| Summary: | 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. Keywords: TiO2, Oxygen reduction reaction, Electrocatalysis, Hydroxyl radicals
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