Facile stir-dried preparation of g-C3N4/TiO2 homogeneous composites with enhanced photocatalytic activity

被引:52
|
作者
Qiu, Jianhao [1 ]
Feng, Yi [1 ]
Zhang, Xiongfei [1 ]
Zhang, Xingguang [1 ]
Jia, Mingmin [1 ]
Yao, Jianfeng [1 ,2 ]
机构
[1] Nanjing Forestry Univ, Coll Chem Engn, Nanjing 210037, Jiangsu, Peoples R China
[2] Jiangsu Key Lab Biomass Based Green Fuels & Chem, Nanjing 210037, Jiangsu, Peoples R China
关键词
GRAPHITIC CARBON NITRIDE; IN-SITU SYNTHESIS; METHYL-ORANGE; THIN-FILMS; TIO2; UV; REMOVAL; HETEROJUNCTIONS; SEMICONDUCTORS; NANOCOMPOSITE;
D O I
10.1039/c7ra00050b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
g- C3N4/ TiO2 composites with homogeneous well-combined structures were prepared by a simple stirdried method, using dicyandiamide (DICY) and tetrabutyl orthotitanate (TBOT) as the precursors, followed by high-temperature calcination. Various characterization techniques including XRD, FTIR, nitrogen adsorption-desorption, SEM and XPS confirm the formation of an interconnected structure between g-C3N4 and TiO2 in the composites. g-C3N4/ TiO2 composites exhibit much higher photocatalytic activity than that of pure g-C3N4 and TiO2 in the degradation of methylene blue under visible light. In particular, the CT-5 composite prepared with DICY/ TBOT at a mass ratio of 5 : 1, exhibited a photodegradation activity that is about 3.8 times that of TiO2 and 2.9 times that of pure gC(3)N(4). The homogeneous g-C3N4/ TiO2 composite CT-5 can be repetitively used without significant loss of activity. The strong synergistic effect between g-C3N4 and TiO2 achieved by this preparation method greatly improves the separation efficiency of photo-generated electrons and holes, thus offering enhanced photocatalytic performances.
引用
收藏
页码:10668 / 10674
页数:7
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