Facile synthesis of Cu sub(2)O/CuO/RGO nanocomposite and its superior cyclability in supercapacitor

A reduced graphene oxide (RGO)-based nanocomposite of redox counterpart of the oxides of Cu(I)-Cu(II) pair for Faradaic reaction, Cu sub(2)O/CuO/RGO, was controllably synthesized through a facile, eco-friendly one-step hydrothermal-assisted redox reaction of elemental Cu and graphene oxide (GO) with...

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Veröffentlicht in:Electrochimica acta 2015-01, Vol.152, p.433-442
Hauptverfasser: Wang, Kun, Dong, Xiangmao, Zhao, Chongjun, Qian, Xiuzhen, Xu, Yunlong
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Sprache:eng
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Zusammenfassung:A reduced graphene oxide (RGO)-based nanocomposite of redox counterpart of the oxides of Cu(I)-Cu(II) pair for Faradaic reaction, Cu sub(2)O/CuO/RGO, was controllably synthesized through a facile, eco-friendly one-step hydrothermal-assisted redox reaction of elemental Cu and graphene oxide (GO) without the addition of any other reagents. The resultant Cu sub(2)O/CuO/RGO nanocomposites were characterized by X-ray diffraction (XRD), Raman spectroscopy, Thermogravimetric analysis (TG), X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscopy (FESEM), and transmission electron microscopy (TEM). It is found that, when dealloyed nanoporous Cu was used as a Cu source, the uniform spherical Cu sub(2)O/CuO nanoparticles with double size scales ( similar to 25 nm and similar to 5 nm) were anchored on RGO sheets. This Cu sub(2)O/CuO/RGO nanocomposite redox counterpart exhibits improved rate capability and excellent cycling stability, i.e., only ca. 21.4% of the capacity was lost when the discharge current density increases from 1 A g super(-1) (173.4 F g super(-1)) to 10 A g super(-1) (136.3 F g super(-1)). Especially, the capacity remains almost unchanged (98.2%) after 100,000 cycles at 10 A g super(-1). The good electrochemical performance and simple accessibility prove that this Cu sub(2)O/CuO/RGO composite consisting of a pair of redox counterparts is a promising material for supercapacitor applications.
ISSN:0013-4686
DOI:10.1016/j.electacta.2014.11.171