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- W3101928854 abstract "Embedded density functional theory (e-DFT) is used to describe the electronic structure of strongly interacting molecular subsystems. We present a general implementation of the Exact Embedding (EE) method [J. Chem. Phys. 133, 084103 (2010)] to calculate the large contributions of the non-additive kinetic potential (NAKP) in such applications. Potential energy curves are computed for the dissociation of Li+-Be, CH3-CF3, and hydrogen-bonded water clusters, and e-DFT results obtained using the EE method are compared with those obtained using approximate kinetic energy functionals. In all cases, the EE method preserves excellent agreement with reference Kohn-Sham calculations, whereas the approximate functionals lead to qualitative failures in the calculated energies and equilibrium structures. We also demonstrate an accurate pairwise approximation to the NAKP that allows for efficient parallelization of the EE method in large systems; benchmark calculations on molecular crystals reveal ideal, size-independent scaling of wall-clock time with increasing system size." @default.
- W3101928854 created "2020-11-23" @default.
- W3101928854 creator A5008965700 @default.
- W3101928854 creator A5028949819 @default.
- W3101928854 creator A5078961588 @default.
- W3101928854 date "2011-04-28" @default.
- W3101928854 modified "2023-10-18" @default.
- W3101928854 title "Embedded density functional theory for covalently bonded and strongly interacting subsystems" @default.
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- W3101928854 doi "https://doi.org/10.1063/1.3582913" @default.
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