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通过有机前体制备热分解方法合成磁性氧化铁纳米粒子的替代低成本方法。

Alternative low-cost approach to the synthesis of magnetic iron oxide nanoparticles by thermal decomposition of organic precursors.

机构信息

CINDECA, CONICET-Universidad Nacional de La Plata, Facultad de Ciencias Exactas, Calle 47 No. 257, La Plata, Argentina.

出版信息

Nanotechnology. 2013 May 3;24(17):175601. doi: 10.1088/0957-4484/24/17/175601. Epub 2013 Apr 3.

DOI:10.1088/0957-4484/24/17/175601
PMID:23548801
Abstract

A new approach to thermal decomposition of organic iron precursors is reported, which results in a simpler and more economical method to produce well crystallized γ-Fe2O3 nanoparticles (NPs) with average sizes within the 3-17 nm range. The NPs were characterized by TEM, SAED, XRD, DLS-QELS, Mössbauer spectroscopy at different temperatures, FT-IR and magnetic measurements. The obtained γ-Fe2O3 NPs are coated with oleic acid and, in a lower quantity, with oleylamine (about 1.5 nm in thickness). It was shown that changing operative variables allows us to tune the average particle diameters and obtain a very narrow or monodisperse distribution of sizes. The γ-Fe2O3 NPs behave superparamagnetically at room temperature and their magnetization saturation is reduced by about 34% in comparison with bulk maghemite. The results indicate that the distance between two neighbour NPs, generated by the coating, of about 3 nm is insufficient to inhibit interparticle magnetic interactions when the average diameter is 8.8 nm. The good quality of the NPs, obtained through the present low-cost and easy-handling process, open a new perspective for future technological applications.

摘要

报道了一种新的有机铁前体热分解方法,该方法可更简单、更经济地制备结晶良好的平均粒径在 3-17nm 范围内的γ-Fe2O3 纳米粒子(NPs)。采用 TEM、SAED、XRD、DLS-QELS、Mössbauer 光谱在不同温度下、FT-IR 和磁测量对 NPs 进行了表征。所得γ-Fe2O3 NPs 用油酸和(厚度约为 1.5nm)较少量的油胺包覆。结果表明,改变操作变量可以调节平均粒径并获得非常窄或单分散的尺寸分布。γ-Fe2O3 NPs 在室温下表现出超顺磁性,其磁化饱和强度与体相磁赤铁矿相比降低了约 34%。结果表明,当平均直径为 8.8nm 时,包覆产生的约 3nm 两个相邻 NPs 之间的距离不足以抑制颗粒间的磁相互作用。通过本低成本且易于处理的方法获得的 NPs 质量好,为未来的技术应用开辟了新的前景。

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