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Exact density functional and wave function embedding schemes based on orbital localization
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DOI：10.1063/1.4960177.png)
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摘要
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Exact schemes for the embedding of density functional theory (DFT) and wave function theory (WFT) methods into lower-level DFT or WFT approaches are introduced utilizing orbital localization. First, a simple modification of the projector-based embedding scheme of Manby and co-workers [J. Chem. Phys. 140, 18A507 (2014)] is proposed. We also use localized orbitals to partition the system, but instead of augmenting the Fock operator with a somewhat arbitrary level-shift projector we solve the Huzinaga-equation, which strictly enforces the Pauli exclusion principle. Second, the embedding of WFT methods in local correlation approaches is studied. Since the latter methods split up the system into local domains, very simple embedding theories can be defined if the domains of the active subsystem and the environment are treated at a different level. The considered embedding schemes are benchmarked for reaction energies and compared to quantum mechanics (QM)/molecular mechanics (MM) and vacuum embedding. We conclude that for DFT-in-DFT embedding, the Huzinaga-equation-based scheme is more efficient than the other approaches, but QM/MM or even simple vacuum embedding is still competitive in particular cases. Concerning the embedding of wave function methods, the clear winner is the embedding of WFT into low-level local correlation approaches, and WFT-in-DFT embedding can only be more advantageous if a non-hybrid density functional is employed. Published by AIP Publishing.
Keyword:
CORRELATED MOLECULAR CALCULATIONS
ELECTRON CORRELATION METHODS
LOCAL CORRELATION APPROACH
GAUSSIAN-BASIS SETS
COUPLED-CLUSTER
AB-INITIO
CORRELATION-ENERGY
PERTURBATION-THEORY
FROZEN ORBITALS
APPROXIMATION
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期刊
IF:
3.1
论文数:
7.2W
被引数:
23.2W
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