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Ta₂O5 도핑에 따른 LATP 고체전해질의 미세구조와 이온전도도의 상관관계

김성현, 황윤찬, 강성현, 박소연, 구상모, 신원호

The Microstructure and Ionic Conductivity of LATP Solid Electrolytes Doped with Ta₂O5

Seong-hyeon Kim, Yun Chan Hwang, Sung Hyun Kang, So Yeon Park, Sang-mo Koo, Weon Ho Shin
J Electr Electron Mater 2026;39(2):210-216.
Published online: March 1, 2026

광운대학교 전자재료공학과

Department of Electronic Materials Engineering, Kwangwoon University, Seoul 01890, Korea
Corresponding author:  Weon Ho Shin
Email: weonho@kw.ac.kr
• Received: September 1, 2025   • Revised: September 14, 2025   • Accepted: September 18, 2025
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The safety and stability concerns of liquid electrolytes in conventional lithium-ion batteries have accelerated the development of solid-state alternatives. NASICON type ceramics Li1.5Al0.5Ti1.5(PO4)3 (LATP) offer promising properties, including high bulk ionic conductivity and good compatibility with lithium anodes. However, their practical application is hindered by grain boundary resistance and relatively low total ionic conductivity. This study investigates the effect of Ta2O5 doping on LATP to overcome these limitations. Doping with 5 wt% Ta2O5 improved the ionic conductivity to 2.95 × 10-4 S/cm by enhancing lattice structure, reducing grain boundary resistance, and suppressing the formation of secondary phase. Additionally, Ta2O5 positively influenced the sintering behavior, resulting in a denser, and more uniform microstructure. These enhancements suggest that Ta2O5-doped LATP is a strong candidate for next-generation all-solid-state lithium-ion batteries.

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The Microstructure and Ionic Conductivity of LATP Solid Electrolytes Doped with Ta₂O5
J Electr Electron Mater. 2026;39(2):210-216.   Published online March 1, 2026
Download Citation

Download a citation file in RIS format that can be imported by all major citation management software, including EndNote, ProCite, RefWorks, and Reference Manager.

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The Microstructure and Ionic Conductivity of LATP Solid Electrolytes Doped with Ta₂O5
J Electr Electron Mater. 2026;39(2):210-216.   Published online March 1, 2026
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