Accuracy of Coupled Cluster Excitation Energies in Diffuse Basis Sets

被引:54
|
作者
Kannar, Daniel [1 ]
Tajti, Attila [1 ]
Szalay, Peter G. [1 ]
机构
[1] Eotvos Lorand Univ, Inst Chem, Lab Theoret Chem, POB 32, H-1518 Budapest 112, Hungary
关键词
EXCITED ELECTRONIC STATES; GAUSSIAN-BASIS SETS; RESPONSE FUNCTIONS; BUILDING-BLOCKS; LINEAR-RESPONSE; NUCLEOBASES; CC3; BENCHMARKING; CCSDR(3);
D O I
10.1021/acs.jctc.6b00875
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 present a comprehensive statistical analysis on the accuracy of various excited state Coupled Cluster methods, accentuating the effect of diffuse basis sets on vertical excitation energies of valence and Rydberg-type states. Many popular approximate doubles and triples methods are benchmarked with basis sets up to aug-cc-pVTZ, with high level EOM-CCSDT results used as reference. The results reveal a serious deficiency of CC2 linear response and CIS(D) techniques in the description of Rydberg states, a feature not shown by the EOM-CCSD(2) and EOM-CCSD variants. The CC3 theory proves to be an accurate choice among the iterative approximate triples methods, while the novel perturbation-based CCSD(T)(a)* variant turns out to be the best way to include the effect of triple excitations in a noniterative way.
引用
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页码:202 / 209
页数:8
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