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.
Authors
- Daeho Han (ORCID: https://orcid.org/0000-0003-2853-6571)
- Seung Kyu Min (ORCID: https://orcid.org/0000-0001-5636-3407)
- Jae‐Hyeok Lee (ORCID: https://orcid.org/0000-0002-4274-7415)
Institutions
- 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)
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