Critical to the development of all-solid-state lithium-ion batteries technology are novel solid-state electrolytes with high ionic conductivity and robust stability under inorganic solid-electrolyte operating conditions. Herein, by using density functional theory and molecular dynamics, a mixed oxygen-sulfur-based Li-superionic conductor is screened out from the local chemical structure of β-Li PS to discover novel Li P Ge S O (LPGSO) with high ionic conductivity and high stability under thermal, moist, and electrochemical conditions, which causes oxygenation at specific sites to improve the stability and selective sulfuration to provide an O-S mixed path by Li-S/O structure units with coordination number between 3 and 4 for fast Li-cooperative conduction. Furthermore, LPGSO exhibits a quasi-isotropic 3D Li-ion cooperative diffusion with a lesser migration barrier (≈0.19 eV) compared to its sulfide-analog Li P Ge S . The theoretical ionic conductivity of this conductor at room temperature is as high as ≈30.0 mS cm , which is among the best in current solid-state electrolytes. Such an oxy-sulfide synergistic effect and Li-ion cooperative migration mechanism would enable the engineering of next-generation electrolyte materials with desirable safety and high ionic conductivity, for possible application in the near future.
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http://dx.doi.org/10.1002/smll.201906374 | DOI Listing |
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