过电位
电解质
硫化物
阴极
电化学
电池(电)
锂(药物)
快离子导体
材料科学
硫化铁
离子
化学
氧化还原
锂离子电池
电压
复合数
电流密度
化学工程
无机化学
电荷(物理)
硫黄
分解
锂电池
硫化铜
充电周期
钠离子电池
电极
作者
Chenxin Huang,Junsheng Fan,Wenxuan Sun,Yongzhu Fu,Wei Guo
出处
期刊:Small methods
[Wiley]
日期:2025-09-20
卷期号:9 (11): e01077-e01077
被引量:1
标识
DOI:10.1002/smtd.202501077
摘要
Abstract Lithium sulfide (Li 2 S), as one of the critical cathodes in all‐solid‐state batteries, shows promising potential. However, its ion and electron blocking characteristics necessitate a high charge overpotential for activation, which can result in the decomposition of sulfide‐based solid‐state electrolytes. In this study, diphenyl chalcogenides are applied as redox mediators to reduce the initial charge voltage and improve the utilization of Li 2 S in all solid‐state lithium‐sulfur batteries. Among them, diphenyl ditelluride (DPDTe) enables the highest initial charge capacity (963.1 mAh g −1 ) of Li 2 S. The Li 2 S‐DPDTe composite cathode, along with Li 7 P 3 S 11 sulfide electrolyte and In‐Li anode, exhibits a low charge voltage of 2.4 V. After 360 cycles, the battery demonstrates an average areal discharge capacity of 0.9 mAh cm −2 at a current density of 0.2 mA cm −2 (706.8 mAh g −1 based on the mass of Li 2 S). This study aims to use diphenyl chalcogenides as mediators to lower the initial overpotential of Li 2 S, thereby aligning with the narrow electrochemical window of sulfide electrolytes and providing valuable insights for high‐energy‐density all‐solid‐state batteries.
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