Relay Catalysis of Multi‐Sites Promotes Oxygen Reduction Reaction
Xuan Luo, Wenkun Wu, Youheng Wang, Youheng Wang, Yuyang Li, Yuyang Li, Jinyu Ye, Haoyu Wang, Qiaorong Jiang, Zhiyou Zhou, Yuguang Li, Yuguang Li, Yucheng Wang, Yucheng Wang, Shi‐Gang Sun
Abstract
Abstract The two‐electron pathway to form hydrogen peroxide (H 2 O 2 ) is undesirable for the oxygen reduction reaction (ORR) in iron and nitrogen doped carbon (Fe–N–C) material as it not only lowers the catalytic efficiency but also impairs the catalyst durability. In this study, a relay catalysis pathway is designed to minimize the two‐electron selectivity of Fe–N–C catalyst. Such a design is achieved by introducing two other sites, that is, MnN 4 site and α‐Fe(110) face. A combination of transmission electron microscopy image and X‐ray absorption spectra verify the three site formation. Electrochemical test coupled with post‐treatment confirm the improvement of MnN 4 site and α‐Fe(110) face on catalyst performance. Theoretical calculation proposes a relay catalysis pathway of three sites, that is, H 2 O 2 released from the FeN 4 site migrates to the MnN 4 site or α‐Fe(110) face, on which the captive H 2 O 2 is further reduced to H 2 O. The relay catalysis pathway positioned the as‐prepared catalyst among the best ORR catalysts in both aqueous electrode and alkaline direct methanol fuel cell test. This study examples an interesting relay catalysis pathway of multi‐sites for the ORR, which offers insights into the design of efficient electrocatalysts for fuel cells or beyond.