Membrane-free redox flow battery with polymer electrolytes
Rajeev K. Gautam,
Xiao Wang and
Jianbing “Jimmy” Jiang ()
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Rajeev K. Gautam: University of Cincinnati
Xiao Wang: University of Cincinnati
Jianbing “Jimmy” Jiang: University of Cincinnati
Nature Communications, 2025, vol. 16, issue 1, 1-12
Abstract:
Abstract Li metal-based nonaqueous batteries are valued for high voltage and energy density, but face challenges like Li instability, volatile electrolytes, and costly ion-exchange membranes. To address these, we develop a membrane-free battery employing an ion-immobilized polymer electrolyte as anolyte and organic solvent as catholyte. Two polymer electrolytes are created for Li negative electrode: solid polymer electrolyte of polyvinylidene fluoride-co-hexafluoropropylene and gel polymer electrolyte with polypropylene carbonate. While the solid-state electrolyte offers an initial approach, it is associated with slower Li+ ions diffusion and lower ionic conductivity. The gel polymer electrolyte, specifically developed to overcome these limitations, improves Li+ diffusion, mass transport, and energy density. These anolytes are coupled with 2,4,6-tri-(1-cyclohexyloxy-4-imino-2,2,6,6-tetramethylpiperidine)−1,3,5-triazine in organic solvents (fluoroethylene carbonate and tetra (ethylene glycol) dimethyl ether) as catholytes, forming membrane-free batteries with solid polymer electrolyte and gel polymer electrolyte. Here we show that, at 0.5 M 2,4,6-tri-(1-cyclohexyloxy-4-imino-2,2,6,6-tetramethylpiperidine)−1,3,5-triazine, the battery with solid polymer electrolyte exhibits capacity retentions of 90.7% and 81.78% and Coulombic efficiencies of 95.4% and 96.7% under static and flow conditions, respectively. The battery with gel polymer electrolyte exhibits capacity retentions of 96.8% and 78.8% and Coulombic efficiencies of 97.8% and 98.4%. These results highlight the polymer electrolyte strategy’s potential for enhancing battery performance and safety.
Date: 2025
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-63878-1
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DOI: 10.1038/s41467-025-63878-1
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