So far, all-solid-state batteries have generally been powered using inorganic sulfides/oxides or polymer-based electrolyte. In addition to these conventional approaches, solid-state Li-ion conductors based on porous crystalline materials (i. e. covalent organic frameworks (COFs) and metal–organic frameworks (MOFs)) have garnered attention due to their directional ion conduction pathways through the ordered pores and versatile structural design. Porous crystalline materials, however, additionally incorporate lithium salts and/or solvents inside the pores of frameworks so that these COFs or MOFs act as conducting medium, not solid-state ion conductors in specific. Herein, we demonstrate a lithium sulfonated covalent organic framework (denoted as TpPa-SO3Li) as a solvent-free, single lithium-ion conductors. Benefiting from the well-designed directional ion channels, high number density of lithium-ions, and covalently tethered anion groups, TpPa-SO3Li exhibits an ionic conductivity of 2.7 × 10–5 S cm–1 with a lithium-ion transference number of 0.9 at room temperature, and an activation energy of 0.18 eV. Moreover, unusual ion transport phenomena of TpPa-SO3Li allow reversible and stable lithium plating/stripping on lithium metal electrodes. These features show promising results to be adopted in next-generation all-solid-state batteries and also demonstrate potential usage for lithium metal batteries.
