Learning the Electrostatic Response of the Electron Density through a Symmetry-Adapted Vector Field Model

A current challenge in atomistic machine learning is that of efficiently predicting the response of the electron density under electric fields. We address this challenge with symmetry-adapted kernel functions that are specifically derived to account for the rotational symmetry of a three-dimensional vector field. We demonstrate the equivariance of the method on a set of rotated water molecules and show its high efficiency with respect to number of training configurations and features for liquid water and naphthalene crystals. We conclude showcasing applications for relaxed configurations of gold nanoparticles, reproducing the scaling law of the electronic polarizability with size, up to systems with more than 2000 atoms. By deriving a natural extension to equivariant learning models of the electron density, our method provides an accurate and inexpensive strategy to predict the electrostatic response of molecules and materials.

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Publication Details

Journal
The Journal of Physical Chemistry Letters
Published
2025-02-24
DOI
https://doi.org/10.1021/acs.jpclett.5c00165
Citations
4
Primary Topic
Machine Learning in Materials Science
Type
article
Field-Weighted Citation Impact
2.07

Funders

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article

Learning the Electrostatic Response of the Electron Density through a Symmetry-Adapted Vector Field Model

Mathieu Salanne, Andrea Grisafi, Alan M. Lewis, Kevin Rossi et al.
4 citations
The Journal of Physical Chemistry Letters
Machine Learning in Materials Science
2.07
article

Learning the Electrostatic Response of the Electron Density through a Symmetry-Adapted Vector Field Model

Mathieu Salanne, Andrea Grisafi, Alan M. Lewis, Kevin Rossi, Mariana Rossi
article en
4 citations

Abstract

A current challenge in atomistic machine learning is that of efficiently predicting the response of the electron density under electric fields. We address this challenge with symmetry-adapted kernel functions that are specifically derived to account for the rotational symmetry of a three-dimensional vector field. We demonstrate the equivariance of the method on a set of rotated water molecules and show its high efficiency with respect to number of training configurations and features for liquid water and naphthalene crystals. We conclude showcasing applications for relaxed configurations of gold nanoparticles, reproducing the scaling law of the electronic polarizability with size, up to systems with more than 2000 atoms. By deriving a natural extension to equivariant learning models of the electron density, our method provides an accurate and inexpensive strategy to predict the electrostatic response of molecules and materials.

The Journal of Physical Chemistry LettersVol. 16(9)
Centre National de la Recherche Scientifique (FR), Institut Universitaire de France (FR), Sorbonne Université (FR), PHENIX laboratory (FR), Max Planck Institute for the Structure and Dynamics of Matter (DE), University of York (GB), Delft University of Technology (NL)
European Cooperation in Science and Technology, Agence Nationale de la Recherche
Openalex Percentile: Top 15%
Machine Learning in Materials Science
2.07
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