Vaida Mihai E, Bernhardt Thorsten M
Institute of Surface Chemistry and Catalysis, University of Ulm, Albert-Einstein-Allee 47, 89069 Ulm, Germany.
Rev Sci Instrum. 2010 Oct;81(10):104103. doi: 10.1063/1.3488098.
A detailed account of the experimental methodology of surface pump-probe femtosecond-laser mass spectrometry is presented. This recently introduced technique enables the direct time-resolved investigation of surface reaction dynamics by monitoring the mass and the relative velocity of intermediates and products of a photoinduced surface reaction via multiphoton ionization. As a model system, the photodissociation dynamics of methyl iodide adsorbed at submonolayer coverage on magnesia ultrathin films is investigated. The magnesia surface preparation and characterization as well as the pulsed deposition of methyl iodide are described. The femtosecond-laser excitation (pump) and, in particular, the resonant multiphoton ionization surface detection (probe) schemas are discussed in detail. Results of pump-probe time-resolved methyl and iodine atom detection experiments are presented and the potential of this method for velocity-resolved photofragment analysis is evaluated.
本文详细介绍了表面泵浦-探测飞秒激光质谱的实验方法。这种最近引入的技术能够通过多光子电离监测光诱导表面反应中间体和产物的质量及相对速度,从而直接对表面反应动力学进行时间分辨研究。作为一个模型系统,研究了亚单层覆盖在氧化镁超薄膜上的碘甲烷的光解离动力学。描述了氧化镁表面的制备与表征以及碘甲烷的脉冲沉积。详细讨论了飞秒激光激发(泵浦),特别是共振多光子电离表面检测(探测)方案。给出了泵浦-探测时间分辨甲基和碘原子检测实验的结果,并评估了该方法在速度分辨光碎片分析方面的潜力。