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Nanostructural evolution during emission of Csl-coated carbon fiber cathodes

机译:Csl涂层碳纤维阴极发射过程中的纳米结构演变

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摘要

Carbon-based nanofiber and microfiber cathodes exhibit very low voltages for the onset of electron emission, and thus provide exciting opportunities for applications ranging from high power microwave sources to field emission displays. CsI coatings have been experimentally shown to lower the work function for emission from the fiber tips, although little is known about the microstructure of the fibers themselves in their as-received state, after coating with CsI, or after being subjected to high voltage cycling. Longitudinal cross sections of the original, unused Csl-coated fibers produced by focused ion beam lift-out revealed a nanostructured graphitic core surrounded by an amorphous carbon shell with submicron sized islands of crystalline CsI on the outer surface. Aberration-corrected high resolution electron microscopy (HREM) of the fiber core achieved 0.10 nm resolution, with the graphite (200) clearly visible in digital fast Fourier transformations of the 2-4 nm highly ordered graphitic domains. As the cathode fibers are cycled at high voltage, HREM demonstrates that the graphitic ordering of the core increases with the number of cycles, however the structure and thickness of the amorphous carbon layer remains unchanged. These results are consistent with micro-Raman measurements of the fiber disordered/graphitic (D/G) band ratios. After high voltage cycling, a uniform ~ 100 nm film at the fiber tip was evident in both bright field transmission electron microscopy (TEM) and high angle annular dark field scanning TEM (STEM). Low-dose electron diffraction techniques confirmed the amorphous nature of this film, and STEM with elemental mapping via x-ray energy dispersive spectroscopy indicates this layer is composed of CsIO. The oxidative evolution of tip composition and morphology due to impurities in the chamber, along with increased graphitization of the fiber core, contributes to changes in emission behavior with cycling.
机译:碳基纳米纤维和超细纤维阴极对于电子发射的开始表现出非常低的电压,因此为从高功率微波源到场发射显示器的各种应用提供了令人兴奋的机会。实验表明,CsI涂层可降低从纤维尖端发射的功函,尽管鲜为人知的是,在用CsI涂层后或经过高压循环后,处于接收状态的纤维本身的微观结构仍不为人所知。通过聚焦离子束提拉产生的原始的,未使用的Csl涂层纤维的纵向横截面显示出纳米结构的石墨核,被无定形碳壳包围,外表面上有亚微米级的晶体CsI岛。光纤纤芯的像差校正高分辨率电子显微镜(HREM)达到了0.10 nm分辨率,而石墨(200)在2-4 nm高阶石墨域的数字快速傅里叶变换中清晰可见。当阴极纤维在高电压下循环时,HREM证明核的石墨有序性随着循环次数的增加而增加,但是非晶碳层的结构和厚度保持不变。这些结果与纤维无序/石墨(D / G)带比的微拉曼测量结果一致。高压循环后,在明场透射电子显微镜(TEM)和大角度环形暗场扫描TEM(STEM)中,在光纤尖端处可见均匀的〜100 nm薄膜。低剂量电子衍射技术证实了该膜的非晶性,通过X射线能量色散光谱进行元素映射的STEM表明该层由CsIO组成。由于腔室中的杂质而引起的尖端组成和形态的氧化演变,以及纤维芯石墨化程度的提高,都导致了循环行为的变化。

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  • 来源
    《Journal of Applied Physics》 |2010年第11期|P.113304.1-113304.6|共6页
  • 作者单位

    ARFL/RXBN, Materials and Manufacturing Directorate, Air Force Research Laboratory, WPAFB, Ohio 43433, USA UES Inc., Dayton, Ohio 45432, USA;

    rnARFL/RXBN, Materials and Manufacturing Directorate, Air Force Research Laboratory, WPAFB, Ohio 43433, USA UES Inc., Dayton, Ohio 45432, USA;

    rnAFRL/RDH, Directed Energy Directorate, Air Force Research Laboratory, Kirtland AFB, New Mexico 87117, USA;

    rnSAIC, Inc., Albuquerque, New Mexico 87106, USA;

    SAIC, Inc., Albuquerque, New Mexico 87106, USA;

    rnARFL/RXBN, Materials and Manufacturing Directorate, Air Force Research Laboratory, WPAFB, Ohio 43433, USA;

    rnARFL/RXBN, Materials and Manufacturing Directorate, Air Force Research Laboratory, WPAFB, Ohio 43433, USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
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  • 正文语种 eng
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