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首页> 外文期刊>Journal of Applied Physics >Anomalous lattice expansion in yttria stabilized zirconia under simultaneous applied electric and thermal fields: A time-resolved in situ energy dispersive x-ray diffractometry study with an ultrahigh energy synchrotron probe
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Anomalous lattice expansion in yttria stabilized zirconia under simultaneous applied electric and thermal fields: A time-resolved in situ energy dispersive x-ray diffractometry study with an ultrahigh energy synchrotron probe

机译:同时施加电场和热场的氧化钇稳定氧化锆中的异常晶格扩展:用超高能量同步加速器探针进行时间分辨的原位能量色散X射线衍射研究

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摘要

Nonisothermal densification in 8% yttria doped zirconia (8YSZ) particulate matter of 250?nm median particle size was studied under 215?V/cm dc electric field and 9?°C/min heating rate, using time-resolved in-situ high temperature energy dispersive x-ray diffractometry with a polychromatic 200?keV synchrotron probe. Densification occurred in the 876–905?°C range, which resulted in 97% of the theoretical density. No local melting at particle-particle contacts was observed in scanning electron micrographs, implying densification was due to solid state mass transport processes. The maximum current draw at 905?°C was 3 A, corresponding to instantaneous absorbed power density of 570?W/cm3. Densification of 8YSZ was accompanied by anomalous elastic volume expansions of the unit cell by 0.45% and 2.80% at 847?°C and 905?°C, respectively. The anomalous expansion at 905?°C at which maximum densification was observed is characterized by three stages: (I) linear stage, (II) anomalous stage, and (III) anelastic recovery stage. The densification in stage I (184?s) and II (15?s) was completed in 199?s, while anelastic relaxation in stage III lasted 130?s. The residual strains (ε) at room temperature, as computed from tetragonal (112) and (211) reflections, are ε(112)?=?0.05% and ε(211)?=?0.13%, respectively. Time dependence of (211) and (112) peak widths (β) show a decrease with both exhibiting a singularity at 905?°C. An anisotropy in (112) and (211) peak widths of {β(112)(211)}?=?(3:1) magnitude was observed. No phase transformation occurred at 905?°C as verified from diffraction spectra on both sides of the singularity, i.e., the unit cell symmetry rem- ins tetragonal. We attribute the reduction in densification temperature and time to ultrafast ambipolar diffusion of species arising from the superposition of mass fluxes due to Fickian diffusion, thermodiffusion (Soret effect), and electromigration, which in turn are a consequence of a superposition of chemical, temperature, and electrical potential gradients. On the other hand, we propose defect pile-up at particle-particle contacts and subsequent tunneling as a mechanism creating the “burst-mode” discontinuous densification at the singularities observed at 847 and 905?°C.
机译:在215?V / cm dc电场和9?C / min的加热速率下,采用时间分辨的原位高温,研究了中值粒径为250?nm的8%氧化钇掺杂的氧化锆(8YSZ)颗粒物中的非等温致密化。能量色散X射线衍射仪,带200?keV彩色同步加速器探头。致密化发生在876–905°C范围内,占理论密度的97%。在扫描电子显微照片中未观察到颗粒与颗粒接触处的局部熔化,这表明致密化是由于固态传质过程所致。 905?C时的最大电流为3 A,对应的瞬时吸收功率密度为570?W / cm 3 。 8YSZ的致密化伴随着在847?C和905?C时晶胞的异常弹性体积膨胀分别为0.45%和2.80%。在905℃下观察到最大致密化的异常膨胀具有三个阶段的特征:(I)线性阶段,(II)异常阶段和(III)非弹性恢复阶段。第一阶段(184?s)和第二阶段(15?s)的致密化在199?s内完成,而第三阶段的非弹性松弛持续了130?s。根据四角形(112)和(211)反射计算出的室温下的残余应变(ε)为ε(112)?=?0.05%和ε(211)(112)(211)}?=?(3:1)幅度的(112)和(211)峰宽各向异性。由奇异性两面的衍射光谱证实,即在905℃,没有相变发生,即晶胞对称性呈四边形。我们将致密化温度和时间的减少归因于由于Fickian扩散,热扩散(Soret效应)和电迁移引起的质量通量的叠加而导致的物质超快速双极性扩散,而化学,温度,和电势梯度。另一方面,我们建议在颗粒与颗粒接触处缺陷堆积并随后进行隧穿,以此作为在847和905?C下观察到的奇异点产生“爆发模式”的不连续致密化的机制。

著录项

  • 来源
    《Journal of Applied Physics》 |2013年第23期|233503-233503|共1页
  • 作者单位

    Department of Materials Science and Engineering, Rutgers University, Piscataway, New Jersey 08854-8065, USA|c|;

  • 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);
  • 原文格式 PDF
  • 正文语种 eng
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