Second-order variational coupled-cluster linear-response method: A Hermitian time-dependent theory
Journal Article
·
· Physical Review. A
- Institute of Physical and Theoretical Chemistry, University of Regensburg, Universitaetsstrasse 31, D-93040 Regensburg (Germany)
The formalism is presented for the linear response of a time-dependent (TD) variational coupled cluster (VCC), truncated according to Moeller-Plesset perturbation theory, i.e., a TD-VCC[n] linear response, where n denotes the order of the corresponding quasienergy with respect to the fluctuation potential. The resulting eigenvalue problem determining the excitation energies is Hermitian and of the simple Tamm-Dancoff form. The VCC excitation energies are equivalent to those of the configuration-interaction singles (CIS) model, while the Casida equation for the TD-Hartree-Fock approach is an approximation to it. The TD-VCC response, the lowest-order method including electron correlation, is discussed in detail and the relations to other second-order methods, such as the CC2 linear response and the algebraic diagrammatic construction at second order [ADC(2)] are explored.
- OSTI ID:
- 21550092
- Journal Information:
- Physical Review. A, Journal Name: Physical Review. A Journal Issue: 6 Vol. 83; ISSN 1050-2947; ISSN PLRAAN
- Country of Publication:
- United States
- Language:
- English
Similar Records
Representation independent algorithms for molecular response calculations in time-dependent self-consistent field theories
Optical potentials for electron-molecule scattering: A comparative study on the N sub 2 sup 2. Pi. sub g resonance
Configuration interaction singles, time-dependent Hartree-Fock, and time-dependent density functional theory for the electronic excited states of extended systems
Journal Article
·
Mon Dec 31 23:00:00 EST 2007
· Journal of Chemical Physics
·
OSTI ID:960966
Optical potentials for electron-molecule scattering: A comparative study on the N sub 2 sup 2. Pi. sub g resonance
Journal Article
·
Tue Nov 14 23:00:00 EST 1989
· Physical Review (Section) A: General Physics; (USA)
·
OSTI ID:5149945
Configuration interaction singles, time-dependent Hartree-Fock, and time-dependent density functional theory for the electronic excited states of extended systems
Journal Article
·
Tue Dec 21 23:00:00 EST 1999
· Journal of Chemical Physics
·
OSTI ID:20217775
Related Subjects
71 CLASSICAL AND QUANTUM MECHANICS
GENERAL PHYSICS
APPROXIMATIONS
CALCULATION METHODS
CLUSTER MODEL
CONFIGURATION INTERACTION
CORRELATIONS
EIGENVALUES
ELECTRON CORRELATION
ENERGY-LEVEL TRANSITIONS
EXCITATION
FLUCTUATIONS
FUNCTIONS
HARTREE-FOCK METHOD
HERMITE POLYNOMIALS
MATHEMATICAL MODELS
NUCLEAR MODELS
PERTURBATION THEORY
POLYNOMIALS
POTENTIALS
TIME DEPENDENCE
VARIATIONAL METHODS
VARIATIONS
GENERAL PHYSICS
APPROXIMATIONS
CALCULATION METHODS
CLUSTER MODEL
CONFIGURATION INTERACTION
CORRELATIONS
EIGENVALUES
ELECTRON CORRELATION
ENERGY-LEVEL TRANSITIONS
EXCITATION
FLUCTUATIONS
FUNCTIONS
HARTREE-FOCK METHOD
HERMITE POLYNOMIALS
MATHEMATICAL MODELS
NUCLEAR MODELS
PERTURBATION THEORY
POLYNOMIALS
POTENTIALS
TIME DEPENDENCE
VARIATIONAL METHODS
VARIATIONS