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dc.contributor.authorWang, K.
dc.contributor.authorCai, R.
dc.contributor.authorYuan, T.
dc.contributor.authorYu, X.
dc.contributor.authorRan, R.
dc.contributor.authorShao, Zongping
dc.date.accessioned2017-01-30T12:37:06Z
dc.date.available2017-01-30T12:37:06Z
dc.date.created2016-09-12T08:36:45Z
dc.date.issued2009
dc.identifier.citationWang, K. and Cai, R. and Yuan, T. and Yu, X. and Ran, R. and Shao, Z. 2009. Process investigation, electrochemical characterization and optimization of LiFePO4/C composite from mechanical activation using sucrose as carbon source. Electrochimica Acta. 54 (10): pp. 2861-2868.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/23414
dc.identifier.doi10.1016/j.electacta.2008.11.012
dc.description.abstract

LiFePO4/C composite was synthesized by mechanical activation using sucrose as carbon source. High-energy ball milling facilitated phase formation during thermal treatment. TG-DSC and TPR experiments demonstrated sucrose was converted to CHx intermediate before completely decomposed to carbon. Ball milling time, calcination temperature and dwelling time all had significant impact on the discharge capacity and rate performance of the resulted power. The optimal process parameters are high-energy ball milling for 2-4 h followed by thermal treatment at 700 °C for 20 h. The product showed a capacity of 174 mAh/g at 0.1C rate and around 117 mAh/g at 20C rate with the capacity fade less than 10% after 50 cycles. Too low calcination temperature or insufficient calcination time, however, could result in the residual of CHx in the electrode and led to a decrease of electrode performance. © 2008 Elsevier Ltd. All rights reserved.

dc.publisherPergamon
dc.titleProcess investigation, electrochemical characterization and optimization of LiFePO4/C composite from mechanical activation using sucrose as carbon source
dc.typeJournal Article
dcterms.source.volume54
dcterms.source.number10
dcterms.source.startPage2861
dcterms.source.endPage2868
dcterms.source.issn0013-4686
dcterms.source.titleElectrochimica Acta
curtin.departmentDepartment of Chemical Engineering
curtin.accessStatusFulltext not available


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