kyoungah; Kim, Sangsig

    2012-07-01

    In this study, Cu/ZnO0.4S0.6Al devices are fabricated on plastic substrates using the sputtering method at room temperature. The ratio of O/S in the zinc oxysulfide thin film is confirmed to be 0.4/0.6 from the Auger depth profiling. The Cu/ZnO0.4S0.6/Al devices show unipolar resistive switching behaviors and the ratio of the measured resistance in the low-resistance state (LRS) to that in the high-resistance state (HRS) is above 10(4). The conduction mechanism of the LRS is governed by Ohm's law. On the other hand, in the HRS, the conduction mechanism at low voltages is controlled by Ohm's law, but that at high voltages results from the Poole-Frenkel emission mechanism. The Ohmic and Poole-Frenkel conduction mechanisms observed in the LRS and HRS support the filament model of unipolar resistive switching. The memory characteristics of the Cu/ZnO0.4S0.6/Al devices are retained for 10(4) sec without any change.

  4. Development of x-ray imaging technique for liquid screening at airport

    NASA Astrophysics Data System (ADS)

    Sulaiman, Nurhani binti; Srisatit, Somyot

    2016-01-01

    X-ray imaging technology is a viable option to recognize flammable liquids for the purposes of aviation security. In this study, an X-ray imaging technology was developed whereby, the image viewing system was built with the use of a digital camera coupled with a gadolinium oxysulfide (GOS) fluorescent screen. The camera was equipped with a software for remote control setting of the camera via a USB cable which allows the images to be captured. The image was analysed to determine the average grey level using a software designed by Microsoft Visual Basic 6.0. The data was obtained for various densities of liquid thickness of 4.5 cm, 6.0 cm and 7.5 cm respectively for X-ray energies ranging from 70 to 200 kVp. In order to verify the reliability of the constructed calibration data, the system was tested with a few types of unknown liquids. The developed system could be conveniently employed for security screening in order to discriminate between a threat and an innocuous liquid.

  5. X-ray imaging with scintillator-sensitized hybrid organic photodetectors

    NASA Astrophysics Data System (ADS)

    Büchele, Patric; Richter, Moses; Tedde, Sandro F.; Matt, Gebhard J.; Ankah, Genesis N.; Fischer, Rene; Biele, Markus; Metzger, Wilhelm; Lilliu, Samuele; Bikondoa, Oier; MacDonald, J. Emyr; Brabec, Christoph J.; Kraus, Tobias; Lemmer, Uli; Schmidt, Oliver

    2015-12-01

    Medical X-ray imaging requires cost-effective and high-resolution flat-panel detectors for the energy range between 20 and 120 keV. Solution-processed photodetectors provide the opportunity to fabricate detectors with a large active area at low cost. Here, we present a disruptive approach that improves the resolution of such detectors by incorporating terbium-doped gadolinium oxysulfide scintillator particles into an organic photodetector matrix. The X-ray induced light emission from the scintillators is absorbed within hundreds of nanometres, which is negligible compared with the pixel size. Hence, optical crosstalk, a limiting factor in the resolution of scintillator-based X-ray detectors, is minimized. The concept is validated with a 256 × 256 pixel detector with a resolution of 4.75 lp mm-1 at a MTF = 0.2, significantly better than previous stacked scintillator-based flat-panel detectors. We achieved a resolution that proves the feasibility of solution-based detectors in medical applications. Time-resolved electrical characterization showed enhanced charge carrier mobility with increased scintillator filling, which is explained by morphological changes.

  6. Rare-earth phosphor laser-induced fluorescence thermal imaging system

    NASA Astrophysics Data System (ADS)

    Bizzak, D. J.; Chyu, M. K.

    1994-01-01

    This article examines the measurement capabilities of a novel, two-dimensional thermal imaging system based on the fluorescence properties of an europium-doped lanthanum oxysulfide (La2O2S:Eu+3) thermographic phosphor. The foundation of the technique (i.e., the fluorescence properties of La2O2S:Eu+3), as well as the design of the thermal imaging system, are also described. The technique that is employed in the design of the system utilizes the tripled output of a pulsed Nd:YAG laser to excite the thin phosphor coating applied to a test surface. The resulting fluorescent emission of the temperature sensitive 512-nm radiative transition, along with that of the relatively temperature independent 620-nm transition, is acquired using an image-intensified charge coupled device camera. The ratio of the intensities of these two emissions, integrated during their decay, is then correlated with temperature. Phosphor calibration data that is presented demonstrate the efficacy of the technique, while results of evaluations to assess the spatial resolution and measurement accuracy provide a quantitative measure of system capabilities.

  7. Use of a laser-induced fluorescence thermal imaging system for film cooling heat transfer measurement

    SciTech Connect

    Chyu, M.K.

    1996-04-01

    This paper describes a novel approach based on fluorescence imaging of thermographic phosphor that enables the simultaneous determination of both local film effectiveness and local heat transfer on a film-cooled surface. The film cooling model demonstrated consists of a single row of three discrete holes on a flat plate. The transient temperature measurement relies on the temperature-sensitive fluorescent properties of europium-doped lanthanum oxysulfide (La{sub 2}O{sub 2}S:Eu{sup +3}) thermographic phosphor. A series of full-field surface temperatures, mainstream temperatures, and coolant film temperatures were acquired during the heating of a test surface. These temperatures are used to calculate the heat transfer coefficients and the film effectiveness simultaneously. Because of the superior spatial resolution capability for the heat transfer data reduced from these temperature frames, the laser-induced fluorescence (LIF) imaging system, the present study observes the detailed heat transfer characteristics over a film-protected surface. The trend of the results agrees with those obtained using other conventional thermal methods, as well as the liquid crystal imaging technique. One major advantage of this technique is the capability to record a large number of temperature frames over a given testing period. This offers multiple-sample consistency.

  8. TiO2 nanotubes supported NiW hydrodesulphurization catalysts: Characterization and activity

    NASA Astrophysics Data System (ADS)

    Palcheva, R.; Dimitrov, L.; Tyuliev, G.; Spojakina, A.; Jiratova, K.

    2013-01-01

    High surface area TiO2 nanotubes (Ti-NT) synthesized by alkali hydrothermal method were used as a support for NiW hydrodesulphurization catalyst. Nickel salt of 12-tungstophosphoric acid - Ni3/2PW12O40 was applied as oxide precursor of the active components. The catalyst was characterized by SBET, XRD, UV-vis DRS, Raman spectroscopy, XPS, TPR and HRTEM. The results obtained were compared with those for the NiW catalysts prepared over high surface area titania and alumina supports. A polytungstate phase evidenced by Raman spectroscopy was observed indicating the destruction of the initial heteropolyanion. The catalytic experiments revealed two times higher thiophene conversion on NiW catalyst supported on Ti-NT than those of catalysts supported on alumina and titania. Increased HDS activity of the NiW catalyst supported on Ti-NT could be related to a higher amount of W oxysulfide entities interacting with Ni sulfide particles as consequence of the electronic effects of the Ti-NT observed with XPS analysis.

  9. A microPET/CT system for invivo small animal imaging

    NASA Astrophysics Data System (ADS)

    Liang, H.; Yang, Y.; Yang, K.; Wu, Y.; Boone, J. M.; Cherry, S. R.

    2007-07-01

    A microCT scanner was designed, fabricated and integrated with a previously reported microPET II scanner (Tai et al 2003 Phys. Med. Biol. 48 1519, Yang et al 2004 Phys. Med. Biol. 49 2527), forming a dual modality system for in vivo anatomic and molecular imaging of the mouse. The system was designed to achieve high-spatial-resolution and high-sensitivity PET images with adequate CT image quality for anatomic localization and attenuation correction with low x-ray dose. The system also has relatively high throughput for screening, and a flexible gantry and user interface. X-rays were produced by a 50 kVp, 1.5 mA fixed tungsten anode tube, with a focal spot size of 70 µm. The detector was a 5 × 5 cm2 photodiode detector incorporating 48 µm pixels on a CMOS array and a fast gadolinium oxysulfide (GOS) intensifying screen. The microCT system has a flexible C-arm gantry design with adjustable detector positioning, which acquires CT projection images around the common microPET/CT bed. The design and the initial characterization of the microCT system is described, and images of the first mouse scans with microPET/CT scanning protocols are shown.

  10. Reaction of Hydrogen Sulfide with Oxygen in the Presence ofSulfite

    SciTech Connect

    Weres, Oleh; Tsao, Leon

    1983-01-01

    Commonly, abatement of hydrogen sulfide emissions from a geothermal powerplant requires that hydrogen sulfide dissolved in the cooling water be eliminated by chemical reaction. Oxidation by atmospheric oxygen is the preferred reaction, but requires a suitable catalyst. Nickel is the most potent and thereby cheapest catalyst for this purpose. One Mg/L nickel in the cooling water would allow 99% removal of hydrogen sulfide to be attained. A major drawback of catalytic air oxidation is that colloidal sulfur is a major reaction product; this causes rapid sludge accumulation and deposition of sulfur scale. The authors studied the kinetics and product distribution of the reaction of hydrogen sulfide with oxygen, catalyzed by nickel. Adding sodium sulfite to the solution completely suppresses formation of colloidal sulfur by converting it to thiosulfate. The oxidation reaction is an autocatalytic, free radical chain reaction. A rate expression for this reaction and a detailed reaction mechanism were developed. Nickel catalyzes the chain initiation step, and polysulfidoradical ions propagate the chains. Several complexes of iron and cobalt were also studied. Iron citrate and iron N-hydroxyEDT are the most effective iron based catalysts. Uncomplexed cobalt is as effective as nickel, but forms a precipitate of cobalt oxysulfide and is too expensive for practical use.

