Preparation of water-dispersible porous g-C3N4 with improved photocatalytic activity by chemical oxidation

被引:291
作者
Li, Hui-Jun [1 ]
Sun, Bo-Wen [1 ]
Sui, Li [2 ]
Qian, Dong-Jin [1 ]
Chen, Meng [1 ]
机构
[1] Fudan Univ, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China
[2] Univ Shanghai Sci & Technol, Sch Med Instrument & Food Engn, Shanghai 200093, Peoples R China
基金
中国国家自然科学基金;
关键词
GRAPHITIC CARBON NITRIDE; HYDROGEN EVOLUTION; AQUEOUS-SOLUTIONS; NANOSHEETS; REDUCTION; PERFORMANCE; C3N4; CO2; ELECTROCATALYSTS; CONDUCTIVITY;
D O I
10.1039/c4cp05020g
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
Hydrophilic treatment of bulk graphene-like carbon nitride (g-C3N4) for future applications has aroused extensive interest, due to its enhanced specific surface area and unusual electronic properties. Herein, water-dispersible g-C3N4 with a porous structure can be obtained by chemical oxidation of bulk g-C3N4 with K2Cr2O7-H2SO4. Acid oxidation results in the production of hydroxyl and carboxyl groups on its basal plane and the formation of a porous structure of g-C3N4 at the same time. The porous g-C3N4 appears as networks with tens of micrometers in width and possesses a high specific surface area of 235.2 m(2) g(-1). The final concentration of porous g-C3N4 can be up to 3 mg mL(-1). Compared with bulk g-C3N4, the as-obtained porous g-C3N4 exhibits excellent water dispersion stability and shows great superiority in photoinduced charge carrier separation and transfer. The photocatalytic activities of porous g-C3N4 towards degradation of organic pollutants are much higher than those of the bulk due to the larger band gap (by 0.2 eV) and specific surface areas.
引用
收藏
页码:3309 / 3315
页数:7
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