Triflate anion chemistry for enhanced four-electron zinc-iodine aqueous batteries
I + hydrolysis, sluggish iodine redox kinetics and the instability of Zn anodes are the primary challenges for aqueous four-electron zinc-iodine batteries (4eZIBs). Herein, the OTf − anion chemistry in aqueous electrolyte is essential for developing advanced 4eZIBs. It is elucidated that OTf − anion...
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2024-07, Vol.6 (58), p.7447-745 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | I
+
hydrolysis, sluggish iodine redox kinetics and the instability of Zn anodes are the primary challenges for aqueous four-electron zinc-iodine batteries (4eZIBs). Herein, the OTf
−
anion chemistry in aqueous electrolyte is essential for developing advanced 4eZIBs. It is elucidated that OTf
−
anions establish weak hydrogen bonds (H bonds) with water to stabilize I
+
species while optimizing a water-lean Zn
2+
coordination structure to mitigate Zn dendrites and corrosion. Moreover, the interaction of the OTf
−
anions with the iodine species results in an increased equilibrium average intermolecular bond length of the iodine species, facilitating the 4e redox kinetics of iodine with improved reversibility.
OTf
−
anions establish weak hydrogen-bonds with water to stabilize I
+
species while optimizing a water-lean Zn
2+
coordination structure to mitigate Zn dendrites and corrosion for developing advanced four-electron zinc-iodine aqueous batteries. |
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ISSN: | 1359-7345 1364-548X 1364-548X |
DOI: | 10.1039/d4cc02266a |