材料科学
弹性体
电解质
复合数
离子电导率
离子键合
复合材料
相容性(地球化学)
导电体
聚合物
热稳定性
储能
阴极
堆栈(抽象数据类型)
纳米技术
模数
电导率
化学工程
极限抗拉强度
化学稳定性
离子
硫化物
作者
Jiaxu Zhang,Shengjie Xia,Shutao Zhang,Zi Wang,Suzhe Liang,Chao Wang,Chao Wang,Pushun Lu,T Liu,Guantai Hu,Mingfeng Wei,Ruizhi Yu,Zhiyun Wu,Ximin Zhai,Deping Wang,Xueliang Sun,Changhong Wang,Changhong Wang
标识
DOI:10.1002/aenm.202504652
摘要
ABSTRACT All‐solid‐state batteries (ASSBs) hold significant promise as next‐generation energy storage systems due to their high energy density and intrinsic safety. However, their practical deployment is impeded by the need for high external pressure (typically tens of megapascals) to maintain solid–solid interfacial contact and ensure long‐term cycling stability. Here, we report an ionic elastomer specifically designed to enable stable ASSB operation under substantially reduced stack pressure. The elastomer combines a mechanically flexible polymer matrix with an ionically conductive phase, delivering high room‐temperature ionic conductivity (0.3 mS cm −1 ), a low elastic modulus (29.8 MPa), excellent thermal stability (≥400°C), and strong chemical compatibility with sulfide‐based solid‐state electrolytes (SSEs). When integrated with sulfide SSEs, the composite exhibits a remarkable room‐temperature ionic conductivity of 5.23 mS cm −1 . Incorporation of this composite into ASSBs with high‐nickel cathodes (Ni ≥ 90%) yields an initial capacity of 200 mAh g −1 at 0.05C and outstanding cycling stability over 700 cycles at 1C under a low stack pressure of just 5 MPa. This ionic‐elastomer strategy mitigates electrochemical‐mechanical degradation, eliminates the high‐pressure requirement, and offers a scalable pathway toward practical, durable ASSBs technologies.
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