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 wavefunctions. Here, we introduce the data-driven CASPT2 (DDCASPT2) method to capture dynamical 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 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 multi-state CASPT2 for capturing dynamical electron correlation with near-CASPT2 quality accuracy.

Authors

Institutions

Publication Details

Journal
ChemRxiv
Published
2025-08-18
DOI
https://doi.org/10.26434/chemrxiv-2025-dl4sb
Primary Topic
Electron and X-Ray Spectroscopy Techniques
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

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

Grier M. Jones, Konstantinos D. Vogiatzis
ChemRxiv
Electron and X-Ray Spectroscopy Techniques
article

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

Grier M. Jones, Konstantinos D. Vogiatzis
article en

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 wavefunctions. Here, we introduce the data-driven CASPT2 (DDCASPT2) method to capture dynamical 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 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 multi-state CASPT2 for capturing dynamical electron correlation with near-CASPT2 quality accuracy.

ChemRxiv
University of Toronto (CA), University of Tennessee at Knoxville (US)
National Science Foundation, Division of Chemistry
Openalex Percentile: Top 80%
Electron and X-Ray Spectroscopy Techniques
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Capturing Electron Correlation with Machine Learning through a Data-Driven CASPT2 Framework — Grier M. Jones, Konstantinos D. Vogiatzis · ChemRxiv (2025) | TGRS Research Map | TGRS