Porous Electrodeposited Cu as a Potential Electrode for Electrochemical Reduction Reactions of CO2

In the present study, a systematic investigation is performed to assess the relationship between electroplating parameters, pore morphology and internal surface area of copper deposits which are promising to serve as electrodes for electrochemical reduction reactions of carbon dioxide (CO2). A set of porous copper deposits are fabricated with the dynamic hydrogen bubble template method. The microstructural and Brunauer-Emmett-Teller (BET) analysis demonstrate that current density, deposition time, and bath composition control pore size, strut size, and hence surface area which could be as high as 20 m(2)/g. Selected sets of porous copper electrodes are then employed in the electrochemical reduction reaction test to determine their conversion performance in comparison to a monolithic copper surface. From the gas chromatography (GC) and nuclear magnetic resonance (NMR) analysis, porous copper is shown to provide higher rates of production of some important chemicals, as compared to copper foil electrodes. Porous copper with fern-like morphology serves as a promising electrode that yields relatively high amounts of acetaldehyde, acetate and ethanol. The study thus presents the opportunities to enhance the electrochemical reduction reaction of CO2 through microstructural engineering of the copper surface, which benefits both CO2 reduction and generation of chemical products of high value.

Automated summary

This study systematically investigates the relationship between electroplating parameters and the pore morphology and internal surface area of copper deposits for electrochemical reduction reactions of CO2. Through microstructural engineering, porous copper electrodes were found to yield higher production rates of acetaldehyde, acetate, and ethanol compared to copper foil electrodes, presenting opportunities for enhancing CO2 reduction reactions.