插层(化学)
阴极
锂(药物)
离子电导率
电解质
氧化物
快离子导体
无定形固体
离子键合
化学
无机化学
能量转换
化学工程
能量转换效率
材料科学
物理化学
离子
有机化学
电极
热力学
医学
物理
光电子学
工程类
内分泌学
作者
X. H. Zhou,Ming Jiang,Yuhao Duan,Zhenghao Jia,Cheng Yuan,Kai Feng,Qiang Fu,Liang Zhang,Xiaofei Yang,Xianfeng Li
标识
DOI:10.1002/ange.202416635
摘要
Abstract All‐solid‐state lithium batteries (ASSLBs) with non‐flammable solid‐state electrolytes offer high energy density and enhanced safety. However, their energy densities are greatly limited by low‐capacity and low‐ionic‐conductivity oxide cathode materials, typically relying on the intercalation‐deintercalation mechanism with a catholyte content of 15–30 wt %. Here we introduce the Li x FeX x+2 (X=Cl, Br) families as high‐capacity and high‐ionic‐conductivity alternatives, operating via a 3 mol e − transfer intercalation‐conversion coupling reaction. Notably, the catholyte‐free ASSLBs using 95 wt % LiFeCl 3 active material delivers a remarkable capacity of 446 mAh g −1 and a high energy density of 912 Wh kg −1 , which surpasses most oxide cathode materials. Of particular interest is the formation of amorphous Fe during the conversion process. The amorphous Fe exhibits high activity, catalyzing the conversion of LiX back to Li x FeX x+2 , which proves instrumental in realizing reversible intercalation‐conversion reactions. These halide cathode materials represent a significant advancement towards high‐energy‐density ASSLBs.
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