期刊
INORGANIC CHEMISTRY COMMUNICATIONS
卷 134, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.inoche.2021.109063
关键词
BiOCl; Heterojunctions; In-situ; Ionic liquid; Separation of carriers
资金
- National Natural Science Foundation of China [21777168]
- Science and Technology Department of Sichuan Province [2019YJ0457, 2019ZYZF0069, 2021YFG0278]
- Chemical Synthesis and Pollution Control Key Laboratory of Sichuan Province [CSPC201903, CSPC202105]
- Key Laboratory of Catalysis and Energy Materials Chemistry of Ministry of Education & Hubei Key Laboratory of Catalysis and Materials Science [CHCL20005]
- Graduate Innovation Fund of the Sichuan University of Science and Engineering [Y2020057]
A flower-like BiOBr/BiOCl heterojunction photocatalyst was successfully constructed in-situ by adding a reactable ionic liquid into the hydrothermal system. The improved photocatalytic performance of the heterojunction can be attributed to the high separation efficiency of photogenerated carriers.
In this study, flower-like BiOBr/BiOCl heterojunction photocatalyst was successfully in-situ constructed by adding a reactable ionic liquid 1-methoxyethyl-3-methylimidazolium bromide ([MOEMIm]Br) into the hydrothermal system. The samples were carefully characterized by specific surface area (BET), X-ray diffraction (XRD), scanning electron microscope (SEM), high resolution transmission electron microscope (HRTEM), energydispersive spectroscopy (EDS), surface photovoltage spectroscopy (SPS), UV-Vis diffuse reflectance spectroscopy (DRS). Electron spin resonance spectroscopy (ESR) and trapping experiments were carried out to identify active free radicals in the reaction system. Using rhodamine B (RhB) as model pollutant, the photocatalytic performance was investigated. The results show that the photoactivity of BiOBr/BiOCl heterojunctions is 5.9 times of that of the bare BiOCl. The boosted photoactivity of BiOBr/BiOCl heterojunctions can be allocated to the relative high separation efficiency of photogenerated carriers owing to the formation of heterojunctions.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据