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Manganese oxide embedded polypyrrole nanocomposites for electrochemical supercapacitor

MnO 2 embedded PPy nanocomposite (MnO 2/PPy) thin film electrodes were electrochemically synthesized over polished graphite susbtrates. Growing PPy polymer chains provides large surface area template that enables MnO 2 to form as nanoparticles embeded within polymer matrix. Co-deposition of MnO 2 an...

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Bibliographic Details
Published in:Electrochimica acta 2008-11, Vol.53 (26), p.7690-7695
Main Authors: Sharma, R.K., Rastogi, A.C., Desu, S.B.
Format: Article
Language:English
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Summary:MnO 2 embedded PPy nanocomposite (MnO 2/PPy) thin film electrodes were electrochemically synthesized over polished graphite susbtrates. Growing PPy polymer chains provides large surface area template that enables MnO 2 to form as nanoparticles embeded within polymer matrix. Co-deposition of MnO 2 and PPy has a complimentary action in which porous PPy matrix provides high active surface area for the MnO 2 nanoparticles and, on the other hand, MnO 2 nanoparticles nucleated over polymer chains contribute to enhanced conductivity and stability of the nanocomposite material by interlinking the PPy polymer chains. The MnO 2/PPy nanocomposite thin film electrodes show significant improvement in the redox performance as cyclic voltammetric studies have shown. Specific capacitance of the nanocomposite is remarkably high (∼620 F g −1) in comparision to its constituents MnO 2 (∼225 F g −1) and PPy (∼250 F g −1). Photoelectron spectroscopy studies show that hydrated manganese oxide in the nanocomposite exists in the mixed Mn(II) to Mn(IV) oxidation states. Accordingly, chemical structures of MnO 2 and PPy constituents in the nanocomposite are not influenced by the co-deposition process. The MnO 2/PPy nanocomposite electrode material however shows significantly improved high specific capacitity, charge–discharge stability and the redox performance properties suitable for application in the high energy density supercapcitors.
ISSN:0013-4686
1873-3859
DOI:10.1016/j.electacta.2008.04.028