首页> 外文期刊>Journal of Applied Physics >Dielectric relaxation and magnetic behavior of bismuth-substituted yttrium iron garnet
【24h】

Dielectric relaxation and magnetic behavior of bismuth-substituted yttrium iron garnet

机译:铋取代钇铁石榴石的介电弛豫和磁行为

获取原文
获取原文并翻译 | 示例
       

摘要

Y_(3-x)Bi_xFe_5O_(12) (x = 0-1.0) was prepared by solid state reaction. X-ray diffraction showed a gradual increase of lattice parameter with the Bi concentration, indicating that Bi had been incorporated into the lattice. Dielectric responses of the samples at room temperature increased initially at low Bi (x < 0.4) and then decreased rapidly at high Bi (x > 0.6). Temperature dependence of dielectric constant showed a huge steplike increase at the temperatures between 20 and 200 ℃, increasing with Bi. X-ray photoelectron spectroscopy revealed the presence of Fe~(2+) and Bi~(2+) in the samples, which might be responsible for the dielectric behaviors. An increase of coercivity and Curie temperature with Bi was observed. This was accompanied by a reduction of the saturation magnetization, whose variation with T follows a modified Bloch law.
机译:通过固相反应制备Y_(3-x)Bi_xFe_5O_(12)(x = 0-1.0)。 X射线衍射显示出随着Bi浓度的增加,晶格参数逐渐增加,表明Bi已经被掺入晶格中。样品在室温下的介电响应最初在低Bi(x <0.4)时增加,然后在高Bi(x> 0.6)时迅速降低。介电常数随温度的变化在20〜200℃之间呈极大的阶梯状增加,随Bi的增加而增加。 X射线光电子能谱表明样品中存在Fe〜(2+)和Bi〜(2+),这可能是介电行为的原因。观察到随着Bi矫顽力和居里温度的增加。这伴随着饱和磁化强度的减小,其饱和磁化强度随T的变化遵循修正的布洛赫定律。

著录项

  • 来源
    《Journal of Applied Physics》 |2011年第2期|p.07A508.1-07A508.3|共3页
  • 作者单位

    Department of Materials Science and Engineering, National Cheng Kung University, Tainan City 70101,Taiwan;

    Department of Materials Science and Engineering, National Cheng Kung University, Tainan City 70101,Taiwan;

    Institute of Nanotechnology and Department of Mechanical Engineering, Southern Taiwan University,Tainan City 71005, Taiwan;

    Department of Physics, National Cheng Kung University, Tainan City 70101, Taiwan;

  • 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
  • 中图分类
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号