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Photo-darkening kinetics and structural anisotropic modifications in the chalcogenide glass arsenic trisulfide: A study of kinetic X-ray absorption spectroscopy.

机译:硫族化物玻璃三硫化二砷中的光变暗动力学和结构各向异性修饰:动力学X射线吸收光谱研究。

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摘要

The purpose of the study is to investigate the mechanisms involved with photo-induced atomic structural modifications in the chalcogenide glass As{dollar}sb2{dollar}S{dollar}sb3{dollar}. This glass exhibits the reversible effects of photo-darkening followed by thermal bleaching. We observed the time behavior of photo-induced properties under the influence of linearly polarized band-gap light. In a macroscopic optical investigation, we monitor optical changes in the photo-darkening process, and in a local structural probe we study kinetic (or time-resolved dispersive) x-ray absorption spectroscopy. Our observations center on kinetic phenomena and structural modifications induced by polarized excitation of lone-pair orbitals in the chalcogenide glass.; Experimental results include the following observations: (i) The polarity of the optically induced anisotropy is critically dependent on the intensity and the polarization of the band-gap irradiation beam. (ii) The near edge peak height in x-ray absorption spectra shows subtle but sensitive change during the photo-darkening process. (iii) Photon intensity dependent dichroic kinetics reflect a connection between the optically probed macroscopic property and the x-ray probed local anisotropic structure. Analysis of the x-ray absorption results includes a computer simulation of the polarized absorption spectra. These results suggest that specific structural units tend to orient themselves with respect to the photon polarization. A substantial part of the analysis involves a major effort in dealing with the x-ray kinetic data manipulation and the experimental difficulties caused by a synchrotron instability problem.; Based on our observations, we propose a possible mechanism for the observed photo-structural modifications. Through a model of computer relaxed photo-darkening kinetics, we support the notion that a twisting of a specific intermediate range order structure is responsible for local directional variations and global network distortions. In the course of this study, we refine knowledge of intermediate range order structural configurations and the bistabilities related to these configurations. The importance of the lone-pair orbital interactions in the chalcogenide glassy network is underscored.
机译:该研究的目的是研究硫族化物玻璃As {dollar} sb2 {dollar} S {dollar} sb3 {dollar}中与光诱导的原子结构修饰有关的机制。这种玻璃具有光变暗和热漂白的可逆作用。我们观察了线性偏振带隙光的影响下光诱导性能的时间行为。在宏观光学研究中,我们监视光变暗过程中的光学变化,在局部结构探针中,我们研究动力学(或时间分辨的色散)x射线吸收光谱。我们的观察集中在由硫族化物玻璃中的孤对轨道的极化激发引起的动力学现象和结构改变。实验结果包括以下观察结果:(i)光学各向异性的极性严格取决于带隙辐照束的强度和偏振。 (ii)在x射线吸收光谱中,近边缘峰高显示出细微但敏感的变化。 (iii)光子强度相关的二向色动力学反映了光学探测的宏观特性与X射线探测的局部各向异性结构之间的联系。 X射线吸收结果的分析包括偏振吸收光谱的计算机模拟。这些结果表明,特定的结构单元趋向于相对于光子极化定向。分析的大部分工作涉及处理X射线动力学数据的操作以及由同步加速器不稳定性问题引起的实验困难。根据我们的观察,我们提出了一种可能的机制,用于观察到的光结构修饰。通过计算机放松的光暗化动力学模型,我们支持以下观点:特定的中间范围有序结构的扭曲是局部方向变化和全局网络畸变的原因。在本研究的过程中,我们完善了对中程级结构构型以及与这些构型有关的双稳态的知识。在硫属化物玻璃状网络中孤对轨道相互作用的重要性被强调。

著录项

  • 作者

    Lee, Jay Min.;

  • 作者单位

    North Carolina State University.;

  • 授予单位 North Carolina State University.;
  • 学科 Physics Condensed Matter.
  • 学位 Ph.D.
  • 年度 1990
  • 页码 200 p.
  • 总页数 200
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 O49;
  • 关键词

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