Search results for "XAFS"

showing 10 items of 93 documents

Structure of the Metal–Support Interface and Oxidation State of Gold Nanoparticles Supported on Ceria

2012

An Au/CeO2 model catalyst was prepared by deposition–precipitation, with the aim of obtaining a sample suitable for a detailed X-ray absorption fine structure (XAFS) analysis of the gold–ceria interface structure. The results demonstrate the existence of a large interface between the gold particle and the support oxide, characterized by well-defined Au–O and Au–Ce interactions extending up to ∼6.4 A. The complex interface structure is retained after CO treatment up to 250 °C and subsequent reoxidation at 400 °C. The analysis of the XANES spectra, and the Au–O distance of 2.21 A, longer than Au–O bond lengths previously reported for Au/ceria catalysts, suggest a low oxidation state for the g…

Materials scienceExtended X-ray absorption fine structureOxideXANESSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysisX-ray absorption fine structureMetalCrystallographychemistry.chemical_compoundGeneral EnergychemistryChemical engineeringColloidal goldOxidation statevisual_artEXAFS ceria catalysis goldvisual_art.visual_art_mediumPhysical and Theoretical ChemistryThe Journal of Physical Chemistry C
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Molecular dynamics simulations of EXAFS in germanium

2011

AbstractClassical molecular dynamics simulations have been performed for crystalline germanium with the aim to estimate the thermal effects within the first three coordination shells and their influence on the single-scattering and multiple-scattering contributions to the Ge K-edge extended x-ray absorption fine structure (EXAFS).

Materials scienceExtended X-ray absorption fine structurePhysicsQC1-999exafsGeneral Physics and Astronomychemistry.chemical_elementGermaniumMolecular physicsmolecular dynamicsMolecular dynamicsgermaniumchemistryThermalmultiple-scatteringAbsorption (electromagnetic radiation)Open Physics
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Formation and Growth of Pd Nanoparticles Inside a Highly Cross-Linked Polystyrene Support: Role of the Reducing Agent

2014

Simultaneous time-resolved SAXS and XANES techniques were employed to follow in situ the formation of Pd nanoparticles in a porous polystyrene support, using palladium acetate as a precursor and gaseous H2 or CO as reducing agents. These results, in conjunction with data obtained by diffuse reflectance UV–vis and DRIFT spectroscopy and TEM measurements, allowed unraveling of the different roles played by gaseous H2 and CO in the formation of the Pd nanoparticles. In particular, it was found that the reducing agent affects (i) the reduction rate (which is faster in the presence of CO) and (ii) the properties of the hosted nanoparticles, in terms of size (bigger with CO), morphology (spherica…

Materials scienceExtended X-ray absorption fine structureReducing agentSmall-angle X-ray scatteringchemistry.chemical_elementNanoparticlePd nanoparticles; SAXS; EXAFSSAXSXANESSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographychemistry.chemical_compoundEXAFSGeneral EnergyPd nanoparticleschemistryChemical engineeringPalladium nanoparticles time-resolved X-ray Absorption Spectroscopy Small Angle X-ray Spectroscopy Transmission Electron MicroscopyDiffuse reflectionPolystyrenePhysical and Theoretical ChemistryPalladium
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Combined small-angle x-ray scattering/extended x-ray absorption fine structure study of coated Co nanoclusters in bis(2-ethylhexyl)sulfosuccinate

2009

Chemically stable cobalt nanostructures have been prepared with Co(II) reduction in the confined space of cobalt bis(2-ethylhexyl)sulfosuccinate, Co(AOT)2, reverse micelles dispersed in n-heptane. The reaction was carried out by adding a solution of sodium borohydride in ethanol (1% weight) to a 0.2M micellar solution of Co(AOT)2 in n-heptane at a reductant to Co(II) molar ratio of 4. This procedure involves the rapid formation of surfactant-coated Co nanoparticles followed by their slow separation as nanostructures embedded in a sodium bis(2-ethylhexyl)sulfosuccinate matrix. The resulting composites, characterized by extended x-ray absorption fine structure and small-angle x-ray scattering…

Materials scienceExtended X-ray absorption fine structureSmall-angle X-ray scatteringInorganic chemistryGeneral Physics and Astronomychemistry.chemical_elementNanoparticleMicelleNanoclustersSodium borohydridechemistry.chemical_compoundchemistrySAXS EXAFS micelle cobalt nanoparticleAbsorption (chemistry)CobaltNuclear chemistry
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Structure of the FeBTC Metal–Organic Framework: A Model Based on the Local Environment Study

2015

The local environment of iron in FeBTC, a metal organic framework commercially known as Basolite F300, is investigated combining XANES and EXAFS studies of the iron K-edge. The building block of the FeBTC can be described as an iron acetate moiety. Dehydration induces a change in the coordination of the first shell while preserving the network. We propose that the local structure around Fe atoms does not undergo a rearrangement, thus, leading to the formation of an open site. The analysis conveys that the FeBTC is a disordered network of locally ordered blocks.

Materials scienceExtended X-ray absorption fine structureStructure (category theory)Shell (structure)Block (periodic table)XANESMetal-Organic FrameworkXANESSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyEXAFSGeneral EnergyLocal environmentMoietyMetal-organic frameworkPhysical and Theoretical Chemistry
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Ab initio molecular dynamics simulations of negative thermal expansion in ScF3: the effect of the supercell size

2020

The authors sincerely thank S. Ali, A. Kalinko, and F. Rocca for providing experimental EXAFS data, as well as M. Isupova, V. Kashcheyevs, and A. I. Popov for stimulating discussions. Financial support provided by project No. 1.1.1.2/VIAA/l/16/147 (1.1.1.2/16/I/001) under the activity “Post-doctoral research aid” realized at the Institute of Solid State Physics, University of Latvia is greatly acknowledged by D.B. A.K and J.P. would like to thank the support of the Latvian Council of Science project No. lzp-2018/2–0353.

