Ionic conductivity of polymer electrolyte membranes based on polyphosphazene with oligo(propylene oxide) side chains

被引:24
作者
Kaskhedikar, N
Paulsdorf, J
Burjanadze, M
Karatas, Y
Wilmer, D
Roling, B
Wiemhöfer, HD
机构
[1] Univ Munster, Inst Inorgan & Analyt Chem, D-48149 Munster, Germany
[2] Univ Munster, SFB 458, D-48149 Munster, Germany
[3] Univ Munster, Inst Chem Phys, D-48149 Munster, Germany
[4] Univ Munster, SFB 458, D-48149 Munster, Germany
[5] Univ Munster, GSC MS, D-48149 Munster, Germany
[6] Univ Marburg, Dept Chem, D-35032 Marburg, Germany
关键词
polymer electrolytes; polyphosphazene; ionic conductivity;
D O I
10.1016/j.ssi.2006.01.011
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
A polyphosphazene [NP(NHR)2](n) with oligo[propylene oxide] side chains -R=-[CH(CH3)-CH2O](m)-CH3 (m=6-10) was synthesized by living cationic polymerisation and polymer-analogue substitution of chlorine from the intermediate precursor [NPCl2](n) using the corresponding primary amine RNH2. The polymer had an average molecular weight of 3.3 x 10(5) D. Polymer electrolytes with different concentrations of dissolved lithium triflate (LiCF3SO3) were prepared. Mechanically stable polymer electrolyte membranes were formed using UV radiation induced crosslinking of the polymer salt mixture in the presence of benzophenone as photoinitiator. The glass transition temperature of the parent polymer was found to be -75 degrees C before cross linking. It increases after crosslinking and with increasing amounts of salt to a maximum of -55 degrees C for 20 wt.% LiCF3SO3. The ionic conductivity was determined by impedance spectroscopy in the temperature range 0-80 degrees C. The highest conductivity was found for a salt concentration of 20 wt.% LiCF3SO3: 6.5 x 10(-6) S(.)cm(-1) at 20 degrees C and 2.8x 10(-4) S cm(-1) at 80 degrees C. The temperature dependence of the conductivities was well described by the MIGRATION concept. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:703 / 707
页数:5
相关论文
共 32 条
[1]  
Allcock H. R., 2003, CHEM APPL POLYPHOSPH
[2]  
Allcock H. R., 1987, POLYM PREPR, V28, P321
[3]   Polyphosphazene block copolymers via the controlled cationic, ambient temperature polymerization of phosphoranimines [J].
Allcock, HR ;
Reeves, SD ;
Nelson, JM ;
Crane, CA ;
Manners, I .
MACROMOLECULES, 1997, 30 (07) :2213-2215
[4]   Ambient-temperature direct synthesis of poly(organophosphazenes) via the ''living'' cationic polymerization of organo-substituted phosphoranimines [J].
Allcock, HR ;
Nelson, JM ;
Reeves, SD ;
Honeyman, CH ;
Manners, I .
MACROMOLECULES, 1997, 30 (01) :50-56
[5]   Influence of reaction parameters on the living cationic polymerization of phosphoranimines to polyphosphazenes [J].
Allcock, HR ;
Reeves, SD ;
de Denus, CR ;
Crane, CK .
MACROMOLECULES, 2001, 34 (04) :748-754
[6]   POLYMER ELECTROLYTES BASED ON POLY-PHOSPHAZENE WITH PENDANT 12-CROWN-4 GROUPS AND MONOVALENT SALTS [J].
ANDREI, M ;
COWIE, JMG ;
PROSPERI, P .
ELECTROCHIMICA ACTA, 1992, 37 (09) :1545-1549
[7]   POLYMER SOLID ELECTROLYTES - AN OVERVIEW [J].
ARMAND, M .
SOLID STATE IONICS, 1983, 9-10 (DEC) :745-754
[8]  
Armand M. B., 1979, Fast Ion Transport in Solids. Electrodes and Electrolytes, P131
[9]   COMPLEX-FORMATION AND IONIC-CONDUCTIVITY OF POLYPHOSPHAZENE SOLID ELECTROLYTES [J].
BLONSKY, PM ;
SHRIVER, DF ;
AUSTIN, P ;
ALLCOCK, HR .
SOLID STATE IONICS, 1986, 18-9 (pt 1) :258-264
[10]   Preparation and conductivity of the composite polymer electrolytes based on poly [bis(methoxyethoxyethoxy)phosphazene], LiClO4 and α-Al2O3 [J].
Chen-Yang, YW ;
Chen, HC ;
Lin, FJ ;
Liao, CW ;
Chen, TL .
SOLID STATE IONICS, 2003, 156 (03) :383-392