Fe oxychloride desorption from an Fe polycrystalline surface

E. Murray, J. Prasad, J.A. Kelber
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引用次数: 1

Abstract

We report the formation of an Fe oxychloride species at the surface of an O- and Cl-covered Fe polycrystalline surface below 230 K under UHV conditions. Our data show that FeOCl (amu 107) desorbs at 230 K. For FeCl2 (amu 126) desorption, two desorption peaks are observed at 230 and 620 K in the presence of chemisorbed oxygen. In the absence of oxygen, only one FeCl2 desorption peak at 620 K is observed. Auger electron spectroscopy and temperature programmed desorption studies reveal that the reaction leading to Fe oxychloride formation involves dissociatively adsorbed O and Cl at the Fe surface. These results indicate that chemisorbed or low coordinate oxygen plays an important and previously unsuspected role in chloride-induced corrosion at ferrous surfaces.

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铁多晶表面氯化铁氧解吸
我们报道了在特高压条件下,在230 K以下,在O-和cl -覆盖的铁多晶表面上形成了铁氯氧化物。我们的数据表明FeOCl (amu107)在230k时解吸。对于FeCl2 (amu126)的解吸,在230和620 K时,在化学吸附氧的存在下观察到两个解吸峰。在无氧条件下,在620k时只观察到一个FeCl2解吸峰。俄热电子能谱和温度程序解吸研究表明,导致铁氯氧化物形成的反应涉及到在铁表面离解吸附的O和Cl。这些结果表明,化学吸附或低配位氧在亚铁表面氯化物腐蚀中起着重要的作用。
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