Facilitating interfacial stability via bilayer heterostructure solid electrolyte toward high-energy, safe and adaptable lithium batteries

• Main Authors: Sun, J., Yao, X., Li, Y., Zhang, Q., Hou, C., Shi, Qiuwei, Wang, H.
• 其他作者: School of Materials Science and Engineering
• 格式: Article
• 語言: English
• 出版: 2022
• 主題: Engineering::Materials; Bilayer Heterostructure Solid Electrolytes; Durable Solid-state Batteries
• 在線閱讀: https://hdl.handle.net/10356/155258
• 機構: Nanyang Technological University

Solid-state electrolytes are widely anticipated to enable the revival of high energy density and safe metallic Li batteries, however, their lower ionic conductivity at room temperature, stiff interfacial contact, and severe polarization during cycling continue to pose challenges in practical applications. Herein, a dual-composite concept is applied to the design of a bilayer heterostructure solid electrolyte composed of Li+ conductive garnet nanowires (Li6.75La3Zr1.75Nb0.25O12)/polyvinylidene fluoride-co-hexafluoropropylene (PVDF-HFP) as a tough matrix and modified metal organic framework particles/polyethylene oxide/PVDF-HFP as an interfacial gel. The integral ionic conductivity of the solid electrolyte reaches 2.0 × 10−4 S cm−1 at room temperature. In addition, a chemically/electrochemically stable interface is rapidly formed, and Li dendrites are well restrained by a robust inorganic shield and matrix. As a result, steady Li plating/stripping for more than 1700 h at 0.25 mA cm−2 is achieved. Solid-state batteries using this bilayer heterostructure solid electrolyte deliver promising battery performance (efficient capacity output and cycling stability) at ambient temperature (25 °C). Moreover, the pouch cells exhibit considerable flexibility in service and unexpected endurance under a series of extreme abuse tests including hitting with a nail, burning, immersion under water, and freezing in liquid nitrogen.