Please use this identifier to cite or link to this item:
http://hdl.handle.net/10397/118590
| DC Field | Value | Language |
|---|---|---|
| dc.contributor | Department of Applied Biology and Chemical Technology | - |
| dc.contributor | Research Institute for Smart Energy | - |
| dc.creator | Chen, X | en_US |
| dc.creator | Wang, Y | en_US |
| dc.creator | Wei, X | en_US |
| dc.creator | Li, Z | en_US |
| dc.creator | Wang, Y | en_US |
| dc.creator | Wong, WY | en_US |
| dc.date.accessioned | 2026-04-28T03:34:46Z | - |
| dc.date.available | 2026-04-28T03:34:46Z | - |
| dc.identifier.issn | 2050-7488 | en_US |
| dc.identifier.uri | http://hdl.handle.net/10397/118590 | - |
| dc.language.iso | en | en_US |
| dc.publisher | Royal Society of Chemistry | en_US |
| dc.title | Tailored quantum dots as a multifunctional electrolyte additive for highly reversible zinc anodes in alkaline batteries | en_US |
| dc.type | Journal/Magazine Article | en_US |
| dc.identifier.spage | 4546 | en_US |
| dc.identifier.epage | 4553 | en_US |
| dc.identifier.volume | 14 | en_US |
| dc.identifier.issue | 8 | en_US |
| dc.identifier.doi | 10.1039/d5ta08181e | en_US |
| dcterms.abstract | Alkaline 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.accessRights | embargoed access | en_US |
| dcterms.bibliographicCitation | Journal of materials chemistry A, 3 Feb. 2026, v. 14, no. 8, p. 4546-4553 | en_US |
| dcterms.isPartOf | Journal of materials chemistry A | en_US |
| dcterms.issued | 2026-02-03 | - |
| dc.identifier.scopus | 2-s2.0-105025233193 | - |
| dc.identifier.eissn | 2050-7496 | en_US |
| dc.description.validate | 202604 bcjz | - |
| dc.description.oa | Not applicable | en_US |
| dc.identifier.SubFormID | G001568/2026-01 | - |
| dc.description.fundingSource | RGC | en_US |
| dc.description.fundingSource | Others | en_US |
| dc.description.fundingText | The 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.pubStatus | Published | en_US |
| dc.date.embargo | 2027-02-03 | en_US |
| dc.description.oaCategory | Green (AAM) | en_US |
| Appears in Collections: | Journal/Magazine Article | |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.



