快离子导体
氧化还原
电解质
离子键合
阴极
固态
电池(电)
材料科学
离子
离子电导率
无机化学
储能
商业化
能量密度
化学工程
化学
工程物理
物理化学
电极
热力学
物理
有机化学
功率(物理)
工程类
法学
政治学
作者
Guangxing Zhang,Zhantao Liu,Yifan Ma,Jakub Pepas,Jianming Bai,Hui Zhong,Yuanzhi Tang,Hailong Chen
标识
DOI:10.1021/acs.chemmater.4c01385
摘要
Solid electrolytes are one of the key challenges that hinder the commercialization of all-solid-state batteries. Most efforts have been made to advance the development of solid electrolytes as separators, while the development of catholytes, particularly redox-active catholytes, has been less extensively studied. The high loading of catholytes in composite cathodes, while facilitating ionic conduction, drastically decreases the energy density of the battery. Here, we report an alternative strategy to improve the energy density by using Li2.9Fe0.9Zr0.1Cl6 as a redox-active catholyte. With a composite cathode containing uncoated LiCoO2 and Li2.9Fe0.9Zr0.1Cl6, the solid-state cell not only shows excellent rate capability and stable long-term cycling, benefiting from the high ionic conductivity of Li2.9Fe0.9Zr0.1Cl6, but also shows a high cathode specific capacity of ∼153 mAh·g-1. This study broadens the chemical space of the materials design for lithium-ion conductors with redox-active elements (e.g., Fe, Ti, V, and Cr), offering new opportunities to reduce the cost and improve the energy density for all-solid-state batteries.
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