Simultaneously Providing Iron Source toward Electro-Fenton Process and Enhancing Hydrogen Peroxide Production via a Fe3O4 Nanoparticles Embedded Graphite Felt Electrode

材料科学 过氧化氢 石墨 电极 化学工程 无机化学 纳米颗粒 纳米技术 冶金 有机化学 物理化学 化学 工程类
作者
Tingting Lian,Chao Huang,Feng Liang,Xinyong Li,Jingyu Xi
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:11 (49): 45692-45701 被引量:44
标识
DOI:10.1021/acsami.9b16236
摘要

Electro-reduction of O2 to generate H2O2 is an attractive alternative to the current anthraquinone process and quite necessary for chemical industries and environmental remediation. In general, sufficient porous structure contributes to expose more catalytic active sites and shorten diffusion paths for the heterogeneous catalysis of O2. In this work, initially the Fe3O4 nanoparticles embedded graphite felt (Fe3O4@GF) is prepared through a mild hydrothermal following with thermal reduction method. This special combination not only provides iron source for the electro-Fenton reaction but also supplies rich active sites from the Fe3O4 embedded structure with abundant cracks, which are beneficial to increase the reaction rate. Compared with raw graphite felt (RGF), fresh Fe3O4@GF exhibits superior pollutant degradation kinetics with more than 400% increase and approximately 37.8% improvement to the removal of total organic carbon. A 98% decolorization of rhodamine B (RhB) can be achieved in just 5 min and quickly completes 100% removal of RhB in the next few seconds. As the electro-Fenton reaction progresses, Fe3O4 dissolves in the electrolyte, leaving a porous structure on the surface of the GF to form a porous GF (PGF), and the rapid radical reaction activates the GF surface. Both the chemical etching of Fe3O4 and the electro-Fenton process can further increase the specific surface area, defects, and actives sites of the electrode. As expected, the active PGF exhibits favorable performance of H2O2 production in electrolytes of different pHs: 1 (320.0 ± 36.5 mg L–1), 3 (301.9 ± 13.2 mg L–1), and 7 (320.4 ± 21.2 mg L–1). The degradation performance of PGF does not significantly decay even after 20 cycles of repeated use, indicating the good structural stability and long-term durability. The superiority of the in situ Fe source and fast reaction kinetics for electro-Fenton of Fe3O4@GF is confirmed, and this holey engineered strategy also provides the possibility to achieve swift water purification and open up a new way for developing efficient carbon-based electrodes.
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