4.8 Article

A cost-effective and humidity-tolerant chloride solid electrolyte for lithium batteries

Journal

NATURE COMMUNICATIONS
Volume 12, Issue 1, Pages -

Publisher

NATURE RESEARCH
DOI: 10.1038/s41467-021-24697-2

Keywords

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Funding

  1. National Key R&D Program of China [2018YFA0209600, 2017YFA0208300]
  2. National Natural Science Foundation of China [22022813, 21878268, 51802302, 11774223, U1732154]
  3. Fundamental Research Funds for the Central Universities [WK3430000006, WK2060190085]
  4. Shanghai talent program

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Li2ZrCl6 is a cost-effective chloride solid electrolyte with high ionic conductivity, deformability, and humidity tolerance, suitable for high-voltage Li metal batteries.
Li-ion-conducting chloride solid electrolytes receive considerable attention due to their physicochemical characteristics such as high ionic conductivity, deformability and oxidative stability. However, the raw materials are expensive, and large-scale use of this class of inorganic superionic conductors seems unlikely. Here, a cost-effective chloride solid electrolyte, Li2ZrCl6, is reported. Its raw materials are several orders of magnitude cheaper than those for the state-of-the-art chloride solid electrolytes, but high ionic conductivity (0.81 mS cm(-1) at room temperature), deformability, and compatibility with 4V-class cathodes are still simultaneously achieved in Li2ZrCl6. Moreover, Li2ZrCl6 demonstrates a humidity tolerance with no sign of moisture uptake or conductivity degradation after exposure to an atmosphere with 5% relative humidity. By combining Li2ZrCl6 with the Li-In anode and the single-crystal LiNi0.8Mn0.1Co0.1O2 cathode, we report a room-temperature all-solid-state cell with a stable specific capacity of about 150 mAh g(-1) for 200 cycles at 200mAg(-1). Stable inorganic solid electrolytes are instrumental in developing high-voltage Li metal batteries. Here, the authors present the synthesis and electrochemical energy storage properties of a cost-effective and humidity-tolerant chloride solid electrolyte.

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