污染物
矿化(土壤科学)
双酚A
光催化
罗丹明B
堆积
环境化学
原位
光化学
氮化碳
化学
聚合
盐酸四环素
化学工程
核化学
材料科学
氮气
聚合物
四环素
催化作用
有机化学
环氧树脂
工程类
生物化学
抗生素
作者
Junpeng Yue,Hanpei Yang,Chen Liu,Qiang Zhang,Yanhui Ao
标识
DOI:10.1016/j.apcatb.2023.122716
摘要
A new strategy to realize efficient removal of organics from water through photo-self-Fenton was investigated. Characterizations and calculations demonstrated that a novel twin carbon nitride with abundant surficial N-defects and compressed π-π layer stacking can be constructed by thermal polymerization of urea under suitable basicity. Synergistically, the twins exhibited an in-situ H2O2 producing at a rate as high as 26.36 mM h−1 g−1 at 420 nm that exceeded most reported C3N4, and their mineralization rates for Tetracycline Hydrochloride, Bisphenol A, Ciprofloxacin, and Rhodamine B reached 8.8, 15.2, 9.1, and 13 times higher than that of pristine C3N4. It is concluded that enriching both of photogenerated electrons and molecular oxygens on specific sites plays a crucial role during photocatalysis-self-Fenton process. Particular attentions have to be paid to build structures achieving one and two-electron reduction of O2, and activation of H2O2 to •OH simultaneously.
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