电催化剂
过氧化氢
钴
催化作用
选择性
可逆氢电极
碳纤维
化学
电解质
化学工程
材料科学
无机化学
电极
电化学
有机化学
工作电极
物理化学
复合材料
工程类
复合数
作者
Longxiang Liu,Liqun Kang,Jianrui Feng,David G. Hopkinson,Christopher S. Allen,Yeshu Tan,Hao Gu,Iuliia Mikulska,Verónica Celorrio,Diego Gianolio,Tianlei Wang,Liquan Zhang,Kaiqi Li,Jichao Zhang,Jiexin Zhu,Georg Held,Pilar Ferrer,David C. Grinter,June Callison,Martin C. Wilding
标识
DOI:10.1038/s41467-024-48209-0
摘要
Electrochemical hydrogen peroxide (H2O2) 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 × 105 A gCo-1 at 0.5 V vs. RHE), and a high practical H2O2 production rate (4.72 mol gcatalyst-1 h-1 cm-2). Compared with the popularly recognized square-planar symmetric Co-N4 configuration, the superiority of asymmetric Co-C/N/O configurations is elucidated by X-ray absorption fine structure spectroscopy analysis and computational studies.
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