Quintuple-ζ quality coupled-cluster correlation energies with triple-ζ basis sets

被引:226
作者
Tew, David P.
Klopper, Wim
Neiss, Christian
Haettig, Christof
机构
[1] Univ Karlsruhe, Inst Phys Chem, Lehrstuhl Theoret Chem, D-76128 Karlsruhe, Germany
[2] Forschungszentrum Karlsruhe, Inst Nanotechnol, D-76344 Karlsruhe, Germany
[3] Ruhr Univ Bochum, Lehrstuhl Theoret Chem, D-44780 Bochum, Germany
关键词
D O I
10.1039/b617230j
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
The explicitly- correlated coupled- cluster method CCSD(T)( R12) is extended to include F12 geminal basis functions that decay exponentially with the interelectronic distance and reproduce the form of the average Coulomb hole more accurately than linear-r(12). Equations derived using the Ansatz 2 strong orthogonality projector are presented. The convergence of the correlation energy with orbital basis set for the new CCSD(T)( F12) method is studied and found to be rapid, 98% of the basis set limit correlation energy is typically recovered using triple-zeta orbital basis sets. The performance for reaction enthalpies is assessed via a test set of 15 reactions involving 23 molecules. The title statement is found to hold equally true for total and relative correlation energies.
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页码:1921 / 1930
页数:10
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