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The heterogeneous electro‐Fenton (EF) process is a promising wastewater treatment technology for the onsite production of H 2 O 2 and avoidance of iron sludge. However, the preparation of the cathode catalysts remains a challenge. Not only must the catalyst surface possesses active sites for both 2e − oxygen reduction reaction and heterogeneous Fenton reaction, preventing active metals from continuous leaching is also crucial to maintain its catalytic activity. Herein, a heterogeneous catalyst (rGO@Fe x P/C) with a vacuumized package‐like structure, where carbon‐supported iron phosphides (Fe x P/C) are tightly covered within interconnected reduced graphene oxide (rGO) sheets, is successfully prepared. The concentration of iron that dissolved from rGO@Fe x P/C after the reaction is only 3.37% of bare Fe x P/C (14.6 mg L −1 ), while rGO@Fe x P/C achieves better performance towards sulfamethoxazole (10 mg L −1 ) degradation than Fe x P/C. Investigation on rGO@Fe x P/C with different thicknesses of outer rGO layer and diverse morphologic structures demonstrate that the unique structure of rGO@Fe x P/C played a decisive role in the simultaneously enhanced activity and stability.
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Cheng et al. (2021) studied this question.
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