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CO在U2N3+xOy薄膜表面反应特性研究

罗丽珠 陆雷 刘柯钊 赵东海

无机材料学报Issue(8):875-879,5.
无机材料学报Issue(8):875-879,5.DOI:10.15541/jim20130641

CO在U2N3+xOy薄膜表面反应特性研究

Surface Behaviors of U2N3+xOy Films in CO Atmosphere

罗丽珠 1陆雷 2刘柯钊 1赵东海1

作者信息

  • 1. 表面物理与化学重点实验室,绵阳 621907
  • 2. 中国工程物理研究院,绵阳 621900
  • 折叠

摘要

Abstract

U2N3+xOy films were deposited on Si substrate by magnetic sputtering deposition method. The behaviors of U2N3+xOy after exposure to CO atmosphere was analyzed by X-ray photoelectron spectroscopy (XPS) to explore its CO corrosion mechanism. Under ultra-high vacuum (UHV) condition, it is found that CO atmosphere is oxidative on the surface of U2N3+xOy film. The dissociated carbon in forms of amorphous is segregated on the outmost surface rather than diffuses inside, and the diffusion of the dissociated oxygen resulted in oxidation of U2N3+xOy, leading to the formation of uranium oxy-nitrides in higher valence state on the surface and an N-rich layer as an intermediacy in the subsurface. The diffusion of oxygen in the film is suppressed on the very surface by the product of uranium oxides or ura-nium oxy-nitrides in higher valence state due to the potential barrier. The distance of the N-rich layer to the outmost surface dominates the intensity variation of satellites at 386.7 eV and 397.5 eV, which is enlarged with the oxidation process. All abore chemical changes play a very important role for understanding the corrosion mechanism of U2N3+xOy films.

关键词

CO/U2N3+xOy/表面腐蚀/氧化

Key words

CO/U2N3+xOy/surface corrosion/oxidation

分类

化学化工

引用本文复制引用

罗丽珠,陆雷,刘柯钊,赵东海..CO在U2N3+xOy薄膜表面反应特性研究[J].无机材料学报,2014,(8):875-879,5.

基金项目

中国工程物理研究院资助项目(2011AO301015) CAEP Research Fund (2011AO301015) (2011AO301015)

无机材料学报

OA北大核心CSCDCSTPCDSCI

1000-324X

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