Institut für Physikalische Chemie und Elektrochemie, Leibniz-Universität Hannover, Callinstr. 3A, D-30167 Hannover, Germany.
Elettra-Sincrotrone Trieste S.C.p.A., SS 14-Km 163.5 in Area Science Park, I-34149 Basovizza, Trieste, Italy.
J Chem Phys. 2018 Apr 21;148(15):154705. doi: 10.1063/1.5020381.
Chemical waves in the H + O reaction on a Rh(111) surface alloyed with Ni [Θ < 1.5 monolayers (ML)] have been investigated in the 10 and 10 mbar range at T = 773 K using scanning photoelectron microscopy and x-ray photoelectron spectroscopy as in situ methods. The local intensity variations of the O 1s and the Ni 2p signal display an anticorrelated behavior. The coincidence of a high oxygen signal with a low Ni 2p intensity, which seemingly contradicts the chemical attraction between O and Ni, has been explained with a phase separation of the oxygen covered Rh(111)/Ni surface into a 3D-Ni oxide and into a Ni poor metallic phase. Macroscopic NiO islands (≈1 μm size) formed under reaction conditions have been identified as 2D-Ni oxide. Titration experiments of the oxygen covered Rh(111)/Ni surface with H demonstrated that the reactivity of oxygen is decreased by an order of magnitude through the addition of 0.6 ML Ni. An excitation mechanism is proposed in which the periodic formation and reduction of NiO modulate the catalytic activity.
在 T = 773 K 下,使用扫描光电显微镜和 X 射线光电子能谱作为原位方法,在 10 和 10 毫巴的范围内研究了 Rh(111)表面与 Ni 合金化(Θ < 1.5 单层)的 H + O 反应中的化学波。O 1s 和 Ni 2p 信号的局部强度变化显示出反相关行为。高氧信号与低 Ni 2p 强度的吻合,似乎与 O 和 Ni 之间的化学吸引力相矛盾,这可以通过氧覆盖的 Rh(111)/Ni 表面的相分离来解释,分为 3D-Ni 氧化物和贫 Ni 的金属相。在反应条件下形成的宏观 NiO 岛(≈1 μm 大小)被鉴定为 2D-Ni 氧化物。用 H 滴定氧覆盖的 Rh(111)/Ni 表面的实验表明,通过添加 0.6 ML Ni,氧的反应性降低了一个数量级。提出了一种激发机制,其中 NiO 的周期性形成和还原调节了催化活性。