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A facile design of Pt nanostructures from submonolayer to monolayer has been realized by ion adsorption–in situ electrochemical reduction on Au nanoparticles supported on multiwall carbon nanotubes (CNTs). The as prepared Au@Pt/CNTs catalysts display coverage-specific electrocatalysis. Au@Pt/CNTs with low Pt coverage is inactive towards methanol oxidation whereas it oxidizes formic acid effectively through a direct pathway with mass specific activity 90 times that of a commercial Pt/C catalyst. Due to its inertness to methanol, it shows high performance in the oxygen reduction reaction (ORR) with high methanol tolerance. In contrast, simply increasing the Pt coverage to above 40% switches the formic acid oxidation process to both direct and indirect catalytic pathways, and also results in high methanol oxidation activity.


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Facile design of Au@Pt core–shell nanostructures: Formation of Pt submonolayers with tunable coverage and their applications in electrocatalysis

Show Author's information Fulin ZhengWing-Tak Wong( )Ka-Fu Yung( )
Department of Applied Biology and Chemical Technology The Hong Kong Polytechnic UniversityHung Hom, Hong Kong SAR China

Abstract

A facile design of Pt nanostructures from submonolayer to monolayer has been realized by ion adsorption–in situ electrochemical reduction on Au nanoparticles supported on multiwall carbon nanotubes (CNTs). The as prepared Au@Pt/CNTs catalysts display coverage-specific electrocatalysis. Au@Pt/CNTs with low Pt coverage is inactive towards methanol oxidation whereas it oxidizes formic acid effectively through a direct pathway with mass specific activity 90 times that of a commercial Pt/C catalyst. Due to its inertness to methanol, it shows high performance in the oxygen reduction reaction (ORR) with high methanol tolerance. In contrast, simply increasing the Pt coverage to above 40% switches the formic acid oxidation process to both direct and indirect catalytic pathways, and also results in high methanol oxidation activity.

Keywords: electrocatalysis, platinum, submonolayer, fuel cell

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Publication history
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Acknowledgements

Publication history

Received: 08 July 2013
Revised: 04 December 2013
Accepted: 29 December 2013
Published: 29 January 2014
Issue date: March 2014

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© Tsinghua University Press and Springer-Verlag Berlin Heidelberg 2014

Acknowledgements

Acknowledgements

K. F. Yung and W. T. Wong acknowledge the financial support from Hong Kong Research Grants Council (RGC No. PolyU 5029/12P) and The Hong Kong Polytechnic University. F. Zheng acknowledges the postgraduate studentship from The Hong Kong Polytechnic University.

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