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Abstract Electrochemical hydrogen peroxide (H 2 O 2 ) production (EHPP) via a two-electron oxygen reduction reaction (2e - ORR) provides a promising alternative to replace the energy-intensive anthraquinone process. M-N-C electrocatalysts, which consist of atomically dispersed transition metals and nitrogen-doped carbon, have demonstrated considerable EHPP efficiency. However, their full potential, particularly regarding the correlation between structural configurations and performances in neutral media, remains underexplored. Herein, a series of ultralow metal-loading M-N-C electrocatalysts are synthesized and investigated for the EHPP process in the neutral electrolyte. CoNCB material with the asymmetric Co-C/N/O configuration exhibits the highest EHPP activity and selectivity among various as-prepared M-N-C electrocatalyst, with an outstanding mass activity (6.1 × 10 5 A g Co −1 at 0.5 V vs. RHE), and a high practical H 2 O 2 production rate (4.72 mol g catalyst −1 h −1 cm −2 ). Compared with the popularly recognized square-planar symmetric Co-N 4 configuration, the superiority of asymmetric Co-C/N/O configurations is elucidated by X-ray absorption fine structure spectroscopy analysis and computational studies.
Liu et al. (Tue,) studied this question.
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