Crystallinity and order of poly(ethylene oxide)/lithium triflate complex confined in nanoporous membranes

被引:26
作者
Bishop, Christina [2 ]
Teeters, Dale [1 ]
机构
[1] Univ Tulsa, Dept Chem & Biochem, Tulsa, OK 74104 USA
[2] Univ Tulsa, Dept Chem Engn, Tulsa, OK 74104 USA
关键词
Nanopores; Ordering; Crystallinity; Electrolyte confinement; Specific conductance; COMPOSITE POLYMER ELECTROLYTES; IONIC-CONDUCTIVITY; LITHIUM BATTERIES; SOLID ELECTROLYTES; SOLVENT-FREE; POLYETHER; OXIDE); BLENDS; SALTS;
D O I
10.1016/j.electacta.2009.02.043
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
070208 [无线电物理];
摘要
The confinement of poly(ethylene oxide), PEO, electrolyte in pores of 13, 35, 55 and 100 nm in diameter in nanoporous alumina membranes was seen to have effects on the ionic conduction properties. Specific conductivity values for the PEC/lithium triflate complex in the 13 and 35 nm pores, for temperatures below the melt temperatures, were increased by a factor of four compared to the non-confined polymer and the 55 and 100 nm pore systems. Thermal analysis data indicate the melting temperature for the PEO electrolyte in the pores is directly proportional to the pore size such that as the pore size of confinement is decreased, the T-m decreases as well. The same behavior is seen for the amount of crystallinity, with less crystallinity being observed as the pores become smaller. Perhaps the observed conduction behavior could be attributed to less crystallinity. However, it is known that confinement of polyethers in pores results in stretching and ordering of the backbone and that such ordering can increase ion conduction. This ordering would seem to be the major factor involved in these results. The enhanced conduction only being seen in the 13 and 35 nm pores and not the 55 and 100 nm pores is attributed to the larger size for the latter which allows a more bulk-like behavior with less ordering. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4084 / 4088
页数:5
相关论文
共 44 条
[1]
[Anonymous], J CHEM SOC PERKIN T
[2]
CONFORMATION AND OPTICAL-ABSORPTION PROPERTIES OF THIOPHENE OLIGOMERS - C-13-NMR, UV, AND MMP2 CALCULATIONS OF DI-QUATERTHIOPHENES AND TETRAMETHYL-QUATERTHIOPHENES [J].
BARBARELLA, G ;
BONGINI, A ;
ZAMBIANCHI, M .
ADVANCED MATERIALS, 1991, 3 (10) :494-496
[3]
Conductivity in amorphous polyether nanocomposite materials [J].
Best, AS ;
Ferry, A ;
MacFarlane, DR ;
Forsyth, M .
SOLID STATE IONICS, 1999, 126 (3-4) :269-276
[4]
ELECTROCHEMICAL PROPERTIES OF POLYETHYLENE OXIDE-LI[(CF3SO2)(2)N]-GAMMA-LIALO2 COMPOSITE POLYMER ELECTROLYTES [J].
BORGHINI, MC ;
MASTRAGOSTINO, M ;
PASSERINI, S ;
SCROSATI, B .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1995, 142 (07) :2118-2121
[5]
Bruce P.G., 1995, Solid state electrochemistry, V1st
[6]
Bruce P.G., 1987, POLYM ELECTROLYTE RE, V1, P252
[7]
ANISOTROPIC IONIC-CONDUCTIVITY IN UNIAXIALLY ORIENTED PERFLUOROSULFONATE IONOMERS [J].
CABLE, KM ;
MAURTIZ, KA ;
MOORE, RB .
CHEMISTRY OF MATERIALS, 1995, 7 (09) :1601-1603
[8]
COMPOSITE POLYMER ELECTROLYTES [J].
CAPUANO, F ;
CROCE, F ;
SCROSATI, B .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1991, 138 (07) :1918-1922
[9]
Impedance Spectroscopy of PEO-lithium triflate confined in nanopores of alumina membranes [J].
Castriota, M ;
Teeters, D .
IONICS, 2005, 11 (3-4) :220-225
[10]
Effect of plasticizers on high molecular weight PEO-LiCF3SO3 complexes [J].
Chintapalli, S ;
Frech, R .
SOLID STATE IONICS, 1996, 86-8 :341-346