Affiliation:
1. Tsinghua Center for Green Chemical Engineering Electrification Beijing Key Laboratory of Green Chemical Reaction Engineering and Technology Department of Chemical Engineering Tsinghua University Beijing 100084 China
2. Tanwei College Tsinghua University Beijing 100084 China
3. Advanced Research Institute of Multidisciplinary Science Beijing Institute of Technology Beijing 100081 China
Abstract
AbstractHalide solid electrolytes (SEs) are attracting strong attention as one of the compelling candidates for the next‐generation of inorganic SEs due to their high ionic conductivity. Nevertheless, unsatisfactory high‐voltage stability restricts the further applications of halide SEs. Herein, the anion‐engineering of F−/O2− is evolved to construct the high‐voltage stable zirconium‐based halide superionic conductors (Li2.5ZrCl5F0.5O0.5, LZCFO). Benefiting from the thermodynamic/kinetic high‐voltage stability of F‐containing SE and the disordered localized structure introduced by O2−, LZCFO displays a practical electrochemical limit of 4.87 V versus Li/Li+ and an ionic conductivity of 1.17 mS cm−1 at 30 °C. With LZCFO and NCM955, the all‐solid‐state lithium battery exhibits a high discharge capacity of 207.1 mAh g−1 at 0.1C and a capacity retention of 81.2% after 500 cycles at 0.5C. The interfacial characterization further demonstrates the formation of the F‐rich cathode–electrolyte interphase (CEI), which inhibits side reactions between the cathode and the SE and boosts excellent cycling stability. This work affords fresh insights on the engineering of SEs with high‐voltage stability, high ionic conductivity, and stable CEI in all‐solid‐state lithium batteries.
Funder
Natural Science Foundation of Beijing Municipality
National Key Research and Development Program of China
National Natural Science Foundation of China
China Postdoctoral Science Foundation
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1 articles.
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