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
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI