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Hierarchical three-dimensional NiMoO.sub.4-anchored rGO/Ni foam as advanced electrode material with improved supercapacitor performance

Designing a novel, efficient and cost-effective nanocomposite with the advantage of robust structure and outstanding conductivity is highly promising for the electrode materials of high-performance supercapacitors. Herein, we designed and synthesized a hierarchical structured NiMoO.sub.4@rGO/NF via...

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Bibliographic Details
Published in:Journal of materials science 2018-06, Vol.53 (11), p.8483
Main Authors: Xu, Yuekui, Xuan, Haicheng, Gao, Jinhong, Liang, Ting, Han, Xiaokun, Yang, Jing, Zhang, Yongqing
Format: Article
Language:English
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Summary:Designing a novel, efficient and cost-effective nanocomposite with the advantage of robust structure and outstanding conductivity is highly promising for the electrode materials of high-performance supercapacitors. Herein, we designed and synthesized a hierarchical structured NiMoO.sub.4@rGO/NF via a facile and scalable approach by growing NiMoO.sub.4 nanowires onto the skeleton of reduced graphene oxide (rGO)/Ni foam (NF). The as-made NiMoO.sub.4@rGO/NF exhibits a superior electrochemical behavior owing to the coupling effect of homogeneous NiMoO.sub.4 nanowires and high conductivity of rGO, and it exhibits a superb capacitance value of 1877 F g.sup.-1 at 1 A g.sup.-1 and shows a ultralong life span with over 98% capacitance retention after 4000 cycles at 5 A g.sup.-1 in 2 M KOH electrolyte. Moreover, an asymmetric device employing NiMoO.sub.4@rGO/NF composite and activated carbon is assembled with an aqueous electrolyte, and it displays a maximum energy density of 40 Wh kg.sup.-1 at a specific power 218.2 W kg.sup.-1. Interestingly, the asymmetric device can remain 111.2% of its initial value even after 8000 charge/discharge cycles. These results demonstrate that the NiMoO.sub.4@rGO/NF binder-free electrode provides greatly enhanced electrochemical performance and shows promising application as an anode for energy storage.
ISSN:0022-2461
1573-4803
DOI:10.1007/s10853-018-2171-1