Dynamic restructuring induced Cu nanoparticles with ideal nanostructure for selective multi-carbon compounds production via carbon dioxide electroreduction

Production of multi-carbon (C 2+ ) products via electrochemical CO 2 reduction reaction (CO 2 RR) has aroused intensive interest in this decade. However, it is still a great challenge in large-scale synthesis of electrocatalysts for C 2+ compounds production with high selectivity and rate in neutral electrolyte. In this study, a robust and scalable aqueous synthesis method was proposed to prepare CuO nanosheets, which was directly used as CO 2 RR electrocatalyst. The catalyst underwent dynamic restructuring during the pre-reduction stage, which significantly changed the morphology, crystalline structure and electrochemical properties of the catalyst. As a result, the pristine CuO nanosheets gradually evolved to coral-like Cu nanoparticle ensembles (CL-Cu NEs). In 0.1 M KHCO 3 at −1.1 V vs. RHE, the CL-Cu NEs exhibited a faradaic efficiency and partial current density of C 2+ products of 72.1% and 25.2 mA cm −2 respectively and no degradation was observed in 15 h running. In contrast to many Cu-based catalysts showing considerable C 2+ products selectivity, the (sub)surface oxygen and Cu + species were unlikely to play a significant role in this study. The strong performance of CL-Cu NEs was ascribed to the synergism between the coral-like morphology and abundant Cu(1 0 0)/Cu(1 1 1) interfaces. This methodology may provide a cost-effective approach for large-scale preparation of CO 2 RR electrocatalysts with ideal nanostructure.