| Literature DB >> 33370108 |
Haobo Dong1, Jianwei Li1, Siyu Zhao1, Yiding Jiao1, Jintao Chen1, Yeshu Tan1, Dan J L Brett2, Guanjie He1,2,3, Ivan P Parkin1.
Abstract
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 δ-Na0.65Mn2O4·1.31H2O cathode. The dissociated Na+ in alginate after gelation directly stabilizes the cathodes by preventing the collapse of layered structures during charge processes. The as-fabricated 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 Na+. 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.Entities:
Keywords: biomass materials; cathode-stabilized electrolyte; flexible devices; hydrogel electrolytes; zinc-ion batteries
Year: 2020 PMID: 33370108 DOI: 10.1021/acsami.0c20388
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229