Electrospun carbon nanofiber electrodes decorated with palladium metal nanoparticles : fabrication and characterization

A new method was investigated to produce a novel oxygen reduction electrode comprised of carbon nanofibers for use in polymer electrolyte membrane (PEM) fuel cells and metal-air batteries. The process involved electrospinning a solution of polymer (polyacrylonitrile), noble metal salt (palladium (II) acetate), and organic solvent (n,n- dimethylformamide) to fabricate a porous, non-woven, free-standing nanofiber mesh. Through experimentation with multiple variables, the optimal electrospinning parameters were quantified. Post-process heating of the electrospun nanofibers included stabilization in air environment at 280⁰C for 2 hours, followed by carbonization in grade 5.0 argon environment to temperatures between 800 and 1100⁰ C for times varying between 1 minute to 1.5 hours. The carbonization step served the purpose of converting insulating polymer into conductive amorphous carbon and precipitating nanoparticles of palladium in a homogeneous distribution throughout the electrode. The electrode was characterized using scanning electron microscopy (SEM), x-ray diffraction (XRD), transmission electron microscopy (TEM), microprobe station, and x-ray adsorption near edge structure (XANES). Electrochemical performance was characterized using cyclic voltammetry (CV), rotating disk electrode (RDE), and testing in a PEM fuel cell. It was demonstrated that palladium crystal size and particle size increased with heat treatment time and temperature. Lower concentrations of PAN in solution had the effect of thinner nanofibers (100-400nm diameters), which led to faster particle growth.

Department dc:contributor.department

Massachusetts Institute of Technology. Dept. of Mechanical Engineering.

Grantor dc:publisher

Massachusetts Institute of Technology

Year dc:date.issued

2005

Author dc:creator

• Kurpiewski, John Paul

Advisor dc:contributor.advisor

• Yang Shao-Horn.

• Mechanical Engineering.

Statement dc:rights

• M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.

Licence dc:rights.uri

• http://dspace.mit.edu/handle/1721.1/7582

Language dc:language.iso

eng

Handle dc:identifier.uri

http://hdl.handle.net/1721.1/32370

OAI identifier oai:identifier

oai:dspace.mit.edu:1721.1/32370