In this study, a dual-carrier catalyst is designed for efficient Fenton-like catalysis following non-radical electron-transfer process (ETP). By using 2D mesoporous carbon sandwiched MXene (MCSMx) nanosheets as dual functional substrates, Co single atoms (Co-SA) were confined within MCSMx (CoSA/MCSMx), in which the coordinated Co-N4 sites in highly ordered mesoporous channels (∼10 nm) facilitated the adsorption of peroxymonosulfate (PMS), while the excellent conductivity of MXene as the substrate enhanced the transport of electron. The unique design of Co-SA anchored on dual carriers endows the CoSA/MCSMx with excellent PMS adsorption and rapid electron transfer, achieved nearly 100 % ETP pathway for bisphenol A (BPA) removal and highly selective degradation towards electron-rich pollutants. Moreover, the ETP-induced polymerization transfer reaction of BPA was discovered in the catalytic system, resulting in total organic carbon (TOC) removal ratios of up to 72 %. This work provides new insights into the rational design ETP-based systems for the efficient removal of organic pollutants.
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