  11. Reaction of hydrogen sulfide with oxygen in the presence of sulfite

    SciTech Connect

    Weres, O.; Tsao, L.

    1983-01-14

    Commonly, abatement of hydrogen sulfide emission from a geothermal powerplant requires that hydrogen sulfide dissolved in the cooling water be eliminated by chemical reaction. Oxidation by atmospheric oxygen is the preferred reaction, but requires a suitable catalyst. Nickel is the most potent and thereby cheapest catalyst for this purpose. One mg/L nickel in the cooling water would allow 99% removal of hydrogen sulfide to be attained. A major drawback of catalytic air oxidation is that colloidal sulfur is a major reaction product; this causes rapid sludge accumulation and deposition of sulfur scale. We studied the kinetics and product distribution of the reaction of hydrogen sulfide with oxygen, catalyzed by nickel. Adding sodium sulfite to the solution completely suppresses formation of colloidal sulfur by converting it to thiosulfate. The oxidation reaction is an autocatalytic, free radical chain reaction. A rate expression for this reaction and a detailed reaction mechanism were developed. Nickel catalyzes the chain initiation step, and polysulfidoradical ions propagate the chains. Several complexes of iron and cobalt were also studied. Iron citrate and iron N-hydroxyEDTA are the most effective iron based catalysts. Uncomplexed cobalt is as effective as nickel, but forms a precipitate of cobalt oxysulfide and is too expensive for practical use. 33 figures, 9 tables.

  12. Use of a laser-induced fluorescence thermal imaging system for film cooling heat transfer measurement

    SciTech Connect

    Chyu, M.K.

    1995-10-01

    This paper describes a novel approach based on fluorescence imaging of thermographic phosphor that enables the simultaneous determination of both local film effectiveness and local heat transfer on a film-cooled surface. The film cooling model demonstrated consists of a single row of three discrete holes on a flat plate. The transient temperature measurement relies on the temperature-sensitive fluorescent properties of europium-doped lanthanum oxysulfide (La{sub 2}O{sub 2}S:EU{sup 3+}) thermographic phosphor. A series of full-field surface temperatures, mainstream temperatures, and coolant film temperatures were acquired during the heating of a test surface. These temperatures are used to calculate the heat transfer coefficients and the film effectiveness simultaneously. Because of the superior spatial resolution capability for the heat transfer data reduced from these temperature frames, the laser-induced fluorescence (LIF) imaging system, the present study observes the detailed heat transfer characteristics over a film-protected surface. The trend of the results agrees with those obtained using other conventional thermal methods, as well as the liquid crystal imaging technique. One major advantage of this technique is the capability to record a large number of temperature frames over a given testing period. This offers multiple-sample consistency.

  13. Laser-induced fluorescence of phosphors for remote cryogenic thermometry

    SciTech Connect

    Beshears, D.L.; Capps, G.J.; Cates, M.R.; Simmons, C.M.; Schwenterly, S.W.

    1990-01-01

    Remote cryogenic temperature measurements can be made by inducing fluorescence in phosphors with temperature-dependent emissions and measuring the emission lifetimes. The thermographic phosphor technique can be used for making precision, non-contact, cryogenic temperature measurements in electrically hostile environments, such as high DC electric or magnetic fields. NASA is interested in utilizing these thermographic phosphors for mapping hot spots on cryogenic tank walls. Europium-doped lanthanum oxysulfide (La{sub 2}O{sub 2}S:Eu) and magnesium fluorogermanate doped with manganese (Mg{sub 4}(F)GeO{sub 6}:Mn) are suitable for low-temperature surface thermometry. Several emission lines, excited by a 337 nm UV laser, provide fluorescence lifetimes having logarithmic dependence with temperatures from 4 to 125 Kelvin. A calibration curve for both La{sub 2}O{sub 2}S:Eu and Mg{sub 4}(F)GeO{sub 6}:Mn are presented as well as emission spectra taken at room temperature and 7 Kelvin.

  14. Monte Carlo simulation of the transit dosimetric response of an a-Si electronic portal imaging device

    NASA Astrophysics Data System (ADS)

    Blake, S. J.; McNamara, A. L.; Vial, P.; Holloway, L.; Greer, P. B.; Kuncic, Z.

    2014-03-01

    Amorphous silicon (a-Si) electronic portal imaging devices (EPIDs) are x-ray detectors frequently used in radiotherapy imaging and dosimetry applications. EPIDs employ a copper plate and gadolinium oxysulfide phosphor screen with an array of a-Si photodiodes to indirectly detect incident radiation. In this study, a previously developed Monte Carlo (MC) model of an a-Si EPID has been extended for transit dosimetry. The GEANT4 MC toolkit was used to integrate an a-Si EPID model with two phantoms and a 6 MV x-ray source. A solid water phantom was used to simulate EPID transmission factors, field size output factors and relative dose profiles and results were compared to experimental measurements. An anthropomorphic head phantom was used to qualitatively compare simulated and measured portal images of humanoid anatomy. Calculated transmission factors and field size output factors agreed to within 2.0% and 1.9% of experimental measurements, respectively. A comparison of calculated and measured relative dose profiles yielded >98% of points passing a gamma analysis with 3%/3 mm criterion for all field sizes. The simulated anthropomorphic head phantom image shows macroscopic anatomical features and qualitatively agrees with the measured image. Results validate the suitability of the MC model for predicting EPID response in transit dosimetry.

  15. ALD Zn(O,S) Thin Films’ Interfacial Chemical and Structural Configuration Probed by XAS

    PubMed Central

    2016-01-01

    The ability to precisely control interfaces of atomic layer deposited (ALD) zinc oxysulfide (Zn(O,S)) buffer layers to other layers allows precise tuning of solar cell performance. The O K- and S K-edge X-ray absorption near edge structure (XANES) of ∼2–4 nm thin Zn(O,S) films reveals the chemical and structural influences of their interface with ZnO, a common electrode material and diffusion barrier in solar cells. We observe that sulfate formation at oxide/sulfide interfaces is independent of film composition, a result of sulfur diffusion toward interfaces. Leveraging sulfur’s diffusivity, we propose an alternative ALD process in which the zinc precursor pulse is bypassed during H2S exposure. Such a process yields similar results to the nanolaminate deposition method and highlights mechanistic differences between ALD sulfides and oxides. By identifying chemical species and structural evolution at sulfide/oxide interfaces, this work provides insights into increasing thin film solar cell efficiencies. PMID:27223620

  16. Inclusions and Microstructure of Ce-Added Weld Metal Coarse Grain Heat-Affected Zone in Twin-Wire Submerged-Arc Welding

    NASA Astrophysics Data System (ADS)

    Yu, S. F.; Yan, N.; Chen, Y.

    2016-06-01

    In high heat-input multi-pass twin-wire submerged-arc welding, weld metal of previous pass will be affected by the heat input of subsequent one and form coarse-grained heat-affected zone (CGHAZ). This study focused on the effects of welding thermal cycle on the inclusions and microstructure of Ce-alloyed weld metal CGHAZ. According to the study of inclusions and microstructure of weld metal CGHAZ, it was found that the composition and type of the inclusions did not change under the effect of welding thermal cycle. Although the inclusions were coarsened slightly, the promoting ability to acicular ferrite (AF) was not deprived after thermal cycling. There are three types of AF in weld metal CGHAZ, which include oxy-sulfides of Ce inclusions-promoted AF, home-position-precipitated AF, and sympathetic AF. Results showed more than 80% of microstructure was AF, which greatly benefited the mechanical properties of weld metal CGHAZ, even though granular bainite and M-A constituents were generated.

  17. ALD Zn(O,S) Thin Films' Interfacial Chemical and Structural Configuration Probed by XAS.

    PubMed

    Dadlani, Anup L; Acharya, Shinjita; Trejo, Orlando; Prinz, Fritz B; Torgersen, Jan

    2016-06-15

    The ability to precisely control interfaces of atomic layer deposited (ALD) zinc oxysulfide (Zn(O,S)) buffer layers to other layers allows precise tuning of solar cell performance. The O K- and S K-edge X-ray absorption near edge structure (XANES) of ∼2-4 nm thin Zn(O,S) films reveals the chemical and structural influences of their interface with ZnO, a common electrode material and diffusion barrier in solar cells. We observe that sulfate formation at oxide/sulfide interfaces is independent of film composition, a result of sulfur diffusion toward interfaces. Leveraging sulfur's diffusivity, we propose an alternative ALD process in which the zinc precursor pulse is bypassed during H2S exposure. Such a process yields similar results to the nanolaminate deposition method and highlights mechanistic differences between ALD sulfides and oxides. By identifying chemical species and structural evolution at sulfide/oxide interfaces, this work provides insights into increasing thin film solar cell efficiencies.

