提取自细菌纤维素的自立电极,用于高效生产过氧化氢

IF 2.6 4区 化学 Q3 ELECTROCHEMISTRY
Shun Zeng, Weiqi Xu, Huiying Chen, Xiao Huang
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引用次数: 0

摘要

通过双电子氧还原反应(ORR)途径生产过氧化氢(H2O2)是传统耗能蒽醌工艺的一种很有前途的替代方法。在这项研究中,利用从细菌纤维素中提取的碳纤维(CF)作为低成本、高效的催化剂来进行 H2O2 电生产。碳纤维电极在不同的气氛下进行处理,其中在惰性气氛下处理的电极具有优异的 H2O2 生成性能。经惰性气氛处理的 CF 电极的 H2O2 产率高达 2200 mg L-1 h-1,远红外效率高达 95%。有趣的是,经过还原气氛处理的电极在循环测试后也显示出较高的 H2O2 产率。物理表征证实,氧官能团和独特的结构造就了 CF 电极的卓越性能。这些结果表明,H2O2 的生产性能应在实际操作条件下进行大规模评估。这些发现为开发用于 H2O2 电合成的低成本电催化剂开辟了一条新途径,并为废弃生物质的利用提供了新机遇。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Self-standing electrode derived from bacterial cellulose for efficient hydrogen peroxide production

Self-standing electrode derived from bacterial cellulose for efficient hydrogen peroxide production

Hydrogen peroxide (H2O2) production through a two-electron oxygen reduction reaction (ORR) pathway presents a promising alternative to the traditional energy-consumed anthraquinone process. In this work, a low-cost and effective catalyst of carbon fiber (CF) derived from bacterial cellulose is utilized for H2O2 electroproduction. The CF electrode is treated under different atmospheres, and the electrode treated under an inert atmosphere exhibits excellent H2O2 production performance. The inert atmosphere-treated CF electrode delivers a high H2O2 production yield of 2200 mg L−1 h−1 with a remarkable faradaic efficiency of 95%. Interestingly, the electrode treated under a reductive atmosphere also shows high H2O2 production rate after cycle test. Physical characterization confirms that the oxygen functional groups and the unique structure contribute to the superior performance of the CF electrode. These results indicate that the H2O2 production performance should be evaluated under practical operating conditions for large-scale. These findings open a new avenue towards the development of low-cost electrocatalysts for H2O2 electrosynthesis, and offer new opportunities for waste biomass utilization.

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来源期刊
CiteScore
4.80
自引率
4.00%
发文量
227
审稿时长
4.1 months
期刊介绍: The Journal of Solid State Electrochemistry is devoted to all aspects of solid-state chemistry and solid-state physics in electrochemistry. The Journal of Solid State Electrochemistry publishes papers on all aspects of electrochemistry of solid compounds, including experimental and theoretical, basic and applied work. It equally publishes papers on the thermodynamics and kinetics of electrochemical reactions if at least one actively participating phase is solid. Also of interest are articles on the transport of ions and electrons in solids whenever these processes are relevant to electrochemical reactions and on the use of solid-state electrochemical reactions in the analysis of solids and their surfaces. The journal covers solid-state electrochemistry and focusses on the following fields: mechanisms of solid-state electrochemical reactions, semiconductor electrochemistry, electrochemical batteries, accumulators and fuel cells, electrochemical mineral leaching, galvanic metal plating, electrochemical potential memory devices, solid-state electrochemical sensors, ion and electron transport in solid materials and polymers, electrocatalysis, photoelectrochemistry, corrosion of solid materials, solid-state electroanalysis, electrochemical machining of materials, electrochromism and electrochromic devices, new electrochemical solid-state synthesis. The Journal of Solid State Electrochemistry makes the professional in research and industry aware of this swift progress and its importance for future developments and success in the above-mentioned fields.
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