Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/117327
DC FieldValueLanguage
dc.contributorDepartment of Mechanical Engineering-
dc.contributorResearch Institute for Smart Energy-
dc.creatorBai, Y-
dc.creatorYang, J-
dc.creatorZhan, C-
dc.creatorYu, X-
dc.date.accessioned2026-02-11T09:07:18Z-
dc.date.available2026-02-11T09:07:18Z-
dc.identifier.issn0013-4686-
dc.identifier.urihttp://hdl.handle.net/10397/117327-
dc.language.isoenen_US
dc.publisherPergamon Pressen_US
dc.subjectAnode freeen_US
dc.subjectElectrolyteen_US
dc.subjectInterfacial electrochemistryen_US
dc.subjectKineticsen_US
dc.subjectSodium metal batteryen_US
dc.subjectStabilityen_US
dc.titleInterfacial electrochemistry engineering via advanced electrolyte design for anode-free sodium metal batteries : innovations and prospectsen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume547-
dc.identifier.doi10.1016/j.electacta.2025.147883-
dcterms.abstractAnode-free sodium metal batteries (AFSMBs) represent promising alternatives to commercial lithium-ion batteries, offering high energy density, simplified configuration, and abundant sodium resources. However, their practical deployment is impeded by uncontrolled electrochemical dendrite growth and irreversible sodium loss. Recent advances integrating electrolyte formulation with solid electrolyte interphase (SEI) engineering have enabled more stable operation under demanding electrochemical conditions. Still, a systematic review correlating these developments from an electrochemical perspective remains lacking. This work fills that gap by providing a critical review and forward-looking perspective on electrolyte design for AFSMBs, emphasizing interfacial electrochemical kinetics/stability of sodium metal anodes. We first outline fundamental electrochemical challenges and the role of electrolyte kinetics and thermodynamics in governing AFSMB performances. Special focus is given to advanced liquid electrolytes tailored for extreme electrochemical conditions, such as low/high temperature and high-voltage operation. The discussion is then extended to semi-solid and all-solid-state systems, with a critical analysis of their interfacial electrochemistry. We examine how gel polymer electrolytes function as electrochemically stabilizing matrices, and how all-solid-state polymer electrolytes regulate ion transport kinetics and suppress dendrite growth via their electrochemical and interfacial characteristics. Finally, we present a research roadmap centered on achieving interfacial electrochemical stability and full cell integration.-
dcterms.accessRightsembargoed accessen_US
dcterms.bibliographicCitationElectrochimica acta, 20 Jan. 2026, v. 547, 147883-
dcterms.isPartOfElectrochimica acta-
dcterms.issued2026-01-20-
dc.identifier.scopus2-s2.0-105023384723-
dc.identifier.eissn1873-3859-
dc.identifier.artn147883-
dc.description.validate202602 bcjz-
dc.description.oaNot applicableen_US
dc.identifier.SubFormIDG000922/2026-01en_US
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThe authors gratefully acknowledge financial support from the Young Collaborative Research Grant of the Hong Kong Research Grant Council (C1002–23Y), The Hong Kong Polytechnic University (U-CDCA), Natural Science Foundation of Guangdong (No. 2025A1515011149), and Innovation and Technology Fund (ITS-322–23FP).en_US
dc.description.pubStatusPublisheden_US
dc.date.embargo2028-01-20en_US
dc.description.oaCategoryGreen (AAM)en_US
Appears in Collections:Journal/Magazine Article
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Embargo End Date 2028-01-20
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