Polyaniline/porous carbon electrodes by chemical polymerisation:: Effect of carbon surface chemistry

被引:46
作者
Bleda-Martinez, M. J.
Morallon, E.
Cazorla-Amoros, D.
机构
[1] Univ Alicante, Dept Quim Inorgan, E-03080 Alicante, Spain
[2] Univ Alicante, Dept Quim Fis, E-03080 Alicante, Spain
关键词
activated carbon; polyaniline; surface oxygen complexes; capacitance; chemical polymerisation;
D O I
10.1016/j.electacta.2007.01.073
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Polyaniline/porous carbon composite electrodes were prepared by chemical polymerisation and characterized in terms of porosity and performance as electrochemical capacitors. To obtain the composite electrodes two methods were used. The first method consisted of mixing, directly, the activated carbon with chemically polymerised polyaniline. The second one consisted of mixing the activated carbon with aniline and subsequent chemical polymerisation. Additionally, the second process was carried out with the porous carbon previously thermally treated in N-2 up to 900 degrees C in order to remove surface oxygen groups. Changes in porosity with the polyaniline addition were analysed. It has been proved that the method used strongly affects the porous structure. Dealing with the electrochemical performance, polyaniline and carbon mechanically mixed seem to work independently, being the composite behaviour a combination of the corresponding performance of both materials separately. The composites prepared by the second method (polymerisation over carbon) reveal the key role of surface chemistry in polyaniline coating. Aniline reacts with the oxygen complexes and their positive effect in capacitance is not observed. The second method (polymerisation over carbon) using a thermally treated carbon seems to be the best one since a more porous (or thinner) polyaniline film is produced. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4962 / 4968
页数:7
相关论文
共 46 条
[31]   Potentiodynamically deposited polyaniline on stainless steel - Inexpensive, high-performance electrodes for electrochemical supercapacitors [J].
Prasad, KR ;
Munichandraiah, N .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2002, 149 (11) :A1393-A1399
[32]   Structural characterization of N-containing activated carbon fibers prepared from a low softening point petroleum pitch and a melamine resin [J].
Raymundo-Piñero, E ;
Cazorla-Amorós, D ;
Linares-Solano, A ;
Find, J ;
Wild, U ;
Schlögl, R .
CARBON, 2002, 40 (04) :597-608
[33]   The influence of porosity and the nature of the charge storage capacitance on the impedance behaviour of electropolymerized polyaniline films [J].
Rossberg, K ;
Paasch, G ;
Dunsch, L ;
Ludwig, S .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1998, 443 (01) :49-62
[34]   Electrochemical capacitor with chemically polymerized conducting polymer based on activated carbon as hybrid electrodes [J].
Ryu, KS ;
Lee, YG ;
Kim, KM ;
Park, YJ ;
Hong, YS ;
Wu, XL ;
Kang, MG ;
Park, NG ;
Song, RY ;
Ko, JM .
SYNTHETIC METALS, 2005, 153 (1-3) :89-92
[35]   Electrochemical supercapacitor based on polyaniline doped with lithium salt and active carbon electrodes [J].
Ryu, KS ;
Lee, YG ;
Han, KS ;
Park, YJ ;
Kang, MG ;
Park, NG ;
Chang, SH .
SOLID STATE IONICS, 2004, 175 (1-4) :765-768
[36]   Symmetric redox supercapacitor with conducting polyaniline electrodes [J].
Ryu, KS ;
Kim, KM ;
Park, NG ;
Park, YJ ;
Chang, SH .
JOURNAL OF POWER SOURCES, 2002, 103 (02) :305-309
[37]  
SALAVAGIONE HJ, 2003, THESIS U NACL RIO CU
[38]   Characterization of the redox processes in polyaniline using capacitance-potential curves [J].
Santiago, EI ;
Pereira, EC ;
Bulhoes, LOS .
SYNTHETIC METALS, 1998, 98 (02) :87-93
[39]   Poly(o-toluidine) for carbon fabric electrode modification to enhance the electrochemical capacitance and conductivity [J].
Sivakumar, C ;
Nian, JN ;
Teng, HS .
JOURNAL OF POWER SOURCES, 2005, 144 (01) :295-301
[40]   Electropolymerization of aniline on carbonized polyacrylonitrile aerogel electrodes: applications for supercapacitors [J].
Talbi, H ;
Just, PE ;
Dao, LH .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 2003, 33 (06) :465-473