Synchronous surface hydroxylation and porous modification of g-C3N4 for enhanced photocatalytic H2 evolution efficiency

被引:40
作者
Wang, Xiao-jing [1 ]
Tian, Xiao [1 ]
Li, Fa-tang [1 ]
Li, Yu-pei [1 ]
Zhao, Jun [1 ]
Hao, Ying-juan [1 ]
Liu, Ying [1 ]
机构
[1] Hebei Univ Sci & Technol, Coll Sci, Shijiazhuang 050018, Peoples R China
基金
中国国家自然科学基金;
关键词
Graphitic carbon nitride; Porous materials; Photocatalysis; H-2; evolution; Ammonium hydroxide; GRAPHITIC CARBON NITRIDE; HYDROGEN-PRODUCTION; WATER; NANOSHEETS; PHOTOREACTIVITY; HETEROJUNCTION; DEGRADATION; PERFORMANCE; CATALYST; MELAMINE;
D O I
10.1016/j.ijhydene.2016.01.004
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
Synchronous strategy of nanocrystallization and surface modification for g-C3N4 was developed via a facile hydrothermal route in ammonium hydroxide solution. The characterization results reveal that the tailored sample possesses not only an irregular porous structure, higher BET specific surface area, larger band gap, but also rich surface H-bond network. The photocurrent responses and electrochemical impedance spectroscopy indicate that the modification process by ammonium hydroxide via hydrothermal reaction can also accelerate the interfacial charge transfer and improve the separation efficiency of photogenerated charges. As a result, the photocatalytic hydrogen generation rate of tailored g-C3N4 is 4.2 times that of bulk g-C3N4. Copyright (C) 2016, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:3888 / 3895
页数:8
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