卤化物
离子键合
钠
离子
离子电导率
无定形固体
材料科学
固态
无机化学
化学工程
化学
化学物理
物理化学
结晶学
有机化学
电解质
冶金
电极
工程类
作者
Meng Wu,Xinyu Liu,Hong Liu,Dabing Li,Xiang Qi,Jianrong Zeng,Lei Gao,Ce‐Wen Nan,Li‐Zhen Fan
标识
DOI:10.1038/s41467-025-58113-w
摘要
Abstract Designing halide solid electrolytes (SEs) with high ionic conductivity and good (electro)chemical stability is essential for the advancement of all-solid-state sodium-ion batteries (ASSIBs). Unfortunately, most sodium-based halide SEs experience limited ionic conductivities and ambiguous correlation between their structure features and ion transport properties. Here we report a novel strategy to significantly boost the conductivities of sodium halides by regulating vacancy and charge carrier concentrations through a facile NaCl-poor method. This approach achieves a balanced structure with optimal vacancy and carrier content, rendering several-fold conductivities enhancement of series sodium halides. Furthermore, a fluorination-induced amorphization protocol is employed to enhance (electro)chemical stability and interfacial compatibility without detrimentally influencing conductivities. When paired with an uncoated Na3V2(PO4)3 cathode and a Na3PS4-coated Na15Sn4 anode, the Na0.5ZrCl4F0.5 catholyte enables the battery to run for 300 cycles, retaining 94.4% of its initial discharge capacity at room temperature. This study provides a versatile pathway for creating inorganic ion conductors with high conductivity and long-term cyclability, advancing the development of ASSIBs.
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