MOLECULAR-MOTION AND ORDERING IN RUBIDIUM CYANIDE, STUDIED WITH DIELECTRIC AND RAMAN TECHNIQUES

被引:48
作者
KONDO, Y
SCHOEMAKER, D
LUTY, F
机构
[1] Physics Department, University of Utah, Salt Lake City
[2] Institute for Solid State Physics, University of Tokyo, Tokyo
[3] University of Antwerp, Wilrijk
来源
PHYSICAL REVIEW B | 1979年 / 19卷 / 08期
关键词
D O I
10.1103/PhysRevB.19.4210
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Rubidium cyanide, so far rarely investigated and apparently for the first time available in high-purity single-crystal form, has been studied with dielectric and optical techniques between 2 and 300 K. Starting from the pseudocubic orientationally disordered phase at room temperature, the crystals show under cooling by a sharp drop in light transmission and dielectric constant the transition into a multidomain structure of elastic dipole order at 132 K. Dielectric measurements give evidence for electric disorder in this phase, showing paraelectric (T-1) behavior down to 47 K, with Debye losses yielding an activation energy for reorientation of 0.107 eV and an effective dipole moment of 0.022 e per CN- dipole. While some indications for the onset of a gradual electric ordering become apparent below 47 K, the freezing-in dipole reorientation prevents its establishment under further cooling, leading most likely at lowest temperatures to an electrically disordered state in nonequilibrium. Raman spectra, taken in both the regimes of librational-translational and CN - stretching modes, are discussed and compared to the behavior in NaCN and KCN. Characteristic trends in the order-disorder phenomena and physical behavior with cation size become apparent among the alkalicyanide family. © 1979 The American Physical Society.
引用
收藏
页码:4210 / 4216
页数:7
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