Li transport properties of sulfolane-based gel polymer electrolyte and effective suppression of lithium polysulfide dissolution in lithium-sulfur batteries

Sulfolane (SL)-based gel polymer electrolytes composed of a polyether-based host polymer were investigated for long-lifecycle lithium-sulfur batteries. The proposed electrolytes were expected to cause chemical and physical suppression of Li 2 S n dissolution and diffusion owing to the low Li 2 S n s...

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Published inSustainable energy & fuels Vol. 6; no. 18; pp. 4218 - 4226
Main Authors Miyauchi, Hibiki, Inaba, Kohei, Takahashi, Keitaro, Arai, Nana, Umebayashi, Yasuhiro, Seki, Shiro
Format Journal Article
LanguageEnglish
Published London Royal Society of Chemistry 13.09.2022
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Summary:Sulfolane (SL)-based gel polymer electrolytes composed of a polyether-based host polymer were investigated for long-lifecycle lithium-sulfur batteries. The proposed electrolytes were expected to cause chemical and physical suppression of Li 2 S n dissolution and diffusion owing to the low Li 2 S n solubility, derived from the highly concentrated SL-based electrolytes, and low Li 2 S n diffusion, derived from the host polymer, respectively. The Li + transport properties, and Li + -SL and Li + -anion interactions, were analyzed by alternating current impedance measurements and Raman spectroscopy, respectively. The relationships between gel polymer electrolyte composition and Li + coordination structure/Li + transport properties were also investigated. The Li-S cells containing gel polymer electrolytes exhibited a sufficient discharge capacity in the first cycle (approx. 1150 mA h g −1 ) and stable charge discharge operation for 100 cycles. Application of the proposed electrolytes resulted in high battery performance owing to chemical and physical control of Li 2 S n dissolution and diffusion, and favorable electrolyte/Li metal interface formation. New-type sulfolane gel electrolytes exhibited high battery performance owing to chemical and physical control of Li 2 S n dissolution and diffusion properties.
Bibliography:https://doi.org/10.1039/d2se00711h
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ISSN:2398-4902
2398-4902
DOI:10.1039/d2se00711h