Mediated Peroxymonosulfate Activation at the Single Atom Fe‐N3O1 Sites: Synergistic Degradation of Antibiotics by Two Non‐Radical Pathways

Abstract

AbstractThe activation of persulfates to degrade refractory organic pollutants is a hot issue in advanced oxidation right now. Here, it is reported that single‐atom Fe‐incorporated carbon nitride (Fe‐CN‐650) can effectively activate peroxymonosulfate (PMS) for sulfamethoxazole (SMX) removal. Through some characterization techniques and DFT calculation, it is proved that Fe single atoms in Fe‐CN‐650 exist mainly in the form of Fe‐N3O1 coordination, and Fe‐N3O1 exhibited better affinity for PMS than the traditional Fe‐N4 structure. The degradation rate constant of SMX in the Fe‐CN‐650/PMS system reached 0.472 min−1, and 90.80% of SMX can still be effectively degraded within 10 min after five consecutive recovery cycles. The radical quenching experiment and electrochemical analysis confirm that the pollutants are mainly degraded by two non‐radical pathways through 1O2 and Fe(IV)═O induced at the Fe‐N3O1 sites. In addition, the intermediate products of SMX degradation in the Fe‐CN‐650/PMS system show toxicity attenuation or non‐toxicity. This study offers valuable insights into the design of carbon‐based single‐atom catalysts and provides a potential remediation technology for the optimum activation of PMS to disintegrate organic pollutants.