Extensions of r12 corrections to CC2-R12 for excited states

被引:35
作者
Neiss, Christian
Haettig, Christof
Klopper, Wim
机构
[1] Forschungszentrum Karlsruhe, Inst Nanotechnol, D-76021 Karlsruhe, Germany
[2] Ruhr Univ Bochum, Lehrstuhl Theoret Chem, D-44780 Bochum, Germany
关键词
D O I
10.1063/1.2335443
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
As known since about two decades, R12 methods, which include terms linear in the interelectronic distance r(12) in the wave function, improve substantially the basis set convergence of the ground state correlation energy. In a previous study, however, it was found that the same approach does not give a similar systematic improvement if applied to excited states in the framework of coupled cluster response theory. In the present work, we examine the reason for this behavior and show that the inclusion of additional orbitals in the construction of the r(12) pair functions leads to an enhanced basis set convergence (and thus a balanced description) also for the excited states. (c) 2006 American Institute of Physics.
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页数:7
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