Probing the Effects of Dimethyl Aluminum Isopropoxide Surface Reaction Byproducts on Atomic Layer Deposition Nucleation

Atomic layer deposition (ALD) processes that leverage a myriad of metal-organic and complementary reactant combinations have been identified to realize precise and conformal thin film growth. However, the effects of the ALD reaction byproducts on nucleation and growth mechanisms are rarely considered. Site-selective ALD processes provide an opportunity for the detailed investigation of uniform surface sites with atomistic accuracy. Intentional pretreatment with a known ALD reaction byproduct - isopropanol - enables a significant improvement in the nucleation rate reproducibility of dimethylaluminum isopropoxide and water ALD on rutile TiO<sub>2</sub>(110). In situ spectroscopic ellipsometry reveals a partially reversible byproduct binding that is site-selective for TiO<sub>2</sub>(110) surface oxygen vacancies. First-principles calculations reveal surface site-specific thermodynamics for adsorption of isopropanol and water that may influence ALD nucleation. The sensitivity of site-selective ALD motivates consideration of secondary surface reactions when designing precision deposition processes, including area- or site-selective ALD reactions.

Authors

Institutions

Publication Details

Journal
ACS Applied Materials & Interfaces
Published
2025-04-22
DOI
https://doi.org/10.1021/acsami.5c00901
Citations
3
Primary Topic
Semiconductor materials and devices
Type
article
Field-Weighted Citation Impact
2.19

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Probing the Effects of Dimethyl Aluminum Isopropoxide Surface Reaction Byproducts on Atomic Layer Deposition Nucleation

Alex B. F. Martinson, Jessica C. Jones, Chang Sheng Yan, Adam S. Hock et al.
3 citations
ACS Applied Materials & Interfaces
Semiconductor materials and devices
2.19
article

Probing the Effects of Dimethyl Aluminum Isopropoxide Surface Reaction Byproducts on Atomic Layer Deposition Nucleation

Alex B. F. Martinson, Jessica C. Jones, Chang Sheng Yan, Adam S. Hock, Jiayi Xu, Ashley R. Bielinski, Mark Muir, Chunxin Luo, Cong Liu
article en
3 citations

Abstract

Atomic layer deposition (ALD) processes that leverage a myriad of metal-organic and complementary reactant combinations have been identified to realize precise and conformal thin film growth. However, the effects of the ALD reaction byproducts on nucleation and growth mechanisms are rarely considered. Site-selective ALD processes provide an opportunity for the detailed investigation of uniform surface sites with atomistic accuracy. Intentional pretreatment with a known ALD reaction byproduct - isopropanol - enables a significant improvement in the nucleation rate reproducibility of dimethylaluminum isopropoxide and water ALD on rutile TiO<sub>2</sub>(110). In situ spectroscopic ellipsometry reveals a partially reversible byproduct binding that is site-selective for TiO<sub>2</sub>(110) surface oxygen vacancies. First-principles calculations reveal surface site-specific thermodynamics for adsorption of isopropanol and water that may influence ALD nucleation. The sensitivity of site-selective ALD motivates consideration of secondary surface reactions when designing precision deposition processes, including area- or site-selective ALD reactions.

ACS Applied Materials & InterfacesVol. 17(18)
Argonne National Laboratory (US), Illinois Institute of Technology (US), Division of Materials Science and Engineering (AU)
Basic Energy Sciences
Openalex Percentile: Top 13%
Semiconductor materials and devices
2.19
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.