化学
电催化剂
电化学
激进的
电子转移
电解
锐钛矿
氧化还原
催化作用
解吸
阴极
无机化学
密度泛函理论
光化学
产量(工程)
吸附
电极
物理化学
材料科学
光催化
有机化学
计算化学
电解质
冶金
作者
Fei Miao,Mingming Gao,Xin Yu,Pengwei Xiao,Mei Wang,Yunkun Wang,Shuguang Wang,Xinhua Wang
标识
DOI:10.1016/j.elecom.2020.106687
摘要
The use of heterogeneous catalysts to improve the Electro-Fenton (EF) process has attracted significant attention. However, complex redox reactions and multiple mass transfer steps during the EF process result in limited current efficiency with only a low rate of generation of hydroxyl radicals (OH). Herein, we establish a three-electron oxygen reduction reaction (ORR) process coupling adsorbed H2O2 (H2O2ad) generation with an in situ EF-like reaction on TiO2 during cathodic electrolysis. Anatase TiO2 was composited with graphite, enabling the electrochemical reduction of Ti4+ to Ti3+. H2O2ad was formed during the ORR, electrocatalyzed by TiO2, then the H2O2ad was reduced in situ to OH without desorption. The generation and decomposition of Ti-OH during the electrochemical reduction were directly observed by in situ Raman spectroscopy. This result was further confirmed by density functional theory (DFT) calculations. Based on this three-electron ORR mechanism, the OH yield reached 2.69 μg cm−2 min−1 and the current efficiency approached 92.8% at a current density of −0.80 mA cm−2 within 2 h during ORR on the TiO2/graphite (TiO2/C) cathode.
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