4.6 Article

Promoting the Electrochemical Water Oxidation Reaction to H2O2 via Bubbles on the Electrode

期刊

ACS SUSTAINABLE CHEMISTRY & ENGINEERING
卷 11, 期 28, 页码 10264-10273

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.3c00630

关键词

surface bubbles; corona; two-electronwateroxidation reaction; electrosynthesis; hydrogen peroxide

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Surface bubbles on the electrode can greatly enhance the electrosynthesis of hydrogen peroxide by a two-electron water oxidation reaction. Contrary to previous assumptions, surface bubbles actually improve the electrochemical reaction due to the high concentration of OH- accumulated by the bubbles. By designing aerophilic PVDF-coated CFP electrodes, the residence time of surface bubbles was prolonged, leading to an increase in 2e-WOR selectivity from 16.3% to 62.5% and a high H2O2 generation rate of 28.4 μmol min(-1) cm(-2). This study challenges conventional thinking about the impact of bubbles on electrodes and provides a theoretical guideline for designing 2-WOR catalysts.
Surfacebubbles on the electrode can significantly improvethe electrosynthesis of hydrogen peroxide by a two-electron wateroxidation reaction. Surfacebubbles on electrodes generated via gas evolution reactionare generally considered harmful to the desired electrochemical reactionas they reduce the electrochemically active area and increase energyconsumption. However, it is shown herein that surface bubbles on theelectrode can significantly improve the electrosynthesis of hydrogenperoxide (H2O2) by a two-electron water oxidationreaction (2e-WOR) due to the high concentration of OH- accumulated by the corona of the bubbles. Inspired by this understanding,aerophilic PVDF-coated CFP electrodes were designed to prolong theresidence time of the in situ generated surface bubbles to improvetheir 2e-WOR selectivity from 16.3 to 62.5%, and the H2O2 generation rate was as high as 28.4 & mu;mol min(-1) cm(-2). This study subverts long-heldassumptions about the effect of the bubbles on the electrode towardelectrochemical reaction and provides a theoretical guideline fordesigning 2-WOR catalysts.

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