Cation‐Anion‐Engineering Modified Oxychloride Zr‐Based Lithium Superionic Conductors for All‐Solid‐State Lithium Batteries
Zongnan Li, Yongbiao Mu, Kunxi Lü, Guojian Kang, Ting Yang, Shuping Huang, Mingdeng Wei, Lin Zeng, Lin Zeng, Yafeng Li, Yafeng Li
Abstract
Abstract Within the family of halide solid electrolytes (SEs), Li 2 ZrCl 6 demonstrates high oxidative stability, cost‐effectiveness, and mechanical deformability, positioning it as a promising candidate for SEs. However, the application of Li 2 ZrCl 6 as a SEs was hindered by its low ionic conductivity at room temperature. Current strategies to enhance the ionic conductivity of Li 2 ZrCl 6 primarily are focused on single cation or anion sublattice‐engineering, each with distinct advantages and limitations. Here, we propose a novel cation and anion‐sublattice‐engineering strategy, termed CASE, to increase the amorphous content and thus enhance ionic conductivity. The incorporation of Cu 2+ and O 2− induces distinctive structural modifications within Li 2 ZrCl 6 . This structure corroborated through analytic data of X‐ray absorption spectroscopy, the neutron diffraction, and ab initio molecular dynamics. Consequently, the amorphous Li 2.1 Zr 0.95 Cu 0.05 Cl 4.4 O 0.8 achieves an enhanced ionic conductivity of 2.05 mS cm −1 at 25 °C. Furthermore, all‐solid‐state lithium batteries utilizing the amorphous Li 2.1 Zr 0.95 Cu 0.05 Cl 4.4 O 0.8 as an electrolyte and LiNi 0.83 Co 0.11 Mn 0.06 O 2 as a cathode exhibit a superior long‐term cycling stability retaining 90.3% of capacity after 1000 cycles at 2 C under room temperature, which are much higher than those of Zr‐based halide electrolytes in publications. Such a result might stimulate the development of more amorphous structures with high ionic conductivity in the CASE strategy.