期刊
SMALL
卷 17, 期 44, 页码 -出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202101845
关键词
binder-free cathodes; cuprous sulfide; hierarchical nanoporous arrays; hybrid magnesium-based batteries
类别
资金
- National Science Fund for Distinguished Young Scholars [51625102]
- National Natural Science Foundation of China [51971065]
- Innovation Program of Shanghai Municipal Education Commission [2019-01-07-00-07-E00028]
This study presents a novel cathode material for magnesium/lithium hybrid batteries, exhibiting high initial and reversible specific capacity, as well as exceptional cycling stability. Utilizing the hierarchical nanoporous array architecture and self-assembly feature, this material provides a guide for designing hierarchical nanoporous materials derived from metal-organic frameworks, and offers a novel strategy of in situ formation for fabricating binder-free cathodes.
On account of easy accessibility, high theoretical volumetric capacity and dendrite-free magnesium (Mg) anode, Mg battery has a great promise to be next generation rechargeable batteries, yet still remains a challenging task in acquiring fast Mg2+ kinetics and effective cathode materials. Herein, hierarchical 3D cuprous sulfide porous nanosheet decorated nanowire cluster arrays with robust adhesion on copper foam (Cu2S HP/CF), which is employed as a binder-free conversion cathode material for magnesium/lithium hybrid battery, delivering impressively initial and reversible specific capacity of 383 and 311 mAh g(-1) at 100 mA g(-1), respectively, which are obviously outperformed corresponding powder cathode in a traditional method by using polymer binder, is reported. Intriguingly, benefiting from the hierarchical nanoporous array architecture and self-assembly feature, Cu2S HP/CF cathode shows a remarkable cycling stability with a high capacity of 129 mAh g(-1) at 300 mA g(-1) over 500 cycles. This work not only highlights a guide for designing hierarchical nanoporous materials derived from metal-organic frameworks, but also provides a novel strategy of in situ formation to fabricate binder-free cathodes.
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