Review of Carbon Support Coordination Environments for Single Metal Atom Electrocatalysts (SACS)

This topical review focuses on the distinct role of carbon support coordination environment of single‐atom catalysts (SACs) for electrocatalysis. The article begins with an overview of atomic coordination configurations in SACs, including a discussion of the advanced characterization techniques and simulation used for understanding the active sites. A summary of key electrocatalysis applications is then provided. These processes are oxygen reduction reaction (ORR), oxygen evolution reaction (OER), hydrogen evolution reaction (HER), nitrogen reduction reaction (NRR), and carbon dioxide reduction reaction (CO2RR). The review then shifts to modulation of the metal atom‐carbon coordination environments, focusing on nitrogen and other non‐metal coordination through modulation at the first coordination shell and modulation in the second and higher coordination shells. Representative case studies are provided, starting with the classic four‐nitrogen‐coordinated single metal atom (MN4) based SACs. Bimetallic coordination models including homo‐paired and hetero‐paired active sites are also discussed, being categorized as emerging approaches. The theme of the discussions is the correlation between synthesis methods for selective doping, the carbon structure–electron configuration changes associated with the doping, the analytical techniques used to ascertain these changes, and the resultant electrocatalysis performance. Critical unanswered questions as well as promising underexplored research directions are identified. Carbon support single‐atom catalysts (SACs) are widely investigated in numerous electrocatalytic systems due to their high selectivity and activity from size effects and unique metal‐support interactions. This review summarizes the recent progress on carbon‐supported SACs in key electrocatalytic systems from the perspective of their coordination environment regulations that greatly affect the electrocatalytic activity and electrocatalytic selectivity.