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A novel approach to fabricate carbon sphere intercalated holey graphene electrode for high energy density electrochemical capacitors

机译:用于制造高能密度电化学电容器的碳球插入碳球的新方法

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摘要

Desirable porous structure and huge ion-accessible surface area are crucial for rapid electronic and ionic pathway electrodes in high-performance graphene-based electrochemical capacitors. However, graphene nanosheets tend to aggregate and restack because of van der Waals interaction among graphene sheets, resulting in the loss of ion-accessible surface area and unsatisfactory electrochemical performance. To resolve this daunting challenge, a novel approach is developed for the self-assembly of holey graphene sheets intercalated with carbon spheres (H-GCS) to obtain freestanding electrodes by using a simple vacuum filtration approach and a subsequent KOH activation process. Through the introduction of carbon spheres as spacers, the restacking of reduced graphene oxide (rGO) sheets during the filtration process is mitigated efficiently. Pores on rGO sheets produced by subsequent KOH activation also provide rapid ionic diffusion kinetics and high ion-accessible electrochemical surface area, both of which favor the formation of electric double-layer capacitance. Furthermore, a higher degree of graphitization of CSs in H-GCS thin film improves the electrical conductivity of the H-GCS electrode. The H-GCS electrode exhibits 207.1 F g(-1) of specific capacitance at a current density of 1 A g(-1) in 6 M KOH aqueous electrolyte. Moreover, the symmetric electrochemical capacitor assembled with H-GCS electrodes and organic electrolyte is capable of delivering a maximum energy density of 29.5 Wh kg(-1) and a power density of 22.6 kW kg(-1). (C) 2017 Elsevier B.V. All rights reserved.
机译:理想的多孔结构和巨大的离子可接近的表面积对于高性能石墨烯基电化学电容器中的快速电子和离子通路电极是至关重要的。然而,石墨烯纳米片倾向于聚集和恢复,因为石墨烯片之间的范德华相互作用,导致离子可接近的表面积和不令人满意的电化学性能的损失。为了解决这种艰难的挑战,开发了一种新的方法,用于通过使用简单的真空过滤方法和随后的KOH活化方法来获得独立的电极和随后的KOH活化过程来开发一种新的方法。通过引入碳球作为间隔物,有效地减轻了过滤过程中的石墨烯氧化物(RGO)片材的重新包装。随后的KOH活化产生的RGO片材上的孔还提供了快速的离子扩散动力学和高离子可接近的电化学表面积,这两者都赞成电动双层电容的形成。此外,H-GCS薄膜中的CSS的较高程度的石墨化改善了H-GCS电极的电导率。 H-GCS电极在6M KOH含水电解质中以1Ag(-1)的电流密度为207.1V(-1)特定电容。此外,与H-GCS电极和有机电解质组装的对称电化学电容器能够提供29.5WH kg(-1)的最大能量密度和22.6kg kg(-1)的功率密度。 (c)2017 Elsevier B.v.保留所有权利。

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