首页> 外文期刊>The journal of physics and chemistry of solids >Single-crystal x-ray diffraction and impedance spectroscopy investigations of the RbxCs1-xH2PO4 (0 = x = 1) proton conductor series
【24h】

Single-crystal x-ray diffraction and impedance spectroscopy investigations of the RbxCs1-xH2PO4 (0 = x = 1) proton conductor series

机译:RBXCS1-XH2PO4(0& = 1)质子导体系列的单晶X射线衍射和阻抗光谱研究

获取原文
获取原文并翻译 | 示例
           

摘要

We have used single-crystal x-ray diffraction to investigate the structural modifications induced by Rb-doping of the superprotonic conductor CsH2PO4. We found that the monoclinic P2(1)/m CsH2PO4 modification persists within the RbxCs1-xH2PO4 (0 = x = 1) series upon Rb-doping from x = 0.1 to x = 0.7. Rb0.8Cs0.2H2PO4 (x = 0.8), however, exhibits a previously unreported P2(1)/c monoclinic phase, where the mirror plane is lost and disorder is present in the PO4 tetrahedra even at room temperature. Higher levels of x display a tetragonal I.42d unit cell isomorphic with the known structure of RbH2PO4. The temperature dependence of the proton conductivity determined from impedance spectroscopy data collected within the 160 degrees C-250 degrees C range is also markedly different at high Rb-doping levels, x = 0.8. Finally, we found that Rb0.9Cs0.1H2PO4 undergoes a transition from its room-temperature tetragonal I-42d phase to an intermediate-temperature monoclinic P2(1)/m modification at a significantly lower temperature (similar to 80 degrees C) than its RbH2PO4 counterpart (similar to 120 degrees C).
机译:我们使用单晶X射线衍射来研究超级旋转导体CSH2PO4的RB掺杂诱导的结构修改。我们发现单斜晶型P2(1)/ m CSH2PO4修改在RBXCS1-XH2PO4(0& = x& = 1)内持续存在于x = 0.1至x = 0.7的RB掺杂时串联。然而,RB0.8CS0.2H2PO4(X = 0.8)呈现先前未报告的P2(1)/ C单斜相,其中镜面损失并且均匀在室温下在PO4 Tetrahedra中存在病症。较高水平的X显示了具有RBH2PO4的已知结构的四方I.42D单元细胞同态。在160摄氏度C-250℃范围内收集的阻抗光谱数据测定的质子电导率的温度依赖性在高RB掺杂水平下也显着不同,x& = 0.8。最后,我们发现RB0.9CS0.1H2PO4经历从其室温四方I-42D相的过渡到中间温度单斜晶型P2(1)/ m改性,明显较低的温度(类似于80℃) RBH2PO4对应(类似于120℃)。

著录项

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