Construction of hydrostable cesium lead bromide-titania for visible-light degradation of tetracycline hydrochloride in water

光催化 盐酸四环素 异质结 钙钛矿(结构) 光降解 卤化物 溴化物 可见光谱 溴化银 四环素 化学 光化学 水溶液 无机化学 材料科学 化学工程 催化作用 纳米技术 有机化学 工程类 卤化银 光电子学 抗生素 图层(电子) 生物化学
作者
Chunxi Liu,Xiaoxiao Qian,Qiyan Wei,Zhi Chen,Jinchao Chen,Weiwei Wang,Xiangyu Chen,Jingyang Gao,Yurong Liu,Lili Xie
出处
期刊:Journal of Cleaner Production [Elsevier BV]
卷期号:365: 132830-132830 被引量:45
标识
DOI:10.1016/j.jclepro.2022.132830
摘要

The poor stability of metal halide perovskite in water is one of the main obstacles restricting its practical application. Hydrostable cesium lead bromide-titania heterojunction was synthesized by the solvothermal method with the following sintering process and applied for the visible-light-driven photodegradation of tetracycline hydrochloride (TC-HCl) in water. The introduced TiO2 components effectively protect CsPbBr3 nanoparticles from phase transition which spurs significantly improved photocatalytic performance and stability on CsPbBr3–TiO2 heterojunction in water. The structure of synthesized CsPbBr3–TiO2 photocatalyst is characterized by XRD, SEM, and TEM. The photoelectric characteristics of prepared photocatalysts investigated through photoelectrochemical and photoluminescent analyses indicate that the enhanced photocatalytic property may be related to the optimized light response and electron-hole separation on heterojunction composites. The active substances in the photocatalytic process are determined through capture experiments, indicating that holes (h+) and superoxide radicals (• O2−) are responsible for photocatalytic activity. A reaction mechanism is suggested in the end. This work provides an alternative for the construction of water-resistant halide perovskite to break through the poor water stability and opens novel applications for halide perovskite-based materials in aqueous environmental control.
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