Cross-Linked Double-Active Centers for Efficient pH-Universal Oxygen Reduction Catalysis

Effective adjustment of the internal electron spin state and the external charge density of the metal is considered important for improving the catalytic activity of metal-nitrogen complex carbon (M/NC) electrocatalysts. Herein, we synthesize a FeMn/NC dual-atom catalyst with a local structure of FeN4–MnN4, which exhibits excellent oxygen reduction reaction (ORR) activity in acidic, neutral, and alkaline environments. In addition, the Zn–air battery based on the FeMn/NC catalyst has a high open-circuit voltage (1.27 V vs RHE), a satisfactory output power density (129 mW cm–2), and a strong charge and discharge stability (500 cycles), all of which are superior to those of commercial Pt/C. Such splendid catalytic performance is due to the change in the charge environment and the transition of the 3d orbital spin state at the metal center. Moreover, density functional theory calculations further demonstrate that the bimetallic synergy mechanism can optimize the adsorption energy of intermediates and improve the ORR efficiency. This work provides a new insight into the rational design of bimetallic catalysts with extraordinary comprehensive ORR capability.