Subsystem real-time time dependent density functional theory

被引:35
|
作者
Krishtal, Alisa [1 ]
Ceresoli, Davide [1 ,2 ]
Pavanello, Michele [1 ]
机构
[1] Rutgers State Univ, Dept Chem, Newark, NJ 07102 USA
[2] CNR ISTM, Inst Mol Sci & Technol, Milan, Italy
来源
JOURNAL OF CHEMICAL PHYSICS | 2015年 / 142卷 / 15期
关键词
CONSTRAINED ELECTRON-DENSITY; KOHN-SHAM EQUATIONS; EXCITED-STATES; ENERGY-TRANSFER; WAVE-FUNCTION; POTENTIALS; PSEUDOPOTENTIALS; EXCITATIONS; DYNAMICS; IMPLEMENTATION;
D O I
10.1063/1.4918276
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
We present the extension of Frozen Density Embedding (FDE) formulation of subsystem Density Functional Theory (DFT) to real-time Time Dependent Density Functional Theory (rt-TDDFT). FDE is a DFT-in-DFT embedding method that allows to partition a larger Kohn-Sham system into a set of smaller, coupled Kohn-Sham systems. Additional to the computational advantage, FDE provides physical insight into the properties of embedded systems and the coupling interactions between them. The extension to rt-TDDFT is done straightforwardly by evolving the Kohn-Sham subsystems in time simultaneously, while updating the embedding potential between the systems at every time step. Two main applications are presented: the explicit excitation energy transfer in real time between subsystems is demonstrated for the case of the Na-4 cluster and the effect of the embedding on optical spectra of coupled chromophores. In particular, the importance of including the full dynamic response in the embedding potential is demonstrated. (C) 2015 AIP Publishing LLC.
引用
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页数:13
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