  18. X-ray performance of a wafer-scale CMOS flat panel imager for applications in medical imaging and nondestructive testing

    NASA Astrophysics Data System (ADS)

    Cha, Bo Kyung; Jeon, Seongchae; Seo, Chang-Woo

    2016-09-01

    This paper presents a wafer-scale complementary metal-oxide semiconductor (CMOS)-based X-ray flat panel detector for medical imaging and nondestructive testing applications. In this study, our proposed X-ray CMOS flat panel imager has been fabricated by using a 0.35 μm 1-poly/4-metal CMOS process. The pixel size is 100 μm×100 μm and the pixel array format is 1200×1200 pixels, which provide a field-of-view (FOV) of 120mm×120 mm. The 14.3-bit extended counting analog-to digital converter (ADC) with built-in binning mode was used to reduce the area and simultaneously improve the image resolution. The different screens such as thallium-doped CsI (CsI:Tl) and terbium gadolinium oxysulfide (Gd2O2S:Tb) scintillators were used as conversion materials for X-rays to visible light photons. The X-ray imaging performance such as X-ray sensitivity as a function of X-ray exposure dose, spatial resolution, image lag and X-ray images of various objects were measured under practical medical and industrial application conditions. This paper results demonstrate that our prototype CMOS-based X-ray flat panel imager has the significant potential for medical imaging and non-destructive testing (NDT) applications with high-resolution and high speed rate.

  19. Efficient plasma-enhanced method for layered LiNi1/3Co1/3Mn1/3O2 cathodes with sulfur atom-scale modification for superior-performance Li-ion batteries

    NASA Astrophysics Data System (ADS)

    Jiang, Qianqian; Chen, Ning; Liu, Dongdong; Wang, Shuangyin; Zhang, Han

    2016-05-01

    In order to improve the electrochemical performance of LiNi1/3Co1/3Mn1/3O2 as a lithium insertion positive electrode material, atom-scale modification was realized to obtain the layered oxysulfide LiNi1/3Co1/3Mn1/3O2-xSx using a novel plasma-enhanced doping strategy. The structure and electrochemical performance of LiNi1/3Co1/3Mn1/3O2-xSx are investigated systematically, which confirms that the S doping can make the structure stable and benefit the electrochemical performance. The phys-chemical characterizations indicate that oxygen atoms in the initial LiNi1/3Co1/3Mn1/3O2 have been partially replaced by S atoms. It should be pointed out that the atom-scale modification does not significantly alter the intrinsic structure of the cathode. Compared to the pristine material, the LiNi1/3Co1/3Mn1/3O2-xSx shows a superior performance with a higher capacity (200.4 mA h g-1) and a significantly improved cycling stability (maintaining 94.46% of its initial discharge capacity after 100 cycles). Moreover, it has an excellent rate performance especially at elevated performance, which is probably due to the faster Li+ transportation after S doping into the layered structure. All the results show that the atom-scale modification with sulfur atoms on LiNi1/3Co1/3Mn1/3O2, which significantly improved the electrochemical performance, offers a novel anionic doping strategy to realize the atom-scale modification of electrode materials to improve their electrochemical performance.In order to improve the electrochemical performance of LiNi1/3Co1/3Mn1/3O2 as a lithium insertion positive electrode material, atom-scale modification was realized to obtain the layered oxysulfide LiNi1/3Co1/3Mn1/3O2-xSx using a novel plasma-enhanced doping strategy. The structure and electrochemical performance of LiNi1/3Co1/3Mn1/3O2-xSx are investigated systematically, which confirms that the S doping can make the structure stable and benefit the electrochemical performance. The phys

  20. Imaging responses of on-site CsI and Gd2O2S flat-panel detectors: Dependence on the tube voltage

    NASA Astrophysics Data System (ADS)

    Jeon, Hosang; Chung, Myung Jin; Youn, Seungman; Nam, Jiho; Lee, Jayoung; Park, Dahl; Kim, Wontaek; Ki, Yongkan; Kim, Ho Kyung

    2015-07-01

    One of the emerging issues in radiography is low-dose imaging to minimize patient's exposure. The scintillating materials employed in most indirect flat-panel detectors show a drastic change of X-ray photon absorption efficiency around their K-edge energies that consequently affects image quality. Using various tube voltages, we investigated the imaging performance of most popular scintillators: cesium iodide (CsI) and gadolinium oxysulfide (Gd2O2S). The integrated detective quantum efficiencies (iDQE) of four detectors installed in the same hospital were evaluated according to the standardized procedure IEC 62220-1 at tube voltages of 40 - 120 kVp. The iDQE values of the Gd2O2S detectors were normalized by those of CsI detectors to exclude the effects of image postprocessing. The contrast-to-noise ratios (CNR) were also evaluated by using an anthropomorphic chest phantom. The iDQE of the CsI detector outperformed that of the Gd2O2S detector over all tube voltages. Moreover, we noted that the iDQE of the Gd2O2S detectors quickly rolled off with decreasing tube voltage under 70 kVp. The CNRs of the two scintillators were similar at 120 kVp. At 60 kVp, however, the CNR of Gd2O2S was about half that of CsI. Compared to the Gd2O2S detectors, variations in the DQE performance of the CsI detectors were relatively immune to variations in the applied tube voltages. Therefore, we claim that Gd2O2S detectors are inappropriate for use in low-tube-voltage imaging (e.g., extremities and pediatrics) with low patient exposure.

  1. Two-dimensional magnetic correlations and partial long-range order in geometrically frustrated CaOFeS with triangle lattice of Fe ions

    NASA Astrophysics Data System (ADS)

    Jin, S. F.; Huang, Q.; Lin, Z. P.; Li, Z. L.; Wu, X. Z.; Ying, T. P.; Wang, G.; Chen, X. L.

    2015-03-01

    We report the results on the structure, transport, and magnetic properties of a layered oxysulfide CaOFeS with a stacked triangle lattice of Fe ions. The susceptibility data show a broad maximum near 120 K, indicating the existence of two-dimensional (2D) short-range ordering in this compound. Features associated with long-range antiferromagnetic (AFM) phase transition are seen below 40 K. Meanwhile, a very small heat-capacity anomaly is detected around 35 K, and most of the measured magnetic entropy is lost during the 2D ordering process. Both crystal and magnetic structures were studied by neutron powder diffraction at 300, 125, 40, and 6 K. The structure was refined based on space group P 63m c with a =3.759 98 (4 ) and c =11.383 51 (16 ) Å at ambient temperature. Low-temperature diffraction reveals 2D magnetic correlations between Fe moments without showing significant structural distortion. Warren peak shape analysis of the neutron-diffraction data at 2 θ near 18° is employed to characterize the correlation length in the 2D magnetic state with lowering temperature. The geometrically frustrated compound is found to gradually condense into a partial long-range ordered state with AFM coupled Fe layers between 40.6 and 26 K. The resulting partially ordered magnetic structure is a G -type Ising AFM with a propagation vector of k =(1 /2 ,1 /2 ,0 ) and an ordered magnetic moment of 2.59 (3 ) μB/Fe along c at 6 K.

  2. TH-C-17A-07: Visualizing and Quantifying Radiation Therapy in Real-Time Using a Novel Beam Imaging Technique

    SciTech Connect

    Jenkins, C; Naczynski, D; Xing, L

    2014-06-15

    Purpose: Radiation therapy uses invisible high energy X-rays to treat an invisible tumor. Proper positioning of the treatment beam relative to the patient's anatomy during dose delivery is critically important to the success of treatment. We develop and characterize a novel radiation therapy beam visualization technique for real-time monitoring of patient treatment. Methods: Custom made flexible scintillator sheets were fabricated from gadolinium oxysulfide (GOS) particles that had been doped with terbium within a silicone elastomer matrix. Sheets of several thicknesses ranging from 0.3 to 1mm were prepared and tested. Sheets were exposed to megavoltage X-ray and electron beams from a Varian linac and the resulting optical signal was collected by multiple CMOS cameras placed in the treatment room. Real-time images were collected for different beam energies and dose rates. Signal intensity and SNR were calculated by processing the acquired images. Results: All signals were detectable in the presence of full room lighting and at an integration time of 45ms. Average signal intensity and SNR increased with both sheet thickness and dose rate and decreased with beam energy and incident light. For a given sheet thickness and beam energy the correlation between dose rate and signal intensity was highly linear. Increased sheet thickness or dose rate results in a linear increase in the detected signal. All results are consistent with analytical approximations. Conclusion: The technique offers a means of accurately visualizing a radiation therapy beam shape and fluence in real time. The effects of salient parameters have been characterized and will enable further optimization of the technique as it is implemented into the clinical workflow. The project described was supported by the National Center for Advancing Translational Sciences of the National Institutes of Health through UL1 TR001085.

