Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/117408
DC FieldValueLanguage
dc.contributorSchool of Fashion and Textilesen_US
dc.creatorLiu, Xen_US
dc.creatorChung, KYen_US
dc.creatorYang, Qen_US
dc.creatorFang, Cen_US
dc.creatorDeng, Sen_US
dc.creatorHan, Jen_US
dc.creatorLu, Jen_US
dc.creatorXu, Ben_US
dc.date.accessioned2026-02-23T07:11:59Z-
dc.date.available2026-02-23T07:11:59Z-
dc.identifier.issn1369-7021en_US
dc.identifier.urihttp://hdl.handle.net/10397/117408-
dc.language.isoenen_US
dc.publisherElsevier Scienceen_US
dc.subjectElectrolyte additiveen_US
dc.subjectMXeneen_US
dc.subjectQuantum dotsen_US
dc.subjectSelf-repairingen_US
dc.subjectZinc anodeen_US
dc.titleMXene quantum dots enable self-repairing and anti-corrosive interphase for high-performance zinc anodeen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage103en_US
dc.identifier.epage113en_US
dc.identifier.volume87en_US
dc.identifier.doi10.1016/j.mattod.2025.05.015en_US
dcterms.abstractZinc-ion batteries (ZIBs) hold great promise owing to their inherent safety and high energy density, yet their practical application is challenged by low Coulombic efficiency (CE), parasitic reactions, and dendrite growth of zinc anode. Herein, we introduce MXene quantum dots (MQDs) as a multifunctional colloid additive to construct a robust solid electrolyte interphase (SEI) and with dynamic self-repairing function. Particularly, MQDs can effectively modify the H-bond environment, provide anti-corrosion benefits, and eliminate dendrites. The strong bonding of MQDs with free water molecules and metallic Zn enhances interfacial stability via modifying localized H-bond network. Depth profile analysis shows that Zn2+ plating coincides with SEI layer formation (ZHS/TiCO), resulting in uniform and dense deposition with mixed crystalline phases. Consequently, this additive strategy achieves dendrite-free deposition with a high Coulombic efficiency of 99.2 %, a reversible lifetime of 3,700 h in symmetric cells, anti-corrosion performance exceeding 4,000 h, along with 3,900 h of self-repairing cycling. Additionally, impressive full-cell cycling retention is further demonstrated with MnO<inf>2</inf>, I<inf>2</inf>, and PANI cathodes. This work paves a new way for more efficient metallic anode in aqueous rechargeable batteries.en_US
dcterms.accessRightsembargoed accessen_US
dcterms.bibliographicCitationMaterials today, Aug. 2025, v. 87, p. 103-113en_US
dcterms.isPartOfMaterials todayen_US
dcterms.issued2025-08-
dc.identifier.scopus2-s2.0-105004800034-
dc.identifier.eissn1873-4103en_US
dc.description.validate202602 bchyen_US
dc.description.oaNot applicableen_US
dc.identifier.SubFormIDG000978/2025-11-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThe authors would like to acknowledge the Hong Kong Polytechnic University for funding support (Project No.: 1-WZ1Y, 1-W34U, 4-YWER) of this work. X. Liu would also like to thank the Hong Kong Polytechnic University for providing him with a postgraduate scholarship.en_US
dc.description.pubStatusPublisheden_US
dc.date.embargo2027-08-31en_US
dc.description.oaCategoryGreen (AAM)en_US
Appears in Collections:Journal/Magazine Article
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Embargo End Date 2027-08-31
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