Capturing Electron Correlation with Machine Learning through a Data-Driven CASPT2 Framework

Multireference perturbation theory methods, such as complete active space second-order perturbation theory (CASPT2), are often employed to recover the missing electron correlation from multiconfigurational zeroth-order wave functions. Here, we introduce the data-driven CASPT2 (DDCASPT2) method to capture dynamic electron correlation using features generated from lower-level electronic structure methods, such as Hartree-Fock and complete active space self-consistent field (CASSCF) theory. We examine the effects of system size, basis set size, and the number of two-electron excitations using a small, but diverse, set of molecules. We also provide insights into our physics-based feature set using SHapley Additive exPlanation (SHAP) analysis, a feature analysis method based on cooperative game theory. In this paper, we utilize these insights to introduce a DDCASPT2 method, which provides a machine-learning-based alternative to traditional single- and multistate CASPT2 for capturing dynamical electron correlation with near-CASPT2 quality accuracy.

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Publication Details

Journal
Journal of Chemical Theory and Computation
Published
2025-10-22
DOI
https://doi.org/10.1021/acs.jctc.5c01333
Citations
1
Primary Topic
Machine Learning in Materials Science
Type
article
Field-Weighted Citation Impact
0.52
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article

Capturing Electron Correlation with Machine Learning through a Data-Driven CASPT2 Framework

Grier M. Jones, Konstantinos D. Vogiatzis
1 citations
Journal of Chemical Theory and Computation
Machine Learning in Materials Science
0.52
article

Capturing Electron Correlation with Machine Learning through a Data-Driven CASPT2 Framework

Grier M. Jones, Konstantinos D. Vogiatzis
article en
1 citations

Abstract

Multireference perturbation theory methods, such as complete active space second-order perturbation theory (CASPT2), are often employed to recover the missing electron correlation from multiconfigurational zeroth-order wave functions. Here, we introduce the data-driven CASPT2 (DDCASPT2) method to capture dynamic electron correlation using features generated from lower-level electronic structure methods, such as Hartree-Fock and complete active space self-consistent field (CASSCF) theory. We examine the effects of system size, basis set size, and the number of two-electron excitations using a small, but diverse, set of molecules. We also provide insights into our physics-based feature set using SHapley Additive exPlanation (SHAP) analysis, a feature analysis method based on cooperative game theory. In this paper, we utilize these insights to introduce a DDCASPT2 method, which provides a machine-learning-based alternative to traditional single- and multistate CASPT2 for capturing dynamical electron correlation with near-CASPT2 quality accuracy.

Journal of Chemical Theory and ComputationVol. 21(21)
University of Toronto (CA), Dairy Farmers of Ontario (CA), University of Tennessee at Knoxville (US), Rogers (United States) (US)
Openalex Percentile: Top 31%
Machine Learning in Materials Science
0.52
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Capturing Electron Correlation with Machine Learning through a Data-Driven CASPT2 Framework — Grier M. Jones, Konstantinos D. Vogiatzis · Journal of Chemical Theory and Computation (2025) | TGRS Research Map | TGRS