DPχ: Constant-Potential Machine-Learning Potentials for Large-Scale Electrocatalysis
We introduce DPχ, a machine-learning potential that enables electrocatalysis simulations at spatiotemporal scales 10^3-10^4 beyond AIMD while retaining near first-principles accuracy. DPχ adopts a Bader-basin-centroid (BC) representation and explicitly decomposes interfacial charge into a neural-predicted chemical component and a conductor component confined to metal sites. The conductor charges are determined on-the-fly by a Siepmann-Sprik-type polarizable-electrode model under an electroneutrality constraint, which adaptively apportions charge between electrodes and yields constant-potential dynamics without imposing the Fermi level. Replacing Wannier-center sites with BCs preserves the far-field accuracy of Wannier-based schemes while permitting fractional charge transfer across electrified metal-water interfaces. On Pt(111)-H2O, DPχ reproduces DFT-level forces, electrode potential, hydrogen-evolution barriers, and vibrational spectra, opening a route to predictive electrocatalysis under realistic conditions.
Authors
- Tao Wang (ORCID: https://orcid.org/0000-0002-3013-1947)
- Junxiang Chen (ORCID: https://orcid.org/0000-0003-3047-0030)
Institutions
- Xiamen University (CN)
- Fujian Institute of Research on the Structure of Matter (CN)
Publication Details
- Journal
- ChemRxiv
- Published
- 2025-08-30
- DOI
- https://doi.org/10.26434/chemrxiv-2025-6vcnc
- Primary Topic
- Machine Learning in Materials Science
- Type
- article
- Field-Weighted Citation Impact
- 0.00