Mandanici Andrea, Huang Wei, Cutroni Maria, Richert Ranko
Dipartimento di Fisica, Università di Messina, 98100 Messina, Italy.
J Chem Phys. 2008 Mar 28;128(12):124505. doi: 10.1063/1.2844797.
The dynamics of ethylcyclohexane are investigated by high resolution dielectric spectroscopy aiming to characterize the relevant relaxational features of this simple system in its fluid, supercooled liquid, and glassy states. The dielectric signature of structural relaxation is a primary loss peak with amplitude Deltaepsilon=0.01, and a secondary loss process is found in the glassy state. This beta relaxation is compared with a "slow" process revealed by ultrasonics and with previously found gamma and chi processes in similar materials containing the cyclohexyl group. The results suggest that this secondary process is an intramolecular mode rather than a Johari-Goldstein process, consistent with its persistence in the liquid state at slow relaxation times which exceed those of the alpha process. The dielectric activity of such a slow process requires that the dipole magnitude changes with the intramolecular transition, whereas a change in dipole direction only would be masked by the faster structural relaxation.
通过高分辨率介电谱研究了乙基环己烷的动力学,旨在表征该简单体系在其液态、过冷液态和玻璃态下的相关弛豫特征。结构弛豫的介电特征是一个幅度为Δε = 0.01的主要损耗峰,并且在玻璃态中发现了一个次要损耗过程。将这种β弛豫与超声揭示的“慢”过程以及先前在含环己基的类似材料中发现的γ和χ过程进行了比较。结果表明,这种次要过程是一种分子内模式,而不是乔哈里 - 戈尔茨坦过程,这与其在慢弛豫时间下在液态中的持续存在一致,该慢弛豫时间超过了α过程的弛豫时间。这种慢过程的介电活性要求偶极矩随分子内跃迁而变化,而仅偶极方向的变化会被更快的结构弛豫所掩盖。