Nonequilibrium solvation for vertical photoemission and photoabsorption processes using the symmetry-adapted cluster-configuration interaction method in the polarizable continuum model

被引:45
|
作者
Fukuda, Ryoichi [1 ,2 ,3 ]
Ehara, Masahiro [1 ,2 ,3 ]
Nakatsuji, Hiroshi [3 ,4 ]
Cammi, Roberto [5 ]
机构
[1] Natl Inst Nat Sci, Inst Mol Sci, Dept Theoret & Computat Mol Sci, Okazaki, Aichi 4448585, Japan
[2] Res Ctr Computat Sci, Okazaki, Aichi 4448585, Japan
[3] Japan Sci & Technol Agcy CREST, Chiyoda Ku, Tokyo 1020075, Japan
[4] Quantum Chem Res Inst, Nishikyo Ku, Kyoto 6158245, Japan
[5] Univ Parma, Dipartmento Chim, I-43100 Parma, Italy
基金
日本学术振兴会;
关键词
ELECTRONIC EXCITATION-ENERGIES; INTEGRAL-EQUATION FORMALISM; DENSITY-FUNCTIONAL THEORY; LINEAR-RESPONSE METHODS; SELF-CONSISTENT-FIELD; EXCITED-STATES; WAVE-FUNCTION; SAC/SAC-CI; BASIS-SETS; FORMULATION;
D O I
10.1063/1.3562211
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
In this paper, we present the theory and implementation of a nonequilibrium solvation model for the symmetry-adapted cluster (SAC) and symmetry-adapted cluster-configuration interaction (SAC-CI) method in the polarizable continuum model. For nonequilibrium solvation, we adopted the Pekar partition scheme in which solvent charges are divided into dynamical and inertial components. With this nonequilibrium solvation scheme, a vertical transition from an initial state to a final state may be described as follows: the initial state is described by equilibrium solvation, while in the final state, the inertial component remains in the solvation for the initial state; the dynamical component will be calculated self-consistently for the final state. The present method was applied to the vertical photoemission and absorption of s-trans acrolein and methylenecyclopropene. The effect of nonequilibrium solvation was significant for a polar solvent. (C) 2011 American Institute of Physics. [doi:10.1063/1.3562211]
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页数:11
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