In Situ X-Ray Photoelectron Spectroscopy Study of Atomic Layer Deposited Cerium Oxide on SiO2: Substrate Influence on the Reaction Mechanism During the Early Stages of Growth

IF 4.4 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY Advanced Materials Interfaces Pub Date : 2024-10-31 DOI:10.1002/admi.202400537
Carlos Morales, Max Gertig, Małgorzata Kot, Carlos Alvarado, Markus Andreas Schubert, Marvin Hartwig Zoellner, Christian Wenger, Karsten Henkel, Jan Ingo Flege
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Abstract

Thermal atomic layer deposition (ALD) of cerium oxide using commercial Ce(thd)4 precursor and O3 on SiO2 substrates is studied employing in-situ X-ray photoelectron spectroscopy (XPS). The system presents a complex growth behavior determined by the change in the reaction mechanism when the precursor interacts with the substrate or the cerium oxide surface. During the first growth stage, non-ALD side reactions promoted by the substrate affect the growth per cycle, the amount of carbon residue on the surface, and the oxidation degree of cerium oxide. On the contrary, the second growth stage is characterized by a constant growth per cycle in good agreement with the literature, low carbon residues, and almost fully oxidized cerium oxide films. This distinction between two growth regimes is not unique to the CeOx/SiO2 system but can be generalized to other metal oxide substrates. Furthermore, the film growth deviates from the ideal layer-by-layer mode, forming micrometric inhomogeneous and defective flakes that eventually coalesce for deposit thicknesses above 10 nm. The ALD-cerium oxide films present less order and a higher density of defects than films grown by physical vapor deposition techniques, likely affecting their reactivity in oxidizing and reducing conditions.

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二氧化硅原子层沉积氧化铈的原位x射线光电子能谱研究:基质对生长早期反应机理的影响
采用原位x射线光电子能谱(XPS)研究了在SiO2衬底上以Ce(thd)4和O3为前驱体制备氧化铈的热原子层沉积(ALD)。当前驱体与底物或氧化铈表面相互作用时,反应机制的变化决定了体系呈现出复杂的生长行为。在第一生长阶段,底物促进的非ald副反应影响每周期的生长、表面残碳量和氧化铈的氧化程度。与此相反,第二生长阶段的特点是每周期生长恒定,与文献一致,碳残量低,氧化铈膜几乎完全氧化。这两种生长体制之间的区别并不是CeOx/SiO2体系所特有的,但可以推广到其他金属氧化物衬底。此外,薄膜的生长偏离了理想的逐层模式,形成微米级的不均匀和有缺陷的薄片,最终在沉积厚度超过10 nm时合并。与物理气相沉积技术相比,ald -铈氧化膜呈现出更少的有序和更高的缺陷密度,可能影响其在氧化和还原条件下的反应性。
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来源期刊
Advanced Materials Interfaces
Advanced Materials Interfaces CHEMISTRY, MULTIDISCIPLINARY-MATERIALS SCIENCE, MULTIDISCIPLINARY
CiteScore
8.40
自引率
5.60%
发文量
1174
审稿时长
1.3 months
期刊介绍: Advanced Materials Interfaces publishes top-level research on interface technologies and effects. Considering any interface formed between solids, liquids, and gases, the journal ensures an interdisciplinary blend of physics, chemistry, materials science, and life sciences. Advanced Materials Interfaces was launched in 2014 and received an Impact Factor of 4.834 in 2018. The scope of Advanced Materials Interfaces is dedicated to interfaces and surfaces that play an essential role in virtually all materials and devices. Physics, chemistry, materials science and life sciences blend to encourage new, cross-pollinating ideas, which will drive forward our understanding of the processes at the interface. Advanced Materials Interfaces covers all topics in interface-related research: Oil / water separation, Applications of nanostructured materials, 2D materials and heterostructures, Surfaces and interfaces in organic electronic devices, Catalysis and membranes, Self-assembly and nanopatterned surfaces, Composite and coating materials, Biointerfaces for technical and medical applications. Advanced Materials Interfaces provides a forum for topics on surface and interface science with a wide choice of formats: Reviews, Full Papers, and Communications, as well as Progress Reports and Research News.
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