Search results for "Absorption"

showing 10 items of 2701 documents

X-ray Absorption under Operating Conditions for Solid-Oxide Fuel Cells Electrocatalysts: The Case of LSCF/YSZ

2019

We describe a novel electrochemical cell for X-ray absorption spectroscopy (XAS) experiments during electrical polarization suitable for high-temperature materials such as those used in solid oxide fuel cells. A half-cell LSCF/YSZ was then investigated under cathodic and anodic conditions (850 &deg

X-ray absorption spectroscopycathodeMaterials scienceAbsorption spectroscopyXAFSOxidein situ02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesX-ray absorption fine structureElectrochemical cellAnodechemistry.chemical_compoundChemical engineeringchemistrySOFC0210 nano-technologyPolarization (electrochemistry)Yttria-stabilized zirconia
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<title>Local structure of Ta-Re mixed oxide thin films studied by x-ray absorption spectroscopy</title>

2003

Mixed Ta-Re oxide thin films were synthesized for the first time by dc magnetron co-sputtering. Local environment around tantalum and rhenium atoms was studied by the Ta and Re L3-edges x-ray absorption spectroscopy in pure Ta2O5 and mixed Ta-Re oxide thin films (Ta:Re = 50:50, 38:62, 20:80 as determined from the ratio of the Ta-to-Re absorption edges). It was found that rhenium atoms are four-fold coordinated by oxygen atoms with R(Re-O) = 1.74 ± 0.01 Å and the mean square relative displacement (MSRD) σ2 = 0.0012 ± 0.0005 Å2. In pure Ta2O5 thin film, tantalum ions are coordinated by six oxygen atoms at R(Ta-O) = 2.02 ± 0.01 Å with the MSRD σ2 = 0.010 ± 0.001 Å2. The addition of rhenium ion…

X-ray absorption spectroscopychemistry.chemical_compoundchemistryExtended X-ray absorption fine structureAbsorption spectroscopyTantalumAnalytical chemistryOxidechemistry.chemical_elementSputter depositionRheniumAbsorption (chemistry)SPIE Proceedings
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Origin of Pressure-Induced Metallization in Cu 3 N: An X-ray Absorption Spectroscopy Study

2018

The authors are grateful to Professor Alain Polian for providing the NDAC cell.

X-ray absorption spectroscopyhigh-pressureMaterials scienceExtended X-ray absorption fine structureCu3NAnalytical chemistry02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesXANESXANES0104 chemical sciencesElectronic Optical and Magnetic MaterialsEXAFSHigh pressureCu K-edge:NATURAL SCIENCES:Physics [Research Subject Categories]0210 nano-technologyphysica status solidi (b)
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Local Structure of Supported Keggin and Wells-Dawson Heteropolyacids and Its Influence on the Catalytic Activity

2019

[EN] Keggin [PW12O40]3– and Wells–Dawson [P2W18O62]6– heteropolyanions are nanosized transition-metal-oxygen clusters belonging to the heteropolyacids (HPAs) family. They are widely used as catalysts due to their high Brønsted acidity, and their dispersion on solid supports favors the accessibility to their acid sites generally increasing the catalytic activity. A series of binary materials composed of Keggin or Wells–Dawson HPAs and SiO2, TiO2, and ZrO2 have been prepared by impregnation or solvothermal methods. Remarkable differences have been found in the catalytic activities among the unsupported and supported HPAs. These differences have been correlated in the past to the structural ch…

X-ray photoelectron spectroscopyX-ray absorption near edge spectroscopy;Cluster chemistryChemistryOxides02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesLocal structureX-ray absorption near edge spectroscopy0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysisCrystallographyGeneral EnergySettore CHIM/03 - Chimica Generale E InorganicaSupported Keggin and Wells-Dawson HeteropolyacidsSettore CHIM/07 - Fondamenti Chimici Delle TecnologiePhysical and Theoretical Chemistryheteropolyacids Keggin Wells-Dawson catalysis polyoxometalates EXAFS0210 nano-technologyMaterials
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Local structure studies of SrTi16O3and SrTi18O3

2014

In this work we report on the local structure of Ti in SrTi 16 O3 (STO16) and SrTi 18 O3 (STO18) investigated in the low temperature range (6‐300K) by extended x-ray absorption fine structure and x-ray absorption near edge structure (XANES) spectroscopy at Ti K-edge and by optical second harmonic generation (SHG). By comparing XANES of STO16 and STO18 we have identified the isotopic effect which produces at T < 100K a noticeable difference in the measured mean square relative displacements (MSRD) of Ti‐O1 bonds: while STO16 follow the expected Einstein-like behavior, for STO18 we have measured an increase of MSRD values with decreasing temperature. This is an indication of an increasing off…

X-ray spectroscopyMaterials scienceAbsorption spectroscopyOctahedronAnalytical chemistrySecond-harmonic generationAtmospheric temperature rangeCondensed Matter PhysicsSpectroscopyAbsorption (electromagnetic radiation)Mathematical PhysicsAtomic and Molecular Physics and OpticsXANESPhysica Scripta
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X-ray Spectroscopy of (Ba,Sr,La)(Fe,Zn,Y)O3-δIdentifies Structural and Electronic Features Favoring Proton Uptake

2020

Mixed protonic–electronic conducting oxides are key functional materials for protonic ceramic fuel cells. Here, (Ba,Sr,La)(Fe,Zn,Y)O3−δ perovskites are comprehensively investigated by X-ray spectroscopy (in oxidized and reduced states). Extended X-ray absorption fine structure shows that Zn,Y doping strongly increases the tendency for Fe–O–Fe buckling. X-ray absorption near-edge spectroscopy at the Fe K-edge and X-ray Raman scattering at the O K edge demonstrate that both iron and oxygen states are involved when the samples are oxidized, and for the Zn,Y doped materials, the hole transfer from iron to oxygen is less pronounced. This can be correlated with the observation that these material…

