Orbital-Based Correlated Electron–Nuclear Dynamics for Extended Systems with Exact Factorization

In this work, we introduce a practical orbital-based framework for simulating correlated electron-nuclear dynamics in extended systems within the exact factorization (XF) formalism. Building on our earlier derivation of time-dependent Kohn-Sham (TDKS) equations that merge real-time time-dependent density functional theory with XF, we apply the classical path approximation and incorporate pairwise XF-derived decoherence corrections in the Kohn-Sham basis. This leads to a new efficient algorithm capable of treating nonadiabatic processes involving thousands of atoms. As a demonstration, we perform nonadiabatic dynamics simulations of two spiro-type hole-transport materials under periodic boundary conditions─the first application of XF-based methods to extended systems. While hole dynamics without decoherence yield unphysical, persistent coherences, the inclusion of XF-derived decoherence produces physically consistent relaxation from lower to higher bands.

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Publication Details

Journal
Journal of Chemical Theory and Computation
Published
2025-11-16
DOI
https://doi.org/10.1021/acs.jctc.5c01575
Citations
1
Primary Topic
Spectroscopy and Quantum Chemical Studies
Type
article
Field-Weighted Citation Impact
1.25
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article

Orbital-Based Correlated Electron–Nuclear Dynamics for Extended Systems with Exact Factorization

Daeho Han, Seung Kyu Min, Jae‐Hyeok Lee
1 citations
Journal of Chemical Theory and Computation
Spectroscopy and Quantum Chemical Studies
1.25
article

Orbital-Based Correlated Electron–Nuclear Dynamics for Extended Systems with Exact Factorization

Daeho Han, Seung Kyu Min, Jae‐Hyeok Lee
article en
1 citations

Abstract

In this work, we introduce a practical orbital-based framework for simulating correlated electron-nuclear dynamics in extended systems within the exact factorization (XF) formalism. Building on our earlier derivation of time-dependent Kohn-Sham (TDKS) equations that merge real-time time-dependent density functional theory with XF, we apply the classical path approximation and incorporate pairwise XF-derived decoherence corrections in the Kohn-Sham basis. This leads to a new efficient algorithm capable of treating nonadiabatic processes involving thousands of atoms. As a demonstration, we perform nonadiabatic dynamics simulations of two spiro-type hole-transport materials under periodic boundary conditions─the first application of XF-based methods to extended systems. While hole dynamics without decoherence yield unphysical, persistent coherences, the inclusion of XF-derived decoherence produces physically consistent relaxation from lower to higher bands.

Journal of Chemical Theory and ComputationVol. 21(22)
Korea Advanced Institute of Science and Technology (KR), InnoCentive (United States) (US), Institute for Basic Science (KR), Ulsan National Institute of Science and Technology (KR)
Openalex Percentile: Top 15%
Spectroscopy and Quantum Chemical Studies
1.25
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Orbital-Based Correlated Electron–Nuclear Dynamics for Extended Systems with Exact Factorization — Daeho Han, Seung Kyu Min, et al. · Journal of Chemical Theory and Computation (2025) | TGRS Research Map | TGRS