石墨烯
微生物燃料电池
阴极
铁质
氧化物
甲基橙
化学工程
材料科学
降级(电信)
复合数
纳米技术
化学
电极
光催化
催化作用
阳极
复合材料
冶金
有机化学
物理化学
工程类
计算机科学
电信
作者
Minmin Sun,Chengxian Wang
出处
期刊:Heliyon
[Elsevier]
日期:2024-01-20
卷期号:10 (3): e24772-e24772
被引量:3
标识
DOI:10.1016/j.heliyon.2024.e24772
摘要
In this work, the ferrous (Fe2+) and graphitic N modified graphene-based composite cathode materials (N-rGO/Fe3O4) were developed through an in-situ reduction method, aiming to facilitate the two-electron pathway in the oxidation-reduction process. This approach generated a specific concentration of H2O2, enabling the construction of a sediment bio-electro-Fenton system using Fe2+ released from the cathode materials. Notably, this system operates without the need for proton exchange membranes. During the cathode material preparation, the utilization of Fe2+ as a reduction agent for graphene oxide (GO), triggered ammonia water to form graphitic N in graphene sheets. This addition enhanced the two-electron pathway, resulting in increased H2O2 production. Specifically, when the Fe2+ concentration was maintained at 0.1 mol/L, precise preparation of N-rGO/Fe3O4 occurred, leading to a maximum output voltage of 0.528 V and a maximum power density of 178.17 mW/m2. The degradation of methyl orange (MO) reached 68.91% within a 25-h period, a phenomenon contributed to the presence of graphitic N in the graphene sheets. H2O2, a byproduct of the two-electron pathway in cathode oxidation reduction reaction, played a crucial role in constructing the bio-electro-Fenton system. This system, in conjunction with Fe2+ released from N-rGO/Fe3O4, facilitated the complete degradation process of MO.
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