Full visible-light absorption of TiO2 nanotubes induced by anionic S22- doping and their greatly enhanced photocatalytic hydrogen production abilities

被引:65
作者
Sun, Shuchao [1 ]
Zhang, Jianjiao [1 ]
Gao, Peng [1 ]
Wang, Ying [1 ]
Li, Xiaobo [1 ]
Wu, Tingting [1 ]
Wang, Yanbo [1 ]
Chen, Yujin [2 ]
Yang, Piaoping [1 ]
机构
[1] Harbin Engn Univ, Coll Mat Sci & Chem Engn, Key Lab Supertight Mat & Surface Technol, Minist Educ, Nantong St 145, Harbin 150001, Heilongjiang, Peoples R China
[2] Harbin Engn Univ, Coll Sci, Nantong St 145, Harbin 150001, Heilongjiang, Peoples R China
关键词
Hydrogen; Layer structure; S-2(2-)-doped TiO2; S-DOPED TIO2; TITANIUM-DIOXIDE; PYRITE FES2; SULFUR; WATER; DEGRADATION; ARRAYS; PERFORMANCE; SURFACES; NITROGEN;
D O I
10.1016/j.apcatb.2017.01.027
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, as a benchmark photocatalyst for hydrogen production through water splitting, has a relatively large band gap (3.2 eV for anatase and 3.0 eV for rutile) requiring UV light (290-400 nm) for electronic excitations from the valence band to the conduction band, hence utilizing only a small part of the solar spectrum. The construction of new electronic band gap, especially in the visible region (400-800 nm), is of great importance for improving TiO2 optical and photocatalytic properties. In this work, though it is deem metastable and can induce a broad visible-light adsorption in previous literatures, anionic S-2(2) has been successfully introduced into TiO2 nanotubes, which is different from the previous works about S-doped TiO2 that contain only cationic S4+ and S6+. Resultantly, the S-2(2-) doped TiO2 nanotubes exhibit a full visible-light absorption (from 400 to 800 nm) and a greatly enhanced photocatalytic H-2-production rate under visible-light irradiation (9610 mu mol h(-1) g(-1), about 13.7 and 37 times of other cationic and anion S-doped TiO2 nanoparticles, respectively, almost highest in all the results reported previously in literatures of TiO2 doped with non-metal elements).(C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:168 / 174
页数:7
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