Microwave-Assisted Synthesis of MoS2/BiVO4 Heterojunction for Photocatalytic Degradation of Tetracycline Hydrochloride

光催化 X射线光电子能谱 异质结 材料科学 高分辨率透射电子显微镜 水热合成 扫描电子显微镜 拉曼光谱 热液循环 盐酸四环素 透射电子显微镜 可见光谱 化学工程 微波食品加热 核化学 纳米技术 催化作用 光电子学 化学 四环素 光学 有机化学 复合材料 生物化学 量子力学 工程类 抗生素 物理
作者
Cixin Cheng,Qin Shi,Weiwei Zhu,Yuheng Zhang,Wanyi Su,Zizheng Lu,Jun Yan,Kao Chen,Qi Wang,Junshan Li
出处
期刊:Nanomaterials [MDPI AG]
卷期号:13 (9): 1522-1522 被引量:13
标识
DOI:10.3390/nano13091522
摘要

Compared with traditional hydrothermal synthesis, microwave-assisted synthesis has the advantages of being faster and more energy efficient. In this work, the MoS2/BiVO4 heterojunction photocatalyst was synthesized by the microwave-assisted hydrothermal method within 30 min. The morphology, structure and chemical composition were characterized by X-ray diffraction (XRD), Raman, X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM), and high-resolution transmission electron microscopy (HRTEM). The results of characterizations demonstrated that the synthesized MoS2/BiVO4 heterojunction was a spherical structure with dimensions in the nanorange. In addition, the photocatalytic activity of the samples was investigated by degrading tetracycline hydrochloride (TC) under visible light irradiation. Results indicated that the MoS2/BiVO4 heterojunction significantly improved the photocatalytic performance compared with BiVO4 and MoS2, in which the degradation rate of TC (5 mg L-1) by compound where the mass ratio of MoS2/BiVO4 was 5 wt% (MB5) was 93.7% in 90 min, which was 2.36 times of BiVO4. The active species capture experiments indicated that •OH, •O2- and h+ active species play a major role in the degradation of TC. The degradation mechanism and pathway of the photocatalysts were proposed through the analysis of the band structure and element valence state. Therefore, microwave technology provided a quick and efficient way to prepare MoS2/BiVO4 heterojunction photocatalytic efficiently.
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