Search results for "Density Functional Theory"

showing 10 items of 981 documents

Accurate ab initio density fitting for multiconfigurational self-consistent field methods

2008

Using Cholesky decomposition and density fitting to approximate the electron repulsion integrals, an implementation of the complete active space self-consistent field (CASSCF) method suitable for large-scale applications is presented. Sample calculations on benzene, diaquo-tetra- μ -acetato-dicopper(II), and diuraniumendofullerene demonstrate that the Cholesky and density fitting approximations allow larger basis sets and larger systems to be treated at the CASSCF level of theory with controllable accuracy. While strict error control is an inherent property of the Cholesky approximation, errors arising from the density fitting approach are managed by using a recently proposed class of auxi…

PhysicsBasis (linear algebra)Field (physics)Ab initioGeneral Physics and AstronomyElectronUNESCO::FÍSICA::Química físicaPhysics and Astronomy (all)Ab initio quantum chemistry methodsComputational chemistryOrganic compoundsDensity functional theorySCF calculationsDensity functional theoryComplete active spaceStatistical physicsAb initio calculationsPhysical and Theoretical ChemistryAb initio calculations ; Density functional theory ; Organic compounds ; SCF calculations:FÍSICA::Química física [UNESCO]Cholesky decomposition
researchProduct

Towards a novel energy density functional for beyond-mean-field calculations with pairing and deformation

2018

We take an additional step towards the optimization of the novel finite-range pseudopotential at constrained Hartree-Fock-Bogolyubov level and implement an optimization procedure within an axial code using harmonic oscillator basis. We perform the optimization using three different numbers of the harmonic oscillator shells. We apply the new parameterizations in the O-Kr part of the nuclear chart and isotopic chain of Sn, and we compare the results with experimental values and those given by a parameterization obtained using a spherical code.

PhysicsBasis (linear algebra)Nuclear Theoryta114[PHYS.NUCL]Physics [physics]/Nuclear Theory [nucl-th]010308 nuclear & particles physicstiheysfunktionaaliteoriaNuclear TheoryFOS: Physical sciencesGeneral Physics and AstronomyDeformation (meteorology)114 Physical sciences01 natural sciencesNuclear Theory (nucl-th)PseudopotentialChain (algebraic topology)Mean field theorySpherical codenuclear physicsPairing0103 physical sciencesStatistical physicsydinfysiikkaHarmonic oscillatordensity functional theory
researchProduct

A comparison of density-functional-theory and coupled-cluster frequency-dependent polarizabilities and hyperpolarizabilities

2005

The frequency-dependent polarizabilities and hyperpolarizabilities of HF, CO, H2O and para-nitroaniline calculated by density-functional theory are compared with accurate coupled-cluster results. Whereas the local-density approximation and the generalized gradient approximation (BLYP) perform very similarly and overestimate polarizabilities and, in particular, the hyperpolarizabilities, hybrid density-functional theory (B3LYP) performs better and produces results similar to those obtained by coupled-cluster singles-and-doubles theory. Comparisons are also made for singlet excitation energies, calculated using linear response theory.

PhysicsBiophysicsHartree–Fock methodCondensed Matter PhysicsPara-nitroanilineMolecular physicsGeneralized gradientCoupled clusterQuantum mechanicsPhysics::Atomic and Molecular ClustersDensity functional theoryPhysics::Atomic PhysicsSinglet statePhysics::Chemical PhysicsPhysical and Theoretical ChemistryMolecular BiologyLinear response theoryExcitationMolecular Physics
researchProduct

Universal correction for the Becke-Johnson exchange potential

2010

The Becke-Johnson exchange potential [A. D. Becke and E. R. Johnson, J. Chem. Phys. 124, 221101 (2006)] has been successfully used in electronic structure calculations within density-functional theory. However, in its original form, the potential may dramatically fail in systems with non-Coulombic external potentials, or in the presence of external magnetic or electric fields. Here, we provide a system-independent correction to the Becke-Johnson approximation by (i) enforcing its gauge-invariance and (ii) making it exact for any single-electron system. The resulting approximation is then better designed to deal with current-carrying states and recovers the correct asymptotic behavior for sy…

PhysicsChemical Physics (physics.chem-ph)Condensed Matter - Materials ScienceHydrogenCondensed Matter - Mesoscale and Nanoscale PhysicsGeneral Physics and Astronomychemistry.chemical_elementMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesElectronElectronic structure//purl.org/becyt/ford/1.3 [https]DFTMagnetic field//purl.org/becyt/ford/1 [https]Chain (algebraic topology)chemistryElectric fieldQuantum electrodynamicsPhysics - Chemical PhysicsMesoscale and Nanoscale Physics (cond-mat.mes-hall)Density functional theoryBecke-Johnson exchange potentialPhysical and Theoretical Chemistry
researchProduct

Sodium atoms and clusters on graphite by density functional theory

2004

Sodium atoms and clusters $(Nl~5)$ on graphite (0001) are studied using density functional theory, pseudopotentials and periodic boundary conditions. A single Na atom is observed to bind at a hollow site 2.45 \AA{} above the surface with an adsorption energy of 0.51 eV. The small diffusion barrier of 0.06 eV indicates a flat potential energy surface. Increased Na coverage results in a weak adsorbate-substrate interaction, which is evident in the larger separation from the surface in the cases of ${\mathrm{Na}}_{3},$ ${\mathrm{Na}}_{4},$ ${\mathrm{Na}}_{5},$ and the $(2\ifmmode\times\else\texttimes\fi{}2)$ Na overlayer. The binding is weak for ${\mathrm{Na}}_{2},$ which has a full valence el…

