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Nanostructured Platinum and Carbon Supported Pt-Ni Catalyst for Polymer Electrolyte Fuel Cell
The Pt-Ni bimetallic nanoparticles supported on nano carbon (Pt x Ni y /C) have been synthesized by the polyol reduction under ultrasonic irradiation. The morphology, structure and specific area of synthesized materials were characterized by X-Ray diffraction (XRD), transmission electron microscopy...
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Main Authors: | , , |
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Format: | Conference Proceeding |
Language: | English |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | The Pt-Ni bimetallic nanoparticles supported on nano carbon (Pt
x
Ni
y
/C) have been synthesized by the polyol reduction under ultrasonic irradiation. The morphology, structure and specific area of synthesized materials were characterized by X-Ray diffraction (XRD), transmission electron microscopy (TEM), nitrogen adsorption (BET). The electrocatalytic activity for alcohol oxidation of the synthesized Pt
x
Ni
y
/C
materials and the commercial 10wt.% Pt loaded on activated carbon catalyst (Aldrich Sigma, Pt/C_com) was investigated by cyclic voltammetry (CV) and chronoamperometry (CA). The catalytic activity for oxygen reduction reaction (ORR) of Pt
x
Ni
y
/C was investigated by CV and linear sweep voltammetry (LSV). The major size of synthesized metallic particles was around 2 nm. The Pt
2
Ni
1
/C exhibited excellent catalytic properties for alcohol oxidation compared to other catalysts on the same support. The CNTs were found to be more effective than carbon Vulcan for use as a support for alcohol oxidation catalysts. The linear sweep voltammograms showed that Pt
x
Ni
y
/C, which has the least coverage of oxygenated species, was the best catalyst for ORR with its onset potential of 0.624 V. From the slope of Koutecky-Levich plot for ORR using Pt
x
Ni
y
/VC materials as catalysts it was found that the overall electron transfer number ranged from 3 to 4, leading to the suggestion of H
2
O
2
formation as an intermediate of the ORR. |
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ISSN: | 1938-5862 1938-6737 |
DOI: | 10.1149/06403.0171ecst |