Non-Debye relaxations in disordered ionic solids

被引:114
作者
Dieterich, W [1 ]
Maass, P
机构
[1] Univ Konstanz, Fachbereich Phys, D-78457 Constance, Germany
[2] Tech Univ Ilmenau, Inst Phys, D-98684 Ilmenau, Germany
关键词
D O I
10.1016/S0301-0104(02)00673-0
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Motions of charged defects in ionic solids, including glassy ionic conductors, defective crystals and composite materials, imply slow relaxation processes, which are observable within a wide range of timescales larger than microscopic (vibrational) times. These processes manifest themselves in numerous dynamical probes, like ac-conductivity, nuclear spin-relaxation, quasi-elastic neutron scattering and mechanical relaxation. The present theoretical understanding of the corresponding response functions is reviewed. Stochastic models based on ion hopping are the most natural approach for systems with structural disorder on microscopic length scales, but more coarse-grained, phenomenological schemes are addressed as well. Macroscopically inhomogeneous systems and interfacial problems are modeled by random impedance networks. Generally, non-exponential relaxation gets enhanced when Coulomb interactions between ions are taken into account. This is demonstrated by large-scale Monte Carlo simulations of disordered lattice gases for ion diffusion and is supported further by new results on random dipolar systems in the context of the "nearly constant dielectric loss response". (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:439 / 467
页数:29
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