双功能
电解质
惰性
材料科学
溶解
锂(药物)
阳极
化学工程
溶剂
无机化学
氧化还原
储能
能量密度
硫黄
卤素
阴极
工作(物理)
电池(电)
惰性气体
离子键合
作者
Peng Wang,Songke Nie,Yike Liu,Na Li,Jiawei Xu,Jinxin Liu,Shu Hong,Jiahao Zhu,Zaowen Zhao,Xiaodong Shi
标识
DOI:10.1002/adfm.202531300
摘要
ABSTRACT Lithium‐sulfur (Li‐S) batteries represent a promising energy storage technology owing to their high energy density and environmental compatibility. However, their practical implementation has been hindered by the growth of lithium dendrites and the accumulation of inactive sulfur species on lithium anode surfaces. NH 4 I is introduced as a bifunctional electrolyte additive to address these issues. Both theoretical and experimental analyses demonstrate that NH 4 + coordinates with solvent molecules, reduces the desolvation energy barrier of Li + , and promotes uniform lithium deposition. Furthermore, during cycling, the reversible I − /I 3 − redox couple reacts with inert lithium sulfides (Li 2 S/Li 2 S 2 ), dissolving them into the electrolyte to alleviate interfacial issues and reduce irreversible active material loss. Consequently, the NH 4 I‐containing electrolyte enables Li‐S batteries to achieve a high reversible capacity of 1097.78 mAh g −1 , and the corresponding capacity retention ration increases from 62.43% to 80.02% after 100 cycles at 0.5C. Moreover, when cycling at 1C for 500 cycles, the capacity attenuation per cycle was only 0.067%. This work gives a novel electrolyte design strategy for long life Li‐S batteries.
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