Improvement of capacitive performances of symmetric carbon/carbon supercapacitors by addition of nanostructured polypyrrole powder

被引:24
作者
Benhaddad, L. [1 ,2 ]
Gamby, J. [2 ]
Makhloufi, L. [1 ]
Pailleret, A. [2 ]
Pillier, F. [2 ]
Takenouti, H. [2 ]
机构
[1] A Mira Univ, Dept Genie Proc, LECVE, Route Targa Ouzemmour, Bejaia 06000, Algeria
[2] Univ Paris 06, Sorbonne Univ, CNRS, LISE,UMR 8235, 4 Pl Jussieu,Case Courrier 133, F-75005 Paris, France
关键词
Carbon/carbon supercapacitor; Double-layer capacitance; Polypyrrole; Electrochemical impedance spectroscopy; Swagelok; Complex capacitance; ELECTRODE MATERIAL; ACTIVATED CARBONS; ELECTROCHEMICAL CAPACITANCE; CONDUCTING POLYMERS; PORE-SIZE; POLYANILINE; COMPOSITES; MNO2; REACTIVITY; NANOWIRES;
D O I
10.1016/j.jpowsour.2015.12.007
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 nanostructured polypyrrole powder was synthesized in a previous work from the oxidation of pyrrole by a nanostructured MnO2 powder used simultaneously as an oxidizing agent and a sacrificial template in a redox heterogeneous mechanism. In this study, this original PPy powder was used as an active additive material with different ratio in carbon/carbon symmetrical supercapacitors whose performances were studied by cyclic voltammetry and electrochemical impedance spectroscopy (EIS) using a Swagelok-type cell. From the EIS spectra, the complex capacitance was extracted using a model involving two Cole-Cole type complex capacitances linked in series. The specific capacitance values evaluated by EIS and cyclic voltammetry are in a good agreement between them. The results show that the addition of nanostructured polypyrrole powder improves significantly the specific capacitance of the carbon electrode and consequently the performances of carbon/carbon supercapacitors. The original and versatile synthesis method used to produce this polypyrrole powder appears to be attractive for large scale production of promising additives for electrode materials of supercapacitors. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:297 / 307
页数:11
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