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High Resolution Image Download MS PowerPoint Slide Garnet-type Li 6.75 La 3 Zr 1.75 Ta 0.25 O 12 (LLZTO) holds significant potential as a solid-state electrolyte (SSE) comprising promising features such as high Li + conductivity, wide electrochemical stability window, and compatibility with Li-metal. However, air exposure forms a thick Li 2 CO 3 passivation layer (∼50 nm), which hinders storage, handling, and interfacial performance, especially for LLZTO nanoparticles (NPs) with a high surface area. This study introduces a scalable, green sonication-assisted method to control the Li 2 CO 3 layer thickness (<10 nm), which enhances air stability without compromising ionic conduction. In-situ ambient-pressure X-ray photoelectron spectroscopy (AP-XPS) further reveals the carbonate formation mechanism under atmospheric conditions. Electrochemical tests in ceramic-in-polymer (CIP) and polymer-in-ceramic (PIC) composite polymer electrolytes (CPEs) confirm that regulated Li 2 CO 3 does not degrade the performance of passivated-LLZTO. The chemical-free, green approach suggested in this work maintains electrochemical properties, which enables scalable use of LLZTO-based SSEs for next-generation Li-metal batteries.
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Srivastava et al. (2025) studied this question.
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