Fabrication of ultrathin CoMoO4 nanosheets modified with chitosan and their improved performance in energy storage device

Ultrathin nanosheet-assembled cobalt molybdate (CoMoO 4 ) with a mesoporous morphology was synthesized by a urea-assisted solution combustion route at a temperature of 400 °C. The as-prepared CoMoO 4 was modified using chitosan cross-linked with glutaraldehyde (glu) and employed as a cathode materia...

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Veröffentlicht in:Dalton transactions : an international journal of inorganic chemistry 2015-04, Vol.44 (13), p.6158-6168
Hauptverfasser: Ramkumar, Ramya, Minakshi, Manickam
Format: Artikel
Sprache:eng
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Zusammenfassung:Ultrathin nanosheet-assembled cobalt molybdate (CoMoO 4 ) with a mesoporous morphology was synthesized by a urea-assisted solution combustion route at a temperature of 400 °C. The as-prepared CoMoO 4 was modified using chitosan cross-linked with glutaraldehyde (glu) and employed as a cathode material in an aqueous hybrid capacitor. The physical and electrochemical behaviour of CoMoO 4 modified with chitosan and the as-prepared (chitosan free) CoMoO 4 has been compared and discussed. The modified CoMoO 4 exhibited excellent electrochemical performance with a specific capacitance of 135 F g −1 at 0.6 A g −1 and an energy density of 31 W h kg −1 . It also exhibited good cycling stability with high coulombic efficiency over 2000 cycles retaining a specific capacitance of 81 F g −1 at 3 A g −1 , comparatively much better than that of nanostructured chitosan free CoMoO 4 which yielded 17 F g −1 . The results indicated that chitosan gel strongly adheres to the molybdate moiety of CoMoO 4 and increases the capacitance four-fold compared to a chitosan free material. The modified CoMoO 4 electrode shows potential for high performance, and is an environmentally friendly and low-cost energy storage device. Ultrathin nanosheet-assembled cobalt molybdate (CoMoO 4 ) with a mesoporous morphology was synthesized by a urea-assisted solution combustion route at a temperature of 400 °C.
ISSN:1477-9226
1477-9234
DOI:10.1039/c5dt00622h