Investigating the kinetics of interfacial ion transfer is imperative for the enhancement of electrochemical energy storage technologies, such as cation batteries. Consequently, we study the enigmatic proton transfer mechanisms that occur at solid-liquid interfaces to evaluate parameters that may modulate the optimization of battery efficiency. Utilizing electrochemical techniques, our objective is to deconvolute the mechanistic and rate-limiting factors associated with proton insertion from an acidic aqueous electrolyte into a thin film of tungsten trioxide (WO 3 ). While WO 3 has been investigated as a battery anode, the kinetics of cation insertion remain inadequately explored despite their effects on system efficiency. Through the Potentiostatic Intermittent Titration Technique (PITT), a developed application of chronoamperometry, along with Butler-Volmer equation fitting, our research endeavors to define the exchange current density and activation energy pertinent to cation insertion. The broader implications of exploring interfacial ion transfer phenomena manifest in advancing the fundamental understanding of energy storage processes.
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Barnard et al. (2024) studied this question.
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