Mixed-Reference Spin-Flip Time-Dependent Density Functional Theory: Multireference Advantages with the Practicality of Linear Response Theory

被引:32
作者
Park, Woojin [1 ]
Komarov, Konstantin [2 ]
Lee, Seunghoon [3 ,4 ]
Choi, Cheol Ho [1 ]
机构
[1] Kyungpook Natl Univ, Dept Chem Educ, Daegu 41566, South Korea
[2] Pohang Univ Sci & Technol, Ctr Quantum Dynam, Pohang 37673, South Korea
[3] CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA
[4] Seoul Natl Univ, Dept Chem, Seoul 151747, South Korea
关键词
POTENTIAL-ENERGY SURFACES; SELF-CONSISTENT-FIELD; NONADIABATIC COUPLING TERMS; MR-CI LEVEL; CONICAL INTERSECTIONS; EXCITED-STATES; ELECTRONIC-STRUCTURE; DOUBLE EXCITATIONS; ANALYTIC EVALUATION; PHOTOEXCITED DNA;
D O I
10.1021/acs.jpclett.3c02296
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
The density functional theory (DFT) and linear response (LR) time-dependent (TD)-DFT are of the utmost importance for routine computations. However, the single reference formulation of DFT suffers in the description of open-shell singlet systems such as diradicals and bond-breaking. LR-TDDFT, on the other hand, finds difficulties in the modeling of conical intersections, doubly excited states, and core-level excitations. In this Perspective, we demonstrate that many of these limitations can be overcome by recently developed mixed-reference (MR) spin-flip (SF)-TDDFT, providing an alternative yet accurate route for such challenging situations. Empowered by the practicality of the LR formalism, it is anticipated that MRSF-TDDFT can become one of the major workhorses for general routine tasks.
引用
收藏
页码:8896 / 8908
页数:13
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