TY - JOUR
T1 - Na-K Interlayer Driven Na-NASICON Solid-State Batteries
AU - Li, Yang
AU - Wang, Zhichao
AU - Sun, Chen
AU - Liu, Shiqiao
AU - Dou, Yankun
AU - Yuan, Xuanyi
AU - Jin, Haibo
AU - Zhao, Yongjie
N1 - Publisher Copyright:
© 2025 Wiley-VCH GmbH.
PY - 2025
Y1 - 2025
N2 - Solid-state sodium batteries are deemed as a highly promising candidate for medium and long-term stationary energy storage. But, the solid-state electrolyte with desirable ionic conductivity and high stability against solid metal electrodes remains a significant challenge for the research and development of solid-state sodium metal batteries. In this research, the approach of in-situ formed Na-K interlayer is put forward, wherein K+ electrochemically migrates from the K-substituted NASICON-structure ceramic electrolyte toward the interface of ceramic electrolyte and Na metal electrode, locally and dynamically forming a Na-K interlayer with Na metal. Therefore, the compatibility between ceramic electrolytes and the Na electrode is obviously enhanced. Accordingly, the area specific resistance of the solid/solid interface contact gets reduced to 29.9 Ω cm2 and a high room temperature critical current density of 1.3 mA cm−2 is achieved. In the meantime, the Na/Na3Zr2Si2PO12-0.005K/Na can steadily operate for 1400 h at 0.2 mA cm−2. Moreover, NASICON-structure ceramic electrolyte-based solid-state sodium metal batteries paired with polyanion and layered sodium ion cathodes are constructed to highlight the superiority of this well-designed ceramic electrolyte/metal electrode interface.
AB - Solid-state sodium batteries are deemed as a highly promising candidate for medium and long-term stationary energy storage. But, the solid-state electrolyte with desirable ionic conductivity and high stability against solid metal electrodes remains a significant challenge for the research and development of solid-state sodium metal batteries. In this research, the approach of in-situ formed Na-K interlayer is put forward, wherein K+ electrochemically migrates from the K-substituted NASICON-structure ceramic electrolyte toward the interface of ceramic electrolyte and Na metal electrode, locally and dynamically forming a Na-K interlayer with Na metal. Therefore, the compatibility between ceramic electrolytes and the Na electrode is obviously enhanced. Accordingly, the area specific resistance of the solid/solid interface contact gets reduced to 29.9 Ω cm2 and a high room temperature critical current density of 1.3 mA cm−2 is achieved. In the meantime, the Na/Na3Zr2Si2PO12-0.005K/Na can steadily operate for 1400 h at 0.2 mA cm−2. Moreover, NASICON-structure ceramic electrolyte-based solid-state sodium metal batteries paired with polyanion and layered sodium ion cathodes are constructed to highlight the superiority of this well-designed ceramic electrolyte/metal electrode interface.
KW - in-situ
KW - Na-K interlayer
KW - NASICON-structure ceramic electrolyte
KW - sodium metal batteries
UR - http://www.scopus.com/inward/record.url?scp=85218822112&partnerID=8YFLogxK
U2 - 10.1002/adfm.202425995
DO - 10.1002/adfm.202425995
M3 - Article
AN - SCOPUS:85218822112
SN - 1616-301X
JO - Advanced Functional Materials
JF - Advanced Functional Materials
ER -