电解质
固态
阴极
材料科学
准固态
快离子导体
化学工程
纳米技术
电极
工程物理
工程类
电气工程
化学
色素敏化染料
物理化学
作者
Fang Hao,Xiaowei Chi,Yanliang Liang,Ye Zhang,Rong Xu,Hua Guo,Tanguy Terlier,Hui Dong,Kejie Zhao,Jun Lou,Yan Yao
出处
期刊:Joule
[Elsevier BV]
日期:2019-04-19
卷期号:3 (5): 1349-1359
被引量:111
标识
DOI:10.1016/j.joule.2019.03.017
摘要
Summary Attaining stable active material-solid electrolyte interfaces is a great challenge in sulfide-based all-solid-state sodium batteries (ASSSBs). A resistive layer forms at the interface upon charging above the anodic stability potential of sulfide electrolytes. In addition, contact failure at the interface during cycling is long known, but a fundamental solution is not yet available. Herein, we use an organic cathode material, pyrene-4,5,9,10-tetraone (PTO), to enable high-performance ASSSBs. We report, for the first time, a reversible active material-electrolyte interfacial resistance evolution during cycling. We further show for the first time that a low-modulus cathode material such as PTO maintains intimate interfacial contact with solid electrolytes during cycling, thus improving cycle life. The PTO-based cells exhibit a high specific energy (587 Wh kg−1) and a record cycling stability (500 cycles) among ASSSBs. This work reveals an effective cathode material design strategy toward compatibility with solid electrolytes and thus high-performance ASSSBs.
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