Boosting lithium ion conductivity of antiperovskite solid electrolyte by potassium ions substitution for cation clusters
Solid-state electrolytes with high ionic conductivities are crucial for the development of all-solid-state lithium batteries, and there is a strong correlation between the ionic conductivities and underlying lattice structures of solid-state electrolytes. Here, we report a lattice manipulation metho...
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Veröffentlicht in: | Nature communications 2023-10, Vol.14 (1), p.6807-10, Article 6807 |
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Hauptverfasser: | , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Solid-state electrolytes with high ionic conductivities are crucial for the development of all-solid-state lithium batteries, and there is a strong correlation between the ionic conductivities and underlying lattice structures of solid-state electrolytes. Here, we report a lattice manipulation method of replacing [Li
2
OH]
+
clusters with potassium ions in antiperovskite solid-state electrolyte (Li
2
OH)
0.99
K
0.01
Cl, which leads to a remarkable increase in ionic conductivity (4.5 × 10
‒3
mS cm
‒1
, 25 °C). Mechanistic analysis indicates that the lattice manipulation method leads to the stabilization of the cubic phase and lattice contraction for the antiperovskite, and causes significant changes in Li-ion transport trajectories and migration barriers. Also, the Li||LiFePO
4
all-solid-state battery (excess Li and loading of 1.78 mg cm
‒2
for LiFePO
4
) employing (Li
2
OH)
0.99
K
0.01
Cl electrolyte delivers a specific capacity of 116.4 mAh g
‒1
at the 150th cycle with a capacity retention of 96.1% at 80 mA g
‒1
and 120 °C, which indicates potential application prospects of antiperovskite electrolyte in all-solid-state lithium batteries.
All-solid-state electrolytes for lithium batteries generally suffer from low ionic conductivity. Here, authors manipulate the lattice of antiperovskite-type Li
2
OHCl by potassium ion substitution, which alters the lattice structure and improves the lithium ion transport properties. |
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ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/s41467-023-42385-1 |