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

机译:来自干净和硫覆盖的Fe金属基材的Fe氧化物的去润湿

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Studies performed in UHV on Fe/Fe-oxide interfaces suggest a mechanism for S-induced thermal instability of the interface. In the absence of sulfur, oxide debonding is initiated by the diffusion of oxygen into the bulk from an Fe-O interfacial "glue" layer. Once diffusion occurs, the polar oxide dewets from the nonpolar metal substrate. In the presence of S, the formation of the FeO layer is inhibited due to site competition between S and O atoms at the interface. Upon heating, S reacts with existing interfacial oxide sites to produce SO_2, and destroying interfacial oxide-metal bonds at a lower temperature (640 K) than that at which oxygen diffusion from the FeO layer occurs (~900 K). At this point there is no interfacial bonding between the polar oxide and the non-polar S-modified substrate, and oxide dewetting occurs. Due to lower Fe coordination at the surface, Fe-S bonds are largely covalent, and therefore the S-modified surface is still nonpolar.
机译:在Fe / Fe氧化物界面上的UHV中进行的研究表明了S诱导界面热不稳定性的机制。在没有硫的情况下,通过Fe-O界面“胶水”层的氧气扩散引发氧化物剥离。一旦发生扩散,极性氧化物从非极性金属基板中脱水。在S存在下,由于界面在S和O原子之间的现场竞争,Feo层的形成被抑制。在加热时,S与现有的界面氧化物位点反应以产生SO_2,并在较低温度(640k)下破坏界面氧化物 - 金属键,而不是从Feo层发生的氧扩散(〜900k)。此时,在极性氧化物和非极性S调制的基材之间没有界面键合,并且发生氧化物脱水。由于表面下的较低的Fe协调,Fe-S键在很大程度上是共价的,因此S改性表面仍然是非极性的。

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