Fabrication and photocatalytic properties of cationic and anionic S-doped TiO2 nanofibers by electrospinning

被引:110
作者
Ma, Dong [1 ,2 ]
Xin, Yanjun [1 ,2 ]
Gao, Mengchun [1 ]
Wu, Juan [2 ]
机构
[1] Ocean Univ China, Coll Environm Sci & Engn, Qingdao 266100, Peoples R China
[2] Qingdao Agr Univ, Coll Resource & Environm, Qingdao 266109, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocatalyst; TiO2; nanofiber; Sulfur doped; Cationic and anionic doping; Electrospinning; VISIBLE-LIGHT PHOTOCATALYSIS; TITANIUM-DIOXIDE; SOL-GEL; FIBERS; DEGRADATION; COMPOSITE; FILMS; PHOTODEGRADATION; TRANSFORMATION; SPECTROSCOPY;
D O I
10.1016/j.apcatb.2013.08.004
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
In present work, S-doped TiO2 nanofibers, with several hundred nanometers in diameter, have been prepared via electrospinning technique using thiourea and CS2 as the sulfur precursors (denoted as UTF and CTF, respectively). The results revealed that sulfur atoms were successfully incorporated into the bulk phase of TiO2 nanofibers. Cationic doping was found with the substitution of Ti4+ by S6+ and Ti-O-S bonds were formed in the UTF sample, but anionic doping was obtained in the CTF sample and O-Ti-S bonds were produced via the S2- substituted for O2-. Meanwhile, evidence showed that chemisorbed SO42- groups were present on the surface of both S-doped samples. Furthermore, S-doping could effectively inhibit the growth of crystalline grain size and obviously increase light absorbance in visible region. The photocatalytic activity of obtained nanofibers was analyzed for the degradation of organic pollutants by visible-light irradiation, and the photocatalytic mechanism was investigated by employing several scavengers for active species. Results showed that photoinduced holes (h(+)) and chemisorbed hydroxyls (OHads-) on catalyst surface played a vital role in the photocatalysis of UTF system, but photoinduced holes (h(+)) and electrons (e(-)) had the nearly equal importance in CTF system. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:49 / 57
页数:9
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