X-ray spectroscopyMaterials scienceProtonGeneral Chemical Engineeringchemistry.chemical_element02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesOxygen0104 chemical sciencesExtended X ray absorption fine structure spectroscopy Functional materials Iron OxygenPerovskite Protonic ceramic fuel cells (PCFC) X ray absorptionCrystallographychemistryvisual_artMaterials Chemistryvisual_art.visual_art_mediumFuel cellsCeramicAbsorption (chemistry)0210 nano-technology
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Using photoelectron emission microscopy with hard-X-rays

2001

We present several successful test cases of using photoelectron emission microscopy (PEEM) for photon energy up to 25 keV. First, the full extended X-ray absorption fine structure analysis was implemented in areas as small as 100 mum(2) for transition-metal K edge absorption spectra and, therefore, demonstrated the feasibility of combining structural and chemical analysis with hard-X-ray absorption spectroscopy with high lateral resolution. We also show that PEEM can be used in a transmission (radiography) mode as an imaging detector for hard-X-ray, This approach again leads to the unprecedented 0.3 mum lateral resolution, particularly critical for the use of coherence-based phase contrast …

X-ray spectroscopyX-ray absorption spectroscopyAbsorption spectroscopyExtended X-ray absorption fine structurebusiness.industryChemistrySynchrotron radiationSurfaces and InterfacesPhoton energyCondensed Matter PhysicsSurfaces Coatings and FilmsOpticsK-edgeX-ray photoelectron spectroscopyMaterials ChemistrybusinessSurface Science
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Jahn-Teller distortion aroundFe4+inSr(FexTi1−x)O3−δfrom x-ray absorption spectroscopy, x-ray diffraction, and vibrational spectroscopy

2007

$\mathrm{Sr}({\mathrm{Fe}}_{x}{\mathrm{Ti}}_{1\ensuremath{-}x}){\mathrm{O}}_{3\ensuremath{-}\ensuremath{\delta}}$ perovskites (strontium titanate ferrite solid solution) with well-defined oxygen stoichiometry have been studied as a function of iron concentration by x-ray diffraction, Fe and Ti $K$-edge x-ray absorption spectroscopy (XAS), and vibrational (Raman and infrared) spectroscopy. In reduced $\mathrm{Sr}({\mathrm{Fe}}_{x}{\mathrm{Ti}}_{1\ensuremath{-}x}){\mathrm{O}}_{3\ensuremath{-}x∕2}$ samples, the analysis of the Fe $K$-edge extended x-ray absorption fine structure indicates the expected presence of oxygen vacancies ${\mathrm{V}}_{\mathrm{O}}^{∙∙}$ in the first coordination shell…

X-ray spectroscopyX-ray absorption spectroscopyCrystallographyMaterials scienceAbsorption spectroscopyJahn–Teller effectX-ray crystallographyCondensed Matter PhysicsSpectroscopyElectronic Optical and Magnetic MaterialsSolid solutionX-ray absorption fine structurePhysical Review B
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Preparation and XAFS studies of organotin(IV) complexes with adenosine and related compounds and calf thymus DNA

2007

Complexes of adenosine and related compounds (adenosine-5’-monophosphate, adenosine-5’-triphosphate and pyridoxal-5-phosphate) with Bu2SnO and/or BuSnCl2 were prepared in the solid state. The compositions of the complexes were determined by standard analytical methods. It was found that the complexes contain the organotin(IV) moiety and the ligand in a ratio of 1:1. The FT-IR spectra demonstrated that Bu2SnO reacts with the D-ribose moiety of the ligands, while Bu2SnCl2 is coordinated to the deprotonated phosphate group. The basic part of the ligands does not participate directly in complex formation. Comparison of the experimental Mossbauer Δ (quadrupole splitting) values with those calcul…

XAFS organotin(IV) DNA Mossbauer FT-IRExtended X-ray absorption fine structureChemistryLigandStereochemistryHealth Toxicology and MutagenesisPublic Health Environmental and Occupational HealthQuadrupole splittingPollutionMedicinal chemistryAnalytical ChemistryX-ray absorption fine structureBond lengthDeprotonationNuclear Energy and EngineeringSettore CHIM/03 - Chimica Generale E InorganicaMössbauer spectroscopyMoietyRadiology Nuclear Medicine and imagingSpectroscopyJournal of Radioanalytical and Nuclear Chemistry
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Comparative Experimental and Theoretical Study of the Fe L-2,L-3-Edges X-ray Absorption Spectroscopy in Three Highly Popular, Low-Spin Organoiron Com…

2019

The occupied and unoccupied electronic structures of three highly popular, closed shell organoiron complexes ([Fe(CO)(5)], [(eta(5)-C5H5 )Fe(CO)(mu-CO)](2), and [(eta(5)-C5H5)(2)Fe]) have been theoretically investigated by taking advantage of density functional theory (DFT) calculations coupled to the isolobal analogy (Elian et al. Inorg. Chem. 1976, 15, 1148). The adopted approach allowed us to look into the relative role played by the ligand -&gt; Fe donation and the Fe -&gt; ligand back-donation in title molecules, as well as to investigate how CO- (terminal or bridging) and [(eta(5)-C5H5)](-)-based pi* orbitals compete when these two ligands are simultaneously present as in [(eta(5)-C5H…

XASXAS spectroscopy Organoiron complexes DFT.High Resolution X-Ray Absorption SpectroscopyFe L23 edgegas phasedensity functional theory
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