4.7 Article

Singlet-Triplet Transitions in Real-Time Time-Dependent Hartree-Fock/Density Functional Theory

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

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资金

  1. NSF [PHY-CDO 0835546, CHE-CAREER 0844999]
  2. ACS Petroleum Research Fund [46487-G6]
  3. Division Of Physics
  4. Direct For Mathematical & Physical Scien [835543] Funding Source: National Science Foundation

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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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