光催化
异质结
材料科学
光降解
X射线光电子能谱
二硫化钼
可见光谱
高分辨率透射电子显微镜
拉曼光谱
光电流
黄药
二氧化钛
吸收边
光化学
化学工程
纳米技术
透射电子显微镜
光电子学
化学
带隙
催化作用
光学
复合材料
有机化学
高分子化学
工程类
物理
作者
Zhen Tang,Longhua Xu,Kaiqian Shu,Jie Yang,Haijun Tang
标识
DOI:10.1016/j.colsurfa.2022.128686
摘要
The spread application of Titanium dioxide (TiO2) is severely limited by the rapid recombination of photogenerated electron-hole pairs (e--h+). For many applications, two-dimensional (2D) molybdenum disulfide (MoS2), with large specific surface area and sufficient active sites, has been widely researched as a beneficial support for TiO2 photocatalytic activity enhancement. The synthesized heterostructures, the 2D MoS2 nanosheets loaded with brown TiO2 particles (b-TiO2@MoS2) were manufactured through an ultrasound aided electrochemical exfoliation of natural bulk molybdenite coupled with sol-gel technique at low temperature (180 ºC). SEM, TEM, HRTEM, XRD, XPS, UV–vis absorption, Raman, PL spectra, and photocurrent analysis were used to investigate the morphology, microstructure, composition, and charge separation property of the samples. It was determined that b-TiO2 @MoS2 heterostructures had photocatalytic activity by observing their degradation of butyl xanthate during 120 min of visible light irradiation. Furthermore, the photocatalytic effectiveness of the 1 wt% b-TiO2 @MoS2 heterostructures is 94.80%, with a maximum rate constant (k value) of 0.01764 min−1. In contrast to brown TiO2, the findings indicated that the b-TiO2 @MoS2 heterostructures enhanced visible light absorption, the expansion of active sites, the separation and transfer of photogenerated charges. A probable degradation mechanism of photodegradation butyl xanthate and charge transfer process of b-TiO2 @MoS2 heterostructures under visible light irradiation were also postulated.
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