Chen Yuanzhi, She Houde, Luo Xiaohua, Yue Guang-Hui, Mi Wen-Bo, Bai Hai-Li, Peng Dong-Liang
Department of Materials Science and Engineering, College of Materials, Research Center for Materials Design and Application, Xiamen University, Xiamen 361005, PR China.
J Nanosci Nanotechnol. 2010 May;10(5):3053-9. doi: 10.1166/jnn.2010.2181.
We report a chemical route for the preparation of monodisperse Fe-Ni nanoparticles with tunable compositions and sizes. Unlike commonly used synthetic approaches that involve the simultaneous reduction of metal precursors in the presence of reducing agents, the approach developed in this study utilizes pre-formed Ni nanoparticles to react with Fe(III) acetylacetonate in high boiling-point solvents, wherein newly-generated Fe atoms diffuse into Ni nanoparticles to form Fe-Ni nanoparticles. The analytic results of powder X-ray diffraction (XRD) and transmission electron microscopy (TEM) show that the as-synthesized Fe-Ni nanoparticles possess a face-centered cubic (fcc) crystalline structure and have a spherical or near-spherical morphology. X-ray photoelectron spectroscopy (XPS) study reveals metallic characteristics for the chemical state of Fe and Ni. The particle morphology and size distribution of the as-synthesized Fe-Ni nanoparticles are regulated by the pre-formed Ni nanoparticles, while the composition can be adjusted to some extent by the ratio of Fe precursor to Ni nanoparticles. Magnetic measurements reveal a superparamagnetic characteristic above the blocking temperature for the as-synthesized Fe-Ni nanoparticles. The synthetic approach may also be applied to other bimetallic nanoparticle systems.
我们报道了一种制备具有可调组成和尺寸的单分散铁镍纳米颗粒的化学方法。与常用的在还原剂存在下同时还原金属前驱体的合成方法不同,本研究开发的方法利用预先形成的镍纳米颗粒在高沸点溶剂中与乙酰丙酮铁(III)反应,其中新生成的铁原子扩散到镍纳米颗粒中形成铁镍纳米颗粒。粉末X射线衍射(XRD)和透射电子显微镜(TEM)的分析结果表明,合成的铁镍纳米颗粒具有面心立方(fcc)晶体结构,并且具有球形或近球形形态。X射线光电子能谱(XPS)研究揭示了铁和镍化学状态的金属特性。合成的铁镍纳米颗粒的颗粒形态和尺寸分布由预先形成的镍纳米颗粒调节,而组成可以通过铁前驱体与镍纳米颗粒的比例在一定程度上进行调整。磁性测量表明,合成的铁镍纳米颗粒在高于阻塞温度时具有超顺磁性特征。该合成方法也可应用于其他双金属纳米颗粒体系。