Exclusive Ni-N4 Sites Realize Near-Unity CO Selectivity for Electrochemical CO2 Reduction

Electrochemical reduction of carbon dioxide (CO2) to value-added carbon products is a promising approach to reduce CO2 levels and mitigate the energy crisis. However, poor product selectivity is still a major obstacle to the development of CO2 reduction. Here we demonstrate exclusive Ni-N-4 sites through a topochemical transformation strategy, bringing unprecedentedly high activity and selectivity for CO2 reduction. Topochemical transformation by carbon layer coating successfully ensures preservation of the Ni-N4 structure to a maximum extent and avoids the agglomeration of Ni atoms to particles, providing abundant active sites for the catalytic reaction. The Ni-N4 structure exhibits excellent activity for electrochemical reduction of CO2 with particularly high selectivity, achieving high faradaic efficiency over 90% for CO in the potential range from -0.5 to -0.9 V and gives a maximum faradaic efficiency of 99% at -0.81 V with a current density of 28.6 mA cm(-2). We anticipate exclusive catalytic sites will shed new light on the design