In situ electrochemical polymerization of a nanorod-PANI-Graphene composite in a reverse micelle electrolyte and its application in a supercapacitor
Highly porous nanorod-PANI-Graphene composite films were prepared by in situ electrochemical polymerization onto an ITO substrate in a reverse micelle electrolyte. The morphology and microstructure of the composite films were analyzed by using a field emission scanning electron microscope. It was ob...
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Veröffentlicht in: | Physical chemistry chemical physics : PCCP 2012-01, Vol.14 (45), p.15652-15656 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Highly porous nanorod-PANI-Graphene composite films were prepared by
in situ
electrochemical polymerization onto an ITO substrate in a reverse micelle electrolyte. The morphology and microstructure of the composite films were analyzed by using a field emission scanning electron microscope. It was observed that the films were highly porous and the nanorod PANI films were inserted by graphene nanosheets. This indicated that a good conductive network between PANI nanorods and graphene sheets was formed. Further electrochemical tests involved cyclic voltammetry (CV), galvanostatic charge-discharge (GCD) and electrochemical impedance spectroscopy (EIS) in 1 mol L
−1
HClO
4
solution. The results showed that the composite film had a favorable capacitance with a high electron transfer rate and low resistance. The highest specific capacitance that could be achieved was as high as 878.57 F g
−1
with the charge loading of 500 mC at a current density of 1 A g
−1
. The GCD at different charge loadings showed good cycle stability with a low fading rate of specific capacitance after 1000 cycles. The results demonstrated that the nanorod-PANI-Graphene composite was proved to be of great potential as an electrode material for supercapacitors.
Highly porous nanorod-PANI-Graphene composite films were prepared by
in situ
electrochemical polymerization onto an ITO substrate in a reverse micelle electrolyte. |
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ISSN: | 1463-9076 1463-9084 |
DOI: | 10.1039/c2cp42192e |