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Article: Highly accurate CCSD(R12) and CCSD(F12) optical response properties using standard triple-ζ basis sets

TitleHighly accurate CCSD(R12) and CCSD(F12) optical response properties using standard triple-ζ basis sets
Authors
Issue Date2009
Citation
Journal of Chemical Physics, 2009, v. 131, n. 7 How to Cite?
AbstractCoupled-cluster response theory for frequency-dependent optical properties within the coupled-cluster singles-and-doubles model (CCSD) has been derived and implemented for ansatz 2 of the explicitly correlated CCSD(R12) and CCSD(F12) methods as part of the program package DALTON. The basis set convergence of static dipole moments, polarizabilities, and parallel averages of first and second hyperpolarizabilities has been investigated for Ne, BH, N2, CO, and BF. The frequency-dependent results are presented for the electronic second-harmonic generation of N2. With triple-ζ basis sets, the CCSD(F12) correlation contributions using ansatz 2 are close to the basis set limits for dipole moments and second hyperpolarizabilities; the CCSD(R12) results are better than the CCSD results obtained with at least quintuple- ζ basis sets for polarizabilities and first hyperpolarizabilities. The exponent of Slater-type correlation factor for CCSD(F12) ground state energy may not be optimal and has to be re-examined for response properties. We also suggest that the remaining one-electron basis set errors arising within the coupled-cluster singles should be reduced by allowing excitations into the auxiliary orbital space. © 2009 American Institute of Physics.
Persistent Identifierhttp://hdl.handle.net/10722/230836
ISSN
2015 Impact Factor: 2.894
2015 SCImago Journal Rankings: 0.959

 

DC FieldValueLanguage
dc.contributor.authorYang, Jun-
dc.contributor.authorHättig, Christof-
dc.date.accessioned2016-09-01T06:06:55Z-
dc.date.available2016-09-01T06:06:55Z-
dc.date.issued2009-
dc.identifier.citationJournal of Chemical Physics, 2009, v. 131, n. 7-
dc.identifier.issn0021-9606-
dc.identifier.urihttp://hdl.handle.net/10722/230836-
dc.description.abstractCoupled-cluster response theory for frequency-dependent optical properties within the coupled-cluster singles-and-doubles model (CCSD) has been derived and implemented for ansatz 2 of the explicitly correlated CCSD(R12) and CCSD(F12) methods as part of the program package DALTON. The basis set convergence of static dipole moments, polarizabilities, and parallel averages of first and second hyperpolarizabilities has been investigated for Ne, BH, N2, CO, and BF. The frequency-dependent results are presented for the electronic second-harmonic generation of N2. With triple-ζ basis sets, the CCSD(F12) correlation contributions using ansatz 2 are close to the basis set limits for dipole moments and second hyperpolarizabilities; the CCSD(R12) results are better than the CCSD results obtained with at least quintuple- ζ basis sets for polarizabilities and first hyperpolarizabilities. The exponent of Slater-type correlation factor for CCSD(F12) ground state energy may not be optimal and has to be re-examined for response properties. We also suggest that the remaining one-electron basis set errors arising within the coupled-cluster singles should be reduced by allowing excitations into the auxiliary orbital space. © 2009 American Institute of Physics.-
dc.languageeng-
dc.relation.ispartofJournal of Chemical Physics-
dc.rightsCreative Commons: Attribution 3.0 Hong Kong License-
dc.titleHighly accurate CCSD(R12) and CCSD(F12) optical response properties using standard triple-ζ basis sets-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1063/1.3204388-
dc.identifier.scopuseid_2-s2.0-69249181243-
dc.identifier.volume131-
dc.identifier.issue7-
dc.identifier.spagenull-
dc.identifier.epagenull-

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