  3. Electrodeposition of ZnO-doped films as window layer for Cd-free CIGS-based solar cells

    NASA Astrophysics Data System (ADS)

    Tsin, Fabien; Vénérosy, Amélie; Hildebrandt, Thibaud; Hariskos, Dimitrios; Naghavi, Negar; Lincot, Daniel; Rousset, Jean

    2016-02-01

    The Cu(In,Ga)Se2 (CIGS) thin film solar cell technology has made a steady progress within the last decade reaching efficiency up to 22.3% on laboratory scale, thus overpassing the highest efficiency for polycrystalline silicon solar cells. High efficiency CIGS modules employ a so-called buffer layer of cadmium sulfide CdS deposited by Chemical Bath Deposition (CBD), which presence and Cd-containing waste present some environmental concerns. A second potential bottleneck for CIGS technology is its window layer made of i-ZnO/ZnO:Al, which is deposited by sputtering requiring expensive vacuum equipment. A non-vacuum deposition of transparent conductive oxide (TCO) relying on simpler equipment with lower investment costs will be more economically attractive, and could increase competitiveness of CIGS-based modules with the mainstream silicon-based technologies. In the frame of Novazolar project, we have developed a low-cost aqueous solution photo assisted electrodeposition process of the ZnO-based window layer for high efficiency CIGS-based solar cells. The window layer deposition have been first optimized on classical CdS buffer layer leading to cells with efficiencies similar to those measured with the sputtered references on the same absorber (15%). The the optimized ZnO doped layer has been adapted to cadmium free devices where the CdS is replaced by chemical bath deposited zinc oxysulfide Zn(S,O) buffer layer. The effect of different growth parameters has been studied on CBD-Zn(S,O)-plated co-evaporated Cu(In,Ga)Se2 substrates provided by the Zentrum für Sonnenenergie-und Wasserstoff-Forschung (ZSW). This optimization of the electrodeposition of ZnO:Cl on CIGS/Zn(S,O) stacks led to record efficiency of 14%, while the reference cell with a sputtered (Zn,Mg)O/ZnO:Al window layer has an efficiency of 15.2%.

  4. Tungsten disulfide nanotubes reinforced biodegradable polymers for bone tissue engineering.

    PubMed

    Lalwani, Gaurav; Henslee, Allan M; Farshid, Behzad; Parmar, Priyanka; Lin, Liangjun; Qin, Yi-Xian; Kasper, F Kurtis; Mikos, Antonios G; Sitharaman, Balaji

    2013-09-01

    In this study, we have investigated the efficacy of inorganic nanotubes as reinforcing agents to improve the mechanical properties of poly(propylene fumarate) (PPF) composites as a function of nanomaterial loading concentration (0.01-0.2 wt.%). Tungsten disulfide nanotubes (WSNTs) were used as reinforcing agents in the experimental group. Single- and multi-walled carbon nanotubes (SWCNTs and MWCNTs) were used as positive controls, and crosslinked PPF composites were used as the baseline control. Mechanical testing (compression and three-point bending) shows a significant enhancement (up to 28-190%) in the mechanical properties (compressive modulus, compressive yield strength, flexural modulus and flexural yield strength) of WSNT-reinforced PPF nanocomposites compared to the baseline control. In comparison to the positive controls, significant improvements in the mechanical properties of WSNT nanocomposites were also observed at various concentrations. In general, the inorganic nanotubes (WSNTs) showed mechanical reinforcement better than (up to 127%) or equivalent to that of carbon nanotubes (SWCNTs and MWCNTs). Sol fraction analysis showed significant increases in the crosslinking density of PPF in the presence of WSNTs (0.01-0.2 wt.%). Transmission electron microscopy (TEM) analysis on thin sections of crosslinked nanocomposites showed the presence of WSNTs as individual nanotubes in the PPF matrix, whereas SWCNTs and MWCNTs existed as micron-sized aggregates. The trend in the surface area of nanostructures obtained by Brunauer-Emmett-Teller (BET) surface area analysis was SWCNTs>MWCNTs>WSNTs. The BET surface area analysis, TEM analysis and sol fraction analysis results taken together suggest that chemical composition (inorganic vs. carbon nanomaterials), the presence of functional groups (such as sulfide and oxysulfide) and individual dispersion of the nanomaterials in the polymer matrix (absence of aggregation of the reinforcing agent) are the key parameters

  5. Platinum Metal-Free Catalysts for Selective Soft Oxidative Methane → Ethylene Coupling. Scope and Mechanistic Observations.

    PubMed

    Peter, Matthias; Marks, Tobin J

    2015-12-01

    Using abundant soft oxidants, a high methane-to-ethylene conversion might be achievable due to the low thermodynamic driving force for over-oxidation. Here we report on the oxidative coupling of methane by gaseous S2 (SOCM). The catalytic properties of Pd/Fe3O4 are compared with those of Fe3O4, and it is found that high ethylene selectivities can be achieved without noble metals; conversion and selectivity on Fe3O4 are stable for at least 48 h at SOCM conditions. SOCM data for 10 oxides are compared, and ethylene selectivities as high as 33% are found; the C2H4/C2H6 ratios of 9-12 observed at the highest S2 conversions are significantly higher than the C2H4/C2H6 ratios usually found in the CH4 coupling with O2. Complementary in-detail analytical studies show that, on Mg, Zr, Sm, W, and La catalysts, which strongly coke during the reaction, lower ethylene selectivities are observed than on Fe, Ti, and Cr catalysts, which only coke to a minor extent. Further catalyst-dependent changes during SOCM in surface area, surface composition, and partial conversion to oxysulfides and sulfides are discussed. Evidence concerning the reaction mechanism is obtained taking into account the selectivity for the different reaction products versus the contact time. CH4 coupling proceeds non-oxidatively with the evolution of H2 on some catalysts, and evidence is presented that C2H4 and C2H2 formation occur via C2H6 and C2H4 dehydrogenation, respectively. PMID:26551955

  6. First principles study of transition metal (TM=Pb, Cu) oxides/sulfides

    NASA Astrophysics Data System (ADS)

    Caudle, Sean; Tao, Meng; Peng, Xihong

    2012-10-01

    Earth-abundant transition meal oxides/sulfides have inspired special research attention recently due to their potential applications in solar cells. A clear understanding of the fundamental properties of these materials, especially the electronic properties and their tunability via chemical doping, are critically important towards the applications. In this presentation, we report first principles density-functional theory (DFT) study on the electronic structures of Pb and Cu oxides/sulfides and their oxysulfides compositions. The band structure and bandgap can be systematically tuned by increasing S component in the metal oxides. For example, the DFT predicted bandgap for PbO is 1.72 eV. While the bandgaps for PbO0.937 S0.063, PbO0.875S0.125, and PbO0.75S0.25 are 1.64 eV, 1.43 eV, and 0.79 eV, respectively. For Cu2O, the standard DFT seriously underestimates the bandgap to be 0.49 eV, compared to the experimental value of 2.17 eV. Two methods, DFT+U and hybrid functional (HSE06), were implemented to overcome this problem. Our results showed that DFT+U method fails and the bandgap doesn't further open up by providing a U potential. The hybrid functional predicts the bandgap to be 2.00 eV, which is in a good agreement with the experimental value.

  7. Improving detector spatial resolution using pixelated scintillators with a barrier rib structure

    NASA Astrophysics Data System (ADS)

    Liu, Langechuan; Lu, Minghui; Cao, Wanqing; Peng, Luke; Chen, Arthur

    2016-03-01

    Indirect conversion flat panel detectors (FPDs) based on amorphous silicon (a-Si) technology are widely used in digital X-ray imaging. In such FPDs a scintillator layer is used for converting X-rays into visible light photons. However, the lateral spread of these photons inside the scintillator layer reduces spatial resolution of the FPD. In this study, FPDs incorporating pixelated scintillators with a barrier rib structure were developed to limit lateral spread of light photons thereby improving spatial resolution. For the pixelated scintillator, a two-dimensional barrier rib structure was first manufactured on a substrate layer, coated with reflective materials, and filled to the rim with the scintillating material of gadolinium oxysulfide (GOS). Several scintillator samples were fabricated, with pitch size varying from 160 to 280 μm and rib height from 200 to 280 μm. The samples were directly coupled to an a-Si flat panel photodiode array with a pitch of 200 μm to convert optical photons to electronic signals. With the pixelated scintillator, the detector modulation transfer function was shown to improve significantly (by 94% at 2 cycle/mm) compared to a detector using an unstructured GOS layer. However, the prototype does show lower sensitivity due to the decrease in scintillator fill factor. The preliminary results demonstrated the feasibility of using the barrier-rib structure to improve the spatial resolution of FPDs. Such an improvement would greatly benefit nondestructive testing applications where the spatial resolution is the most important parameter. Further investigation will focus on improving the detector sensitivity and exploring its medical applications.

  8. Efficient plasma-enhanced method for layered LiNi1/3Co1/3Mn1/3O2 cathodes with sulfur atom-scale modification for superior-performance Li-ion batteries.

    PubMed

    Jiang, Qianqian; Chen, Ning; Liu, Dongdong; Wang, Shuangyin; Zhang, Han

    2016-06-01

    In order to improve the electrochemical performance of LiNi1/3Co1/3Mn1/3O2 as a lithium insertion positive electrode material, atom-scale modification was realized to obtain the layered oxysulfide LiNi1/3Co1/3Mn1/3O2-xSx using a novel plasma-enhanced doping strategy. The structure and electrochemical performance of LiNi1/3Co1/3Mn1/3O2-xSx are investigated systematically, which confirms that the S doping can make the structure stable and benefit the electrochemical performance. The phys-chemical characterizations indicate that oxygen atoms in the initial LiNi1/3Co1/3Mn1/3O2 have been partially replaced by S atoms. It should be pointed out that the atom-scale modification does not significantly alter the intrinsic structure of the cathode. Compared to the pristine material, the LiNi1/3Co1/3Mn1/3O2-xSx shows a superior performance with a higher capacity (200.4 mA h g(-1)) and a significantly improved cycling stability (maintaining 94.46% of its initial discharge capacity after 100 cycles). Moreover, it has an excellent rate performance especially at elevated performance, which is probably due to the faster Li(+) transportation after S doping into the layered structure. All the results show that the atom-scale modification with sulfur atoms on LiNi1/3Co1/3Mn1/3O2, which significantly improved the electrochemical performance, offers a novel anionic doping strategy to realize the atom-scale modification of electrode materials to improve their electrochemical performance.

