Physicochemical characterization of Fe3O4/SiO2/Au multilayer nanostructure

被引:16
|
作者
Khosroshahi, Mohammad E. [1 ]
Ghazanfari, Lida [1 ]
机构
[1] Amirkabir Univ Technol, Biomat Grp, Fac Biomed Engn, Laser & Nanobiophoton Lab, Tehran 158754413, Iran
关键词
Nanostructures; Magnetic materials; Optical properties; Atomic force microscopy (AFM); IRON-OXIDE NANOPARTICLES; GOLD NANOSHELLS; MAGNETIC-PROPERTIES; OPTICAL-PROPERTIES; SIZE; NANOCOMPOSITES; PARTICLES; SURFACE; CORE;
D O I
10.1016/j.matchemphys.2011.12.047
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The purpose of this research was to synthesize and characterize gold-coated Fe3O4/SiO2 nanoshells for biomedical applications. Magnetite nanoparticles (NPs) were prepared using co-precipitation method. Smaller particles were synthesized by decreasing the NaOH concentration, which in our case this corresponded to 35 nm using 0.9M of NaOH at 750 rpm with a specific surface area of 41 m(2) g(-1). For uncoated Fe3O4 NPs, the results showed an octahedral geometry with saturation magnetization range of 80-100 emu g(-1) and coercivity of 80-120 Oe for particles between 35 and 96 nm, respectively. The magnetic NPs were modified with a thin layer of silica using Stober method. Small gold colloids (1-3 nm) were synthesized using Duff method and covered the amino functionalized particle surface. Magnetic and optical properties of gold nanoshells were assessed using Brunauer-Emmett-Teller (BET), vibrating sample magnetometer (VSM), UV-Vis spectrophotometer, atomic and magnetic force microscope (AFM, MFM), and transmission electron microscope (TEM). Based on the X-ray diffraction (XRD) results, three main peaks of Au (111), (200) and (220) were identified. The formation of each layer of a nanoshell is also demonstrated by Fourier transform infrared (FTIR) results. The Fe3O4/SiO2/Au nanostructures, with 85 nm as particle size, exhibited an absorption peak at similar to 550 nm with a magnetization value of 1.3 emu g(-1) with a specific surface area of 71 m(2) g(-1). (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:55 / 62
页数:8
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