电解质
阴极
电池(电)
材料科学
氧化还原
快离子导体
碘化物
电极
化学工程
动力学
无机化学
碘化钠
降级(电信)
纳米技术
导线
导电体
容量损失
工作温度
电化学
熔点
化学动力学
钾离子电池
化学
储能
作者
Shufeng Song,Hongyang Shan,Wei Xue,Zhixu Long,Chengtao Xiang,Weihua Liang,Chaohe Xu,Guangsheng Huang
摘要
Challenges such as polyselenide shuttling and poor reaction kinetics persist in sodium–selenium (Na–Se) batteries. While solid-state Na–Se batteries could potentially eliminate the shuttle effect, they have received limited attention due to poor solid–solid interfacial contact and intrinsically sluggish conversion kinetics. Herein, we report a solid-state Na–Se2I2 battery that employs a low-melting point Se2I2 molecular cathode and a tailored hybrid solid electrolyte. At an operating temperature above its melting point, liquid Se2I2 establishes favorable liquid–liquid interfaces and enables a facile liquid–solid conversion pathway. Furthermore, the sodium super ion conductor (NASICON)/poly(ethylene oxide) hybrid electrolyte simultaneously dissolves polyselenides to promote redox kinetics and physically blocks their shuttling to ensure cycling stability. As a result, a reversible six-electron conversion reaction is achieved, and the solid-state Na–Se2I2 battery delivers a high specific capacity of 336 mAh g−1 at 0.1 C and a stable cycling over 200 cycles with 88.2% capacity retention at 0.5 C. The electrochemically active Se2I2 molecular design opens an alternative chemistry for selenium-based electrodes and provides a promising direction for future solid-state battery research.
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