材料科学
电解质
卤化物
快离子导体
离子电导率
电导率
极化率
化学工程
无定形固体
离子键合
无机化学
工作(物理)
硫化物
化学物理
堆栈(抽象数据类型)
钙钛矿(结构)
陶瓷
氯化物
电荷(物理)
介孔材料
复合数
离子
电阻率和电导率
声子
异质结
光电子学
作者
Jiacong Li,Y Cao,Pushun Lu,Kehao Tao,Wujie Dong,Junchao Chen,W Tang,Z-F Yu,Hong Zhu,Fuqiang Huang
摘要
ABSTRACT The commercialization of all‐solid‐state batteries (ASSBs) is hindered by the lack of a solid electrolyte (SE) that simultaneously delivers high ionic conductivity, resilience to humidity, and efficient low‐temperature operation. Herein, we propose to develop solid‐state electrolytes (SEs) by reacting Li 2 CO 3 with chloride frameworks. The CO 3 2− group serves a dual function: it forms a rigid, hydrolysis‐resistant scaffold via non‐hydrolysable metal‐carbonate bonds, while its high polarizability and charge delocalization soften local phonon modes, significantly reducing the activation energy for Li + migration. Ta‐based SE achieves an ionic conductivity of 7.1 mS cm −1 at 25°C, ranking among the highest for amorphous SEs; Zr‐based SE retains 80% of its conductivity after direct exposure to humid air (20% RH, 2 h), outperforming commercial sulfide and halide counterparts. ASSBs employing these SEs demonstrate ultralong cycling stability (>1000 cycles with 90% capacity retention at 25°C) and unprecedented low‐temperature performance, operating effectively down to −60°C. This work establishes a generalizable design principle for next‐generation SEs that unify high conductivity, stability, and practicality.
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