Effects of pressure, temperature and volume on the electrical conductivity of polymer electrolytes

被引:1
|
作者
Bendler, J. T. [2 ]
Fontanella, J. J. [1 ]
Shlesinger, M. F. [1 ,3 ]
Wintersgill, M. C. [1 ]
机构
[1] USN Acad, Dept Phys, Annapolis, MD 21402 USA
[2] BSC Inc, Rapid City, SD 57702 USA
[3] Off Naval Res, Arlington, VA 22203 USA
关键词
Polymer electrolytes; Electrical conductivity; High pressure; Scaling; Defect diffusion model; GLASS-FORMING LIQUIDS; DEFECT DIFFUSION-MODEL; ION-ION INTERACTION; POLY(PROPYLENE GLYCOL); TRANSITION DYNAMICS; RELAXATION; DEPENDENCE; LICF3SO3; DENSITY; SALTS;
D O I
10.1016/j.electacta.2011.07.010
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Three features of the electrical conductivity of ion conducting polymers are described. First, it is shown how the ratio of the apparent isochoric activation energy to the isobaric activation enthalpy. E(V)*/H*, can be used to separate the contributions of volume and temperature to the electrical conductivity. Next, the effect of pressure on the conductivity is considered. Finally, the concept of scaling is discussed and is applied to poly(propylene glycol) containing LiCF(3)SO(3). All results are interpreted in terms of the defect diffusion model (DDM). First, it is shown how E(V)*/H* can be calculated using the DDM. Next, the effect of pressure on the conductivity is given a physical interpretation. Finally, it is pointed out that in the DDM, scaling arises because the critical temperature can be represented approximately by a power law. Consequently, in the DDM scaling is always approximate. (C) 2011 Elsevier Ltd. All rights reserved.
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页码:160 / 164
页数:5
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