Freindl K, Partyka-Jankowska E, Karaś W, Zając M, Madej E, Spiridis N, Slęzak M, Slęzak T, Wiśnios D, Korecki J
Jerzy Haber Institute of Catalysis and Surface Chemistry, Polish Academy of Sciences, ul. Niezapominajek 8, 30-239 Kraków, Poland.
Faculty of Physics, University of Vienna, Strudlhofgasse 4, A-1090 Vienna, Austria.
Surf Sci. 2013 Nov;617(100):183-191. doi: 10.1016/j.susc.2013.07.011.
The adsorption of oxygen on a pseudomorphic iron monolayer deposited on a W(110) surface was studied experimentally and theoretically. Standard surface characterization methods, such as Auger electron spectroscopy and low energy electron diffraction, and specific nuclear methods, such as conversion electron Mössbauer spectroscopy (CEMS) and nuclear resonant scattering of synchrotron radiation, combined with theoretical calculations based on the density functional theory allowed us to determine the structure of the oxygen adsorbate and the electronic properties of iron atoms with different oxygen coordinations. The oxygen-(3 × 2) structure on the iron monolayer was recognized and was interpreted to be a state with oxygen chemisorbed on the non-reconstructed surface with modest electron transfer from iron to oxygen. A transition from chemisorbed oxygen to the onset of Fe-oxidation is revealed by distinct changes in the CEMS spectra.
对沉积在W(110)表面的赝形铁单层上氧气的吸附进行了实验和理论研究。采用标准表面表征方法,如俄歇电子能谱和低能电子衍射,以及特定的核方法,如转换电子穆斯堡尔谱(CEMS)和同步辐射的核共振散射,并结合基于密度泛函理论的理论计算,使我们能够确定氧吸附质的结构以及具有不同氧配位的铁原子的电子性质。识别出了铁单层上的氧-(3×2)结构,并将其解释为氧化学吸附在未重构表面上且有适度电子从铁转移到氧的状态。CEMS光谱的明显变化揭示了从化学吸附氧到铁氧化开始的转变。