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Interplay between porous texture and surface-active sites for efficient oxygen reduction reactions in N-inherited carbon.

Abstract

Nitrogen-doped porous carbon materials have excellent oxygen reduction reaction (ORR) activity due to their synergistic effect caused by the electron-accepting ability from the adjacent Sp2 bonded carbon atoms leading to the redistribution of charge density. However, the nitrogen doping in the carbon matrix usually involves a tedious chemical synthesis process with toxic compounds. So, the synthesis of nitrogen-doped carbon from nitrogen-containing biomass with simpler carbonization methods would be advantageous. Herein we report a facile synthesis of nitrogen-enriched porous activated carbon from mandarin peel biomass. The prepared carbon possesses uniform pore distribution, highly mesoporous and defective nature with enriched nitrogen and oxygen species over the carbon surface. The excellent ORR activity is confirmed from the rotating ring electrode (RDE) measurements. The onset potential of ORR is 0.83, 0.81, 0.87 V vs RHE and a half-wave potential is 0.7,0.71,0.75 V vs RHE for open-air, KOH and NaOH treated samples respectively. All samples follow the conventional four-electron transfer process with good stability in an alkaline medium. We have observed a correlation between the onset potential with a nitrogen content of carbon. Moreover, the kinetic current increases with an increase of specific surface area due to higher electrochemical active surface sites. The honeycomb-like morphology allows the electrolyte to penetrate through the porous network and enhance the ORR activity. This study reveals a trade-off between nitrogen content, porous texture, and surface-active sites.

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Supplementary files

Article information


Submitted
17 Feb 2020
Accepted
08 Apr 2020
First published
13 Apr 2020

New J. Chem., 2020, Accepted Manuscript
Article type
Paper

Interplay between porous texture and surface-active sites for efficient oxygen reduction reactions in N-inherited carbon.

D. Chinnadurai, R. rajendiran , S. Aravindharaja, H. Kim and K. Prabakar, New J. Chem., 2020, Accepted Manuscript , DOI: 10.1039/D0NJ00841A

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