On the density matrix based approach to time-dependent density functional response theory

被引:380
|
作者
Furche, F [1 ]
机构
[1] Univ Karlsruhe, Inst Phys Chem, D-76128 Karlsruhe, Germany
来源
JOURNAL OF CHEMICAL PHYSICS | 2001年 / 114卷 / 14期
关键词
D O I
10.1063/1.1353585
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
The formulation of time-dependent Kohn-Sham (TDKS) response theory based on the noninteracting one-particle density matrix is reanalyzed in detail. A transparent derivation starting from a von-Neumann-type equation of motion for the TDKS one-particle density matrix is presented. The resulting scheme has a simple structure and leads to compact expressions for frequency-dependent response properties. A systematic treatment of excited states is inferred from a pole analysis of the frequency-dependent density matrix response. A variational principle for excitation energies is established. Excited state properties are straightforward by analytical derivative techniques. The theory provides a particularly suitable starting point for linear scaling implementations. Magneto-optic properties such as rotatory strengths and the rotatory dispersion are accessible from the TDKS current-density response. The formalism is gauge-invariant. Various new sum rules within the adiabatic approximation (AA) are derived. It is shown that there is no "assignment problem" for excited states in the density matrix based formulation; the common density based approach is included as a special case. Merits and limitations of the AA are discussed. (C) 2001 American Institute of Physics.
引用
收藏
页码:5982 / 5992
页数:11
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