4.6 Article

Superionic Lithium Argyrodite Electrolytes by Bromine-Doping for All-Solid-State Lithium Batteries

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出版社

ELECTROCHEMICAL SOC INC
DOI: 10.1149/1945-7111/ac67b4

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资金

  1. National Key Research and Development Program of China [2016YFB0100105]
  2. National Natural Science Foundation of China [U1964205, 51872303, 51902321, 52172253]
  3. Ningbo S&T Innovation 2025 Major Special Programme [2018B10061, 2018B10087, 2019B10044, 2021Z122]
  4. Zhejiang Provincial Key R&D Program of China [2022C01072]
  5. Youth Innovation Promotion Association CAS [Y2021080]

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A promising all-solid-state lithium battery electrolyte material with high ionic conductivity and favorable stability has been developed in this study, demonstrating potential applications with its high lithium ion conductivity and good cycling stability.
High energy density all-solid-state rechargeable batteries with excellent safety are considered as reliable alternative to the current lithium-ion battery. The major challenge of all-solid-state rechargeable batteries is to develop new electrolyte material with high conductivity and good stability against lithium. In this work, the argyrodite electrolytes Li5.4PS4.4Cl1.6-xBrx (0 <= x <= 0.8) are synthesized through wet-milling method. Benefit from higher concentration of Br and the lattice softening of crystal structure, Li5.4PS4.4Cl1.2Br0.4 electrolyte with the highest lithium ion conductivity of 8.17 mS cm(-1) is realized. The Li/Li5.4PS4.4Cl1.2Br0.4/Li symmetric battery can stable cycle for 2500 h at 0.1 mA cm(-2), showing favorable stability against lithium. The assembled LiCoO2/Li5.4PS4.4Cl1.2Br0.4/Li battery delivers an initial reversible capacity of 122.4 mAh g(-1) with a capacity retention of 82.8% after 100 cycles. These results demonstrate a promising argyrodite electrolyte Li5.4PS4.4Cl1.2Br0.4 with high ionic conductivity and favorable electrochemical stability for all-solid-state lithium battery. (C) 2022 The Electrochemical Society (ECS). Published on behalf of ECS by IOP Publishing Limited.

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