Influence of lithium salt addition on ionic conductivity and transporting properties of lithium bis(trifluoromethanesulfonyl)imide-doped glycine-based ionic liquid electrolyte

被引:10
|
作者
Kuo, Chung-Wen [1 ]
Hao, Lin [2 ]
Kuo, Ping-Lin [3 ]
Chen, Pin-Rong [4 ]
Wu, Tzi-Yi [4 ]
机构
[1] Natl Kaohsiung Univ Appl Sci, Dept Chem & Mat Engn, Kaohsiung 80778, Taiwan
[2] Natl Cheng Kung Univ, Dept Chem, Tainan 70101, Taiwan
[3] Natl Cheng Kung Univ, Dept Chem Engn, Tainan 701, Taiwan
[4] Natl Yunlin Univ Sci & Technol, Dept Chem & Mat Engn, Yunlin 64002, Taiwan
关键词
Ionic liquid electrolyte; Ionic conductivity; Glycine; Walden's rule; Self-diffusion coefficient; Lithium ion transference number; PHYSICOCHEMICAL PROPERTIES; THERMOPHYSICAL PROPERTIES; ORGANIC-DYES; TEMPERATURE; DIFFUSION; GLYCOL; HEXAFLUOROPHOSPHATE; MIXTURES; SOLVENTS; CATIONS;
D O I
10.1016/j.jtice.2013.10.017
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The effects of the incorporation of lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) on the ionic transporting and physicochemical properties of a glycine-based ionic liquid (IL) are studied. The ionization conditions of each ionic species in LiTFSI-doped glycine-based ionic liquid electrolytes ([MGlyA][TFSI]), are characterized by diffusion coefficients of the species measured using the pulsed gradient spin-echo (PGSE) NMR technique. Temperature-dependent viscosity, ionic conductivity, molar conductivity, and self diffusion coefficient in neat [MGlyA][TFSI] and LiTFSI-doped [MGlyA][TFSI] followed the Vogel-Tamman-Fulcher equation at all concentrations. The experimental molar conductivity (Lambda) of neat [MGlyA][TFSI] and LiTFSI-doped [MGlyA][TFSI] is lower than that of the calculated molar conductivity (Lambda(NMR)) from PGSE NMR technique over the entire temperature range, demonstrating that not all the diffusive species contribute to the ionic conduction, that is, free-ions, ionic pairs, and/or clusters coexist in ILs. (C) 2013 Taiwan Institute of Chemical Engineers. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1270 / 1279
页数:10
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