Investigates oxygen evolution efficiency in manganese-based catalysts, highlighting new design insights.
A series of Ni and Co codoped manganese dioxide catalysts with varying Ni/Co ratios were prepared via a two-step hydrothermal-assisted calcination process, in which Birnessite-type δ-MnO 2 precursors were first synthesized hydrothermally and then calcined at different temperatures. The optimally performing Ca-NCMO11–500 (Ni/Co = 1:1, calcined at 500 °C) was identified. Systematic investigations revealed that bimetallic doping modulates the local structure and electronic states of the manganese oxide framework. The Ca-NCMO11–500 catalyst exploits Ni–Co synergistic effects to activate lattice oxygen and promote O–O coupling, resulting in superior oxygen evolution reaction activity. Electrochemical measurements demonstrate that Ca-NCMO11–500 achieves 50 mA cm –2 at an overpotential of 237 mV and maintains excellent durability with negligible activity loss over 300 h at 400 mA cm –2 . This study elucidates the microscopic mechanism by which Ni and Co codoping strengthens metal–oxygen bonds and enhances lattice oxygen reactivity, providing a rational basis for the design of high-performance manganese-based electrocatalysts.
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Wei et al. (2026) studied this question.
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