NiO hybrid nanoarchitecture-based pseudocapacitor in organic electrolyte with high rate capability and cycle life
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Accepted version
Date
2015-04-26
Authors
Padmanathan, Narayanasamy
Selladurai, Subramanian
Rahulan, K. Mani
O'Dwyer, Colm
Razeeb, Kafil M.
Journal Title
Journal ISSN
Volume Title
Publisher
Springer Verlag
Published Version
Abstract
A 3D hierarchical NiO nanostructures with combined microstructure of nanoflakes and nanoflowers have been fabricated on carbon fibre cloth (CFC). Unique nano-micro structural features of NiO/CFC electrode showed an enhanced electrochemical activity in organic electrolyte (1 M tetraethylammonium tetrafluorborate (TEABF4) in propylene carbonate) in terms of rate capability, specific energy and power performance as well as potential limit. The electrode showed a specific capacitance of 170 Fg−1 for a current density of 5 Ag−1. Configured as a two-electrode symmetric supercapacitor, the device showed a specific capacitance of 34.9 Fg−1 at 1 Ag−1 current density. It delivered a maximum specific energy density of 19.4 Wh kg−1 at a high power density of 1002.8 W kg−1 at a constant current density of 1 Ag−1. The cell is also capable of long-term cycling stability with an efficiency of 58 % after 25,000 cycles with a potential window of 0 to ±2 V. This superior electrochemical activity of the NiO electrode is due to their structural benefits of well-connected hybrid nano/mesoporous structure and rapid ion intercalation within the porous electrode surface.
Description
Keywords
Nickel oxide , Nanomaterials , Flexible electrode , Pseudocapacitor , Supercapacitor
Citation
Padmanathan, N., Selladurai, S., Rahulan, K. M., O’Dwyer, C. and Razeeb, K. M. (2015) 'NiO hybrid nanoarchitecture-based pseudocapacitor in organic electrolyte with high rate capability and cycle life', Ionics, 21(9), pp. 2623-2631. doi: 10.1007/s11581-015-1444-9
Copyright
© Springer-Verlag Berlin Heidelberg 2015. This is a post-peer-review, pre-copyedit version of an article published in Ionics. The final authenticated version is available online at: http://dx.doi.org/10.1007/s11581-015-1444-9