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Treated carbon felt as electrode material in vanadium redox flow batteries: a study of the use of carbon nanotubes as electrocatalyst

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Abstract

Electrodes for large-scale usage in vanadium redox flow battery are usually fabricated without any electrocatalyst due to the lack of good, viable options. The best performance is achieved of carbon-based materials. Recently, some researchers have been reported regarding the use of carbon nanotube as the electrocatalyst in the vanadium redox flow batteries. However, these researches have been carried out without making any comparison between the performance of the traditional method and the carbon nanotube electrocatalyst. In the present study, the loading of multi-walled carbon nanotube, the acid–heat treatment, and their combination were used to modify the carbon felt electrode to be applied in the vanadium redox flow battery. The obtained results showed better electrochemical properties for acid–heat-treated carbon felt electrode compared to the carbon nanotube-loaded one. The best electrode was obtained for using in a vanadium redox flow battery in terms of electrochemical and surface properties after applying a combination of two modification strategies. Applying this proposed method in modification of the carbon felt electrode increased its hydrophilicity more than 17 times and its capability to absorb VOSO4 solution more than eight times. Also, the charge transfer resistance of a modified electrode, by the combination of the carbon nanotube and the acid–heat treatment, significantly decreased in both positive and negative poles of vanadium redox flow battery. Consequently, the exchange current density enhanced more than 100- and 175-fold in positive and negative poles, respectively, in comparison with carbon felt electrode.

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Correspondence to Sahar Rashid-Nadimi.

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Jelyani, M.Z., Rashid-Nadimi, S. & Asghari, S. Treated carbon felt as electrode material in vanadium redox flow batteries: a study of the use of carbon nanotubes as electrocatalyst. J Solid State Electrochem 21, 69–79 (2017). https://doi.org/10.1007/s10008-016-3336-y

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  • DOI: https://doi.org/10.1007/s10008-016-3336-y

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