光催化
矿化(土壤科学)
降级(电信)
材料科学
激进的
羟基自由基
化学工程
污染物
光化学
环境化学
催化作用
核化学
化学
有机化学
计算机科学
氮气
工程类
电信
作者
Le Chen,Xinxia He,Zehan Gong,Jia-Lian Li,Yang Liao,Xiaoting Li,Jun Ma
出处
期刊:Rare Metals
[Springer Nature]
日期:2022-03-28
卷期号:41 (7): 2429-2438
被引量:30
标识
DOI:10.1007/s12598-022-01963-w
摘要
Photocatalysis-self-Fenton system, i.e., photocatalytic H2O2 generation and utilization in situ for ·OH radials production to remove organic pollutants with high-fluent degradation and mineralization performance possesses such advantages as cleanliness, efficiency and safety. However, its degradation activity always suffers from the Fe(III)/Fe(II) cycle. For this reason, graphitic carbon interface-modified g-C3N4 (CUCN) was fabricated to remarkably improve photocatalysis-self-Fenton degradation activity. The experiment results indicated that CUCN-2% photocatalyst, in which the loading percentage of graphitic carbon was 2%, demonstrated the optimum degradation performance among all the counterparts. The mineralization degree for RhB in 3 h over CUCN-2% reached 63.77%, nearly 3.35-fold higher than the pristine g-C3N4. The significantly improved mineralization efficiency was ascribed to the promoted Fe(III)/Fe(II) cycle by photogenerated electrons, which leading to the higher utilization efficiency of H2O2 through Fenton reaction, thereby producing more hydroxyl radicals. It is anticipated that our work could provide new insights for the design of photocatalysis-self-Fenton system with exceptional degradation performance for actual photocatalytic applications.Graphical abstract
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