Accelerated O2 adsorption and stabilized *OOH for electrocatalytic H2O2 production

被引:1
|
作者
Deng, Danni [1 ]
Wang, Jinxian [1 ]
Wang, Meng [1 ]
Wang, Yuchao [1 ]
Jiang, Jiabi [1 ]
Chen, Yingbi [1 ]
Bai, Yu [1 ]
Wu, Qiumei [1 ]
Lei, Yongpeng [1 ]
机构
[1] Cent South Univ, State Key Lab Powder Met, Changsha 410083, Peoples R China
关键词
Pyrrolic nitrogen; Electrocatalytic hydrogen peroxide; production; Two-electron oxygen reduction reaction; Non-metal; *OOH intermediates; 2-ELECTRON OXYGEN REDUCTION; HYDROGEN-PEROXIDE; EFFICIENT; ELECTROSYNTHESIS; CATALYSTS; SITES;
D O I
10.1016/j.jmst.2024.12.017
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Electrocatalytic hydrogen peroxide (H2O2) production via the two-electron oxygen reduction reaction (2e- ORR) is promising, but non-metal catalysts with high selectivity are lacking. Herein, a high content of pyrrolic N doped carbon (HPNC) with small mesopores is constructed. Over 80 % H2O2 selectivity at a wide potential of 0.2-0.6 V is achieved. The finite element simulation reveals that small pore-size mesopores are beneficial to O2 adsorption. And in-situ characterization proves that HPNC suppresses the breakage of O-O bond and enhances the stabilization of *OOH intermediates, thus improving the 2e- ORR performance. This work highlights the combination of non-metal active sites and geometry for 2e- ORR electrocatalysis. (c) 2025 Published by Elsevier Ltd on behalf of The editorial office of Journal of Materials Science & Technology.
引用
收藏
页码:76 / 81
页数:6
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