Understanding the molecular and electronic structure of electrolytes at interfaces requires an analysis of the interactions between the electrode surface, the ions, and the solvent environment on equal footing. Here, we tackle this challenge by exploring the initial stages of Cs+ hydration on a Cu(111) surface by combining experiment and theory. Remarkably, we observe "inside out" solvation of Cs ions, i.e, their preferential location at the perimeter of the water clusters on the metal surface. In addition, water-Cs complexes containing multiple Cs+ ions are observed to form at these surfaces. Established models based on maximum ion-water coordination and the double layer notion cannot account for this situation and the complex interplay of microscopic interactions is the key to a fundamental understanding.
@article{arxiv.2207.00882,
title = {Hydration at highly crowded interfaces},
author = {Christopher Penschke and John Thomas and Cord Bertram and Angelos Michaelides and Karina Morgenstern and Peter Saalfrank and Uwe Bovensiepen},
journal= {arXiv preprint arXiv:2207.00882},
year = {2023}
}