Graphitic-C3N4-hybridized TiO2 nanosheets with reactive {001} facets to enhance the UV- and visible-light photocatalytic activity

被引:268
作者
Gu, Liuan [2 ]
Wang, Jingyu [1 ,2 ]
Zou, Zhijuan [2 ]
Han, Xijiang [2 ]
机构
[1] Huazhong Univ Sci & Technol, Sch Chem & Chem Engn, Wuhan 430074, Peoples R China
[2] Harbin Inst Technol, Dept Chem, Harbin 150001, Peoples R China
基金
中国国家自然科学基金;
关键词
TiO2; Graphitic-C3N4; {001} facets; Hybrid materials; Photocatalysis; GRAPHITIC CARBON NITRIDE; ANATASE TIO2; COMPOSITE PHOTOCATALYST; HIGH PERCENTAGE; DEGRADATION; ACTIVATION; PERFORMANCE; OXIDATION; PHOTODEGRADATION; ABSORPTION;
D O I
10.1016/j.jhazmat.2014.01.021
中图分类号
X [环境科学、安全科学];
学科分类号
083001 [环境科学];
摘要
Anatase TiO2 nanosheets with dominant {0 0 1} facets were hybridized with graphitic carbon nitride (g-C3N4) using a facile solvent evaporation method. On top of the superior photocatalytic performance of highly reactive {0 0 1} facets, the hybridization with g-C3N4 is confirmed to further improve the reactivity through degrading a series of organic molecules under both UV- and visible-light irradiation. It is proposed that an effective charge separation between g-C3N4 and TiO2 exists in the photocatalytic process, i.e., the transferring of photogenerated holes from the valence band (VB) of TiO2 to the highest occupied molecular orbital (HOMO) of g-C3N4, and the injecting of electrons from the lowest unoccupied molecular orbital (LUMO) of g-C3N4 to the conduction band (CB) of TiO2. Due to this synergistic effect, the enhancement of UV- and visible-light photoactivity over the hybrid is achieved. Furthermore, it has been revealed that holes were the main factor for the improved photoactivity under UV-light, while the (OH)-O-center dot radicals gained the predominance for degrading organic molecules under visible-light. Overall, this work would be significant for fabricating efficient UV-/visible-photocatalysts and providing deeper insight into the enhanced mechanisms of pi-conjugated molecules hybridized semiconductors. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:216 / 223
页数:8
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