4.7 Article

Amplitude Determinant Coupled Cluster with Pairwise Doubles

Journal

JOURNAL OF CHEMICAL THEORY AND COMPUTATION
Volume 12, Issue 12, Pages 5841-5850

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jctc.6b00812

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Funding

  1. Office of Science, Office of Basic Energy Sciences, the US Department of Energy [DE-AC02-05CH11231]

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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.

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