Quasi-degenerate perturbation theory using matrix product states

被引:43
作者
Sharma, Sandeep [1 ]
Jeanmairet, Guillaume [1 ]
Alavi, Ali [1 ,2 ]
机构
[1] Max Planck Inst Solid State Res, Heisenbergstr 1, D-70569 Stuttgart, Germany
[2] Univ Cambridge, Dept Chem, Lensfield Rd, Cambridge CB2 1EW, England
关键词
CORRELATED MOLECULAR CALCULATIONS; FIELD REFERENCE FUNCTIONS; GAUSSIAN-BASIS SETS; RENORMALIZATION-GROUP; CONFIGURATION-INTERACTION; QUANTUM-CHEMISTRY; AB-INITIO; CONICAL INTERSECTIONS; UNITARY-INVARIANT; ELECTRONIC STATES;
D O I
10.1063/1.4939752
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
In this work, we generalize the recently proposed matrix product state perturbation theory (MPSPT) for calculating energies of excited states using quasi-degenerate (QD) perturbation theory. Our formulation uses the Kirtman-Certain-Hirschfelder canonical Van Vleck perturbation theory, which gives Hermitian effective Hamiltonians at each order, and also allows one to make use of Wigner's 2n + 1 rule. Further, our formulation satisfies Granovsky's requirement of model space invariance which is important for obtaining smooth potential energy curves. Thus, when we use MPSPT with the Dyall Hamiltonian, we obtain a model space invariant version of quasi-degenerate n-electron valence state perturbation theory (NEVPT), a property that the usual formulation of QD-NEVPT2 based on a multipartitioning technique lacked. We use our method on the benchmark problems of bond breaking of LiF which shows ionic to covalent curve crossing and the twist around the double bond of ethylene where significant valence-Rydberg mixing occurs in the excited states. In accordance with our previous work, we find that multi-reference linearized coupled cluster theory is more accurate than other multi-reference theories of similar cost. (C) 2016 AIP Publishing LLC.
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页数:7
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