Literature DB >> 27959525

Accuracy of Coupled Cluster Excitation Energies in Diffuse Basis Sets.

Dániel Kánnár1, Attila Tajti1, Péter G Szalay1.   

Abstract

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.

Entities:  

Year:  2016        PMID: 27959525     DOI: 10.1021/acs.jctc.6b00875

Source DB:  PubMed          Journal:  J Chem Theory Comput        ISSN: 1549-9618            Impact factor:   6.006


  2 in total

1.  Reduced-cost linear-response CC2 method based on natural orbitals and natural auxiliary functions.

Authors:  Dávid Mester; Péter R Nagy; Mihály Kállay
Journal:  J Chem Phys       Date:  2017-05-21       Impact factor: 3.488

2.  Multilevel CC2 and CCSD in Reduced Orbital Spaces: Electronic Excitations in Large Molecular Systems.

Authors:  Sarai Dery Folkestad; Eirik F Kjønstad; Linda Goletto; Henrik Koch
Journal:  J Chem Theory Comput       Date:  2021-01-08       Impact factor: 6.006

  2 in total

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