4.7 Article

A highly stable microporous boron-doped diamond electrode etched by oxygen plasma for enhanced electrochemical ozone generation

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.jece.2021.106369

关键词

Boron-doped diamond; Oxygen plasma etching; Electrochemical ozone generation; Microporous structure

资金

  1. National Key Research and Development Program of China [2016YFB0301400]
  2. National Natural Science Foundation of China [52071345, 51874370]
  3. Key Research and Development Program of Guangdong Province [2020B010185001]
  4. Natural Science Foundation of Hunan Province [2019JJ40375, 2019JJ50793]
  5. State Key Laboratory of Powder Metallurgy

向作者/读者索取更多资源

The study introduces a microporous BDD electrode etched by oxygen plasma (p-BDD) to enhance electrochemical ozone generation performance, with optimized etching parameters and significantly improved electrochemically active surface area and charge transfer resistance compared to bare BDD, resulting in 3.76 times higher ozone generation capacity under the same unit energy consumption.
The boron-doped diamond (BDD) electrode, having ultra-high oxygen evolution potential and anodic stability, is potentially considered the ideal candidate for the next-generation ozone generator despite the relatively low current efficiency. In this work, we first report using a microporous BDD electrode etched by oxygen plasma, denoted as p-BDD, to improve the performance of electrochemical ozone generation. Two parameters, including O-2 plasma etching temperature and time, are experimentally optimized. We demonstrated that the electrochemically active surface area (ECSA) of the optimal p-BDD is 2.51 times that of the bare BDD, and this p-BDD shows about one-quarter lower charge transfer resistance than the latter. Under the same unit energy consumption, the p-BDD has 3.76 times the ozone generation capacity compared to the latter. The p-BDD shows excellent long-term stability, only having 4.2% of the decrease in the current density up to 40 h of consecutive water electrolysis under the steady-state period, and it also remains a 100% recovery rate in its capability of electrochemical performance after mild treatment by cycling at a diluted sulfuric acid solution for 200 s

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