Search results for "Electronic structure"

showing 10 items of 722 documents

Modeling of Point Defects in Corundum Crystals

1994

Several different approaches including Hartree-Fock ab initio cluster calculations, semiempirical INDO calculations, and atom-atom potentials were used for modeling of the spatial and electronic structure as well as migration mechanisms of both intrinsic defects (self-trapped and defect-trapped holes, O and Al vacancies) and impurities (transition-metal ions like Co, Fe, Mg, Mn, Ti). The atomic structure of all hole centers is found to be similar to V[sub K] centers in alkali halides (two-site model); their formation is energetically favorable. The energy required for 60[degree] hole reorientations inside the basic oxygen triangles is found to be similar to both the energy for hops between …

Arrhenius equationMaterials scienceAb initioIonic bondingElectronic structureActivation energyMolecular physicsIonsymbols.namesakeAb initio quantum chemistry methodsVacancy defectPhysics::Atomic and Molecular ClustersMaterials ChemistryCeramics and CompositessymbolsPhysical chemistryJournal of the American Ceramic Society
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A theoreticalab initiostudy on the H2NO + O3reaction

2003

The deviation of the NH2 pseudo-first-order decay Arrhenius plots of the NH2 + O3 reaction at high ozone pressures measured by experimentalists, has been attributed to the regeneration of NH2 radicals due to the subsequent reactions of the products of this reaction with ozone. Although these products have not yet been characterized experimentally, the radical H2NO has been postulated, because it can regenerate NH2 radicals through the reactions: H2NO + O3 NH2 + O2 and H2NO + O3 HNO + OH + O2. With the purpose of providing a reasonable explanation from a theoretical point of view to the kinetic observed behaviour of the NH2 + O3 system, we have carried ab initio electronic structure calculat…

Arrhenius equationReaction mechanismChemistryRadicalAb initioGeneral ChemistryElectronic structureKinetic energyComputational Mathematicssymbols.namesakeAb initio quantum chemistry methodsComputational chemistryAtmospheric chemistrysymbolsJournal of Computational Chemistry
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Many-body perturbation theory calculations using the yambo code

2019

Abstract yambo is an open source project aimed at studying excited state properties of condensed matter systems from first principles using many-body methods. As input, yambo requires ground state electronic structure data as computed by density functional theory codes such as Quantum ESPRESSO and Abinit. yambo’s capabilities include the calculation of linear response quantities (both independent-particle and including electron–hole interactions), quasi-particle corrections based on the GW formalism, optical absorption, and other spectroscopic quantities. Here we describe recent developments ranging from the inclusion of important but oft-neglected physical effects such as electron–phonon i…

BETHE-SALPETER EQUATION02 engineering and technology01 natural sciencesSoftwarereal-time dynamicsGeneral Materials Sciencequasi-particleCondensed Matter - Materials Scienceparallelismelectron-phononreal-time dynamicComputational Physics (physics.comp-ph)021001 nanoscience & nanotechnologySupercomputerMANY-BODY PERTURBATION THEORYCondensed Matter Physicsbethe-salpeter-equationoptical-propertiesoptical propertietemperature-dependence[PHYS.COND.CM-MS]Physics [physics]/Condensed Matter [cond-mat]/Materials Science [cond-mat.mtrl-sci]User interface0210 nano-technologyGround statePhysics - Computational Physicsoptical propertiesmonte-carloMaterials scienceExploitFOS: Physical sciencesabinitSettore FIS/03 - Fisica della MateriaComputational scienceKerr effect0103 physical scienceskerr effect010306 general physicselectronic excitationsTHEORETICAL SPECTROSCOPYpolarizationspin and spinorsbusiness.industrysoftwareMaterials Science (cond-mat.mtrl-sci)Rangingelectronic structureABINITInterfacingelectron-phonon; electronic structure; Kerr effect; optical properties; parallelism; real-time dynamics; spin and spinorsbusinessabsorption
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Ab initio calculations of the atomic and electronic structure of BaZrO3 (111) surfaces

2013

Abstract The paper presents and discusses the results of calculations of surface relaxations and energetics for the polar (111) surface of BaZrO 3 using a hybrid B3LYP description of exchange and correlation. On the (111) surface, both Zr- and BaO 3 -terminations were analyzed. For both Zr and BaO 3 -terminated BaZrO 3 (111) surface upper layer atoms, with the sole exception of BaO 3 -terminated surface Ba atoms, relax inwards. The Zr-terminated BaZrO 3 (111) surface second layer Ba atoms exhibit the strongest relaxation between all Zr and BaO 3 -terminated BaZrO 3 (111) surface atoms. The calculated surface relaxation energy for Zr-terminated BaZrO 3 (111) surface is almost fifteen times l…

Band gapAb initio quantum chemistry methodsChemistryRelaxation (NMR)Ab initioGeneral Materials ScienceGeneral ChemistrySurface phononElectronic structureAtomic physicsCondensed Matter PhysicsSurface energySurface statesSolid State Ionics
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Comparative analysis of the electronic structures of mono- and bi-atomic chains of IV, III–V and II–VI group elements calculated using the DFT LCAO a…

2015

Using the first principle non-relativistic linear combination of atomic orbitals (LCAO) and relativistic linearized augmented cylindrical wave (LACW) methods, the band structure of the covalent and partially ionic ANB8−N single atom width chain is calculated. Both the LCAO and LACW methods show that the chains of C, Si, Ge, Sn, and Pb are metallic. However, there is a great difference between the relativistic and non-relativistic band structures. The π bands crossing the Fermi level are orbitally doubly degenerate in the non-relativistic model. The relativistic LACW calculations demonstrate that the spin and orbital motion of electrons are coupled, thereby splitting the π bands. The spin–or…