  9. Microstructure, texture evolution and magnetic properties of strip-casting non-oriented 6.5 wt.% Si electrical steel doped with cerium

    SciTech Connect

    Li, Hao-Ze Liu, Hai-Tao; Liu, Zhen-Yu Wang, Guo-Dong

    2015-05-15

    A 0.3 mm thick non-oriented 6.5 wt.% Si electrical steel sheet doped with cerium is produced by twin-roll strip casting, hot rolling, warm rolling and annealing. A detailed study of the cerium precipitates in the as-cast strip, microstructure and texture evolution at different processing stages is carried out by electron probe micro-analysis, optical microscopy, X-ray diffraction and electron backscattered diffraction analysis. Grain interior distributing precipitates identified as Ce-oxides, Ce-oxysulfides and Ce-phosphides, and boundary distributing Ce-oxides and Ce-phosphides are observed in the as-cast strip. The initial as-cast strip is characterized by a much finer solidification microstructure and dominated by obvious < 001 >//ND texture through the strip thickness. After hot and warm rolling, inhomogeneous microstructure containing large amounts of in-grain shear bands is characterized by mixed < 110 >//RD and < 111 >//ND textures. The texture of the annealed sheet with a relatively large average grain size is far more optimized by the domination of the beneficial cube, rotated cube, (001)< 120 > to (001)< 130 > and Goss texture components, and the elimination of the detrimental γ-fiber texture, leading to a superior magnetic induction and improved iron loss. - Highlights: • An Fe–6.5 wt.% Si as-cast strip doped with cerium was produced. • A thin warm rolled sheet with limited edge cracks was obtained. • Microstructure and texture evolution at each stage were investigated. • Strong λ-fiber and Goss recrystallization textures were formed. • The magnetic properties of the annealed sheet were significantly improved.

  10. In situ sulfiding of Ni-W hydrocracking catalysts : differentiation of different preparation procedures using EXAFS and HRTEM.

    SciTech Connect

    Kelly, S. D.; Yang, N.; Mickelson, G. E.; Greenlay, N.; Karapetrova, E.; Sinkler, W.; Bare, S. R.; UOP LLC; EXAFS Analysis

    2009-01-01

    The detailed structural characterization of the metal function of two fully formulated Ni-W hydrocracking catalysts was investigated by time resolved in situ X-ray absorption spectroscopy (EXAFS and XANES) at both the Ni K-edge and W L{sub 3}-edge, and by high resolution transmission electron microscopy. These two hydrocracking catalysts (designated as HCA and HCB) contained the same wt% of Ni and W, the same wt% of the other constituents ({gamma}-Al{sub 2}O{sub 3}/silico-aluminate), and were calcined at the same temperature, but were prepared by different methods in order to highlight the sensitivity of the characterization techniques to the structural differences. The morphology of the WS{sub 2} particles in the sulfided catalyst is substantially different between the two catalysts: in the HCA catalyst there are many more particles with multiple WS{sub 2} layers whereas in HCB there are more single layers. The average diameter of the WS{sub 2} plates is similar in both. The catalysts show a difference in the amount of W sulfidation after the 410 C sulfidation treatment in 10% H{sub 2}S/H{sub 2}. The W of HCA catalyst was completely sulfided whereas 16% W of HCB catalyst was unsulfided. Similarly there is a difference in the amount of sulfided Ni: 16% Ni in HCA and 60% Ni in HCB remain unsulfided. In the sulfided form of both catalysts the Ni exists in three different morphologies: oxidized Ni (six-fold coordinate as a nickel aluminate), nanoparticulate Ni{sub 3}S{sub 2}, and Ni decorating the edge sites of the WS{sub 2}. In both the Ni{sub 3}S{sub 2}, and Ni decorating the edge sites of the WS{sub 2}, the Ni is in a tetrahedral coordination with sulfur. In both catalysts the sulfidation of the Ni and W occurs essentially simultaneously over most of the temperature range and the sulfidation of the W proceeds through the same tungsten oxysulfide in both samples. The characterization methodology presented here is a powerful one for elucidating the structural

  11. Hybrid x-ray/optical luminescence imaging: Characterization of experimental conditions

    SciTech Connect

    Carpenter, C. M.; Sun, C.; Pratx, G.; Rao, R.; Xing, L.

    2010-08-15

    Purpose: The feasibility of x-ray luminescence imaging is investigated using a dual-modality imaging system that merges x-ray and optical imaging. This modality utilizes x-ray activated nanophosphors that luminesce when excited by ionizing photons. By doping phosphors with lanthanides, which emit light in the visible and near infrared range, the luminescence is suitable for biological applications. This study examines practical aspects of this new modality including phosphor concentration, light emission linearity, detector damage, and spectral emission characteristics. Finally, the contrast produced by these phosphors is compared to that of x-ray fluoroscopy. Methods: Gadolinium and lanthanum oxysulfide phosphors doped with terbium (green emission) or europium (red emission) were studied. The light emission was imaged in a clinical x-ray scanner with a cooled CCD camera and a spectrophotometer; dose measurements were determined with a calibrated dosimeter. Using these properties, in addition to luminescence efficiency values found in the literature for a similar phosphor, minimum concentration calculations are performed. Finally, a 2.5 cm agar phantom with a 1 cm diameter cylindrical phosphor-filled inclusion (diluted at 10 mg/ml) is imaged to compare x-ray luminescence contrast with x-ray fluoroscopic contrast at a superficial location. Results: Dose to the CCD camera in the chosen imaging geometry was measured at less than 0.02 cGy/s. Emitted light was found to be linear with dose (R{sup 2}=1) and concentration (R{sup 2}=1). Emission peaks for clinical x-ray energies are less than 3 nm full width at half maximum, as expected from lanthanide dopants. The minimum practical concentration necessary to detect luminescent phosphors is dependent on dose; it is estimated that subpicomolar concentrations are detectable at the surface of the tissue with typical mammographic doses, with the minimum detectable concentration increasing with depth and decreasing with dose. In

  12. WE-D-17A-02: Evaluation of a Two-Dimensional Optical Dosimeter On Measuring Lateral Profiles of Proton Pencil Beams

    SciTech Connect

    Hsi, W; Lee, T; Schultz, T; Arjomandy, B; Park, S; Gao, M; Pankuch, M; Boyer, S; Mah, D; Pillainayagam, M; Schreuder, A

    2014-06-15

    Purpose: To evaluate the accuracy of a two-dimensional optical dosimeter on measuring lateral profiles for spots and scanned fields of proton pencil beams. Methods: A digital camera with a color image senor was utilized to image proton-induced scintillations on Gadolinium-oxysulfide phosphor reflected by a stainless-steel mirror. Intensities of three colors were summed for each pixel with proper spatial-resolution calibration. To benchmark this dosimeter, the field size and penumbra for 100mm square fields of singleenergy pencil-scan protons were measured and compared between this optical dosimeter and an ionization-chamber profiler. Sigma widths of proton spots in air were measured and compared between this dosimeter and a commercial optical dosimeter. Clinical proton beams with ranges between 80 mm and 300 mm at CDH proton center were used for this benchmark. Results: Pixel resolutions vary 1.5% between two perpendicular axes. For a pencil-scan field with 302 mm range, measured field sizes and penumbras between two detection systems agreed to 0.5 mm and 0.3 mm, respectively. Sigma widths agree to 0.3 mm between two optical dosimeters for a proton spot with 158 mm range; having widths of 5.76 mm and 5.92 mm for X and Y axes, respectively. Similar agreements were obtained for others beam ranges. This dosimeter was successfully utilizing on mapping the shapes and sizes of proton spots at the technical acceptance of McLaren proton therapy system. Snow-flake spots seen on images indicated the image sensor having pixels damaged by radiations. Minor variations in intensity between different colors were observed. Conclusions: The accuracy of our dosimeter was in good agreement with other established devices in measuring lateral profiles of pencil-scan fields and proton spots. A precise docking mechanism for camera was designed to keep aligned optical path while replacing damaged image senor. Causes for minor variations between emitted color lights will be investigated.

  13. The energy transfer phenomena and colour tunability in Y2O2S:Eu(3+)/Dy(3+) micro-fibers for white emission in solid state lighting applications.

