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
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
相关论文
共 52 条
  • [1] Stability analysis for solutions of the closed shell Kohn-Sham equation
    Bauernschmitt, R
    Ahlrichs, R
    [J]. JOURNAL OF CHEMICAL PHYSICS, 1996, 104 (22) : 9047 - 9052
  • [2] Treatment of electronic excitations within the adiabatic approximation of time dependent density functional theory
    Bauernschmitt, R
    Ahlrichs, R
    [J]. CHEMICAL PHYSICS LETTERS, 1996, 256 (4-5) : 454 - 464
  • [3] Experiment versus time dependent density functional theory prediction of fullerene electronic absorption
    Bauernschmitt, R
    Ahlrichs, R
    Hennrich, FH
    Kappes, MM
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (20) : 5052 - 5059
  • [4] Calculation of excitation energies within time-dependent density functional theory using auxiliary basis set expansions
    Bauernschmitt, R
    Haser, M
    Treutler, O
    Ahlrichs, R
    [J]. CHEMICAL PHYSICS LETTERS, 1997, 264 (06) : 573 - 578
  • [5] Casida M. E., 1995, RECENT ADV DENSITY F, V1, P155, DOI [10.1142/9789812830586_0005, DOI 10.1142/9789812830586_0005]
  • [6] Christiansen O, 1998, INT J QUANTUM CHEM, V68, P1, DOI 10.1002/(SICI)1097-461X(1998)68:1<1::AID-QUA1>3.0.CO
  • [7] 2-Z
  • [8] CIZEK J, 1967, J CHEM PHYS, V47, P3976
  • [9] Time-dependent density functional theory beyond linear response: An exchange-correlation potential with memory
    Dobson, JF
    Bunner, MJ
    Gross, EKU
    [J]. PHYSICAL REVIEW LETTERS, 1997, 79 (10) : 1905 - 1908
  • [10] Circular dichroism of helicenes investigated by time-dependent density functional theory
    Furche, F
    Ahlrichs, R
    Wachsmann, C
    Weber, E
    Sobanski, A
    Vögtle, F
    Grimme, S
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (08) : 1717 - 1724