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dc.contributor.authorZhao, Guixia
dc.contributor.authorHuang, Xiubing
dc.contributor.authorWang, X.
dc.contributor.authorConnor, Paul Alexander
dc.contributor.authorLi, J.
dc.contributor.authorZhang, S.
dc.contributor.authorIrvine, John Thomas Sirr
dc.date.accessioned2015-10-31T00:11:31Z
dc.date.available2015-10-31T00:11:31Z
dc.date.issued2015-01-07
dc.identifier.citationZhao , G , Huang , X , Wang , X , Connor , P A , Li , J , Zhang , S & Irvine , J T S 2015 , ' Synthesis and lithium-storage properties of MnO/reduced graphene oxide composites derived from graphene oxide plus the transformation of Mn(vi) to Mn(ii) by the reducing power of graphene oxide ' , Journal of Materials Chemistry A , vol. 3 , no. 1 , pp. 297-303 . https://doi.org/10.1039/c4ta05376aen
dc.identifier.issn2050-7488
dc.identifier.otherPURE: 160060996
dc.identifier.otherPURE UUID: ea94fad8-cba5-4d92-b93e-470f61de6025
dc.identifier.otherScopus: 84915746857
dc.identifier.otherWOS: 000345962800037
dc.identifier.otherORCID: /0000-0002-1492-7590/work/60427181
dc.identifier.otherORCID: /0000-0002-8394-3359/work/68280537
dc.identifier.urihttps://hdl.handle.net/10023/7721
dc.descriptionThe authors acknowledge the financial support from the National Natural Science Foundation of China (21272236, 21225730, 21207136 and 91326202), the Ministry of Science and Technology of China (2011CB933700), the Jiangsu Provincial Key Laboratory of Radiation Medicine and Protection and the Priority Academic Program Development of Jiangsu Higher Education Institutions.en
dc.description.abstractIn this report, a novel method is proposed to prepare MnO/reduced graphene oxide (rGO) composites via calcining the precursors (i.e. δ-MnO2/graphene oxide composites) at 500 °C in Ar using no external reducing gas, in which graphene oxide (GO) successfully serves as a reductant by releasing CO during its thermolysis for the first time. By controlling the initial ratios of GO to KMnO4, differently composed precursors can be obtained via the redox reaction between GO and KMnO4, then leading to the formation of composites with different MnO/rGO ratios and dispersion of MnO on the rGO surface (denoted as MGC1 and MGC2). When applied as an active material in lithium ion batteries, MGC1 shows excellent cycling performance and capacity retention. Under 100 and 200 mA g−1, MGC1 could deliver reversible capacities as high as 900 and 750 mA h g−1, respectively, after more than 100 cycles. Considering the simple operation and low energy consumption in the whole material synthesis processes, the present strategy is feasible and effective for practical application. Even more importantly, the reductibility of graphene oxide upon thermolysis is utilized for the first time, which is meaningful for its extension in synthesis of functional nanomaterials.
dc.format.extent7
dc.language.isoeng
dc.relation.ispartofJournal of Materials Chemistry Aen
dc.rightsCopyright 2015 the Authors. This work is made available online in accordance with the publisher’s policies. This is the author created, accepted version manuscript following peer review and may differ slightly from the final published version. The final published version of this work is available at https://dx.doi.org/10.1039/C4TA05376Aen
dc.subjectQD Chemistryen
dc.subjectNDASen
dc.subjectSDG 7 - Affordable and Clean Energyen
dc.subject.lccQDen
dc.titleSynthesis and lithium-storage properties of MnO/reduced graphene oxide composites derived from graphene oxide plus the transformation of Mn(vi) to Mn(ii) by the reducing power of graphene oxideen
dc.typeJournal articleen
dc.contributor.sponsorEPSRCen
dc.description.versionPostprinten
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. St Andrews Sustainability Instituteen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doihttps://doi.org/10.1039/c4ta05376a
dc.description.statusPeer revieweden
dc.date.embargoedUntil2015-10-31
dc.identifier.urlhttp://www.rsc.org/suppdata/ta/c4/c4ta05376a/c4ta05376a1.pdfen
dc.identifier.grantnumberEP/K015540/1en


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