Carbon-Supported Single Metal Site Catalysts for Electrochemical CO2 Reduction to CO and Beyond

The electrochemical CO2 reduction reaction (CO2RR) is a promising strategy to achieve electrical-to-chemical energy storage while closing the global carbon cycle. The carbon-supported single-atom catalysts (SACs) have great potential for electrochemical CO2RR due to their high efficiency and low cost. The metal centers' performance is related to the local coordination environment and the long-range electronic intercalation from the carbon substrates. This review summarizes the recent progress on the synthesis of carbon-supported SACs and their application toward electrocatalytic CO2 reduction to CO and other C-1 and C-2 products. Several SACs are involved, including MNx catalysts, heterogeneous molecular catalysts, and the covalent organic framework (COF) based SACs. The controllable synthesis methods for anchoring single-atom sites on different carbon supports are introduced, focusing on the influence that precursors and synthetic conditions have on the final structure of SACs. For the CO2RR performance, the intrinsic activity difference of various metal centers and the corresponding activity enhancement strategies via the modulation of the metal centers' electronic structure are systematically summarized, which may help promote the rational design of active and selective SACs for CO2 reduction to CO and beyond.

Automated summary

This passage describes the application of carbon-supported single-atom catalysts in the electrochemical CO2 reduction reaction, and summarizes research progress on synthesis methods, intrinsic activity differences of metal centers, and strategies for enhancing activity.