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dc.contributor.authorCai, R.
dc.contributor.authorYu, X.
dc.contributor.authorLiu, X.
dc.contributor.authorShao, Zongping
dc.date.accessioned2017-01-30T10:50:24Z
dc.date.available2017-01-30T10:50:24Z
dc.date.created2016-09-12T08:36:45Z
dc.date.issued2010
dc.identifier.citationCai, R. and Yu, X. and Liu, X. and Shao, Z. 2010. Li4Ti5O12/Sn composite anodes for lithium-ion batteries: Synthesis and electrochemical performance. Journal of Power Sources. 195 (24): pp. 8244-8250.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/6060
dc.identifier.doi10.1016/j.jpowsour.2010.07.059
dc.description.abstract

Li4Ti5O12/tin phase composites are successfully prepared by cellulose-assisted combustion synthesis of Li 4Ti5O12 matrix and precipitation of the tin phase. The effect of firing temperature on the particulate morphologies, particle size, specific surface area and electrochemical performance of Li 4Ti5O12/tin oxide composites is systematically investigated by SEM, XRD, TG, BET and charge-discharge characterizations. The grain growth of tin phase is suppressed by forming composite with Li 4Ti5O12 at a calcination of 500 °C, due to the steric effect of Li4Ti5O12 and chemical interaction between Li4Ti5O12 and tin oxide. The experimental results indicate that Li4Ti5O 12/tin phase composite fired at 500 °C has the best electrochemical performance. A capacity of 224 mAh g-1 is maintained after 50 cycles at 100 mA g-1 current density, which is still higher than 195 mAh g-1 for the pure Li4Ti5O 12 after the same charge/discharge cycles. It suggests Li 4Ti5O12/tin phase composite may be a potential anode of lithium-ion batteries through optimizing the synthesis process. © 2010 Elsevier B.V. All rights reserved.

dc.publisherElsevier SA
dc.titleLi4Ti5O12/Sn composite anodes for lithium-ion batteries: Synthesis and electrochemical performance
dc.typeJournal Article
dcterms.source.volume195
dcterms.source.number24
dcterms.source.startPage8244
dcterms.source.endPage8250
dcterms.source.issn0378-7753
dcterms.source.titleJournal of Power Sources
curtin.departmentDepartment of Chemical Engineering
curtin.accessStatusFulltext not available


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