摘要
Zr-based halide solid-state electrolytes (SSEs) hold significant commercial potential owing to their cost-effectiveness, excellent mechanical deformability, and superior oxidative stability. However, their practical applications are still hindered by limited room-temperature ionic conductivity and insufficient compatibility with high-voltage oxide cathodes. Here, a oxygen-doped high-entropy SSE (HESSEO, Li 2.89 Zr 0.72 Nb 0.07 Mo 0.07 Ta 0.07 Hf 0.07 Cl 4.9 O 1.1 ) was synthesized by introducing M (M = Nb, Mo, Ta, and Hf) and O ions into Li 2 ZrCl 6 (LZC), achieving a high ionic conductivity of 2.13 mS cm −1 at room temperature. Density functional theory (DFT) calculations confirmed that HESSEO exhibits higher Li + diffusion coefficients and lower diffusion barriers compared with those of LZC. All-solid-state batteries (ASSBs) with HESSEO demonstrated excellent long-term cycling stability, delivering an initial discharge capacity of 187.2 mAh g −1 and retaining 78.8% of the capacity after 1000 cycles at 2 C with the cutoff voltage of 4.3 V (vs. Li + /Li). Moreover, the batteries maintained stable operation for over 300 cycles even at 1 C with a higher cutoff voltage of 4.5 V. This multi-ion synergistic design provides a viable strategy to simultaneously enhance the ionic conductivity and high-voltage stability of halide SSEs, offering a practical approach for the development of commercially relevant ASSBs.
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