Botez Cristian E, Hermosillo Juan D, Zhang Jianzhong, Qian Jiang, Zhao Yusheng, Majzlan Juraj, Chianelli Russell R, Pantea Cristian
Department of Physics, University of Texas at El Paso, 500 W. University Avenue, El Paso, TX 79968, USA.
J Chem Phys. 2007 Nov 21;127(19):194701. doi: 10.1063/1.2804774.
To clarify the microscopic origin of the temperature-induced three-order-of-magnitude jump in the proton conductivity of CsH(2)PO(4) (superprotonic behavior), we have investigated its crystal structure modifications within the 25-300 degrees C temperature range under both ambient- and high-pressure conditions using synchrotron x-ray diffraction. Our high-pressure data show no indication of the thermal decomposition/polymerization at the crystal surface recently proposed as the origin of the enhanced proton conductivity [Phys. Rev. B 69, 054104 (2004)]. Instead, we found direct evidence that the superprotonic behavior of the title material is associated with a polymorphic structural transition to a high-temperature cubic phase. Our results are in excellent agreement with previous high-pressure ac impedance measurements.
为了阐明磷酸二氢铯(CsH₂PO₄)质子电导率中温度诱导的三个数量级跃升(超质子行为)的微观起源,我们利用同步辐射X射线衍射,在环境压力和高压条件下,研究了其在25 - 300℃温度范围内的晶体结构变化。我们的高压数据没有显示出最近提出的作为质子电导率增强起源的晶体表面热分解/聚合迹象[《物理评论B》69, 054104 (2004)]。相反,我们发现了直接证据,表明该材料的超质子行为与向高温立方相的多晶型结构转变有关。我们的结果与之前的高压交流阻抗测量结果非常吻合。