The Differential Capacitance as a probe for the electric double layer structure and the electrolyte bulk composition

TL;DR

This study uses classical Density Functional Theory to show how differential capacitance measurements can reveal detailed information about the electric double layer and electrolyte composition, especially the influence of trace divalent ions.

Contribution

It introduces a new expression for differential capacitance derived from mechanical equilibrium, emphasizing the role of the first ion layer near the electrode.

Findings

Trace divalent ions significantly affect capacitance.

Small ions dominate behavior at high electrode potentials.

New theoretical expression links capacitance to ion layer structure.

Abstract

In this work we theoretically study the differential capacitance of an aqueous electrolyte in contact with a planar electrode, using classical Density Functional Theory, and show how this measurable quantity can be used as a probe to better understand the structure and composition of the electric double layer at play. Specifically, we show how small trace amounts of divalent ions can influence the differential capacitance greatly, and also how small ions dominate its behaviour for high electrode potentials. In this study, we consider primitive model electrolytes, and not only use the standard definition of the differential capacitance, but also derive a new expression from mechanical equilibrium in a planar geometry. This expression reveals explicitly that the first layer of ions near the charged surface is key to its understanding. Our insights might be used as a guide in experiments to better understand the electrolyte-electrode interface as well as the (composition of the) bulk electrolyte.