Fluorine-oxygen co-coordination of lithium in fluorinated polymers for broad temperature quasi-solid-state batteries.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 41115961.
- Also identified by DOI 10.1038/s41467-025-64356-4 and PMC identifier 12537920.
- Licence recorded as CC BY-NC-ND.
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Abstract
Polymer-based solid-state batteries operable across broad temperatures are critical for advanced energy storage but face limitations from sluggish ion transport kinetics in polymer electrolytes. Here, we develop a fluorinated quasi-solid polymer electrolyte that balances weak Li⁺-polymer interactions with efficient salt dissociation. This electrolyte was fabricated by in situ polymerization of 2,2,3,4,4,4-hexafluorobutyl acrylate. The incorporation of -CF<sub>2</sub>- groups within 2,2,3,4,4,4-hexafluorobutyl acrylate promotes the formation a fluorine-oxygen co-coordination structure that decouples ion conduction from polymer relaxation. This mechanism creates more efficient Li⁺ transport pathways along polymer chains and surrounding solvent molecules, promoting uniform Li⁺ flux at the Li metal electrode interface. Consequently, the electrolyte exhibits 0.27 mS cm<sup>-1</sup> conductivity at -40 °C, enabling 10 C rates and operation from -50 to 70 °C in Li | |LiNi<sub>0.8</sub>Co<sub>0.1</sub>Mn<sub>0.1</sub>O<sub>2</sub> cells. At 20 mA g<sup>-1</sup> and -30 °C, the 4.5 V coin cell retains 64.3% capacity of its 30 °C capacity, while cells maintain 86% capacity after 200 cycles at 60 mA g<sup>-1</sup> and 30 °C. Extending this coordination-tuning strategy to sodium-based systems yields similar ion-transport enhancements, highlighting its broad applicability for next-generation solid-state batteries.