Search results for " Electronic Structure"

showing 10 items of 29 documents

Nuclear anapole moment interaction in BaF from relativistic coupled-cluster theory

2018

We present high accuracy relativistic coupled cluster calculations of the P-odd interaction coefficient $W_A$ describing the nuclear anapole moment effect on the molecular electronic structure. The molecule under study, BaF, is considered a promising candidate for the measurement of the nuclear anapole moment, and the preparation for the experiment is now underway [Altunas et al., Phys. Rev. Lett. 120, 142501 (2018)]. Influence of various computational parameters (size of the basis set, treatment of relativistic effects, and treatment of electron correlation) on the calculated $W_A$ coefficient is investigated and a recommended value of 147.7 Hz with an estimated uncertainty of 1.5% is prop…

ATOMIC PARITY NONCONSERVATIONDIATOMIC-MOLECULESP-ODDVIOLATIONAtomic Physics (physics.atom-ph)Nuclear TheoryDENSITY FUNCTIONALSFOS: Physical sciences01 natural sciences010305 fluids & plasmasPhysics - Atomic PhysicsENHANCEMENTMolecular electronic structure0103 physical sciencesIMPLEMENTATIONNuclear Experiment010306 general physicsBasis setPhysicsElectronic correlationELECTRIC-FIELD GRADIENTSDiatomic moleculeWEAK-INTERACTIONSCoupled clusterMoment (physics)Atomic physicsRelativistic quantum chemistryAPPROXIMATIONPhysical Review A
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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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General occurrence of polar twisted minima in the ionic singlet excited surfaces of polyenes

1982

Except for a few cases, the lowest closed shell SCF solutions for the twisted geometries of polyenes involves delocalized nonpolarized MO’s, and represents a meaningless mixture of radicalar gound state and ionic excited states. Higher (quasi) solutions allow a realistic approach of the polarized ionic states. Orthogonality to the radicalar ground state may be imposed without important loss of energy. Further extensive CI does not modify significantly the situation. These statements are illustrated through ab initio calculations of butadiene and hexatriene. This approach allows us to show that slight distortions stablize polar minima even in ’’homosymmetric’’ molecules such as all‐trans hex…

ChemistryUNESCO::FÍSICAGeneral Physics and AstronomyIonic bondingElectronic structurePolyenesExcited StatesSelf−Consistent FieldDelocalized electronElectronic StructureAb initio quantum chemistry methods:FÍSICA [UNESCO]Polyenes ; Self−Consistent Field ; Electronic Structure ; Excited StatesExcited statePhysics::Atomic and Molecular ClustersSinglet statePhysical and Theoretical ChemistryAtomic physicsPhysics::Chemical PhysicsGround stateOpen shell
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The integral‐direct coupled cluster singles and doubles model

1996

An efficient and highly vectorized implementation of the coupled cluster singles and doubles (CCSD) model using a direct atomic integral technique is presented. The minimal number of n6processes has been implemented for the most time consuming terms and point group symmetry is used to further reduce operation counts and memory requirements. The significantly increased application range of the CCSD method is illustrated with sample calculations on several systems with more than 500 basis functions. Furthermore, we present the basic trends of an open ended algorithm and discuss the use of integral prescreening. © 1996 American Institute of Physics.

Computer scienceClose Coupling ApproximationSymmetry GroupsGeneral Physics and AstronomyBasis functionSymmetry groupUNESCO::FÍSICA::Química físicaComputational scienceCluster ModelClose Coupling Approximation ; Algorithms ; Cluster Model ; Electronic Structure ; Molecular Orbital Method ; Symmetry GroupsPhysics and Astronomy (all)Range (mathematics)Coupled clusterElectronic StructureComputational chemistryCluster (physics)Molecular symmetryMolecular Orbital MethodPhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]Direct-coupled amplifierAlgorithmsThe Journal of Chemical Physics
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Pyrazolium- and 1,2-Cyclopentadiene-Based Ligands as σ-Donors: a Theoretical Study of Electronic Structure and Bonding

2012

A high-level theoretical investigation of 1,2-cyclopentadiene (4) was performed using density functional theory and wave function methods. The results reveal that, in contrast to earlier assumptions, the ground state of this ephemeral “allene” is carbene-like with a small diradical component. Furthermore, the electronic structure and chemistry of 4 are found to parallel that of 1,2,4,6-cycloheptatetraene: both molecules possess a low-lying excited singlet state with a closed-shell carbenic structure, enabling rich coordination chemistry. Energy decomposition analyses conducted for currently unknown metal complexes of 4 as well as those involving stable carbenes based on the pyrazolium frame…

CyclopentadieneChemistrysyklopentadieeniContrast (music)Electronic structurecyclopentadieneCombinatorial chemistryelektronirakenneInorganic Chemistrychemistry.chemical_compoundComputational chemistrymetal complexes electronic structureDensity functional theoryPhysical and Theoretical ChemistryWave functionta116metallikompleksitInorganic Chemistry
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Selected dissociation‐ and correlation‐consistent configuration interaction by a perturbative criterion

1990

We propose a perturbative criterion to select the most important dissociation‐ or correlation‐consistent type of contributions to perform generalized valence bond‐configuration interaction (GVB‐CI) calculations, dissociation‐consistent configuration interaction (DCCI) or correlation‐consistent configuration interaction (CCCI) approach, respectively. The procedure presented is computationally less demanding than the CCCI proposed by Goddard and co‐workers. To ensure the distance consistency of the MOs used, the nonvalence virtual orbitals are obtained by a projection technique. The results obtained for a few test calculations show the ability of the suggested approach to get close results to…

