激进的
硫黄
未成对电子
化学
金属
溶剂化电子
电解质
光化学
无机化学
放射分析
有机化学
物理化学
电极
作者
Xiaosheng Song,Chenxiao Wang,Zhengyuan Shen,Keying Guo,Jietao Wu,Zhijie Guo,Xiao Liu,Yong Zhao
出处
期刊:eScience
[Elsevier]
日期:2024-08-01
卷期号:4 (4): 100225-100225
被引量:22
标识
DOI:10.1016/j.esci.2023.100225
摘要
Free radicals can improve the reaction rate, but most of them are unstable due to unpaired electrons. Simultaneously maintaining their stability and activity is challenging. Herein, taking sulfur (S) radicals as an example, we propose a strategy in which solvated metal complexes constructed by Al(acetylacetonate)3 and different solvents can stabilize high concentrations of S radicals with good activity through ion–dipole interactions. Based on this strategy, it is first demonstrated that S4•− is selectively stabilized by controlling the configurations of the solvated complexes. As a result, the reaction rate of S↔Li2S is increased by 8 times, and the energy efficiency and rate capability of the Li–S batteries are significantly improved, especially the 5-fold increase in cell capacities at a low electrolyte/sulfur ratio. This work provides an important strategy in which solvated metal complexes balance the activity and stability of free radicals to accelerate reactions and their application in various fields.
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