催化作用
电化学
法拉第效率
碳纤维
过氧化氢
兴奋剂
化学工程
硼
材料科学
无机化学
化学
电极
有机化学
物理化学
复合材料
工程类
复合数
光电子学
作者
Ayeong Byeon,Jae Won Choi,Hong Woo Lee,Won Chan Yun,Wenjun Zhang,Chang‐Kyu Hwang,Seung Yong Lee,Sang Soo Han,Jong Min Kim,Jae Woo Lee
标识
DOI:10.1016/j.apcatb.2023.122557
摘要
Electrochemical hydrogen peroxide (H2O2) synthesis via the two-electron oxygen reduction reaction (2e- ORR) is considered a promising alternative to the anthraquinone process due to its eco-friendliness and on-site production. Recently, although B-doped carbon (BC) has been suggested as a promising 2e- ORR catalyst, the question of whether BC can further improve catalytic activity by tuning the doping configuration and site still remains unanswered. This work demonstrates CO2-derived edge-B-doped porous carbon (E-BPC) for highly effective electrochemical H2O2 production. Herein, it is revealed that the oxygenated B-doping configurations (BCO2 and BC2O) at edge sites are responsible for enhanced 2e- ORR activity and stability. Outstanding mass activity (54.7 A g−1 at 0.65 V vs. RHE) is demonstrated with the highest high production rate in a flow reactor among the reported studies, of 24.3 mol gcat−1 h−1. The faradaic efficiency of the E-BPC was maintained (∼82%) for over 100 h without performance degradation.
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