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- W3136793071 abstract "Tailored coupled cluster theory represents a computationally inexpensive way to describe static and dynamical electron correlation effects. In this work, we scrutinize the performance of various tailored coupled cluster methods externally corrected by electronic wave functions of polynomial cost. Specifically, we focus on frozen-pair coupled-cluster (fpCC) methods, which are externally corrected by pair-coupled cluster doubles (pCCD), and coupled cluster theory tailored by matrix product state wave functions optimized by the density matrix renormalization group (DMRG) algorithm. As test system, we selected a set of various small- and medium-sized molecules containing diatomics (N$_2$, F$_2$, C$_2$, CN$^+$, BN, BO$^+$, and Cr$_2$) and molecules (ammonia, ethylene, cyclobutadiene, benzene) for which conventional single-reference coupled cluster singles and doubles (CCSD) is not able to produce accurate results for spectroscopic constants, potential energy surfaces, and barrier heights. Most importantly, DMRG-tailored and pCCD-tailored approaches yield similar errors in spectroscopic constants and potential energy surfaces compared to multireference and/or experimental reference data and generally outrank the conventional single-reference CCSD approach. Although fpCC methods provide a reliable description for the dissociation pathway of molecules featuring single and quadruple bonds, they fail in the description of triple or hextuple bond-breaking processes or avoided crossing regions." @default.
- W3136793071 created "2021-03-29" @default.
- W3136793071 creator A5018343508 @default.
- W3136793071 creator A5037649922 @default.
- W3136793071 creator A5047955091 @default.
- W3136793071 creator A5070016694 @default.
- W3136793071 date "2021-03-23" @default.
- W3136793071 modified "2023-10-18" @default.
- W3136793071 title "Assessing the accuracy of tailored coupled cluster methods corrected by electronic wave functions of polynomial cost" @default.
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