In-situ observation of hydrogenation of ethylene on a Pt(111) surface under atmospheric pressure by infrared reflection absorption spectroscopy

被引:58
作者
Ohtani, T [1 ]
Kubota, J [1 ]
Kondo, JN [1 ]
Hirose, C [1 ]
Domen, K [1 ]
机构
[1] Tokyo Inst Technol, Resources Utilizat Res Lab, Midori Ku, Yokohama, Kanagawa, Japan
关键词
D O I
10.1021/jp9907241
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hydrogenation of ethylene on a Pt(111) surface in the presence of gaseous ethylene and hydrogen in the 10(3) Pa range was investigated by infrared reflection absorption spectroscopy (IRAS). The IRA peaks assigned to di-sigma-bonded ethylene and ethylidyne were observed on Pt(111) under the flow of 1.3 x 10(2) Pa of ethylene and 6.5 x 10(3) Pa of hydrogen at 200-300 K, and the apparent activation energy of ethylene hydrogenation was estimated to be 37 +/- 5 kJ mol(-1) from the rate of temperature-dependent ethane production. The ethylene hydrogenation on ethylidyne-covered Pt(111) was also examined under the same condition. The peak due to the di-sigma-bonded ethylene was not observed on ethylidyne-covered Pt(111), although the similar rate of hydrogenation and the similar activation energy (39 +/- 5 kJ mol(-1)) were obtained as those on clean Pt(111). The pi-bonded ethylene, which has been previously proposed as an intermediate by the sum-frequency generation (SFG) experiment under the catalytic hydrogenation condition and by IRAS under the low-temperature condition, was not detected in the present study. The similarity of the rate and activation energy for clean and ethylidyne-covered Pt(111) surfaces suggests that-the rate of hydrogenation does not depend on either coverage of di-sigma-bonded ethylene or ethylidyne. The role of the observed species in the hydrogenation of ethylene is discussed.
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页码:4562 / 4565
页数:4
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