Electric double layer capacitors with gelled polymer electrolytes based on poly(ethylene oxide) cured with poly(propylene oxide) diamines

被引:53
作者
Tien, Chien-Ping [1 ,2 ]
Liang, Wuu-Jyh [1 ,2 ]
Kuo, Ping-Lin [1 ,2 ]
Teng, Hsi-Sheng [1 ,2 ]
机构
[1] Natl Cheng Kung Univ, Dept Chem Engn, Tainan 70101, Taiwan
[2] Natl Cheng Kung Univ, Ctr Micro Nano Sci & Technol, Tainan 70101, Taiwan
关键词
gel electrolyte; PEO-copolyrner-PPO; ionic conductivity; electric double layer capacitor; activated carbon electrode;
D O I
10.1016/j.electacta.2008.01.021
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Using a gel electrolyte for electric double layer capacitors usually encountered a drawback of poor contact between the electrolyte and the electrode surface. A gel electrolyte consisting of poly(ethylene oxide) crosslinked with poly(propylene oxide) as a host, propylene carbonate (PC) as a plasticizer, and LiClO4 as a electrolytic salt was synthesized for double layer capacitors. Diglycidyl ether of bisphenol-A was blended with the polymer precursors to enhance the mechanical properties and increase the internal free volume. This gel electrolyte showed an ionic conductivity as high as 2 x 10(-3) S cm(-1) at 25 degrees C and was electrochemically stable over a wide potential range (ca. 5 V). By sandwiching this get-electrolyte film with two activated carbon cloth electrodes (1100m(2) g(-1) in surface area), we obtained a capacitor with a specific capacitance of 86 F g(-1) discharged at 0.5 mA cm(-2), while the capacitance was 82 Fg(-1) for a capacitor equipped with a liquid electrolyte of I M LiClO4/PC. The capacitance decrease with the current density was less significant for the gel-electrolyte capacitor. We found that the less restricted ion diffusion near the electrolyte/electrode interface led to the smaller overall resistance of the gel-electrolyte capacitor. The high performance of the gel-electrolyte capacitor has demonstrated that the developed polymer network not only facilitated ion motion in the electrolyte bulk phase but also gave an intimate contact with the carbon surface. The side chains of the polymer in the amorphous phase could stretch across the boundary layer at the electrolyte/electrode interface to come into contact with the carbon surface, thus improving transport of Li+ ions by the segmental mobility in polymer. (c) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4505 / 4511
页数:7
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