过氧化氢
杂原子
法拉第效率
化学
电解质
电催化剂
电解
无机化学
碳纤维
材料科学
析氧
可逆氢电极
氮气
电极
电化学
有机化学
工作电极
烷基
复合材料
物理化学
复合数
作者
Junyu Zhang,Gong Zhang,Shengyao Jin,Yujun Zhou,Qinghua Ji,Huachun Lan,Huijuan Liu,Jiuhui Qu
出处
期刊:Carbon
[Elsevier BV]
日期:2020-03-09
卷期号:163: 154-161
被引量:188
标识
DOI:10.1016/j.carbon.2020.02.084
摘要
Electrocatalytic two-electron oxygen reduction reaction (2e− ORR) is a promising strategy to achieve hydrogen peroxide (H2O2) production, which can replace the anthraquinone method in industrial processes. Nitrogen-doped carbon materials are active and selective electrocatalysts for 2e− ORR; however, it remains challenging to develop N-doped carbons for practical H2O2 production and pinpoint the exact role of nitrogen functionalities. Here, we examine covalent organic framework-derived nitrogen-doped carbons with well-defined porous structure and tunable N species for electrocatalytic H2O2 production. Electrochemical studies show their highest ORR activity and H2O2 selectivity of up to 75% in alkaline electrolyte. Notably, chronoamperometric bulk electrolysis achieves an unprecedented carbon-catalyzed H2O2 yield rate of 1286.9 mmol gcatalyst−1 h−1 and a faradaic efficiency of 69.8% at pH 13. X-ray photoelectron spectroscopy analysis combined with control experiments reveals that graphitic N is responsible for H2O2 production from 2e− ORR on N-doped carbons. Our work provides insights into the rational development of heteroatom-doped carbon electrocatalysts for efficient H2O2 generation.
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