材料科学
四方晶系
离子
电解质
快离子导体
硫化物
固溶体
溶解
降水
离子键合
相(物质)
结晶学
分析化学(期刊)
晶体结构
物理化学
化学
冶金
物理
气象学
有机化学
色谱法
电极
作者
Jongwook W. Heo,Abhik Banerjee,Kern Ho Park,Yoon Seok Jung,Seung‐Tae Hong
标识
DOI:10.1002/aenm.201702716
摘要
Abstract Sulfide Na‐ion solid electrolytes (SEs) are key to enable room‐temperature operable all‐solid‐state Na‐ion batteries that are attractive for large‐scale energy storage applications. To date, few sulfide Na‐ion SEs have been developed and most of the SEs developed contain P and suffer from poor chemical stability. Herein, discovery of a new structural class of tetragonal Na4−xSn1−xSbxS4 (0.02 ≤ x ≤ 0.33) with space group I41/acd is described. The evolution of a new phase, distinctly different from Na4SnS4 or Na3SbS4, allows fast ionic conduction in 3D pathways (0.2–0.5 mS cm−1 at 30 °C). Moreover, their excellent air stability and reversible dissolution in water and precipitation are highlighted. Specifically, TiS2/Na–Sn all‐solid‐state Na‐ion batteries using Na3.75Sn0.75Sb0.25S4 demonstrates high capacity (201 mA h (g of TiS2)−1) with excellent reversibility.
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