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A high-performance supercapacitor electrode based on tremella-like NiCO@NiO core/shell hierarchical nanostructures on nickel foam. | LitMetric

A high-performance supercapacitor electrode based on tremella-like NiCO@NiO core/shell hierarchical nanostructures on nickel foam.

Dalton Trans

State Key Laboratory on Integrated Optoelectronics, College of Electronic Science and Engineering, Jilin University, Changchun, Jilin 130012, PR China.

Published: February 2017

AI Article Synopsis

  • Researchers created tremella-like nickel oxalate@nickel oxide (NiCO@NiO) core/shell nanostructures on nickel foam using a hydrothermal method and electrochemical activation.
  • These structures act as effective binder-free electrodes for supercapacitors, improving energy storage capabilities.
  • The material shows impressive specific capacitance of 2287.09 F g, excellent cycling stability (95% after 10,000 cycles), and maintains 83.2% capacity retention when current density increases.

Article Abstract

Tremella-like nickel oxalate@nickel oxide (NiCO@NiO) core/shell hierarchical nanostructures have been successfully synthesized on nickel foam, using Ni foam as a current collector, a Ni source and a three-dimensional (3D) substrate, through a facile hydrothermal method followed by an electrochemical activation process. The prepared samples can be directly used as binder-free electrodes for supercapacitors. The tremella-like morphology, together with the NiCO nanoblocks on 3D Ni foam, significantly increases the amount of active sites for redox reactions and the conductivity of the electrode material, shortens the diffusion pathway for ions, facilitates the effective penetration of the electrolyte, and lowers the intrinsic equivalent series resistance, demonstrating good potential for energy storage application. This material has a high specific capacitance of 2287.09 F g at 1 A g, a good cycling stability (remaining 95% after 10 000 cycles) and a good rate capability (83.2% retention upon increasing the current density by 10 times).

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Source
http://dx.doi.org/10.1039/c6dt04500fDOI Listing

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