电解质
离子电导率
材料科学
电化学
电池(电)
导电体
氧化物
快离子导体
纳米复合材料
锂(药物)
电导率
化学工程
电极
氟
离子键合
纳米技术
相间
无机化学
离子
电化学窗口
锂离子电池
电化学电池
锂电池
化学稳定性
电阻率和电导率
作者
Qiaodong Li,Jingming Yao,Yue Wang,Xinyu Liu,Jiuwei Lei,Wen Yin,Zhixuan Yu,Shaojie Wang,Li Li,Xinlin Yan,Zongpu Shao,Zhenyu Wang,Wei Xia,Yue Chen,Chuang Yu,Lin Wang,Bin Wen,Bo Xu,Jianyu Huang,Long Zhang
标识
DOI:10.1038/s41467-026-74773-8
摘要
The development of high-energy all-solid-state batteries is critically hindered by the electrochemical instability of solid electrolytes against high-voltage oxide positive electrodes. While fluorination is a promising strategy to enhance electrolyte stability, conventional methods are ineffective, resulting in insufficient fluorine content and a debilitating trade-off with ionic conductivity. Here, we report a solid-state anion-exchange strategy that overcomes these limitations by producing core-shell Li-fluoride/LiCl nanocomposite precursors. These precursors enable the synthesis of heavily fluorinated lithium-halide and lithium-sulfide electrolytes that combine high ionic conductivity with good oxidative stability. This stability originates from the formation of a robust, self-limiting LiF-rich interphase at the positive electrode. Consequently, an all-solid-state battery using a Li-rich oxide positive electrode achieves high performance, retaining over 77.5% capacity after 2000 cycles at a high rate of 3 C (1 C = 275 mA/g) and a 5.0 V cutoff. This anion-exchange approach is broadly applicable to other systems and establishes a versatile platform for designing advanced fluorinated materials for next-generation batteries. Conventional fluorination cannot resolve the stability/ion-transport trade-off in solid electrolytes. Here, authors report core-shell Li-fluoride/LiCl nanocomposite precursors to synthesize heavily fluorinated Li-halide and Li-sulfide electrolytes with both high ionic conductivity and good oxidative stability.
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