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In relation to this article, we declare that there is no conflict of interest.
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Received July 31, 2009
Accepted October 20, 2009
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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The effect of PtRuW ternary electrocatalysts on methanol oxidation reaction in direct methanol fuel cells

Petroleum Displacement Technology Research Center, Korea Research Institute of Chemical Technology (KRICT), Sinseongno, Yuseong-gu, Daejeon 305-600, Korea 1Department of Hydrogen and Fuel Cells Engineering, Specialized Graduate School, Chonbuk National University, Jeonju 561-756, Korea 2Department of Mineral Resources & Energy Engineering, Chonbuk National University, Jeonju 561-756, Korea 3Faculty of Environmental Engineering, University of Seoul, Seoul 130-743, Korea
jmsohn@jbnu.ac.kr
Korean Journal of Chemical Engineering, March 2010, 27(3), 802-806(5), 10.1007/s11814-010-0146-2
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Abstract

PtRu and PtRuW ternary electrocatalysts were synthesized using an NaBH4 reduction method. A uniform distribution of particles, with average particle size of 3-3.5 nm was indentified from X-ray diffraction (XRD) and transmission electron microscopy (TEM). The electrochemically active surface area was slightly decreased after the addition of W into PtRu. When W was added to PtRu, the specific and mass activity of methanol electro-oxidation was increased. The most active catalyst was Pt5Ru4W, of which specific and mass activities were 265.38 mA/m2 and 6.21 A/g.catal, respectively. The specific and mass activity was 390 and 320% higher than that of PtRu.

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