A High‐Performance Alginate Hydrogel Binder for Aqueous Zn−Ion Batteries
The binder is an indispensable battery component that maintains the integrity of the electrode. Polyvinylidene fluoride (PVDF) is most commonly used as a binder in rechargeable batteries; however, it is associated with the toxic and expensive N‐methyl‐2‐pyrrolidone organic solvent. Here, through the...
Gespeichert in:
Veröffentlicht in: | Chemphyschem 2022-09, Vol.23 (17), p.e202200106-n/a |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | The binder is an indispensable battery component that maintains the integrity of the electrode. Polyvinylidene fluoride (PVDF) is most commonly used as a binder in rechargeable batteries; however, it is associated with the toxic and expensive N‐methyl‐2‐pyrrolidone organic solvent. Here, through the cross‐linking of sodium alginate (SA) with metal cations, a high‐performance hydrogel binder is developed that maintains the stability of MnO2 cathodes in an aqueous electrolyte. Owing to the strong adhesion, high hydrophilicity, and good mechanical stability resulting from the strong bonding of Ca2+ with SA, a commercial microsized MnO2 cathode with a Ca−SA binder delivered a capacity above 300 mAh/g at 1 C, which was larger than those of Mn−SA and Zn−SA (∼200 mAh/g) and PVDF (∼150 mAh/g) binders, and a capacity of 250 mAh/g at 3 C for over 200 cycles. These encouraging results could unlock the enormous potential of aqueous binders for practical applications in aqueous batteries.
An aqueous alginate hydrogel binder is developed through the cross‐linking of sodium alginate (SA) with metal cations to improve the electrochemical performance of MnO2 cathodes in aqueous electrolytes. The enhancement can be attributed to the strong adhesion, high hydrophilicity, and good mechanical stability resulting from the strong bonding of Ca2+ with SA. |
---|---|
ISSN: | 1439-4235 1439-7641 |
DOI: | 10.1002/cphc.202200106 |