4.8 Article

3D Graphene-Ni Foam as an Advanced Electrode for High-Performance Nonaqueous Redox Flow Batteries

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 9, Issue 27, Pages 22502-22508

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.7b04777

Keywords

nonaqueous redox flow battery; electrode; Ni metal foam; graphene; energy storage system

Funding

  1. Energy Efficiency & Resources Core Technology Program of the Korea Institute of Energy Technology Evaluation and Planning (KETEP) of the Ministry of Trade, Industry, and Energy, Republic of Korea [20162020107060, 20152000000350]
  2. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education [NRF-2016R1D1A1B01015557]
  3. Korea Evaluation Institute of Industrial Technology (KEIT) [20162020107060, 20152000000350] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Electrodes composed of multilayered graphene grown on a metal foam (GMF) were prepared by directly growing multilayer graphene sheets on a three-dimensional (3D) Ni-foam substrate via a self-catalyzing chemical vapor deposition process. The multilayer graphene sheets are successfully grown on the Ni-foam substrate surface, maintaining the unique 3D macroporous structure of the Ni foam. The potential use of GMF electrodes in nonaqueous redox flow batteries (RFBs) is carefully examined using [Co(bpy)(3)](+/2+) and [Fe(bpy)(3)](2+/3+) redox couples. The GMF electrodes display a much improved electrochemical activity and enhanced kinetics toward the [Co(bpy)(3)](+/2+) (anolyte) and [Fe(bpy)(3)](2+/3+) (catholyte) redox couples, compared with the bare Ni metal foam electrodes, suggesting that the 2D graphene sheets having lots of interdomain defects provide sufficient reaction sites and secure electric-conduction pathways. Consequently, a nonaqueous RFB cell assembled with GMF electrodes exhibits high Coulombic and voltage efficiencies of 87.2 and 90.9%, respectively, at the first cycle. This performance can be maintained up to the 50th cycle without significant efficiency loss. Moreover, the importance of a rational electrode design for improving electrochemical performance is addressed.

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