Exploration of the active center structure of nitrogen-doped graphene-based catalysts for oxygen reduction reaction

We present two different ways to fabricate nitrogen-doped graphene (N-graphene) and demonstrate its use as a metal-free catalyst to study the catalytic active center for the oxygen reduction reaction (ORR). N-graphene was produced by annealing of graphene oxide (G-O) under ammonia or by annealing...

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Bibliographic Details
Main Authors: Lai, Linfei, Potts, Jeffrey R., Zhan, Da, Wang, Liang, Poh, Chee Kok, Tang, Chunhua, Ruoff, Rodney S., Gong, Hao, Shen, Zexiang, Lin, Jianyi
Other Authors: School of Physical and Mathematical Sciences
Format: Journal Article
Language:English
Published: 2013
Online Access:https://hdl.handle.net/10356/98056
http://hdl.handle.net/10220/13284
Description
Summary:We present two different ways to fabricate nitrogen-doped graphene (N-graphene) and demonstrate its use as a metal-free catalyst to study the catalytic active center for the oxygen reduction reaction (ORR). N-graphene was produced by annealing of graphene oxide (G-O) under ammonia or by annealing of a N-containing polymer/reduced graphene oxide (RG-O) composite (polyaniline/RG-O or polypyrrole/ RG-O). The effects of theNprecursors and annealing temperature on the performance of the catalyst were investigated. The bonding state of the N atom was found to have a significant effect on the selectivity and catalytic activity for ORR. Annealing of G-O with ammonia preferentially formed graphitic N and pyridinic N centers, while annealing of polyaniline/RG-O and polypyrrole/RG-O tended to generate pyridinic and pyrrolic N moieties, respectively.Most importantly, the electrocatalytic activity of the catalyst was found to be dependent on the graphitic N content which determined the limiting current density, while the pyridinicNcontent improved the onset potential forORR.However, the totalNcontent in the graphene-based non-precious metal catalyst does not play an important role in the ORR process.