Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/100543
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dc.contributorDepartment of Electrical and Electronic Engineering-
dc.creatorZhang, Len_US
dc.creatorHui, KNen_US
dc.creatorHui, KSen_US
dc.creatorOr, SWen_US
dc.date.accessioned2023-08-11T03:10:15Z-
dc.date.available2023-08-11T03:10:15Z-
dc.identifier.issn1477-9226en_US
dc.identifier.urihttp://hdl.handle.net/10397/100543-
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.rightsThis journal is © The Royal Society of Chemistry 2019en_US
dc.rightsThe following publication Zhang, L., Hui, K. N., Hui, K. S., & Or, S. W. (2019). 3D heterostructured cobalt oxide@ layered double hydroxide core–shell networks on nickel foam for high-performance hybrid supercapacitor. Dalton Transactions, 48(1), 150-157 is available at https://doi.org/10.1039/C8DT03350A.en_US
dc.title3D heterostructured cobalt oxide@layered double hydroxide core-shell networks on nickel foam for high-performance hybrid supercapacitoren_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage150en_US
dc.identifier.epage157en_US
dc.identifier.volume48en_US
dc.identifier.issue1en_US
dc.identifier.doi10.1039/C8DT03350Aen_US
dcterms.abstractHigh performance of an electrode relies largely on scrupulous design of nanoarchitectures and smart hybridization of bespoke active materials. Here, a 3D heterostructured core–shell architecture was fabricated as a supercapacitor electrode, in which Co3O4 nanowire cores were grown on nickel foam prior to the in situ deposition of layered double hydroxide (LDH) nanosheet shells. Owing to the unique configuration and hybridization, the as-fabricated Co3O4@LDH core–shell electrode exhibited high capacities of 818.6 C g−1 at 2 A g−1 and 479.3 C g−1 at 40 A g−1 (3.2 C cm−2 at 7.8 mA cm−2 and 1.87 C cm−2 at 156 mA cm−2), which were much higher than those of the individual components, namely, Co3O4 and LDH. A hybrid supercapacitor with Co3O4@LDH as the positive electrode and graphene nanosheets as the negative electrode yielded an energy density of 53.2 W h kg−1 and a power density of 16.4 kW kg−1, which outperformed devices reported in the literature; the device also exhibited long-term cycling stability and retained 71% of its initial capacity even after 10 000 cycles at 6 A g−1. The rational design of the core–shell architecture may lead to the development of new strategies for fabricating promising electrode materials for electrochemical energy storage.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationDalton transactions : an international journal of inorganic chemistry, 7 Jan. 2019, v. 48, no. 1, p. 150-157en_US
dcterms.isPartOfDalton transactions : an international journal of inorganic chemistryen_US
dcterms.issued2019-01-07-
dc.identifier.scopus2-s2.0-85058752751-
dc.identifier.pmid30516189-
dc.identifier.eissn1477-9234en_US
dc.description.validate202307 bckw-
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberEE-0262-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextPostdoctoral Fellowships Scheme of The Hong Kong Polytechnic University; Innovation and Technology Commission of the HKSAR Goverment to the Hong Kong Branch of National Rail Transit Electrification and Automation Engineering Technology Research Center; Science and Technology Development Fund of the Macau SAR; Multi-year Research Grant from the Research Services and Knowledge Transfer Office at the University of Macauen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS26218794-
dc.description.oaCategoryGreen (AAM)en_US
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