Search results for " Quantum chemistry"

showing 10 items of 549 documents

Ab initio calculations of the Ni K ‐edge XANES in Ni c Mg 1‐c O solid solutions

2005

An interpretation of the Ni K-edge X-ray absorption near edge structure (XANES) in pure NiO and NicMg1-cO solid solutions is given based on three types of ab initio theoretical calculations: the full-multiple-scattering (FMS) approach, the finite difference method (FDM) and the full potential linear muffin-tin orbital (FP-LMTO) method within the LSDA+U approach. The first two methods differ in the cluster potential approximation: the spherically symmetric muffin-tin potential is used in the FMS approach, whereas a non-muffin-tin numerical potential makes the core of the FDM. We found that the FMS and FDM techniques allow rather accurate description of the experimental XANES signal especiall…

CrystallographyAbsorption edgeK-edgeAb initio quantum chemistry methodsChemistryAb initioCluster (physics)Absorption (electromagnetic radiation)Molecular physicsXANESSolid solutionphysica status solidi (c)
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Hybrid functional calculations on the Na and K impurities in substitutional and interstitial positions in Cu2ZnSnSe4

2015

We studied the energetics, atomic and electronic structure of Na and K extrinsic defects in Cu2ZnSnSe4 by ab initio calculations using the HSE06 hybrid functional. Our results show that (i) among all substitutional positions, the Cu-site is the most favorable position for both Na and K. (ii) The tetrahedrally coordinated interstitial site has a lower formation energy than the octahedrally coordinated interstitial site. (iii) Based on the band structure calculations we can conclude, Se-related defects lead to the formation of defect states within the band gap.

CrystallographyChemistryImpurityAb initio quantum chemistry methodsBand gapInorganic chemistryElectronic structureElectronic band structureHybrid functional2015 IEEE 42nd Photovoltaic Specialist Conference (PVSC)
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Ab Initio Studies of Disilazanes:  Structures and Vibrational Properties of Hexachloro-, Hexamethyl-, and Tetrachlorodisilazane

1999

The structures of hexachlorodisilazane, NH(SiCl3)2, and hexamethyldisilazane, NH(SiMe3)2, have been calculated at HF/6-31G* and MP2/6-31G* levels. Both contain planar HNSi2 skeletons and show the expected staggering of the substituents as seen along the Si‚‚‚Si direction, as previously found in the electron diffraction structure of the hexamethyl compound. Unlike the latter, however, the ab initio structures both belong to the C2 point group. Force fields for these two molecules and for tetrachlorodisilazane, NH(SiHCl 2)2, were calculated at the HF level and scaled to produce vibration frequencies for comparison with previously obtained spectra. For NH(SiCl3)2, all but five of the fundament…

CrystallographyElectron diffractionComputational chemistryBond strengthChemistryAb initio quantum chemistry methodsAb initioMoleculePhysical and Theoretical ChemistryInductive effectConformational isomerismSpectral lineThe Journal of Physical Chemistry A
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Ab initio calculation of wurtzite‐type GaN nanowires

2007

Ab initio calculations of wurtzite-type GaN nanowires have been performed using density functional theory. Different shapes of nanowires of with similar diameters of around 2 nm have been considered to determine the stability of the structures. The quantitative similarities in the local properties obtained and dangling bond energies of nanowires and bulk surfaces have lead to a simple model model for a calculation of effective Young's modulus of nanowires of arbitrary diameters and shapes. The size dependence of the Young's modulus reveals a softening of GaN nanowires with the decrease of the diameter. (© 2007 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim)

CrystallographyMaterials scienceCondensed matter physicsAb initio quantum chemistry methodsNanowireAb initioDangling bondModulusDensity functional theoryCondensed Matter PhysicsSofteningWurtzite crystal structurephysica status solidi c
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Spectroscopic Investigation of the System TeCl4/[NEt4]PF6 in Solution and the Crystal Structure of [NEt4]2[Te2Cl10].

2005

Solutions containing TeCl 4 and [NEt 4 ][PF 6 ] in CH 2 Cl 2 were investigated by means of UV/vis and NMR spectroscopy in order to study the complex chemistry of TeCl 4 with the [PF 6 ] - anion. The results show formation of [TeCl 5 ] - and strong interactions of [PF 6 ] - with a tellurium containing species, presumably [TeCl 3 ] + . The life time of the Te I V -PF 6 complex is long enough to give different signals in the 1 9 F NMR spectrum of a solution containing excess [PF 6 ] - . Even a fivefold excess of Cl - ions over [PF 6 ] - does hardly lead to a dissociation of [TeCl 3 ...PF 6 ]. Crystals of [NEt 4 ] 2 [Te 2 Cl 1 0 ] were obtained from a 4:1 solution of [NEt 4 ]PF 6 and TeCl 4 in …

CrystallographyStereochemistryChemistryAb initio quantum chemistry methodsHalogenchemistry.chemical_elementGeneral MedicineNuclear magnetic resonance spectroscopyCrystal structureTriclinic crystal systemTelluriumDissociation (chemistry)IonChemInform
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A 'Butterfly'-shaped Water Tetramer in a Cu4 Complex Supported by a Hydrazone Ligand: Synthesis, Crystal Structure, Magnetic Properties, and Quantum …

