Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/94998
Title: Electrochemical energy storage in a β-Na0.33V2O5 nanobelt network and its application for supercapacitors
Authors: Khoo, Eugene
Wang, Jinmin
Ma, Jan
Lee, Pooi See
Keywords: DRNTU::Engineering::Materials
Issue Date: 2010
Source: Khoo, E., Wang, J., Ma, J., & Lee, P. S. (2010). Electrochemical energy storage in a β-Na0.33V2O5 nanobelt network and its application for supercapacitors. Journal of Materials Chemistry, 20(38), 8368-8374.
Series/Report no.: Journal of materials chemistry
Abstract: We report a nanostructured oxide pseudocapacitor electrode utilizing a sodium-doped vanadium oxide (β-Na0.33V2O5) nanobelt network with a three dimensional framework crystal structure, which has been successfully synthesized under mild hydrothermal conditions and heat treatment. Cyclic voltammetry, galvanostatic charge-discharge and cycling tests have been carried out on the nanobelt network in 1 M LiClO4/propylene carbonate (PC) electrolyte for a 1 V potential window. A high specific capacitance of 320 F g−1 at 5 mV s−1 scan rate has been achieved with two sets of redox peaks being identified, corresponding to the half occupancy at M3 and M2 intercalation sites along the tunnel in the β-Na0.33V2O5 crystal lattice. The β-Na0.33V2O5 nanobelt electrode is able to deliver a high energy density of 47 W h kg−1 at a high power density of 5 kW kg−1. Slight degradation in energy density at high power density has been observed. This can be attributed to the charge storage in the nanobelt network which is dominated by the fast surface dependent reaction. Superior cycling stability, with only 34% degradation in specific capacitance, is observed in the β-Na0.33V2O5 nanobelts after 4000 cycles. The results clearly indicate the promising potential of these doped vanadium oxide electrodes for electrochemical energy storage devices.
URI: https://hdl.handle.net/10356/94998
http://hdl.handle.net/10220/8692
DOI: http://dx.doi.org/10.1039/c0jm00652a
Rights: © 2010 The Royal Society of Chemistry. This is the author created version of a work that has been peer reviewed and accepted for publication by Journal of Materials Chemistry , The Royal Society of Chemistry. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.1039/c0jm00652a].
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:MSE Journal Articles

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