Article ; Online: Finite-temperature-based time-dependent density-functional theory method for static electron correlation systems.
The Journal of chemical physics
2020 Volume 152, Issue 24, Page(s) 244111
Abstract: In this study, we developed a time-dependent density-functional theory (TDDFT) with a finite-temperature (FT) scheme, denoted as FT-TDDFT. We introduced the concept of fractional occupation numbers for random phase approximation equation and evaluated ... ...
Abstract | In this study, we developed a time-dependent density-functional theory (TDDFT) with a finite-temperature (FT) scheme, denoted as FT-TDDFT. We introduced the concept of fractional occupation numbers for random phase approximation equation and evaluated the excited-state electronic entropy terms with excited-state occupation number. The orbital occupation numbers for the excited state were evaluated from the change in the ground-state electron configuration with excitation and deexcitation coefficients. Furthermore, we extended the FT formulation to the time-dependent density-functional tight-binding (TDDFTB) method for larger systems, denoted as FT-TDDFTB. Numerical assessment for the FT-(TD)DFT method showed smooth potential curves for double-bond rotation of ethylene in both ground and excited states. Excited-state calculations based on the FT-TDDFTB method were applied to the uniform π-stacking columns composed of trioxotriangulene, possessing neutral radicals in strong correlation systems. |
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Language | English |
Publishing date | 2020-06-17 |
Publishing country | United States |
Document type | Journal Article |
ZDB-ID | 3113-6 |
ISSN | 1089-7690 ; 0021-9606 |
ISSN (online) | 1089-7690 |
ISSN | 0021-9606 |
DOI | 10.1063/1.5144527 |
Database | MEDical Literature Analysis and Retrieval System OnLINE |
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