Subspace Density Matrix Functional Embedding Theory: Theory, Implementation, and Applications to Molecular Systems

被引:17
|
作者
Zhang, Xing [1 ]
Carter, Emily A. [2 ]
机构
[1] Princeton Univ, Dept Mech & Aerosp Engn, Princeton, NJ 08544 USA
[2] Princeton Univ, Sch Engn & Appl Sci, Princeton, NJ 08544 USA
基金
美国国家科学基金会;
关键词
GAUSSIAN-BASIS SETS; AB-INITIO; EXCITATION-ENERGIES; BAND-STRUCTURE; WAVE-FUNCTIONS; STATE; POTENTIALS; SOLIDS;
D O I
10.1021/acs.jctc.8b00990
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 introduce the subspace density matrix functional embedding theory (sDMFET), in which optimization of the nonlocal embedding potential and subsequent embedded correlated wave function calculations are carried out within a truncated subspace determined by a Schmidt decomposition. As compared to the original density matrix functional embedding theory [K. Yu and E. A. Carter, Proceedings of the National Academy of Sciences 2017, 114, E10861], the computational cost of sDMFET is significantly reduced while the accuracy is preserved. We perform test calculations for both covalently and noncovalently bound molecular systems to demonstrate the feasibility of our theory.
引用
收藏
页码:949 / 960
页数:12
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