Effect of the support properties on the preparation and performance of platinum catalysts supported on carbon nanofibers

Platinum nanoparticles were supported on carbon nanofibers (CNFs) for their use as electrocatalyst for PEM fuel cells. Before platinum deposition, CNFs were oxidized using concentrated HNO 3 or a HNO 3–H 2SO 4 mixture as oxidizing agents. During these treatments, new surface oxygen groups were creat...

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Bibliographic Details
Published inJournal of power sources Vol. 192; no. 1; pp. 144 - 150
Main Authors Calvillo, L., Gangeri, M., Perathoner, S., Centi, G., Moliner, R., Lázaro, M.J.
Format Journal Article Conference Proceeding
LanguageEnglish
Published Amsterdam Elsevier B.V 01.07.2009
Elsevier
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Summary:Platinum nanoparticles were supported on carbon nanofibers (CNFs) for their use as electrocatalyst for PEM fuel cells. Before platinum deposition, CNFs were oxidized using concentrated HNO 3 or a HNO 3–H 2SO 4 mixture as oxidizing agents. During these treatments, new surface oxygen groups were created. Moreover, the most severe treatments resulted in the shortening of CNFs. Both effects allow to study the influence of both the morphology and the surface chemistry of CNFs on the preparation and performance of Pt electrocatalysts. Catalysts were prepared by the incipient wetness impregnation method. CNFs and electrocatalysts were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) and N 2-physisorption. Furthermore, the performance of Pt/CNF based electrodes was compared with that of a commercial Pt/carbon black electrode (E-TEK) in a 1-cm 2 PEM fuel cell. The results showed that both the surface chemistry and the morphology of the support have an important effect on the dispersion, particle size and activity of Pt catalysts. An increase in the agglomeration degree of Pt particles as the severity of oxidation treatments increased was observed. However, the performance of Pt/CNF electrodes was better than that of the commercial one. This was attributed to the CNF porous structure and to the better Pt–support interaction through the surface oxygen groups of the support.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0378-7753
1873-2755
DOI:10.1016/j.jpowsour.2009.01.005