Explicitly correlated geminal-based perturbation theory

An explicitly correlated extension of a pair-function based perturbation theory is presented. The reference is obtained as the antisymmetrized product of strongly orthogonal geminals, termed Strictly Localized Geminals (SLG), which can capture static correlation at mean-field cost. Geminals entering SLG are spin unrestricted, in general, and are expanded in the one-electron basis of the natural orbitals of the unrestricted Hartree-Fock wavefunction. Dynamic correlation is accounted for by perturbation theory (PT) at second order via a Dyall-like Hamiltonian acting as the zero-order operator [Földvári et al., J. Chem. Phys. 150, 034103 (2019)]. Here, an explicitly correlated (F12) correction is added to SLGPT2 to improve the description of dynamic correlation and enhance convergence with respect to the basis size. The resulting SLGPT2-F12 scheme inherits the fragmented structure of the SLGPT2 method, facilitating an efficient solution scheme. For numerical illustration, the SLGPT2-F12 approach is applied to small diradical systems, mainly focusing on singlet-triplet splittings.

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Publication Details

Journal
The Journal of Chemical Physics
Published
2025-09-10
DOI
https://doi.org/10.1063/5.0283207
Primary Topic
Advanced Chemical Physics Studies
Type
article
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article

Explicitly correlated geminal-based perturbation theory

Jozef Noga, Zsuzsanna É. Mihálka
The Journal of Chemical Physics
Advanced Chemical Physics Studies
article

Explicitly correlated geminal-based perturbation theory

Jozef Noga, Zsuzsanna É. Mihálka
article en

Abstract

An explicitly correlated extension of a pair-function based perturbation theory is presented. The reference is obtained as the antisymmetrized product of strongly orthogonal geminals, termed Strictly Localized Geminals (SLG), which can capture static correlation at mean-field cost. Geminals entering SLG are spin unrestricted, in general, and are expanded in the one-electron basis of the natural orbitals of the unrestricted Hartree-Fock wavefunction. Dynamic correlation is accounted for by perturbation theory (PT) at second order via a Dyall-like Hamiltonian acting as the zero-order operator [Földvári et al., J. Chem. Phys. 150, 034103 (2019)]. Here, an explicitly correlated (F12) correction is added to SLGPT2 to improve the description of dynamic correlation and enhance convergence with respect to the basis size. The resulting SLGPT2-F12 scheme inherits the fragmented structure of the SLGPT2 method, facilitating an efficient solution scheme. For numerical illustration, the SLGPT2-F12 approach is applied to small diradical systems, mainly focusing on singlet-triplet splittings.

The Journal of Chemical PhysicsVol. 163(10)
Comenius University Bratislava (SK)
Openalex Percentile: Top 82%
Advanced Chemical Physics Studies
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