Journal
MACROMOLECULAR RAPID COMMUNICATIONS
Volume 42, Issue 4, Pages -Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/marc.202000607
Keywords
anionic ring-opening polymerization; polythioethers; redox-active polymers; solid-state electrolytes
Categories
Funding
- MEXT, Japan [17H03072, 18K19120, 18H05515, 20H05298, 19K15638]
- Research Institute for Science and Engineering
- Grants-in-Aid for Scientific Research [19K15638, 20H05298] Funding Source: KAKEN
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A poly(ethylene sulfide) backbone is used as the main chain in a radical polymer, synthesized through anionic ring-opening polymerization of an episulfide monomer with TEMPO. This new polythioether exhibits a lower glass transition temperature and significantly higher solid-state ionic conductivity compared to traditional poly(ethylene oxide) backbones. Additionally, it improves the charge/discharge properties of a cathode in solid-state lithium-ion batteries.
A poly(ethylene sulfide) backbone is introduced as the main chain of a radical polymer. Anionic ring-opening polymerization of an episulfide monomer substituted with 2,2,6,6tetramethylpiperidin1oxyl (TEMPO), a robust nitroxide radical, yields the corresponding polythioether. Compared to the traditional poly(ethylene oxide) backbone, the new polymer shows a lower glass transition temperature (-10 degrees C), and about threefold higher solid-state ionic conductivity. The polythioether is also shown to improve the charge/discharge properties of a cathode in solid-state lithium-ion batteries.
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