电解质
离子电导率
锂(药物)
无机化学
电导率
金属
离子键合
材料科学
金属有机骨架
离解(化学)
化学工程
阴极
电化学
盐(化学)
化学
吸附
离子
电极
有机化学
物理化学
冶金
医学
工程类
内分泌学
作者
Youlan Zou,Zhuoran Ao,Zhehao Zhang,Nantao Chen,Haiyan Zou,Yiyang Lv,Yuxing Huang
标识
DOI:10.1016/j.ces.2023.118705
摘要
All-solid-state lithium metal batteries (ASSLMBs) are expected to provide a next-generation solution for energy storage. However, intrinsic low ionic conductivity of PEO-based electrolyte causes inferior capacity seriously hinders their widespread commercial application. Here, a new kind of solid electrolyte is explored by incorporation of PEO with metal–organic framework ZIF-67 to enhance the ionic conductivity to 1 × 10-4 S cm−1 at room temperature. Lewis acid-base interaction that forms between Co element and TFSI- promotes the dissociation of lithium salt and enhances Li+ transport. Moreover, NH bonds of ZIF-67 combine with the lone pair of electrons of O on the PEO segment to form hydrogen bonds (NH…O), reducing the strong interaction between Li+ and PEO. The cathode with 6 mg cm−2 of LiFePO4 loading delivers a high capacity of 129.7 mAhg-1 at 0.1C. Furthermore, the assembled batteries delivered a capacity of 147 mAhg-1 at room temperature after 300 cycles.
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