Institute of Chemical Sciences and Engineering (ISIC), École Polytechnique Fédérale de Lausanne (EPFL), 1015 Lausanne, Switzerland.
Max Planck-EPFL Center for Molecular Nanoscience and Technology, Göttingen, Germany.
J Chem Phys. 2023 Jun 7;158(21). doi: 10.1063/5.0150009.
We describe a novel ultrahigh vacuum state-to-state molecule/surface scattering apparatus with quantum state preparation of the incident molecular beam and angle-resolved quantum state detection of the scattered molecules. State-resolved detection is accomplished using a tunable mid-infrared laser source combined with a cryogenic bolometer detector and is applicable to any molecule with an infrared-active vibrational transition. Results on rotationally inelastic scattering of CH4 methane from a Ni(111) surface and NiO(111)/Ni(111) oxide film, obtained by the new apparatus, are presented. Molecules scattering from the oxidized surface, compared to those scattering from the bare nickel surface, are more highly excited rotationally and scatter into a broader distribution of angles. The internal alignment of molecular rotation is in addition found to be stronger in molecules scattering from the bare surface. Furthermore, the maxima of the state-resolved angular distributions shift toward and away from surface normal with increasing rotational quantum number J for the oxidized and bare surface, respectively. Finally, the rotational state populations produced in scattering from the oxidized surface are well-described by a Boltzmann distribution, while those produced in scattering from the bare surface exhibit large deviations from their best-fit Boltzmann distributions. These results point toward a marked enhancement in molecule-surface collisional energy exchange induced by oxidation of the nickel surface.
我们描述了一种新颖的超高真空态态分子/表面散射装置,具有入射分子束的量子态制备和散射分子的角度分辨量子态检测功能。通过可调谐中红外激光源与低温量热计探测器相结合,实现了态分辨检测,可适用于任何具有红外活性振动跃迁的分子。我们利用新装置获得了 CH4 甲烷从 Ni(111)表面和 NiO(111)/Ni(111)氧化膜上的非弹性散射的旋转结果。与从裸露镍表面散射的分子相比,从氧化表面散射的分子在旋转中受到更高的激发,并散射到更广泛的角度分布中。此外,还发现分子从裸露表面散射时,分子旋转的内部对准更强。此外,对于氧化表面和裸露表面,随着转动量子数 J 的增加,态分辨角分布的最大值分别向和远离表面法线移动。最后,从氧化表面散射产生的转动态分布很好地符合玻尔兹曼分布,而从裸露表面散射产生的转动态分布则与其最佳拟合的玻尔兹曼分布有很大偏差。这些结果表明,镍表面氧化显著增强了分子-表面碰撞能量交换。