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Surface engineering of inorganic solid-state electrolytes via interlayers strategy for developing long-cycling quasi-all-solid-state lithium batteries

Lithium metal batteries (LMBs) with inorganic solid-state electrolytes are considered promising secondary battery systems because of their higher energy content than their Li-ion counterpart. However, the LMB performance remains unsatisfactory for commercialization, primarily owing to the inability...

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Detalles Bibliográficos
Autores principales: Kim, Ju-Sik, Yoon, Gabin, Kim, Sewon, Sugata, Shoichi, Yashiro, Nobuyoshi, Suzuki, Shinya, Lee, Myung-Jin, Kim, Ryounghee, Badding, Michael, Song, Zhen, Chang, JaeMyung, Im, Dongmin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9922298/
https://www.ncbi.nlm.nih.gov/pubmed/36774375
http://dx.doi.org/10.1038/s41467-023-36401-7
Descripción
Sumario:Lithium metal batteries (LMBs) with inorganic solid-state electrolytes are considered promising secondary battery systems because of their higher energy content than their Li-ion counterpart. However, the LMB performance remains unsatisfactory for commercialization, primarily owing to the inability of the inorganic solid-state electrolytes to hinder lithium dendrite propagation. Here, using an Ag-coated Li(6.4)La(3)Zr(1.7)Ta(0.3)O(12) (LLZTO) inorganic solid electrolyte in combination with a silver-carbon interlayer, we demonstrate the production of stable interfacially engineered lab-scale LMBs. Via experimental measurements and computational modelling, we prove that the interlayers strategy effectively regulates lithium stripping/plating and prevents dendrite penetration in the solid-state electrolyte pellet. By coupling the surface-engineered LLZTO with a lithium metal negative electrode, a high-voltage positive electrode with an ionic liquid-based liquid electrolyte solution in pouch cell configuration, we report 800 cycles at 1.6 mA/cm(2) and 25 °C without applying external pressure. This cell enables an initial discharge capacity of about 3 mAh/cm(2) and a discharge capacity retention of about 85%.