铁在O(100)单晶表面氧化还原行为的常压光电子能谱研究

Q1 Materials Science Catalysis Structure & Reactivity Pub Date : 2017-03-03 DOI:10.1080/2055074X.2016.1275379
L. Merte, J. Gustafson, M. Shipilin, Chu Zhang, E. Lundgren
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引用次数: 7

摘要

摘要采用常压XPS和NEXAFS研究了铁掺杂MgO单晶中铁的氧化还原过程。升高的温度和气体气氛使晶体的表面充电变得容易控制。铁的氧化态在两种状态之间可逆地转换,速率极不对称;氧化在点或在点几乎完成,而还原在点开始,在点仍未完成。晶体的掠射XRD表征表明,镁铁素体尖晶石存在八面体纳米级夹杂物()。有人提出,观察到的氧化还原行为涉及岩盐(O)和尖晶石相之间的相互转化,与还原相比,更开放的晶格包含更快速的离子扩散,因此更容易氧化。
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Redox behavior of iron at the surface of an O(100) single crystal studied by ambient-pressure photoelectron spectroscopy
Graphical Abstract We have studied the oxidation and reduction of iron in an Fe-doped MgO single crystal by , and using ambient-pressure XPS and NEXAFS. Surface charging of the crystal was rendered manageable by the elevated temperatures and the gas atmospheres. The oxidation state of iron was found to shift reversibly between the and states, with a strong asymmetry in the rates; while oxidation by or was nearly complete at , reduction by began at , and was still incomplete at . Grazing-incidence XRD characterization of the crystal indicated the presence of octahedral, nanoscale inclusions assigned to the magnesioferrite spinel (). It is proposed that the redox behavior observed involves interconversion between the rock-salt (O) and spinel phases, with the more open lattice containing enabling more rapid ion diffusion and thus more facile oxidation compared to reduction.
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Catalysis Structure & Reactivity
Catalysis Structure & Reactivity CHEMISTRY, PHYSICAL-
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