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Pseudocapacitive Effects of Multi-Walled Carbon Nanotubes-Functionalised Spinel Copper Manganese Oxide

Spinel copper manganese oxide nanoparticles combined with acid-treated multi-walled carbon nanotubes (CuMn(2)O(4)/MWCNTs) were used in the development of electrodes for pseudocapacitor applications. The CuMn(2)O(4)/MWCNTs preparation involved initial synthesis of Mn(3)O(4) and CuMn(2)O(4) precursors...

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Detalles Bibliográficos
Autores principales: Nolly, Christopher, Ikpo, Chinwe O., Ndipingwi, Miranda M., Ekwere, Precious, Iwuoha, Emmanuel I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9565235/
https://www.ncbi.nlm.nih.gov/pubmed/36234643
http://dx.doi.org/10.3390/nano12193514
Descripción
Sumario:Spinel copper manganese oxide nanoparticles combined with acid-treated multi-walled carbon nanotubes (CuMn(2)O(4)/MWCNTs) were used in the development of electrodes for pseudocapacitor applications. The CuMn(2)O(4)/MWCNTs preparation involved initial synthesis of Mn(3)O(4) and CuMn(2)O(4) precursors followed by an energy efficient reflux growth method for the CuMn(2)O(4)/MWCNTs. The CuMn(2)O(4)/MWCNTs in a three-electrode cell assembly and in 3 M LiOH aqueous electrolyte exhibited a specific capacitance of 1652.91 F g(−1) at 0.5 A g(−1) current load. Similar investigation in 3 M KOH aqueous electrolyte delivered a specific capacitance of 653.41 F g(−1) at 0.5 A g(−1) current load. Stability studies showed that after 6000 cycles, the CuMn(2)O(4)/MWCNTs electrode exhibited a higher capacitance retention (88%) in LiOH than in KOH (64%). The higher capacitance retention and cycling stability with a Coulombic efficiency of 99.6% observed in the LiOH is an indication of a better charge storage behaviour in this electrolyte than in the KOH electrolyte with a Coulombic efficiency of 97.3%. This superior performance in the LiOH electrolyte than in the KOH electrolyte is attributed to an intercalation/de-intercalation mechanism which occurs more easily in the LiOH electrolyte than in the KOH electrolyte.