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氧化铁薄膜的表面结构演变。

Surface structural evolution in iron oxide thin films.

机构信息

Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, P.O. Box 603, Beijing 100190, PR China.

出版信息

Langmuir. 2011 Jan 4;27(1):11-4. doi: 10.1021/la103732r. Epub 2010 Dec 8.

Abstract

Ordered iron oxide ultrathin films were fabricated on a single-crystal Mo(110) substrate under ultrahigh vacuum conditions by either depositing Fe in ambient oxygen or oxidizing preprepared Fe(110) films. The surface structure and electronic structure of the iron oxide films were investigated by various surface analytical techniques. The results indicate surface structural transformations from metastable FeO(111) and O-terminated Fe(2)O(3)(0001) to Fe(3)O(4)(111) films, respectively. The former depends strongly on the oxygen pressure and substrate temperature, and the latter relies mostly upon the annealing temperature. Our experimental observations are helpful in understanding the mechanisms of surface structural evolution in iron oxides. The model surfaces of Fe-oxide films, particularly O-terminated surfaces, can be used for further investigation in chemical reactions (e.g., in catalysis).

摘要

有序氧化铁超薄膜在超高真空条件下通过在环境氧气中沉积 Fe 或氧化预先制备的 Fe(110) 薄膜在单晶 Mo(110) 衬底上制备。通过各种表面分析技术研究了氧化铁膜的表面结构和电子结构。结果表明,表面结构从亚稳态 FeO(111)和 O 终止的 Fe(2)O(3)(0001)分别转变为 Fe(3)O(4)(111)膜。前者强烈依赖于氧压和衬底温度,后者主要依赖于退火温度。我们的实验观察有助于理解氧化铁表面结构演化的机制。氧化铁膜的模型表面,特别是 O 终止表面,可用于进一步研究化学反应(例如,在催化中)。

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