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Preparation and characterization of flower-like gold nanomaterials and iron oxide/gold composite nanomaterials

We have successfully synthesized flower-like gold nanomaterials and Fe3O4/Au composite nanomaterials through the use of wet chemical methods in aqueous solution. In the presence of 0.5 mM citrate, 0.313 mM poly(ethylene glycol), and 109.72 mM sodium acetate (NaOAc), we prepared Au nanoflowers (NFs)...

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Bibliographic Details
Published in:Nanotechnology 2007-06, Vol.18 (25), p.255606-255606 (7)
Main Authors: Yang, Zusing, Hong Lin, Zong, Tang, Chih-Yuan, Chang, Huan-Tsung
Format: Article
Language:English
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Summary:We have successfully synthesized flower-like gold nanomaterials and Fe3O4/Au composite nanomaterials through the use of wet chemical methods in aqueous solution. In the presence of 0.5 mM citrate, 0.313 mM poly(ethylene glycol), and 109.72 mM sodium acetate (NaOAc), we prepared Au nanoflowers (NFs) having diameters ranging from 300 to 400 nm in aqueous solution after the reduction of Au ions at room temperature for 10 min. In the presence of spherical Fe3O4 nanomaterials, we applied a similar synthetic method to prepare Fe3O4/Au composite nanomaterials, including nanowires (NWs) that have a length of 1.58 mum and a width of 28.3 nm. We conducted energy-dispersive x-ray analysis, scanning electron microscopy, transmission electron microscopy (TEM), ultraviolet-visible (UV-vis) absorption, and x-ray powder diffraction measurements to characterize the as-prepared flower-like Au nanomaterials and Fe3O4/Au composite nanomaterials. From time-evolution TEM measurements, we suggested that Au atoms that were bound to the Fe3O4 nanomaterials grew to form Fe3O4/Au composite nanomaterials. The as-prepared Au NFs absorbed light strongly in the visible-near-infrared (Vis-NIR) region (500-1200 nm). The Fe3O4/Au composite nanomaterials had electronic conductivities greater than 100 nA at an applied voltage of 20 mV, which induced a temperature increase of 20.5 +/- 0.5 deg C under an alternating magnetic field (62 muT).
ISSN:0957-4484
1361-6528
DOI:10.1088/0957-4484/18/25/255606