A visible-light-driven heterojunction for enhanced photocatalytic water splitting over Ta2O5 modified g-C3N4 photocatalyst

被引:127
|
作者
Hong, Yuanzhi [1 ]
Fang, Zhenyuan [2 ]
Yin, Bingxin [2 ]
Luo, Bifu [2 ]
Zhao, Yong [2 ]
Shi, Weidong [2 ]
Li, Changsheng [1 ]
机构
[1] Jiangsu Univ, Sch Mat Sci & Engn, Zhenjiang 212013, Peoples R China
[2] Jiangsu Univ, Sch Chem & Chem Engn, Zhenjiang 212013, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
g-C3N4; Ta2O5; Heterojunction; Water splitting; Photocatalytic activity; Hydrogen evolution; CARBON NITRIDE NANOSHEETS; CDS QUANTUM DOTS; HYDROGEN-EVOLUTION; H-2; EVOLUTION; EFFICIENT PHOTOCATALYST; Z-SCHEME; GENERATION; NANOCOMPOSITES; FABRICATION; IRRADIATION;
D O I
10.1016/j.ijhydene.2016.12.055
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The photocatalytic water splitting for generation of clean hydrogen energy has received increasingly attention in the field of photocatalysis. In this study, the Ta2O5/g-C3N4 heterojunctions were successfully fabricated via a simple one-step heating strategy. The photocatalytic activity of as-prepared photocatalysts were evaluated by water splitting for hydrogen evolution under visible-light irradiation (lambda > 420 nm). Compared to the pristine g-C3N4, the obtained heterojunctions exhibited remarkably improved hydrogen production performance. It was found that the 7.5%TO/CN heterojunction presented the best photo catalytic hydrogen evolution efficiency, which was about 4.2 times higher than that of pure g-C3N4. Moreover, the 7.5%TO/CN sample also displayed excellent photochemical stability even after 20 h photocatalytic test. By further experimental study, the enhanced photo catalytic activity is mainly attributed to the significantly improve the interfacial charge separation in the heterojunction between g-C3N4 and Ta2O5. This work provides a facile approach to design g-C3N4-based photocatalyst and develops an efficient visible-light driven heterojunction for application in solar energy conversion. (C) 2016 Published by Elsevier Ltd on behalf of Hydrogen Energy Publications LLC.
引用
收藏
页码:6738 / 6745
页数:8
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