Investigation of a Biomass Hydrogel Electrolyte Naturally Stabilizing Cathodes for Zinc-Ion Batteries
Aqueous zinc-ion batteries (AZIBs) have the potential to be utilized in a grid-scale energy storage system owing to their high energy density and cost-effective properties. However, the dissolution of cathode materials and the irreversible extraction of preintercalated metal ions in the electrode ma...
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Veröffentlicht in: | ACS applied materials & interfaces 2021-01, Vol.13 (1), p.745-754 |
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Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Aqueous zinc-ion batteries (AZIBs) have the potential to be utilized in a grid-scale energy storage system owing to their high energy density and cost-effective properties. However, the dissolution of cathode materials and the irreversible extraction of preintercalated metal ions in the electrode materials restrict the stability of AZIBs. Herein, a cathode-stabilized ZIB strategy is reported based on a natural biomass polymer sodium alginate as the electrolyte coupling with a Na+ preintercalated delta-Na0.65Mn2O4 center dot 1.31H(2)O cathode. The dissociated Na+ in alginate after gelation directly stabilizes the cathodes by preventing the collapse of layered structures during charge processes. The asfabricated ZIBs deliver a high capacity of 305 mA h g(-1) at 0.1 A g(-1), 10% higher than the ZIBs with an aqueous electrolyte. Further, the hybrid polymer electrolyte possessed an excellent Coulombic efficiency above 99% and a capacity retention of 96% within 1000 cycles at 2 A g(-1). A detailed investigation combining ex situ experiments uncovers the charge storage mechanism and the stability of assembled batteries, confirming the reversible diffusions of both Zn2+ and preintercalated Nat. A flexible device of ZIBs fabricated based on vacuum-assisted resin transfer molding possesses an outstanding performance of 160 mA h g(-1) at 1 A g(-1), which illustrates their potential for wearable electronics in mass production. |
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ISSN: | 1944-8244 1944-8252 |
DOI: | 10.1021/acsami.0c20388 |