Controlling the All-Solid Surface Reaction Between an Li1.3Al0.3Ti1.7(PO4)3 Electrolyte and Anode Through the Insertion of Ag and Al2O3 Nano-Interfacial Layers

Solid-state lithium batteries are considered ideal due to the safety of solid-state electrolytes. The Na superionic conductor-type Li1.3Al0.3Ti1.7(PO4)3 (LATP) is a solid electrolyte with high ionic conductivity, low cost, and stability. However, LATP is reduced upon contact with metallic lithium, leading to lithium dendrite growth on the anode during charging. In this study, LATP was synthesized, and the relationship between crystallinity and ionic conductivity was investigated at different heat treatment temperatures. Optimal sintering conditions and ionic conductivity were analyzed for sintering temperatures from 800 to 1000 °C. To suppress reactions with Li metal, 50 nm thick Ag and 10 nm thick Al2O3 layers were deposited on LATP via DC sputtering and plasma-enhanced atomic layer deposition. The electrochemical stability was tested under three conditions: uncoated LATP, Al2O3-coated LATP, and Ag+Al2O3-coated LATP. The stability improved in the following order: uncoated < Al2O3-coated < Ag+Al2O3-coated. The Al2O3 coating suppressed secondary phase formation by preventing direct contact between LATP and Li, while Ag coating mitigated charge concentration, inhibiting dendrite growth. These findings demonstrate that Ag and Al2O3 nano-layers enhance electrolyte stability, advancing solid-state battery reliability and commercialization.