卤化物
纳米技术
材料科学
相容性(地球化学)
阴极
锂(药物)
电解质
离子电导率
快离子导体
电极
金属锂
工程物理
兴奋剂
电导率
作者
Kai Zhang,Songjia Kong,Keqi Chen,Siwen Zhang,Yanguang Li,Feipeng Zhao
标识
DOI:10.1021/acsaem.5c04039
摘要
The growing demand for high-energy-density batteries has positioned all-solid-state lithium batteries (ASSBs) as a leading technology with the potential for significant impact. As a key material for ASSBs, halide solid electrolytes (SEs) have emerged as a current research hotspot, especially for non-close-packed halide SEs with ultrahigh ionic conductivity (>10 mS cm –1 at room temperature). However, they still suffer from insufficient compatibility with high-voltage cathode materials (>4.3 V vs Li/Li + ) and poor reduction limit (>0.9 V vs Li/Li + ). Based on the recent advancements, those challenges have been alleviated through cation/anion regulation engineering and the introduction of extra interlayers. This review distinguishes itself from previous works by systematically examining interfacial failure mechanisms and modification strategies for emerging non-close-packed halide SEs. Surpassing conventional halide SEs with close-packed structures, the non-close-packed ones enable broader cationic/anionic doping versatility, including multi-element co-doping and facilitate the improvement of interfacial engineering through more diverse interlayers. This focused review is expected to inspire more research on improving the interfacial stability between non-close-packed halide SEs and electrode materials, which would promote the development of high-performance ASSBs.
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