    PubMed

    Som, S; Mitra, P; Kumar, Vijay; Kumar, Vinod; Terblans, J J; Swart, H C; Sharma, S K

    2014-07-14

    This paper reports on the structural, optical and photometric characterization of an Eu(3+)/Dy(3+) doped yttrium oxysulfide phosphor (Y2O2S:Eu(3+)/Dy(3+)) for near white emission in solid state lighting. A series of Y2O2S phosphors doped with Eu(3+)/Dy(3+) were prepared by the hydrothermal method. The microstructures of the as-synthesized phosphors were investigated by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The XRD results reveal that the obtained powder phosphors have a single-phase hexagonal structure and also indicate that the incorporation of the dopants/co-dopants did not affect the crystal structure. The SEM images reveal the morphology of the prepared phosphors as an intense interpenetrating network of interconnected micro-fibers with a diameter of about 0.15 μm. The band gap of the phosphors was calculated from diffuse reflectance spectra using the Kubelka-Munk function. The Eu(3+), Dy(3+) doped and Eu(3+)/Dy(3+) co-doped phosphors illuminated with ultraviolet light showed characteristic red luminescence corresponding to the (5)D0→(7)FJ transitions of Eu(3+) and characteristic blue and yellow luminescence corresponding to the (4)F9/2→(6)H15/2 or (4)F9/2→(6)H13/2 transitions of Dy(3+). The luminescence spectra, the energy transfer efficiency and the decay curves of the phosphors indicated that there exists a strong energy transfer from Dy(3+) to Eu(3+) and this was demonstrated to be a resonant type via a dipole-quadrupole reaction. Furthermore, the critical distance of the Eu(3+) and Dy(3+) ions have also been calculated. By utilizing the principle of energy transfer it was also demonstrated that with an appropriate tuning of the activator content the Y2O2S:Eu(3+)/Dy(3+) phosphors can exhibit a great potential to act as single-emitting component phosphors for white light emission in solid state lighting technology.

  14. (Mn 1-xPb x)Pb 10+ySb 12-yS 26-yCl 4+yO, a new oxy-chloro-sulfide with ˜2 nm-spaced (Mn,Pb)Cl 4 single chains within a waffle-type crystal structure

    NASA Astrophysics Data System (ADS)

    Doussier, Charlotte; Moëlo, Yves; Léone, Philippe; Meerschaut, Alain

    2007-08-01

    The new oxy-chloro-sulfide (Mn 1-xPb x)Pb 10+ySb 12-yS 26-yCl 4+yO ( x ∈ [0.2-0.3]; y ∈ [0.3-1.6]) was synthesized by dry way at 500-600 °C. A single crystal ˜Mn 0.7Pb 11.0Sb 11.3S 25.3Cl 4.7O indicates a monoclinic symmetry, space group C2 /m, with a = 37.480(8), b = 4.1178(8), c = 18.167(4) Å, β = 106.37(3)°, V = 2690.2(9) Å 3, Z = 2. Its crystal structure was determined by X-ray single crystal diffraction, with a final R = 5.11%. Modular analysis of the crystal structure reveals a "waffle" architecture, where complex rods with lozenge section delimitate an internal channel filled by a single chain of (Mn 0.7Pb 0.3)Cl 6 octahedra connected by opposite edges. Minimal inter-chain distances are close to 18 Å. The rod wall, two-atom thick, presents, in alternation with S atoms, Pb or (Pb,Sb) cations with prismatic coordination in the internal atom layer, while the external atom layer is constituted exclusively by Sb cations with dissymmetric square pyramidal coordination. A (Pb,Sb) 2S 2 fragment connects two successive rods along (2 0 1) to form a waffle-type palissadic layer. The unique O position, half filled, presents the same environment than the isolated O positions in the oxy-sulfide Pb 14Sb 30S 54O 5, or oxy-chloro-sulfides Pb 18Sb 20S 46Cl 2O and (Cu,Ag) 2Pb 21Sb 23S 55ClO. This compound belongs to a pseudo-homologous series of chalcogenides with waffle structure, ordered according to the size of their lozenge shape channel. Such a complex senary compound of the oxy-chloro-sulfide type illustrates the structural competition between three cations, on one hand, and, on the other hand, three anions. This compound is of special interest regarding the 1D distribution of magnetic Mn 2+ atoms at the ˜2 nm scale.

  15. Towards an ab initio description of correlated materials

    NASA Astrophysics Data System (ADS)

    Yee, Chuck-Hou

    the superconducting transition temperatures across the cuprate families. In the second, we extend this idea towards first-principles design of cuprates by exploring a new family of copper oxysulfides.

  16. Optimization of phosphor-based detector design for oblique x-ray incidence in digital breast tomosynthesis

    SciTech Connect

    Acciavatti, Raymond J.; Maidment, Andrew D. A.

    2011-11-15

    Purpose: In digital breast tomosynthesis (DBT), a volumetric reconstruction of the breast is generated from a limited range of x-ray projections. One trade-off of DBT is resolution loss in the projections due to non-normal (i.e., oblique) x-ray incidence. Although degradation in image quality due to oblique incidence has been studied using empirical data and Monte Carlo simulations, a theoretical treatment has been lacking. The purpose of this work is to extend Swank's calculations of the transfer functions of turbid granular phosphors to oblique incidence. The model is ultimately used as a tool for optimizing the design of DBT detectors. Methods: A quantum-limited system and 20 keV x-rays are considered. Under these assumptions, the modulation transfer function (MTF) and noise power spectra (NPS) are derived using the diffusion approximation to the Boltzmann equation to model optical scatter within the phosphor. This approach is applicable to a nonstructured scintillator such as gadolinium oxysulfide doped with terbium (Gd{sub 2}O{sub 2}S:Tb), which is commonly used in breast imaging and which can reasonably approximate other detector materials. The detective quantum efficiency (DQE) is then determined from the Nishikawa formulation, where it is written as the product of the x-ray quantum detection efficiency, the Swank factor, and the Lubberts fraction. Transfer functions are calculated for both front- and back-screen configurations, which differ by positioning the photocathode at the exit or entrance point of the x-ray beam, respectively. Results: In the front-screen configuration, MTF and DQE are found to have considerable angular dependence, while NPS is shown to vary minimally with projection angle. As expected, the high frequency MTF and DQE are degraded substantially at large angles. By contrast, all transfer functions for the back-screen configuration have the advantage of significantly less angular dependence. Using these models, we investigated the

  17. Metal oxide electrocatalysts for alternative energy technologies

    NASA Astrophysics Data System (ADS)

    Pacquette, Adele Lawren

    This dissertation focuses on the development of metal oxide electrocatalysts with varying applications for alternative energy technologies. Interest in utilizing clean, renewable and sustainable sources of energy for powering the planet in the future has received much attention. This will address the growing concern of the need to reduce our dependence on fossil fuels. The facile synthesis of metal oxides from earth abundant metals was explored in this work. The electrocatalysts can be incorporated into photoelectrochemical devices, fuel cells, and other energy storage devices. The first section addresses the utilization of semiconductors that can harness solar energy for water splitting to generate hydrogen. An oxysulfide was studied in order to combine the advantageous properties of the stability of metal oxides and the visible light absorbance of metal chalcogenides. Bi 2O2S was synthesized under facile hydrothermal conditions. The band gap of Bi2O2S was smaller than that of its oxide counterpart, Bi2O3. Light absorption by Bi 2O2S was extended to the visible region (>600 nm) in comparison to Bi2O3. The formation of a composite with In 2O3 was formed in order to create a UV irradiation protective coating of the Bi2O2S. The Bi2O2S/In 2O3 composite coupled with a dye CrTPP(Cl) and cocatalysts Pt and Co3O4 was utilized for water splitting under light irradiation to generate hydrogen and oxygen. The second section focuses on improving the stability and light absorption of semiconductors by changing the shapes and morphologies. One of the limitations of semiconductor materials is that recombination of electron-hole pairs occur within the bulk of the materials instead of migration to the surface. Three-dimensional shapes, such as nanorods, can prevent this recombination in comparison to spherical particles. Hierarchical structures, such as dendrites, cubes, and multipods, were synthesized under hydrothermal conditions, in order to reduce recombination and improve

  18. Anode materials for sour natural gas solid oxide fuel cells

    NASA Astrophysics Data System (ADS)

    Danilovic, Nemanja

    Novel anode catalysts have been developed for sour natural gas solid oxide fuel cell (SOFC) applications. Sour natural gas comprises light hydrocarbons, and typically also contains H2S. An alternative fuel SOFC that operates directly on sour natural gas would reduce the overall cost of plant construction and operation for fuel cell power generation. The anode for such a fuel cell must have good catalytic and electrocatalytic activity for hydrocarbon conversion, sulfur-tolerance, resistance to coking, and good electronic and ionic conductivity. The catalytic activity and stability of ABO3 (A= La, Ce and/or Sr, B=Cr and one or more of Ti, V, Cr, Fe, Mn, or Co) perovskites as SOFC anode materials depends on both A and B, and are modified by substituents. The materials have been prepared by both solid state and wet-chemical methods. The physical and chemical characteristics of the materials have been fully characterized using electron microscopy, XRD, calorimetry, dilatometry, particle size and area, using XPS and TGA-DSC-MS. Electrochemical performance was determined using potentiodynamic and potentiostatic cell testing, electrochemical impedance analysis, and conductivity measurements. Neither Ce0.9Sr0.1VO3 nor Ce0.9 Sr0.1Cr0.5V0.5O3 was an active anode for oxidation of H2 and CH4 fuels. However, active catalysts comprising Ce0:9Sr0:1V(O,S)3 and Ce0.9Sr 0.1Cr0.5V0.5(O,S)3 were formed when small concentrations of H2S were present in the fuels. The oxysulfides formed in-situ were very active for conversion of H2S. The maximum performance improved from 50 mW cm-2 to 85 mW cm -2 in 0.5% H2S/CH4 at 850°C with partial substitution of V by Cr in Ce0.9Sr0.1V(O,S)3. Selective conversion of H2S offers potential for sweetening of sour gas without affecting the hydrocarbons. Perovskites La0.75Sr0.25Cr0.5X 0.5O3--delta, (henceforth referred to as LSCX, X=Ti, Mn, Fe, Co) are active for conversion of H2, CH4 and 0.5% H2S/CH4. The order of activity in the different fuels depends on

  19. Geochemical Exploration Techniques Applicable in the Search for Copper Deposits

    USGS Publications Warehouse

    Chaffee, Maurice A.

