Photocatalytic and antibacterial properties of Au-decorated Fe3O4@mTiO2 core-shell microspheres

被引:58
作者
Li, Cuiyan [1 ,3 ]
Younesi, Reza [1 ]
Cai, Yanling [2 ]
Zhu, Yihua [3 ]
Ma, Mingguo [4 ]
Zhu, Jiefang [1 ]
机构
[1] Uppsala Univ, Dept Chem, Angstrom Lab, S-75121 Uppsala, Sweden
[2] Uppsala Univ, Div Nanotechnol & Funct Mat, Angstrom Lab, S-75121 Uppsala, Sweden
[3] E China Univ Sci & Technol, Key Lab Ultrafine Mat, Minist Educ, Shanghai 200237, Peoples R China
[4] Beijing Forestry Univ, Coll Mat Sci & Technol, Inst Biomass Chem & Technol, Beijing 100083, Peoples R China
关键词
Fe3O4; microsphere; Mesoporous TiO2; Core-shell structure; Au nanoparticle; Photocatalysis; Antibacterial effect; Recycle; CORE/SHELL MICROSPHERES; HIGHLY EFFICIENT; ACTIVITY TIO2; DEGRADATION; PARTICLES; SURFACE; ANATASE; ARRAYS; WATER; PH;
D O I
10.1016/j.apcatb.2014.03.031
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
A facile approach for the fabrication of Au-decorated mesoporous Fe3O4@TiO2 (Fe3O4@mTiO(2)) core-shell microspheres is demonstrated. The protocol involved the coating of a successive layer of TiO2 onto a magnetic Fe3O4 core via a sol-gel process, followed by TiO2 crystallization and mesopore-formation by a hydrothermal treatment, and then the deposition of Au nanoparticles onto Fe3O4@mTiO(2) microspheres through an in situ reduction of perchloric acid. The mesoporous microspheres (Fe3O4@mTiO(2)) showed stronger magnetic properties than the dense sample (Fe3O4@TiO2) before the hydrothermal treatment. The size and loading amount of Au nanoparticles were controlled by the reduction temperature and concentration of Au salt, respectively. Compared to unmodified Fe3O4@mTiO(2) microspheres, Fe3O4@mTiO(2)@Au microspheres showed higher photocatalytic activity for organic degradation and antibacterial action in water. These core-shell Fe3O4@mTiO(2)@Au microspheres can serve as efficient and recyclable photocatalysts, which have promising applications in environmental treatment. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:314 / 322
页数:9
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