Towards Direct Electroanalysis in Seawater: Understanding the Role of the Buffer Capacity of Seawater in Proton-Coupled Electron Transfer Reactions

The study of electrochemical reactions in seawater requires understanding of the associated coupled chemistry with the components of seawater, especially the role of the carbonate-bicarbonate buffer system in the case of proton-coupled electron transfer reactions. We report the comparative paradigmatic voltam-metric response of the reversible hydrogen oxidation reaction in the absence or presence of dibasic phosphate, formate, or bicarbonate. Electrochemically and chemically reversible voltammetry is seen in aqueous 0.7 M NaCl at platinum macroelectrodes in the absence of a buffer, while the presence of chemically stable buffer systems, such as phosphate or formate, leads either to a cathodic shift in the oxidation potential for high buffer concentrations or to a split wave for concentrations approximately a factor of 2 less than the dissolved H-2. In the case of bicarbonate buffer, the dehydration of carbonic acid on the voltammetric timescale leads to chemically irreversible voltammetric behavior, with a similar response measured in authentic seawater. Numerical simulations based on a simple Nernstian model with literature values for kinetic and thermodynamic parameters are reported, which display excellent agreement with the experiment.

Automated summary

This study explores the electrochemical reactions in seawater, focusing on the coupled chemistry with the components of seawater, especially the role of the carbonate-bicarbonate buffer system in proton-coupled electron transfer reactions. The presence or absence of various buffer systems, such as phosphate, formate, or bicarbonate, influences the voltammetric response of reversible hydrogen oxidation reactions. The research findings are supported by numerical simulations based on a simple Nernstian model, showing excellent agreement with experimental results.