4.8 Article

Ultrafast Self-Assembly of Graphene Oxide-Induced Monolithic NiCo-Carbonate Hydroxide Nanowire Architectures with a Superior Volumetric Capacitance for Supercapacitors

期刊

ADVANCED FUNCTIONAL MATERIALS
卷 25, 期 14, 页码 2109-2116

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.201404019

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资金

  1. Natural Science Foundation of China (NSFC) [21336001, U1203292]
  2. Fundamental Research Funds for the Central Universities [DUT14LAB06]
  3. Education Department of the Liaoning Province of China [T2013001]

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The monolithic electrodes with high volumetric capacitance demonstrate a great potential in practical industrial applications for supercapacitors. Herein, a novel strategy for ultrafast self-assembly of graphene oxides (GO)-induced monolithic NiCo-carbonate hydroxide (NiCo-CH) nanowire composite films (G-CH) is reported. The oxygen-containing functional groups on the GO surface help effectively to induce formation of the monodisperse NiCo-CH nanowires. Such a nanowire-shaped structure further functions as a scaffold and/or support, leading to 25 s of ultrafast self-assembly for G-CH composite films and a relatively loose and open channel that contributes to fast electrolyte transport. The as-obtained monolithic G-CH architectures show an excellent supercapacitor performance as binder-and conductive agent-free electrode, evidenced by a superior volumetric capacitance of 2936 F cm(-3) and good electrochemical stability. Combining highly conductive carbon nanotubes (CNTs) into the monolithic composite films can further create well-interconnected conductive networks within the electrode matrix, thus to improve the reaction kinetics and rate capability. The present strategy that can modulate the growth of the high-electroactive pseudocapacitive hydroxides and achieve an ultrafast self-assembly of monolithic composites may pave a promising new way for development of high-performance supercapacitors and shed a new light on the configuration of carbon-based electrode materials in energy storage and conversion devices.

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