Extended Mixed-Reference Spin-Flip Time-Dependent Density Functional Theory for Charge-Transfer State

We propose a novel extended mixed-reference spin-flip time-dependent density functional theory (EMRSF-TDDFT). This approach extends MRSF-TDDFT by incorporating electronic configurations present in linear-response TDDFT but absent in conventional MRSF-TDDFT. The formulation is based on the connection between linear-response and MRSF time-dependent Hartree-Fock theories and is extended to TDDFT. Benchmark calculations for representative molecular systems show that the newly introduced configurations capture a major contribution to orbital relaxation effects. This stabilizes both ground and excited states described in the triplet-reference orbital basis and improves agreement with reference theoretical best estimates. We expect that the new EMRSF-TDDFT model is applicable to photochemical processes involving charge transfer.

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Publication Details

Journal
Journal of Chemical Theory and Computation
Published
2026-06-09
DOI
https://doi.org/10.1021/acs.jctc.6c00454
Primary Topic
Magnetism in coordination complexes
Type
article
Field-Weighted Citation Impact
0.00

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article

Extended Mixed-Reference Spin-Flip Time-Dependent Density Functional Theory for Charge-Transfer State

YounJoon Jung, Nakhyun Kim, Minseok Oh, Cheol Ho Choi et al.
Journal of Chemical Theory and Computation
Magnetism in coordination complexes
article

Extended Mixed-Reference Spin-Flip Time-Dependent Density Functional Theory for Charge-Transfer State

YounJoon Jung, Nakhyun Kim, Minseok Oh, Cheol Ho Choi, Seunghoon Lee
article en

Abstract

We propose a novel extended mixed-reference spin-flip time-dependent density functional theory (EMRSF-TDDFT). This approach extends MRSF-TDDFT by incorporating electronic configurations present in linear-response TDDFT but absent in conventional MRSF-TDDFT. The formulation is based on the connection between linear-response and MRSF time-dependent Hartree-Fock theories and is extended to TDDFT. Benchmark calculations for representative molecular systems show that the newly introduced configurations capture a major contribution to orbital relaxation effects. This stabilizes both ground and excited states described in the triplet-reference orbital basis and improves agreement with reference theoretical best estimates. We expect that the new EMRSF-TDDFT model is applicable to photochemical processes involving charge transfer.

Journal of Chemical Theory and Computation
Seoul National University (KR), Kyungpook National University (KR)
POSCO TJ Park Foundation, Seoul National University, National Research Foundation of Korea, Ministry of Science and ICT, South Korea
Openalex Percentile: Top 16%
Magnetism in coordination complexes
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