Glyme-Lithium Salt Equimolar Molten Mixtures: Concentrated Solutions or Solvate Ionic Liquids?

被引:367
作者
Ueno, Kazuhide [1 ]
Yoshida, Kazuki [1 ]
Tsuchiya, Mizuho [1 ]
Tachikawa, Naoki [1 ]
Dokko, Kaoru [1 ]
Watanabe, Masayoshi [1 ]
机构
[1] Yokohama Natl Univ, Dept Chem & Biotechnol, Hodogaya Ku, Yokohama, Kanagawa 2408501, Japan
基金
日本科学技术振兴机构;
关键词
PHYSICOCHEMICAL PROPERTIES; POLYMER ELECTROLYTES; TRANSPORT-PROPERTIES; LOW-VISCOSITY; COMPLEXES; CONDUCTIVITY; DIFFUSION; BIS(TRIFLUOROMETHANESULFONYL)IMIDE; BIS(TRIFLUOROMETHYLSULFONE)IMIDE; CONFORMATION;
D O I
10.1021/jp307378j
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
To demonstrate a new family of ionic liquids (ILs), i.e., "solvate" ionic liquids, the properties (thermal, transport, and electrochemical properties, Lewis basicity, and ionicity) of equimolar molten mixtures of glymes (triglyme (G3) and tetraglyme (G4)) and nine different lithium salts (LiX) were investigated. By exploring the anion-dependent properties and comparing them with the reported data on common aprotic ILs, two different classes of liquid regimes, i.e., ordinary concentrated solutions and "solvate" ILs, were found in the glyme-Li salt equimolar mixtures ([Li(glyme)]X) depending on the anionic structures. The class a given [Li(glyme)]X belonged to was governed by competitive interactions between the glymes and Li cations and between the counteranions (X) and Li cations. [Li(glyme)]X with weakly Lewis basic anions can form long-lived [Li(glyme)](+) complex cations. Thus, they behaved as typical ionic liquids. The lithium "solvate" ILs based on [Li(glyme)]X have many desirable properties for lithium-conducting electrolytes, including high ionicity, a high lithium transference number, high Li cation concentration, and high oxidative stability, in addition to the common properties of ionic liquids. The concept of "solvate" ionic liquids can be utilized in an unlimited number of combinations of other metal salts and ligands, and will thus open a new field of research on ionic liquids.
引用
收藏
页码:11323 / 11331
页数:9
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