化学
光化学
激进的
降级(电信)
猝灭(荧光)
石墨氮化碳
高级氧化法
电子转移
糠醇
光降解
辐照
光催化
催化作用
荧光
有机化学
物理
核物理学
电信
量子力学
计算机科学
作者
Pengfei Gan,Yi Lu,Yunyi Li,Wen Liu,Long Chen,Meiping Tong,Jialiang Liang
标识
DOI:10.1016/j.jhazmat.2022.130549
摘要
In this work, an excitonic energy transfer (EET) based non-radical mechanism was proposed for the degradation of organic pharmaceuticals by graphitic carbon nitride (g-C3N4) under visible light irradiation. Using diclofenac (DCF) as a model molecule, the competition between single electron transfer (SET) and EET was studied through modulating the exciton binding energy of g-C3N4. The different mechanisms of SET and EET for DCF degradation were predicted by DFT calculation, and further confirmed by their different degradation pathways. When EET played an important role, the rationality of some very popular radical scavengers, such as p-BQ, TEMPOL and furfuryl alcohol must be reconsidered. In addition, humic acid (HA) had a distinct effect on EET and SET. Specifically, HA enhanced the EET process through photosensitization, but suppressed SET through radical quenching effect. The effect of HA on DCF degradation depended on the contribution ratio of SET and ET.
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