Issue 21, 2012

Metal-free nitrogen-doped hollow carbon spheres synthesized by thermal treatment of poly(o-phenylenediamine) for oxygen reduction reaction in direct methanol fuel cell applications

Abstract

This study described a facile and effective route for the synthesis of structurally uniform and electrochemically active nitrogen-doped hollow carbon spheres (NHCSs) via pyrolysis of hollow poly(o-phenylenediamine) (PoPD) spheres. The characters and the mechanism of the transformation between the as-prepared PoPD and the NHCSs were studied. Results showed that the ladder aromatic structure of the as-prepared PoPD was transformed into a polycyclic-type structure in which nitrogen atoms were successfully incorporated into the graphitic structures to replace the carbon atoms. The as-prepared NHCSs showed a much higher electrocatalytic current than multi-wall carbon nanotubes and nitrogen-doped carbon nanotubes for the oxygen reduction reaction through a four-electron pathway in alkaline solution. The enhanced catalytic activity of NHCSs for ORR arose from the doping of nitrogen in the form of quaternary nitrogen, along with pyridinic N and pyrrolic N. The NHCSs also presented high methanol tolerance and long-term operational stability. The results showed that the NHCSs had a promising application in direct methanol fuel cells and provided a new method to synthesize carbon-based metal-free electrocatalysts from organic polymers.

Graphical abstract: Metal-free nitrogen-doped hollow carbon spheres synthesized by thermal treatment of poly(o-phenylenediamine) for oxygen reduction reaction in direct methanol fuel cell applications

Supplementary files

Article information

Article type
Paper
Submitted
09 Feb 2012
Accepted
28 Mar 2012
First published
29 Mar 2012

J. Mater. Chem., 2012,22, 10911-10917

Metal-free nitrogen-doped hollow carbon spheres synthesized by thermal treatment of poly(o-phenylenediamine) for oxygen reduction reaction in direct methanol fuel cell applications

Y. Li, T. Li, M. Yao and S. Liu, J. Mater. Chem., 2012, 22, 10911 DOI: 10.1039/C2JM30781B

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