Materials scienceGeneral Computer ScienceGeneral Physics and AstronomyFOS: Physical sciences02 engineering and technologyCP2K010402 general chemistry01 natural sciencesMolecular physicsNegative thermal expansionchemistry.chemical_compoundLattice constantNegative thermal expansion:NATURAL SCIENCES:Physics [Research Subject Categories]General Materials ScienceScF3Condensed Matter - Materials ScienceExtended X-ray absorption fine structureAb initio molecular dynamicsMaterials Science (cond-mat.mtrl-sci)General ChemistryAtmospheric temperature range021001 nanoscience & nanotechnologyScandium fluoride0104 chemical sciencesEXAFSComputational MathematicsMolecular geometrychemistryMechanics of MaterialsSupercell (crystal)0210 nano-technologyCP2K
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Synchrotron Radiation and Chemistry: Studies of Materials for Renewable Energy Sources

2014

We present an overview of selected applications of synchrotron radiation methods to topical chemical research. The analysis is limited to the studies on materials for renewable energy sources, focussing on topics peculiar to chemical research, such as reactivity and synthesis routes; in particular, the paper takes into account subjects having some relevance for the production and storage of energy based on hydrogen. Hydrogen production and storage are taken into account in the sections concerning: (i) Dye-sensitized solar cells, (ii) Metal-organic frameworks and (iii) Hydrides for hydrogen storage; production of energy by fuel cell devices is treated in (iv) Oxide ion and proton conductors …

Materials scienceHydrogenbusiness.industrysynchrotron radiationXRDSynchrotron radiationchemistry.chemical_elementSAXSElectrochemistryXRPDEngineering physicsXANESRenewable energyCatalysishydrogen storagefuel cellHydrogen storageEXAFSchemistrydye-sensitized solar cellSR-XRDReactivity (chemistry)businessNuclear chemistryHydrogen production
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Dopants and defects: local structure and dynamics in barium cerates and zirconates

2010

In this paper we present an overview of state-of-the-art EXAFS measurements and data analysis on Ba, Ce, Zr, Y, In and Gd local environments in Y:BaCeO3, In:BaCeO3, Gd:BaCeO3, Y:BaZrO3, and In:BaZrO3, at different temperatures, hydration degrees and doping levels. This approach allows to reach unprecedented insights on the peculiar role of the dopant, and its interactions with the other lattice defects. In particular, we evidence that each different dopant shows unique behavior, depending mainly on its electronic structure, and that the usual criterion of ionic radius matching is not useful to outline an effective doping strategy of proton-conducting perovskites. As what concerns the struct…

Materials scienceIonic radiusExtended X-ray absorption fine structureDopantInorganic chemistryDopingEXAFS perovskite proton conductorGeneral ChemistryElectronic structureConductivityCondensed Matter PhysicsChemical physicsGeneral Materials ScienceProton conductorPerovskite (structure)EXAFS perovskite proton conductor barium zirconate barium cerate
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Evidence for a Double Doping Regime in Nd:YAG nanopowders

2009

Nanopowders of Yttrium Aluminium Garnet doped with neodymium (Nd:YAG) were investigated by X-Ray Absorption Fine Structure (XAFS) at the Nd LIII-edge in the 1.3 - 20.8 % doping range. XANES spectra appear similar in the full range of the Nd concentration. However, a significant decrease in the white line intensity of XANES is revealed as the quantity of Nd doping ions increases. Plotting the white line intensity as a function of Nd doping ions reveals two linear trends with two different slopes, identifying a threshold value where the neodymium concentration reaches 5 at.% This experimental finding provides support for the existence of a double doping regime in Nd:YAG nanopowders.

Materials scienceMechanical EngineeringDopingAnalytical chemistrychemistry.chemical_elementNeodymiumXANESXANESSpectral lineND:YAGIonX-ray absorption fine structureNANOPOWDERSEXAFSchemistry.chemical_compoundchemistryMechanics of MaterialsYttrium aluminium garnetGeneral Materials ScienceNd:YAG EXAFS XanesAbsorption (electromagnetic radiation)Settore CHIM/02 - Chimica Fisica
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High-temperature X-ray absorption spectroscopy study of thermochromic copper molybdate

2019

Financial support provided by Scientific Research Project for Students and Young Researchers Nr. SJZ/2017/5 and SJZ/2018/1 realized at the Institute of Solid State Physics, University of Latvia is greatly acknowledged. The work was also supported by philanthropist MikroTik and administrated by the University of Latvia Foundation . The experiment at the Elettra synchrotron was performed within the project No. 20150303 .

Materials sciencePolymers and PlasticsAbsorption spectroscopyAnalytical chemistrychemistry.chemical_element02 engineering and technologyMolybdate01 natural sciences7. Clean energychemistry.chemical_compound0103 physical sciences:NATURAL SCIENCES:Physics [Research Subject Categories]010302 applied physicsReverse Monte Carlo simulationsX-ray absorption spectroscopyThermochromismExtended X-ray absorption fine structureCuMoO4Metals and AlloysAtmospheric temperature range021001 nanoscience & nanotechnologyCopperXANESXANESElectronic Optical and Magnetic MaterialsEXAFSchemistryMolybdenumCeramics and Composites0210 nano-technologyActa Materialia
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