Facilitating Redox Cycles of Copper Species by Pollutants in Peroxymonosulfate Activation

The redox behavior of metal active sites determines the rate of heterogeneous catalysis in peroxymonosulfate activation. Previous reports focused on the construction of catalysts for accelerating interfacial electron transfer. In this work, a new strategy was proposed for facilitating valence cycles of Cu+/Cu2+ by using pollutants. The 2.5Cu/CeO2/PMS system was capable of achieving the efficient removal of pollutants, including tetracycline, oxytetracycline, and rhodamine B, in a wide pH working range. In the presence of tetracycline, a Cu-N bond was formed between the -NH2 group of tetracycline and the Cu site of the catalyst, showing that the coordination of Cu active sites changed to CuO4N1. The charge of CuO4N1 active sites rearranged, making it easier to obtain electrons and promote the PMS oxidation, thereby accelerating the reduction of Cu2+ to Cu+ and PMS activation. The PMS activation system showed excellent sustainability and selectivity for the removal of organic pollutants. This study provides a novel routine to promote peroxymonosulfate activation by utilizing pollutants to accelerate the redox behavior of metal species.

Automated summary

The redox behavior of metal active sites plays a significant role in the rate of peroxymonosulfate activation catalyzed by metals. Previous studies have focused on developing catalysts that enhance interfacial electron transfer. This study proposes a new strategy for facilitating the valence cycles of Cu+/Cu2+ by utilizing pollutants. The 2.5Cu/CeO2/PMS system demonstrates efficient removal of pollutants over a wide pH range and exhibits excellent sustainability and selectivity for the removal of organic pollutants.