Pure non-local machine-learned density functional theory for electron correlation

Johannes T. Margraf () and Karsten Reuter
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Johannes T. Margraf: Technische Universität München
Karsten Reuter: Technische Universität München

Nature Communications, 2021, vol. 12, issue 1, 1-7

Abstract: Abstract Density-functional theory (DFT) is a rigorous and (in principle) exact framework for the description of the ground state properties of atoms, molecules and solids based on their electron density. While computationally efficient density-functional approximations (DFAs) have become essential tools in computational chemistry, their (semi-)local treatment of electron correlation has a number of well-known pathologies, e.g. related to electron self-interaction. Here, we present a type of machine-learning (ML) based DFA (termed Kernel Density Functional Approximation, KDFA) that is pure, non-local and transferable, and can be efficiently trained with fully quantitative reference methods. The functionals retain the mean-field computational cost of common DFAs and are shown to be applicable to non-covalent, ionic and covalent interactions, as well as across different system sizes. We demonstrate their remarkable possibilities by computing the free energy surface for the protonated water dimer at hitherto unfeasible gold-standard coupled cluster quality on a single commodity workstation.

Date: 2021
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DOI: 10.1038/s41467-020-20471-y

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