2009

A potentially tetradentate NOOO donor hydrazone ligand, LH2 (condensation product of benzhydrazide with O-vanillin) generates a tetranuclear CuII complex [Cu4(L)4]·4H2O (1), whose void spaces are occupied by water tetramers presenting a ‘butterfly’ conformation with the highest dihedral angle reported to date, as revealed by its X-ray crystal structure. 1 has also been characterized using various spectroscopic techniques, including IR, UV-vis, and elemental analysis. Variable temperature magnetic susceptibility measurements reveal the presence of moderate antiferromagnetic intra-tetramer coupling between the four CuII centres connected through simple oxo groups of the hydrazone ligand with…

CrystallographyTetramerChemistryAb initio quantum chemistry methodsSupramolecular chemistryPhysical chemistryDensity functional theoryGeneral ChemistryCrystal structureDihedral angleMagnetic susceptibilityQuantum chemistryAustralian Journal of Chemistry
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Fast vibrational configuration interaction using generalized curvilinear coordinates and self-consistent basis

2010

In this paper, we couple a numerical kinetic-energy operator approach to the direct-vibrational self-consistent field (VSCF)/vibrational configuration interaction (VCI) method for the calculation of vibrational anharmonic frequencies. By combining this with fast-VSCF, an efficient direct evaluation of the ab initio potential-energy surface (PES), we introduce a general formalism for the computation of vibrational bound states of molecular systems exhibiting large-amplitude motion such as methyl-group torsion. We validate our approach on an analytical two-dimensional model and apply it to the methanol molecule. We show that curvilinear coordinates lead to a significant improvement in the VSC…

Curvilinear coordinatesClassical mechanicsAb initio quantum chemistry methodsChemistryComputationAnharmonicityBound stateAb initioGeneral Physics and AstronomyTorsion (mechanics)Physics::Chemical PhysicsPhysical and Theoretical ChemistryConfiguration interactionThe Journal of Chemical Physics
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Ab initio determination of the ionization potentials of DNA and RNA nucleobases

2006

Quantum chemical high level ab initio coupled-cluster and multiconfigurational perturbation methods have been used to compute vertical and adiabatic ionization potentials of the five canonical DNA and RNA nucleobases: uracil, thymine, cytosine, adenine, and guanine. Several states of their cations have been also calculated. The present results represent a systematic compendium of these magnitudes, establishing theoretical reference values at a level not reported before, calibrating computational strategies, and guiding the assignment of the features in the experimental photoelectron spectra. Daniel.Roca@uv.es Mercedes.Rubio@uv.es Manuela.Merchan@uv.es Luis.Serrano@uv.es

DNA ; Macromolecules ; Ionisation potential ; Photoelectron spectra ; Molecular biophysics ; Ab initio calculations ; Coupled cluster calculations ; Perturbation theoryGuanineGuaninePhotochemistryAb initioBiophysicsGeneral Physics and AstronomyIonisation potentialPerturbation theoryNucleobasechemistry.chemical_compoundCytosinePhotoelectron spectraCoupled cluster calculationsAb initio quantum chemistry methodsComputational chemistryIonizationPhysics::Atomic and Molecular ClustersPhysical and Theoretical ChemistryUracil:FÍSICA::Química física [UNESCO]IonsPhysics::Biological PhysicsQuantitative Biology::BiomoleculesBase CompositionChemistry PhysicalAdenineUracilDNAMolecular biophysicsQuantitative Biology::GenomicsThymineUNESCO::FÍSICA::Química físicachemistryMacromoleculesCalibrationQuantum TheoryRNAAb initio calculationsCytosineSoftwareThymine
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Pressure-induced phase transformation in zircon-type orthovanadate SmVO4from experiment and theory

2016

The compression behavior of zircon-type samarium orthovanadate, SmVO4, has been investigated using synchrotron-based powder x-ray diffraction and ab-initio calculations up to 21 GPa. The results indicate the instability of ambient zircon phase at around 6 GPa, which transforms to a high-density scheelite-type phase. The high-pressure phase remains stable up to 21 GPa, the highest pressure reached in the present investigations. On pressure release, the scheelite phase is recovered. Crystal structure of high-pressure phase and equations of state (EOS) for the zircon- and scheelite-type phases have been determined. Various compressibilities such as bulk, axial and bond, estimated from the expe…

Diffraction86Materials scienceFOS: Physical scienceschemistry.chemical_elementThermodynamics02 engineering and technologyCrystal structure01 natural sciencesInstabilityPhysics::GeophysicsCondensed Matter::Materials Sciencechemistry.chemical_compoundAb initio quantum chemistry methodsPhase (matter)0103 physical sciencesGeneral Materials Science010306 general physicsCondensed Matter - Materials ScienceMaterials Science (cond-mat.mtrl-sci)021001 nanoscience & nanotechnologyCondensed Matter PhysicsSamariumchemistryScheelite0210 nano-technologyZirconJournal of Physics: Condensed Matter
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Electronic structure and transport properties of the Heusler compound Co2TiAl

2009

The properties of the Heusler compound Co2TiAl were investigated in detail by experimental techniques and theoretical methods. X-ray diffraction measurements indicate that as-cast samples of the compound exhibit the L21 structure with a small amount of B2-type disorder. This leads to a reduced saturation magnetization per formula unit of 0.747 μB. The Curie temperature is approximately 120 K. The transport properties are influenced by the change in the electronic structure at the Curie temperature, as revealed experimentally by conductivity, thermal transport and specific heat measurements. Different theoretical models based on ab initio calculations of the electronic structure are used to …

DiffractionAcoustics and UltrasonicsCondensed matter physicsChemistryElectronic structureengineering.materialConductivityCondensed Matter PhysicsHeusler compoundSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsThermal transportAb initio quantum chemistry methodsFormula unitengineeringCurie temperatureJournal of Physics D: Applied Physics
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