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Reaction Mechanisms of Non-hydrolytic Atomic Layer Deposition of Al2O3with a Series of Alcohol Oxidants
  • Seo, Seunggi ;
  • Woo, Whang Je ;
  • Lee, Yujin ;
  • Yoon, Hwi ;
  • Kim, Miso ;
  • Oh, Il Kwon ;
  • Chung, Seung Min ;
  • Kim, Hyungjun ;
  • Shong, Bonggeun
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Publication Year
2021-08-26
Publisher
American Chemical Society
Citation
Journal of Physical Chemistry C, Vol.125, pp.18151-18160
Mesh Keyword
Carbon impuritiesExperimental methodsHydrogen transferInterfacial oxidesReaction mechanismReaction pathwaysSubstrate oxidationTrimethylaluminum
All Science Classification Codes (ASJC)
Electronic, Optical and Magnetic MaterialsEnergy (all)Physical and Theoretical ChemistrySurfaces, Coatings and Films
Abstract
Atomic layer deposition (ALD) of Al2O3 using trimethylaluminum (TMA) and H2O is the most widely and deeply studied ALD process owing to the superior properties of the deposited Al2O3 thin films and usability of TMA and H2O. However, H2O can cause undesirable substrate oxidation during ALD. While previous studies have shown that alcohol oxidants can be used to deposit Al2O3 thin films with less substrate oxidation, the reaction mechanism of ALD Al2O3 with alcohol oxidants has not been elucidated yet. In this study, the reaction mechanism of ALD of Al2O3 thin films using various alcohol oxidants was systematically investigated by computational and experimental methods. Various possible reaction pathways are considered for the oxidation of Al-CH3 with methanol (MeOH), ethanol (EtOH), and propanol (n-PrOH). It is found that the feasible reaction mechanism for removal of the surface-adsorbed alkoxy group is autocatalytic liberation of alkene through β-hydrogen transfer. ALD processes were developed using the alcohol oxidants. Our process using EtOH showed a growth rate of 0.96 Å/cycle and a moderate level of carbon impurities (2.6%). In addition, we investigated the properties of ALD-deposited Al2O3 thin films with alcohol oxidants, which indicated superior electrical properties and decreased formation of interfacial oxide on the Si substrate.
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/32239
DOI
https://doi.org/10.1021/acs.jpcc.1c03518
Fulltext

Type
Article
Funding
This research was supported by the National Research Foundation of Korea (NRF) funded by the Korean Government (Ministry of Science and ICT; no. 2019R1F1A1058615), by Korea Institute for Advancement of Technology (KIAT) grant funded by the Korea Government(MOTIE)(P0012451, The Competency Development Program for Industy Specialist), by the Materials and Components Technology Development Program of MOTIE/KEIT (10080642, Development on precursors for carbon/halogen-free thin film and their delivery system for high- k/metal gate application, and 20012460, Research support group for localization of ALD precursor and parts for 10 nm class semiconductor devices), and by Samsung Display Co., LTD. This work was also supported by the National Supercomputing Center including supercomputing resources and technical support (KSC-2020-CRE-0140).
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Oh, Il-Kwon 오일권
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