石墨氮化碳
吸附
降级(电信)
光催化
污染物
氮化碳
材料科学
激进的
电子转移
化学工程
氧化还原
化学
光化学
无机化学
催化作用
有机化学
电信
计算机科学
工程类
作者
Fan Li,Zhicong Lu,Peng Zhang,Yang Jin,Tong Li,Chun Hu
出处
期刊:ACS ES&T engineering
[American Chemical Society]
日期:2022-04-07
卷期号:2 (7): 1296-1305
被引量:16
标识
DOI:10.1021/acsestengg.1c00459
摘要
The adsorption of organic pollutants on the surface defects of photocatalysts can directly change the surface redox reaction to improve the photocatalytic degradation efficiency; however, the interaction mechanism remains unclear. In this study, graphitic carbon nitride (g-C3N4) with C vacancies enabling more C–NHx exposure (HTCN) was synthesized and used to study the effect of organic pollutant adsorption on photocatalytic properties. The exposure of C–NHx distinctly separates the highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital of HTCN and avoids the competitive adsorption between O2 and organic pollutants on the HTCN surface, facilitating the generation of O2•– and direct pollutant oxidation by h+. More importantly, the pollutants exactly adsorbed on the HOMO distribution area of HTCN derived from C vacancies further regulate the energy band structure by spontaneous electron transfer, which promotes more electrons to be captured by O2 for O2•– generation and high-performance degradation of pollutants.
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