Template-free synthesis of nanocage-like g-C3N4 with high surface area and nitrogen defects for enhanced photocatalytic H2 activity

被引:140
|
作者
Wu, Mao [1 ]
Gong, Yansheng [1 ]
Nie, Tao [1 ]
Zhang, Jin [1 ]
Wang, Rui [1 ]
Wang, Huanwen [1 ]
He, Beibei [2 ]
机构
[1] China Univ Geosci, Fac Mat Sci & Chem, Wuhan 430074, Hubei, Peoples R China
[2] China Univ Geosci, Minist Educ, Engn Res Ctr Nanogeomat, 388 Lumo Rd, Wuhan 430074, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
GRAPHITIC CARBON NITRIDE; OXYGEN-DOPED G-C3N4; HYDROGEN EVOLUTION; DEFICIENT G-C3N4; FACILE SYNTHESIS; WATER; NANOSHEETS; FABRICATION; EFFICIENCY; PHOSPHORUS;
D O I
10.1039/c8ta12076e
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
Nanocage-like 3D porous graphitic carbon nitride (g-C3N4) with a high surface area and nitrogen defects was successfully prepared via a novel, template-free, cost-effective and hydrothermal-copolymerization route. Compared with pristine g-C3N4, the synergetic effect of nitrogen vacancies combined with a nanocage-like structure endowed it with a broad visible-light-responsive range, more exposed active lateral edges and catalytically active sites, as well as efficient separation of photogenerated carriers. As a consequence, the modified g-C3N4 exhibited prominent photocatalytic performance in water splitting for the hydrogen evolution reaction under visible light illumination. The optimized photocatalyst (DCN-550) showed a maximum photocatalytic H-2 evolution rate of 92.57 mol h(-1), almost 20.3 times higher than that of pristine g-C3N4. Moreover, a possible mechanism for the photocatalytic hydrogen evolution and nanostructure formation process based on the experimental results was proposed. The new growth strategy developed here could inspire similar attempts to modify novel visible-light-driven photocatalysts through nanostructure design.
引用
收藏
页码:5324 / 5332
页数:9
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