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首页> 外文期刊>Journal of Materials Chemistry, A. Materials for energy and sustainability >Porous nitrogen-rich carbon materials from carbon self-repairing g-C3N4 assembled with graphene for high-performance supercapacitor
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Porous nitrogen-rich carbon materials from carbon self-repairing g-C3N4 assembled with graphene for high-performance supercapacitor

机译:碳自修复g-C3N4与石墨烯组装而成的多孔富氮碳材料,可用于高性能超级电容器

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摘要

Nitrogen-rich carbon material derived from carbon self-repairing g-C3N4 is self-assembled with graphene oxide (GO) to form a porous structure. Different from the pristine g-C3N4, which has scarcely been employed in supercapacitors because of its low charge mobility, the carbon self-repairing g-C3N4 (C-C3N4) shows an improved electrochemical activity. After carbon-repairing, a delocalized big p-bond can be formed by the homogeneous C-substitution for N atoms or the formation of new interstitial C-N bond. The extending p-conjugation planar layer of C-C3N4 possesses a closer contact with GO to form a three-dimensional (3D) pore structure, which ensures good mobility for electrons and quick access for electrolytes. Under the optimum C-repairing content of 5.99 at%, the C-C3N4@rGO exhibited high specific capacity of 379.7 F g(-1) and energy density of 52.7 W h kg(-1) at a current density of 0.25 A g(-1). Moreover, the electrode kept 85% capacity retention after 10 000 cycles at a high constant current density of 10 A g(-1). The active sites of pseudocapacitance can be confirmed in the oxygen-containing groups and the carbon atoms close to the nitrogen by the XPS results.
机译:源自碳自我修复g-C3N4的富氮碳材料与氧化石墨烯(GO)进行自组装以形成多孔结构。不同于由于电荷迁移率低而几乎没有用于超级电容器的原始g-C3N4,碳自修复g-C3N4(C-C3N4)的电化学活性得到改善。碳修复后,可以通过对N原子进行均一的C取代或形成新的间隙C-N键来形成离域的大p键。 C-C3N4的扩展p共轭平面层与GO紧密接触,形成三维(3D)孔结构,从而确保了良好的电子迁移率和电解质的快速通道。在5.99 at%的最佳C修复含量下,C-C3N4 @ rGO在0.25 A g的电流密度下显示出379.7 F g(-1)的高比容和52.7 W h kg(-1)的能量密度。 (-1)。此外,在10 A g(-1)的高恒定电流密度下,10000次循环后,电极保持了85%的容量保持率。通过XPS结果,可以在含氧基团和接近氮的碳原子上确定假电容的活性位点。

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