期刊
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
卷 45, 期 11, 页码 6024-6035出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2019.12.178
关键词
Supercapacitor; Core-shell architecture; CoMoO4@CoS composite; Asymmetric supercapacitors; Energy density
资金
- Natural Science Foundation of Shanxi Province, China [201801D121100]
- Program for the Outstanding Innovative Teams of Higher Learning Institutions of Shanxi (OIT)
- Scientific and Technological Innovation Programs of Higher Education Institutions in Shanxi (STIP) [201802033]
- Collaborative Innovation Center for Shanxi Advanced Permanent Magnetic Materials and Technology [2016-06]
Engineering multicomponent active materials as an advanced electrode with the rational designed core-shell structure is an effective way to enhance the electrochemical performances for supercapacitors. Herein, three-dimensional self-supported hierarchical CoMoO4@CoS core-shell heterostructures supported on reduced graphene oxide/Ni foam have been rationally designed and prepared via a facile approach. The unique structure and the synergistic effects between two different materials, as well as excellent electronic conductivity of the reduced graphene oxide, contribute to the increased electrochemically active site and enhanced capacitance. The core-shell CoMoO4@CoS composite displays the superior specific capacitance of 3380.3 F g(-1) (1 A g(-1)) in the three-electrode system and 81.1% retention of the initial capacitance even after 6000 cycles. Moreover, an asymmetric device was successfully prepared using CoMoO4@CoS and activated carbon as positive/negative electrodes. It is worth mentioning that the device delivered the high energy density of 59.2 W h kg(-1) at the power density of 799.8 W kg(-1) and the excellent cycle performance (about 91.5% capacitance retention over 6000 cycles). These results indicate that the core-shell CoMoO4@CoS composites offers the novelty strategy for preparation of electrodes for energy conversion and storage devices. (C) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
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