Identification and Understanding of Active Sites of Non‐Noble Iron‐Nitrogen‐Carbon Catalysts for Oxygen Reduction Electrocatalysis

Non‐noble iron‐nitrogen‐carbon (Fe‐N‐C) catalysts have been explored as one type of the most promising alternatives of precious platinum (Pt) in catalyzing the oxygen reduction reaction (ORR). However, their catalytic ORR activity and stability still cannot meet the requirement of practical applications. Active sites in such catalysts are the key factors determining the catalytic performance. This review gives a critical overview on identification and understanding of active sties of non‐pyrolytic and pyrolytic Fe‐N‐C catalysts in terms of design strategies, synthesis, characterization, functional mechanisms and performance validation. The diversity and complexity of active sites that greatly dominate the progress of Fe‐N‐C catalysts include Fe‐containing sites (Fe‐based nanoparticles and single‐atom Fe‐species) and metal‐free sites (heteroatoms doping and defects). Meanwhile, synergistic effects are also discussed in this review with emphasis on the interaction among multiple active sites. Although substantial endeavors have been devoted to develop the efficient Fe‐N‐C catalysts, some challenges still remain. To facilitate further research on Fe‐N‐C catalysts toward practical applications, some research perspectives are prospected in the aspects of innovative synthesis methods, active‐sites modulation strategies, high‐resolution ex situ/in situ/operando characterization techniques, theoretical calculations, and so on. This review may provide a guideline for identifying and understanding active‐sites for developing high‐performance Fe‐N‐C catalysts. Z. Yang, Y. Chen, S. Zhang, J. Zhang Non‐noble iron‐nitrogen‐carbon (Fe‐N‐C) catalysts have been considered as one of the most promising alternatives of precious platinum (Pt) in catalyzing the oxygen reduction reaction. This review summarizes the identification and understanding of active sites in non‐pyrolytic and pyrolytic Fe‐N‐C catalysts by advanced design strategies for the expected highly‐efficient oxygen reduction electrocatalysis.