Tensor Hypercontraction Form of the Perturbative Triples Energy in Coupled-Cluster Theory

被引:6
|
作者
Jiang, Andy [2 ]
Turney, Justin M. [1 ]
Schaefer III, Henry F. [1 ]
机构
[1] Georgia Inst Technol, Ctr Computat Mol Sci & Technol, Sch Chem & Biochem, Sch Computat Sci & Engn, Atlanta, GA 30332 USA
[2] Univ Georgia, Ctr Computat Quantum Chem, Dept Chem, Athens, GA 30602 USA
关键词
CORRELATED MOLECULAR CALCULATIONS; GAUSSIAN-BASIS SETS; PARALLEL IMPLEMENTATION; CONFIGURATION-INTERACTION; NATURAL ORBITALS; AB-INITIO; ACCURACY; CCSD; APPROXIMATION; EQUATIONS;
D O I
10.1021/acs.jctc.2c00996
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
We present the working equations for a reduced scaling method of evaluating the perturbative triples (T) energy in coupled-cluster theory, through the tensor hypercontraction (THC) of the triples amplitudes (t(ijk)(abc)). Through our method, we can reduce the scaling of the (T) energy from the traditional O(N-7) to a more modest O(N-5). We also discuss implementation details to aid future research, development, and software realization of this method. Additionally, we show that this method yields submillihartree (mEh) differences from CCSD(T) when evaluating absolute energies and sub-0.1 kcal/mol energy differences when evaluating relative energies. Finally, we demonstrate that this method converges to the true CCSD(T) energy through the systematic increasing of the rank or eigenvalue tolerance of the orthogonal projector, as well as exhibiting sublinear to linear error growth with respect to system size.
引用
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页码:1476 / 1486
页数:11
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