Conductivity in polymer ionics. Dynamic disorder and correlation

M. Ratner, A. Nitzan
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引用次数: 115

Abstract

Theoretical constructs are developed for discussing diffusivity and conductivity in polymer ionic materials. Such materials are characterized by extensive disorder, either static (lack of long-range order) or static and dynamic (lack of long-range order with short-range order evolving with time). Beginning with a dynamic percolation model, we show that, in general, so long as the mean-square displacement of the charged particle obeys a certain growth law, the observed charged-particle motion will be diffusive, both in the ballistic regime, corresponding to electronic motion with strong scattering, and in the ionic-hopping regime, corresponding to dynamic disorder renewal of the hopping situation. Some general behaviour for transport under these conditions is predicted, including definite statements about the frequency dependence of the conduction, the relationship between the growth law in a single interval and the growth law for observation times long compared to scattering or renewal times, and the behaviour in the neighbourhood of the percolation threshold for the static problem. Interpretations are suggested both for ion and electron-hopping situations.A statistical thermodynamic model is developed for analysis of contact ion pair formation and its effect on conductivity in ion-conducting polymer systems. In this model, the energy (due to solvation and polarization) favouring formation of a homogeneous complex in which the cations are solvated by the polymer host, competes with an entropic term favouring the separated structures (free polymer and contact ion pairs). We derive general conditions for this phase separation, and an expression for the number of polymer-bound, homogeneously solvated ions. We show that this number will, in general, decrease monotonically with increase in temperature, due to entropic favouring of the phase-separated material, this is reminiscent of the lower consolute temperature phenomenon in liquid mixtures.
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聚合物离子中的电导率。动态失序和相关
建立了讨论聚合物离子材料的扩散率和电导率的理论结构。这类材料具有广泛无序的特点,要么是静态的(缺乏长程秩序),要么是静态和动态的(缺乏长程秩序,而短程秩序随时间演变)。从一个动态渗流模型出发,我们表明,一般来说,只要带电粒子的均方位移服从一定的生长规律,观察到的带电粒子运动将是扩散的,无论是在弹道状态下,对应于强散射的电子运动,还是在离子跳跃状态下,对应于跳跃状态的动态无序更新。预测了这些条件下输运的一些一般行为,包括关于传导频率依赖性的明确陈述,单个间隔内的生长规律与与散射或更新时间相比较长的观察时间的生长规律之间的关系,以及静态问题的渗透阈值附近的行为。对离子跳跃和电子跳跃的情况都提出了解释。建立了一个统计热力学模型,用于分析离子导电聚合物体系中接触离子对的形成及其对电导率的影响。在该模型中,能量(由于溶剂化和极化)有利于形成均相配合物,其中阳离子被聚合物主体溶剂化,与熵项竞争有利于分离结构(自由聚合物和接触离子对)。我们推导了相分离的一般条件,以及聚合物结合的均溶剂化离子的数量表达式。我们表明,由于相分离物质的熵倾向,这个数字一般会随着温度的升高而单调减少,这让人想起液体混合物中较低的溶质温度现象。
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