Photocatalytic performance of Sn-doped TiO2/reduced graphene oxide composite materials

被引:34
作者
Thuy-Duong Nguyen-Phan [1 ]
Viet Hung Pham [1 ]
Chung, Jin Suk [1 ]
Chhowalla, Manish [2 ]
Asefa, Tewodros [3 ,4 ]
Kim, Woo-Jae [5 ]
Shin, Eun Woo [1 ]
机构
[1] Univ Ulsan, Sch Chem Engn & Bioengn, Ulsan 680749, South Korea
[2] Rutgers State Univ, Dept Mat Sci & Engn, Piscataway, NJ 08854 USA
[3] Rutgers State Univ, Dept Chem & Chem Biol, Piscataway, NJ 08854 USA
[4] Rutgers State Univ, Dept Chem & Biochem Engn, Piscataway, NJ 08854 USA
[5] Gachon Univ, Dept Chem & Environm Engn, Songnam 461701, Gyeonggi Do, South Korea
基金
新加坡国家研究基金会; 美国国家科学基金会;
关键词
TiO2; Sn doping; Graphene; Nanocomposite; Photocatalysis; TIO2; DEGRADATION; NANOCOMPOSITES; SPECTROSCOPY; ENHANCEMENT; MECHANISMS; TITANIA; ZNO;
D O I
10.1016/j.apcata.2013.12.030
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
Composite materials of Sn-doped TiO2 nanoparticles (4-6 nm) uniformly anchored onto reduced graphene oxide (RGO) sheets were fabricated by a hydrothermal process. When compared with an undoped TiO2/RGO composite material, the partial substitution of Sn4+ for Ti4+ in TiO2/RGO in different doping concentrations not only increased the specific surface area, but also narrowed the band gap energy of the material. It also resulted in a shift in the photoresponse of the material into the visible light region, an increase in the relative intensity of its Raman (DIG) band, and changes in its X-ray photoelectron spectra; these results implied strong interactions between the Sn species and nanosized TiO2 as well as between the TiO2 and RGO layers. The presence of RGO led to enhanced adsorptivity of methyl orange onto the material compared with that of either pure TiO2 or Sn-doped TiO2. Increasing the Sn dopant content to optimal value facilitated photoactivity under both UV and visible light irradiation. The incorporation of both RGO and Sn dopants significantly modified the electronic structure of TiO2, altering the electron transfer direction and efficiently prohibiting the recombination of photo-induced charge carriers. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:21 / 30
页数:10
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