光催化
聚丙烯腈
材料科学
复合数
纳米片
化学工程
比表面积
复合材料
纳米技术
催化作用
碳纳米管
有机化学
化学
工程类
聚合物
作者
Fang He,Gang Chen,Jianwei Miao,Zhenxing Wang,Dongmeng Su,Song Liu,Weizheng Cai,Liping Zhang,Sue Hao,Bin Liu
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2016-10-12
卷期号:1 (5): 969-975
被引量:98
标识
DOI:10.1021/acsenergylett.6b00398
摘要
Hollow one-dimensional (1-D) nanostructures have drawn great attention in heterogeneous photocatalysis. Herein, we report that tapered polyacrylonitrile-derived carbon (C-PAN)/g-C3N4 composite nanotubes can be synthesized through a facile sulfur-mediated self-templating method via thermal condensation of polyacrylonitrile (PAN), melamine, and sulfur. The hollow tapered C-PAN/g-C3N4 composite nanotubes exhibit superior photocatalytic H2 evolution performance under visible light irradiation. The 5 wt % C-PAN/g-C3N4 composite nanotubes show a 16.7 times higher photocatalytic H2 evolution rate than that of pure g-C3N4, which is even 4.7 times higher than that of a 5 wt % C-PAN/g-C3N4 nanosheet composite obtained without sulfur. The hollow nanotubular composite structure provides g-C3N4 with higher specific surface area, enhanced light absorption, and better charge carrier separation and transfer, which synergistically contribute to the superior photocatalytic activity. Our work provides a new strategy to develop carbon-based architected photocatalysts.
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