异质结
X射线光电子能谱
降级(电信)
氧化还原
电子转移
甲基橙
材料科学
反应速率常数
反应性(心理学)
辐照
光催化
光化学
化学工程
化学
催化作用
动力学
光电子学
有机化学
冶金
物理
工程类
病理
电信
核物理学
医学
替代医学
量子力学
计算机科学
作者
Yiqian Gao,Donghui Wang,Zehui Yu,Feng Chen
标识
DOI:10.1016/j.colsurfa.2023.131553
摘要
As-synthesized MoS2/α-FeOOH heterojunction exhibits efficient reactivities for Fenton and photo-Fenton degradation of acid orange 7 (AO7) and sulfamethoxazole. Work functions investigated by DFT method suggest a spontaneous electron transfer from MoS2 to α-FeOOH by constructing a type II heterojunction. The electron transfer across the heterojunction was further confirmed by XPS observation. The carrier transfer can be maintained and intensified by surface redox reaction of H2O2 with the accumulated carriers, which amplifies the role of heterojunction. The reaction rate constant for photo-Fenton degradation of AO7 with MoS2/α-FeOOH-10 is 6.6 times higher than that of α-FeOOH. Notably, although α-FeOOH cannot absorb the 660 nm irradiation, a much-enhanced photo-Fenton degradation of AO7 with MoS2/α-FeOOH-10 under 660 nm irradiation further verifies the occurrence of electron transfer from MoS2 to α-FeOOH. This work provides an in-depth observation on the role of type II heterojunction in promoting the photo-Fenton reactivity for organic degradation.
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