Short-Range Solvent-Solvent and Ion-Solvent Correlations at Metal-Electrolyte Interfaces: Parameterization and Benchmarking

Abstract

Short-range correlations in electrolyte solutions lead to oscillatory profiles of water polarization and ionic concentration at electrode-electrolyte interfaces. The recently developed density-potential-polarization functional theory (DPPFT) provides a comprehensive framework to incorporate these short-range correlation effects. In the present work, the parameters describing short-range solvent-solvent and ion-solvent correlations in DPPFT are determined from the wavenumber-dependent dielectric susceptibility spectrum of pure water and from ion solvation energies derived within nonlocal electrostatics, respectively. The experimental ionic-radius-dependent hydration energies of alkali metal cations and halide anions are well reproduced by the solvation model. The charge hydration asymmetry is explained as the stronger short-range repulsion between cations and water molecules compared to that between anions and water molecules. Using these parameters, DPPFT is then applied to investigate short-range correlation effects at the Ag(111)-NaF aqueous electrolyte interface. The water polarization profiles obtained from DPPFT calculations agree with AIMD simulations. Furthermore, as the strength of short-range ion-solvent repulsion increases, the peaks of anionic/layers shift from regions near centers of positive/negative polarization charges toward those of opposite sign, thereby preserving solvation configurations similar to those in bulk solution. This work develops a consistent procedure for parameterizing short-range correlation effects within the DPPFT framework, thereby enabling a more quantitative and computationally efficient description of atomic-scale phenomena at electrochemical interfaces.