Please use this identifier to cite or link to this item: https://doi.org/10.1021/jp1005692
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dc.titlePreparation, characterization, and electrochemical performance of lithium trivanadate rods by a surfactant-assisted polymer precursor method for lithium batteries
dc.contributor.authorSakunthala, A.
dc.contributor.authorReddy, M.V.
dc.contributor.authorSelvasekarapandian, S.
dc.contributor.authorChowdari, B.V.R.
dc.contributor.authorSelvin, P.C.
dc.date.accessioned2014-10-16T09:37:05Z
dc.date.available2014-10-16T09:37:05Z
dc.date.issued2010-05-06
dc.identifier.citationSakunthala, A., Reddy, M.V., Selvasekarapandian, S., Chowdari, B.V.R., Selvin, P.C. (2010-05-06). Preparation, characterization, and electrochemical performance of lithium trivanadate rods by a surfactant-assisted polymer precursor method for lithium batteries. Journal of Physical Chemistry C 114 (17) : 8099-8107. ScholarBank@NUS Repository. https://doi.org/10.1021/jp1005692
dc.identifier.issn19327447
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/97595
dc.description.abstractLithium trivanadate (LiV3O8) compound was prepared under different conditions and characterized by the Rietveld-refined X-ray diffraction, scanning electron microscopy (SEM), and Brunauer-Emmett-Teller (BET) surface area and density techniques. The electrochemical performances of the LiV3O8 compounds prepared under different conditions were compared. LiV3O8 rods prepared by the surfactant-assisted polymer precursor method were found to perform well, delivering a discharge capacity of 230 (±5) mA·h/g at the end of the second cycle, with an excellent capacity retention of 99.52% at the end of the 20th cycle, for a current density of 30 mA/g. LiV3O8 rods delivered a discharge capacity of 135 (±5) mA·h/g at the end of 350 cycles, for a current density of 240 mA/g, and reasonably high capacity values were achieved at the different current rates. Impedance spectroscopic studies during the first and eighth cycles at various voltages are analyzed and discussed. © 2010 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/jp1005692
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentPHYSICS
dc.description.doi10.1021/jp1005692
dc.description.sourcetitleJournal of Physical Chemistry C
dc.description.volume114
dc.description.issue17
dc.description.page8099-8107
dc.identifier.isiut000277053600079
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