Transforming Plastics to Single Atom Catalysts for Peroxymonosulfate Activation: Axial Chloride Coordination Intensified Electron Transfer Pathway.
basic_science · Level V
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- Record sourced from PubMed, PMID 39757509.
- Also identified by DOI 10.1002/adma.202415339.
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Abstract
Transforming plastics into single-atom catalysts is a promising strategy for upcycling waste plastics into value-added functional materials. Herein, a graphene-based single-atom catalyst with atomically dispersed FeN<sub>4</sub>Cl sites (Fe─N/Cl─C) is produced from high-density polyethylene wastes via one-pot catalytic pyrolysis. The Fe─N/Cl─C catalyst exhibited much higher turnover frequency and surface area normalized activity (K<sub>ac</sub>) compared with the Fe─N─C catalyst without axial Cl modulation. Both experiments and density functional theory (DFT) computations demonstrated that the axial incorporation of chloride fine-tuned the coordination environment of FeN<sub>4</sub> sites and enhanced peroxymonosulfate (PMS) activation because of improved conductivity and modulated spin state. In situ, Raman, and infrared spectroscopic techniques revealed that PMS is activated by the Fe─N/Cl─C catalyst through an electron transfer process. The formation of a key PMS<sup>*</sup> intermediate at the Fe site effectively elevated the redox capacity of the catalyst surface to realize a fast degradation of diverse pollutants. The non-radical oxidation manner secures high selectivity toward target pollutants and high chemical utilization efficiency. A continuous operation in a column reactor also demonstrated the high efficiency and stability of the (Fe─N/Cl─C + PMS) system for practical water treatment.