Frozen‐density embedding‐based many‐body expansions. Issue 21 (7th April 2020)

• Record Type: Journal Article
• Authors: Schmitt‐Monreal, Daniel; Jacob, Christoph R.
• Other Names: Wasserman Adam guestEditor.; Pavanello Michele guestEditor.
• Is Part Of: International journal of quantum chemistry. Volume 120:Issue 21(2020)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2020-04-07
• Subjects: frozen‐density embedding -- many‐body expansion -- molecular clusters -- quantum embedding; Quantum chemistry -- Periodicals; 541.28
• DOI: 10.1002/qua.26228
• Languages: English
• ISSNs: 0020-7608

Abstract

Abstract: Fragmentation methods allow for the accurate quantum chemical (QC) treatment of large molecular clusters and materials. Here we explore the combination of two complementary approaches to the development of such fragmentation methods: the many‐body expansion (MBE) on the one hand, and subsystem density‐functional theory (DFT) or frozen‐density embedding (FDE) theory on the other hand. First, we assess potential benefits of using FDE to account for the environment in the subsystem calculations performed within the MBE. Second, we use subsystem DFT to derive a density‐based MBE, in which a many‐body expansion of the electron density is used to calculate the system's total energy. This provides a correction to the energies calculated with a conventional energy‐based MBE that depends only on the subsystem's electron densities. For the test case of clusters of water and of aspirin, we show that such a density‐based MBE converges faster than the conventional energy‐based MBE. For our test cases, truncation errors in the interaction energies are below chemical accuracy already with a two‐body expansion. The density‐based MBE thus provides a promising avenue for accurate QC calculation of molecular clusters and materials. Abstract : The combination of the many‐body expansion with frozen‐density embedding theory is explored. A density‐based many‐body expansion is presented, which is able to provide interaction energies of molecular clusters with chemical accuracy already with a two‐body expansion.