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Taming Active Material-Solid Electrolyte Interfaces with Organic Cathode for All-Solid-State Batteries

delete2019-05-01
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OA
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F
Fang Hao
迟晓伟 (Xiaowei Chi)
Y
Yanliang Liang
Y
Ye Zhang
许瑞珍 cover
许瑞珍 (Rong Xu)
H
Hua Guo
T
Tanguy Terlier
H
Hui Dong
K
Kejie Zhao
J
Jun Lou
Y
Yan Yao *
DOI:10.1016/j.joule.2019.03.017delete
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Abstract

Abstract

En 中文
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.
Keywords:
SODIUM-ION BATTERIES
NA3PS4
CONDUCTION
DESIGN
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Joule
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Purdue University System
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