阴极
电解质
材料科学
电池(电)
纳米技术
聚合物电解质
快离子导体
接口(物质)
电池容量
化学工程
复合材料
电极
电气工程
离子电导率
物理化学
化学
热力学
工程类
功率(物理)
毛细管作用
物理
毛细管数
作者
Hanwen An,Qingsong Liu,Biao Deng,Jian Wang,Menglu Li,Xin Li,Shuaifeng Lou,Jiajun Wang
标识
DOI:10.1002/adfm.202305186
摘要
Abstract The design of practical cathodes with high areal capacity in polymer‐based all‐solid‐state batteries remains challenged by the absence of an effective guiding principle that prolongs battery life‐span. Unlike liquid batteries, the notorious interface incompatibility between cathodes and electrolytes limited the cycling life of the all‐solid‐state batteries. Herein, this study proposes a dynamically stable cathode design with a fully covered surface, effectively mitigating interface failure and enabling the cyclic time of batteries with a cathode loading of 12.7 mg cm ‒2 over 10 000 h. This study unveils the importance of local state of charge in affecting the interfacial properties of particles through local oxidative‐stability of electrolytes on the interface. This study shows that the phenomena can be strongly influenced by the porosity of the cathode through the perspective of discreteness of ion transport. These insights and approach provide a broader promise for solid batteries for long lifetime.
科研通智能强力驱动
Strongly Powered by AbleSci AI