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Microwave synthesis and electrochemical performance of a PtPb alloy catalyst for methanol and formic acid oxidation
► Microwave was used to rapidly synthesize PtPb alloy catalyst for methanol and formic acid oxidation. ► A core–shell structure with Pt core and shell of PtPb alloying. ► PtPb/C catalyst has much higher catalytic activity compared with commercial Pt/C and PtRu/C catalysts. ► Prominent advantages are...
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Published in: | Electrochimica acta 2012-02, Vol.63, p.346-353 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | ► Microwave was used to rapidly synthesize PtPb alloy catalyst for methanol and formic acid oxidation. ► A core–shell structure with Pt core and shell of PtPb alloying. ► PtPb/C catalyst has much higher catalytic activity compared with commercial Pt/C and PtRu/C catalysts. ► Prominent advantages are excellent anti-poisoning ability and high stability. ► Peak current densities of methanol oxidation in 950th cycle on PtPb/C, PtRu/C and Pt/C are 870.6, 596.4 and 472.9mAmg−1Pt (or 4.53, 1.30 and 1.05mAcm−2), respectively.
A PtPb alloy catalyst with a uniform core–shell structure was synthesized in a two-step rapid microwave-assisted polyol process. The X-ray diffraction (XRD) and transmission electron microscopy (TEM) data demonstrate that the core of this catalyst is a Pt particle, and the shell or completely alloyed nanoparticles are composed of a PtPb alloy with an hcp structure. The average diameter of the catalyst is approximately 5.9nm. The PtPb alloy catalyst exhibits enhanced catalytic activity and durability for methanol or formic acid oxidation. The anodic peak current densities for methanol oxidation at the 950th cycle on PtPb/C, PtRu/C (JM) and Pt/C (JM) catalysts are 870.6, 596.4 and 472.9mAmg−1 Pt, respectively. The formation of large numbers of oxides on the PtPb/C catalyst surface can enhance the anti-poisoning ability and catalytic durability of the catalyst. |
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ISSN: | 0013-4686 1873-3859 |
DOI: | 10.1016/j.electacta.2011.12.112 |