催化作用
光催化
化学
石墨氮化碳
可见光谱
光化学
降级(电信)
激活剂(遗传学)
材料科学
有机化学
计算机科学
光电子学
生物化学
电信
基因
作者
Gang Zhao,Wenchao Li,Huayu Zhang,Wei Wang,Yueping Ren
标识
DOI:10.1016/j.cej.2021.132937
摘要
A highly efficient single atom Fe-dispersed g-C3N4 catalyst with a Fe-N4 coordination structure for peroxymonosulfate (PMS) photocatalytic activation and sulfamethoxazole (SMX) degradation was synthesized. The dominant role of Fe single atoms in the activation of PMS and SMX removal was revealed, and the contribution of photo-generated electrons (e−) and holes (h+) to the enhanced catalytic performance of the catalyst in PMS activation was elucidated. Under visible light irradiation, 98.7% of the SMX with the initial concentration of 10 mg/L was quickly degraded within 6 min using 50 mg/L catalyst. The turnover efficiency (TOF) of the catalyst is as high as 5.27 min−1, which is 2–6 orders of magnitude higher than normal Fe-containing catalysts for SMX degradation. Moreover, this catalyst exhibits excellent stability and reusability. The dominating reaction active species involved in the degradation of SMX were identified, and the possible SMX degradation mechanism was proposed based on the detected degradation intermediates. This work provide a highly efficient visible light response single atom Fe catalyst for the sulfate radical-based advanced oxidation process.
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