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• W2045649029 abstract "Non-expanded dispersion energies are calculated from time-dependent coupled-perturbed density functional theory (DFT) employing various non-hybrid and hybrid exchange-correlation potentials and suitable adiabatic local density approximations for the exchange-correlation kernel. Considering the dimer systems He2, Ne2, Ar2, NeAr, NeHF, ArHF, (H2)2, (HF)2, and (H2O)2 it is shown that the effects of intramonomer electron correlation on the dispersion energy are accurately reproduced with the PBE0AC exchange-correlation potential. In contrast, the uncoupled sum-over-states approximation yields inacceptable errors. These are mainly due to neglect of the Coulomb and exchange-correlation kernels and therefore, not substantially improved through an asymptotic correction of the exchange-correlation potential." @default.
• W2045649029 created "2016-06-24" @default.
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• W2045649029 date "2003-01-01" @default.
• W2045649029 modified "2023-10-17" @default.
• W2045649029 title "Intermolecular dispersion energies from time-dependent density functional theory" @default.
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• W2045649029 doi "https://doi.org/10.1016/s0009-2614(02)01796-7" @default.
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