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

被引:45
|
作者
Isborn, Christine M. [1 ]
Li, Xiaosong [1 ]
机构
[1] Univ Washington, Dept Chem, Seattle, WA 98195 USA
基金
美国国家科学基金会;
关键词
EXCITATION-ENERGIES; LARGE MOLECULES; STATES;
D O I
10.1021/ct900264b
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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.
引用
收藏
页码:2415 / 2419
页数:5
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