Please use this identifier to cite or link to this item: https://doi.org/10.1039/c2jm30422h
DC FieldValue
dc.titleNitrogen-doped carbon-encapsulation of Fe 3O 4 for increased reversibility in Li + storage by the conversion reaction
dc.contributor.authorMa, Y.
dc.contributor.authorZhang, C.
dc.contributor.authorJi, G.
dc.contributor.authorLee, J.Y.
dc.date.accessioned2014-10-09T06:55:30Z
dc.date.available2014-10-09T06:55:30Z
dc.date.issued2012-04-28
dc.identifier.citationMa, Y., Zhang, C., Ji, G., Lee, J.Y. (2012-04-28). Nitrogen-doped carbon-encapsulation of Fe 3O 4 for increased reversibility in Li + storage by the conversion reaction. Journal of Materials Chemistry 22 (16) : 7845-7850. ScholarBank@NUS Repository. https://doi.org/10.1039/c2jm30422h
dc.identifier.issn09599428
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/89586
dc.description.abstractOne great challenge in designing anode materials for lithium-ion batteries is to satisfy the concurrent requirements for good capacity retention, high rate performance and low first cycle losses. We report here the design and synthesis of a nitrogen-doped carbon encapsulated Fe 3O 4 composite which performed very well in all these areas. The composite with the optimized carbon content not only showed a high reversible capacity of ∼850 mA h g -1 for 50 cycles at 100 mA g -1, but was also able to maintain a stable cycling performance at a twenty-fold increase in current density to 2000 mA g -1. More importantly, the composite significantly lowered the irreversible capacity loss in the first cycle compared with other iron oxide anodes reported in the literature. Characterization of the electrode/electrolyte interface indicated the presence of a protective solid electrolyte interface (SEI) layer in which chemically stable LiF and FeF 3 were the major constituents. Thus, it is believed that the N-doped carbon coating had effectively modified the surface chemistry at the anode/electrolyte interface to increase the columbic efficiency of cycling and to reduce the secondary reactions in the first cycle of use. © 2012 The Royal Society of Chemistry.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c2jm30422h
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1039/c2jm30422h
dc.description.sourcetitleJournal of Materials Chemistry
dc.description.volume22
dc.description.issue16
dc.description.page7845-7850
dc.description.codenJMACE
dc.identifier.isiut000302026100031
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