Synthesis and characterization of novel urethane cross-linked ormolytes for solid-state lithium batteries

被引:68
作者
Bermudez, VD
Alcácer, L
Acosta, JL
Morales, E
机构
[1] Univ Tras os Montes & Alto Douro, Seccao Quim, Quinta Prados, P-5001 Vila Real, Portugal
[2] Inst Super Tecn, Dept Engn Quim, P-1092 Lisbon, Portugal
[3] CSIC, Inst Ciencia & Tecnol Polimeros, Madrid 28007, Spain
关键词
lithium batteries; lithium triflate; polymer electrolytes; sol-gel;
D O I
10.1016/S0167-2738(98)00346-4
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 novel family of Li+-based organic/inoganic materials obtained by the sol-gel process is proposed. The compounds, named urethanesils, are obtained as thin, transparent, elastomeric and amorphous monolithic films. They incorporate solvating pendant methyl end-capped short poly(oxyethylene) chains which are covalently bonded to the silica backbone by means of urethane cross-links. The urethane linkages are formed by reacting 3-isocyanatepropyltriethoxysilane with hepta(ethylene glycol) methyl ether (HEGME). Li+ has been introduced in the urethanesils as lithium triflate (LiCF3SO3). Two compositions of salt have been considered: n = 100 and 8, where n represents the molar ratio of (OCH2CH2) units per lithium ion. infrared spectroscopy provides conclusive evidence that, although the oligopolyether chains of HEGME become less disordered upon formation of the inorganic network, the addition of salt induces disorder. The FTIR spectrum of the most concentrated urethanesil strongly suggests that the triflate ions are essentially coordinated in the material. The thermal and mechanical properties of the undoped and doped urethanesils have been investigated by DSC and DMTA. At 90 degrees C, the highest ionic conductivity (approximately 10(-6) Ohm(-1) cm(-1)) is observed for composition n = 8. The electrochemical stability domain of the least concentrated urethanesil spans 5 V. (C) 1999 Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:197 / 209
页数:13
相关论文
共 48 条
[41]   POLYCONDENSATION OF AMINOSILANES IN METHANOL [J].
ROUSSEAU, F ;
POINSIGNON, C ;
GARCIA, J ;
POPALL, M .
CHEMISTRY OF MATERIALS, 1995, 7 (05) :828-839
[42]  
SANCHEZ JY, 1993, POLYM ADVAN TECHNOL, V4, P99
[43]  
SCHMIDT H, 1990, 2ND INT S POL EL, P325
[44]  
SCROSATI B, 1990, P 2 INT S POL EL
[45]  
SHANTZ S, 1993, SOLID STATE IONICS, V60, P47
[46]   INFRARED SPECTRA-STRUCTURE CORRELATIONS FOR ORGANOSILICON COMPOUNDS [J].
SMITH, AL .
SPECTROCHIMICA ACTA, 1960, 16 (1-2) :87-105
[47]   STRUCTURE, DYNAMICS AND MORPHOLOGY IN THE SYSTEM M(CF3SO3)2 PEON FOR M=ZN AND PB [J].
WENDSJO, A ;
LINDGREN, J ;
PALUSZKIEWICZ, C .
ELECTROCHIMICA ACTA, 1992, 37 (09) :1689-1693
[48]  
Wright P. V., 1975, British Polymer Journal, V7, P319, DOI 10.1002/pi.4980070505