Soft matter electrolytes based on polymethylmetacrylate dispersions in lithium bis(trifluoromethanesulfonyl)imide/1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide ionic liquids

被引:20
作者
Duluard, S.
Litas, I.
Bhattacharyya, A. J. [2 ]
Mauvy, F.
Campet, G.
Delville, M-H [1 ]
机构
[1] Univ Bordeaux, ICMCB, CNRS, Dept Chem,UPR 9048, F-33608 Pessac, France
[2] Indian Inst Sci, Solid State & Struct Chem Unit, Bangalore 560012, Karnataka, India
关键词
Ion transport; Transparent polymer-ionic liquid membrane; Ionic conductivity; VTF model; Electrochromism; POLYMER; SOLVATION; VISCOSITY; TRANSPORT; DIFFUSION; RAMAN; PMMA;
D O I
10.1016/j.electacta.2010.08.014
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Ion transport in a polymer-ionic liquid (IL) soft matter composite electrolyte is discussed here in detail in the context of polymer-ionic liquid interaction and glass transition temperature The dispersion of polymethylmetacrylate (PMMA) in 1-butyl-3-methylimidazolium hexafluorophosphate (BMIPF6) and 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide (BMITFSI) resulted in transparent composite electrolytes with a jelly-like consistency The composite ionic conductivity measured over the range -30 C to 60 C was always lower than that of the neat BMITFSI/BMIPF6 and LiTFSI-BMITFSI/LiTFSI-BMIPF6 electrolytes but still very high (>1 mS/cm at 25 degrees C up to 50 wt% PMMA) While addition of LiTFSI to IL does not influence the glass T-g and T-m melting temperature significantly dispersion of PMMA (especially at higher contents) resulted in increase in T-g and disappearance of T-m In general the profile of temperature-dependent ionic conductivity could be fitted to Vogel-Tamman-Fulcher (VTF) suggesting a solvent assisted ion transport However for higher PMMA concentration sharp demarcation of temperature regimes between thermally activated and solvent assisted ion transport were observed with the glass transition temperature acting as the reference point for transformation from one form of transport mechanism to the other Because of the beneficial physico-chemical properties and interesting ion transport mechanism we envisage the present soft matter electrolytes to be promising for application in electrochromic devices (C) 2010 Elsevier Ltd All rights reserved
引用
收藏
页码:8839 / 8846
页数:8
相关论文
共 45 条
[1]  
Armand M, 2009, NAT MATER, V8, P621, DOI [10.1038/NMAT2448, 10.1038/nmat2448]
[2]   FAST-ION TRANSPORT IN NEW LITHIUM ELECTROLYTES GELLED WITH PMMA .2. INFLUENCE OF LITHIUM SALT CONCENTRATION [J].
BOHNKE, O ;
FRAND, G ;
REZRAZI, M ;
ROUSSELOT, C ;
TRUCHE, C .
SOLID STATE IONICS, 1993, 66 (1-2) :105-112
[3]   Ionic liquids in electrochromic devices [J].
Brazier, A. ;
Appetecchi, G. B. ;
Passerini, S. ;
Vuk, A. Surca ;
Orel, B. ;
Donsanti, F. ;
Decker, F. .
ELECTROCHIMICA ACTA, 2007, 52 (14) :4792-4797
[4]   POLYMER ELECTROLYTES [J].
BRUCE, PG ;
VINCENT, CA .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1993, 89 (17) :3187-3203
[5]  
BRUCE PG, 1995, SOLID STATE ELECTRON, P130
[6]  
Callister W.D., 2000, MAT SCI ENG INTRO, V5th, P871
[7]  
CAMPET G, 2001, Patent No. 2803951
[8]   Electrochemistry of poly(3,4-ethylenedioxythiophene)-polyaniline/Prussian blue electrochromic devices containing an ionic liquid based gel electrolyte film [J].
Deepa, Melepurath ;
Awadhia, Arvind ;
Bhandari, Shweta .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2009, 11 (27) :5674-5685
[9]   Lithium solvation in a PMMA membrane plasticized by a lithium-conducting ionic liquid based on 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide [J].
Duluard, Sandrine ;
Grondin, Joseph ;
Bruneel, Jean-Luc ;
Campet, Guy ;
Delville, Marie-Helene ;
Lassegues, Jean-Claude .
JOURNAL OF RAMAN SPECTROSCOPY, 2008, 39 (09) :1189-1194
[10]   Lithium solvation and diffusion in the 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide ionic liquid [J].
Duluard, Sandrine ;
Grondin, Joseph ;
Bruneel, Jean-Luc ;
Pianet, Isabelle ;
Grelard, Axelle ;
Campet, Guy ;
Delville, Marie-Helene ;
Lassegues, Jean-Claude .
JOURNAL OF RAMAN SPECTROSCOPY, 2008, 39 (05) :627-632