Classical theory of electron-ion correlations at electrochemical interfaces: Closing the circuit from double-layer charging to ion adsorption
Nils Bruch, Michael Eikerling, Tobias Binninger

TL;DR
This paper develops a classical, first-principles theory of the electric double layer at electrochemical interfaces that incorporates electron-ion correlations, unifying double-layer charging and ion adsorption phenomena, and aligns well with experimental data.
Contribution
It introduces a correlation-inclusive classical theory derived from statistical mechanics that extends beyond mean-field models for better accuracy.
Findings
Quantitative agreement with experimental capacitance data
Unification of double-layer charging and ion adsorption
Resolution of discrepancies in traditional models
Abstract
The electric double layer (EDL) that forms at the interface between metals and ionic solutions is at the heart of various energy technologies. Recent experimental data have challenged our traditional understanding of the EDL charging behavior, which is based on mean-field Gouy-Chapman-Stern-type (GCS) models. In this article, we present a classical theory for the EDL, derived from first-principles statistical mechanics, that accounts for electron-ion correlation effects using the method of image charges and systematically extends beyond the mean-field level. Such electron-ion correlations introduce an additional interaction between the metal surface and electrolyte ions, significantly altering the EDL structure. Our theory, valid in the limit of dilute electrolyte solutions and weakly charged metal surfaces, achieves quantitative agreement with experimental capacitance data across a…
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