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Atomistic analysis of the surface reactivity, roughness, and crystallinity of plasma-deposited amorphous silicon thin films.

机译:等离子体沉积非晶硅薄膜的表面反应性,粗糙度和结晶度的原子分析。

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摘要

Hydrogenated amorphous silicon (a-Si:H) and nanocrystalline silicon (nc-Si:H) thin films grown by plasma-enhanced chemical vapor deposition from silane-containing discharges are widely used in electronic devices such as solar cells and flat-panel displays. The reactivities and mobilities of reactive species from the plasma, which impinge on the growth surface during film deposition or on the surface of the deposited film during its post-deposition treatment, determine the film properties such as crystallinity and surface roughness. These film properties, in turn, are crucial in determining the performance of the resulting optoelectronic or photovoltaic devices. Specifically, smooth, device-quality a-Si:H films are deposited under conditions where the dominant deposition precursor is the SiH3 radical. Furthermore, the exposure of a-Si:H films to H atoms from an H2 plasma leads to the deposition of nc-Si:H thin films.; In this dissertation, an integrated atomic-scale computational analysis of the fundamental interactions of the SiH3 radical and H atoms with a-Si:H deposition surfaces is presented. The analysis is based on a synergistic approach that combines molecular-dynamics simulations of radical precursor impingement on a-Si:H growth surfaces and H atom impingement on surfaces of smooth a-Si:H films with targeted, accurate first-principles density functional theory calculations of the corresponding diffusion and reaction pathways. Following this approach, we have addressed a number of outstanding problems in the plasma deposition of a-Si:H thin films and provided a comprehensive interpretation to a large body of measurements from silicon thin-film growth and characterization experiments. Specifically, three major unresolved issues in a-Si:H literature are addressed: analysis of the reactions of the SiH 3 radical on a-Si:H growth surfaces to explain the temperature independent surface reactivity and growth rate of a-Si:H films, elucidation of the atomic-scale mechanisms responsible for the surface smoothness of a-Si:H films, and, finally, comprehensive analysis of the key reaction and transport processes of atomic H, which mediate the amorphous-to-nanocrystalline transition during the post-deposition exposure of a-Si:H films to H atoms.
机译:通过等离子体增强化学气相沉积法从含硅烷的放电中生长的氢化非晶硅(a-Si:H)和纳米晶硅(nc-Si:H)薄膜广泛用于电子设备,例如太阳能电池和平板显示器。来自等离子体的反应性物种的反应性和迁移率决定了薄膜的性质,例如结晶度和表面粗糙度,所述等离子体在薄膜沉积期间撞击在生长表面上或在其沉积后处理期间撞击在沉积的薄膜表面上。这些膜性质反过来对于确定所得光电或光伏器件的性能至关重要。具体而言,在主要沉积前驱物为SiH3自由基的条件下沉积光滑,器件质量好的a-Si:H膜。此外,a-Si:H膜从H2等离子体暴露于H原子会导致nc-Si:H薄膜的沉积。本文对SiH3自由基和H原子与a-Si:H沉积表面的基本相互作用进行了原子级的综合计算分析。该分析基于一种协同方法,该方法结合了针对性的,精确的第一原理密度泛函理论,将分子前驱体撞击a-Si:H生长表面上的自由基前体和光滑a-Si:H薄膜表面上的H原子的分子动力学模拟与目标精确的第一原理密度泛函理论相结合相应的扩散和反应途径的计算。遵循这种方法,我们已经解决了a-Si:H薄膜的等离子体沉积中的许多突出问题,并为硅薄膜生长和表征实验中的大量测量提供了全面的解释。具体来说,解决了a-Si:H文献中三个主要未解决的问题:分析a-Si:H生长表面上SiH 3自由基的反应,以解释与温度无关的a-Si:H膜的表面反应性和生长速率,阐明造成a-Si:H薄膜表面光滑度的原子尺度机理,最后,全面分析原子H的关键反应和传输过程,这些原子和原子在后阶段介导了非晶态向纳米晶态的转变。 a-Si:H膜对H原子的沉积曝光。

著录项

  • 作者

    Valipa, Mayur S.;

  • 作者单位

    University of California, Santa Barbara.;

  • 授予单位 University of California, Santa Barbara.;
  • 学科 Engineering Chemical.
  • 学位 Ph.D.
  • 年度 2005
  • 页码 356 p.
  • 总页数 356
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化工过程(物理过程及物理化学过程);
  • 关键词

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