Amplitude Determinant Coupled Cluster with Pairwise Doubles

被引:14
|
作者
Zhao, Luning [1 ]
Neuscamman, Eric [1 ,2 ]
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[2] Lawrence Berkeley Natl Lab, Div Chem Sci, Berkeley, CA 94720 USA
关键词
MOLECULAR-ORBITAL METHODS; BOND DISSOCIATIONS; QUANTUM-CHEMISTRY; BERYLLIUM ATOM; WAVE-FUNCTIONS; GEMINALS; OPTIMIZATION; SYSTEMS; MATRIX; STATES;
D O I
10.1021/acs.jctc.6b00812
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
Recently developed pair coupled cluster doubles (pCCD) theory successfully reproduces doubly occupied configuration interaction (DOCI) with mean field cost. However, the projective nature of pCCD makes the method nonvariational and thus hard to improve systematically. As a variational alternative, we explore the idea of coupled-cluster-like expansions based on amplitude determinants and develop a specific theory similar to pCCD based on determinants of pairwise doubles. The new ansatz admits a variational treatment through Monte Carlo methods while remaining size-consistent and, crucially, polynomial cost. In the dissociations of LiH, HF, H2O, and N-2, the method performs very similarly to pCCD and DOCI, suggesting that coupled-cluster-like ansatzes and variational evaluation may not be mutually exclusive. In an attractive pairing model, the method retains its accuracy even when pCCD suffers a severe variational violation.
引用
收藏
页码:5841 / 5850
页数:10
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