
Citation: Yi Zhang, Wei Feng, Fan Yang, Xinhe Bao. Interface-controlled synthesis of CeO2(111) and CeO2(100) and their structural transition on Pt(111)[J]. Chinese Journal of Catalysis, 2019, 40(2): 204-213. doi: 10.1016/S1872-2067(18)63171-7

CeO2(111)和CeO2(100)的界面调控合成及在Pt(111)上的结构转变
在Pt(111)上生长的氧化铈薄膜通常暴露CeO2(111)表面.我们发现Pt(111)表面厚度在三层以内的氧化铈薄膜,其结构是高度动态且随着退火温度升高而变化的,这种动态结构变化可归因于Pt和氧化铈间的界面电子作用.当氧化铈薄膜的厚度增大到三层以上,其负载的氧化铈团簇开始表现出迥异于三层以下氧化铈纳米岛的优异的热稳定性,表明Pt与CeOx之间的界面电子作用主要影响厚度在三层以内的氧化铈纳米结构.采用常规的反应沉积方法难以获得完全覆盖Pt(111)衬底的规整氧化铈薄膜,而我们通过采取一种两步的动力学限制生长方法,制备出了完全覆盖Pt(111)衬底的氧化铈薄膜.对于Pt(111)上厚度约为3-4层的氧化铈薄膜,在超高真空中于1000K退火会导致氧化铈薄膜表面形成CeO2(100)结构.这是因为高温还原促进了c-Ce2O3(100)缓冲层的形成,该缓冲层被Pt的界面电子转移以及相匹配的超晶格所稳定,并进一步成为顶层CeO2(100)结构生长的模板.进一步在900 K的氧气中处理则可将薄膜CeO2(100)表面完全转变为CeO2(111)表面.
因此,Pt(111)上氧化铈纳米岛和薄膜所展现的结构动态变化是由Pt-CeOx界面作用与氧化铈层间作用相互竞争所决定.本研究提供了对氧化铈负载Pt催化剂的原子级理解,虽然Pt/CeO2催化剂活性增强的原因常被简单归结于界面强相互作用,我们的研究在原子尺度上进一步表明Pt/CeO2在还原条件下易形成界面Ce2O3层.此外,本研究提供了不同晶面二氧化铈模型催化剂的构筑方法,可将对氧化铈晶面效应和Pt/CeOx催化剂的研究推进到分子尺度.
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关键词:
- 界面作用
- / Pt/CeOx催化剂
- / CeO2(111)
- / CeO2(100)
- / c-Ce2O3(100)
English
Interface-controlled synthesis of CeO2(111) and CeO2(100) and their structural transition on Pt(111)
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Key words:
- Interfacial interaction
- / Pt/CeOx catalyst
- / CeO2(111)
- / CeO2(100)
- / c-Ce2O3(100)
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