Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/117170
DC FieldValueLanguage
dc.contributorDepartment of Mechanical Engineering-
dc.contributorResearch Institute for Smart Energy-
dc.contributorResearch Institute for Advanced Manufacturing-
dc.creatorBai, Y-
dc.creatorHuo, X-
dc.creatorTang, M-
dc.creatorFu, E-
dc.creatorLong, X-
dc.creatorShi, X-
dc.creatorWei, L-
dc.creatorAn, L-
dc.date.accessioned2026-02-05T08:30:30Z-
dc.date.available2026-02-05T08:30:30Z-
dc.identifier.issn1613-6810-
dc.identifier.urihttp://hdl.handle.net/10397/117170-
dc.language.isoenen_US
dc.publisherWiley-VCHen_US
dc.subjectElectrochemical kineticsen_US
dc.subjectElectrodeen_US
dc.subjectMass transferen_US
dc.subjectMulticore-shell structureen_US
dc.subjectVanadium redox flow batteriesen_US
dc.titleIn situ preparation of bismuth nanoparticles encapsulated in porous carbon spheres on graphite felt electrodes for vanadium redox flow batteriesen_US
dc.typeJournal/Magazine Articleen_US
dc.description.otherinformationTitle on author's file: In-situ Preparation of Bismuth Nanoparticles Encapsulated in Porous Carbon Spheres on Graphite Felt Electrodes for Vanadium Redox Flow Batteries-
dc.identifier.volume22-
dc.identifier.issue6-
dc.identifier.doi10.1002/smll.202511775-
dcterms.abstractVanadium redox flow batteries (VRFBs) attract significant interest for large-scale energy storage. However, the inherently low catalytic activity and restricted specific surface area of the pristine graphite felt electrodes hinder the further development of VRFBs. Herein, a facile in situ synthesis is reported of Bi nanoparticles encapsulated in N-doped carbon spheres on graphite felt (Bi@NC/GF). The resulting multicore-shell nanostructure exhibits enhanced electrocatalytic activity toward the V³⁺/V²⁺ redox couple, attributed to the synergistic effect between dispersed Bi cores and N-doped carbon matrix. Density functional theory analysis further verifies that the electronic structure at the core–shell interface significantly enhances vanadium-ion adsorption. Meanwhile, the porous carbon shell not only facilitates electron transfer but also enlarges the electrolyte-accessible surface area, thereby promoting electrolyte penetration. As a result, the battery employing Bi@NC/GF achieves an energy efficiency of 79.22% at 300 mA cm⁻² and a peak power density of 1254.32 mW cm⁻². Furthermore, the battery demonstrates outstanding cycling stability, with minimal performance decay over 1000 cycles. This work offers a promising strategy for advancing composite electrode design for next-generation VRFBs.-
dcterms.accessRightsembargoed accessen_US
dcterms.bibliographicCitationSmall, 27 Jan. 2026, v. 22, no. 6, e11775-
dcterms.isPartOfSmall-
dcterms.issued2026-01-27-
dc.identifier.scopus2-s2.0-105024248861-
dc.identifier.eissn1613-6829-
dc.identifier.artne11775-
dc.description.validate202602 bcjz-
dc.description.oaNot applicableen_US
dc.identifier.SubFormIDG000874/2026-01en_US
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThis work was supported by a grant from the Research Institute for Smart Energy (CDB2), a grant from the Research Institute for Advanced Manufacturing (CDJQ) at The Hong Kong Polytechnic University, and a grant from the Research Grants Council of the Hong Kong Special Administrative Region, China (Project No. 15308024).en_US
dc.description.pubStatusPublisheden_US
dc.date.embargo2027-01-27en_US
dc.description.oaCategoryGreen (AAM)en_US
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