Hydrothermal Synthesis g-C3N4/Nano-InVO4 Nanocomposites and Enhanced Photocatalytic Activity for Hydrogen Production under Visible Light Irradiation

被引:167
作者
Hu, Bo [1 ]
Cai, Fanpeng [2 ]
Chen, Tianjun [1 ]
Fan, Mingshan [1 ]
Song, Chengjie [3 ]
Yan, Xu [1 ]
Shi, Weidong [1 ]
机构
[1] Jiangsu Univ, Sch Chem & Chem Engn, Zhenjiang 212013, Peoples R China
[2] Jiangsu Univ Sci & Technol, Sch Biol & Chem Engn, Zhenjiang 212003, Peoples R China
[3] Changzhou Univ, Sch Environm & Safety Engn, Changzhou 213000, 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; InVO4; nanocomposites; interface; H-2 production from water splitting; heterojunction; Z-SCHEME; EVOLVING PHOTOCATALYST; INVO4; MICROSPHERES; CARBON NITRIDE; H-2; PRODUCTION; G-C3N4; EVOLUTION; WATER; PERFORMANCE; COMPOSITE;
D O I
10.1021/acsami.5b05715
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
We synthesized g-C3N4/nano-InVO4 heterojunction-type photocatalyts by in situ growth of InVO4, nanopartides onto the surface of g-C3N4 sheets via a hydrothermal process. The results of SEM and TEM showed that the obtained InVO4 nanopartides 20 nm in size dispersed uniformly on the surface of g-C3N4 sheets, which revealed that g-C3N4 sheets was probably a promising support for in situ growth of nanosize materials. The achieved intimate interface promoted the charge transfer and inhibited the recombination rate of photogenerated electron hole pairs, which significantly improved the photocatalytic activity. A possible growth process of g-C3N4/nano-InVO4 nanocomposites was proposed based on different mass fraction of g-C3N4 content. The obtained g-C3N4/nano-InVO4 nanocomposites could achieve effective separation of charge-hole pairs and stronger reducing power, which caused enhanced H-2 evolution from water-splitting compared with bare g-C3N4 sheets and g-C3N4/micro-InVO4 composites, respectively. As a result, the g-C3N4/nano-InVO4 nanocomposite with a mass ratio of 80:20 possessed the maximum photocatalytic activity for hydrogen production under visible-light irradiation.
引用
收藏
页码:18247 / 18256
页数:10
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