Engineering highly active TiO2 photocatalysts via the surface-phase junction strategy employing a titanate nanotube precursor

被引:86
作者
Liu, Yuanxu
Wang, Zhonglei
Wang, Wendong [1 ]
Huang, Weixin [1 ]
机构
[1] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Peoples R China
关键词
Photocatalytic H-2 production; TiO2; photocatalyst; Titanate; Surface-phase junction; Phase transition; TITANIUM-DIOXIDE NANOMATERIALS; HIGH QUANTUM EFFICIENCY; HYDROGEN-PRODUCTION; CONTROLLABLE SYNTHESIS; RAMAN-SPECTRUM; ANATASE TIO2; PT-PDS/CDS; BROOKITE; TRANSFORMATION; NANOSTRUCTURES;
D O I
10.1016/j.jcat.2013.03.024
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
TiO2 photocatalysts were synthesized by the hydrothermal treatment of titanate nanotube precursor at different HNO3 concentrations. Their structures were characterized, and their photocatalytic activity in H-2 production from water was evaluated. The phase structure of TiO2 photocatalysts is dependent on the HNO3 concentration employed during the hydrothermal treatment and varies from pure anatase to pure rutile with increasing HNO3 concentration, with the heterophase in-between. The heterophase TiO2 photocatalysts exhibit large specific surface areas and intimately contacting anatase-brookite and anatase-rutile surface junctions. The presence of anatase-brookite and anatase-rutile-phase junctions on heterophase TiO2 photocatalysts was found to efficiently suppress recombination of photoinduced charge carriers in TiO2. The heterophase TiO2 photocatalysts are photocatalytically active in H-2 production from water. TiO2 photocatalysts consisting of 72.9 wt% anatase, 24.6 wt% brookite, and 2.5 wt% rutile exhibits a photocatalytic H-2 yield of 179 mu mol h(-1) g(-1) under Xe lamp irradiation, about four times that of P25 (45.3 mu mol h(-1) g(-1)) under the same reaction conditions. These results demonstrate that the surface-phase junction strategy is very useful for engineering highly active TiO2 photocatalysts, and there still exists plenty of space to explore. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:16 / 23
页数:8
相关论文
共 48 条
[41]   Understanding polymorphic phase transformation behavior during growth of nanocrystalline aggregates:: Insights from TiO2 [J].
Zhang, HZ ;
Banfield, JF .
JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (15) :3481-3487
[42]   UV Raman spectroscopic study on TiO2.: I.: Phase transformation at the surface and in the bulk [J].
Zhang, J ;
Li, MJ ;
Feng, ZC ;
Chen, J ;
Li, C .
JOURNAL OF PHYSICAL CHEMISTRY B, 2006, 110 (02) :927-935
[43]   Importance of the relationship between surface phases and photocatalytic activity of TiO2 [J].
Zhang, Jing ;
Xu, Qian ;
Feng, Zhaochi ;
Li, Meijun ;
Li, Can .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2008, 47 (09) :1766-1769
[44]   Photocatalytic Degradation of Rhodamine B on Anatase, Rutile, and Brookite TiO2 [J].
Zhang Jing ;
Yan Song ;
Fu Lu ;
Wang Fei ;
Yuan Mengqiong ;
Luo Genxiang ;
Xu Qian ;
Wang Xiang ;
Li Can .
CHINESE JOURNAL OF CATALYSIS, 2011, 32 (06) :983-991
[45]   Phase transition and morphological evolution of titania/titanate nanomaterials under alkalescent hydrothermal treatment [J].
Zhao, Bin ;
Chen, Feng ;
Jiao, Yanchao ;
Zhang, Jinlong .
JOURNAL OF MATERIALS CHEMISTRY, 2010, 20 (37) :7990-7997
[46]   Phase transformation of TiO2 nanobelts and TiO2(B)/anatase interface heterostructure nanobelts with enhanced photocatalytic activity [J].
Zhou, Weijia ;
Gai, Ligang ;
Hu, Peiguang ;
Cui, Jingjie ;
Liu, Xiaoyan ;
Wang, Dongzhou ;
Li, Guohong ;
Jiang, Huaidong ;
Liu, Duo ;
Liu, Hong ;
Wang, Jiyang .
CRYSTENGCOMM, 2011, 13 (22) :6643-6649
[47]   Hydrogen titanate nanofibers covered with anatase nanocrystals: A delicate structure achieved by the wet chemistry reaction of the titanate nanofibers [J].
Zhu, HY ;
Gao, XP ;
Lan, Y ;
Song, DY ;
Xi, YX ;
Zhao, JC .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (27) :8380-8381
[48]   Phase transition between nanostructures of titanate and titanium dioxides via simple wet-chemical reactions [J].
Zhu, HY ;
Lan, Y ;
Gao, XP ;
Ringer, SP ;
Zheng, ZF ;
Song, DY ;
Zhao, JC .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (18) :6730-6736