Ionic liquid-assisted hydrothermal preparation of BiOI/BiOCl heterojunctions with enhanced separation efficiency of photo-generated charge pairs and photocatalytic performance

光催化 罗丹明B 异质结 X射线光电子能谱 材料科学 水溶液 热液循环 离子液体 化学工程 激进的 光化学 化学 光电子学 催化作用 有机化学 工程类
作者
Huanhuan Liu,Yang Cai,Jiao Huang,Jiufu Chen,Junbo Zhong,Jianzhang Li
出处
期刊:Inorganic Chemistry Communications [Elsevier BV]
卷期号:113: 107806-107806 被引量:60
标识
DOI:10.1016/j.inoche.2020.107806
摘要

In this contribution, BiOI/BiOCl heterojunctions were successfully synthesized with the assistance of reactable ionic liquid (IL) 1-propyl-3-methylimidazolium iodide ([PrMIm]I) via a hydrothermal method. The crystal structures, morphologies, chemical compositions, optical properties and separation efficiency of photo-generated charge pairs of the as-prepared BiOI/BiOCl heterojunctions were characterized by various analytic methods. Surface photovoltage spectroscopy (SPS) and photoelectrochemical measurements reveal that the BiOI/BiOCl heterojunctions exhibit higher separation efficiency of photo-generated charge pairs than the reference BiOCl and BiOI. XPS results reveal that I element exists in the as-prepared samples with a chemical valence of −1, and when the mass ratio of [PrMIm]I/BiOCl is 8%, the sample holds the highest surface hydroxyl content. Photocatalytic performance of the as-fabricated photocatalysts was evaluated by abatement of rhodamine B (RhB) aqueous solution under simulated sunlight irradiation. BiOI/BiOCl heterojunctions exhibit enhanced photocatalytic performance; the 8% sample displays the highest photocatalytic activity. Trapping experiments certify that the superoxide radicals (O2−) is the predominant active free radicals in the photocatalytic degradation process of RhB over the BiOI/BiOCl heterojunctions. In light of experimental results, a possible Z-scheme photocatalytic degradation mechanism was discussed to elaborate the separation and migration of the photo-induced electron-hole pairs. This study provides a useful reference for ILs assisted fabrication of high efficiency photocatalytic materials.
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