Electropolymerization of PEDOT on CNTs conductive network assembled at water/oil interface

被引:21
作者
Gao, Lili [1 ,2 ]
Mao, Xuhui [1 ]
Zhu, Hua [1 ]
Xiao, Wei [1 ]
Gan, Fuxing [1 ]
Wang, Dihua [1 ]
机构
[1] Wuhan Univ, Sch Resource & Environm Sci, Wuhan 430072, Peoples R China
[2] Taiyuan Univ Technol, Sch Environm Sci & Engn, Taiyuan 030024, Peoples R China
基金
山西省青年科学基金;
关键词
liquid-liquid interface; electropolymerization; composite; PEDOT film; carbon nanotube; WALLED CARBON NANOTUBES; 3-PHASE JUNCTION; COMPOSITE FILMS; POLYMER; POLY(3,4-ETHYLENEDIOXYTHIOPHENE); POLYANILINE; FABRICATION; ELECTRODEPOSITION; SUPERCAPACITORS; CAPACITANCE;
D O I
10.1016/j.electacta.2014.05.053
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
We demonstrate an interfacial electrochemical process for the preparation of composite film of poly(3,4-ethylenedioxythiophene) (PEDOT) and carbon nanotubes (CNTs) at a water/oil (w/o) interface. The 3,4-ethylenedioxythiophene (EDOT) monomer and lithium perchlorate electrolyte were supplied from the oil phase (dichloromethane) and water phase, respectively. Firstly, acid-oxidized carbon nanotubes were assembled at the w/o interface with the assistance of a trace dosage of cationic surfactant, forming a CNTs network. And then the CNTs network acted as a "working electrode" and "reinforcement bars" for the electropolymerization of PEDOT, resulting in the production of PEDOT@CNTs composite film. Higher CNTs areal density (mu g/mm(2) CNTs) caused a faster radial growth of PEDOT at the CNTs network, namely a faster growth of "apparent area" of the composite film. The current-time curves of the electropolymerization demonstrated that there was an optimal areal density of CNTs network (0.40 mu g/mm(2)) to achieve the largest amount of polymerized PEDOT. These observations suggested that the assembled CNTs network and the formed PEDOT@CNTs composite film not only functioned as an electrical conductor for the electrochemical process, but also affected the mass transfer of the reactants. The prepared PEDOT@CNTs composite film showed heterogeneous structures with a capacitance of 0.148 F/C. The pre-assembled nano-particles network involved liquid-liquid interfacial eletropolymerization may be developed for the preparation of a series of conductive polymer@nanoparticle composite film. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:97 / 104
页数:8
相关论文
共 29 条
[1]   Electropolymerization of an immiscible monomer in aqueous electrolytes using acoustic emulsification [J].
Asami, R ;
Atobe, M ;
Fuchigami, T .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (38) :13160-13161
[2]   Three-phase electrochemistry. Influence of temperature on ion transfer [J].
Bak, Elzbieta ;
Donten, Mikolaj ;
Stojek, Zbigniew .
ELECTROCHEMISTRY COMMUNICATIONS, 2008, 10 (07) :1074-1077
[3]   Electrodeposition of poly(N-vinylcarbazole) at the three-phase junction.: Formation of very different polymer structures [J].
Bak, Elzbieta ;
Donten, Mikolaj ;
Skompska, Magdalena ;
Stojek, Zbigniew .
JOURNAL OF PHYSICAL CHEMISTRY B, 2006, 110 (48) :24635-24641
[4]   Oxygen reduction on oxide/polypyrrole composite electrodes: effect of doping anions [J].
Cong, HN ;
El Abbassi, K ;
Gautier, JL ;
Chartier, P .
ELECTROCHIMICA ACTA, 2005, 50 (06) :1369-1376
[5]  
Downs C, 1999, ADV MATER, V11, P1028, DOI 10.1002/(SICI)1521-4095(199908)11:12<1028::AID-ADMA1028>3.0.CO
[6]  
2-N
[7]   Electropolymerization of 3-methylthiophene at liquid 3-methylthlophene | aqueous solution | graphite three-phase junction [J].
Gergely, A ;
Inzelt, G .
ELECTROCHEMISTRY COMMUNICATIONS, 2001, 3 (12) :753-757
[8]   High performance electrochemical supercapacitor from electrochemically synthesized nanostructured polyaniline [J].
Gupta, V ;
Miura, N .
MATERIALS LETTERS, 2006, 60 (12) :1466-1469
[9]   Chemical sensors based on highly conductive poly(3,4-ethylenedioxythiophene) nanorods [J].
Jang, J ;
Chang, M ;
Yoon, H .
ADVANCED MATERIALS, 2005, 17 (13) :1616-+
[10]   Supercapacitors from nanotubes/polypyrrole composites [J].
Jurewicz, K ;
Delpeux, S ;
Bertagna, V ;
Béguin, F ;
Frackowiak, E .
CHEMICAL PHYSICS LETTERS, 2001, 347 (1-3) :36-40