材料科学
多硫化物
介孔材料
电解质
化学工程
纳米片
锂(药物)
异质结
催化作用
电化学
碳纤维
纳米技术
复合数
电极
化学
有机化学
光电子学
物理化学
复合材料
医学
工程类
内分泌学
作者
Xiang Li,Qinghua Guan,Zechao Zhuang,Yongzheng Zhang,Yuhang Lin,Jian Wang,Chunyin Shen,Hongzhen Lin,Yanli Wang,Liang Zhan,Licheng Ling
出处
期刊:ACS Nano
[American Chemical Society]
日期:2023-01-06
卷期号:17 (2): 1653-1662
被引量:120
标识
DOI:10.1021/acsnano.2c11663
摘要
Lithium–sulfur (Li–S) batteries exhibit unparalleled theoretical capacity and energy density than conventional lithium ion batteries, but they are hindered by the dissatisfactory "shuttle effect" and the sluggish conversion kinetics owing to the low lithium ion transport kinetics, resulting in rapid capacity fading. Herein, a catalytic two-dimensional heterostructure composite is prepared by evenly grafting mesoporous carbon on the MXene nanosheet (denoted as OMC-g-MXene), serving as interfacial kinetic accelerators in Li–S batteries. In this design, the grafted mesoporous carbon in the heterostructure can not only prevent the stack of MXene nanosheets with the enhanced mechanical property but also offer a facilitated pump for accelerating ion diffusion. Meanwhile, the exposed defect-rich OMC-g-MXene heterostructure inhibits the polysulfide shuttling with chemical interactions between OMC-g-MXene and polysulfides and thus simultaneously enhances the electrochemical conversion kinetics and efficiency, as fully investigated by in situ/ex situ characterizations. Consequently, the cells with OMC-g-MXene ion pumps achieve a high cycling capacity (966 mAh g–1 at 0.2 C after 200 cycles), a superior rate performance (537 mAh g–1 at 5 C), and an ultralow decaying rate of 0.047% per cycle after 800 cycles at 1 C. Even employed with a high sulfur loading of 7.08 mg cm–2 under lean electrolyte, an ultrahigh areal capacity of 4.5 mAh cm–2 is acquired, demonstrating a future practical application.
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