Cheng Cixin, Shi Qin, Zhu Weiwei, Zhang Yuheng, Su Wanyi, Lu Zizheng, Yan Jun, Chen Kao, Wang Qi, Li Junshan
Guangxi Colleges and Universities Key Laboratory of Environmental-Friendly Materials and New Technology for Carbon Neutralization, Guangxi Key Laboratory of Advanced Structural Materials and Carbon Neutralization, School of Materials and Environment, Guangxi Minzu University, Nanning 530105, China.
Guangxi Research Institute of Chemical Industry Co., Ltd., Nanning 530006, China.
Nanomaterials (Basel). 2023 Apr 30;13(9):1522. doi: 10.3390/nano13091522.
Compared with traditional hydrothermal synthesis, microwave-assisted synthesis has the advantages of being faster and more energy efficient. In this work, the MoS/BiVO 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 MoS/BiVO 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 MoS/BiVO heterojunction significantly improved the photocatalytic performance compared with BiVO and MoS, in which the degradation rate of TC (5 mg L) by compound where the mass ratio of MoS/BiVO was 5 wt% (MB5) was 93.7% in 90 min, which was 2.36 times of BiVO. The active species capture experiments indicated that •OH, •O 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 MoS/BiVO heterojunction photocatalytic efficiently.
与传统水热合成相比,微波辅助合成具有速度更快、更节能的优点。在本工作中,通过微波辅助水热法在30分钟内合成了MoS/BiVO异质结光催化剂。采用X射线衍射(XRD)、拉曼光谱、X射线光电子能谱(XPS)、扫描电子显微镜(SEM)和高分辨率透射电子显微镜(HRTEM)对其形貌、结构和化学成分进行了表征。表征结果表明,合成的MoS/BiVO异质结为纳米级尺寸的球形结构。此外,通过在可见光照射下降解盐酸四环素(TC)研究了样品的光催化活性。结果表明,与BiVO和MoS相比,MoS/BiVO异质结显著提高了光催化性能,其中MoS/BiVO质量比为5 wt%的复合物(MB5)对5 mg L的TC在90分钟内的降解率为93.7%,是BiVO 的2.36倍。活性物种捕获实验表明,•OH、•O和h活性物种在TC的降解中起主要作用。通过对能带结构和元素价态的分析,提出了光催化剂的降解机理和途径。因此,微波技术为高效制备MoS/BiVO异质结光催化剂提供了一种快速有效的方法。