材料科学
卤化物
电解质
离子电导率
阴极
离子键合
电导率
失真(音乐)
格子(音乐)
离子
化学工程
化学物理
理论(学习稳定性)
无机化学
晶格常数
电阻率和电导率
导电体
化学稳定性
电荷密度
分析化学(期刊)
溶解过程
纳米技术
电阻抗
结构稳定性
作者
Qian Zhao,Weizong Wang,Cheng Ruan,Zhengping Ding,Peng Wei,Xiangqun Zhuge,Yurong Ren
标识
DOI:10.1021/acsami.5c19063
摘要
Developing advanced halide solid-state electrolytes (SSEs) with both high ionic conductivity and high-voltage stability is crucial for high-energy all-solid-state batteries (ASSBs). However, conventional strategies such as simple cation substitution or anion engineering for achieving these properties simultaneously often require compromising one for the other. Herein, a high-entropy strategy is employed to design and synthesize Li3–4xIn1–6xFexYxZr2xHf2xCl6 (0 ≤ x ≤ 0.05) through multication substitution in Li3InCl6 (LIC). Li2.92In0.88Fe0.02Y0.02Zr0.04Hf0.04Cl6 (HE-LIC) featuring moderate lattice distortion achieves the highest ionic conductivity of 1.136 mS cm–1 at 25 °C and improved high-voltage stability. Based on theoretical calculations and experimental findings, the tailored distortion elongates Li1–Cl bonds (2.6616 vs 2.6531 Å in LIC) to facilitate Li+ conduction, while confining Cl– distribution to inhibit oxidation. ASSBs with HE-LIC and LiCoO2 cathode deliver a discharge capacity of 151.13 mAh g–1 and 81.17% capacity retention after 100 cycles at 0.5 C under 4.5 V. Even at 4.6 V, a discharge capacity of 165.98 mAh g–1 with 80.63% retention after 50 cycles at 0.5 C is achieved. These findings demonstrate the potential of high-entropy-driven moderate lattice distortion for advanced SSEs in high-voltage ASSBs.
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