Saint-Lager M-C, Bailly A, Dolle P, Baudoing-Savois R, Taunier P, Garaudée S, Cuccaro S, Douillet S, Geaymond O, Perroux G, Tissot O, Micha J-S, Ulrich O, Rieutord F
Institut Néel, CNRS and Université Joseph Fourier, BP 166, F-38042, Grenoble Cedex 9, France.
Rev Sci Instrum. 2007 Aug;78(8):083902. doi: 10.1063/1.2766821.
A new experimental setup has been developed to enable in situ studies of catalyst surfaces during chemical reactions by means of surface x-ray diffraction (SXRD) and grazing incidence small angle x-ray scattering. The x-ray reactor chamber was designed for both ultrahigh-vacuum (UHV) and reactive gas environments. A laser beam heating of the sample was implemented; the sample temperature reaches 1100 K in UHV and 600 K in the presence of reactive gases. The reactor equipment allows dynamical observations of the surface with various, perfectly mixed gases at controlled partial pressures. It can run in two modes: as a bath reactor in the pressure range of 1-1000 mbars and as a continuous flow cell for pressure lower than 10(-3) mbar. The reactor is connected to an UHV preparation chamber also equipped with low energy electron diffraction and Auger spectroscopy. This setup is thus perfectly well suited to extend in situ studies to more complex surfaces, such as epitaxial films or supported nanoparticles. It offers the possibility to follow the chemically induced changes of the morphology, the structure, the composition, and growth processes of the model catalyst surface during exposure to reactive gases. As an example the Pd(8)Ni(92)(110) surface structure was followed by SXRD under a few millibars of hydrogen and during butadiene hydrogenation while the reaction was monitored by quadrupole mass spectrometry. This experiment evidenced the great sensitivity of the diffracted intensity to the subtle interaction between the surface atoms and the gas molecules.
一种新的实验装置已被开发出来,通过表面X射线衍射(SXRD)和掠入射小角X射线散射,能够在化学反应过程中对催化剂表面进行原位研究。X射线反应腔室设计用于超高真空(UHV)和反应性气体环境。实现了对样品的激光束加热;在超高真空下样品温度可达1100 K,在有反应性气体存在时可达600 K。该反应设备允许在可控分压下用各种完全混合的气体对表面进行动态观察。它可以在两种模式下运行:作为压力范围为1 - 1000毫巴的浴式反应器,以及作为压力低于10^(-3)毫巴的连续流通池。该反应器连接到一个同样配备了低能电子衍射和俄歇光谱的超高真空制备腔室。因此,这种装置非常适合将原位研究扩展到更复杂的表面,如外延膜或负载型纳米颗粒。它提供了在暴露于反应性气体期间跟踪模型催化剂表面的形态、结构、组成和生长过程的化学诱导变化的可能性。例如,在几毫巴氢气下以及丁二烯氢化过程中,通过SXRD跟踪Pd(8)Ni(92)(110)表面结构,同时用四极质谱监测反应。该实验证明了衍射强度对表面原子与气体分子之间微妙相互作用的高度敏感性。