Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/118590
DC FieldValueLanguage
dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.contributorResearch Institute for Smart Energy-
dc.creatorChen, Xen_US
dc.creatorWang, Yen_US
dc.creatorWei, Xen_US
dc.creatorLi, Zen_US
dc.creatorWang, Yen_US
dc.creatorWong, WYen_US
dc.date.accessioned2026-04-28T03:34:46Z-
dc.date.available2026-04-28T03:34:46Z-
dc.identifier.issn2050-7488en_US
dc.identifier.urihttp://hdl.handle.net/10397/118590-
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.titleTailored quantum dots as a multifunctional electrolyte additive for highly reversible zinc anodes in alkaline batteriesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage4546en_US
dc.identifier.epage4553en_US
dc.identifier.volume14en_US
dc.identifier.issue8en_US
dc.identifier.doi10.1039/d5ta08181een_US
dcterms.abstractAlkaline aqueous zinc batteries (AZBs) are promising for high safety and high-energy density but are plagued by the poor reversibility of the zinc anode, manifesting as severe corrosion, hydrogen evolution, and passivation. While electrolyte additives can mitigate these issues, most of them fail to address the sluggish kinetics of the essential Zn/Zn(OH)₄²⁻/ZnO solid–liquid–solid conversion. Herein, we introduce cadmium selenide quantum dots (CdSe QDs) with tailored abundant Cd²⁺ dangling bonds as a multifunctional electrolyte additive. The QD species form a uniform dispersion across the electrode interface, significantly suppressing corrosion and hydrogen evolution. Simultaneously, the positively charged Cd dangling bonds act as active sites that adsorb OH⁻, which lowers the activation energy for the conversion reaction and enhances ion transport. As a result, Zn‖Zn symmetric batteries with the QD additive exhibit longer cycle stability, lasting over 220 000 s at 5 mA cm⁻², while that of KOH + ZnO is just around 30 000 s. This superiority is also validated in Zn–Ni full batteries, which demonstrate longer cycle life and higher capacity for the CdSe QD system. This work presents a novel strategy of using functional QDs as electrolyte additives to simultaneously stabilize the interface and promote reaction dynamics, paving the way for high-performance alkaline zinc-based batteries.-
dcterms.accessRightsembargoed accessen_US
dcterms.bibliographicCitationJournal of materials chemistry A, 3 Feb. 2026, v. 14, no. 8, p. 4546-4553en_US
dcterms.isPartOfJournal of materials chemistry Aen_US
dcterms.issued2026-02-03-
dc.identifier.scopus2-s2.0-105025233193-
dc.identifier.eissn2050-7496en_US
dc.description.validate202604 bcjz-
dc.description.oaNot applicableen_US
dc.identifier.SubFormIDG001568/2026-01-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThe authors gratefully acknowledge the financial support from the RGC Senior Research Fellowship Scheme (SRFS2021-5S01), the Hong Kong Research Grants Council (PolyU 15307321), the Research Institute for Smart Energy (CDAQ), the Research Centre for Nanoscience and Nanotechnology (CE2H), the Research Centre for Carbon-Strategic Catalysis (CE01 and CE41), Miss Clarea Au for the Endowed Professorship in Energy (847S), the National Natural Science Foundation of China (22309156) and the start-up fund of the Hong Kong Polytechnic University (BD2G).en_US
dc.description.pubStatusPublisheden_US
dc.date.embargo2027-02-03en_US
dc.description.oaCategoryGreen (AAM)en_US
Appears in Collections:Journal/Magazine Article
Open Access Information
Status embargoed access
Embargo End Date 2027-02-03
Access
View full-text via PolyU eLinks SFX Query
Show simple item record

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.