A multireference perturbation method using non-orthogonal Hartree-Fock determinants for ground and excited states

被引:29
|
作者
Yost, Shane R. [1 ]
Kowalczyk, Tim [1 ]
Van Voorhis, Troy [1 ]
机构
[1] MIT, Dept Chem, Cambridge, MA 02139 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2013年 / 139卷 / 17期
基金
美国国家科学基金会;
关键词
SELF-CONSISTENT-FIELD; DENSITY-FUNCTIONAL THEORY; PHOTOINDUCED ELECTRON-TRANSFER; COUPLED-CLUSTER METHOD; REFERENCE WAVE-FUNCTIONS; CONFIGURATION-INTERACTION; QUANTUM-CHEMISTRY; EXCITATION-ENERGIES; HYDROGEN-FLUORIDE; LARGE MOLECULES;
D O I
10.1063/1.4827456
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 article we propose the Delta SCF(2) framework, a multireference strategy based on second-order perturbation theory, for ground and excited electronic states. Unlike the complete active space family of methods, Delta SCF(2) employs a set of self-consistent Hartree-Fock determinants, also known as Delta SCF states. Each Delta SCF electronic state is modified by a first-order correction from Moller-Plesset perturbation theory and used to construct a Hamiltonian in a configuration interactions like framework. We present formulas for the resulting matrix elements between nonorthogonal states that scale as (NoccNvirt3)-N-2. Unlike most active space methods, Delta SCF(2) treats the ground and excited state determinants even-handedly. We apply Delta SCF(2) to the H-2, hydrogen fluoride, and H-4 systems and show that the method provides accurate descriptions of ground- and excited-state potential energy surfaces with no single active space containing more than 10 Delta SCF states. (C) 2013 AIP Publishing LLC.
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页数:9
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