Chem. J. Chinese Universities

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In situ Electrochemical FTIR Spectroscopy of Adsorption and Oxidation Process of Methanol on PtRu/C Electrocatalyst

WANG Qi1,2, SUN Gong-Quan1, YAN Shi-You1, WANG Guo-Xiong1, XIN Qin1, CHEN Qing-Song3, LI Jun-Tao3, JIANG Yan-Xia3, SUN Shi-Gang3   

    1. Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China;
    2. Graduate School of the Chinese Academy of Sciences, Beijing 100039, China;
    3. State Key Laboratory for Physical Chemistry of Solid Surfaces, Department of Chemistry, Xiamen University, Xiamen 361005, China
  • Received:2005-12-14 Revised:1900-01-01 Online:2006-11-10 Published:2006-11-10
  • Contact: SUN Shi-Gang

Abstract: A modified polyol process was used to prepare Pt/C, PtRu/C and Ru/C electrocatalysts. Calculated from XRD patterns, the mean particle size of PtRu/C electrocatalyst was 2.2 nm and the percentage of Ru alloyed was 71%, respectively. Adsorption and electrooxidation progress of methanol on PtRu/C electrocatalyst was investigated by in situ FTIRS, combined with electrochemical experiments. It is revealed that the activity of PtRu/C electrocatalyst for methanol oxidation was much higher than that of Pt/C. Addition of Ru in PtRu/C electrocatalyst changed the characteristic of methanol adsorption, and Ru—OH species could oxidize linear bonded CO(COL) at a lower potential, thus inhibited the catalyst poisoning. In addition, from FTIRs results, COL was evidently identified to the main poisonous species and the major product was CO2. Methyl formate was also identified. Based on these results, the mechanism of methanol oxidation was discussed.

Key words: Direct methanol fuel cell, PtRu/C, Methanol oxidation, Electrochemistry, In situ FTIR

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