Metal-Free Electrocatalysts for H2O2 Electrosynthesis: From Sites Identification to Electrochemical Advanced Oxidation Process

IF 3.9 3区 化学 Q2 CHEMISTRY, PHYSICAL ChemCatChem Pub Date : 2025-01-22 DOI:10.1002/cctc.202401889
Yu Chen, Yajing Di, Haixing Zhang, Yiming An, Jie Miao, Hui Wang, Prof. Jing Ji, Prof. Zhilin Li, Prof. Masatsugu Fujishige, Prof. Morinobu Endo, Prof. Zhengping Zhang, Prof. Feng Wang
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Abstract

Carbonaceous materials, especially the metal-free carbons, have attracted widespread attention owing to their risk-free nature with metal dissolving during the electrocatalysis process, but their further developments are still hindered by missing a suitable scenario on practical applications. Herein, we demonstrate a successful case of using the oxygen-containing-groups-modified carbons for the H2O2 electrosynthesis and the derivative electrochemical advanced oxidation process. The active sites with the more C─O rather than C═O groups are easily obtained by controlling the temperature and time in the wet chemical treatment. Identified by theoretical calculations and electrochemical testing, the modified carbons with the highest ratio of C─O/C═O groups exhibit high activity with above 90% H2O2 selectivity over the entire potential during 2e-transfer oxygen reduction reaction, attributing to their enlarged charge delocalization. In addition, the corresponding gas diffusion electrodes with the high-speed and high-stability H2O2 electrosynthesis (2.78 µg s−1 cm−2 with the above 80% current efficiency) are applied for the electro-peroxone process on the simulant and practical phenolic wastewater, where the chemical oxygen demand removal reaches above 90%. The long-term operation in the harsh electrochemical environment for over 200 h also confirms its great potential for practical electrochemical applications.

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无金属电催化剂用于H2O2电合成:从位点识别到电化学高级氧化过程
碳质材料,特别是无金属碳,由于其在电催化过程中无金属溶解的特性而受到广泛关注,但由于缺乏合适的实际应用场景,其进一步发展仍然受到阻碍。在此,我们展示了一个使用含氧基团修饰碳进行H2O2电合成及其衍生的电化学高级氧化过程的成功案例。在湿化学处理中,通过控制温度和时间,容易得到含有较多C─O而不是C = O基团的活性位点。通过理论计算和电化学测试发现,在e-转移氧还原反应中,C─O/C = O基团比例最高的改性碳具有较高的活性,在整个电位上具有90%以上的H2O2选择性,这是由于它们的电荷离域扩大。此外,将相应的具有高速高稳定性H2O2电合成(2.78µg s−1 cm−2,电流效率在80%以上)的气体扩散电极应用于模拟和实际酚类废水的电-过氧酮工艺,化学需氧量去除率达到90%以上。在恶劣的电化学环境下长达200 h以上的长期运行也证实了其在实际电化学应用中的巨大潜力。
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来源期刊
ChemCatChem
ChemCatChem 化学-物理化学
CiteScore
8.10
自引率
4.40%
发文量
511
审稿时长
1.3 months
期刊介绍: With an impact factor of 4.495 (2018), ChemCatChem is one of the premier journals in the field of catalysis. The journal provides primary research papers and critical secondary information on heterogeneous, homogeneous and bio- and nanocatalysis. The journal is well placed to strengthen cross-communication within between these communities. Its authors and readers come from academia, the chemical industry, and government laboratories across the world. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies, and is supported by the German Catalysis Society.
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