Synergistic degradation of p-nitrophenol using peroxymonosulfate activated with a bimetallic Mn3O4–Cu2O catalyst: Investigation of strong interactions between metal oxides

Abstract

The use of efficient, eco-friendly catalysts is essential for activating peroxymonosulfate (PMS) to degrade organic contaminants in aqueous media. In this study, we developed a novel approach to fabricating bimetallic MnCu catalysts (Mn:Cu molar ratios: 10:1, 5:1, 3:1, and 2:1) comprising tetragonal Mn3O4 and cubic Cu2O. MnCu-5:1 exhibited superior catalytic activity for the degradation of p-nitrophenol (PNP) using PMS because of the synergistic interplay between Mn and Cu. Experimental and density functional theory (DFT) calculation data revealed that the mixed valence states and strong interactions between Mn and Cu in the MnCu-5:1 system increased the electron transfer efficiency and promoted electron transfer to PMS. The results of quenching experiments elucidated a primary radical mechanism and minor nonradical pathway for the PNP degradation over the MnCu-5:1/PMS system. DFT calculations confirmed a relatively high adsorption energy of the Mn3O4–Cu2O (MnCu) composite, indicating enhanced catalytic performance. The superior reactivity of the composite was verified by analyzing its density of states and electrostatic difference potential. Our findings offer fresh perspectives for harnessing the synergistic potential of less toxic mixed metal oxides for controlling catalytic properties and help achieve a better understanding of the activation mechanism for contaminant degradation over MnCu catalysts.