光催化
材料科学
可见光谱
甲基橙
三元运算
硫化锌
分解水
锰
硫化镉
化学工程
无机化学
催化作用
锌
化学
光电子学
冶金
程序设计语言
工程类
生物化学
计算机科学
作者
Hui Feng,Wenhua Zhou,Xiangyang Zhang,Songbai Zhang,Bo Liu,Deshuai Zhen
标识
DOI:10.1177/2633366x19895020
摘要
The exploration of highly efficient visible-light-driven photocatalysts for dye degradation has received great concerns in wastewater treatment. Here, molybdenum disulfide (MoS 2 ) and cadmium sulfide–manganese (CdS-Mn) were sequentially assembled onto titanium dioxide (TiO 2 ) nanotube by a simple hydrothermal method coupled with successive ionic layer adsorption and reaction. A zinc sulfide (ZnS) layer was introduced as a potential barrier for performance improvement; the resultant material exhibits prominent visible-light-induced photocatalytic activity in degrading methyl orange (MO) and 9-anthracenecarboxylic acids, which is 3.16-fold, 2.00-fold, and 1.69-fold or 2.86-fold, 1.56-fold, and 1.47-fold of TiO 2 , MoS 2 /TiO 2 , and CdS-Mn/TiO 2 systems, respectively. Furthermore, the synthesized ZnS/CdS-Mn/MoS 2 /TiO 2 composite also possesses a high hydrogen production rate of 408.27 mmol/cm 2 /h out of water under visible light illumination, which is about 30.08 times greater than that of pure TiO 2 and 5.18-fold and 2.52-fold of MoS 2 /TiO 2 and CdS-Mn/TiO 2 , respectively. The enhanced photocatalyst performances are mainly attributed to the synergetic effects of CdS-Mn, MoS 2 , and TiO 2 , forming a Z-scheme system in the CdS-Mn/MoS 2 /TiO 2 electrode, which not only accelerates the interfacial charge transfer efficiency but also preserves the strong redox ability of the photogenerated electrons and holes. In addition, the prepared photoelectrode is highly stable and completely recyclable over hydrogen evolution reaction and organic degradation.
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