Please use this identifier to cite or link to this item: https://doi.org/10.1149/1.1647571
DC FieldValue
dc.titleMicroemulsion Syntheses of Sn and SnO 2-Graphite Nanocomposite Anodes for Li-Ion Batteries
dc.contributor.authorWang, Y.
dc.contributor.authorLee, J.Y.
dc.contributor.authorChen, B.-H.
dc.date.accessioned2014-10-09T06:53:26Z
dc.date.available2014-10-09T06:53:26Z
dc.date.issued2004
dc.identifier.citationWang, Y., Lee, J.Y., Chen, B.-H. (2004). Microemulsion Syntheses of Sn and SnO 2-Graphite Nanocomposite Anodes for Li-Ion Batteries. Journal of the Electrochemical Society 151 (4) : A563-A570. ScholarBank@NUS Repository. https://doi.org/10.1149/1.1647571
dc.identifier.issn00134651
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/89408
dc.description.abstractNanostructured SnO 2, SnO 2-graphite, and Sn-graphite composites were prepared by microemulsion techniques using Tergitol 15-S-5 as the surfactant. The particle size of the pristine SnO 2 nanoparticles was typically between 12 and 14 nm. For the composites, Sn and SnO 2 nanoparticles 7-10 nm in size with narrow size distribution were uniformly dispersed on graphite, indicating the positive effect of graphite in maintaining smaller particle size. These Sn-based nanocomposites are multiple Li host systems with good cycling performance in Li-ion battery applications. The improved cyclability is perceived to be a combination of the use of well dispersed Sn or SnO 2 nanoparticles resistant to particle agglomeration, and the presence of a soft graphite matrix to buffer the volume changes in the Li-Sn reactions. In addition, the Sn-graphite nanocomposites exhibited a SnO-shell-Sn-core structure and slightly lower first cycle capacity losses. © 2004 The Electrochemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1149/1.1647571
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.contributor.departmentCHEMICAL & ENVIRONMENTAL ENGINEERING
dc.contributor.departmentSINGAPORE-MIT ALLIANCE
dc.description.doi10.1149/1.1647571
dc.description.sourcetitleJournal of the Electrochemical Society
dc.description.volume151
dc.description.issue4
dc.description.pageA563-A570
dc.description.codenJESOA
dc.identifier.isiut000220560700011
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