Mechanistic Insights into the Enhanced Activity and Stability of Agglomerated Cu Nanocrystals for the Electrochemical Reduction of Carbon Dioxide to n-Propanol

Abstract

The reduction of carbon dioxide (CO2) to n-propanol (CH3CH2CH2OH) using renewable electricity is a potentially sustainable route to the production of this valuable engine fuel. In this study, we report that agglomerates of ∼15 nm sized copper nanocrystals exhibited unprecedented catalytic activity for this electrochemical reaction in aqueous 0.1 M KHCO3. The onset potential for the formation of n-propanol was 200-300 mV more positive than for an electropolished Cu surface or Cu(0) nanoparticles. At -0.95 V (vs RHE), n-propanol was formed on the Cu nanocrystals with a high current density (jn-propanol) of -1.74 mA/cm(2), which is ∼25× larger than that found on Cu(0) nanoparticles at the same applied potential. The Cu nanocrystals were also catalytically stable for at least 6 h, and only 14% deactivation was observed after 12 h of CO2 reduction. Mechanistic studies suggest that n-propanol could be formed through the C-C coupling of carbon monoxide and ethylene precursors. The enhanced activity of the Cu nanocrystals toward n-propanol formation was correlated to their surface population of defect sites.