4.8 Article

Advanced High-Voltage All-Solid-State Li-Ion Batteries Enabled by a Dual-Halogen Solid Electrolyte

Journal

ADVANCED ENERGY MATERIALS
Volume 11, Issue 32, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/aenm.202100836

Keywords

all-solid-state Li-ion batteries; anodic (oxidation) stability; cathode-electrolyte interface; F-rich passivating interface; ultrahigh voltage

Funding

  1. Natural Sciences and Engineering Research Council of Canada (NSERC)
  2. Canada Research Chair Program (CRC)
  3. Canada Foundation for Innovation (CFI)
  4. Ontario Research Foundation (ORF)
  5. China Automotive Battery Research Institute Co., Ltd.
  6. Glabat Solid-State Battery Inc.
  7. University of Western Ontario (UWO)
  8. CFI
  9. NSERC
  10. National Research Council (NRC)
  11. Canadian Institutes of Health Research (CIHR)
  12. Government of Saskatchewan
  13. University of Saskatchewan
  14. National Science Foundation [1550423]
  15. Ontario Trillium Scholarship (OTS)
  16. Direct For Computer & Info Scie & Enginr
  17. Office of Advanced Cyberinfrastructure (OAC) [1550423] Funding Source: National Science Foundation

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This study addresses the stability issue of solid-state electrolytes in high-voltage operations by designing a dual-halogen Li-ion conductor, improving both ionic conductivity and stability. The dual-halogen solid electrolyte shows great potential for high-voltage all-solid-state Li-ion batteries and provides a new design strategy for fast Li-ion conductors with high oxidation stability.
Solid-state electrolytes (SEs) with high anodic (oxidation) stability are essential for achieving all-solid-state Li-ion batteries (ASSLIBs) operating at high voltages. Until now, halide-based SEs have been one of the most promising candidates due to their compatibility with cathodes and high ionic conductivity. However, the developed chloride and bromide SEs still show limited electrochemical stability that is inadequate for ultrahigh voltage operations. Herein, this challenge is addressed by designing a dual-halogen Li-ion conductor: Li3InCl4.8F1.2. F is demonstrated to selectively occupy a specific lattice site in a solid superionic conductor (Li3InCl6) to form a new dual-halogen solid electrolyte (DHSE). With the incorporation of F, the Li3InCl4.8F1.2 DHSE becomes dense and maintains a room-temperature ionic conductivity over 10(-4) S cm(-1). Moreover, the Li3InCl4.8F1.2 DHSE exhibits a practical anodic limit over 6 V (vs Li/Li+), which can enable high-voltage ASSLIBs with decent cycling. Spectroscopic, computational, and electrochemical characterizations are combined to identify a rich F-containing passivating cathode-electrolyte interface (CEI) generated in situ, thus expanding the electrochemical window of Li3InCl4.8F1.2 DHSE and preventing the detrimental interfacial reactions at the cathode. This work provides a new design strategy for the fast Li-ion conductors with high oxidation stability and shows great potential to high-voltage ASSLIBs.

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