Source data: Distinct solvation patterns of OH− versus H3O+ charge defects at electrified gold/water interfaces govern their properties

This dataset is meant to give access to the source data for other researchers to enable comparison and further research into this topic. Understanding the solvation structures of OH– and H3O+ at metal interfaces is crucial for developing efficient electrochemical devices.

In this paper, we present a detailed investigation of the solvation structures of OH– and H3O+ near gold electrodes under alkaline and acidic aqueous conditions, using ab initio molecular dynamics simulations at controlled surface charge density conditions. Our findings reveal that the adsorption tendencies of OH– and H3O+ are strongly influenced by the oscillating net atomic charge of water normal to the electrified interface in concert with the distinct solvation patterns of these charge defects.