In Situ Synthesis of Vertical Standing Nanosized NiO Encapsulated in Graphene as Electrodes for High‐Performance Supercapacitors

NiO is a promising electrode material for supercapacitors. Herein, the novel vertically standing nanosized NiO encapsulated in graphene layers (G@NiO) are rationally designed and synthesized as nanosheet arrays. This unique vertical standing structure of G@NiO nanosheet arrays can enlarge the access...

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Veröffentlicht in:Advanced science 2018-03, Vol.5 (3), p.1700687-n/a
Hauptverfasser: Lin, Jinghuang, Jia, Henan, Liang, Haoyan, Chen, Shulin, Cai, Yifei, Qi, Junlei, Qu, Chaoqun, Cao, Jian, Fei, Weidong, Feng, Jicai
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Sprache:eng
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Zusammenfassung:NiO is a promising electrode material for supercapacitors. Herein, the novel vertically standing nanosized NiO encapsulated in graphene layers (G@NiO) are rationally designed and synthesized as nanosheet arrays. This unique vertical standing structure of G@NiO nanosheet arrays can enlarge the accessible surface area with electrolytes, and has the benefits of short ion diffusion path and good charge transport. Further, an interconnected graphene conductive network acts as binder to encapsulate the nanosized NiO particles as core–shell structure, which can promote the charge transport and maintain the structural stability. Consequently, the optimized G@NiO hybrid electrodes exhibit a remarkably enhanced specific capacity up to 1073 C g−1 and excellent cycling stability. This study provides a facial strategy to design and construct high‐performance metal oxides for energy storage. The novel vertical‐standing nanosized NiO encapsulated in graphene (G@NiO) is rationally designed and synthesized while maintaining the nanosheet morphology. This study feasibly offers insight into the in situ forming graphene on nanosized transition metal oxides (TMOs) particles directly as electrodes for maximizing their electrochemical performances, which may help to accelerate development of TMOs as electrode for high‐performance supercapacitors.
ISSN:2198-3844
2198-3844
DOI:10.1002/advs.201700687