光催化
制氢
煅烧
贵金属
十二面体
材料科学
分解水
催化作用
光催化分解水
金属
纳米技术
无机化学
化学工程
化学
冶金
结晶学
工程类
生物化学
作者
Xiao‐li Wang,Yang Xiao,Hui Yu,Ying Yang,Xiangting Dong,Long Xia
出处
期刊:Chemcatchem
[Wiley]
日期:2020-08-15
卷期号:12 (22): 5669-5678
被引量:24
标识
DOI:10.1002/cctc.202001118
摘要
Abstract Inspired by the rich morphology of ZnO and cation‐exchange technology, regular dodecahedron‐like CeO 2 /ZnO was obtained by the calcination of Ce doped ZIF‐8 precursor in this study, and CeO 2 /ZnS was obtained by the in‐situ vulcanization of CeO 2 /ZnO. This design not only maintained the morphology of ZIF‐8, but also enhanced the oxidation‐reduction capacity of the catalyst. When the Ce content was 10 wt %, 10‐CeO 2 /ZnS sample showed the best photocatalytic hydrogen production performance in all X−CeO 2 /ZnS samples. Loading of co‐catalysts can effectively enhance the surface hydrogen reduction in photocatalytic water splitting by introducing a positive Schottky barrier. CuS was regarded as a promising cocatalyst to replace the noble metals due to its low cost and equivalent or even better performance. The in‐situ cation exchange method was used to load co‐catalyst CuS on the 10‐CeO 2 /ZnS composites to obtain the 10‐CeO 2 /ZnS‐CuS composites which had the large specific surface area, regular dodecahedral structure and much excellent photolysis of water to produce hydrogen characters. This work provided a new strategy for the advantages combining of co‐catalyst, p‐n junction as well as the porous structure to enhance the photocatalytic characters.
科研通智能强力驱动
Strongly Powered by AbleSci AI