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首页> 外文期刊>Journal of Applied Physics >Dielectric Dissipation in NaCl and KCl below 4.2°K
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Dielectric Dissipation in NaCl and KCl below 4.2°K

机译:低于4.2°K的NaCl和KCl中的介电耗散

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摘要

Dielectric loss tangents for NaCl and KCl single crystals are presented for the frequency range 40–1000 Mc/sec from 4.2° to 1.8°K. The tan δ‐frequency‐reciprocal temperature surface shows considerable structure with loss tangents in the range of 2–9×10-5. Debye relaxation associated with crystal defects appears to be the dominant mechanism, with individual peaks becoming resolved above the background caused by peaks at other frequencies. A NaCl sample shows a loss peak near 300 Mc/sec at 4.2°K, with its high‐frequency shoulder distorted by an adjacent peak. At lower temperatures the peaks move closer and to lower frequencies. The activation energy is estimated to be 0.0011 eV and occurs at approximately one lattice site in 5×1010. The loss mechanism suggested is electron relaxation between neighboring multivalent impurities. The loss would be indistinguishable at room temperature, but is calculated to occur at 4.6 Gc/sec with a peak loss tangent of 3.2×10-7.
机译:给出了NaCl和KCl单晶的介电损耗正切,其频率范围为4.2°至1.8°K,范围为40-1000 Mc / sec。 tanδ频率倒数温度表面显示出相当大的结构,损耗角正切在2–9×10-5的范围内。与晶体缺陷相关的德拜弛豫似乎是主要的机理,单个峰在其他频率的峰引起的背景以上被分辨。 NaCl样品在4.2°K处显示出接近300 Mc / sec的损耗峰,其高频肩峰被相邻峰扭曲。在较低的温度下,峰值移近并移向较低的频率。活化能估计为0.0011 eV,发生在5×1010的大约一个晶格位置。建议的损耗机理是相邻多价杂质之间的电子弛豫。该损耗在室温下无法区分,但计算得出为4.6 Gc / sec,峰值损耗角正切为3.2×10-7。

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  • 来源
    《Journal of Applied Physics 》 |1966年第13期| 共6页
  • 作者单位

    The University of Texas, Austin, Texas;

  • 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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