Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/118487
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dc.contributorSchool of Fashion and Textiles-
dc.contributorDepartment of Civil and Environmental Engineering-
dc.creatorChen, D-
dc.creatorMing, Y-
dc.creatorCai, W-
dc.creatorWang, Z-
dc.creatorTawiah, B-
dc.creatorShi, S-
dc.creatorHu, X-
dc.creatorYu, R-
dc.creatorPoon, CS-
dc.creatorFei, B-
dc.date.accessioned2026-04-17T09:20:39Z-
dc.date.available2026-04-17T09:20:39Z-
dc.identifier.issn1613-6810-
dc.identifier.urihttp://hdl.handle.net/10397/118487-
dc.language.isoenen_US
dc.publisherWiley-VCH Verlag GmbH & Co. KGaAen_US
dc.rights© 2024 Wiley-VCH GmbHen_US
dc.rightsThis is the peer reviewed version of the following article: Chen, D., Ming, Y., Cai, W., Wang, Z., Tawiah, B., Shi, S., ... & Fei, B. (2025). Enhancing Potassium‐Ion Storage through Nanostructure Engineering and Ion‐Doped: A Case Study of Cu2+‐Doped Co0. 85Se with Yolk‐Shell Structure. Small, 21(3), 2408792, which has been published in final form at https://doi.org/10.1002/smll.202408792. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited.en_US
dc.subjectCu²⁺-dopeden_US
dc.subjectElectronic structureen_US
dc.subjectPotassium-ion batteriesen_US
dc.subjectReaction kineticsen_US
dc.subjectYolk-shell structureen_US
dc.titleEnhancing potassium-ion storage through nanostructure engineering and ion-doped : a case study of Cu²⁺-doped Co₀.₈₅Se with yolk-shell structureen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume21-
dc.identifier.issue3-
dc.identifier.doi10.1002/smll.202408792-
dcterms.abstractFabricating transition metal selenide (TMSe) anode materials with rapid K⁺ diffusion and high-rate performance is crucial for the advancement of potassium-ion batteries (PIBs), yet it remains a challenge. In this study, a Cu²⁺-doped Co₀.₈₅Se@N-doped carbon anode with an optimal concentration of Cu²⁺-doped and yolk-shell structure (denoted as Cu-Co₀.₈₅Se@NC-2) is developed to enhance the reaction kinetics and cycling life. The Cu²⁺-doped modulates the electronic structure of the Co₀.₈₅Se interface, improves the diffusion and adsorption of K⁺, and further promotes the charge transport efficiency, as demonstrated by theoretical calculations and experimental results. In addition, an optimal Cu²⁺-doped content is identified that is conducive to achieving the best structure and electrochemical performance. Moreover, the N-doped carbon shell effectively enhances the conductivity of the electrode and alleviates the volume change of Co₀.₈₅Se yolk during cycling. Benefiting from the above advantages, the obtained Cu-Co₀.₈₅Se@NC-2 anode exhibits excellent rate performance (208.1 mA h g⁻¹ at 10 A g⁻¹) and cycling stability (239.7 mA h g⁻¹ at 2 A g⁻¹ after 500 cycles, the capacity retention rate is up to 80.4%). This work integrates nanostructure engineering and ion-doped to provide a straightforward and effective strategy for designing advanced high-rate TMSe anodes for next-generation PIBs.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationSmall, 22 Jan. 2025, v. 21, no. 3, 2408792-
dcterms.isPartOfSmall-
dcterms.issued2025-01-22-
dc.identifier.scopus2-s2.0-85210743652-
dc.identifier.pmid39618005-
dc.identifier.eissn1613-6829-
dc.identifier.artn2408792-
dc.description.validate202604 bcjz-
dc.description.oaAccepted Manuscripten_US
dc.identifier.SubFormIDG001471/2026-03en_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThe authors gratefully acknowledge financial support from the PolyU Postdoc Matching Fund 1-W34P, ITF project ITP/023/22TP, PolyU RCRE fund 1-BBCB, and IWEAR fund 1-CD8E.en_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryGreen (AAM)en_US
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