Search results for "Full configuration interaction"

showing 10 items of 25 documents

High excitations in coupled-cluster series: vibrational energy levels of ammonia

2004

The ammonia molecule containing large amplitude inversion motion is a revealing system in examining high-order correlation effects on potential energy surfaces. Correlation contributions to the equilibrium and saddle point geometries, inversion barrier height and vibrational energy levels, including inversion splittings, have been investigated. A six-dimensional Taylor-type series expansion of the Born–Oppenheimer potential energy surface, which is scaled to different levels of theory, is used to determine vibrational energy levels and inversion splittings variationally. The electronic energies are calculated by coupled-cluster methods, combining explicitly correlated R12 theory (which incl…

010304 chemical physicsElectronic correlationChemistryBiophysics010402 general chemistryCondensed Matter Physics01 natural sciencesPotential energyFull configuration interaction0104 chemical sciencesCoupled clusterSaddle point0103 physical sciencesPotential energy surfacePhysical and Theoretical ChemistryAtomic physicsWave functionSeries expansionMolecular BiologyMolecular Physics
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Full configuration interaction calculation of singlet excited states of Be3

2004

The full configuration interaction (FCI) study of the singlets vertical spectrum of the neutral beryllium trimer has been performed using atomic natural orbitals [3s2p1d] basis set. The FCI triangular equilibrium structure of the ground state has been used to calculate the FCI vertical excitation energies up to 4.8 eV. The FCI vertical ionization potential for the same geometry and basis set amounts to 7.6292 eV. The FCI dipole and quadrupole transition moments from the ground state are reported as well. The FCI electric quadrupole moment of the X (3)A(1) (') ground state has been also calculated with the same basis set (Theta(zz)=-2.6461 a.u., Theta(xx)=Theta(yy)=-1/2Theta(zz)). Twelve of …

Atomic clustersElectron correlationsIonisation potentialGeneral Physics and AstronomyFull configuration interactionBeryllium ; Configuration interactions ; Excited states ; Orbital calculations ; Ground states ; Ionisation potential ; Molecular configurations ; Transition moments ; Quadrupole moments ; Molecular moments ; Electron correlations ; Atomic clustersPhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]Basis setElectronic correlationChemistryConfiguration interactionsExcited statesPhysics::Physics EducationMolecular configurationsTransition momentsUNESCO::FÍSICA::Química físicaOrbital calculationsGround statesDipoleExcited stateQuadrupoleQuadrupole momentsMolecular momentsBerylliumAtomic physicsIonization energyGround stateThe Journal of Chemical Physics
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Equation-of-motion coupled-cluster methods for ionized states with an approximate treatment of triple excitations.

2005

The accuracy of geometries and harmonic vibrational frequencies is evaluated for two equation-of-motion ionization potential coupled-cluster methods including CC3 and CCSDT-3 triples corrections. The first two Sigma states and first Pi state of the N2 +, CO+, CN, and BO diatomic radicals are studied. The calculations show a tendency for the CC3 variant to overestimate the bond lengths and to underestimate the vibrational frequencies, while the CCSDT-3 variant seems to be more reliable. It is also demonstrated that the accuracy of such methods is comparable to sophisticated traditional multireference approaches and the full configuration interaction method.

Bond lengthCoupled clusterChemistryIonizationHarmonicGeneral Physics and AstronomyEquations of motionPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsIonization energyFull configuration interactionDiatomic moleculeThe Journal of chemical physics
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Generalized Many-Body Expanded Full Configuration Interaction Theory

2019

Facilitated by a rigorous partitioning of a molecular system's orbital basis into two fundamental subspaces - a reference and an expansion space, both with orbitals of unspecified occupancy - we generalize our recently introduced many-body expanded full configuration interaction (MBE-FCI) method to allow for electron-rich model and molecular systems dominated by both weak and strong correlation to be addressed. By employing minimal or even empty reference spaces, we show through calculations on the one-dimensional Hubbard model with up to 46 lattice sites, the chromium dimer, and the benzene molecule how near-exact results may be obtained in a entirely unbiased manner for chemical and physi…

Chemical Physics (physics.chem-ph)010304 chemical physicsBasis (linear algebra)Computer scienceFOS: Physical sciences010402 general chemistrySpace (mathematics)01 natural sciencesFull configuration interactionMany body0104 chemical sciencesTheoretical physicsAtomic orbitalPhysics - Chemical Physics0103 physical sciencesGeneral Materials ScienceAstrophysics::Earth and Planetary AstrophysicsPhysical and Theoretical Chemistry
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Many-Body Expanded Full Configuration Interaction. II. Strongly Correlated Regime

2019

In this second part of our series on the recently proposed many-body expanded full configuration interaction (MBE-FCI) method, we introduce the concept of multideterminantal expansion references. Through theoretical arguments and numerical validations, the use of this class of starting points is shown to result in a focussed compression of the MBE decomposition of the FCI energy, thus allowing chemical problems dominated by strong correlation to be addressed by the method. The general applicability and performance enhancements of MBE-FCI are verified for standard stress tests such as the bond dissociations in H$_2$O, N$_2$, C$_2$, and a linear H$_{10}$ chain. Furthermore, the benefits of em…

Chemical Physics (physics.chem-ph)010304 chemical physicsThe RenaissanceFOS: Physical sciences010402 general chemistry01 natural sciencesFull configuration interactionMany body0104 chemical sciencesComputer Science ApplicationsFormalism (philosophy of mathematics)Physics - Chemical Physics0103 physical sciencesStatistical physicsPhysical and Theoretical ChemistryGround state
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Virtual Orbital Many-Body Expansions: A Possible Route towards the Full Configuration Interaction Limit

