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• W2033733316 abstract "Building on the framework recently reported for determining general response properties for frozen-density embedding [S. Höfener, A. S. P. Gomes, and L. Visscher, J. Chem. Phys. 136, 044104 (2012)]10.1063/1.3675845, in this work we report a first implementation of an embedded coupled-cluster in density-functional theory (CC-in-DFT) scheme for electronic excitations, where only the response of the active subsystem is taken into account. The formalism is applied to the calculation of coupled-cluster excitation energies of water and uracil in aqueous solution. We find that the CC-in-DFT results are in good agreement with reference calculations and experimental results. The accuracy of calculations is mainly sensitive to factors influencing the correlation treatment (basis set quality, truncation of the cluster operator) and to the embedding treatment of the ground-state (choice of density functionals). This allows for efficient approximations at the excited state calculation step without compromising the accuracy. This approximate scheme makes it possible to use a first principles approach to investigate environment effects with specific interactions at coupled-cluster level of theory at a cost comparable to that of calculations of the individual subsystems in vacuum." @default.
• W2033733316 created "2016-06-24" @default.
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• W2033733316 creator A5050604856 @default.
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• W2033733316 date "2013-09-11" @default.
• W2033733316 modified "2023-10-18" @default.
• W2033733316 title "Solvatochromic shifts from coupled-cluster theory embedded in density functional theory" @default.
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• W2033733316 doi "https://doi.org/10.1063/1.4820488" @default.
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