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The negligible role of C-H stretch excitation in the physisorption of CH4 on Pt(111).

机译:C-H拉伸激发在pt(111)上CH4的物理吸附中可忽略不计的作用。

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摘要

We report a molecular beam study of the effect of vibrational excitation on the physisorption of methane on a Pt(111) surface. Our experiments use a continuous molecular beam of CH4, prepared in its antisymmetic C-H stretch mode nu(3) by infrared laser pumping via rapid adiabatic passage. Physisorbed CH4(ads) is detected on a Pt(111) surface by reflection absorption infrared spectroscopy. At a surface temperature of 77 K, the desorption lifetime of CH4(ads) is observed to be 0.4 +/- 0.2 s. Trapping probabilities for the incident CH4 are measured by the King and Wells beam reflectivity method with and without vibrational excitation. Vibrational excitation of the incident CH4 with one quantum of nu(3) vibration does not produce a measurable effect (less than 0.2% change) on the trapping probability, in sharp contrast to the dissociative chemisorption process. The effect of resonant vibrational excitation of physisorbed CH4(ads) on its dissociation rate was also investigated.
机译:我们报告了分子束研究振动激发对Pt(111)表面上甲烷的物理吸附的影响。我们的实验使用CH4的连续分子束,该束分子通过快速绝热通道的红外激光泵浦以其反对称C-H拉伸模式nu(3)制备。通过反射吸收红外光谱法在Pt(111)表面检测到物理吸附的CH4(ads)。在表面温度为77 K时,观察到CH4(ads)的解吸寿命为0.4 +/- 0.2 s。通过King和Wells光束反射率方法在有和没有振动激发的情况下测量入射CH4的俘获概率。与nu(3)振动的一个量子的入射CH4的振动激发不会对捕获概率产生可测量的影响(变化小于0.2%),这与解离性化学吸附过程形成了鲜明的对比。还研究了物理吸附的CH4(ads)的共振振动激发对其离解速率的影响。

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