Band gapChemistryGeneral Chemical EngineeringFermi levelIonic bondingGeneral ChemistryElectronic structuresymbols.namesakeLinear combination of atomic orbitalsAtomsymbolsDensity of statesAtomic physicsElectronic band structureRSC Advances
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Electron delocalization in mixed-valence Keggin polyoxometalates. Ab initio calculation of the local effective transfer integrals and its consequence…

2002

We present a quantitative evaluation of the influence of the electron transfer on the magnetic properties of mixed-valence polyoxometalates reduced by two electrons. For that purpose, we extract from valence-spectroscopy ab initio calculations on embedded fragments the value of the transfer integrals between W nearest-neighbor atoms in a mixed-valence alphaPW(12)O(40) polyoxowolframate Keggin anion. In contradiction with what is usually assumed, we show that the electron transfer between edge-sharing and corner-sharing WO(6) octahedra have very close values. Considering fragments of various ranges, we analyze the accuracy of calculations on fragments based on only two WO(5) pyramids which s…

Band gapelectron delocalizationAb initioElectronic structureElectron010402 general chemistry01 natural sciencesBiochemistryMolecular physicsCatalysisIonElectron transferColloid and Surface ChemistryAb initio quantum chemistry methodsComputational chemistrypolyoxometalesmixed-valenceValence (chemistry)010405 organic chemistryChemistryGeneral MedicineGeneral ChemistryConfiguration interaction0104 chemical sciencesmagnetismDiamagnetism[PHYS.COND.CM-SCE]Physics [physics]/Condensed Matter [cond-mat]/Strongly Correlated Electrons [cond-mat.str-el]
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Ab Initio Study of BiFeO3: Thermodynamic Stability Conditions

2015

BiFeO3 is investigated intensively, mainly as a multiferroic material. In this paper, the state-of-the-art ab initio hybrid functional approach with atomic basis sets was employed for a study of the stability range of BiFeO3 with respect to its decomposition into binary oxides and elementary metals, as a function of temperature and oxygen partial pressure. The calculated atomic and electronic structure of BiFeO3 was compared with previous LDA+U calculations using plane-wave basis sets. Based on performed calculations, the phase diagram was constructed, which allows us to predict the stability region of stoichiometric BiFeO3.

Basis (linear algebra)ChemistryAb initioThermodynamicsNanotechnologyElectronic structureFunction (mathematics)7. Clean energyHybrid functionalCondensed Matter::Materials ScienceGeneral Materials ScienceChemical stabilityPhysical and Theoretical ChemistryStoichiometryPhase diagramThe Journal of Physical Chemistry Letters
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The accuracy of molecular dipole moments in standard electronic structure calculations

2000

Abstract A systematic investigation has been carried out of the accuracy of calculated molecular equilibrium dipole moments of 11 polar closed-shell molecules, using the HF, MP2, CCSD and CCSD(T) models and correlation-consistent basis sets. Augmented basis sets are important for improving the basis-set convergence, but the quality of the results depends more on the correlation treatment than on the cardinal number of the basis set. Augmented triple-zeta basis sets are sufficient for most calculations. The mean absolute error of the HF calculations is 0.16 D, which is reduced at the MP2 and CCSD levels to 0.048 and 0.025 D, respectively. The CCSD(T) errors are small – typically

Basis (linear algebra)ChemistryCardinal numberGeneral Physics and AstronomyElectronic structureComputational physicsDipoleQuality (physics)Convergence (routing)Physics::Atomic and Molecular ClustersPolarPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsBasis set
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Cation Environment in BaCeO3-Based Protonic Conductors: a Computational Study

2009

Geometry calculations were performed on pure BaCeO(3) fragments and on Y- and In-doped derivatives. HF and DFT approaches were used to investigate monoclinic and orthorhombic structures. The computational methods, structural models, and electronic structure investigation protocols were tuned taking into consideration and balancing the consistency of the results against the computational cost. The calculated structures and energetics parameter, as well as the detailed orbital analysis performed on the corresponding BaCeO(3) derivatives allowed us to explain experimental findings and to develop a procedure to study the cationic octahedral environment of doped X:BaCeO(3) (X = Y, In) and undope…

Basis (linear algebra)ChemistryDopingElectronic structureCondensed Matter::Materials ScienceOctahedronComputational chemistryChemical physicsOrthorhombic crystal systemperovskite computational chemistryPhysical and Theoretical ChemistryElectrical conductorOrbital analysisMonoclinic crystal system
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Q-Chem 2.0: a high-performanceab initio electronic structure program package

2000

ABSTRACT: Q-Chem 2.0 is a new release of an electronic structure programpackage, capable of performing first principles calculations on the ground andexcited states of molecules using both density functional theory and wavefunction-based methods. A review of the technical features contained withinQ-Chem 2.0 is presented. This article contains brief descriptive discussions of thekey physical features of all new algorithms and theoretical models, together withsample calculations that illustrate their performance. c 2000 John Wiley S electronic structure; density functional theory;computer program; computational chemistry Introduction A reader glancing casually at this article mightsuspect on t…

Basis (linear algebra)Computer programProgramming languageComputer sciencePrincipal (computer security)Theoretical modelsAb initioGeneral ChemistryElectronic structurecomputer.software_genreComputational scienceComputational MathematicsKey (cryptography)Density functional theorycomputerJournal of Computational Chemistry
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