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Article: Unusual formation of α-Fe2O3 hexagonal nanoplatelets in N-doped sandwiched graphene chamber for high-performance lithium-ions batteries

TitleUnusual formation of α-Fe2O3 hexagonal nanoplatelets in N-doped sandwiched graphene chamber for high-performance lithium-ions batteries
Authors
Keywordsα-Fe2O3
Graphene
Lithium-ions batteries
N-doped
Nanoplatelets
Sandwich
Issue Date2013
Citation
Nano Energy, 2013, v. 2, n. 2, p. 257-267 How to Cite?
AbstractNowadays, 2D nanosheets or nanoplatelets have attracted great attention due to their wide applications. However, the synthesis of 2D α-Fe2O3 nanosheets with well-defined hexagonal shape is extremely challenging, because the selective growth along one specific facet is very hard to be realized. In our work, we studied the non-capping ligand mediated reaction within graphene layer chamber, and successfully synthesized α-Fe2O3 hexagonal nanoplatelets sandwiched between graphene layers (HP-Fe-G). These materials exhibit an improved electrochemical performance compared with the pre-existing α-Fe2O3 nanoparticles loaded graphene (G-Fe2O3) composites because of the uniqueness of such architectures: thin nanoplatelets, large enough sandwiched spaces to buffer the volume expansion and N-doped graphene. HP-Fe-G delivered an ultrahigh reversible capacity of 1100mAh/g after 50 cycles, thus higher than their theoretical value (926mAh/g); while G-Fe2O3 composites showed relatively low capacity retention even after only 20 cycles (582mAh/g). In addition, HP-Fe-G also reveal superior rate capability, 887mAh/g at 1C; in comparison, this value was only 135mAh/g at 1C for G-Fe2O3. © 2012 Elsevier Ltd.
Persistent Identifierhttp://hdl.handle.net/10722/359922
ISSN
2023 Impact Factor: 16.8
2023 SCImago Journal Rankings: 4.685

 

DC FieldValueLanguage
dc.contributor.authorWang, Xi-
dc.contributor.authorTian, Wei-
dc.contributor.authorLiu, Dequan-
dc.contributor.authorZhi, Chunyi-
dc.contributor.authorBando, Yoshio-
dc.contributor.authorGolberg, Dmitri-
dc.date.accessioned2025-09-10T09:04:02Z-
dc.date.available2025-09-10T09:04:02Z-
dc.date.issued2013-
dc.identifier.citationNano Energy, 2013, v. 2, n. 2, p. 257-267-
dc.identifier.issn2211-2855-
dc.identifier.urihttp://hdl.handle.net/10722/359922-
dc.description.abstractNowadays, 2D nanosheets or nanoplatelets have attracted great attention due to their wide applications. However, the synthesis of 2D α-Fe<inf>2</inf>O<inf>3</inf> nanosheets with well-defined hexagonal shape is extremely challenging, because the selective growth along one specific facet is very hard to be realized. In our work, we studied the non-capping ligand mediated reaction within graphene layer chamber, and successfully synthesized α-Fe<inf>2</inf>O<inf>3</inf> hexagonal nanoplatelets sandwiched between graphene layers (HP-Fe-G). These materials exhibit an improved electrochemical performance compared with the pre-existing α-Fe<inf>2</inf>O<inf>3</inf> nanoparticles loaded graphene (G-Fe<inf>2</inf>O<inf>3</inf>) composites because of the uniqueness of such architectures: thin nanoplatelets, large enough sandwiched spaces to buffer the volume expansion and N-doped graphene. HP-Fe-G delivered an ultrahigh reversible capacity of 1100mAh/g after 50 cycles, thus higher than their theoretical value (926mAh/g); while G-Fe<inf>2</inf>O<inf>3</inf> composites showed relatively low capacity retention even after only 20 cycles (582mAh/g). In addition, HP-Fe-G also reveal superior rate capability, 887mAh/g at 1C; in comparison, this value was only 135mAh/g at 1C for G-Fe<inf>2</inf>O<inf>3</inf>. © 2012 Elsevier Ltd.-
dc.languageeng-
dc.relation.ispartofNano Energy-
dc.subjectα-Fe2O3-
dc.subjectGraphene-
dc.subjectLithium-ions batteries-
dc.subjectN-doped-
dc.subjectNanoplatelets-
dc.subjectSandwich-
dc.titleUnusual formation of α-Fe2O3 hexagonal nanoplatelets in N-doped sandwiched graphene chamber for high-performance lithium-ions batteries-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.nanoen.2012.09.004-
dc.identifier.scopuseid_2-s2.0-84875072910-
dc.identifier.volume2-
dc.identifier.issue2-
dc.identifier.spage257-
dc.identifier.epage267-

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