Synthesis and characterization of ethanol electro-oxidation catalysts

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2010
Demir-Kıvrak, Hilal
In this study, the role of defects, the role of Sn in relation to defects, and the role of oxide phase of tin in ethanol electro-oxidation reaction were investigated. Firstly, adsorption calorimetry measurements were conducted on monometallic (1%Pt, 2%Pt, and 5%Pt) and bi-metallic (5% Pt-Sn) γ-Al2O3 supported Pt catalysts. It was observed that while saturation coverage values decreased, intermediate heats remained same for Pt-Sn catalysts by the increasing amount of tin. The effect of particle size was investigated on Pt/C (pH=5), Pt/C (pH=11) catalysts at different scan rates. At high scan rates (quite above diffusion limitations), current per site activities were nearly the same for 20% Pt/C (E-Tek), Pt/C (pH=11), and Pt/C (pH=5) catalysts, which explained as electro-oxidation reaction takes place at the defects sites. Furthermore, the effect of support on ethanol electro-oxidation was investigated on CNT supported Pt catalyst. Results indicate that only the metal dispersions improved ethanol electro-oxidation reaction and support did not have any effect on ethanol electro-oxidation reaction. Results on the 20% Pt-Sn/C (15:1 to 1:1 Pt: Sn atomic ratios) and 20% Pt-SnO2/C (6:1 and 1:1) catalysts indicated that ethanol electro-oxidation activity increased by increasing tin amount. For 20% Pt-Sn/C catalysts, Pt-Sn (6:1)/C indicated best activity. On the other hand, 20% Pt-SnO2 (6:1)/C catalyst was better than Pt-Sn (6:1)/C in terms of ethanol electro-oxidation activity due to the fact that there was low contact between Pt and tin oxide particles.

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Citation Formats
H. Demir-Kıvrak, “Synthesis and characterization of ethanol electro-oxidation catalysts,” Ph.D. - Doctoral Program, Middle East Technical University, 2010.