Preparation and photocatalytic properties of Fe3+-doped Ag@TiO2 core-shell nanoparticles

被引:114
作者
Wang, Wenjiao [1 ,2 ]
Zhang, Jinlong [1 ,2 ]
Chen, Feng [1 ,2 ]
He, Dannong [3 ]
Anpo, Masakazu [4 ]
机构
[1] E China Univ Sci & Technol, Adv Mat Lab, Shanghai 200237, Peoples R China
[2] E China Univ Sci & Technol, Inst Fine Chem, Shanghai 200237, Peoples R China
[3] Shanghai Natl Engn Res Ctr Nanotechnol, Shanghai 200237, Peoples R China
[4] Osaka Prefecture Univ, Grad Sch Engn, Dept Appl Chem, Osaka 5998531, Japan
关键词
titanium oxide; photodegradation; Ag@TiO2; Fe3+ doping; core-shell structure;
D O I
10.1016/j.jcis.2008.03.043
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
Ag@TiO2 core-shell-type nanophotocatalysts have been prepared using a simple and convenient method. The products were characterized by TEM, XRD, and UV-vis spectra. To make the catalysts achieve the highest photocatalytic activity under UV light illumination, the Ag content of Ag@TiO2 was optimized. The results showed that Ag@TiO2-doped Fe3+ extend their absorption into the visible region. Among the Fe3+-doped samples, Ag@Fe-TiO2 with low Ag content showed higher photocatalytic activity under visible light illumination. An excessive added amount of Ag would reduce Fe3+ to Fe2+ and make them difficult to be incorporated into the lattice of titania. From the experiments, we found that Fe3+ ions could stabilize the Ag@TiO2 colloid by holding back the aggregation of the core-shell nanoparticles. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:182 / 186
页数:5
相关论文
共 20 条
[1]   Kinetics of hydrogen production upon reduction of aqueous TiO2 nanoparticles catalyzed by Pd0, Pt0, or Au0 coatings and an unusual hydrogen abstraction;: Steady state and pulse radiolysis study [J].
Behar, D ;
Rabani, J .
JOURNAL OF PHYSICAL CHEMISTRY B, 2006, 110 (17) :8750-8755
[2]   Preparation of highly uniform Ag/TiO2 and Au/TiO2 supported nanoparticle catalysts by photodeposition [J].
Chan, SC ;
Barteau, MA .
LANGMUIR, 2005, 21 (12) :5588-5595
[3]   THE ROLE OF METAL-ION DOPANTS IN QUANTUM-SIZED TIO2 - CORRELATION BETWEEN PHOTOREACTIVITY AND CHARGE-CARRIER RECOMBINATION DYNAMICS [J].
CHOI, WY ;
TERMIN, A ;
HOFFMANN, MR .
JOURNAL OF PHYSICAL CHEMISTRY, 1994, 98 (51) :13669-13679
[4]  
Fujishima A., 2000, Journal of Photochemistry and Photobiology C: Photochemistry Reviews, V1, P1, DOI [10.1016/S1389-5567(00)00002-2, DOI 10.1016/S1389-5567(00)00002-2]
[5]   Charge separation and catalytic activity of Ag@TiO2 core-shell composite clusters under UV-irradiation [J].
Hirakawa, T ;
Kamat, PV .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (11) :3928-3934
[6]   ENVIRONMENTAL APPLICATIONS OF SEMICONDUCTOR PHOTOCATALYSIS [J].
HOFFMANN, MR ;
MARTIN, ST ;
CHOI, WY ;
BAHNEMANN, DW .
CHEMICAL REVIEWS, 1995, 95 (01) :69-96
[7]   Photocatalytic degradation of triazine-containing azo dyes in aqueous TiO2 suspensions [J].
Hu, C ;
Yu, JC ;
Hao, ZP ;
Wong, PK .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2003, 42 (01) :47-55
[8]   PHOTOCHEMISTRY ON NONREACTIVE AND REACTIVE (SEMICONDUCTOR) SURFACES [J].
KAMAT, PV .
CHEMICAL REVIEWS, 1993, 93 (01) :267-300
[9]   Visible light active platinum-ion-doped TiO2 photocatalyst [J].
Kim, S ;
Hwang, SJ ;
Choi, WY .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (51) :24260-24267
[10]   Study of Au/Au3+-TiO2 photocatalysts toward visible photooxidation for water and wastewater treatment [J].
Li, XZ ;
Li, FB .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2001, 35 (11) :2381-2387