光催化
异质结
电子转移
降级(电信)
光化学
热液循环
激进的
可见光谱
材料科学
化学
表面等离子共振
化学工程
催化作用
纳米技术
光电子学
纳米颗粒
有机化学
计算机科学
工程类
电信
作者
Zhuangzhuang Wang,Lisha Jiang,Kai Wang,Yuan Li,Gaoke Zhang
标识
DOI:10.1016/j.jhazmat.2020.124948
摘要
Herein, we constructed a novel AgI/BiSbO4 heterojunction via a hydrothermal-precipitation method. The heterojunction structure boosts the generation of hydroxyl and superoxide radicals for efficient degradation of organic pollutants. The photocatalytic activities of the optimal sample for ARG and TC degradation are 10 and 1.6 times higher than those of bare AgI, respectively. Characterizations and theoretical calculations together confirm a strong interfacial charge transfer exists between the interlayer in AgI and BiSbO4 by the formation of Ag‒O bond, making O atoms obtain rich free electrons from Ag atoms of AgI, thus forming an ultrahigh electron transfer tunnel, and ultimately accelerating the separation of photoinduced electrons. More interestingly, low amounts of Ag0 NPs formed during the photocatalytic process, enhancing the visible light absorption because of its SPR (surface plasmon resonance) effect and further promoting the separation of photoinduced carriers. Furthermore, photocatalytic degradation pathways were proposed in detail by analyzing intermediates and a reasonable photocatalytic mechanism was unearthed. This work extends the development of AgI-based heterojunction photocatalysts.
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