New Cost-Effective Halide Solid Electrolytes for All-Solid-State Batteries: Mechanochemically Prepared Fe3+-Substituted Li2ZrCl6

Hiram Kwak, Daseul Han, Jeyne Lyoo, Juhyoun Park, Sung Hoo Jung, Yoonjae Han, Gihan Kwon, Hansu Kim, Seung Tae Hong, Kyung Wan Nam, Yoon Seok Jung

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3 Citations (Scopus)

Abstract

Owing to the combined advantages of sulfide and oxide solid electrolytes (SEs), that is, mechanical sinterability and excellent (electro)chemical stability, recently emerging halide SEs such as Li3YCl6 are considered to be a game changer for the development of all-solid-state batteries. However, the use of expensive central metals hinders their practical applicability. Herein, a new halide superionic conductors are reported that are free of rare-earth metals: hexagonal close-packed (hcp) Li2ZrCl6 and Fe3+-substituted Li2ZrCl6, derived via a mechanochemical method. Conventional heat treatment yields cubic close-packed monoclinic Li2ZrCl6 with a low Li+ conductivity of 5.7 × 10−6 S cm−1 at 30 °C. In contrast, hcp Li2ZrCl6 with a high Li+ conductivity of 4.0 × 10−4 S cm−1 is derived via ball-milling. More importantly, the aliovalent substitution of Li2ZrCl6 with Fe3+, which is probed by complementary analyses using X-ray diffraction, pair distribution function, X-ray absorption spectroscopy, and Raman spectroscopy measurements, drastically enhances the Li+ conductivity up to ≈1 mS cm−1 for Li2.25Zr0.75Fe0.25Cl6. The superior interfacial stability when using Li2+xZr1−xFexCl6, as compared to that when using conventional Li6PS5Cl, is proved. Furthermore, an excellent electrochemical performance of the all-solid-state batteries is achieved via the combination of Li2ZrCl6 and single-crystalline LiNi0.88Co0.11Al0.01O2.

Original languageEnglish
Article number2003190
JournalAdvanced Energy Materials
Volume11
Issue number12
DOIs
Publication statusPublished - 2021 Mar 25

Bibliographical note

Funding Information:
H.K. and D.H. contributed equally to this work. This research was supported by the Technology Development Program to Solve Climate Changes and by Basic Science Research Program of the National Research Foundation (NRF) funded by the Ministry of Science & ICT (grant no. NRF-2017M1A2A2044501, 2018R1A2B6004996, and 2017M1A2A2044502), by the Technology Innovation Program (grant no. 20007045) funded by the Ministry of Trade, Industry & Energy (MOTIE, Korea). The PDF research used beamline 28-ID-1(PDF) of the National Synchrotron Light Source II, a US Department of Energy (DOE) Office of Science User Facility operated for the DOE Office of Science by Brookhaven National Laboratory under contract no. DE-SC0012704. The facility support from beamline 16A1 of Taiwan Light Source (TLS) is also acknowledged.

Funding Information:
H.K. and D.H. contributed equally to this work. This research was supported by the Technology Development Program to Solve Climate Changes and by Basic Science Research Program of the National Research Foundation (NRF) funded by the Ministry of Science & ICT (grant no. NRF‐2017M1A2A2044501, 2018R1A2B6004996, and 2017M1A2A2044502), by the Technology Innovation Program (grant no. 20007045) funded by the Ministry of Trade, Industry & Energy (MOTIE, Korea). The PDF research used beamline 28‐ID‐1(PDF) of the National Synchrotron Light Source II, a US Department of Energy (DOE) Office of Science User Facility operated for the DOE Office of Science by Brookhaven National Laboratory under contract no. DE‐SC0012704. The facility support from beamline 16A1 of Taiwan Light Source (TLS) is also acknowledged.

Publisher Copyright:
© 2021 Wiley-VCH GmbH

All Science Journal Classification (ASJC) codes

  • Renewable Energy, Sustainability and the Environment
  • Materials Science(all)

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