Beta-Al2O3-based solid-state sodium metal batteries are some of the best options for large-scale energy storage systems because of their high energy density, high-level safety, and low cost. Nevertheless, their room-/low-temperature operation remains challenging due to low ionic conductivity of Beta-Al2O3 electrolyte and weak solid-solid contact of the Na/Beta-Al2O3 interface. Herein, an integrated strategy was developed via electrolyte optimization and interface regulation, in which Cu2+ as a stabilizing agent was incorporated into Beta-Al2O3 to improve density and ionic conductivity and the In2S3 interface layer was introduced between the Na anode and solid electrolyte to induce the in situ formation of a mixed conductive layer (Na-In alloy and Na2S). The integrated strategy bolstered the interfacial electrochemical stability and promoted fluent Na+ transport, allowing the symmetric battery to cycle steadily for more than 2670 h at room temperature with a current density of 0.2 mA cm-2. Impressively, it demonstrated remarkable endurance, cycling at 0.025 mA cm-2 for more than 3315 h at -15 °C. The Na3V2(PO4)3|Beta-Al2O3-0.5 wt.% Cu2+@In2S3|Na full battery demonstrated outstanding cyclic stability and rate performance at -15 °C and room temperature, underscoring its potential for low-temperature solid-state sodium-metal batteries.
Keywords: Beta-Al2O3 electrolyte; Mixed conductive layer; Na dendrites; Solid-state sodium−metal batteries; ion doping.