锂(药物)
材料科学
法拉第效率
电解质
金属锂
硼
共价键
离子电导率
多孔性
化学工程
阴极
无机化学
共价有机骨架
金属
离子键合
电导率
硼酸锂
枝晶(数学)
离子
电化学
金属有机骨架
磷酸钒锂电池
电阻率和电导率
作者
Ye Tian,Xiaolong Cheng,Lei Cheng,Y. L. Chang,Jixin Wu,Muhua Gu,Ki‐Taek Bang,Rui Wang,Ran Tao,Yufeng Wang,소순용,Yanming Wang,Yoonseob Kim
标识
DOI:10.1002/advs.202513879
摘要
ABSTRACT To advance lithium metal batteries, novel solid‐state electrolytes are crucial. Covalent Organic Frameworks (COFs) are promising due to their crystalline, porous structure, light composition, strong bonds, high surface area, and stability. COFs can be engineered for enhanced ion conduction, with their porosity and ion‐functional groups enabling fast ion movement and uniform lithium deposition. We synthesized a single‐crystalline 3D borate COF (B‐COF), achieving an ionic conductivity of 8.1 mS cm −1 at room temperature and a lithium‐ion transference number of 0.98 in a quasi‐solid‐state. In symmetric cells, B‐COF supported stable lithium deposition/stripping for 2000 h, suppressing dendrite formation. Full cells with LiFePO 4 cathodes cycled stably at 0.5C, delivering 147 mAh g −1 initial capacity, 91.8% retention, and 99.98% Coulombic efficiency over 600 cycles. These results highlight B‐COF's potential as a high‐performance solid electrolyte for lithium metal batteries.
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