Please use this identifier to cite or link to this item:
https://doi.org/10.1039/c2jm30422h
DC Field | Value | |
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dc.title | Nitrogen-doped carbon-encapsulation of Fe 3O 4 for increased reversibility in Li + storage by the conversion reaction | |
dc.contributor.author | Ma, Y. | |
dc.contributor.author | Zhang, C. | |
dc.contributor.author | Ji, G. | |
dc.contributor.author | Lee, J.Y. | |
dc.date.accessioned | 2014-10-09T06:55:30Z | |
dc.date.available | 2014-10-09T06:55:30Z | |
dc.date.issued | 2012-04-28 | |
dc.identifier.citation | Ma, 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.issn | 09599428 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/89586 | |
dc.description.abstract | One 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.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c2jm30422h | |
dc.source | Scopus | |
dc.type | Article | |
dc.contributor.department | CHEMICAL & BIOMOLECULAR ENGINEERING | |
dc.description.doi | 10.1039/c2jm30422h | |
dc.description.sourcetitle | Journal of Materials Chemistry | |
dc.description.volume | 22 | |
dc.description.issue | 16 | |
dc.description.page | 7845-7850 | |
dc.description.coden | JMACE | |
dc.identifier.isiut | 000302026100031 | |
Appears in Collections: | Staff Publications |
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