Yadav Ruchika, Swain Diptikanta, Kundu Partha P, Nair Harikrishnan S, Narayana Chandrabhas, Elizabeth Suja
Department of Physics, Indian Institute of Science, Bangalore - 560012, India.
Phys Chem Chem Phys. 2015 May 14;17(18):12207-14. doi: 10.1039/c5cp00906e.
Temperature-dependent Raman and dielectric measurements have been carried out on (C2H5NH3)2CdCl4 single crystals. Raman studies reveal the presence of two structural phase transitions below room temperature at 216 K and 114 K. The phase transitions are marked by anomalies in temperature dependence of wave-number and full width half maximum (FWHM) of several vibrational modes. The transitions are also accompanied by anomalies in dielectric measurements. Raman and dielectric data indicate that the transition at 216 K is order-disorder in nature and is driven by re-orientation of organic ions, while the transition at 114 K is due to coupling between the CdCl6 octahedron and the organic chain. Further high temperature dielectric measurements reveal the presence of one more structural phase transition around 473 K across which dispersion in dielectric parameters is observed. The activation energies and relaxation time obtained for high temperature dielectric phases are characteristic of combined reorientation motions of alkyl ammonium cations.
已对(C2H5NH3)2CdCl4单晶进行了温度相关的拉曼和介电测量。拉曼研究表明,在室温以下216 K和114 K处存在两个结构相变。相变的特征是几个振动模式的波数和半高宽(FWHM)的温度依赖性出现异常。这些转变还伴随着介电测量中的异常。拉曼和介电数据表明,216 K处的转变本质上是有序-无序的,是由有机离子的重新取向驱动的,而114 K处的转变是由于CdCl6八面体与有机链之间的耦合。进一步的高温介电测量表明,在473 K左右还存在一个结构相变,在此相变过程中观察到介电参数的色散。高温介电相的活化能和弛豫时间是烷基铵阳离子组合重新取向运动的特征。