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首页> 外文期刊>The Journal of Chemical Physics >Dynamics of glass-forming liquids. XIX. Rise and decay of field induced anisotropy in the non-linear regime
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Dynamics of glass-forming liquids. XIX. Rise and decay of field induced anisotropy in the non-linear regime

机译:玻璃形成液体的动力学。十九。非线性条件下场感应各向异性的兴衰

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For glycerol and three monohydroxy alcohols, we have measured the non-linear dielectric effects resulting from the application and removal of a high dc bias electric field. The field effects are detected by virtue of a small amplitude harmonic field, from which time resolved changes in the dielectric loss are derived. The changes in permittivity are dominated by modifications of the time constants (rather than amplitudes) which display two contributions: a heating-like decrease of relaxation times that originates from the time dependent field when the bias is switched on and off and a slowing down of the dynamics resulting from the field induced reduction of configurational entropy. As observed for the electro-optical Kerr effect, the rise of the entropy change is slower than its decay, a feature that we rationalize on the basis of the quadratic dependence of the entropy change on polarization. For glycerol, the observed steady state level of the field induced shift of the glass transition temperature (+84 mK) matches the expectation based on the entropy change and its impact on dynamics via the Adam-Gibbs relation (+88 mK). For the alcohols, these non-linear effects rise and decay on the time scales of the prominent dielectric Debye process, underscoring the relation of these features to polarization anisotropy, opposed to mechanical or enthalpy relaxation which are orders of magnitude faster in these systems. A model is discussed which captures the observed magnitudes as well as time dependences in a near quantitative fashion. It is demonstrated that the high bias field modifies the response of polarization to the ac field, including a temporary change in the low field susceptibility. (C) 2015 AIP Publishing LLC.
机译:对于甘油和三种单羟基醇,我们已经测量了由于施加和去除高直流偏置电场而产生的非线性介电效应。借助于小的振幅谐波场来检测场效应,从中可以导出介电损耗的分辨分辨时间。介电常数的变化主要由时间常数(而不是幅度)的变化决定,这表现出两个作用:像加热一样的弛豫时间的减少,这是由于在打开和关闭偏置时随时间变化的磁场引起的;以及由场引起的动力学降低了结构熵。正如对电光Kerr效应所观察到的,熵变化的上升比其衰减慢,这是我们根据熵变化对偏振的二次依赖性来合理化的一个特征。对于甘油,观察到的稳态引起的玻璃化转变温度位移的稳态水平(+84 mK)与基于熵变及其通过Adam-Gibbs关系对动力学的影响(+88 mK)的期望相符。对于醇类而言,这些非线性效应会在突出的介电德拜过程的时间尺度上上升和下降,这凸显了这些特征与极化各向异性的关系,与机械或焓弛豫相反,后者在这些系统中的速度要快几个数量级。讨论了一个模型,该模型以接近定量的方式捕获了观察到的幅度以及时间依赖性。事实证明,高偏压场会改变极化对交流场的响应,包括低场磁化率的暂时变化。 (C)2015 AIP Publishing LLC。

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