    1975-01-01

    Geochemical exploration is an important part of copper-resource evaluation. A large number of geochemical exploration techniques, both proved and untried, are available to the geochemist to use in the search for new copper deposits. Analyses of whole-rock samples have been used in both regional and local geochemical exploration surveys in the search for copper. Analyses of mineral separates, such as biotite, magnetite, and sulfides, have also been used. Analyses of soil samples are widely used in geochemical exploration, especially for localized surveys. It is important to distinguish between residual and transported soil types. Orientation studies should always be conducted prior to a geochemical investigation in a given area in order to determine the best soil horizon and the best size of soil material for sampling in that area. Silty frost boils, caliche, and desert varnish are specialized types of soil samples that might be useful sampling media. Soil gas is a new and potentially valuable geochemical sampling medium, especially in exploring for buried mineral deposits in arid regions. Gaseous products in samples of soil may be related to base-metal deposits and include mercury vapor, sulfur dioxide, hydrogen sulfide, carbon oxysulfide, carbon dioxide, hydrogen, oxygen, nitrogen, the noble gases, the halogens, and many hydrocarbon compounds. Transported materials that have been used in geochemical sampling programs include glacial float boulders, glacial till, esker gravels, stream sediments, stream-sediment concentrates, and lake sediments. Stream-sediment sampling is probably the most widely used and most successful geochemical exploration technique. Hydrogeochemical exploration programs have utilized hot- and cold-spring waters and their precipitates as well as waters from lakes, streams, and wells. Organic gel found in lakes and at stream mouths is an unproved sampling medium. Suspended material and dissolved gases in any type of water may also be useful

  20. UT-CT: A National Resource for Applications of High-Resolution X-ray Computed Tomography in the Geological Sciences

    NASA Astrophysics Data System (ADS)

    Carlson, W. D.; Ketcham, R. A.; Rowe, T. B.

    2002-12-01

    An NSF-sponsored (EAR-IF) shared multi-user facility dedicated to research applications of high-resolution X-ray computed tomography (CT) in the geological sciences has been in operation since 1997 at the University of Texas at Austin. The centerpiece of the facility is an industrial CT scanner custom-designed for geological applications. Because the instrument can optimize trade-offs among penetrating ability, spatial resolution, density discrimination, imaging modes, and scan times, it can image a very broad range of geological specimens and materials, and thus offers significant advantages over medical scanners and desktop microtomographs. Two tungsten-target X-ray sources (200-kV microfocal and 420-kV) and three X-ray detectors (image-intensifier, high-sensitivity cadmium tungstate linear array, and high-resolution gadolinium-oxysulfide radiographic line scanner) can be used in various combinations to meet specific imaging goals. Further flexibility is provided by multiple imaging modes: second-generation (translate-rotate), third-generation (rotate-only; centered and variably offset), and cone-beam (volume CT). The instrument can accommodate specimens as small as about 1 mm on a side, and as large as 0.5 m in diameter and 1.5 m tall. Applications in petrology and structural geology include measuring crystal sizes and locations to identify mechanisms governing the kinetics of metamorphic reactions; visualizing relationships between alteration zones and abundant macrodiamonds in Siberian eclogites to elucidate metasomatic processes in the mantle; characterizing morphologies of spiral inclusion trails in garnet to test hypotheses of porphyroblast rotation during growth; measuring vesicle size distributions in basaltic flows for determination of elevation at the time of eruption to constrain timing and rates of continental uplift; analysis of the geometry, connectivity, and tortuosity of migmatite leucosomes to define the topology of melt flow paths, for numerical

  1. A piecewise-focused high DQE detector for MV imaging

    PubMed Central

    Star-Lack, Josh; Shedlock, Daniel; Swahn, Dennis; Humber, Dave; Wang, Adam; Hirsh, Hayley; Zentai, George; Sawkey, Daren; Kruger, Isaac; Sun, Mingshan; Abel, Eric; Virshup, Gary; Shin, Mihye; Fahrig, Rebecca

    2015-01-01

    Purpose: Electronic portal imagers (EPIDs) with high detective quantum efficiencies (DQEs) are sought to facilitate the use of the megavoltage (MV) radiotherapy treatment beam for image guidance. Potential advantages include high quality (treatment) beam’s eye view imaging, and improved cone-beam computed tomography (CBCT) generating images with more accurate electron density maps with immunity to metal artifacts. One approach to increasing detector sensitivity is to couple a thick pixelated scintillator array to an active matrix flat panel imager (AMFPI) incorporating amorphous silicon thin film electronics. Cadmium tungstate (CWO) has many desirable scintillation properties including good light output, a high index of refraction, high optical transparency, and reasonable cost. However, due to the 0 1 0 cleave plane inherent in its crystalline structure, the difficulty of cutting and polishing CWO has, in part, limited its study relative to other scintillators such as cesium iodide and bismuth germanate (BGO). The goal of this work was to build and test a focused large-area pixelated “strip” CWO detector. Methods: A 361  ×  52 mm scintillator assembly that contained a total of 28 072 pixels was constructed. The assembly comprised seven subarrays, each 15 mm thick. Six of the subarrays were fabricated from CWO with a pixel pitch of 0.784 mm, while one array was constructed from BGO for comparison. Focusing was achieved by coupling the arrays to the Varian AS1000 AMFPI through a piecewise linear arc-shaped fiber optic plate. Simulation and experimental studies of modulation transfer function (MTF) and DQE were undertaken using a 6 MV beam, and comparisons were made between the performance of the pixelated strip assembly and the most common EPID configuration comprising a 1 mm-thick copper build-up plate attached to a 133 mg/cm2 gadolinium oxysulfide scintillator screen (Cu-GOS). Projection radiographs and CBCT images of phantoms were acquired. The work

  2. Analysis of a free-running synchronization artifact correction for MV-imaging with aSi:H flat panels

    SciTech Connect

    Mooslechner, Michaela; Mitterlechner, Bernhard; Weichenberger, Harald; Sedlmayer, Felix; Deutschmann, Heinz; Huber, Stefan

    2013-03-15

    Purpose: Solid state flat panel electronic portal imaging devices (EPIDs) are widely used for megavolt (MV) photon imaging applications in radiotherapy. In addition to their original purpose in patient position verification, they are convenient to use in quality assurance and dosimetry to verify beam geometry and dose deposition or to perform linear accelerator (linac) calibration procedures. However, native image frames from amorphous silicon (aSi:H) detectors show a range of artifacts which have to be eliminated by proper correction algorithms. When a panel is operated in free-running frame acquisition mode, moving vertical stripes (periodic synchronization artifacts) are a disturbing feature in image frames. Especially for applications in volumetric intensity modulated arc therapy (VMAT) or motion tracking, the synchronization (sync) artifacts are the limiting factor for potential and accuracy since they become even worse at higher frame rates and at lower dose rates, i.e., linac pulse repetition frequencies (PRFs). Methods: The authors introduced a synchronization correction method which is based on a theoretical model describing the interferences of the panel's readout clocking with the linac's dose pulsing. Depending on the applied PRF, a certain number of dose pulses is captured per frame which is readout columnwise, sequentially. The interference of the PRF with the panel readout is responsible for the period and the different gray value levels of the sync stripes, which can be calculated analytically. Sync artifacts can then be eliminated multiplicatively in precorrected frames without additional information about radiation pulse timing. Results: For the analysis, three aSi:H EPIDs of various types were investigated with 6 and 15 MV photon beams at varying PRFs of 25, 50, 100, 200, and 400 pulses per second. Applying the sync correction at panels with gadolinium oxysulfide scintillators improved single frame flood field image quality drastically

  3. (Mn{sub 1-x}Pb{sub x})Pb{sub 10+y}Sb{sub 12-y}S{sub 26-y}Cl{sub 4+y}O, a new oxy-chloro-sulfide with {approx}2 nm-spaced (Mn,Pb)Cl{sub 4} single chains within a waffle-type crystal structure

