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构建二维/二维介孔WO/CeO层状异质结以优化光催化性能。

Construction of 2D/2D Mesoporous WO/CeO Laminated Heterojunctions for Optimized Photocatalytic Performance.

作者信息

Wang Wenjie, Yang Decai, Mou Yifan, Liao Lijun, Wang Shijie, Guo Liping, Wang Xuepeng, Li Zhenzi, Zhou Wei

机构信息

Shandong Provincial Key Laboratory of Molecular Engineering, School of Chemistry and Chemical Engineering, Qilu University of Technology (Shandong Academy of Sciences), Jinan 250353, China.

出版信息

Nanomaterials (Basel). 2023 Jun 4;13(11):1798. doi: 10.3390/nano13111798.

DOI:10.3390/nano13111798
PMID:37299701
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10254501/
Abstract

Photocatalytic elimination of antibiotics from the environment and drinking water is of great significance for human health. However, the efficiency of photoremoval of antibiotics such as tetracycline is severely limited by the prompt recombination of electron holes and slow charge migration efficacy. Fabrication of low-dimensional heterojunction composites is an efficient method for shortening charge carrier migration distance and enhancing charge transfer efficiency. Herein, 2D/2D mesoporous WO/CeO laminated Z-scheme heterojunctions were successfully prepared using a two-step hydrothermal process. The mesoporous structure of the composites was proved by nitrogen sorption isotherms, in which sorption-desorption hysteresis was observed. The intimate contact and charge transfer mechanism between WO nanoplates and CeO nanosheets was investigated using high-resolution transmission electron microscopy and X-ray photoelectron spectroscopy measurements, respectively. Photocatalytic tetracycline degradation efficiency was noticeably promoted by the formation of 2D/2D laminated heterojunctions. The improved photocatalytic activity could be attributed to the formation of Z-scheme laminated heterostructure and 2D morphology favoring spatial charge separation, confirmed by various characterizations. The optimized 5WO/CeO (5 wt.% WO) composites can degrade more than 99% of tetracycline in 80 min, achieving a peak TC photodegradation efficiency of 0.0482 min, which is approximately 3.4 times that of pristine CeO. A Z-scheme mechanism is proposed for photocatalytic tetracycline by from WO/CeO Z-scheme laminated heterojunctions based on the experimental results.

摘要

光催化消除环境和饮用水中的抗生素对人类健康具有重要意义。然而,四环素等抗生素的光去除效率受到电子空穴快速复合和电荷迁移效率缓慢的严重限制。制备低维异质结复合材料是缩短载流子迁移距离和提高电荷转移效率的有效方法。在此,采用两步水热法成功制备了二维/二维介孔WO/CeO层状Z型异质结。通过氮吸附等温线证明了复合材料的介孔结构,其中观察到吸附-解吸滞后现象。分别使用高分辨率透射电子显微镜和X射线光电子能谱测量研究了WO纳米片和CeO纳米片之间的紧密接触和电荷转移机制。二维/二维层状异质结的形成显著提高了光催化四环素的降解效率。通过各种表征证实,光催化活性的提高可归因于Z型层状异质结构的形成和有利于空间电荷分离的二维形态。优化后的5WO/CeO(5 wt.% WO)复合材料在80分钟内可降解超过99%的四环素,达到0.0482 min的四环素光降解效率峰值,约为原始CeO的3.4倍。基于实验结果,提出了WO/CeO Z型层状异质结光催化四环素的Z型机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac8/10254501/6fb948bcead6/nanomaterials-13-01798-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac8/10254501/47b011b8d480/nanomaterials-13-01798-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac8/10254501/691c7452dd9e/nanomaterials-13-01798-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac8/10254501/faf9e03e63ae/nanomaterials-13-01798-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac8/10254501/c62536edd4dc/nanomaterials-13-01798-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac8/10254501/98804be0f12c/nanomaterials-13-01798-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac8/10254501/ebc061b17211/nanomaterials-13-01798-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac8/10254501/bb0413684c50/nanomaterials-13-01798-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac8/10254501/6fb948bcead6/nanomaterials-13-01798-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac8/10254501/47b011b8d480/nanomaterials-13-01798-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac8/10254501/691c7452dd9e/nanomaterials-13-01798-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac8/10254501/faf9e03e63ae/nanomaterials-13-01798-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac8/10254501/c62536edd4dc/nanomaterials-13-01798-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac8/10254501/98804be0f12c/nanomaterials-13-01798-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac8/10254501/ebc061b17211/nanomaterials-13-01798-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac8/10254501/bb0413684c50/nanomaterials-13-01798-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac8/10254501/6fb948bcead6/nanomaterials-13-01798-g007.jpg

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