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Updated: Jul 13, 2026

Computation of Atmospheric Concentrations of Molecular Clusters from ab initio Thermochemistry
Published on: April 8, 2020
Second- and third-order triples and quadruples corrections to coupled-cluster singles and doubles in the ground and
Toru Shiozaki1, Kimihiko Hirao, So Hirata
1Department of Applied Chemistry, Graduate School of Engineering, The University of Tokyo, Tokyo 113-8656, Japan.
Abstract:
Second- and third-order perturbation corrections to equation-of-motion coupled-cluster singles and doubles (EOM-CCSD) incorporating excited configurations in the space of triples [EOM-CCSD(2)T and (3)T] or in the space of triples and quadruples [EOM-CCSD(2)TQ] have been implemented. Their ground-state counterparts--third-order corrections to coupled-cluster singles and doubles (CCSD) in the space of triples [CCSD(3)T] or in the space of triples and quadruples [CCSD(3)TQ]--have also been implemented and assessed. It has been shown that a straightforward application of the Rayleigh-Schrodinger perturbation theory leads to perturbation corrections to total energies of excited states that lack the correct size dependence. Approximations have been introduced to the perturbation corrections to arrive at EOM-CCSD(2)T, (3)T, and (2)TQ that provide size-intensive excitation energies at a noniterative O(n(7)), O(n(8)), and O(n(9)) cost (n is the number of orbitals) and CCSD(3)T and (3)TQ size-extensive total energies at a noniterative O(n(8)) and O(n(10)) cost. All the implementations are parallel executable, applicable to open and closed shells, and take into account spin and real Abelian point-group symmetries. For excited states, they form a systematically more accurate series, CCSD
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