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Electron energy loss spectroscopy and ab initio investigation of iron oxide nanomaterials grown by a hydrothermal process

机译:水热法制备氧化铁纳米材料的电子能量损失谱和从头算研究

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摘要

We first describe with the help of reference experiments (at the Fe 2p and O 1s edges) and ab initio calculations how electron energy loss spectroscopy (EELS) can be used in order to characterize phases of iron oxide and/or hydroxide nanomaterials. In particular we show that dehydration of iron hydroxides such as goethite can easily appear under the electron beam but might be followed by monitoring the O K peak. Indeed both local spin-density approximation (LSDA) and LSDA+ U calculations confirm that intensity of the prepeak of O K should increase while H atoms are removed. We also demonstrate that different magnetic orders do not change significantly the O K EELS fine structure of goethite. Thus, nanomaterials (particles and wires) synthesized by a hydrothermal treatment of nanoscale (10-40 nm) magnetite particles have been conducted. Among them, crystalline iron oxide nanowires with average diameter of 20 nm and length of up to 10 μm are reported. The O K edge and Fe L_(2,3) edges were studied by EELS for these nanostructures. The results indicated that the valence of iron is 3+ in the wires while it is the mixture of 2+ and 3+ in the particles. From these combined EELS, scanning transmission electron microscopy, diffraction, and high-resolution electron microscopy, the complexity of the produced phases from these hydrothermal treatments can be revealed. This work shows how EELS with high-energy resolution is a unique tool to differentiate iron oxide compounds such as the tricky magnetite-maghemite solid solution or the case of partially dehydrated phases, even on a nanometer scale.
机译:我们首先借助参考实验(在Fe 2p和O 1s边缘)和从头算开始来描述如何使用电子能量损失谱(EELS)来表征铁氧化物和/或氢氧化物纳米材料的相。特别是,我们表明,在针状电子束下很容易出现氢氧化铁如针铁矿的脱水现象,但随后可能会监测到O K峰。实际上,局部自旋密度近似(LSDA)和LSDA + U计算都证实,在去除H原子的同时,O K的前峰强度应增加。我们还证明了不同的磁序不会显着改变针铁矿的O K EELS精细结构。因此,已经进行了通过对纳米级(10-40nm)磁铁矿颗粒进行水热处理而合成的纳米材料(颗粒和线)。其中,据报道晶体氧化铁纳米线的平均直径为20 nm,长度最大为10μm。 EELS研究了这些纳米结构的O K边缘和Fe L_(2,3)边缘。结果表明,铁在链中的化合价为3+,而在粒子中则为2+和3+的混合物。从这些组合的EELS,扫描透射电子显微镜,衍射和高分辨率电子显微镜可以看出,这些水热处理产生的相的复杂性。这项工作表明,具有高能量分辨率的EELS如何独特地区分氧化铁化合物,例如棘手的磁铁矿-磁赤铁矿固溶体或部分脱水相(即使是纳米级)。

著录项

  • 来源
    《Physical review》 |2009年第10期|126-135|共10页
  • 作者单位

    Department of Polymer Engineering, National Taiwan University of Science and Technology, Taipei, Taiwan Laboratoire de Physique des Solides, CNRS-UMR 8502, Universite Paris Sud, 91405 Orsay, France;

    Laboratoire de Physique des Solides, CNRS-UMR 8502, Universite Paris Sud, 91405 Orsay, France;

    Center for Condensed Matter Sciences, National Taiwan University, Taipei, Taiwan;

    Center for Condensed Matter Sciences, National Taiwan University, Taipei, Taiwan;

    Center for Condensed Matter Sciences, National Taiwan University, Taipei, Taiwan;

    Laboratoire de Physique des Solides, CNRS-UMR 8502, Universite Paris Sud, 91405 Orsay, France;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    X-ray standing waves;

    机译:X射线驻波;

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