材料科学
阴极
电解质
电池(电)
双层
电化学
离子
离子电导率
快离子导体
储能
锂(药物)
纳米技术
化学物理
化学工程
电极
膜
物理化学
化学
热力学
内分泌学
功率(物理)
工程类
有机化学
物理
医学
生物化学
作者
Chaoyi Yan,Ying Zhou,Hui Cheng,Raphael Orenstein,Pei Zhu,Özkan Yıldız,Philip D. Bradford,Jesse S. Jur,Nianqiang Wu,Mahmut Dirican,Xiangwu Zhang
标识
DOI:10.1016/j.ensm.2021.10.014
摘要
All-solid-state lithium (Li) batteries with high energy density are a promising solution for the next-generation energy storage systems in large-scale devices. To simultaneously overcome the challenges of poor ionic conduction of solid electrolytes and shuttling of active materials, we introduce a functional electrolyte-cathode bilayer framework with interconnected LLAZO channels from the electrolyte into the cathode for advanced solid-state Li-S batteries. Differing from the traditional solid-state batteries with separated layer compositions, the introduced bilayer framework provides ultrafast and continuous ion/electron conduction. Instead of transferring Li+ across the polymer and garnet phases which involve huge interfacial resistance, Li+ is directly conducted through the LLAZO channels created continuously from the cathode layer to the solid electrolyte layer, significantly shortening the diffusion distance and facilitating the redox reaction of sulfur and sulfides. A stable cycle life is demonstrated in the prototype Li-S solid-state batteries assembled with the introduced [email protected] interconnected bilayer framework. High capacity is obtained at room temperature, indicating the superior electrochemical properties of the bilayer framework that result from the unique design of the interconnected LLAZO garnet phase.
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