Diatomic MoleculesValence (chemistry)ChemistryConfiguration Interaction ; Electronic Structure ; Dissociation Energy ; Perturbation Theory ; Diatomic Molecules ; Polyatomic MoleculesGeneral Physics and AstronomyDissociation EnergyElectronic structureConfiguration interactionBond-dissociation energyDiatomic moleculeDissociation (chemistry)Polyatomic MoleculesUNESCO::FÍSICA::Química físicaConfiguration InteractionElectronic StructureAtomic orbitalComputational chemistryPerturbation TheoryPerturbation theory (quantum mechanics)Statistical physicsPhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]The Journal of Chemical Physics
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EPR on Radiation-Induced Defects in SiO2

2014

Continuous-wave electron paramagnetic resonance (EPR) spectroscopy has been the technique of choice for the studies of radiation-induced defects in silica (SiO2) for 60 years, and has recently been expanded to include more sophisticated techniques such as high-frequency EPR, pulse electron nuclear double resonance (ENDOR), and pulse electron spin echo envelope modulation (ESEEM) spectroscopy. Structural models of radiation-induced defects obtained from single-crystal EPR analyses of crystalline SiO2 (alfa-quartz) are often applicable to their respective analogues in amorphous silica (a-SiO2), although significant differences are common.

Electron nuclear double resonanceMaterials sciencePulse (signal processing)Settore FIS/01 - Fisica SperimentaleRadiation inducedOxygen vacancylaw.inventionNuclear magnetic resonancelawSingle-crystal and glass EPR multi-frequency EPR pulse ENDOR pulse ESEEM coordinate system oxygen vacancy silicon vacancy impurity defects electronic structures dynamic propertiesAmorphous silicaElectron paramagnetic resonanceSpectroscopyEnvelope (waves)
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Linear and nonlinear optical properties of a series of Ni-dithiolene derivatives

2009

Some linear and nonlinear optical (NLO) properties of Ni(SCH)4 and several of its derivatives have been computed by employing a series of basis sets and a hierarchy of methods (e.g., HF, DFT, coupled cluster, and multiconfigurational techniques). The electronic structure of Ni(SCH)4 has been also analyzed by using CASSCF/CASPT2, ab initio valence bond, and DFT methods. In particular we discuss how the diradicaloid character (DC) of Ni(SCH)4 significantly affects its NLO properties. The quasidegeneracy of the two lowest-energy singlet states 1 mathg and 1 math1u, the clear DC nature of the former, and the very large number of low-lying states enhance the NLO properties values. These particul…

Electronic structureNonlinear opticsSeries (mathematics)Optical propertiesChemistryAb initioGeneral Physics and AstronomyNonlinear opticsElectronic structureAb initio calculations ; Electronic structure ; Nonlinear optics ; Optical materials ; Optical properties ; Organic compounds ; VB calculationsUNESCO::FÍSICA::Química físicaCoupled clusterVB calculationsAb initio quantum chemistry methodsComputational chemistryOptical materialsOrganic compoundsPhysical chemistryValence bond theorySinglet stateAb initio calculationsPhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]
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The VN2 negatively charged defect in diamond. A quantum mechanical investigation of the EPR response

2020

Abstract The VN 2 − defect in diamond consists of a vacancy surrounded by two substitutional nitrogen atoms, which lower the local symmetry from Td to C2v. Calculations of the doublet ground state geometry, electronic structure, EPR parameters, and IR spectra of this defect are reported along with a preliminary investigation of the observed optical transition. For the most part our results were obtained using a uniform charge compensated supercell approach together with the B3LYP functional and all-electron Gaussian basis sets designed for the properties studied. In particular, the computed hyperfine and quadrupolar EPR parameters for the carbon and nitrogen atoms adjacent to the vacancy ag…

Electronic structuredefectMaterials scienceVNPhonon2002 engineering and technologyElectronic structureengineering.materialBand structure; Comparison simulation-experiment; Diamond; Electron paramagnetic resonance response; Electronic structure; IR spectrum; VN; 2; 0; defect; VN; 2; −; defect010402 general chemistry01 natural sciencesMolecular physicslaw.inventionlawSpin waveVacancy defectGeneral Materials ScienceIR spectrumElectron paramagnetic resonanceHyperfine structureDiamondBand structureGeneral ChemistryComparison simulation-experiment021001 nanoscience & nanotechnology0104 chemical sciencesengineeringDiamond0210 nano-technologyGround stateElectron paramagnetic resonance responseCarbon
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The composite operator method route to the 2D Hubbard model and the cuprates

2018

In this review paper, we illustrate a possible route to obtain a reliable solution of the 2D Hubbard model and an explanation for some of the unconventional behaviours of underdoped high-$T_\text{c}$ cuprate superconductors within the framework of the composite operator method. The latter is described exhaustively in its fundamental philosophy, various ingredients and robust machinery to clarify the reasons behind its successful applications to many diverse strongly correlated systems, controversial phenomenologies and puzzling materials.

Electronic structureСильно скорельованi системиHubbard modelPhysics and Astronomy (miscellaneous)Hubbard modelFOS: Physical sciencesЕлектронна структура01 natural sciencesComposite operatorПсевдощiлинаTheoretical physicsCondensed Matter - Strongly Correlated ElectronsCupratesCondensed Matter::Superconductivity0103 physical sciencesCuprateбагаточастинковi методи010306 general physicsStrongly correlated systemsКупрати010302 applied physicsPhysicsPseudogapCuprates; Electronic structure; Hubbard model; Many-body techniques; Pseudogap; Strongly correlated systems; багаточастинковi методи; Електронна структура; Купрати; Модель Хаббарда; Псевдощiлина; Сильно скорельованi системи;Strongly Correlated Electrons (cond-mat.str-el)Many-body techniquesCondensed Matter Physicslcsh:QC1-999Модель ХаббардаCondensed Matter::Strongly Correlated Electronslcsh:Physics
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