    SciTech Connect

    Doussier, Charlotte; Moelo, Yves Leone, Philippe; Meerschaut, Alain

    2007-08-15

    The new oxy-chloro-sulfide (Mn{sub 1-x}Pb{sub x})Pb{sub 10+y}Sb{sub 12-y}S{sub 26-y}Cl{sub 4+y}O (x element of [0.2-0.3]; y element of [0.3-1.6]) was synthesized by dry way at 500-600 deg. C. A single crystal {approx}Mn{sub 0.7}Pb{sub 11.0}Sb{sub 11.3}S{sub 25.3}Cl{sub 4.7}O indicates a monoclinic symmetry, space group C2/m, with a = 37.480(8), b 4.1178(8), c = 18.167(4) A, {beta} = 106.37(3){sup o}, V = 2690.2(9) A{sup 3}, Z = 2. Its crystal structure was determined by X-ray single crystal diffraction, with a final R = 5.11%. Modular analysis of the crystal structure reveals a 'waffle' architecture, where complex rods with lozenge section delimitate an internal channel filled by a single chain of (Mn{sub 0.7}Pb{sub 0.3})Cl{sub 6} octahedra connected by opposite edges. Minimal inter-chain distances are close to 18 A. The rod wall, two-atom thick, presents, in alternation with S atoms, Pb or (Pb,Sb) cations with prismatic coordination in the internal atom layer, while the external atom layer is constituted exclusively by Sb cations with dissymmetric square pyramidal coordination. A (Pb,Sb){sub 2}S{sub 2} fragment connects two successive rods along (2 0 1) to form a waffle-type palissadic layer. The unique O position, half filled, presents the same environment than the isolated O positions in the oxy-sulfide Pb{sub 14}Sb{sub 30}S{sub 54}O{sub 5}, or oxy-chloro-sulfides Pb{sub 18}Sb{sub 20}S{sub 46}Cl{sub 2}O and (Cu,Ag){sub 2}Pb{sub 21}Sb{sub 23}S{sub 55}ClO. This compound belongs to a pseudo-homologous series of chalcogenides with waffle structure, ordered according to the size of their lozenge shape channel. Such a complex senary compound of the oxy-chloro-sulfide type illustrates the structural competition between three cations, on one hand, and, on the other hand, three anions. This compound is of special interest regarding the 1D distribution of magnetic Mn{sup 2+} atoms at the {approx}2 nm scale. - Graphical abstract: Projection of the crystal structure of (Mn

  4. Solid State Ionics Advanced Materials for Emerging Technologies

    NASA Astrophysics Data System (ADS)

    Chowdari, B. V. R.; Careem, M. A.; Dissanayake, M. A. K. L.; Rajapakse, R. M. G.; Seneviratne, V. A.

    2006-06-01

    SiO[symbol]) ceramics via solid state sintering of Zr)[symbol] and SiO[symbol] and the effect of dopants on the zircon yield / U. Dhanayake, B. S. B. Karunaratne. Preparation and properties of vanadium doped ZnTe cermet thin films / M. S. Hossain, R. Islam, K. A. Khan. Dynamical properties and electronic structure of lithium-ion conductor / M. Kobayashi ... [et al.]. Cuprous ion conducting Montmorillonite-Polypyrrole nanocomposites / D. M. M. Krishantha ... [et al.]. Frequency dependence of conductivity studies on a newly synthesized superionic solid solution/mixed system: [0.75AgI: 0.25AgCl] / R. K. Nagarch, R. Kumar. Diffuse X-ray and neutron scattering from Powder PbS / X. Lian ... [et al.]. Electron affinity and work function of Pyrolytic MnO[symbol] thin films prepared from Mn(C[symbol]H[symbol]O[symbol])[symbol].4H[symbol]) / A. K. M. Farid Ul Islam, R. Islam, K. A. Khan. Crystal structure and heat capacity of Ba[symbol]Ca[symbol]Nb[symbol]O[symbol] / T. Shimoyama ... [et al.]. XPS and impedance investigations on amorphous vanadium oxide thin films / M. Kamalanathan ... [et al.]. Sintering and mixed electronic-ionic conducting properties of La[symbol]Sr[symbol]NiO[symbol] derived from a polyaminocarboxylate complex precursor / D.-P. Huang ... [et al.]. Preparation and characteristics of ball milled MgH[symbol] + M (M= Fe, VF[symbol] and FeF[symbol]) nanocomposites for hydrogen storage / N. W. B. Balasooriya, Ch. Poinsignon. Structural studies of oxysulfide glasses by X-ray diffraction and molecular dynamics simulation / R. Prasada Rao, M. Seshasayee, J. Dheepa. Synthesis, sintering and oxygen ionic conducting properties of Bi[symbol]V[symbol]Cu[symbol]O[symbol] / F. Zhang ... [et al.]. Synthesis and transport characteristics of PbI[symbol]-Ag[symbol]O-Cr[symbol]O[symbol] superioninc system / S. A. Suthanthiraraj, V. Mathew. Electronic conductivity of La[symbol]Sr[symbol]Ga[symbol]Mg[symbol]Co[symbol]O[symbol] electrolytes / K. Yamaji ... [et al.] -- pt. II. Electrode materials

  5. Photoelectrochemical Hydrogen Production

    SciTech Connect

    Hu, Jian

    2013-12-23

    -circuit photocurrent density of the hybrid device (measured in a 2-electrode configuration) increased significantly without assistance of any external bias, i.e. from ≤1 mA/cm{sup 2} to ~5 mA/cm{sup 2}. With the copper chalcopyrite compounds, we have achieved a STH efficiency of 3.7% in a coplanar configuration with 3 a-Si solar cells and one CuGaSe{sub 2} photocathode. This material class exhibited good durability at a photocurrent density level of -4 mA/cm{sup 2} (“5% STH” equivalent) at a fixed potential (-0.45 VRHE). A poor band-edge alignment with the hydrogen evolution reaction (HER) potential was identified as the main limitation for high STH efficiency. Three new pathways have been identified to solve this issue. First, PV driver with bandgap lower than that of amorphous silicon were investigated. Crystalline silicon was identified as possible bottom cell. Mechanical stacks made with one Si solar cell and one CuGaSe{sub 2} photocathode were built. A 400 mV anodic shift was observed with the Si cell, leading to photocurrent density of -5 mA/cm{sup 2} at 0VRHE (compared to 0 mA/cm{sup 2} at the same potential without PV driver). We also investigated the use of p-n junctions to shift CuGaSe{sub 2} flatband potential anodically. Reactively sputtered zinc oxy-sulfide thin films was evaluated as n-type buffer and deposited on CuGaSe{sub 2}. Ruthenium nanoparticles were then added as HER catalyst. A 250 mV anodic shift was observed with the p-n junction, leading to photocurrent density at 0VRHE of -1.5 mA/cm{sup 2}. Combining this device with a Si solar cell in a mechanical stack configuration shifted the onset potential further (+400 mV anodically), leading to photocurrent density of -7 mA/cm{sup 2} at 0VRHE. Finally, we developed wide bandgap copper chalcopyrite thin film materials. We demonstrated that Se can be substituted with S using a simple annealing step. Photocurrent densities in the 5-6 mA/cm{sub 2} range were obtained with red 2.0eV CuInGaS{sub 2} photocathodes

  6. Solid State Ionics Advanced Materials for Emerging Technologies

    NASA Astrophysics Data System (ADS)

    Chowdari, B. V. R.; Careem, M. A.; Dissanayake, M. A. K. L.; Rajapakse, R. M. G.; Seneviratne, V. A.

    2006-06-01

    SiO[symbol]) ceramics via solid state sintering of Zr)[symbol] and SiO[symbol] and the effect of dopants on the zircon yield / U. Dhanayake, B. S. B. Karunaratne. Preparation and properties of vanadium doped ZnTe cermet thin films / M. S. Hossain, R. Islam, K. A. Khan. Dynamical properties and electronic structure of lithium-ion conductor / M. Kobayashi ... [et al.]. Cuprous ion conducting Montmorillonite-Polypyrrole nanocomposites / D. M. M. Krishantha ... [et al.]. Frequency dependence of conductivity studies on a newly synthesized superionic solid solution/mixed system: [0.75AgI: 0.25AgCl] / R. K. Nagarch, R. Kumar. Diffuse X-ray and neutron scattering from Powder PbS / X. Lian ... [et al.]. Electron affinity and work function of Pyrolytic MnO[symbol] thin films prepared from Mn(C[symbol]H[symbol]O[symbol])[symbol].4H[symbol]) / A. K. M. Farid Ul Islam, R. Islam, K. A. Khan. Crystal structure and heat capacity of Ba[symbol]Ca[symbol]Nb[symbol]O[symbol] / T. Shimoyama ... [et al.]. XPS and impedance investigations on amorphous vanadium oxide thin films / M. Kamalanathan ... [et al.]. Sintering and mixed electronic-ionic conducting properties of La[symbol]Sr[symbol]NiO[symbol] derived from a polyaminocarboxylate complex precursor / D.-P. Huang ... [et al.]. Preparation and characteristics of ball milled MgH[symbol] + M (M= Fe, VF[symbol] and FeF[symbol]) nanocomposites for hydrogen storage / N. W. B. Balasooriya, Ch. Poinsignon. Structural studies of oxysulfide glasses by X-ray diffraction and molecular dynamics simulation / R. Prasada Rao, M. Seshasayee, J. Dheepa. Synthesis, sintering and oxygen ionic conducting properties of Bi[symbol]V[symbol]Cu[symbol]O[symbol] / F. Zhang ... [et al.]. Synthesis and transport characteristics of PbI[symbol]-Ag[symbol]O-Cr[symbol]O[symbol] superioninc system / S. A. Suthanthiraraj, V. Mathew. Electronic conductivity of La[symbol]Sr[symbol]Ga[symbol]Mg[symbol]Co[symbol]O[symbol] electrolytes / K. Yamaji ... [et al.] -- pt. II. Electrode materials