Frequency-dependent polarizabilities, hyperpolarizabilities, and excitation energies from time-dependent density-functional theory based on the quasienergy derivative method

被引:22
|
作者
Aiga, F [1 ]
Tada, T [1 ]
Yoshimura, R [1 ]
机构
[1] Toshiba Co Ltd, Mat & Devices Res Lab, Saiwai Ku, Kawasaki, Kanagawa 2108582, Japan
来源
JOURNAL OF CHEMICAL PHYSICS | 1999年 / 111卷 / 07期
关键词
D O I
10.1063/1.479570
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
A time-dependent density-functional theory for systems in periodic external potentials in time is formulated on the assumption of the existence of the Floquet states from the quasienergy viewpoint. Coupling strength integration, which connects a noninteracting system with an interacting system, is introduced by using the time-dependent Hellmann-Feynman theorem. Coupled perturbed time-dependent Kohn-Sham equations are derived from the variational condition to the quasienergy functional with respect to parameters. Explicit expressions for frequency-dependent polarizability and first hyperpolarizability are given by the quasienergy derivative method. Excitation energies and transition moments are defined from poles and residues of frequency-dependent polarizabilities, respectively. In contrast to the previous theory, our formulation has the following three advantages: (1) The time-dependent exchange-correlation potential is defined by the functional derivative of the exchange-correlation quasienergy. (2) The formal expression for frequency-dependent polarizability, which corresponds to the exact sumover-states expression, can be obtained. (3) Explicit expressions for response properties which satisfy the 2n+1 rule can be automatically obtained. (C) 1999 American Institute of Physics. [S0021-9606(99)31031-X].
引用
收藏
页码:2878 / 2888
页数:11
相关论文
共 50 条
  • [31] SINGULAR POINTS OF FREQUENCY-DEPENDENT POLARIZABILITIES FROM TIME-DEPENDENT HARTREE-FOCK THEORY
    SANTRY, DP
    JOURNAL OF CHEMICAL PHYSICS, 1979, 70 (02): : 1008 - 1010
  • [32] Analysis of environment response effects on excitation energies within subsystem-based time-dependent density-functional theory
    Scholz, Linus
    Toelle, Johannes
    Neugebauer, Johannes
    INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, 2020, 120 (21)
  • [33] Direct calculation of exciton binding energies with time-dependent density-functional theory
    Yang, Zeng-hui
    Ullrich, Carsten A.
    PHYSICAL REVIEW B, 2013, 87 (19):
  • [34] Fragment-based time-dependent density-functional theory
    Jensen, Daniel S.
    Wasserman, Adam
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2013, 246
  • [35] Local Excitation Approximations to Time-Dependent Density Functional Theory for Excitation Energies in Solution
    Liu, Jie
    Herbert, John M.
    JOURNAL OF CHEMICAL THEORY AND COMPUTATION, 2016, 12 (01) : 157 - 166
  • [36] The calculation of frequency-dependent polarizabilities using current density functional theory
    Ioannou, AG
    Colwell, SM
    Amos, RD
    CHEMICAL PHYSICS LETTERS, 1997, 278 (4-6) : 278 - 284
  • [37] Multicomponent Time-Dependent Density Functional Theory: Proton and Electron Excitation Energies
    Yang, Yang
    Culpitt, Tanner
    Hammes-Schiffer, Sharon
    JOURNAL OF PHYSICAL CHEMISTRY LETTERS, 2018, 9 (07): : 1765 - +
  • [38] FREQUENCY-DEPENDENT V-REPRESENTABILITY IN DENSITY-FUNCTIONAL THEORY
    MEARNS, D
    KOHN, W
    PHYSICAL REVIEW A, 1987, 35 (11): : 4796 - 4799
  • [39] LOCAL DENSITY-FUNCTIONAL THEORY OF FREQUENCY-DEPENDENT LINEAR RESPONSE
    GROSS, EKU
    KOHN, W
    PHYSICAL REVIEW LETTERS, 1985, 55 (26) : 2850 - 2852
  • [40] Highly Efficient Implementation of Pseudospectral Time-Dependent Density-Functional Theory for the Calculation of Excitation Energies of Large Molecules
    Cao, Yixiang
    Hughes, Thomas
    Giesen, Dave
    Halls, Mathew D.
    Goldberg, Alexander
    Vadicherla, Tati Reddy
    Sastry, Madhavi
    Patel, Bhargav
    Sherman, Woody
    Weisman, Andrew L.
    Friesner, Richard A.
    JOURNAL OF COMPUTATIONAL CHEMISTRY, 2016, 37 (16) : 1425 - 1441