Surface-immobilized cross-linked cationic polyelectrolyte enables CO₂ reduction with metal cation-free acidic electrolyte

Electrochemical CO2 reduction in acidic electrolytes is a promising strategy to achieve high utilization efficiency of CO2. Although alkali cations in acidic electrolytes play a vital role in suppressing hydrogen evolution and promoting CO2 reduction, they also cause precipitation of bicarbonate on the gas diffusion electrode (GDE), flooding of electrolyte through the GDE, and drift of the electrolyte pH. In this work, we realize the electroreduction of CO2 in a metal cation-free acidic electrolyte by covering the catalyst with cross-linked poly-diallyldimethylammonium chloride. This polyelectrolyte provides a high density of cationic sites immobilized on the surface of the catalyst, which suppresses the mass transport of H+ and modulates the interfacial field strength. By adopting this strategy, the Faradaic efficiency (FE) of CO reaches 953% with the Ag catalyst and the FE of formic acid reaches 76 +/- 3% with the In catalyst in a 1.0pH electrolyte in a flow cell. More importantly, with the metal cation-free acidic electrolyte the amount of electrolyte flooding through the GDE is decreased to 2.5 +/- 0.6% of that with alkali cation-containing acidic electrolyte, and the FE of CO maintains above 80% over 36h of operation at -200mA center dot cm(-2). Alkali bicarbonate precipitation hinders electrochemical CO2 reduction in acidic electrolytes. Here, the authors report CO2 reduction in a metal cation-free acidic electrolyte by covering the catalyst with crosslinked polyelectrolyte, achieving 36-hour stability in a flow cell.