材料科学
电解质
离子电导率
快离子导体
化学工程
电池(电)
无定形固体
电导率
复合数
储能
自行车
金属
钠
金属锂
离子键合
电极
电流密度
钠离子电池
容量损失
复合材料
工作(物理)
纳米技术
合金
能量密度
锂(药物)
无机化学
固溶体
作者
Anqi Zhu,Pengtao Qiu,Yang Luo,Feng Ning,Guang‐Jing Feng,Shujun Li,Liqing He,Yiying Wu,Xuenian Chen
标识
DOI:10.1021/acsami.6c10920
摘要
Solid-state sodium metal batteries are promising candidates for grid-scale energy storage due to their inherent safety and low cost. However, the development of solid electrolytes that support high-rate (>20 C) cycling for fast-charging applications remains a major challenge. Herein, we explore how adding SiO2 affects the ionic conductivity and dendrite suppression of NaB3H8, to develop superior solid electrolytes for high-rate batteries. The composites featuring an amorphous passivating layer with B-O bonds were fabricated via ball milling. Among them, NaB3H8-40%SiO2 exhibits the best conductivity, reaching 0.62 mS cm-1 at 25 °C, 2 orders of magnitude higher than that of pristine NaB3H8. Crucially, by reducing electronic conductivity and enhancing mechanical strength, it possesses a high critical current density of up to 6.5 mA cm-2, significantly higher than that of other reported hydridoborates. The Na/NaB3H8-40%SiO2/TiS2 batteries exhibit superior rate capability (216.4 mAh g-1 at 1 C and 143.1 mAh g-1 at 20 C) and long-term cycling stability (nearly 100.0% capacity retention after 2000 cycles at 20 C) at 30 °C. This work offers a promising approach for the development of innovative solid electrolytes in fast-charging or high-power-density sodium metal batteries.
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