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Bimolecular Reaction Mechanism in the Amido Complex-Based Atomic Layer Deposition of HfO(2)

[Image: see text] The surface chemistry of the initial growth during the first or first few precursor cycles in atomic layer deposition is decisive for how the growth proceeds later on and thus for the quality of the thin films grown. Yet, although general schemes of the surface chemistry of atomic...

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Detalles Bibliográficos
Autores principales: D’Acunto, Giulio, Tsyshevsky, Roman, Shayesteh, Payam, Gallet, Jean-Jacques, Bournel, Fabrice, Rochet, François, Pinsard, Indiana, Timm, Rainer, Head, Ashley R., Kuklja, Maija, Schnadt, Joachim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9879184/
https://www.ncbi.nlm.nih.gov/pubmed/36711051
http://dx.doi.org/10.1021/acs.chemmater.2c02947
Descripción
Sumario:[Image: see text] The surface chemistry of the initial growth during the first or first few precursor cycles in atomic layer deposition is decisive for how the growth proceeds later on and thus for the quality of the thin films grown. Yet, although general schemes of the surface chemistry of atomic layer deposition have been developed for many processes and precursors, in many cases, knowledge of this surface chemistry remains far from complete. For the particular case of HfO(2) atomic layer deposition on a SiO(2) surface from an alkylamido-hafnium precursor and water, we address this lack by carrying out an operando atomic layer deposition experiment during the first cycle of atomic layer deposition. Ambient-pressure X-ray photoelectron spectroscopy and density functional theory together show that the decomposition of the metal precursor on the stoichiometric SiO(2) surface in the first half-cycle of atomic layer deposition proceeds via a bimolecular reaction mechanism. The reaction leads to the formation of Hf-bonded methyl methylene imine and free dimethylamine. In addition, ligand exchange takes place involving the surface hydroxyls adsorbed at defect sites of the SiO(2) surface.