Enhancing Zinc-Ion-Transport Kinetics in Solid-State Zinc Batteries via an Internal/Surface Dual Acceleration Strategy.
basic_science · Level V
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- Record sourced from PubMed, PMID 40315015.
- Also identified by DOI 10.1021/acs.nanolett.5c01076.
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Abstract
Solid polymer electrolytes (SPEs) hold substantial potential for enabling highly flexible and stable zinc-ion batteries (ZIBs) due to their nearly anhydrous nature. However, the development of SPEs is still hindered by their poor zinc-ion-transport kinetics. Herein, utilizing CALF-20 as both a filler and a functional coating, a bilayer solid-state electrolyte (BSSE) was designed. On the one hand, the intermediate CALF-20 filled poly(ethylene oxide) hybrid gel demonstrates strong interaction with CF<sub>3</sub>SO<sub>3</sub><sup>-</sup> anions, thus promoting Zn<sup>2+</sup> dissociation and transmission. On the other hand, the outer single CALF-20 layer supports Zn<sup>2+</sup> ions with abundant transmission paths and a low Zn<sup>2+</sup> migration energy barrier, which doubly accelerates ion migration at the interface. This internal/surface dual acceleration strategy allows the BSSE to deliver high ionic conductivity and Zn<sup>2+</sup> transference number. Both the Zn∥Zn symmetric and Zn∥MnO<sub>2</sub> full cells exhibit an obvious prolonged cycle life. This dual acceleration strategy sheds light on the design of high-ionic-conductivity, steady, and practical ZIBs.