Molecular Connectors Boosting the Performance of MoS2 Cathodes in Zinc-Ion Batteries

被引:7
|
作者
Guo, Haipeng [1 ]
Montes-Garcia, Veronica [1 ]
Peng, Haijun [1 ]
Samori, Paolo [1 ]
Ciesielski, Artur [1 ]
机构
[1] Univ Strasbourg, CNRS, ISIS, 8 Allee Gaspard Monge, F-67000 Strasbourg, France
关键词
electrochemical reaction mechanism; molecular strategy; MoS2; zinc ion batteries; STORAGE; NANOSHEETS;
D O I
10.1002/smll.202310338
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Zinc-ion batteries (ZIBs) are promising energy storage systems due to high energy density, low-cost, and abundant availability of zinc as a raw material. However, the greatest challenge in ZIBs research is lack of suitable cathode materials that can reversibly intercalate Zn2+ ions. 2D layered materials, especially MoS2-based, attract tremendous interest due to large surface area and ability to intercalate/deintercalate ions. Unfortunately, pristine MoS2 obtained by traditional protocols such as chemical exfoliation or hydrothermal/solvothermal methods exhibits limited electronic conductivity and poor chemical stability upon charge/discharge cycling. Here, a novel molecular strategy to boost the electrochemical performance of MoS2 cathode materials for aqueous ZIBs is reported. The use of dithiolated conjugated molecular pillars, that is, 4,4 '-biphenyldithiols, enables to heal defects and crosslink the MoS2 nanosheets, yielding covalently bridged networks (MoS2-SH2) with improved ionic and electronic conductivity and electrochemical performance. In particular, MoS2-SH2 electrodes display high specific capacity of 271.3 mAh g(-1) at 0.1 A g(-1), high energy density of 279 Wh kg(-1), and high power density of 12.3 kW kg(-1). With its outstanding rate capability (capacity of 148.1 mAh g(-1) at 10 A g(-1)) and stability (capacity of 179 mAh g(-1) after 1000 cycles), MoS2-SH2 electrodes outperform other MoS2-based electrodes in ZIBs.
引用
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页数:9
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