Electrochemical upgrade of CO2 from amine capture solution

CO2 capture technologies based on chemisorption present the potential to lower net emissions of CO2 into the atmosphere. The electrochemical upgrade of captured CO2 to value-added products would be particularly convenient. Here we find that this goal is curtailed when the adduct of the capture molecule with CO2 fails to place the CO2 sufficiently close to the site of the heterogeneous reaction. We investigate tailoring the electrochemical double layer to achieve the valorization of chemisorbed CO2 in an aqueous monoethanolamine electrolyte. We reveal, using electrochemical studies and in situ surface-enhanced Raman spectroscopy, that a smaller double layer distance correlates with improved activity for CO2 to CO from amine solutions. With the aid of an alkali cation and accelerated mass transport by system design-temperature and concentration-we demonstrate amine-CO2 conversion to CO with 72% Faradaic efficiency at 50 mA cm(-2). Electrochemical conversion of CO2 into high-value products is attractive for lowering net carbon emissions. Lee et al. present the valorization of chemisorbed CO2 to CO in an aqueous monoethanolamine electrolyte via tailoring of the electrochemical double layer, with 72% Faradaic efficiency at 50 mA cm(-2).

Automated summary

CO2 capture technologies based on chemisorption have the potential to lower net emissions of CO2, with electrochemical upgrade of captured CO2 to value-added products being particularly convenient. Tailoring the electrochemical double layer in an aqueous monoethanolamine electrolyte can enhance the activity for CO2 to CO conversion from amine solutions, achieving 72% Faradaic efficiency at 50 mA cm(-2).