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This paper presents a novel coupled cluster method designed specifically for multireference and open-shell quantum systems, addressing critical challenges in accurately modeling complex electronic structures. By restricting excitations to ensure commutativity among operators, the approach captures significantly more dynamical correlation than standard methods without similarity transformations. This advancement represents a substantive contribution to the theoretical foundations of computational chemistry and quantum simulation capabilities.
Coupled cluster theory for multireference and open-shell molecules
arXiv:2610.07440v1 Announce Type: cross Abstract: We introduce a simple coupled cluster approach for multireference and open-shell systems. In the restricted active space coupled cluster framework, the cluster operator only includes excitations from doubly occupied to virtual orbitals, and this ensures the individual operators commute among each other. The ground and excited states are obtained by diagonalisation of the coupled cluster similarity transformed Hamiltonian in a restricted active space. We demonstrate the framework for the RAS-CCSD model, where single and double excitations are included in the cluster operator, and likewise for a complete active space. We consider systems with multireference character and open-shell systems in a spin-adapted manner. The approach captures significantly more dynamical correlation than without the coupled cluster similarity transformation.
Abstract:We introduce a simple coupled cluster approach for multireference and open-shell systems. In the restricted active space coupled cluster framework, the cluster operator only includes excitations from doubly occupied to virtual orbitals, and this ensures the individual operators commute among each other. The ground and excited states are obtained by diagonalisation of the coupled cluster similarity transformed Hamiltonian in a restricted active space. We demonstrate the framework for the RAS-CCSD model, where single and double excitations are included in the cluster operator, and likewise for a complete active space. We consider systems with multireference character and open-shell systems in a spin-adapted manner. The approach captures significantly more dynamical correlation than without the coupled cluster similarity transformation.
Chemical Physics (physics.chem-ph); Quantum Physics (quant-ph)
arXiv:2610.07440 [physics.chem-ph]
(or arXiv:2610.07440v1 [physics.chem-ph] for this version)
https://doi.org/10.48550/arXiv.2610.07440 Focus to learn more arXiv-issued DOI via DataCite (pending registration)
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Full text under the publisher's open licence · 213 words
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