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氧化铈上薄氧化铁薄膜的电子和结构性质

Electronic and Structural Properties of Thin Iron Oxide Films on CeO.

作者信息

Piliai Lesia, Castro-Latorre Pablo, Pchálek František, Oveysipoor Shiva, Kosto Yuliia, Khalakhan Ivan, Skála Tomáš, Neyman Konstantin M, Alemany Pere, Vorochta Michael, Bruix Albert, Matvija Peter, Matolínová Iva

机构信息

Department of Surface and Plasma Science, Faculty of Mathematics and Physics, Charles University, V Holešovičkách 2, Prague 8 180 00, Czech Republic.

Departament de Ciència de Materials i Química Física and Institut de Química Teòrica i Computacional (IQTCUB), Universitat de Barcelona, Barcelona 08028, Spain.

出版信息

ACS Appl Mater Interfaces. 2024 Sep 4;16(35):46858-46871. doi: 10.1021/acsami.4c05542. Epub 2024 Aug 21.

Abstract

Modification of CeO (ceria) with 3d transition metals, particularly iron, has been proven to significantly enhance its catalytic efficiency in oxidation or combustion reactions. Although this phenomenon is widely reported, the nature of the iron-ceria interaction responsible for this improvement remains debated. To address this issue, we prepared well-defined model FeO/CeO(111) catalytic systems and studied their structure and interfacial electronic properties using photoelectron spectroscopy, scanning tunneling microscopy, and low-energy electron diffraction, coupled with density functional theory (DFT) calculations. Our results show that under ultrahigh vacuum conditions, Fe deposition leads to the formation of small FeO clusters on the ceria surface. Subsequent annealing results in the growth of large amorphous FeO particles and a 2D FeO layer. Annealing in an oxygen-rich atmosphere further oxidizes iron up to the Fe state and improves the crystallinity of both the 2D layer and the 3D particles. Our DFT calculations indicate that the 2D FeO layer interacts strongly with the ceria surface, exhibiting structural corrugations and transferred electrons between Fe/Fe and Ce/Ce redox pairs. The novel 2D FeO/CeO(111) phase may explain the enhancement of the catalytic properties of CeO by iron. Moreover, the corrugated 2D FeO layer can serve as a template for the ordered nucleation of other catalytically active metals, in which the redox properties of the 2D FeO/CeO(111) system are exploited to modulate the charge of the supported metals.

摘要

用3d过渡金属,特别是铁对二氧化铈(CeO₂)进行改性,已被证明能显著提高其在氧化或燃烧反应中的催化效率。尽管这一现象已被广泛报道,但导致这种改善的铁-二氧化铈相互作用的本质仍存在争议。为了解决这个问题,我们制备了定义明确的模型FeO/CeO₂(111)催化体系,并使用光电子能谱、扫描隧道显微镜和低能电子衍射,结合密度泛函理论(DFT)计算,研究了它们的结构和界面电子性质。我们的结果表明,在超高真空条件下,铁的沉积导致在二氧化铈表面形成小的FeO团簇。随后的退火导致大的非晶态FeO颗粒的生长和二维FeO层的形成。在富氧气氛中退火进一步将铁氧化至Fe³⁺状态,并改善了二维层和三维颗粒的结晶度。我们的DFT计算表明,二维FeO层与二氧化铈表面强烈相互作用,表现出结构起伏以及Fe/Fe³⁺和Ce/Ce³⁺氧化还原对之间的电子转移。这种新型的二维FeO/CeO₂(111)相可能解释了铁对CeO₂催化性能的增强作用。此外,起伏的二维FeO层可以作为其他催化活性金属有序成核的模板,其中利用二维FeO/CeO₂(111)体系的氧化还原性质来调节负载金属的电荷。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfd1/11378155/4a895fb3c571/am4c05542_0001.jpg

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