Universal Framework for Multiconfigurational DFT

Strong correlation remains a significant challenge for DFT with no satisfying solutions found yet within the standard Kohn-Sham framework. Instead, for decades, a number of different approaches have been suggested to combine the accuracy of multiconfigurational methods with the efficiency of DFT. In this article, we demonstrate that many of these methods are or would be significantly improved by being reformulated as variants of multiconfigurational pair-density functional theory (MC-PDFT). This work presents the first implementation of these methods within the recently proposed variational formulation of MC-PDFT. It also provides for the first time a systematic comparison of their accuracy across representative examples of strongly correlated systems. By analyzing their accuracy and formal properties, we provide design guidelines to inform the development of future functionals.

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Publication Details

Journal
Journal of Chemical Theory and Computation
Published
2025-03-07
DOI
https://doi.org/10.1021/acs.jctc.4c01687
Citations
3
Primary Topic
Semiconductor materials and devices
Type
article
Field-Weighted Citation Impact
2.19

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article

Universal Framework for Multiconfigurational DFT

Mickaël G. Delcey
3 citations
Journal of Chemical Theory and Computation
Semiconductor materials and devices
2.19
article

Universal Framework for Multiconfigurational DFT

Mickaël G. Delcey
article en
3 citations

Abstract

Strong correlation remains a significant challenge for DFT with no satisfying solutions found yet within the standard Kohn-Sham framework. Instead, for decades, a number of different approaches have been suggested to combine the accuracy of multiconfigurational methods with the efficiency of DFT. In this article, we demonstrate that many of these methods are or would be significantly improved by being reformulated as variants of multiconfigurational pair-density functional theory (MC-PDFT). This work presents the first implementation of these methods within the recently proposed variational formulation of MC-PDFT. It also provides for the first time a systematic comparison of their accuracy across representative examples of strongly correlated systems. By analyzing their accuracy and formal properties, we provide design guidelines to inform the development of future functionals.

Journal of Chemical Theory and ComputationVol. 21(6)
Lund University (SE), Computational Physics (United States) (US)
Vetenskapsrådet
Openalex Percentile: Top 13%
Semiconductor materials and devices
2.19
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