Search results for "Spectroscopy"

showing 10 items of 10293 documents

Microscopic origin of the charge transfer in single crystals based on thiophene derivatives: A combined NEXAFS and density functional theory approach

2016

We have investigated the charge transfer mechanism in single crystals of DTBDT-TCNQ and DTBDT-F4TCNQ (where DTBDT is dithieno[2,3-d;2',3'-d'] benzo[1,2-b;4,5-b']dithiophene) using a combination of near-edge X-ray absorption spectroscopy (NEXAFS) and density functional theory calculations (DFT) including final state effects beyond the sudden state approximation. In particular, we find that a description that considers the partial screening of the electron-hole Coulomb correlation on a static level as well as the rearrangement of electronic density shows excellent agreement with experiment and allows to uncover the details of the charge transfer mechanism in DTBDT-TCNQ and DTBDT-F4 TCNQ, as w…

Absorption spectroscopyExtended X-ray absorption fine structureChemistryAnalytical chemistryGeneral Physics and Astronomy02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesMolecular physicsXANES0103 physical sciencesAtomCoulombDensity functional theoryAtomic numberPhysical and Theoretical Chemistry010306 general physics0210 nano-technologyElectronic densityThe Journal of Chemical Physics
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Interpretation of the Ni K-edge EXAFS in nanocrystalline nickel oxide using molecular dynamics simulations

2011

Abstract Analysis of atomic structure at the nanoscale is a challenging task, complicated by relaxation phenomena and thermal disorder. In this work, the x-ray absorption spectroscopy at the Ni K-edge was used to address this problem in nanocrystalline NiO (nano-NiO) at 300 K. The analysis of the first two coordination shells using conventional two-shell single-scattering approximation allowed us to determine the expansion of the average lattice but contraction of the Ni―O bonds in the first coordination shell in nano-NiO in comparison with the bulk nickel oxide. The EXAFS signal generated within the first six coordination shells (up to ~ 6.5 A) was successfully interpreted using classical …

Absorption spectroscopyExtended X-ray absorption fine structureChemistryNickel oxideAb initioAnalytical chemistry02 engineering and technology021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesNanocrystalline materialElectronic Optical and Magnetic MaterialsCondensed Matter::Materials ScienceMolecular dynamicsK-edgeChemical physicsSurface-extended X-ray absorption fine structure0103 physical sciencesMaterials ChemistryCeramics and Compositesddc:660010306 general physics0210 nano-technology
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Probing NiO nanocrystals by EXAFS spectroscopy

2010

Abstract The structure relaxation in nanocrystalline NiO (nano-NiO, 13 nm crystallite size) has been studied by X-ray absorption spectroscopy at the Ni K-edge at 300 K. Conventional single-scattering analysis of the EXAFS signals from the first two coordination shells showed a lattice volume expansion by about 1% and a contraction of the Ni–O bonds by about 0.5% in nano-NiO compared to microcrystalline NiO. A more sophisticated approach, based on a combination of classical molecular dynamics and ab initio multiple-scattering EXAFS theory, allowed us to interpret both static relaxation and lattice dynamics in nano-NiO.

Absorption spectroscopyExtended X-ray absorption fine structureChemistryNon-blocking I/OAb initio02 engineering and technologyGeneral ChemistryCrystal structure021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesNanocrystalline materialCondensed Matter::Materials ScienceAb initio quantum chemistry methodsComputational chemistry0103 physical sciencesMaterials ChemistryPhysical chemistryCondensed Matter::Strongly Correlated ElectronsCrystallite010306 general physics0210 nano-technologySolid State Communications
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EXAFS and XRD study of Pd–Ag bimetallic catalysts supported on pumice from organometallic precursors

2001

Abstract Silver–palladium bimetallic catalysts were supported on pumice following different procedures, based on mild treatments of organometallic precursors. The experiments for the structural characterization of the synthesized samples, wide angle X-ray diffraction (XRD) and X-ray absorption spectroscopy, were carried out at the beamline GILDA of the European Synchrotron Radiation Facility. The analysis of the data demonstrated that alloying took place with a degree of homogeneity depending on the different preparation routes.

Absorption spectroscopyExtended X-ray absorption fine structureChemistrychemistry.chemical_elementCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsCatalysisCrystallographyTransition metalPumiceX-ray crystallographyMaterials ChemistryCeramics and CompositesBimetallic stripPalladiumNuclear chemistryJournal of Non-Crystalline Solids
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External pressure and composition effects on the atomic and electronic structure of SnWO4

2015

The atomic and electronic structure of tin tungstates, α-SnWO4, α-Sn1.03W0.99O4 and β-SnWO4 ,w as studied by the W L3-edge X-ray absorption spectroscopy and first-principles linear combination of atomic orbital (LCAO) calculations based on the hybrid exchange-correlation density functional (DFT)/ Hartree–Fock (HF) scheme. It was found that the crystal structure of both α-phases is built up of strongly distorted WO6 octahedra, whereas that of β-SnWO4 is composed of nearly regular WO4 tetrahedra. In addition, there are distorted SnO6 octahedra in both α- and β-phases. The metal–oxygen octahedra distortion is explained by the second-order Jahn–Teller effect. The influence of pressure on the st…

Absorption spectroscopyExtended X-ray absorption fine structureRenewable Energy Sustainability and the EnvironmentBand gapChemistryElectronic structureCrystal structureMolecular physicsSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyAtomic orbitalOctahedronLinear combination of atomic orbitalsddc:530
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Temperature and pH Dependence XAFS Study of Gd(DOTA)(-) and Gd(DTPA)(2)(-) Complexes: Solid State and Solution Structures.

