化学
离子电导率
卤化物
逆向蒙特卡罗
无定形固体
离子键合
对分布函数
电导率
电化学
快离子导体
化学物理
离子
化学工程
无机化学
物理化学
结晶学
有机化学
晶体结构
电解质
电极
工程类
中子衍射
数学分析
数学
作者
Shumin Zhang,Feipeng Zhao,Lo‐Yueh Chang,Yu‐Chun Chuang,Zhen Zhang,Yuanmin Zhu,Xiaoge Hao,Jiamin Fu,Jiatang Chen,Jing Luo,Minsi Li,Yingjie Gao,Yining Huang,Tsun‐Kong Sham,Meng Gu,Yuanpeng Zhang,Graham King,Xueliang Sun
摘要
The recently surged halide-based solid electrolytes (SEs) are great candidates for high-performance all-solid-state batteries (ASSBs), due to their decent ionic conductivity, wide electrochemical stability window, and good compatibility with high-voltage oxide cathodes. In contrast to the crystalline phases in halide SEs, amorphous components are rarely understood but play an important role in Li-ion conduction. Here, we reveal that the presence of amorphous component is common in halide-based SEs that are prepared via mechanochemical method. The fast Li-ion migration is found to be associated with the local chemistry of the amorphous proportion. Taking Zr-based halide SEs as an example, the amorphization process can be regulated by incorporating O, resulting in the formation of corner-sharing Zr–O/Cl polyhedrons. This structural configuration has been confirmed through X-ray absorption spectroscopy, pair distribution function analyses, and Reverse Monte Carlo modeling. The unique structure significantly reduces the energy barriers for Li-ion transport. As a result, an enhanced ionic conductivity of (1.35 ± 0.07) × 10–3 S cm–1 at 25 °C can be achieved for amorphous Li3ZrCl4O1.5. In addition to the improved ionic conductivity, amorphization of Zr-based halide SEs via incorporation of O leads to good mechanical deformability and promising electrochemical performance. These findings provide deep insights into the rational design of desirable halide SEs for high-performance ASSBs.
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