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自支撑CFP@CoFeO电极实现高效电芬顿催化

Efficient electro-Fenton catalysis by self-supported CFP@CoFeO electrode.

作者信息

Guo Meiting, Lu Mingjie, Zhao Heng, Lin Feifei, He Fengting, Zhang Jinqiang, Wang Shuaijun, Dong Pei, Zhao Chaocheng

机构信息

State Key Laboratory of Petroleum Pollution Control, China University of Petroleum (East China), Qingdao 266580, PR China.

School of Engineering, Edith Cowan University, 270 Joondalup Drive, Joondalup, WA 6027, Australia.

出版信息

J Hazard Mater. 2022 Feb 5;423(Pt A):127033. doi: 10.1016/j.jhazmat.2021.127033. Epub 2021 Aug 25.

Abstract

In this work, the bimetallic iron oxide self-supported electrode was prepared by a simple solvothermal as well as thermal method. CoFeO magnetic nanoparticles were grown in situ on the CFP surface and characterized to reveal the morphology, composition, and electrochemical properties of the electrode. Compared to CFP and CFP@Co-Fe, CFP@CoFeO equipped more efficient mineralization current efficiency and lower energy consumption due to the improved electrocatalytic capacity of CoFeO properly grown on the conductive substrate surface. Further studies showed that the manufactured electrode maintained a high level of stability after continuous operation. According to the free radical trapping experiment, EPR, and liquid mass spectrometry analysis, the rational reaction mechanism of p-nitrophenol was finally proposed, in which ·OH and SO· were considered as the main active oxidants. This work demonstrated the great potential of establishing an electro-Fenton system based on CoFeO immobilized self-supporting cathode for environmental remediation.

摘要

在本工作中,通过简单的溶剂热法以及热法制备了双金属氧化铁自支撑电极。CoFeO磁性纳米颗粒原位生长在CFP表面,并对其进行表征以揭示电极的形貌、组成和电化学性质。与CFP和CFP@Co-Fe相比,CFP@CoFeO由于在导电基底表面适当生长的CoFeO的电催化能力提高,具有更高的矿化电流效率和更低的能耗。进一步的研究表明,制造的电极在连续运行后保持了高水平的稳定性。根据自由基捕获实验、电子顺磁共振和液相质谱分析,最终提出了对硝基苯酚的合理反应机理,其中·OH和SO·被认为是主要的活性氧化剂。这项工作展示了基于固定化CoFeO自支撑阴极建立电芬顿系统用于环境修复的巨大潜力。

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