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Hydrolysis of Electrolyte Cations Enhances the Electrochemical Reduction of CO2 over Ag and Cu

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posted on 18.11.2017 by Meenesh R. Singh, Youngkook Kwon, Yanwei Lum, Joel W. Ager III, Alexis T. Bell
Electrolyte cation size is known to influence the electrochemical reduction of CO2 over metals; however, a satisfactory explanation for this phenomenon has not been developed. We report here that these effects can be attributed to a previously unrecognized consequence of cation hydrolysis occurring in vicinity of the cathode. With increasing cation size, the pKa for cation hydrolysis decreases and is sufficiently low for hydrated K+ , Rb+ , and Cs+ to serve as buffering agents. Buffering lowers the pH near the cathode leading to an increase in the local concentration of dissolved CO2. The consequences of these changes are an increase in cathode activity, a decrease in Faradaic efficiencies for H2 and CH4 and an increase in Faradaic efficiencies for CO, C2H4, and C2H5OH in full agreement with experimental observations for CO2 reduction over Ag and Cu.

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Publisher Statement

Post print version of article may differ from published version. The definitive version is available through American Chemical Society at DOI:10.1021/jacs.6b07612

Publisher

American Chemical Society

issn

00027863

Issue date

05/10/2016

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