Improved method for generating exchange-correlation potentials from electronic wave functions

被引:42
|
作者
Ospadov, Egor [1 ]
Ryabinkin, Ilya G. [2 ]
Staroverov, Viktor N. [1 ]
机构
[1] Univ Western Ontario, Dept Chem, London, ON N6A 5B7, Canada
[2] Univ Toronto Scarborough, Dept Physiol & Environm Sci, Scarborough, ON M1C 1A4, Canada
来源
JOURNAL OF CHEMICAL PHYSICS | 2017年 / 146卷 / 08期
基金
加拿大自然科学与工程研究理事会;
关键词
KOHN-SHAM POTENTIALS; OPTIMIZED EFFECTIVE POTENTIALS; HARTREE-FOCK ENERGIES; GAUSSIAN-BASIS SETS; KOOPMANS THEOREM; MOLECULAR CALCULATIONS; IONIZATION-POTENTIALS; DENSITY FUNCTIONALS; ORBITAL ENERGIES; ATOMS;
D O I
10.1063/1.4975990
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
Ryabinkin, Kohut, and Staroverov (RKS) [Phys. Rev. Lett. 115, 083001 (2015)] devised an iterative method for reducing many-electron wave functions to Kohn-Sham exchange-correlation potentials, v(XC)(r). For a given type of wave function, the RKS method is exact (Kohn-Sham-compliant) in the basis-set limit; in a finite basis set, it produces an approximation to the corresponding basis-setlimit v(XC)(r). The original RKS procedure works very well for large basis sets but sometimes fails for commonly used (small and medium) sets. We derive a modification of the method's working equation that makes the RKS procedure robust for all Gaussian basis sets and increases the accuracy of the resulting exchange-correlation potentials with respect to the basis-set limit. Published by AIP Publishing.
引用
收藏
页数:8
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