Ultrafine metal nanoparticles loaded on TiO2 nanorods: Synthesis strategy and photocatalytic activity

被引:15
作者
Dai, Weijiong [1 ]
Yan, Junqing [3 ]
Dai, Ke [2 ]
Li, Landong [3 ]
Guan, Naijia [3 ]
机构
[1] Huazhong Agr Univ, Coll Sci, Wuhan 430070, Hubei, Peoples R China
[2] Huazhong Agr Univ, Coll Resources & Environm, Wuhan 430070, Hubei, Peoples R China
[3] Nankai Univ, Sch Mat Sci & Engn, Key Lab Adv Energy Mat Chem, Minist Educ, Tianjin 300071, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocatalyst; Hydrogen production; Rutile; Brookite; Co-catalyst; TITANIUM-DIOXIDE NANOMATERIALS; DOPED TIO2; REDUCTION; ANATASE; BROOKITE; HYDROGEN; NITRATE; WATER; PHOTOREACTIVITY; DEGRADATION;
D O I
10.1016/S1872-2067(15)60954-8
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Ultrafine noble metal nanoparticles (Pt, Pd, or Au) co-catalyst loaded on the surface of rutile and brookite TiO2 were prepared via a simple photo-deposition strategy under high vacuum conditions. The properties of the prepared samples were determined by different characterization techniques, including X-ray diffraction, transmission electron microscopy, diffuse reflectance ultraviolet-visible spectroscopy, and photoluminescence spectroscopy. The photocatalytic performance of the samples was evaluated by monitoring the reforming of methanol. Co-catalyst loading greatly improved the photocatalytic activity of TiO2. Specifically, Pt-TiO2 displayed the highest photocatalytic activity among all samples studied, followed by Pd-TiO2 and then Au-TiO2. Furthermore, this photocatalytic behavior was not influenced by the intrinsic nature of the TiO2 semiconductor photocatalyst. Similar photocatalytic activity trends were achieved with both sets of noble metal-loaded photocatalysts prepared using rutile and brookite TiO2 as supports. By examining the physicochemical and photocatalytic properties, the factors controlling the photocatalytic activity of the noble metal-loaded TiO2 samples were discussed in detail. (C) 2015, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1968 / 1975
页数:8
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