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- W4387057879 abstract "While CCSD(T) is often considered the ``gold standard'' of computational chemistry, the scaling of its computational cost as N^7 limits is applicability for large and complex molecular systems. In this work, we apply the density-based many-body expansion [Int. J. Quantum Chem. 2020, 120, e26228] in combination with CCSD(T). The accuracy of this approach is assessed for neutral, protonated, and deprotonated water hexamers as well as (H2O)16 and (H2O)17 clusters. For the neutral water clusters, we find that already with a density-based two-body expansion, we are able to approximate the supermolecular CCSD(T) energies within chemical accuracy (4 kJ/mol). This surpasses the accuracy that is achieved with a conventional, energy-based three-body expansion. We show that this accuracy can be maintained even when approximating the electron densities using Hartree-Fock instead of using coupled-cluster densities. The density-based many-body expansion thus offers a simple, resource efficient, and highly parallelizable approach that makes CCSD(T)-quality calculations feasible where they would otherwise be prohibitively expensive." @default.
- W4387057879 created "2023-09-27" @default.
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- W4387057879 date "2023-09-26" @default.
- W4387057879 modified "2023-09-27" @default.
- W4387057879 title "Coupled-Cluster Density-Based Many-Body Expansion" @default.
- W4387057879 doi "https://doi.org/10.26434/chemrxiv-2023-lhl0f-v2" @default.
- W4387057879 hasPublicationYear "2023" @default.
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