Green Strategyfor Li<sub>2</sub>CO<sub>3</sub> Regulationin Garnet-Type Solid-State Electrolytes via Acoustic Cavitation

Garnet-type Li<sub>6.75</sub>La<sub>3</sub>Zr<sub>1.75</sub>Ta<sub>0.25</sub>O<sub>12</sub> (LLZTO) holds significant potential as a solid-state electrolyte (SSE) comprising promising features such as high Li<sup>+</sup> conductivity, wide electrochemical stability window, and compatibility with Li-metal. However, air exposure forms a thick Li<sub>2</sub>CO<sub>3</sub> 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<sub>2</sub>CO<sub>3</sub> layer thickness (<10 nm), which enhances air stability without compromising ionic conduction. <i>In-situ</i> 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<sub>2</sub>CO<sub>3</sub> 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.

Publication Details

Journal
Figshare
Published
2025-03-17
DOI
https://doi.org/10.1021/acsenergylett.5c00368.s001
Primary Topic
Advanced Battery Materials and Technologies
Type
article
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article

Green Strategyfor Li2CO3 Regulationin Garnet-Type Solid-State Electrolytes via Acoustic Cavitation

Figshare
Advanced Battery Materials and Technologies
article

Green Strategyfor Li2CO3 Regulationin Garnet-Type Solid-State Electrolytes via Acoustic Cavitation

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Abstract

Garnet-type Li<sub>6.75</sub>La<sub>3</sub>Zr<sub>1.75</sub>Ta<sub>0.25</sub>O<sub>12</sub> (LLZTO) holds significant potential as a solid-state electrolyte (SSE) comprising promising features such as high Li<sup>+</sup> conductivity, wide electrochemical stability window, and compatibility with Li-metal. However, air exposure forms a thick Li<sub>2</sub>CO<sub>3</sub> 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<sub>2</sub>CO<sub>3</sub> layer thickness (<10 nm), which enhances air stability without compromising ionic conduction. <i>In-situ</i> 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<sub>2</sub>CO<sub>3</sub> 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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Advanced Battery Materials and Technologies
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