PVDF-HFP@Nafion-based quasisolid polymer electrolyte for high migration number in working rechargeable Na-O<sub>2</sub> batteries.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 38809713.
- Also identified by DOI 10.1073/pnas.2320012121 and PMC identifier 11161764.
- Licence recorded as CC BY-NC-ND.
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Abstract
Rechargeable sodium-oxygen (Na-O<sub>2</sub>) battery is deemed as a promising high-energy storage device due to the abundant sodium resources and high theoretical energy density (1,108 Wh kg<sup>-1</sup>). A series of quasisolid electrolytes are constantly being designed to restrain the dendrites growth, the volatile and leaking risks of liquid electrolytes due to the open system of Na-O<sub>2</sub> batteries. However, the ticklish problem about low operating current density for quasisolid electrolytes still hasn't been conquered. Herein, we report a rechargeable Na-O<sub>2</sub> battery with polyvinylidene fluoride-hexafluoropropylene recombination Nafion (PVDF-HFP@Nafion) based quasisolid polymer electrolyte (QPE) and MXene-based Na anode with gradient sodiophilic structure (M-GSS/Na). QPE displays good flame resistance, locking liquid and hydrophobic properties. The introduction of Nafion can lead to a high Na<sup>+</sup> migration number (<i>t</i><sub>Na</sub><sup>+</sup> = 0.68) by blocking the motion of anion and promote the formation of NaF-rich solid electrolyte interphase, resulting in excellent cycling stability at relatively high current density under quasisolid environment. In the meantime, the M-GSS/Na anode exhibits excellent dendrite inhibition ability and cycling stability. Therefore, with the synergistic effect of QPE and M-GSS/Na, constructed Na-O<sub>2</sub> batteries run more stably and exhibit a low potential gap (0.166 V) after an initial 80 cycles at 1,000 mA g<sup>-1</sup> and 1,000 mAh g<sup>-1</sup>. This work provides the reference basis for building quasisolid state Na-O<sub>2</sub> batteries with long-term cycling stability.