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Accuracy of Coupled Cluster Excitation Energies in Diffuse Basis Sets.
Kánnár, Dániel; Tajti, Attila; Szalay, Péter G.
Affiliation
  • Kánnár D; Laboratory of Theoretical Chemistry, Institute of Chemistry, Eötvös Loránd University , P.O. Box 32, H-1518, Budapest 112, Hungary.
  • Tajti A; Laboratory of Theoretical Chemistry, Institute of Chemistry, Eötvös Loránd University , P.O. Box 32, H-1518, Budapest 112, Hungary.
  • Szalay PG; Laboratory of Theoretical Chemistry, Institute of Chemistry, Eötvös Loránd University , P.O. Box 32, H-1518, Budapest 112, Hungary.
J Chem Theory Comput ; 13(1): 202-209, 2017 01 10.
Article in En | MEDLINE | ID: mdl-27959525
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.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Chem Theory Comput Year: 2017 Document type: Article Affiliation country: Hungary Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Chem Theory Comput Year: 2017 Document type: Article Affiliation country: Hungary Country of publication: United States