Elsevier

Materials Letters

Volume 64, Issue 22, 30 November 2010, Pages 2462-2464
Materials Letters

An easy fabrication of monodisperse oleic acid-coated Fe3O4 nanoparticles

https://doi.org/10.1016/j.matlet.2010.08.025Get rights and content

Abstract

An easy route is described for the synthesis of monodisperse oleic acid-coated Fe3O4 nanoparticles with uniform size and shape via a thermal decomposition of Fe(acac)3 in the presence of oleic acid (OA). The prepared Fe3O4 samples are characterized by X-ray diffraction, transmission electron microscopy, Fourier transform infrared spectrometry, and vibrating sample magnetometer. The results show that the resulting OA-coated Fe3O4 nanoparticles have an average diameter of about 24 nm and an OA layer, around 3 nm in thickness. The magnetic saturation value of the prepared OA-coated Fe3O4 nanoparticles is determined to be 78.68 emu/g, indicating a well-established superparamagnetic property.

Introduction

The development of nanoparticles has been intensively pursued not only for the fundamental scientific interest, but also for many technological applications [1]. The synthesis of monodisperse nanoparticles is of key importance, because the electrical, optical, and magnetic properties of these nanoparticles depend strongly on their dimensions. For example, monodisperse magnetic nanoparticles have drawn much attention due to their numerous applications, e.g., magnetic storage, magnetic resonance imaging, immunoassay, and drug delivery [2], [3], [4], [5]. Magnetite (Fe3O4) is a common magnetic iron oxide that has a cubic inverse spinel structure with oxygen forming a fcc closed packing and Fe cations occupying interstitial tetrahedral sites and octahedral sites [6]. Over the past decades, there have been a number of synthetic routes to the Fe3O4 nanoparticles, such as coprecipitation, reverse micelle method, hydrothermal method, and thermal decomposition of organometallic or coordination compounds [7], [8], [9], [10], [11], [12]. Among these, thermal decomposition of iron complex (e.g., FeCup3, Fe(CO)5, Fe(acac)3, or Fe(oleate)2) was demonstrated to be a very promising route to the monodisperse Fe3O4 nanoparticles with uniform and controllable size and shape [13], [14], [15]. However, some expensive agents such as 1,2-hexadecanediol or 1-octadece, were often used in these syntheses, which will add cost to the overall fabrication process of the Fe3O4 nanoparticles. Therefore, a large-scale, economic preparation of the monodisperse Fe3O4 nanoparticles without using external expensive reagents will be highly desirable.

One problem faced in the formation of the Fe3O4 nanoparticles is that nanoscale particles with a large surface-to-volume ratio will cause aggregation during particle formation through van der Waals interparticle attractions [16]. To address this issue, stabilizing agents which can attach to the surface of the particles and provide spatial isolation in the synthesis system were used. Wooding et al. prepared stable aqueous magnetic nanoparticles dispersions with various saturated and unsaturated fatty acids as primary and secondary surfactants [17]. Zhao et al. [18] synthesized the Fe3O4 nanoparticles in an aqueous solution coated with bilayer oleic acid (OA). Recently, Lan et al. produced Fe3O4 nanoparticles coated with OA bilayer (a diameter about 12 nm), which are stable over a period of more than 3 months [19]. In this study, we developed a facile, low-cost synthesis of the monodisperse OA-coated Fe3O4 nanoparticles with uniform size and shape via a thermal decomposition of Fe(acac)3 in the presence of OA. Furthermore, the process does not require a size-selection procedure and is readily scaled up for the mass production of magnetic nanoparticles.

Section snippets

Materials

Fe(acac)3 (CP), OA (CP), absolute ethanol (AR), and cyclohexane (AR) were purchased from Sinopharm Chemical Reagent Co. Ltd. (China) and used directly without any further purification.

Preparation of OA-coated Fe3O4 nanoparticles

OA-coated Fe3O4 was synthesized via a facile thermal decomposition of Fe(acac)3 only in the presence of OA. In a typical procedure, 3.6 g of Fe(acac)3 was added to 15 mL of OA at room temperature. The reaction mixture was heated to 120 °C under nitrogen atmosphere with vigorous stirring, and then kept at that

Results and discussion

To determine the crystallinity and structure of the resultant magnetic nanoparticles, powder X-ray diffraction (XRD) was utilized. Fig. 1 shows the XRD pattern of the as-synthesized OA-coated Fe3O4 nanoparticles. All the reflections in the pattern can be indexed from those of a standard sample of the Fe3O4 spinel structure [JC-PDS card No: 26-1136], indicating that the pure Fe3O4 has been obtained. By use of Debye–Scherrer equation for the full width at half-maximum (fwhm) of the (311)

Conclusions

In summary, we have demonstrated a simple, low-cost synthesis of the monodisperse OA-coated Fe3O4 nanoparticles with uniform size and shape by the thermal decomposition of Fe(acac)3 in the presence of OA. Without using any expensive surfactant, such as 1,2-hexadecanediol or 1-octadece, only OA was utilized as the solvent in the synthetic process. The resultant spherical OA-coated Fe3O4 nanoparticles have an average diameter of around 24 nm and an OA layer with thickness of around 3 nm. The

Acknowledgement

This work was supported by the financial supports of the Research Foundation for Talented Scholars of Jiangsu University (08JDG052), the National Natural Science Foundation of China (No. 30772117), and the Natural Science Foundation of Jiangsu Province (No. BK2007096).

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