Search results for "ELECTRONIC.STRUCTURE"

showing 10 items of 734 documents

EXAFS and XANES Studies of CoxMg1−xO Solid Solutions Using a Laboratory EXAFS Spectrometer

1993

Studies of the local electronic structure and the short-range order in solid solutions CoxMg1−xO with x varying from 0.02 to 1.00 are carried out on the CoK-edge X-ray absorption spectra using a laboratory EXAFS spectrometer. A non-monotonous change of the CoO distance in the first coordination shell with a bent at about x = 0.5 is established. The second coordination shell of cobalt is formed by cobalt and magnesium atoms with a distribution close to a statistical one. [Russian Text Ignored.]

Absorption spectroscopySpectrometerExtended X-ray absorption fine structureInorganic chemistryAnalytical chemistrychemistry.chemical_elementElectronic structureCondensed Matter PhysicsXANESElectronic Optical and Magnetic MaterialsBond lengthchemistryCobaltSolid solutionPhysica Status Solidi (a)
researchProduct

Optical absorption of divalent metal tungstates: Correlation between the band-gap energy and the cation ionic radius

2008

We have carried out optical-absorption and reflectance measurements at room temperature in single crystals of AWO4 tungstates (A = Ba, Ca, Cd, Cu, Pb, Sr, and Zn). From the experimental results their band-gap energy has been determined to be 5.26 eV (BaWO4), 5.08 eV (SrWO4), 4.94 eV (CaWO4), 4.15 eV (CdWO4), 3.9-4.4 eV (ZnWO4), 3.8-4.2 eV (PbWO4), and 2.3 eV (CuWO4). The results are discussed in terms of the electronic structure of the studied tungstates. It has been found that those compounds where only the s electron states of the A2+ cation hybridize with the O 2p and W 5d states (e.g BaWO4) have larger band-gap energies than those where also p, d, and f states of the A2+ cation contribu…

Accelerator Physics (physics.acc-ph)Condensed Matter - Materials ScienceMaterials scienceIonic radiusBand gapAnalytical chemistryMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesGeneral Physics and AstronomyElectronic structureElectronReflectivityDivalent metalValence bandPhysics - Accelerator PhysicsAbsorption (electromagnetic radiation)EPL (Europhysics Letters)
researchProduct

Electronic properties of Co2MnSi thin films studied by hard x-ray photoelectron spectroscopy

2009

This work reports on the electronic properties of thin films of the Heusler compound Co2MnSi studied by means of hard x-ray photoelectron spectroscopy (HAXPES). The results of photoelectron spectroscopy from multilayered thin films excited by photons of 2?8?keV are presented. The measurements were performed on (substrate/buffer layer/Co2MnSi(z)/capping layer) multilayers with a thickness z ranging from 0 to 50?nm. It is shown that high energy spectroscopy is a valuable tool for non-destructive depth profiling. The experimentally determined values of the inelastic electron mean free path in Co2MnSi increase from about 19.5 to 67?? on increasing the kinetic energy from about 1.9 to 6.8?keV. T…

Acoustics and UltrasonicsChemistryMean free pathAnalytical chemistryElectronic structureThermal treatmentengineering.materialCondensed Matter PhysicsHeusler compoundElectron spectroscopySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsX-ray photoelectron spectroscopyengineeringThin filmSpectroscopyJournal of Physics D: Applied Physics
researchProduct

Cu–Cu interactions in the transparent p-type conductors: CuAlO2 and SrCu2O2

2003

Abstract Electronic structures of the p-type Transparent Conducting Oxides (TCO): CuAlO2 and SrCu2O2 are calculated using the Tight Binding Linearized Muffin Tin Orbital within the Atomic Sphere Approximation method (TB-LMTO-ASA). The band structures indicate two gaps for CuAlO2 (an indirect one with ΔE≈0.45 eV and a direct one with ΔE≈1.25 eV) and one direct gap for SrCu2O2 (with ΔE≈2 eV). In both oxides the Cu states are dominant at the top of the valence band, close to the Fermi level and the existence of weak Cu–Cu bonding interactions is revealed through the Integrated Crystal Orbital Hamiltonian Population (ICOHP). The presence of such interactions suggests that for the hole doped oxi…