1998

We present an X-ray absorption spectroscopy study of the local structures of Gd(DTPA)(2)(-) and Gd(DOTA)(-) complexes in the crystalline state (at room and low temperatures) and in aqueous solutions exhibiting various pH values (0.15-7) at different temperatures (25-90 degrees C). Using X-ray absorption fine structure (XAFS) analysis procedures and ab initio multiple scattering calculations of XAFS spectra at the Gd L(3) edge, we reconstructed the Gd(3+) local environment, and compared it with existing structural models. From neutral pH to a value of 1.5, we found that the local environment and complex dynamics around the gadolinium ions were conserved up to 4.5 Å, and the structure agreed …

Absorption spectroscopyGadoliniumAb initiochemistry.chemical_elementX-ray absorption fine structureInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryDOTAMoleculeCarboxylatePhysical and Theoretical ChemistryAbsorption (chemistry)Inorganic chemistry
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XAFS study of gadolinium and samarium bisporphyrinate complexes.

2001

The comparative X-ray absorption spectroscopy study of gadolinium and samarium bisporphyrinate complexes represented by the formulas Gd(III)H(oep)(tpp), Gd(III)(oep)(2), Gd(III)H(tpp)(2) and Sm(III)H(oep)(tpp), Sm(III)(oep)(2), Sm(III)H(tpp)(2) is reported. The XAFS spectra are recorded on the LURE-DCI storage ring (Orsay, France) in transmission mode on the microcrystalline samples at the Gd and Sm L(3) edges. The local environment for Ln(3+) ions has been reconstructed applying one-shell and two-shell XAFS analysis procedures. The protonated and nonprotonated bisporphyrinate complexes present different XAFS features. After our analysis on the title derivatives, the gadolinium ion (at 80 K…

Absorption spectroscopyGadoliniumInorganic chemistrychemistry.chemical_elementProtonationNitrogenSpectral lineIonX-ray absorption fine structureInorganic ChemistrySamariumCrystallographychemistryPhysical and Theoretical ChemistryInorganic chemistry
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Interaction of Cd(II) and Ni(II) terpyridine complexes with model polynucleotides: A multidisciplinary approach

2016

Two metal complexes of 2,2′:6′,2′′-terpyridine (terpy), i.e. Cd(terpy)Cl2 and Ni(terpy)Cl2·3H2O, have been prepared and extensively characterized. The interaction of Cd(terpy)Cl2 with synthetic DNA models, poly(dA-dT)·poly(dA-dT) (polyAT) and poly(dG-dC)·poly(dG-dC) (polyGC), has been studied by CD, fluorescence and UV-vis electronic absorption spectroscopy at several metal/polynucleotide–phosphate ratios and for different NaCl concentrations. All the experimental results indicate an intercalative mechanism of interaction. The optimized geometry of the cadmium complex intercalated between the sixth and seventh base pairs of (AT) and (GC) dodecanucleotide duplexes, obtained by quantum mechan…

Absorption spectroscopyGeneral Chemical EngineeringInorganic chemistryIntercalation (chemistry)chemistry.chemical_element010402 general chemistry01 natural sciencesMetalchemistry.chemical_compoundDNA-bindingChemical Engineering (all)SpectroscopyDNA-binding; circular-dichroism; chelate complexes010405 organic chemistryChemistry (all)chelate complexesGeneral Chemistry0104 chemical sciencesNickelCrystallographycircular-dichroismchemistryOctahedronPolynucleotideSettore CHIM/03 - Chimica Generale E Inorganicavisual_artvisual_art.visual_art_mediumTerpyridine
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Conformational Properties of Nickel(II) Octaethylporphyrin in Solution. 2. A Low-Temperature Optical Absorption Spectroscopy Study

1996

We have measured the absorption spectrum of Ni(II) octaethylporphyrin in CH2Cl2 and in a 50% v/v isopentane/ethyl ether mixture as a function of temperature between 150 and 300 K and 40 and 300 K, respectively. The Soret band can be decomposed into two subbands whose frequencies differ by 220 cm-1. By analogy with resonance Raman results (Jentzen et al. J. Phys. Chem. 1996, 100, 14184−14191 (preceding paper)), we attribute the low-frequency subband to a conformer with a nonplanar macrocycle structure, whereas the high-frequency subband is interpreted as resulting from a planar conformer. The subbands' intensity ratios exhibit a solvent-dependent van't Hoff behavior between 300 and 160 K. Cr…

Absorption spectroscopyGeneral EngineeringAnalytical chemistryResonancechemistry.chemical_elementEtherlaw.inventionsymbols.namesakeIsopentanechemistry.chemical_compoundNickelchemistrylawsymbolsPhysical and Theoretical ChemistryCrystallizationRaman spectroscopyConformational isomerismThe Journal of Physical Chemistry
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Double-Electron Excitations in L-edges X-ray-Absorption Spectra of W, Ir and Cs Oxide Compounds

1993

Very strong double-electron excitations have been observed for the first time in the W, Ir L 3-edge and Cs L 1,2,3-edges X-ray-absorption spectra of tungsten and iridium oxide thin films and cesium oxide containing glasses. They are expressed as peaks with a width of several electron-volts located at the absorption background above the edge. The positions of these features are in good agreement with atomic calculations in the Z+1 approximation. They can be attributed to the transitions 2p4d → 5d5d for the L 2,3-edges and 2s4d → 6p5d for the L 1-edge with the dipole selection rules for the angular and total angular momentum ΔL=±1, ΔJ=0,±1.

Absorption spectroscopyGeneral EngineeringOxideGeneral Physics and Astronomychemistry.chemical_elementElectronTungstenSpectral lineDipolechemistry.chemical_compoundchemistryTotal angular momentum quantum numberAtomic physicsAbsorption (electromagnetic radiation)Japanese Journal of Applied Physics
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