期刊
JOURNAL OF CHEMICAL THEORY AND COMPUTATION
卷 5, 期 9, 页码 2415-2419出版社
AMER CHEMICAL SOC
DOI: 10.1021/ct900264b
关键词
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资金
- NSF [PHY-CDO 0835546, CHE-CAREER 0844999]
- ACS Petroleum Research Fund [46487-G6]
- Division Of Physics
- Direct For Mathematical & Physical Scien [835543] Funding Source: National Science Foundation
Real-time time-dependent Hartree-Fock (TDHF)/density functional theory (TDDFT) has been gaining in popularity because of its ability to treat phenomena beyond the linear response and because it has the potential to be more computationally powerful than frequency domain TDHF/TDDFT. Within real-time TDHF/TDDFT, we present a method that gives the excited state triplet energies starting from a singlet ground state. Using a spin-dependent field, we break the spin-symmetry of the alpha and beta density matrices, which incorporates a triplet contribution into the superposition state. The alpha electron density follows the applied field, and the beta electron density responds to the perturbation from the changing alpha electron density. We examine the individual alpha/beta responses during the electron density propagation. Singlet-triplet transitions appear as 'dark' states: they are present in the alpha/beta responses but are absent from the total electron density response.
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