Issue 9, 2024

Self-constructing a lattice-oxygen-stabilized interface in Li-rich cathodes to enable high-energy all-solid-state batteries

Abstract

Employing lithium-rich oxides as cathode materials offers an ideal option for achieving high-energy all-solid-state lithium batteries (ASSLBs), while lithium-rich cathode materials are usually hard to directly match with solid-state electrolytes (SSEs), severely limiting the capacity utilization of the high-capacity cathodes in ASSLBs. Here, a composite cathode system with only SSEs and lithium-rich oxides is used to investigate the compatibility, where the single-crystal Li2RuO3 (LRO) with high electronic conductivity is selected as a model lithium-rich oxide to avoid additional conductive carbon interfaces. By matching with two classical SSEs, Li6PS5Cl and Li3InCl6 (LIC), we reveal that the interface compatibility of SSEs/LRO, especially the compatibility of SSEs with the oxidized lattice oxygen (O(2−n)−, 0 < n < 2) of LRO, is the dominant factor of the electrochemical properties. Furthermore, a self-constructed lattice-oxygen-stabilized interface formed by the interaction of indium with O(2−n)− is first reported, which effectively prevents the O loss and interface degradation of LRO, resulting in a reversible capacity of 294.0 mA h g−1 with an initial coulombic efficiency of 98.1% and a capacity retention of 99.6% after 300 cycles, as well as a specific energy of 495 W h kg−1 based on the mass of a 30 wt%-LIC/70 wt%-LRO composite cathode and Li anode.

Graphical abstract: Self-constructing a lattice-oxygen-stabilized interface in Li-rich cathodes to enable high-energy all-solid-state batteries

Supplementary files

Article information

Article type
Paper
Submitted
29 Feb 2024
Accepted
04 Apr 2024
First published
05 Apr 2024

Energy Environ. Sci., 2024,17, 3052-3059

Self-constructing a lattice-oxygen-stabilized interface in Li-rich cathodes to enable high-energy all-solid-state batteries

X. Xu, S. Chu, S. Xu, S. Guo and H. Zhou, Energy Environ. Sci., 2024, 17, 3052 DOI: 10.1039/D4EE00938J

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