Unlocking Solid-State Sodium–Metal Batteries at −15 °C by Electrolyte Optimization and Interface Regulation

作者：Hongbin Chen, Tongyu Wang, Zhenjun Wang, Andong Li, Shangxu Cen, Zhiyong Mao, Jingjing Chen, Xinxin Wang, Chenlong Dong · 发表于：ACS Applied Materials & Interfaces · 年份：2024 · DOI：10.1021/acsami.4c16791 · 被引用次数：5 · 研究领域：Advanced Battery Materials and Technologies、Advancements in Battery Materials、Thermal Expansion and Ionic Conductivity

Beta-Al 2 O 3 -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-Al 2 O 3 electrolyte and weak solid–solid contact of the Na/Beta-Al 2 O 3 interface. Herein, an integrated strategy was developed via electrolyte optimization and interface regulation, in which Cu 2+ as a stabilizing agent was incorporated into Beta-Al 2 O 3 to improve density and ionic conductivity and the In 2 S 3 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 Na 2 S). 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 Na 3 V 2 (PO 4 ) 3 |Beta-Al 2 O 3 -0.5 wt .% Cu 2+ @In 2 S 3 |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.