2017

In the present letter, it is demonstrated how full configuration interaction (FCI) results in extended basis sets may be obtained to within sub-kJ/mol accuracy by decomposing the energy in terms of many-body expansions in the virtual orbitals of the molecular system at hand. This extension of the FCI application range lends itself to two unique features of the current approach, namely that the total energy calculation can be performed entirely within considerably reduced orbital subspaces and may be so by means of embarrassingly parallel programming. Facilitated by a rigorous and methodical screening protocol and further aided by expansion points different from the Hartree-Fock solution, al…

Chemical Physics (physics.chem-ph)Physics010304 chemical physicsBasis (linear algebra)Embarrassingly parallelFOS: Physical sciences010402 general chemistry01 natural sciencesFull configuration interactionLinear subspace0104 chemical sciencesRange (mathematics)Atomic orbitalComputational chemistryPhysics - Chemical Physics0103 physical sciencesGeneral Materials ScienceLimit (mathematics)Statistical physicsPhysical and Theoretical ChemistryEnergy (signal processing)
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Convergence of coupled cluster perturbation theory.

2016

The convergence of a recently proposed coupled cluster (CC) family of perturbation series [Eriksen, J. J. et al., J. Chem. Phys. 140, 064108 (2014)], in which the energetic difference between two CC models - a low-level parent and a high-level target model - is expanded in orders of the M{\o}ller-Plesset (MP) fluctuation potential, is investigated for four prototypical closed-shell systems (Ne, singlet methylene, distorted HF, and the fluoride anion) in standard and augmented basis sets. In these investigations, energy corrections of the various series have been calculated to high orders and their convergence radii determined by probing for possible front- and back-door intruder states, the…

Chemical Physics (physics.chem-ph)Physics010304 chemical physicsFOS: Physical sciencesGeneral Physics and AstronomyPerturbation (astronomy)010402 general chemistry01 natural sciencesFull configuration interaction0104 chemical sciencesIonCoupled clusterPhysics - Chemical Physics0103 physical sciencesSinglet stateStatistical physicsPhysical and Theoretical ChemistryThe Journal of chemical physics
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Incremental Treatments of the Full Configuration Interaction Problem

2020

The recent many-body expanded full configuration interaction (MBE-FCI) method is reviewed by critically assessing its advantages and drawbacks in the context of contemporary near-exact electronic structure theory. Besides providing a succinct summary of the history of MBE-FCI to date within a generalized and unified theoretical setting, its finer algorithmic details are discussed alongside our optimized computational implementation of the theory. A selected few of the most recent applications of MBE-FCI are revisited, before we close by outlining its future research directions as well as its place among modern near-exact wave function-based methods.

Chemical Physics (physics.chem-ph)Theoretical computer science010304 chemical physicsComputer scienceFOS: Physical sciencesContext (language use)010402 general chemistry01 natural sciencesBiochemistryFull configuration interaction0104 chemical sciencesComputer Science ApplicationsComputational MathematicsPhysics - Chemical Physics0103 physical sciencesMaterials ChemistryPhysical and Theoretical Chemistry
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Full configuration interaction calculation of BeH adiabatic states.

2008

An all-electron full configuration interaction (FCI) calculation of the adiabatic potential energy curves of some of the lower states of BeH molecule is presented. A moderately large ANO basis set of atomic natural orbitals (ANO) augmented with Rydberg functions has been used in order to describe the valence and Rydberg states and their interactions. The Rydberg set of ANOs has been placed on the Be at all bond distances. So, the basis set can be described as 4s3p2d1f3s2p1d(BeH)+4s4p2d(Be). The dipole moments of several states and transition dipole strengths from the ground state are also reported as a function of the R(Be-H) distance. The position and the number of states involved in sever…

ChemistryConfiguration interactionsGeneral Physics and AstronomyBond lengthsBeryllium compounds ; Bond lengths ; Configuration interactions ; Ground states ; Molecular moments ; Potential energy surfaces ; Rydberg states ; Vibrational statesRydberg statesPotential energyFull configuration interactionGround statesUNESCO::FÍSICA::Química físicaDipolesymbols.namesakeAtomic orbitalBeryllium compoundsPotential energy surfacesRydberg formulasymbolsMolecular momentsVibrational statesPhysical and Theoretical ChemistryAtomic physicsGround stateAdiabatic process:FÍSICA::Química física [UNESCO]Basis setThe Journal of chemical physics
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Multireference equation-of-motion coupled cluster theory.

2012

A generalization of the equation-of-motion coupled cluster theory is proposed, which is built upon a multireference parent state. This method is suitable for a number of electronic states of a system that can be described by similar active spaces, i.e., different linear combinations of the same set of active space determinants. One of the suitable states is chosen as the parent state and the dominant dynamical correlation is optimized for this state using an internally contracted multireference coupled cluster ansatz. The remaining correlation and orbital relaxation effects are obtained via an uncontracted diagonalization of the transformed Hamiltonian, Ĥ = e(-T) Ĥe(T), in a compact multire…

ChemistryGeneral Physics and AstronomyMultireference configuration interactionEquations of motionFull configuration interactionsymbols.namesakeCoupled clusterClassical mechanicsExcited statesymbolsPhysical and Theoretical ChemistryAtomic physicsHamiltonian (quantum mechanics)Linear combinationAnsatzThe Journal of chemical physics
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