快离子导体
材料科学
电解质
离子电导率
钠
电化学
碳化
无定形固体
化学工程
固态
电导率
无机化学
金属
离子键合
化学
离子
电极
冶金
物理化学
复合材料
结晶学
扫描电子显微镜
有机化学
工程类
作者
Qiangqiang Zhang,Yaxiang Lu,Weichang Guo,Yuanjun Shao,Lilu Liu,Jiaze Lu,Xiaohui Rong,Xiaogang Han,Hong Li,Liquan Chen,Yong‐Sheng Hu
标识
DOI:10.34133/2021/9870879
摘要
NASICON- (Na superionic conductor-) based solid-state electrolytes (SSEs) are believed to be attracting candidates for solid-state sodium batteries due to their high ionic conductivity and prospectively reliable stability. However, the poor interface compatibility and the formation of Na dendrites inhibit their practical application. Herein, we directly observed the propagation of Na dendrites through NASICON-based Na 3.1 Zr 2 Si 2.1 P 0.9 O 12 SSE for the first time. Moreover, a fluorinated amorphous carbon (FAC) interfacial layer on the ceramic surface was simply developed by in situ carbonization of PVDF to improve the compatibility between Na metal and SSEs. Surprisingly, Na dendrites were effectively suppressed due to the formation of NaF in the interface when molten Na metal contacts with the FAC layer. Benefiting from the optimized interface, both the Na||Na symmetric cells and Na 3 V 2 (PO 4 ) 3 ||Na solid-state sodium batteries deliver remarkably electrochemical stability. These results offer benign reference to the maturation of NASICON-based solid-state sodium batteries.
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