Layered MoS2 Grown on Anatase TiO2 {001} Promoting Interfacial Electron Transfer to Enhance Photocatalytic Evolution of H2 From H2S

光催化 X射线光电子能谱 材料科学 光电流 锐钛矿 光致发光 电子转移 半导体 带隙 介电谱 分解水 纳米技术 化学工程 光化学 光电子学 电化学 催化作用 化学 物理化学 电极 生物化学 工程类
作者
Qing Cai,Fang Wang,Jianglai Xiang,Meng Dan,Shan Yu,Ying Zhou
出处
期刊:Frontiers in environmental chemistry [Frontiers Media SA]
卷期号:1 被引量:2
标识
DOI:10.3389/fenvc.2020.591645
摘要

The treatment of hazardous hydrogen sulfide (H 2 S) via photocatalysis technology has been known as one of the most promising green technologies. Photocatalytic production of hydrogen (H 2 ) from H 2 S by two-dimensional (2D) semiconductor materials has gathered great attention owing to its large surface area and high catalytic activity. In this work, layered MoS 2 has been successfully grown on TiO 2 {001} surface to fabricate the 2D MoS 2 /TiO 2 {001} composites for H 2 evolution from H 2 S, which can be confirmed by the X-ray diffraction (XRD) and transmission electron microscopy (TEM) tests. Band structures and UV-Vis spectra provide important evidences that MoS 2 loading can significantly narrow the band gap and broaden the light absorbance into the visible light region. Electron transfer is obviously visualized at the interface of MoS 2 /TiO 2 , resulting in the built-in potential from TiO 2 to MoS 2 , which is determined by the density functional theory (DFT) calculations and X-ray photoelectron spectroscopy (XPS) test. Consequently, the photo-induced electrons and holes are accumulated at the sides of TiO 2 and MoS 2 under the illumination, respectively, which largely promote the interfacial electron transfer and prolong the lifetime of photo-generated electrons that participate in the photocatalytic reactions of H 2 evolution from H 2 S. This efficient separation of photo-induced carriers can be further proved by photoluminescence (PL) spectra, photocurrent responses, and electrochemical impedance spectra. As a result, the photocatalytic activity of H 2 evolution is largely increased by 9.4 times compared to the pristine TiO 2 . This study could offer a new and facile way to design highly efficient 2D photocatalysts for the application of H 2 S treatment.

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