光催化
异质结
催化作用
三元运算
热液循环
X射线光电子能谱
硫黄
材料科学
硫化物
可见光谱
氮气
光化学
金属
电子转移
化学工程
无机化学
化学
有机化学
光电子学
工程类
冶金
程序设计语言
计算机科学
作者
Qian Zhang,Shaozheng Hu,Zhiping Fan,Dao-Sheng Liu,Yanfeng Zhao,Hongyan Ma,Fayun Li
出处
期刊:Dalton Transactions
[The Royal Society of Chemistry]
日期:2016-01-01
卷期号:45 (8): 3497-3505
被引量:88
摘要
Nitrogen fixation is the second most important chemical process in nature, next to photosynthesis. Herein, we report a novel g-C3N4/ZnMoCdS heterojunction photocatalyst with outstanding nitrogen photofixation ability under visible light prepared by hydrothermal post-treatment. The as-prepared ZnMoCdS is the ternary metal sulfide Zn(0.12)Mo(0.12)Cd(0.9)S(1.14) with many sulfur vacancies, not a mixture of ZnS, MoS2 and CdS. Strong electronic coupling, as evidenced by the UV-Vis, XPS and EIS results, exists between two components in g-C3N4/ZnMoCdS heterojunction photocatalysts, leading to more effective separation of photogenerated electron-hole pairs and faster interfacial charge transfer. The sulfur vacancies on ternary metal sulfides not only serve as active sites to adsorb and activate N2 molecules but also promote interfacial charge transfer from the catalyst to N2 molecules, thus significantly improving their nitrogen photofixation ability. With an optimal ZnMoCdS mass percentage of 80%, the as-prepared heterojunction photocatalyst exhibits the highest NH4(+) generation rate under visible light, which is 13.5-fold and 1.75-fold greater than those of individual g-C3N4 and ZnMoCdS, respectively.
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