Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/103916
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dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.contributorResearch Institute for Smart Energy-
dc.creatorChen, Xen_US
dc.creatorShi, Xen_US
dc.creatorRuan, Pen_US
dc.creatorTang, Yen_US
dc.creatorSun, Yen_US
dc.creatorWong, WYen_US
dc.creatorLu, Ben_US
dc.creatorZhou, Jen_US
dc.date.accessioned2024-01-10T02:41:25Z-
dc.date.available2024-01-10T02:41:25Z-
dc.identifier.urihttp://hdl.handle.net/10397/103916-
dc.language.isoenen_US
dc.publisherWiley-VCH GmbHen_US
dc.rights© 2023 The Authors. Small Science published by Wiley-VCH GmbHen_US
dc.rightsThis is an open access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited.en_US
dc.rightsThe following publication Chen, X., Shi, X., Ruan, P., Tang, Y., Sun, Y., Wong, W. Y., ... & Zhou, J. (2023). Construction of an Artificial Interfacial Layer with Porous Structure toward Stable Zinc‐Metal Anodes. Small Science, 3(6), 2300007 is available at https://doi.org/10.1002/smsc.202300007.en_US
dc.subjectNH4V4O10en_US
dc.subjectOrganic acid etchingen_US
dc.subjectSurface modificationen_US
dc.subjectZinc-metal anodesen_US
dc.subjectZinc-ion batteriesen_US
dc.titleConstruction of an artificial interfacial layer with porous structure toward stable zinc-metal anodesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume3en_US
dc.identifier.issue6en_US
dc.identifier.doi10.1002/smsc.202300007en_US
dcterms.abstractAqueous zinc-ion batteries possess great potential in stationary energy storage devices. Nevertheless, the occurrence of zinc dendrite growth and hydrogen evolution reaction severely hinders the utilization efficiency and service life of zinc-metal anodes. Herein, an in situ etching strategy is proposed to construct an interfacial layer with porous structure on the surface of zinc foil under the assistance of tartaric acid (denoted as TA@Zn). The optimized anode surface is beneficial to not only achieve uniform Zn deposition behavior due to the low nucleation overpotential, but also enhance the interfacial reaction kinetics due to the reduced activation energy barrier. As expected, the TA@Zn-based symmetric cell delivers small voltage hysteresis and superior stability for 5000 h at the current density of 1 mA cm(-2). Moreover, the TA@Zn|NH4V4O10 cell also exhibits high specific capacity and long-term cycling stability.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationSmall science, June 2023, v. 3, no. 6, 2300007en_US
dcterms.isPartOfSmall scienceen_US
dcterms.issued2023-06-
dc.identifier.isiWOS:000969311200001-
dc.identifier.scopus2-s2.0-85168325728-
dc.identifier.eissn2688-4046en_US
dc.identifier.artn2300007en_US
dc.description.validate202401 bcvc-
dc.description.oaVersion of Recorden_US
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Natural Science Foundation of China; Natural Science Foundation of Hunan Province; Hunan Natural Science Fund for Distinguished Young Scholar; Fundamental Research Funds for the Central Universities; Natural Science Foundation of Changsha; RGC Senior Research Fellowship Scheme; Research Institute for Smart Energy (CDAQ); Miss Clarea Au for the Endowed Professorship in Energyen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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