Cofactor-Assisted Artificial Enzyme with Multiple Li-Bond Networks for Sustainable Polysulfide Conversion in Lithium-Sulfur Batteries

被引:28
作者
Zhou, Suya [1 ]
Yang, Shuo [1 ,2 ]
Cai, Dong [1 ]
Liang, Ce [1 ]
Yu, Shuang [1 ]
Hu, Yue [1 ]
Nie, Huagui [1 ]
Yang, Zhi [1 ]
机构
[1] Wenzhou Univ, Key Lab Carbon Mat Zhejiang Prov, Wenzhou 325035, Peoples R China
[2] Wenzhou Univ, Coll Elect & Elect Engn, Wenzhou 325035, Peoples R China
基金
中国国家自然科学基金;
关键词
biomimetic catalysts; covalent amide bonds; FeN5 coordination structures; lithium-sulfur batteries; multiple Li-bond networks; PERFORMANCE; REDUCTION; INTERLAYER; POINTS;
D O I
10.1002/advs.202104205
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lithium-sulfur batteries possess high theoretical energy density but suffer from rapid capacity fade due to the shuttling and sluggish conversion of polysulfides. Aiming at these problems, a biomimetic design of cofactor-assisted artificial enzyme catalyst, melamine (MM) crosslinked hemin on carboxylated carbon nanotubes (CNTs) (i.e., [CNTs-MM-hemin]), is presented to efficiently convert polysulfides. The MM cofactors bind with the hemin artificial enzymes and CNT conductive substrates through FeN5 coordination and/or covalent amide bonds to provide high and durable catalytic activity for polysulfide conversions, while pi-pi conjugations between hemin and CNTs and multiple Li-bond networks offered by MM endow the cathode with good electronic/Li+ transmission ability. This synergistic mechanism enables rapid sulfur reaction kinetics, alleviated polysulfide shuttling, and an ultralow (<1.3%) loss of hemin active sites in electrolyte, which is approximate to 60 times lower than those of noncovalent crosslinked samples. As a result, the Li-S battery using [CNTs-MM-hemin] cathode retains a capacity of 571 mAh g(-1) after 900 cycles at 1C with an ultralow capacity decay rate of 0.046% per cycle. Even under raising sulfur loadings up to 7.5 mg cm(-2), the cathode still can steadily run 110 cycles with a capacity retention of 83%.
引用
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页数:13
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