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Received December 15, 2015
Accepted January 11, 2016
- 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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Enhanced activity of carbon-supported PdCo electrocatalysts toward electrooxidation of ethanol in alkaline electrolytes
Department of Chemical Engineering, Pohang University of Science & Technology (POSTECH), San 31 Hyoja-dong, Pohang 37673, Korea 1School of Energy & Chemical Engineering, Ulsan National University of Science & Technology (UNIST), 60 UNIST-gil, Ulsan 44919, Korea
jlee1234@unist.ac.kr
Korean Journal of Chemical Engineering, June 2016, 33(6), 1799-1804(6), 10.1007/s11814-016-0015-8
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Abstract
Carbon-supported Pd and PdCo (1 : 2, 1 : 1, 2 : 1 and 3 : 1) catalysts were synthesized by chemical reduction with NaBH4. Their electrochemical properties were investigated by cyclic voltammetry, chronoamperometry and CO stripping voltammetry in alkaline electrolytes, and compared with commercial Pt/C and PtRu(1 : 1)/C catalysts. In electrochemical oxidation of ethanol in an alkaline electrolyte, marked improvements in the current density and onset potential were observed by incorporating Co into Pd/C to form PdCo/C alloy electrocatalysts. The best catalyst PdCo (1 : 1)/C showed performance superior to the commercial Pt/C or PtRu/C catalysts. It is shown that the incorporated Co facilitates the oxidation of strongly-adsorbed carbonaceous intermediate species on the surface of Pd by forming OH. group and reacts away the intermediates from Pd surface. Thus, PdCo(1 : 1)/C catalyst is a promising anode catalyst for direct ethanol fuel cells with alkaline electrolytes.
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