Excellent bisphenol A removal performance triggered by electron-transfer regime on cobalt phosphide embedded in...

The non-radical pathway dominated by the electron transfer process (ETP) has gained considerable attention for the removal of organic contaminants in persulfate-based advanced oxidation processes. Rationally designing new catalysts with optimized composition and structural merits and further elucidating the enhanced removal mechanism are of great importance. In this work, we successfully synthesized a nitrogen-sulfur co-doped carbon encapsulated cobalt phosphide (Co₂P) on both sides of MXene nanosheets (MZPC) to degrade bisphenol A (BPA) from organic wastewater. The results indicated that BPA was degraded by 98.2 % in a mere 5 min using 0.1 g L^-1 of peroxymonosulfate (PMS) and 0.05 g L^-1 of the optimized catalyst (MZPC-9), exhibiting an excellent pseudo-first-order kinetics rate constant (k = 1.485 min^-1). Uniformly dispersed Co₂P nanoparticles (approximately 9.4 nm, calculated using the Scherrer equation) on both sides of MXene exhibited enhanced binding affinity with PMS, forming the MZPC-9-PMS* metastable complexes with potent oxidative capability. The resultant MZPC-9-PMS* complexes induced the polymerization reaction of BPA and achieved 81 % total organic carbon (TOC) removal. This study offers a novel perspective on the design of metal active centers to enhance the ETP-dominated non-radical pathway for pollutant degradation.