potential applications in lithium-metal batteries (LiMBs) due to their high-energy densities and high-capacity with easy processability and lightweight. [1-5] Ceramic based electrolytes for LiMBs are real rising power sources for portable electronic, electrical, hybrid charged vehicles penetrating to heavy scale energy storage/ transportation systems owing to their safe electrochemical and high mechanical properties. [6-8] However, the applications of ceramic-based lithium-metal batteries with large capacities and power densities have been restricted due to interfacial incompatibility and thermal runway which further complicates the serious safety issues. [9,10] Therefore, extensive research has been devoted to overcome these issues, including the structural and interfacial design of ceramic electrolytes to face the key challenges of dendritic expansion and limiting the side reactions among Li-metal anode and electrolytes. [11,12] It is worth mentioning that the Li-metal is a supreme anode candidate for LiMBs to get the high energy density due to the large theoretical capacities (3860 mAh g −1) and the lowest negative potential (−3.040 V vs the hydrogen electrode). [13] Nevertheless, there is much harm when combining Li metal anode with conventional liquid electrolytes possesses (lowest unoccupied molecular orbital) lower to Fermi level of alkali metals anode, [14] such electrolytes can easily react with Li metal to form heterogeneous products and produce unstable Lithium-metal batteries (LiMBs) are promising energy storage devices due to the high capacity and minimum negative electrochemical potential. Nevertheless, their concrete applications remain disturbed by unbalanced electrolyte-electrode interfaces, limited electrochemical window, and high risk. Herein, a novel strategy to obtain dual ceramic-based electrolytes that possesses a great potential in energy storages and higher level of energy densities in LiMBs. Dual-ceramic (lithium aluminum titanium phosphate-lithium lanthanum titanium oxide (LATP-LLTO)) gel polymer electrolyte (DCGPE) film developed via the curable system aims to prepare flexible Li + interpenetrating network film to integrate the two ceramic structures with polyethylene oxide (PEO) to yield the free-standing electrolytes film for better battery safety and desired interfacial stability. The DCGPEs films present a satisfactory electrochemical performance, including good ionic conductivity, large transference number, and wide electrochemical stability window at room temperature. Most importantly, the fundamental function of LATP and LLTO is to support building a stable solid-electrolyte-interphase and limits the growth of dendrites. Thus, prepared dual ceramic-based electrolytes effectively render to inhibit lithium dendrite growth in a symmetrical cell Li//PEO + 10% LATP + 15% LLTO//Li test during charge/discharge at a current density of 2 and 0.25 mA cm −2 above 2400 h without short-circuiting occurrence at room temperature. Besides, the battery assembled of LiFePO 4 /PEO + 10% LATP + 20%...