Propagator corrections to adiabatic time-dependent density-functional theory linear response theory

被引:99
作者
Casida, ME [1 ]
机构
[1] Univ Grenoble 1, LEDSS, ECT, UMR 5616,Inst Chim Mol Grenoble,FR 2607, F-38041 Grenoble, France
关键词
D O I
10.1063/1.1836757
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
It has long been known that only one-electron excitations are available from adiabatic time-dependent density functional theory (TDDFT). This is particularly clear in Casida's formulation of TDDFT linear response theory [M. E. Casida, in Recent Advances in Density Functional Methods, Part I, edited by D. P. Chong (World Scientific, Singapore, 1995), p. 155]. Nevertheless the explicit inclusion of two- and higher-electron excitations is necessary for an adequate description of some excited states, notably the first excited singlet states of butadiene and quartet excited states of molecules with a doublet ground state. The equation-of-motion superoperator approach is used here to derive a Casida-like propagator equation which can be clearly separated into an adiabatic part and a nonadiabatic part. The adiabatic part is identified as corresponding to Casida's equation for adiabatic TDDFT linear response theory. This equivalence is confirmed by deriving a general formula which includes the result that Gonze and Scheffler derived to show the equivalence of TDDFT and Gorling-Levy adiabatic connection perturbation theory for the exchange-only optimized effective potential [X. Gonze and M. Scheffler, Phys. Rev. Lett. 82, 4416 (1999)]. The nonadiabatic part explicitly corrects adiabatic TDDFT for two- and higher-electron excitations. The "dressed TDDFT" of Maitra, Zhang, Cave, and Burke is obtained as a special case where the ground state is closed shell [N. T. Maitra, F. Zhang, R. J. Cave, and K. Burke, J. Chem. Phys. 120, 5932 (2004)]. The extension of dressed TDDFT to the case where the ground state is an open-shell doublet is presented, highlighting the importance of correctly accounting for symmetry in this theory. The extension to other ground state spin symmetries is a straightforward consequence of the present work. (C) 2005 American Institute of Physics.
引用
收藏
页数:9
相关论文
共 58 条
[41]   Electronic states of the phenoxyl radical [J].
Radziszewski, JG ;
Gil, M ;
Gorski, A ;
Spanget-Larsen, J ;
Waluk, J ;
Mróz, BJ .
JOURNAL OF CHEMICAL PHYSICS, 2001, 115 (21) :9733-9738
[42]   Restricted density functional theory of linear time-dependent properties in open-shell molecules [J].
Rinkevicius, Z ;
Tunell, I ;
Salek, P ;
Vahtras, O ;
Ågren, H .
JOURNAL OF CHEMICAL PHYSICS, 2003, 119 (01) :34-46
[43]   DENSITY-FUNCTIONAL THEORY FOR TIME-DEPENDENT SYSTEMS [J].
RUNGE, E ;
GROSS, EKU .
PHYSICAL REVIEW LETTERS, 1984, 52 (12) :997-1000
[44]   DENSITY-FUNCTIONAL THEORY OF THE ENERGY-GAP [J].
SHAM, LJ ;
SCHLUTER, M .
PHYSICAL REVIEW LETTERS, 1983, 51 (20) :1888-1891
[45]   The spin-flip approach within time-dependent density functional theory: Theory and applications to diradicals [J].
Shao, YH ;
Head-Gordon, M ;
Krylov, AI .
JOURNAL OF CHEMICAL PHYSICS, 2003, 118 (11) :4807-4818
[46]   A VARIATIONAL APPROACH TO THE UNIPOTENTIAL MANY-ELECTRON PROBLEM [J].
SHARP, RT ;
HORTON, GK .
PHYSICAL REVIEW, 1953, 90 (02) :317-317
[47]   Electronic structure of the trimethylenemethane diradical in its ground and electronically excited states: Bonding, equilibrium geometries, and vibrational frequencies [J].
Slipchenko, LV ;
Krylov, AI .
JOURNAL OF CHEMICAL PHYSICS, 2003, 118 (15) :6874-6883
[48]   Potential energy curves for PO, calculated using DFT and MRCI methodology [J].
Spielfiedel, A ;
Handy, NC .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 1999, 1 (10) :2401-2409
[49]   OPTIMIZED EFFECTIVE ATOMIC CENTRAL POTENTIAL [J].
TALMAN, JD ;
SHADWICK, WF .
PHYSICAL REVIEW A, 1976, 14 (01) :36-40
[50]   Resonant nonlinear polarizabilities in the time-dependent density functional theory [J].
Tretiak, S ;
Chernyak, V .
JOURNAL OF CHEMICAL PHYSICS, 2003, 119 (17) :8809-8823