Effect of binder polymer structures used in composite cathodes on interfacial charge transfer processes in lithium polymer batteries

被引:26
作者
Seki, S
Tabata, S
Matsui, S
Watanabe, M
机构
[1] Yokohama Natl Univ, Dept Chem & Biotechnol, Hodogaya Ku, Yokohama, Kanagawa 2408501, Japan
[2] CREST, JST, Hodogaya Ku, Yokohama, Kanagawa 2408501, Japan
[3] DAISO Co Ltd, Amagasaki, Hyogo 6600842, Japan
关键词
polymer electrolyte; ionic conductivity; interfacial resistance; composite cathode; lithium polymer battery;
D O I
10.1016/j.electacta.2003.12.065
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The effect of binder polymer structures used in composite cathodes on the interfacial charge transfer processes in lithium polymer batteries (LPB) has been studied in detail. A cross-linked comb-copolymer, consisting of ethylene oxide (EO), 2-(2-methoxyethoxy)ethyl glycidyl ether (MEEGE), and allyl glycidyl ether (AGE), was used as a solid polymer electrolyte (SPE). LiCoO2 composite cathodes were fabricated using binder comb-copolymers, consisting of EO and MEEGE with different compositions. Ionic conductivity of the SPE, and the interfacial charge transfer processes between the SPE and metallic lithium and between the SPE and the composite cathode at several cathode potentials versus Li/Li+, were electrochemically explored. With increasing MEEGE composition in the binder copolymers, the interfacial resistances between the SPE and the composite cathode appreciably decreased. As the result, discharge capacity of the LPB also enhanced with increasing the MEEGE composition. The introduction of the branched-side-chains to the polymer backbone to the binder polymers for the composite cathodes caused to facilitate the interfacial charge transport processes, while the introduction had also been found to be very effective in terms of the enhancement of ionic conductivity of SPE. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:379 / 383
页数:5
相关论文
共 10 条
[1]   Network polymer electrolytes with free chain ends as internal plasticizer [J].
Kono, M ;
Hayashi, E ;
Watanabe, M .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1998, 145 (05) :1521-1527
[2]  
MacCallum J.R., 1989, POLYM ELECTROLYTE RE, V2
[3]  
MacCallum J. R., 1987, POLYM ELECTROLYTE RE, V1
[4]   Liquid-free rechargeable Li polymer battery [J].
Matsui, S ;
Muranaga, T ;
Higobashi, H ;
Inoue, S ;
Sakai, T .
JOURNAL OF POWER SOURCES, 2001, 97-8 :772-774
[5]  
MIURA K, Patent No. 9568336
[6]   High ionic conductivity of polyether-based network polymer electrolytes with hyperbranched side chains [J].
Nishimoto, A ;
Agehara, K ;
Furuya, N ;
Watanabe, T ;
Watanabe, M .
MACROMOLECULES, 1999, 32 (05) :1541-1548
[7]   High ionic conductivity of new polymer electrolytes based on high molecular weight polyether comb polymers [J].
Nishimoto, A ;
Watanabe, M ;
Ikeda, Y ;
Kohjiya, S .
ELECTROCHIMICA ACTA, 1998, 43 (10-11) :1177-1184
[8]   Template synthesis of polypyrrole-coated spinel LiMn2O4 nanotubules and their properties as cathode active materials for lithium batteries [J].
Nishizawa, M ;
Mukai, K ;
Kuwabata, S ;
Martin, CR ;
Yoneyama, H .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1997, 144 (06) :1923-1927
[9]   Sol-gel-based template synthesis and Li-insertion rate performance of nanostructured vanadium pentoxide [J].
Patrissi, CJ ;
Martin, CR .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1999, 146 (09) :3176-3180
[10]   High ionic conductivity and electrode interface properties of polymer electrolytes based on high molecular weight branched polyether [J].
Watanabe, M ;
Endo, T ;
Nishimoto, A ;
Miura, K ;
Yanagida, M .
JOURNAL OF POWER SOURCES, 1999, 81 :786-789