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Nanoscale. 2016 Jun 16;8(24):12330-8. doi: 10.1039/c6nr02013e.

Hierarchical networks of redox-active reduced crumpled graphene oxide and functionalized few-walled carbon nanotubes for rapid electrochemical energy storage.

Author information

1
George W. Woodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, USA. seung.lee@me.gatech.edu.
2
Rare Metals Research Center, Korea Institute of Geoscience and Mineral Resources, Yuseong-gu, Deajeon 305-350, Korea. hdjang@kigam.re.kr and Department of Nanomaterials Science and Engineering, University of Science & Technology, Deajeon 305-350, Korea. hdjang@kigam.re.kr.
3
School of Chemical & Biomolecular Engineering, Center for Innovative Fuel Cell and Battery Technologies, Georgia Institute of Technology, Atlanta, GA 30332, USA.
4
Department of Applied Chemistry, Waseda University, 3-4-1 Okubo, Shinjuku-ku, Tokyo 169-8555, Japan.

Abstract

Crumpled graphene is known to have a strong aggregation-resistive property due to its unique 3D morphology, providing a promising solution to prevent the restacking issue of graphene based electrode materials. Here, we demonstrate the utilization of redox-active oxygen functional groups on the partially reduced crumpled graphene oxide (r-CGO) for electrochemical energy storage applications. To effectively utilize the surface redox reactions of the functional groups, hierarchical networks of electrodes including r-CGO and functionalized few-walled carbon nanotubes (f-FWNTs) are assembled via a vacuum-filtration process, resulting in a 3D porous structure. These composite electrodes are employed as positive electrodes in Li-cells, delivering high gravimetric capacities of up to ∼170 mA h g(-1) with significantly enhanced rate-capability compared to the electrodes consisting of conventional 2D reduced graphene oxide and f-FWNTs. These results highlight the importance of microstructure design coupled with oxygen chemistry control, to maximize the surface redox reactions on functionalized graphene based electrodes.

PMID:
27273722
DOI:
10.1039/c6nr02013e

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