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Magnetic properties of self-assembled iron nanoparticle arrays.

机译:自组装铁纳米颗粒阵列的磁性。

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摘要

Nanoparticles of Fe were synthesized via thermal decomposition of iron pentacarbonyl, Fe(CO)5, in the presence of surfactants. Heterogeneously nucleating particles from Pt seeds led to high moment, minimally oxidized Fe particles 4.5–9 nm in diameter. Homogeneous nucleation of particles in the presence of an excess of oleic acid led to formation of partially oxidized particles, consisting of an Fe core and an oxide shell, 9–19 nm in diameter. Once synthesized, the particles were dispersed in hexane, and the hexane evaporated from the dispersion. During the evaporation, the particles self-assembled to form particle superlattices. The size and quality of the particle arrays depended on particle and surfactant concentration and drying conditions. Transmission electron microscopy (TEM) was used to characterize the size and structure of both particles and particle superlattices. Structural evidence for magnetic interactions between particles in the arrays was observed. Samples of hcp superlattices of 6.6 nm, high moment Fe particles displayed a preference for odd numbers of layers. This was not observed in arrays of low moment particles, and has not been reported for non-magnetic particles. The magnetic properties of dilute particle suspensions and dried particle arrays were measured using a Quantum Design MPMS magnetometer. The hysteretic and remanent behavior of both the dispersions and dried assemblies were indicative of the existence of dipole interactions between particles. Differences in the magnetic behavior of dispersions and arrays indicated that dipole interaction effects depend on the size and structure of particle assemblies. Magnetizing interactions play a larger role in the large, close-packed arrays than in the smaller, loosely-associated clusters contained in the dispersions. The magnetizing effects in the arrays can be enhanced by decreasing the interparticle spacing. The arrays were also magnetically anisotropic, with magnetic properties depending on the angle between the applied field direction and the array plane.
机译:在表面活性剂存在下,通过热分解五羰基铁Fe(CO) 5 合成Fe的纳米颗粒。 Pt晶种的异质成核颗粒导致高矩,直径4.5–9 nm的最小氧化的Fe颗粒。在过量油酸的存在下,颗粒的均相成核导致形成部分氧化的颗粒,该颗粒由铁核和直径为9-19 nm的氧化物壳组成。合成后,将颗粒分散在己烷中,并将己烷从分散液中蒸发。在蒸发过程中,粒子自组装形成粒子超晶格。颗粒阵列的大小和质量取决于颗粒和表面活性剂的浓度以及干燥条件。透射电子显微镜(TEM)用于表征颗粒和颗粒超晶格的尺寸和结构。观察到阵列中颗粒之间的磁性相互作用的结构证据。 6.6 nm高矩Fe颗粒的hcp超晶格样品显示出对奇数层的偏爱。在低矩粒子阵列中未观察到这种现象,对于非磁性粒子也未见报道。使用Quantum Design MPMS磁力计测量稀颗粒悬浮液和干燥颗粒阵列的磁性。分散体和干燥组件的滞后和剩余行为表明颗粒之间存在偶极相互作用。分散体和阵列的磁行为差异表明,偶极相互作用效应取决于粒子组件的大小和结构。磁化相互作用在较大的密排阵列中比在分散体中包含的较小的,松散关联的簇中起更大的作用。阵列中的磁化效应可以通过减小粒子间距来增强。阵列也是磁各向异性的,其磁性取决于所施加的场方向和阵列平面之间的角度。

著录项

  • 作者

    Farrell, Dorothy.;

  • 作者单位

    Carnegie Mellon University.;

  • 授予单位 Carnegie Mellon University.;
  • 学科 Physics Condensed Matter.
  • 学位 Ph.D.
  • 年度 2002
  • 页码 134 p.
  • 总页数 134
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 O49;
  • 关键词

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