Search results for "Size consistency and size extensivity"

showing 5 items of 5 documents

Application of the open-shell size-consistent self-consistent singles and doubles configuration interaction method to multielectronic transitions in …

2000

The size-consistent self-consistent matrix dressing method has been applied on an open-shell single-configuration reference state. Once the reference state is converged, several low-lying roots can be obtained for the dressed configuration interaction (CI) matrices of appropriate symmetry. The CI matrices were built with a complete-active-space singles and doubles CI method in order to deal properly with multiconfiguration excited states. The vertical ionization and ionization–excitation transitions are obtained from the difference to the closed shell ground-state energy of the neutral molecule. The method has been applied to NH+3 and N+2 using atomic natural orbital basis sets and state-av…

ChemistryPhotoemission spectroscopyIonizationExcited stateMolecular orbitalPhysical and Theoretical ChemistryConfiguration interactionAtomic physicsSize consistency and size extensivityOpen shellSpectral lineTheoretical Chemistry Accounts: Theory, Computation, and Modeling (Theoretica Chimica Acta)
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Pilot applications of internally contracted multireference coupled cluster theory, and how to choose the cluster operator properly.

2011

The internally contracted multireference coupled cluster (icMRCC) method allows a highly accurate description of both static and dynamic correlation with a computational scaling similar to single reference coupled cluster theory. The authors show that the method can lose its orbital invariance and size consistency when no special care is taken in the elimination of redundant excitations. Using the BeH(2) model system, four schemes are compared which differ in their treatment of linear dependencies between excitations of different rank (such as between singles and doubles). While the energy curves agree within tens of μE(h) when truncating the cluster operator at double excitations (icMRCCSD…

Coupled clusterRank (linear algebra)ChemistryOperator (physics)Cluster (physics)General Physics and AstronomySpecial careStatistical physicsPhysical and Theoretical ChemistryAtomic physicsSize consistency and size extensivityLinear combinationEnergy (signal processing)The Journal of chemical physics
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Communication: Restoring full size extensivity in internally contracted multireference coupled cluster theory.

2012

The reason for the lack of size extensivity in the valence space in current implementations of internally contracted multireference coupled cluster theories is the procedure used to eliminate redundant components from the cluster operator. We present a simple way to restore full size extensivity by performing this critical step in a basis of excitation operators that are normal ordered with respect to the multiconfigurational reference function.

Operator (computer programming)Coupled clusterComputer scienceQuantum mechanicsGeneral Physics and AstronomyStatistical physicsPhysical and Theoretical ChemistryReference functionSize consistency and size extensivityWave functionThe Journal of chemical physics
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New quantum Monte Carlo formulation for modeling trans-polyacetylene properties: specific heat calculation

2004

Abstract In this paper we propose a new hybridization scheme for numerical simulation based on the determinantal quantum Monte Carlo and analytical model to treat the vibration mode of one-dimensional trans -polyacetylene chain. We use both of the extended Hubbard model (EHM) and Peierls–Hubbard model to compute the specific heat for different assumptions. For both the two models, our results indicate that the behavior of the specific heat is characterized by a maximum. We also introduce the effect of dimerization through Peierls–Hubbard model. In this case it is found that the specific heat magnitude is slightly more important when compared to specific heat value found with the EHM case. M…

Polymers and PlasticsComputer simulationHubbard modelChemistryQuantum Monte CarloOrganic ChemistryMonte Carlo methodSize consistency and size extensivityMaterials ChemistryCondensed Matter::Strongly Correlated ElectronsSolitonStatistical physicsGround stateQuantum fluctuationPolymer
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Reducing CAS-SDCI space. Using selected spaces in configuration interaction calculations in an efficient way

2002

A new method is presented, which allows an important reduction of the size of some Configuration Interaction (CI) matrices. Starting from a Complete Active Space (CAS), the numerous configurations that have a small weight in the CAS wave function are eliminated. When excited configurations (e.g., singly and doubly excited) are added to the reference space, the resulting MR-SDCI space is reduced in the same proportion as compared with the full CAS–SDCI. A set of active orbitals is chosen, but some selection of the most relevant excitations is performed because not all the possible excitations act as SDCI generators. Thanks to a new addressing technique, the computational time is drastically …

Reduction (complexity)Computational MathematicsExcited stateMultireference configuration interactionGeneral ChemistryComplete active spaceAtomic physicsConfiguration interactionSize consistency and size extensivitySpace (mathematics)Wave functionComputational physicsMathematicsJournal of Computational Chemistry
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