Unravelingthe Origin of Grain Boundary Lithium Deficiencyin Ceramic Solid Electrolytes

Realizing solid electrolytes with low grain-boundary (GB) resistance is critical for advancing all-solid-state batteries. High GB resistance in SEs is often attributed to deficiencies in mobile ions at these boundaries; yet, when and how these deficiencies form during synthesis remain unclear. Here, we use a unique in situ scanning transmission electron microscopy setup to guide solid electrolyte crystallization during annealing, enabling real-time observation of GB formation at the atomic scale, with Li<sub>0.33</sub>La<sub>0.56</sub>TiO<sub>3</sub> as a model SE. We reveal an ultrathin, less than 1.5 nm thick, lithium-deficient layer that emerges at the crystallization front upon crystallization and persists as two adjacent crystals fuse to form a GB. We offer two hypotheses for the origin of the lithium-deficient layer, one based on thermodynamic stabilization and the other on kinetic constraints. Our results provide guidelines for designing synthesis strategies to reduce GB resistance in solid electrolytes.

Publication Details

Journal
Figshare
Published
2025-03-24
DOI
https://doi.org/10.1021/acsenergylett.5c00117.s001
Primary Topic
Advanced Battery Materials and Technologies
Type
article
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article

Unravelingthe Origin of Grain Boundary Lithium Deficiencyin Ceramic Solid Electrolytes

Figshare
Advanced Battery Materials and Technologies
article

Unravelingthe Origin of Grain Boundary Lithium Deficiencyin Ceramic Solid Electrolytes

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Abstract

Realizing solid electrolytes with low grain-boundary (GB) resistance is critical for advancing all-solid-state batteries. High GB resistance in SEs is often attributed to deficiencies in mobile ions at these boundaries; yet, when and how these deficiencies form during synthesis remain unclear. Here, we use a unique in situ scanning transmission electron microscopy setup to guide solid electrolyte crystallization during annealing, enabling real-time observation of GB formation at the atomic scale, with Li<sub>0.33</sub>La<sub>0.56</sub>TiO<sub>3</sub> as a model SE. We reveal an ultrathin, less than 1.5 nm thick, lithium-deficient layer that emerges at the crystallization front upon crystallization and persists as two adjacent crystals fuse to form a GB. We offer two hypotheses for the origin of the lithium-deficient layer, one based on thermodynamic stabilization and the other on kinetic constraints. Our results provide guidelines for designing synthesis strategies to reduce GB resistance in solid electrolytes.

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Advanced Battery Materials and Technologies
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