Conducting-polymer-based supercapacitor devices and electrodes

被引:3077
作者
Snook, Graeme A. [1 ]
Kao, Pon [2 ]
Best, Adam S. [2 ]
机构
[1] CSIRO Proc Sci & Engn, Clayton, Vic 3169, Australia
[2] CSIRO Energy Technol, Clayton, Vic 3169, Australia
关键词
Supercapacitor; Ultracapacitor; Conducting polymer; Cycle-life; Specific energy; Specific power; NI12+ ION IRRADIATION; CARBON NANOTUBES; ELECTROCHEMICAL CAPACITOR; ACTIVATED CARBON; NANOCOMPOSITE MATERIALS; PERFORMANCE EVALUATION; REDOX SUPERCAPACITOR; NANOHYBRID MATERIALS; COMPOSITE CATHODE; PPY/V2O5; HYBRID;
D O I
10.1016/j.jpowsour.2010.06.084
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
Supercapacitor electrodes and devices that utilise conducting polymers are envisaged to bridge the gap between existing carbon-based supercapacitors and batteries to form units of intermediate specific energy. This review looks at the major conducting polymer materials, namely, polyaniline, polypyrrole, polythiophene and derivatives of polythiophene, as well as composites of these materials with carbon nanotubes and inorganic battery materials. Various treatments of the conducting polymer materials to improve their properties are considered and comparisons are made with other supercapacitor materials such as carbon and with inorganic battery materials. Conducting polymers are pseudo-capacitive materials, which means that the bulk of the material undergoes a fast redox reaction to provide the capacitive response and they exhibit superior specific energies to the carbon-based supercapacitors (double-layer capacitors). In general conducting polymers are more conductive than the inorganic battery materials and consequently have greater power capability. On the downside, conducting polymers swell and contract substantially on charge and discharge, respectively. Consequently, cycle-life is poor compared with carbon-based supercapacitors which generally only charge via adsorption and desorption of ions (giving typically a few thousand cycles for conducting polymers compared with >500 000 cycles for carbon-based devices). (c) 2010 Elsevier B.V. All rights reserved.
引用
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页码:1 / 12
页数:12
相关论文
共 134 条
[1]   Polypyrrole/polymer electrolyte composites prepared by in situ electropolymerization of pyrrole as cathode/electrolyte material for facile electron transfer at the solid interface [J].
Amanokura, J ;
Suzuki, Y ;
Imabayashi, S ;
Watanabe, M .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2001, 148 (04) :D43-D48
[2]  
An HF, 2009, PROG CHEM, V21, P1832
[3]  
Aouada FA, 2007, E-POLYMERS
[4]   Li1.01Mn1.97O4 surface modification by poly (3,4-ethylenedioxythiophene) [J].
Arbizzani, C ;
Balducci, A ;
Mastragostino, M ;
Rossi, M ;
Soavi, F .
JOURNAL OF POWER SOURCES, 2003, 119 :695-700
[5]   CHARACTERIZATION BY IMPEDANCE SPECTROSCOPY OF A POLYMER-BASED SUPERCAPACITOR [J].
ARBIZZANI, C ;
MASTRAGOSTINO, M ;
MENEGHELLO, L .
ELECTROCHIMICA ACTA, 1995, 40 (13-14) :2223-2228
[6]   N-DOPED AND P-DOPED POLYDITHIENO[3,4-B-3',4'-D] THIOPHENE - A NARROW-BAND GAP POLYMER FOR REDOX SUPERCAPACITORS [J].
ARBIZZANI, C ;
CATELLANI, M ;
MASTRAGOSTINO, M ;
MINGAZZINI, C .
ELECTROCHIMICA ACTA, 1995, 40 (12) :1871-1876
[7]   Preparation and electrochemical characterization of a polymer Li1.03Mn1.97O4/pEDOT composite electrode [J].
Arbizzani, C ;
Mastragostino, M ;
Rossi, M .
ELECTROCHEMISTRY COMMUNICATIONS, 2002, 4 (07) :545-549
[8]  
Arbizzani C, 1996, ADV MATER, V8, P331, DOI 10.1002/adma.19960080409
[9]   New trends in electrochemical supercapacitors [J].
Arbizzani, C ;
Mastragostino, M ;
Soavi, F .
JOURNAL OF POWER SOURCES, 2001, 100 (1-2) :164-170
[10]   Cycling stability of a hybrid activated carbon//poly(3-methylthiophene) supercapacitor with N-butyl-N-methylpyrrolidinium bis(trifluoromethanesulfonyl)imide ionic liquid as electrolyte [J].
Balducci, A ;
Henderson, WA ;
Mastragostino, M ;
Passerini, S ;
Simon, P ;
Soavi, F .
ELECTROCHIMICA ACTA, 2005, 50 (11) :2233-2237