Ionic Associations and Hydration in the Electrical Double Layer of Water-in-Salt Electrolytes

TL;DR

This paper develops a theory for the electrical double layer in Water-in-Salt Electrolytes, accounting for ionic associations and validating predictions with molecular dynamics simulations and electrochemical measurements.

Contribution

The study introduces a novel theoretical framework for the EDL of WiSEs that includes thermoreversible ionic associations and validates it with simulations and experiments.

Findings

Asymmetric EDL structure predicted by the theory.

Hydrated Li+ clusters are enhanced at negative voltages and diminished at positive voltages.

Good qualitative agreement between theory, MD simulations, and electrochemical measurements.

Abstract

Water-in-Salt-Electrolytes (WiSEs) are an exciting class of concentrated electrolytes finding applications in energy storage devices because of their expanded electrochemical stability window, good conductivity and cation transference number, and fire-extinguishing properties. These distinct properties are thought to originate from the presence of an anion-dominated ionic network and interpenetrating water channels for cation transport, which indicates that associations in WiSEs are crucial to understanding their properties. Currently, associations have mainly been investigated in the bulk, while little attention has been given to the electrolyte structure near electrified interfaces. Here, we develop a theory for the electrical double layer (EDL) of WiSEs, where we consistently account for the thermoreversible associations of species into Cayley tree aggregates. The theory predicts an asymmetric structure of the EDL. At negative voltages, hydrated Li$^+$ dominate and cluster aggregation is initially slightly enhanced before disintegration at larger voltages. At positive voltages when compared to the bulk, clusters are strictly diminished. Performing atomistic molecular dynamics (MD) simulations of the EDL of WiSE provides EDL data for validation and bulk data for parameterization of our theory. Validating the predictions of our theory against MD showed good qualitative agreement. Furthermore, we performed electrochemical impendence measurements to determine the differential capacitance of the studied LiTFSI WiSE and also found reasonable agreement with our theory. Overall, the developed approach can be used to investigate ionic aggregation and solvation effects in the EDL, which amongst other properties, can be used to understand the pre-cursers for solid-electrolyte interphase formation.