Reduced Scaling Real-Time Coupled Cluster Theory

被引:4
|
作者
Peyton, Benjamin G. [1 ]
Wang, Zhe [1 ]
Crawford, T. Daniel [1 ]
机构
[1] Virginia Tech, Dept Chem, Blacksburg, VA 24061 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY A | 2023年 / 127卷 / 40期
基金
美国国家科学基金会;
关键词
ELECTRON CORRELATION METHODS; POLARIZED BASIS-SETS; FREQUENCY-DEPENDENT POLARIZABILITIES; CORRELATED MOLECULAR CALCULATIONS; LOCAL-DENSITY APPROXIMATION; GAUSSIAN-BASIS SETS; CORRELATION-ENERGY; RESPONSE FUNCTIONS; NATURAL ORBITALS; NUCLEAR-DYNAMICS;
D O I
10.1021/acs.jpca.3c05151
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
Real-time coupled cluster (CC) methods have several advantages over their frequency-domain counterparts, namely, response and equation of motion CC theories. Broadband spectra, strong fields, and pulse manipulation allow for the simulation of complex spectroscopies that are unreachable using frequency-domain approaches. Due to the high-order polynomial scaling, the required numerical time propagation of the CC residual expressions is a computationally demanding process. This scaling may be reduced by local correlation schemes, which aim to reduce the size of the (virtual) orbital space by truncation according to user-defined parameters. We present the first application of local correlation to real-time CC. As in previous studies of locally correlated frequency-domain CC, traditional local correlation schemes are of limited utility for field-dependent properties; however, a perturbation-aware scheme proves promising. A detailed analysis of the amplitude dynamics suggests that the main challenge is a strong time dependence of the wave function sparsity.
引用
收藏
页码:8486 / 8499
页数:14
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