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DE-WETTING OF Fe OXIDE FROM CLEAN AND SULFUR-COVERED Fe METAL SUBSTRATES

机译:清洁和硫覆盖的铁金属母液中氧化铁的去湿

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摘要

Studies performed in UHV on Fe/Fe-oxide interfaces suggest a mechanism for S-inducedrnthermal instability of the interface. In the absence of sulfur, oxide debonding is initiated byrnthe diffusion of oxygen into the bulk from an Fe-O interfacial "glue" layer. Once diffusionrnoccurs, the polar oxide dewets from the nonpolar metal substrate. In the presence of S, thernformation of the FeO layer is inhibited due to site competition between S and O atoms atrnthe interface. Upon heating, S reacts with existing interfacial oxide sites to produce SO_2,rnand destroying interfacial oxide-metal bonds at a lower temperature (640 K) than that atrnwhich oxygen diffusion from the FeO layer occurs (~900 K). At this point there is norninterfacial bonding between the polar oxide and the non-polar S-modified substrate, andrnoxide dewetting occurs. Due to lower Fe coordination at the surface, Fe-S bonds are largelyrncovalent, and therefore the S-modified surface is still nonpolar.
机译:在UHV中对Fe / Fe-氧化物界面进行的研究表明,S诱导界面的热不稳定性是一种机制。在不存在硫的情况下,通过氧从Fe-O界面“胶”层扩散到主体中而引发氧化物脱键。一旦发生扩散现象,极性氧化物便会从非极性金属基材上润湿。在S的存在下,由于S和O原子在界面处的位竞争,FeO层的形成受到抑制。加热后,S与现有的界面氧化物位点反应生成SO_2,并在比氧从FeO层扩散的温度更低的温度(〜900 K)下(640 K)破坏界面氧化物-金属键。在这一点上,在极性氧化物和非极性S-改性的底物之间存在正界面结合,并且发生了氮氧化物反润湿。由于表面上较低的Fe配位,Fe-S键大部分为共价键,因此S修饰的表面仍为非极性。

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  • 来源
  • 会议地点 San Diego CA(US)
  • 作者单位

    Department of Chemistry, P.O. Box 305070, University of North Texas, Denton, TX-76203;

    Department of Chemistry, P.O. Box 305070, University of North Texas, Denton, TX-76203;

    Cherry Semiconductor Corporation, North Kingstown, RI-02852;

    Department of Chemistry and Biochemistry, University of Texas at Austin, Austin, TX-78712;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 燃料电池;
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