Aluminium oxideseducation.field_of_studyCondensed matter physicsChemistryFermi levelPopulationDopingchemistry.chemical_elementGeneral MedicineGeneral ChemistryElectronic structureCondensed Matter PhysicsMolecular physicsCrystalsymbols.namesakeTight bindingAtomic orbitalsymbolsGeneral Materials ScienceHamiltonian (quantum mechanics)TineducationElectronic band structureSolid State Sciences
researchProduct

TASCAを用いたCn, Nh, Fl化学実験のためのHg, Tl, PbのSiO2及びAu表面に対するオンライン化学吸着研究

2018

Online gas-solid adsorption studies with single atom quantities of Hg, Tl, and Pb on SiO$_{2}$ and Au surfaces were carried out using short-lived radioisotopes with half-lives in the range of 4-49 s. This is a model study to measure adsorption enthalpies of superheavy elements Cn, Nh, and Fl. The short-lived isotopes were produced and separated by the gas-filled recoil separator TASCA at GSI. The products were stopped in He gas, and flushed into gas chromatography columns made of Si detectors whose surfaces were covered by SiO$_{2}$ or Au. The short-lived Tl and Pb were successfully measured by the Si detectors with the SiO$_{2}$ surface at room temperature. On the other hand, the Hg did no…

Analytical chemistrychemistry.chemical_elementElectronic structure010402 general chemistry01 natural sciencesadsorption studiethermochromatographyHomologs of superheavy elementRELATIVISTIC PERIODIC DFTMetalGSIAdsorptionCHEMISTRY0103 physical sciencesisothermal chromatographyPhysical and Theoretical ChemistrySUPERHEAVY ELEMENTS010306 general physicsCoperniciumChemistryQUARTZ SURFACE0104 chemical sciencesgas phase chromatography of single atomHEAVIEST ELEMENTSFleroviumELECTRONIC-STRUCTUREvisual_artYield (chemistry)METALvisual_art.visual_art_mediumGas chromatographyRelativistic quantum chemistryphysical preseparationSYSTEMRadiochimica acta
researchProduct

Ab initiomodeling of sulphur doped TiO2nanotubular photocatalyst for water-splitting hydrogen generation

2012

In order to construct an efficient visible-light-driven TiO2 photocatalyst for water splitting applications, one has to perform improvements of its electronic structure. In this theoretical study we consider single-walled anatase TiO2 nanotubes having following morphologies: (101) 3-layered wall with chirality indexes (n,0) and (n,n), (101) 6-layered wall with (n,0) and (0,n), (001) 6-layered wall with (n,0) and (0,n), and (001) 9-layered wall with (n,0) and (0,n). The latter configuration occurs to be the most energetically stable, due to possessing negative strain energy. In our study the most stable 9-layered anatase (001) (0,n) nanotube has been doped with sulphur. According to obtained…

AnataseNanotubeMaterials scienceDopantDopingPhotocatalysisAb initioWater splittingPhysical chemistryNanotechnologyElectronic structureIOP Conference Series: Materials Science and Engineering
researchProduct

The Electronic Structure of Hexagonal BaCoO3

1999

Abstract TB–LMTO–ASA band structure calculations within the local spin density approximation have been performed to explain the magnetic and transport properties of BaCoO3. The calculations predict a magnetic and metallic ground state as energetically favored. BaCoO3 shows no long-range magnetic ordering, however, and only poor conductivity. The magnetic energy is low and the compound shows glassy susceptibility behavior at low temperatures. From the band structure we find Mott–Hubbard localization to be unlikely, and instead propose Anderson localization as a possible origin of the observed behavior. Calculations on slightly distorted structures exclude the possibility of a Peierls distort…

