Benchmarking third-order cluster perturbation theory for electronically excited states

In this study, we investigate the reliability of cluster perturbation (CP) theory applied to the calculation of electronically excited states through a comprehensive benchmark. In CP theory, perturbative corrections are added to the properties of a parent excitation space, which converge toward the properties of a target excitation space. For the CPS(D-n) model, perturbative corrections through order n are added to the coupled cluster singles (CCS) excitation energies to target the coupled cluster singles and doubles (CCSD) excitation energies. Through a comparative analysis of excitation energy calculations across a diverse set of molecules and wavefunction methods, we present a comprehensive evaluation of the accuracy of the third-order CPS(D) model, CPS(D-3), in calculating excitation energies. Our findings demonstrate that CPS(D-3) is a reliable alternative to established methods, particularly CCSD, while systematically overestimating the excitation energies compared to high-level coupled cluster methods such as CC3. These results highlight the strengths and limitations of CPS(D-3), as well as the promising directions for its future development.

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Publication Details

Journal
The Journal of Chemical Physics
Published
2025-03-05
DOI
https://doi.org/10.1063/5.0253976
Primary Topic
Advanced Chemical Physics Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Benchmarking third-order cluster perturbation theory for electronically excited states

Magnus Bukhave Johansen, Héctor H. Corzo, Andreas Erbs Hillers‐Bendtsen, Kurt V. Mikkelsen et al.
The Journal of Chemical Physics
Advanced Chemical Physics Studies
article

Benchmarking third-order cluster perturbation theory for electronically excited states

Magnus Bukhave Johansen, Héctor H. Corzo, Andreas Erbs Hillers‐Bendtsen, Kurt V. Mikkelsen, Dmytro Bykov
article en

Abstract

In this study, we investigate the reliability of cluster perturbation (CP) theory applied to the calculation of electronically excited states through a comprehensive benchmark. In CP theory, perturbative corrections are added to the properties of a parent excitation space, which converge toward the properties of a target excitation space. For the CPS(D-n) model, perturbative corrections through order n are added to the coupled cluster singles (CCS) excitation energies to target the coupled cluster singles and doubles (CCSD) excitation energies. Through a comparative analysis of excitation energy calculations across a diverse set of molecules and wavefunction methods, we present a comprehensive evaluation of the accuracy of the third-order CPS(D) model, CPS(D-3), in calculating excitation energies. Our findings demonstrate that CPS(D-3) is a reliable alternative to established methods, particularly CCSD, while systematically overestimating the excitation energies compared to high-level coupled cluster methods such as CC3. These results highlight the strengths and limitations of CPS(D-3), as well as the promising directions for its future development.

The Journal of Chemical PhysicsVol. 162(9)
University of Copenhagen (DK), Oak Ridge National Laboratory (US), Pulse Biosciences (United States) (US), Stanford University (US)
U.S. Department of Energy, European Commission, Danmarks Frie Forskningsfond, Office of Science, Danish Agency for Science and Higher Education, Oak Ridge National Laboratory
Affordable and clean energy
Openalex Percentile: Top 97%
Advanced Chemical Physics Studies
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