Study of Pd-Au/MWCNTs formic acid electrooxidation catalysts

被引:12
|
作者
Mikolajczuk, Anna [1 ]
Borodzinski, Andrzej [1 ]
Stobinski, Leszek [1 ,2 ]
Kedzierzawski, Piotr [1 ]
Lesiak, Beata [1 ]
Laszlo Koever [3 ]
Jozsef Toth [3 ]
Lin, Hong-Ming [4 ]
机构
[1] Polish Acad Sci, Inst Phys Chem, PL-01224 Warsaw, Poland
[2] Warsaw Univ Technol, Fac Mat Sci & Engn, PL-02507 Warsaw, Poland
[3] Hungarian Acad Sci ATOMKI, Inst Nucl Res, H-4001 Debrecen, Hungary
[4] Tatung Univ, Dept Mat Engn, Taipei 104, Taiwan
来源
关键词
Au-Pd/MWCNTs catalysts; electrooxidation reaction; electron spectroscopy methods; METAL-CLUSTERS; PALLADIUM;
D O I
10.1002/pssb.201000271
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
The Pd-Au multiwall carbon nanotubes (MWCNTs) supported catalyst exhibits higher power density in direct formic acid fuel cell (DFAFC) than similar Pd/MWCNTs catalyst. The Pd-Au/MWCNTs catalyst also exhibits higher activity and is more stable in electrooxidation reaction of formic acid during cyclic voltammetry (CV) measurements. After preparation by polyol method, the catalyst was subjected to two type of treatments: (I) annealing at 250 degrees C in 100% of Ar, (II) reducing in 5% of H-2 in Ar atmosphere at 200 degrees C. It was observed that the catalyst after treatment I was completely inactive, whereas after treatment II exhibited high activity. In order to explain this effect the catalysts were characterized by electron spectroscopy methods. The higher initial catalytic activity of Pd-Au/MWCNTs catalyst than Pd/MWCNTs catalyst in reaction of formic acid electrooxidation was attributed to electronic effect of gold in Pd-Au solution, and larger content of small Au nanoparticles of 1 nm size. The catalytic inactivity of Pd-Au/MWCNTs catalysts annealed in argon is attributed to carbon amorphous overlayer covering of Pd oxide shell on the metallic nanoparticles. (C) 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
引用
收藏
页码:2717 / 2721
页数:5
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