电合成
过氧化氢
析氧
法拉第效率
电化学
材料科学
电催化剂
阳极
化学
硼
纳米技术
兴奋剂
分解水
催化作用
制氢
化学工程
电极
无机化学
光电子学
光催化
物理化学
有机化学
工程类
作者
Sotirios Mavrikis,Maximilian Göltz,Samuel C. Perry,Felix Bogdan,Puiki Leung,Stefan Rosiwal,Ling Wang,Carlos Ponce de León
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2021-06-03
卷期号:6 (7): 2369-2377
被引量:100
标识
DOI:10.1021/acsenergylett.1c00904
摘要
The two-electron water oxidation reaction (2e– WOR) is progressively gaining traction as a sustainable approach for in situ electrosynthesis of hydrogen peroxide (H2O2). State-of-the-art 2e– WOR electrocatalysts have shown great promise at low electrical currents yet exhibit diminished electrocatalytic capabilities at larger current densities. Herein, by tailoring the boron doping level of boron-doped diamond (BDD) microfilms, we have fabricated an active, selective, and stable electrocatalyst for the 2e– WOR. Experimentally, we find that our modulated BDD films achieve a peak faradaic efficiency of 87%, as well as a record H2O2 production rate of 76.4 μmol cm–2 min–1, while maintaining a stable electrochemical performance for 10 h at 200 mA cm–2 in carbonate-based solutions. The results reported in this work firmly establish BDD as a primary catalyst candidate for large-scale implementation of the 2e– WOR and synchronously unlock new research avenues for the next-generation design of sp3-structured carbonaceous materials for anodic H2O2 electrosynthesis from water.
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