Promoting the Electrocatalytic Reduction of CO 2 on Ultrathin Porous Bismuth Nanosheets with Tunable Surface-Active Sites and Local pH Environments

Electrochemical CO reduction reaction (CO RR) yielding value-added chemicals provides a sustainable approach for renewable energy storage and conversion. Bismuth-based catalysts prove to be promising candidates for converting CO and water into formate but still suffer from poor selectivity and activity and/or sluggish kinetics. Here, we report that ultrathin porous Bi nanosheets (Bi-PNS) can be prepared through a controlled solvothermal protocol. Compared with smooth Bi nanoparticles (Bi-NPs), the ultrathin, rough, and porous Bi-PNS provide more active sites with higher intrinsic reactivities for CO RR. Moreover, such high activity further increases the local pH in the vicinity of the catalyst surfaces during electrolysis and thus suppresses the competing hydrogen evolution reaction. As a result, the Bi-PNS exhibit significantly boosted CO RR properties, showing a Faradaic efficiency of 95% with an effective current density of 45 mA cm for formate evolution at the potential of -1.0 V versus reversible hydrogen electrode.