Enhanced ionic conductivity of Ga/Nb Co-doped LLZO ceramic electrolyte via sintering regime optimization
To enhance the room-temperature lithium-ion conductivity and interfacial stability of Li 7 La 3 Zr 2 O[Formula: see text] (LLZO) solid-state electrolytes, a co-doping strategy with Ga[Formula: see text] and Nb[Formula: see text] was employed. By systematically optimizing the sintering protocol — including heating rate, temperature, and dwell time — highly dense and phase-pure cubic-phase LLZO ceramics were successfully synthesized. The co-doping approach effectively stabilized the cubic garnet structure and regulated the lattice framework to facilitate Li[Formula: see text] transport pathways. Under optimized conditions, compared to undoped LLZO (0.31 mS cm[Formula: see text], 0.362 eV), the co-doped ceramic exhibited significantly enhanced total ionic conductivity (0.81 mS cm[Formula: see text]) and reduced activation energy (0.207 eV), confirming the superior transport performance enabled by the co-doping strategy. Furthermore, the electrolyte showed good wettability and interfacial compatibility with metallic lithium, enabling stable cycling performance in symmetric Li——Ga/Nb-LLZO——Li cells over short durations. These results confirm the practical potential of the co-doped LLZO electrolyte in all-solid-state lithium batteries. This study provides a viable pathway for the material design and processing of high-performance LLZO-based solid electrolytes.
Authors
- Zhao Jie (ORCID: https://orcid.org/0000-0003-3618-094X)
- Saifang Huang (ORCID: https://orcid.org/0000-0002-4315-4494)
- Can Cui (ORCID: https://orcid.org/0000-0002-9517-7823)
- Ming Guan (ORCID: https://orcid.org/0000-0001-7217-426X)
Institutions
- Jiangsu University of Science and Technology (CN)
- China Railway Group (China) (CN)
Publication Details
- Journal
- Functional Materials Letters
- Published
- 2025-11-01
- DOI
- https://doi.org/10.1142/s1793604725510786
- Primary Topic
- Advanced Battery Materials and Technologies
- Type
- article
- Field-Weighted Citation Impact
- 0.00