异质结
氧化剂
过氧化氢
二硫化钼
氮化碳
石墨氮化碳
降级(电信)
材料科学
氮化物
制氢
光化学
化学
纳米技术
化学工程
光电子学
光催化
催化作用
有机化学
计算机科学
图层(电子)
工程类
冶金
电信
作者
Guofei Jiang,Xuehui You,Beiya An,Benjie Zhu,Fang Liu,Xiaoguang Duan,Yongqiang Wang,Ruiyu Zhao
标识
DOI:10.1016/j.apsusc.2023.156656
摘要
In this work, we first applied molybdenum disulfide with S vacancy (MoS2-v) /carbon nitride nanotube (TCN) composite (MoS2-v/TCN) to drive the iron-free photo-Fenton-like reaction. The well-designed band structure enables MoS2-v/TCN to construct direct Z-scheme heterostructures, realizing the rapid separation of photoinduced-e− and h+, and effectively improving the photocatalytic efficiency of MoS2-v/TCN. DFT calculation showed that Z-scheme heterojunction greatly reduced the energy barrier for generating *OOH and *HO2–, affording MoS2/TCN high performance and stability toward H2O2 generation (pure water: 254.8–269.9 μmol·g−1·h−1, 10 % isopropanol: 1879 μmol·g−1·h−1) over a wide pH range (3–9). The photoinduced-e− and Mo4+ on the surface of MoS2-v/TCN rapidly converted H2O2 in situ to strong oxidizing •OH, realizing the efficient degradation of organic pollutants and rapid inactivation of bacteria. This work provides a new approach to solving the technical bottlenecks in traditional Fenton oxidation via synthesizing multifunctional heterojunction for in situ H2O2 generation and activation.
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