Regulating Asymmetric C–C Coupling with Interfacial Alkalinity for Efficient CO2 to C2+ Electroconversion

Abstract The electrocatalytic reduction of CO 2 in neutral electrolytes is a promising avenue to minimize energy losses linked to carbonate formation. However, selectivity for multi‐carbon (C 2+ ) products is hampered by kinetic barriers in C–C coupling. Here, the regulation of asymmetric C–C coupling is achieved with interfacial alkalinity, facilitating efficient CO 2 to C 2+ electroconversion. This is realized by co‐engineering copper electrodes with ZrO 2 sites and CeO x sites to enable a favorable microenvironment that greatly boosts intrinsic catalytic activity. In situ spectroscopic results and theoretical analyses demonstrates that CeO x facilitates the dissociation of H 2 O into *H and *OH, effectively regulating *H coverage at the catalytic interface and promoting the protonation of *CO to *COH. Meanwhile, ZrO 2 sites significantly enhance the adsorption of in situ‐produced *OH, optimize the local pH on the Cu surface, and enable the formation of C 2+ products via a low‐energy *OC–COH coupling pathway. A notable CO 2 to C 2+ electroconversion in 1.0 M KCl electrolyte, with Faraday efficiency of 67.2 ± 2.1% and a partial current density of 413.0 ± 9.9 mA cm −2 is achieved. This synergistic enhancement of hydroxyl adsorption and stabilization at the catalytic interface, driven by the activation of H 2 O, is crucial for boosting the overall catalytic performance of the system.