首页> 外文会议>Conference on Inorganic Optical Materials Ⅲ Aug 2, 2001, San Diego, USA >Control of defect concentrations in single crystals: Insights from micro-IR on natural quartz crystals
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Control of defect concentrations in single crystals: Insights from micro-IR on natural quartz crystals

机译:控制单晶中的缺陷浓度:微型红外对天然石英晶体的见解

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The physical properties of single crystals are highly dependent on trace impurities contained within them. For synthesis of single crystals with prescribed properties, precise and accurate control of impurity content can be extremely desirable. We review and expand on studies of crystals from the natural environment that document systematic order-of-magnitude variations in defect abundances. Using high-resolution FTIR, we demonstrate that the dominant control on the uptake of defects in growing quartz crystals is the growth rate of the advancing crystal face. We show that the uptake of different kinds of defects have the same functional dependence both on crystal growth rate and on the crystallographic orientation of the growth face. In unaltered quartz crystals, concentrations of LiOH, HOH species (which reside in voids), and Al-bearing species (which substitute for Si within the crystal structure) are proportional to one another despite fast and slow growth on both 'r' and 'z' rhombohedral growth faces. In addition, our measurements can distinguish the effects of processes, such as internal diffusion and fluid exchange, which have re-set the abundances of defect species after crystal growth; A1OH, HOH, and LiOH show increasing propensities for secondary mobility and are dependent on the crystallographic orientation of the original growth face which incorporated them.
机译:单晶的物理性质高度依赖于其中所含的微量杂质。为了合成具有规定性能的单晶,非常需要精确和准确地控制杂质含量。我们回顾并扩展了自然环境中晶体的研究,这些研究记录了缺陷丰度中系统的数量级变化。使用高分辨率的FTIR,我们证明了对生长的石英晶体中缺陷吸收的主要控制是前进的晶体面的生长速率。我们表明,摄取不同种类的缺陷对晶体生长速率和生长面的晶体学取向都具有相同的功能依赖性。在未改变的石英晶体中,尽管“ r”和“ r”都快速而缓慢地生长,但LiOH,HOH种类(存在于空隙中)和含Al种类(在晶体结构中替代Si)的浓度彼此成正比。 z的菱面体生长面。另外,我们的测量可以区分过程的影响,例如内部扩散和流体交换,这些影响在晶体生长后重新设置了缺陷种类的丰度。 AlOH,HOH和LiOH显示出第二迁移率的增加的趋势,并且取决于结合它们的原始生长面的晶体学取向。

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