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Engineering a High-Voltage Durable Cathode/Electrolyte Interface for All-Solid-State Lithium Metal Batteries via In Situ Electropolymerization.

Qi LiXiaoyu ZhangJian PengZhihao WangZhixiang RaoYuyu LiZhen LiChun FangJiantao HanYunhui Huang
Published in: ACS applied materials & interfaces (2022)
Poly(ethylene oxide) (PEO)-based polymer electrolytes have been widely studied as a result of their flexibility, excellent interface contact, and high compatibility with a lithium metal anode. Owing to the poor oxidation resistance of ethers, however, the PEO-based electrolytes are only compatible with low-voltage cathodes, which limits their energy density. Here, a high-voltage stable solid-state interface layer based on polyfluoroalkyl acrylate was constructed via in situ solvent-free bulk electropolymerization between the LiNi 0.8 Mn 0.1 Co 0.1 O 2 (NCM811) cathode and the PEO-based solid polymer electrolyte. The electrochemical oxidation window of the as-synthesized electrolyte was therefore expanded from 4.3 V for the PEO-based matrix electrolyte to 5.1 V, and the ionic conductivity was improved to 1.02 × 10 -4 S cm -1 at ambient temperature and 4.72 × 10 -4 S cm -1 at 60 °C as a result of the improved Li + migration. This fabrication process for the interface buffer layer by an in situ electrochemical process provides an innovative and universal interface engineering strategy for high-performance and high-energy-density solid-state batteries, which has not been explicitly discussed before, paving the way toward the large-scale production of the next generation of solid-state lithium batteries.
Keyphrases
  • solid state
  • ion batteries
  • ionic liquid
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  • particulate matter
  • electron transfer
  • molecularly imprinted
  • visible light