Lehrstuhl für Theoretische Chemie, Universität Erlangen-Nürnberg, Egerlandstr. 3, 91058 Erlangen, Germany.
Phys Chem Chem Phys. 2011 Sep 28;13(36):16227-35. doi: 10.1039/c1cp21694e. Epub 2011 Aug 8.
We studied the adsorption and reactivity of SO(2) on clean and oxygen precovered Pd(100) with high resolution X-ray photoelectron spectroscopy and density functional calculations. Upon adsorption at 120 K two different SO(2) species were detected, which were identified as upright-standing and flat-lying molecules by comparing the calculated core level shifts. In agreement with the relative stabilities determined by the calculations the intensities of the photoelectron spectra indicate that the majority species are upright-standing SO(2). Upon heating the quantitative analysis of the data indicates desorption of SO(3) and formation of atomic sulfur. On the oxygen precovered surface small amounts of SO(3) are formed already upon SO(2) adsorption at low temperatures. Upon heating stepwise oxidation of SO(2) to SO(3) and, eventually, to SO(4) is found. Two different SO(4) species were detected, which are assigned to SO(4) bound in the proximity of or remote from oxygen adatoms, according to core level shift estimates.
我们使用高分辨率 X 射线光电子能谱和密度泛函计算研究了清洁和氧预覆盖 Pd(100)表面上 SO(2)的吸附和反应性。在 120 K 下吸附时,检测到两种不同的 SO(2)物种,通过比较计算得出的芯能级位移,将其鉴定为垂直站立和平面分子。与计算确定的相对稳定性一致,光电子能谱的强度表明大多数物种为垂直站立的 SO(2)。加热时,数据分析表明 SO(3)脱附和硫原子的形成。在氧预覆盖的表面上,在低温下 SO(2)吸附时就已经形成少量的 SO(3)。随着温度升高,逐步发现 SO(2)氧化为 SO(3),最终氧化为 SO(4)。根据芯能级位移的估计,检测到两种不同的 SO(4)物种,它们被分配到与氧原子吸附物附近或远离的 SO(4)结合。