Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/115307
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dc.titleSynthesis and electrochemical studies of layer-structured metastable α i-LiVOPO 4
dc.contributor.authorShahul Hameed, A.
dc.contributor.authorNagarathinam, M.
dc.contributor.authorReddy, M.V.
dc.contributor.authorChowdari, B.V.R.
dc.contributor.authorVittal, J.J.
dc.date.accessioned2014-12-12T07:13:51Z
dc.date.available2014-12-12T07:13:51Z
dc.date.issued2012-04-21
dc.identifier.citationShahul Hameed, A., Nagarathinam, M., Reddy, M.V., Chowdari, B.V.R., Vittal, J.J. (2012-04-21). Synthesis and electrochemical studies of layer-structured metastable α i-LiVOPO 4. Journal of Materials Chemistry 22 (15) : 7206-7213. ScholarBank@NUS Repository.
dc.identifier.issn09599428
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/115307
dc.description.abstractThe layer structured α I-LiVOPO 4 was obtained via a two step chemical synthesis. In the first step, a hydrated phase, LiVOPO 4·2H 2O, was obtained by a simple hydrothermal route at 120 °C. Single crystal X-ray diffraction analysis revealed the structure of LiVOPO 4·2H 2O to be orthorhombic with lattice parameters: a = 8.9454(7) Å, b = 9.0406(7) Å and c = 12.7373(10) Å. Dehydration of the parent compound led to its structural transformation to tetragonal α I-LiVOPO 4, which was only identified previously during the lithium insertion in VOPO 4. We have investigated the solid-state dehydration of LiVOPO 4· 2H 2O and proposed a possible mechanism for the crystal structure transformation. Electrochemical characterization of this rarely studied tetragonal phase revealed its good lithium cycling at high operating voltage. Galvanostatic charge-discharge cycling of α I-LiVOPO 4 was studied in a voltage window of 2.5-4.5 V, which shows a stable reversible capacity of 103(±3) mA h g -1 at a current density of 16 mA g -1 (0.1 C). At higher current rates, although it exhibited good cyclability, the capacity was found to decrease with increasing current rates. The long term cycling stability of the above material was demonstrated at a current rate of 0.5 C up to 200 cycles. © 2012 The Royal Society of Chemistry.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c2jm00062h
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.contributor.departmentPHYSICS
dc.description.sourcetitleJournal of Materials Chemistry
dc.description.volume22
dc.description.issue15
dc.description.page7206-7213
dc.description.codenJMACE
dc.identifier.isiut000301957300018
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