Approaches to, and Problems with, Ionic Liquid Electrolytes for Alkali Metal Electrochemical Devices: The Case of Low-Melting Chloroaluminate Binary Solutions
Approaches to, and Problems with, Ionic Liquid Electrolytes for Alkali Metal Electrochemical Devices: The Case of Low-Melting Chloroaluminate Binary Solutions
复制标题
用于碱金属电化学装置的离子液体电解质的方法和问题:以低熔点氯铝酸盐二元溶液为例
DOI:
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发表时间:
2014
期刊:
影响因子:
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通讯作者:
C. Angell
中科院分区:
文献类型:
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作者:
T. Tucker;C. Angell
Despite many attempts to use ionic liquid media with dissolved lithium salts as the electrolyte component of electrochemical cells, there has been only limited success. Despite its small size, Li+ seems to be the slowest species in the electrolyte, so the cells polarize. As sodium batteries gain attention, the needed Na+-containing ionic liquid electrolytes are likely to encounter similar, but more serious, kinetic problems. Here we first review past attempts to use, as an alternative, inorganic salts and quasi-salts of high conductivity, where conductivity increases with alkali content. Then we provide a detailed study of one organic cation system which confirms and extends earlier work by the Wilkes laboratory that showed how the opposite trend applied for mixtures of NaAlCl4 with the ionic liquid ethylmethylimidazolium tetrachloroaluminate [EMI][AlCl4]. In the present work the depression of conductivity for the Na+ case is fully characterized and is discussed in terms of a 1983 coulomb field alkali trapping concept for low-melting mixtures. This itself is an adaptation of earlier molten salt electrostatic and ionic polarizability models. The apparent exceptionalism of lithium salts in inorganic quasi-ionic liquid solutions is reviewed and possible ways of sidestepping the identified problems for sodium ion conductors are considered. © 2014 The Electrochemical Society. [DOI: 10.1149/2.0471412jes] All rights reserved.
影响因子:
3.9
作者:
Ye, Hui;Huang, Jian;Greenbaum, Steve G.
通讯作者:
Greenbaum, Steve G.