dc.contributor.author |
Chidembo, AT
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|
dc.contributor.author |
Ozoemena, KI
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|
dc.date.accessioned |
2012-04-18T10:45:33Z |
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dc.date.available |
2012-04-18T10:45:33Z |
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dc.date.issued |
2010-11 |
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dc.identifier.citation |
Chidembo, AT and Ozoemena, KI. 2010. Electrochemical capacitive behaviour of multiwalled carbon nanotubes modified with electropolymeric films of nickel tetraaminophthalocyanine. Electroanalysis, vol. 22(21), pp 2529-2535 |
en_US |
dc.identifier.issn |
1040-0397 |
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dc.identifier.uri |
http://onlinelibrary.wiley.com/doi/10.1002/elan.201000290/pdf
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|
dc.identifier.uri |
http://hdl.handle.net/10204/5787
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dc.description |
Copyright: 2010 Wiley-VCH Verlag GmbH & Co. This is an ABSTRACT ONLY |
en_US |
dc.description.abstract |
Electrochemical capacitive behaviour of the electropolymeric nickel tetra-aminophthalocyanine (poly-NiTAPc) supported on multiwalled carbon nanotube (MWCNT) platform is described. From the data in 1 M H2SO4, the MWCNT-poly-NiTAPc exhibited superior capacitance (112 mF cm2 or 777 F g1). The supercapacitance of the MWCNT-polyNiTAPc was found to be much better in 1 M H2SO4 than in 1 M NaOH medium. Impedance data proved that most of the stored energy of the MWCNT-poly-NiTAPc could be accessible at high frequency (1.6 kHz). The electrode is capable of undergoing continuous charge-discharge process for more than a 1000 cycles without any significant deterioration in the stability. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
Wiley-VCH Verlag GmbH & Co |
en_US |
dc.relation.ispartofseries |
Workflow;6127 |
|
dc.subject |
Supercapacitance |
en_US |
dc.subject |
Nickel tetraaminophthalocyanine electropolymer |
en_US |
dc.subject |
MWCNTs |
en_US |
dc.subject |
Cyclic voltammetry |
en_US |
dc.subject |
Galvanostatic charge-discharge |
en_US |
dc.title |
Electrochemical capacitive behaviour of multiwalled carbon nanotubes modified with electropolymeric films of nickel tetraaminophthalocyanine |
en_US |
dc.type |
Article |
en_US |
dc.identifier.apacitation |
Chidembo, A., & Ozoemena, K. (2010). Electrochemical capacitive behaviour of multiwalled carbon nanotubes modified with electropolymeric films of nickel tetraaminophthalocyanine. http://hdl.handle.net/10204/5787 |
en_ZA |
dc.identifier.chicagocitation |
Chidembo, AT, and KI Ozoemena "Electrochemical capacitive behaviour of multiwalled carbon nanotubes modified with electropolymeric films of nickel tetraaminophthalocyanine." (2010) http://hdl.handle.net/10204/5787 |
en_ZA |
dc.identifier.vancouvercitation |
Chidembo A, Ozoemena K. Electrochemical capacitive behaviour of multiwalled carbon nanotubes modified with electropolymeric films of nickel tetraaminophthalocyanine. 2010; http://hdl.handle.net/10204/5787. |
en_ZA |
dc.identifier.ris |
TY - Article
AU - Chidembo, AT
AU - Ozoemena, KI
AB - Electrochemical capacitive behaviour of the electropolymeric nickel tetra-aminophthalocyanine (poly-NiTAPc) supported on multiwalled carbon nanotube (MWCNT) platform is described. From the data in 1 M H2SO4, the MWCNT-poly-NiTAPc exhibited superior capacitance (112 mF cm2 or 777 F g1). The supercapacitance of the MWCNT-polyNiTAPc was found to be much better in 1 M H2SO4 than in 1 M NaOH medium. Impedance data proved that most of the stored energy of the MWCNT-poly-NiTAPc could be accessible at high frequency (1.6 kHz). The electrode is capable of undergoing continuous charge-discharge process for more than a 1000 cycles without any significant deterioration in the stability.
DA - 2010-11
DB - ResearchSpace
DP - CSIR
KW - Supercapacitance
KW - Nickel tetraaminophthalocyanine electropolymer
KW - MWCNTs
KW - Cyclic voltammetry
KW - Galvanostatic charge-discharge
LK - https://researchspace.csir.co.za
PY - 2010
SM - 1040-0397
T1 - Electrochemical capacitive behaviour of multiwalled carbon nanotubes modified with electropolymeric films of nickel tetraaminophthalocyanine
TI - Electrochemical capacitive behaviour of multiwalled carbon nanotubes modified with electropolymeric films of nickel tetraaminophthalocyanine
UR - http://hdl.handle.net/10204/5787
ER -
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en_ZA |