Surface Co-Modification of Halide Anions and Potassium Cations Promotes High-Rate CO₂ -to-Ethanol Electrosynthesis

The high-rate electrochemical CO₂ conversion to ethanol with high partial current density is attractive but challenging, which requires competing with other reduction products as well as hydrogen evolution. This work demonstrates the in situ reconstruction of KCuF₃ perovskite under CO₂ electroreduction conditions to fabricate a surface fluorine-bonded, single-potassium-atom-modified Cu(111) nanocrystal (K-F-Cu-CO₂ ). Density functional theory calculations reveal that the co-modification of both F and K atoms on the Cu(111) surface can promote the ethanol pathway via stabilization of the CO bond and selective hydrogenation of the CC bond in the CH₂ CHO* intermediate, while the single modification of either F or K is less effective. The K-F-Cu-CO₂ electrocatalyst exhibits an outstanding CO₂ -to-ethanol partial current density of 423 ± 30 mA cm^-2 with the corresponding Faradaic efficiency of 52.9 ± 3.7%, and a high electrochemical stability at large current densities, thus suggesting an attractive means of surface co-modification of halide anions and alkali-metal cations on Cu catalysts for high-rate CO₂ -to-ethanol electrosynthesis.