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
收藏
页码:202 / 209
页数:8
相关论文
共 50 条
  • [31] Fock space multireference coupled cluster theory: noniterative inclusion of triples for excitation energies
    Nayana Vaval
    Sourav Pal
    Debashis Mukherjee
    Theoretical Chemistry Accounts, 1998, 99 : 100 - 105
  • [33] Cluster perturbation theory. III. Perturbation series for coupled cluster singles and doubles excitation energies
    Baudin, Pablo
    Pawlowski, Filip
    Bykov, Dmytro
    Liakh, Dmitry
    Kristensen, Kasper
    Olsen, Jeppe
    Jorgensen, Poul
    JOURNAL OF CHEMICAL PHYSICS, 2019, 150 (13):
  • [34] Intermediate Hamiltonian coupled cluster methods: meV accuracy for alkaline earth transition energies
    Koren, Tal
    Eliav, Ephraim
    Ishikawa, Yasuyuki
    Kaldor, Uzi
    JOURNAL OF MOLECULAR STRUCTURE-THEOCHEM, 2006, 768 (1-3): : 127 - 132
  • [35] Performance of Property-Optimized Basis Sets for Optical Rotation with Coupled Cluster Theory
    Howard, J. Coleman
    Sowndarya, Shree S. V.
    Ansari, Imaad M.
    Mach, Taylor J.
    Baranowska-Laczkowska, Angelika
    Crawford, T. Daniel
    JOURNAL OF PHYSICAL CHEMISTRY A, 2018, 122 (28): : 5962 - 5969
  • [36] Selection of Basis Sets in Coupled-Cluster Calculations with Spin-Orbit Coupling
    Yi Shuhe
    Wang Fan
    ACTA CHIMICA SINICA, 2024, 82 (06) : 604 - 612
  • [37] A pair natural orbital implementation of the coupled cluster model CC2 for excitation energies
    Helmich, Benjamin
    Haettig, Christof
    JOURNAL OF CHEMICAL PHYSICS, 2013, 139 (08):
  • [38] A local framework for calculating coupled cluster singles and doubles excitation energies (LoFEx-CCSD)
    Baudin, Pablo
    Bykov, Dmytro
    Liakh, Dmitry
    Ettenhuber, Patrick
    Kristensen, Kasper
    MOLECULAR PHYSICS, 2017, 115 (17-18) : 2135 - 2144
  • [39] Reduction of the virtual space for coupled-cluster excitation energies of large molecules and embedded systems
    Send, Robert
    Kaila, Ville R. I.
    Sundholm, Dage
    JOURNAL OF CHEMICAL PHYSICS, 2011, 134 (21):
  • [40] OPEN-SHELL COUPLED-CLUSTER METHOD - DIRECT CALCULATION OF EXCITATION-ENERGIES
    KALDOR, U
    HAQUE, A
    CHEMICAL PHYSICS LETTERS, 1986, 128 (01) : 45 - 48