材料科学
电解质
快离子导体
陶瓷
复合数
电导率
锂(药物)
延展性(地球科学)
脆性
制作
离子电导率
复合材料
化学工程
蠕动
电极
化学
物理化学
工程类
医学
替代医学
病理
内分泌学
作者
Bingqing Xiong,Jianwei Zhang,Qingshun Nian,Xiaoye Liu,Jinyu Jiang,Zihong Wang,Zhenzhong Yang,Xiaodi Ren
标识
DOI:10.1002/ange.202413502
摘要
Garnet Li7La3Zr2O12 (LLZO)‐based solid‐state electrolytes (SSEs) hold promise for realizing next‐generation lithium metal batteries with high energy density. However, the high stiffness of high‐temperature sintered LLZO makes it brittle and susceptible to strain during the fabrication of solid‐state batteries. Cold‐pressed LLZO exhibits improved ductility but suffers from insufficient Li+ conductivity. Here, we report cold‐pressed Ta‐doped LLZO (Ta‐LZ) particles integrated with ductile Li6PS5Cl (LPSC) via a Li+ conductive Li‐containing Ta‐Cl structure. This configuration creates a continuous Li+ conduction network by enhancing the Li+ exchange at the Ta‐LZ/LPSC interface. The resulting Ta‐LZ/LPSC SSE exhibits Li+ conductivity of 4.42 × 10–4 S cm–1 and a low activation energy of 0.31 eV. Li symmetric cells with Ta‐LZ/LPSC SSE demonstrate excellent Li dendrite suppression ability, with an improved critical current density of 5.0 mA cm−2 and a prolonged cycle life exceeding 600 h at 1 mA cm‐2. Our finding provides valuable insights into developing cold‐pressed ceramic powder electrolytes for high‐performance all‐solid‐state batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI