4.6 Article

Proposal of a Facile Method to Fabricate a Multi-Dope Multiwall Carbon Nanotube as a Metal-Free Electrocatalyst for the Oxygen Reduction Reaction

Journal

SUSTAINABILITY
Volume 14, Issue 2, Pages -

Publisher

MDPI
DOI: 10.3390/su14020965

Keywords

multiwall carbon nanotube; heteroatom doping; electrocatalyst; oxygen reduction reaction; fuel cell

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In this study, a one-pot, low-temperature synthesis method was used to fabricate heteroatom doped multiwall carbon nanotubes as electrocatalysts for oxygen reduction reaction. The characterization results showed that the doping of N, B, and S atoms increased the defects in the CNT structure, leading to improved electrochemistry performance and electron transfer rate. NB-MWCNT catalyst exhibited the best performance and electrochemical activity.
In this study, a one-pot, low-temperature synthesis method is considered for the fabrication of heteroatom dope multiwall carbon nanotubes (MWCNT). Doped MWCNT is utilized as an effective electrocatalyst for oxygen reduction reaction (ORR). Single, double, and triple doping of boron, nitrogen and sulfur elements are utilized as the dopants. A reflux system with temperature of 180 degrees C is implemented in the doping procedure. Actually, unlike the previous studies in which doping on the carbon structures was performed using a furnace at temperatures above 700 degrees C, in this green and sustainable method, the triple doping on MWCNT is conducted at atmospheric pressure and low temperature. The morphology and structure of the fabricated catalysts were evaluated by Fourier-transform infrared spectroscopy (FTIR), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM) and Raman spectroscopy. According to the results, the nanoparticles were encapsulated in the carbon nanotubes. Aggregated clusters of the sulfur in the case of S-MWCNT are considerable. Cyclic voltammetry (CV), rotating disk electrode, linear sweep voltammetry (LSV), and chronoamperometry electrochemical tests are employed for assessing the oxygen reduction activity of the catalysts. The results illustrate that by using this doping method, the onset potential shifts to positive values towards the oxidized MWCNT. It can be deduced that by doping the N, B, and S atoms on MWCNTs, the defects in the CNT structure, which serve as active sites for ORR application, increase. The N/S/B-doped graphitic layers have a more rapid electron transfer rate at the electrode/electrolyte interface. Thus, this can improve the electrochemistry performance and electron transfer of the MWCNTs. The best performance and electrochemical activity belonged to the NB-MWCNT catalyst (-0.122 V vs. Ag/AgCl). Also, based on the results gained from the Koutecky-Levich (KL) plot, it can be said that the ORR takes place through the 4 e(-) pathway.

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