晶界
材料科学
离子电导率
电导率
电解质
离子键合
快离子导体
钙钛矿(结构)
化学物理
微观结构
凝聚态物理
矿物学
离子
结晶学
冶金
物理化学
化学
电极
物理
有机化学
作者
Cong Gao,Xuefeng Zhou,Runsheng Yu,Chengyu Li,Xiang Gao,Wenge Yang,Dongliang Chao,Yongjin Chen
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-03-14
标识
DOI:10.1021/acsnano.4c15481
摘要
The ABO3 perovskite oxide solid state electrolyte Li3xLa2/3-xTiO3 (LLTO) has gained significant attention. Despite their potential, both the bulk and grain boundary conductivity values observed in practice fall short of theoretical expectations. In terms of structures, domain boundaries and grain boundaries play a crucial role in hindering ionic transport, and there has been no comprehensive study that enhances both the bulk and grain boundary conductivity by modification of these microstructures. Here, we have employed the multiscale method and demonstrated that Ta and Sr codoping strategy balances the structural symmetry, Li+ concentration, grain boundaries, domain boundaries, and the lattice defects, which simultaneously enhances the bulk and grain boundary conductivity. The highest total ionic conductivity achieved is 3.0 × 10-4 S cm-1 in the Li0.33La0.54Sr0.03Ti0.9625Ta0.03O3 sample, with an 280% enhancement over the pristine sample. Our work highlights the coupling effects of domain and grain boundaries for further improving the ionic conductivity of perovskite solid state electrolyte.
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