Hierarchical spheres assembled from large ultrathin anatase TiO2 nanosheets for photocatalytic hydrogen evolution from water splitting

被引:33
作者
Ding, Zixuan [1 ,2 ]
Hu, Haihua [3 ]
Xu, Juan [1 ,2 ]
Lin, Ping [1 ,2 ]
Cui, Can [1 ,2 ]
Qian, Degui [1 ,2 ]
Wang, Peng [1 ,2 ]
Xu, Lingbo [1 ,2 ]
Pan, Jiaqi [1 ,2 ]
Li, Chaorong [1 ,2 ]
机构
[1] Zhejiang Sci Tech Univ, Zhejiang Prov Key Lab Fiber Mat & Mfg Technol, Hangzhou 310018, Zhejiang, Peoples R China
[2] Zhejiang Sci Tech Univ, Dept Phys, Hangzhou 310018, Zhejiang, Peoples R China
[3] Zhejiang Univ City Coll, Hangzhou 310015, Zhejiang, Peoples R China
关键词
TiO2; Hierarchical spheres; Photocatalyst; Water splitting; EXPOSED; 001; FACETS; CARBON-DOPED TIO2; TITANIUM-DIOXIDE; OXYGEN VACANCIES; NANOSTRUCTURES; COMPOSITE; MICROSPHERES; NANOFIBER;
D O I
10.1016/j.ijhydene.2018.05.071
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
We report the synthesis of TiO2 hierarchical spheres (THS) with large specific surface area via a facile one-pot solvothermal method. The as-prepared THS are self-assembled by ultrathin TiO2 nanosheets with thickness of several nanometers and they show a uniform spherical morphology with an average size of 500-700 nm. However, the as-prepared light yellow THS exhibit inferior photocatalytic activity for hydrogen evolution from water splitting due to the poor crystallization of TiO2 and the existence of oxygen vacancies. Significantly, a subsequent thermal treatment improves the crystallinity of THS, reduces the oxygen vacancies, and thereby enhances the photocatalytic performance. It demonstrates that the sample annealed at 550 degrees C (THS550) exhibits the highest photocatalytic activity, about 5 times higher than that of commercial TiO2 nanoparticles (C-TiO2). Moreover, the THS550 sample loaded with 1 wt% Pt exhibits an hydrogen evolution rate as high as 17.9 mmol h(-1)g(-1), and the corresponding apparent quantum efficiency has been determined to be 28.46% under 350 nm light irradiation. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:13190 / 13199
页数:10
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