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Structural and dynamical studies of molecular and network forming chalcogenide glasses and supercooled liquids with NMR and Raman spectroscopy.

机译:利用NMR和拉曼光谱研究分子和网络形成的硫族化物玻璃和过冷液体的结构和动力学。

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摘要

The techniques of Nuclear Magnetic Resonance (NMR) and Raman spectroscopy have been employed to study structure and dynamics in Ge-Se, Ge/As-Te, and As-S binary and complex Ge-As-Te and P-As-S ternary chalcogenide glasses. Structural studies were conducted on Ge-Se glasses and on binary Ge/As-Te and ternary Ge-As-Te systems. The structure of the GexSe100-x glass series, with 5≤x≤33, is investigated with 77Se Magic Angle Spinning (MAS) NMR and then compared with three different proposed structural models. For the binary Ge-Te and As-Te and ternary Ge-As-Te glass systems the structure is studied using Raman spectroscopy and correlated with physical properties such as molar volume, viscosity, optical band gap and thermophysical properties.;Studies on glass transition dynamics were conducted on systems with a range of structural features including an As4S3 inorganic molecular glass former, an As-P-S system where molecules are bonded to the As-S network, and network glasses in the Ge-Se system. Timescales of the rotational dynamics of As4S3 cage molecules in the molecular As-sulfide glass and supercooled liquid show remarkably large decoupling from the timescales of viscous flow and shear relaxation at temperatures below and near Tg (312K). Next, the dynamic behavior of a (As 2S3)90(P2S5)10 glass, which is proposed to consist of As2P2S8 molecular structures which are connected to an As-S network, is investigated with 31P NMR. The rotational dynamics of selenium chains in network forming GexSe100-x glasses and supercooled liquids with 5≤x≤23 are investigated with variable temperature 77Se NMR spectroscopy to determine the relationship between rigidity percolation and dynamic behavior. The timescale of the motion of the Se atoms is observed to be nearly identical for x≤17 and r>≤2.36. However, for the x=20 and 23 compositions where r>≤2.4, above the rigidity percolation threshold, the timescale slows down abruptly. Finally, the Ge20Se 80 glass and supercooled liquid have been the focus of a variable temperature Raman spectroscopy study to investigate the vibrational mode softening behavior and the importance of vibrational entropy in glass transition.
机译:已采用核磁共振(NMR)和拉曼光谱技术研究Ge-Se,Ge / As-Te和As-S二元以及复杂的Ge-As-Te和P-As-S三元的结构和动力学硫属化物眼镜。在Ge-Se玻璃以及二元Ge / As-Te和三元Ge-As-Te系统上进行了结构研究。使用77Se魔角旋转(MAS)NMR对5≤x≤33的GexSe100-x玻璃系列的结构进行了研究,然后与三种不同的拟议结构模型进行了比较。对于二元Ge-Te和As-Te以及三元Ge-As-Te玻璃系统,使用拉曼光谱研究结构,并与诸如摩尔体积,粘度,光学带隙和热物理性质等物理性质相关。对具有一系列结构特征的系统进行了动力学研究,其中包括As4S3无机分子玻璃形成剂,将分子结合到As-S网络上的As-PS系统以及Ge-Se系统中的网络玻璃。硫化氢分子玻璃和过冷液体中As4S3笼形分子旋转动力学的时标与低于Tg(312K)时和接近Tg(312K)时的粘性流动和剪切松弛时标表现出显着的去耦关系。接下来,用31 P NMR研究了被建议由与As-S网络相连的As2P2S8分子结构组成的(As 2S3)90(P2S5)10玻璃的动力学行为。用变温77Se NMR光谱研究了形成GexSe100-x玻璃和5≤x≤23的过冷液体中网络中硒链的旋转动力学,以确定刚性渗流与动力学行为之间的关系。对于x≤17且≤2.36,观察到Se原子运动的时间尺度几乎相同。但是,对于x = 20和23 ≤2.4的成分,在刚度渗透阈值之上,时间尺度突然变慢。最后,Ge20Se 80玻璃和过冷液体已成为可变温度拉曼光谱研究的重点,以研究振动模式的软化行为以及振动熵在玻璃化转变中的重要性。

著录项

  • 作者

    Gjersing, Erica Lee.;

  • 作者单位

    University of California, Davis.;

  • 授予单位 University of California, Davis.;
  • 学科 Physics Low Temperature.;Engineering Materials Science.
  • 学位 Ph.D.
  • 年度 2010
  • 页码 138 p.
  • 总页数 138
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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