PhysicsChemical bondPotential energy surfaceAtomPhysics::Atomic and Molecular ClustersCharge densityCharge (physics)Density functional theoryAtomic physicsCondensed Matter PhysicsValence electronOpen shellElectronic Optical and Magnetic MaterialsPhysical Review B
researchProduct

Molecular dynamics simulations of elementary chemical processes in liquid water using combined density functional and molecular mechanics potentials.…

1997

A new approach to carry out molecular dynamics simulations of chemical reactions in solution using combined density functional theory/molecular mechanics potentials is presented. We focus our attention on the analysis of reactive trajectories, dynamic solvent effects and transmission coefficient rather than on the evaluation of free energy which is another important topic that will be examined elsewhere. In a previous paper we have described the generalities of this hybrid molecular dynamics method and it has been employed to investigate low energy barrier proton transfer process in water. The study of processes with activation energies larger than a few kT requires the use of specific tech…

PhysicsChemical processReaction stepMolecular dynamics method ; Chemical reactions ; Solvent effects ; Density functional theory ; WaterWaterGeneral Physics and AstronomyMolecular dynamics methodContext (language use)UNESCO::FÍSICA::Química físicaMolecular dynamicsChemical physicsChemical reactionsQuantum mechanicsSolvent effectsDensity functional theoryDensity functional theoryTransmission coefficientPhysical and Theoretical ChemistrySolvent effects:FÍSICA::Química física [UNESCO]QuantumThe Journal of Chemical Physics
researchProduct

2021

Electronic circular dichroism (ECD) is a powerful spectroscopy method for investigating chiral properties at the molecular level. ECD calculations with the commonly used linear-response time-dependent density functional theory (LR-TDDFT) framework can be prohibitively costly for large systems. To alleviate this problem, we present here an ECD implementation within the projector augmented-wave method in a real-time-propagation TDDFT framework in the open-source GPAW code. Our implementation supports both local atomic basis sets and real-space finite-difference representations of wave functions. We benchmark our implementation against an existing LR-TDDFT implementation in GPAW for small chir…

PhysicsCircular dichroism010304 chemical physicsBasis (linear algebra)General Physics and AstronomyTime-dependent density functional theory010402 general chemistry01 natural sciences0104 chemical sciencesComputational physics0103 physical sciencesPhysics::Atomic and Molecular ClustersCluster (physics)Density functional theoryPhysical and Theoretical ChemistryWave functionSpectroscopyBasis setThe Journal of Chemical Physics
researchProduct

Theory of Current-Induced Angular Momentum Transfer Dynamics in Spin-Orbit Coupled Systems.

2020

Motivated by the importance of understanding competing mechanisms to current-induced spin-orbit torque in complex magnets, we develop a unified theory of current-induced spin-orbital coupled dynamics. The theory describes angular momentum transfer between different degrees of freedom in solids, e.g., the electron orbital and spin, the crystal lattice, and the magnetic order parameter. Based on the continuity equations for the spin and orbital angular momenta, we derive equations of motion that relate spin and orbital current fluxes and torques describing the transfer of angular momentum between different degrees of freedom. We then propose a classification scheme for the mechanisms of the c…

PhysicsCondensed Matter - Materials ScienceAngular momentumCondensed Matter - Mesoscale and Nanoscale PhysicsCondensed matter physicsEquations of motionMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesArticleMagnetizationFerromagnetismHall effectMesoscale and Nanoscale Physics (cond-mat.mes-hall)Spin Hall effectTorqueddc:530Density functional theoryAstrophysics::Earth and Planetary AstrophysicsPhysical review research
researchProduct

The quantum paraelectric phase of SrTiO$_3$ from first principles

2021

We demonstrate how the quantum paraelectric ground state of SrTiO$_3$ can be accessed via a microscopic $ab~initio$ approach based on density functional theory. At low temperature the quantum fluctuations are strong enough to stabilize the paraelectric phase even though a classical description would predict a ferroelectric phase. We find that accounting for quantum fluctuations of the lattice and for the strong coupling between the ferroelectric soft mode and lattice elongation is necessary to achieve quantitative agreement with experimental frequency of the ferroelectric soft mode. The temperature dependent properties in SrTiO$_3$ are also well captured by the present microscopic framework.

PhysicsCondensed Matter - Materials ScienceCondensed matter physicsAb initioLattice (group)Materials Science (cond-mat.mtrl-sci)FOS: Physical sciencesCavity material02 engineering and technologySoft modes021001 nanoscience & nanotechnology01 natural sciencesFerroelectricitySettore FIS/03 - Fisica Della MateriaCondensed Matter::Materials Science0103 physical sciencesDensity functional theory010306 general physics0210 nano-technologyGround stateQuantumQuantum fluctuation
researchProduct

Comparison of first-principles methods to extract magnetic parameters in ultra-thin films: Co/Pt(111)

2019

We compare three distinct computational approaches based on first-principles calculations within density functional theory to explore the magnetic exchange and the Dzyaloshinskii-Moriya interactions (DMI) of a Co monolayer on Pt(111), namely, (i) the method of infinitesimal rotations of magnetic moments based on the Korringa-Kohn-Rostoker (KKR) Green function method, (ii) the generalized Bloch theorem applied to spiraling magnetic structures and (iii) supercell calculations with noncollinear magnetic moments, the latter two being based on the full-potential linearized augmented plane wave (FLAPW) method. In particular, we show that the magnetic interaction parameters entering micromagnetic …

PhysicsCondensed Matter - Materials ScienceCondensed matter physicsMagnetic momentExchange interactionPlane waveMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciences02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesCondensed Matter::Materials ScienceFerromagnetism0103 physical sciencesCurie temperatureDensity functional theoryddc:530010306 general physics0210 nano-technologySpin-½Bloch wave
researchProduct