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Article: Overcharge protection in aqueous zinc-ion batteries via self-sacrificial additives

TitleOvercharge protection in aqueous zinc-ion batteries via self-sacrificial additives
Authors
Issue Date2024
Citation
Energy and Environmental Science, 2024, v. 17, n. 19, p. 7424-7434 How to Cite?
AbstractIn pursuing zinc-ion batteries (ZIBs) with extended lifetimes, considerable research has been devoted to enhancing their stability, specifically cycling stability, by developing stable cathodes and Zn anodes. However, the durability, that is, reliability of ZIBs under abuse operations, particularly overcharge conditions, has long been overlooked in past research. This work investigates the durability of two typical aqueous ZIBs under overcharge conditions (Mn2+ expanded hydrated vanadium (MnVO) and manganese dioxide (MnO2) as cathode materials). Experimental findings highlight the detrimental effects of overcharging on ZIBs, leading to rapid battery failure primarily attributed to electrolyte decomposition and subsequent deterioration of interfacial contact. Subsequently, self-sacrificial electrolytes are developed by introducing bromine-based additives into the electrolyte (tetrabutylammonium and benzyl trimethylammonium bromine). These additives undergo oxidation before the electrolyte decomposition, introducing an additional Br/Br2 redox couple. Consequently, this approach effectively stabilizes the electrolyte environment. It provides efficient overcharge protection for extended periods, enabling the Zn‖MnVO and Zn‖MnO2 batteries to sustain for over 650 hours and 550 hours, even under harsh 200% state-of-charge conditions, respectively.
Persistent Identifierhttp://hdl.handle.net/10722/360336
ISSN
2023 Impact Factor: 32.4
2023 SCImago Journal Rankings: 10.935

 

DC FieldValueLanguage
dc.contributor.authorYang, Shuo-
dc.contributor.authorMei, Liang-
dc.contributor.authorWu, Zhuoxi-
dc.contributor.authorZhu, Jiaxiong-
dc.contributor.authorLi, Pei-
dc.contributor.authorHong, Hu-
dc.contributor.authorZeng, Zhiyuan-
dc.contributor.authorLi, Hongfei-
dc.contributor.authorMo, Funian-
dc.contributor.authorZhi, Chunyi-
dc.date.accessioned2025-09-10T09:06:19Z-
dc.date.available2025-09-10T09:06:19Z-
dc.date.issued2024-
dc.identifier.citationEnergy and Environmental Science, 2024, v. 17, n. 19, p. 7424-7434-
dc.identifier.issn1754-5692-
dc.identifier.urihttp://hdl.handle.net/10722/360336-
dc.description.abstractIn pursuing zinc-ion batteries (ZIBs) with extended lifetimes, considerable research has been devoted to enhancing their stability, specifically cycling stability, by developing stable cathodes and Zn anodes. However, the durability, that is, reliability of ZIBs under abuse operations, particularly overcharge conditions, has long been overlooked in past research. This work investigates the durability of two typical aqueous ZIBs under overcharge conditions (Mn<sup>2+</sup> expanded hydrated vanadium (MnVO) and manganese dioxide (MnO<inf>2</inf>) as cathode materials). Experimental findings highlight the detrimental effects of overcharging on ZIBs, leading to rapid battery failure primarily attributed to electrolyte decomposition and subsequent deterioration of interfacial contact. Subsequently, self-sacrificial electrolytes are developed by introducing bromine-based additives into the electrolyte (tetrabutylammonium and benzyl trimethylammonium bromine). These additives undergo oxidation before the electrolyte decomposition, introducing an additional Br<sup>−</sup>/Br<inf>2</inf> redox couple. Consequently, this approach effectively stabilizes the electrolyte environment. It provides efficient overcharge protection for extended periods, enabling the Zn‖MnVO and Zn‖MnO<inf>2</inf> batteries to sustain for over 650 hours and 550 hours, even under harsh 200% state-of-charge conditions, respectively.-
dc.languageeng-
dc.relation.ispartofEnergy and Environmental Science-
dc.titleOvercharge protection in aqueous zinc-ion batteries via self-sacrificial additives-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1039/d4ee01759e-
dc.identifier.scopuseid_2-s2.0-85204136380-
dc.identifier.volume17-
dc.identifier.issue19-
dc.identifier.spage7424-
dc.identifier.epage7434-
dc.identifier.eissn1754-5706-

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