Wang Zhuangzhuang, Jiang Lisha, Wang Kai, Li Yuan, Zhang Gaoke
Hubei Key Laboratory of Mineral Resources Processing and Environment, State Key Laboratory of Silicate Materials for Architectures, Wuhan University of Technology, 122 Luoshi Road, Wuhan 430070, People's Republic of China.
Hubei Key Laboratory of Mineral Resources Processing and Environment, State Key Laboratory of Silicate Materials for Architectures, Wuhan University of Technology, 122 Luoshi Road, Wuhan 430070, People's Republic of China; Henan Institute of Advanced Technology, Zhengzhou University, Zhengzhou 450052, People's Republic of China.
J Hazard Mater. 2021 May 15;410:124948. doi: 10.1016/j.jhazmat.2020.124948. Epub 2020 Dec 24.
Herein, we constructed a novel AgI/BiSbO 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 BiSbO 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 Ag 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.
在此,我们通过水热沉淀法构建了一种新型的AgI/BiSbO异质结。该异质结结构促进了羟基和超氧自由基的生成,以有效降解有机污染物。最佳样品对ARG和TC降解的光催化活性分别比纯AgI高10倍和1.6倍。表征和理论计算共同证实,通过形成Ag‒O键,在AgI和BiSbO的中间层之间存在强烈的界面电荷转移,使O原子从AgI的Ag原子获得丰富的自由电子,从而形成超高电子转移隧道,并最终加速光生电子的分离。更有趣的是,在光催化过程中形成了少量的Ag NPs,由于其表面等离子体共振(SPR)效应增强了可见光吸收,并进一步促进了光生载流子的分离。此外,通过分析中间体详细提出了光催化降解途径,并揭示了合理的光催化机理。这项工作拓展了基于AgI的异质结光催化剂的发展。