LAUSR

Developing nonflammable electrolytes with wide electrochemical windows is of great importance for energy storage devices. Water-in-salt electrolytes (WiSE) have attracted great interests due to their widely opened electrochemical windows and high stability. Previous theoretical investigations have revealed changes in solvation shell of water molecules result in opening of HOMO-LUMO gaps of water, leading to the formation of an anion-derived solid-electrolyte-interphase (SEI) in WiSE. However, how solvation structures affect electrochemical windows at atomic level is still a puzzle, which hinders optimization and design of aqueous electrolytes. Herein, machine learning molecular dynamics and free energy calculation method are applied to compute redox potentials of anions of Li-salts and water of aqueous electrolytes at a range of salt concentrations. Furthermore, an analysis based on local solvation structures is employed to demonstrate the structure-property relations. Our calculation shows that the hydrogen evolution reaction is impeded in WiSE due to switching of the order of redox levels of the anion and H2O, leading to formation of SEI and high reductive stability. Level switching is caused by the special solvation environments of isolated water molecules. Our work provides new insight into the electrochemistry of aqueous electrolytes which would benefit the electrolyte design in energy storage devices.