电导率
粘度
碳酸乙烯酯
电解质
溶剂
碳酸丙烯酯
化学
热力学
盐(化学)
分析化学(期刊)
分数(化学)
质量分数
碳酸盐
色谱法
物理化学
有机化学
电极
物理
作者
Michael S. Ding,T. Richard Jow
出处
期刊:Journal of The Electrochemical Society
[The Electrochemical Society]
日期:2003-01-01
卷期号:150 (5): A620-A620
被引量:82
摘要
Conductivity κ and viscosity η of propylene carbonate (PC)-diethyl carbonate (DEC) and PC-ethylene carbonate (EC) solutions of were experimentally determined, the former at salt molalities from 0.2 to solvent compositions from 0 to 0.7 weight fraction of DEC and 0 to 0.6 weight fraction of EC, and temperatures θ from 60 to the latter indirectly and qualitatively through measuring the glass transition temperature in the same ranges of and The increased with and decreased with of DEC but increased with of EC, indicating a concurrent change in the η of the solutions. The κ of the PC-DEC solution of peaked in both and thus forming a dome in its 3D presentation in the coordinates, while that of the PC-EC solution peaked only in resulting in an arch-shaped surface. As θ lowered, these κ surfaces fell in height and shifted in the direction of low η. These observations correlated well with the changes of dielectric constant ɛ and viscosity η of the solutions with the same set of variables. More detailed study of the effects of DEC and EC on the κ of PC solution of demonstrated the benefit of having a low-η solvent component in an electrolyte for it to have a decent κ at low θ and the independence on θ of ion association in these solutions in support of an earlier finding. The data of the PC-DEC solution of were fit with the Vogel-Tamman-Fulcher equation for an evaluation of its apparent activation energy and its vanishing mobility temperature the former shown to be a simple surface in the coordinates slanting up in the direction of high η, and the latter another one slanting up in the same direction and lying beneath the surface of by more than ten degrees. © 2003 The Electrochemical Society. All rights reserved.
科研通智能强力驱动
Strongly Powered by AbleSci AI