同核分子
材料科学
电解质
铜
催化作用
锂硫电池
同种类的
锂(药物)
硫黄
无机化学
金属锂
化学工程
有机化学
冶金
电极
分子
物理化学
化学
医学
物理
工程类
热力学
内分泌学
作者
Qin Yang,Shiying Shen,Zhiyuan Han,Guanwu Li,Dong Liu,Qingchun Zhang,Lixian Song,Xiaogang Wang,Guangmin Zhou,Yingze Song
标识
DOI:10.1002/adma.202405790
摘要
Lithium-sulfur (Li-S) batteries suffer from severe polysulfide shuttle, retarded sulfur conversion kinetics and notorious lithium dendrites, which has curtailed the discharge capacity, cycling lifespan and safety. Engineered catalysts act as a feasible strategy to synchronously manipulate the evolution behaviors of sulfur and lithium species. Herein, a chlorine bridge-enabled binuclear copper complex (Cu-2-T) is in situ synthesized in electrolyte as homogeneous catalyst for rationalizing the Li-S redox reactions. The well-designed Cu-2-T provides completely active sites and sufficient contact for homogeneously guiding the Li
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