Improvement in photocatalytic H2 evolution over g-C3N4 prepared from protonated melamine

被引:132
作者
Zhong, Yujiao [1 ]
Wang, Zhiqiang [1 ]
Feng, Jianyong [1 ]
Yan, Shicheng [1 ]
Zhang, Haitao [2 ]
Li, Zhaosheng [1 ]
Zou, Zhigang [1 ]
机构
[1] Nanjing Univ, Natl Lab Solid State Microstruct, Coll Engn & Appl Sci, ERERC, Nanjing 210093, Jiangsu, Peoples R China
[2] Univ Jinan, Sch Chem & Chem Engn, Guangzhou, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
g-C3N4; Protonation; Porous structure; Photocatalytic H-2 evolution; Condensation degree; GRAPHITIC CARBON NITRIDE; HYDROGEN-PRODUCTION; MESOPOROUS G-C3N4; WATER; PHOTODEGRADATION; NANOPARTICLES; MORPHOLOGY; MPG-C3N4; CATALYST; SOLIDS;
D O I
10.1016/j.apsusc.2014.01.008
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
Porous g-C3N4 (pm-g-C3N4) samples were prepared by sintering protonated melamine. Photocatalytic activities for H-2 production over the g-C3N4 samples were evaluated under visible-light irradiation. Specific surface areas and condensation degree of the g-C3N4 samples prepared from protonated melamine turn larger as the calcination temperatures increase (400 degrees C, 450 degrees C, 500 degrees C, 550 degrees C, and 580 degrees C for 1 h). Also, their bandgaps are narrowed and PL peak red shifts, and thus their photocatalytic activities are enhanced. Compared with the reference g-C3N4 samples synthesized by sintering melamine without any protonation (m-g-C3N4), the pm-g-C3N4 samples exhibit better photocatalytic performances, owing to larger specific surface area, less recombination of photogenerated carriers and higher degree of condensation. By optimizing the preparation parameters and the amount of Pt cocatalyst, the highest hydrogen evolution rate of 417 mu mol h(-1) g(-1) was achieved over the pm-g-C3N4 samples synthesized at 550 degrees C for 2 h, when irradiated by 300-W Xe lamp with a cutoff filter (lambda > 420 nm). (C) 2014 Elsevier B. V. All rights reserved.
引用
收藏
页码:253 / 259
页数:7
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