Anderson localizationMagnetic energyCondensed matter physicsChemistryElectronic structureCondensed Matter PhysicsElectron localization functionElectronic Optical and Magnetic MaterialsInorganic ChemistryTight bindingMaterials ChemistryCeramics and CompositesCondensed Matter::Strongly Correlated ElectronsPhysical and Theoretical ChemistryElectronic band structureGround stateAnderson impurity modelJournal of Solid State Chemistry
researchProduct

Ab initio quasi-relativistic calculations on angular momentum and magnetic couplings of molecular electronic states.

2002

Abstract We formulate an ab initio method of quasirelativistic calculations on angular momentum and magnetic transition matrix elements between adiabatic electronic states of molecules. Our approach is based on the construction of a state-selective effective Hamiltonian and transition density matrices by means of the multireference many-body perturbation theory. Pilot applications to the evaluation of B 0 + u → B ″1 u predissociation matrix elements in I 2 and interactions in the B 0 + u ∼ B 1 u complex of Te 2 are reported.

Angular momentumChemistryAb initioGeneral Physics and AstronomyElectronic structureDiatomic moleculesymbols.namesakeMatrix (mathematics)Ab initio quantum chemistry methodssymbolsPhysical and Theoretical ChemistryAtomic physicsHamiltonian (quantum mechanics)Adiabatic process
researchProduct

The Ã 1Au state and the T2 potential surface of acetylene: Implications for triplet perturbations in the fluorescence spectra of the à state

1996

The cis–trans isomerization reaction on the T2 surface of acetylene and the lowest excited singlet state of acetylene, A 1Au, are investigated by ab initio electronic structure theory. We report optimized geometries, dipole moments, and harmonic vibrational frequencies of stationary points and adiabatic energy differences between them using basis sets as large as triple‐ζ plus double polarization with higher angular momentum functions, TZ(2df,2pd), and theoretical methods up to coupled‐cluster singles and doubles with a perturbative triples correction [CCSD(T)] and the equation‐of‐motion coupled‐cluster method (EOM‐CCSD). Our theoretical predictions should aid the interpretation of observat…

Angular momentumZeeman effectChemistryAb initioGeneral Physics and AstronomyElectronic structureQuantum chemistryPotential energyDipolesymbols.namesakechemistry.chemical_compoundAcetylenePhysics::Atomic and Molecular ClusterssymbolsPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsThe Journal of Chemical Physics
researchProduct

A computational study of the lowest singlet and triplet states of neutral and dianionic 1,2-substituted icosahedral and octahedralo-carboranes

2006

This work introduces a calibrated B3LYP/6-31G(d) study on the electronic structure of singlet and triplet neutral species of 1,2-substituted icosahedral 1,2-R(2)-1,2-C(2)B(10)H(10) and octahedral 1,2-R(2)-1,2-C(2)B(4)H(4) molecules with R = {H, OH, SH, NH(2), PH(2), CH(3), SiH(3)} and their respective dianions formed by proton removal on each R group. A variety of small adiabatic singlet-triplet gaps DeltaE(ST) are obtained from these systems ranging from 2.93 eV (R = NH(2)) <or= DeltaE(ST) <or= 3.98 eV (R = SiH(3)) for the icosahedral neutrals and 1.56 eV (R = NH(2)) <or= DeltaE(ST) <or= 4.13 eV (R = SiH(3)) for the octahedral neutrals, these gaps being globally smaller for the dianionic s…

AnionsBoron CompoundsModels MolecularChemical PhenomenaProtonChemistry PhysicalChemistryIcosahedral symmetryMolecular ConformationGeneral ChemistryElectronic structureComputational MathematicsCrystallographyOctahedronComputational chemistryMoleculeComputer SimulationSinglet stateAlgorithmsJournal of Computational Chemistry
researchProduct