Miniaturization of microelectronic devices necessitates atomic precision in manufacturing techniques, particularly in the deposition of thin films. Atomic layer deposition (ALD) is recognized for its precision in controlling film thickness and composition on intricate three-dimensional structures. This study focuses on the ALD nucleation and growth mechanisms of ruthenium (Ru), a metal that has significant future implications for microelectronics. Despite its advantages, the deposition of a high surface-free energy material like Ru on a low surface-free energy material such as an oxide often faces challenges of large nucleation delays and non-uniform growth. To address these challenges, we explored the effectiveness of organometallic surface pretreatments using trimethylaluminum (TMA) or diethylzinc (DEZ) to enhance Ru film nucleation and growth. Our study employed a less-studied Ru precursor, cyclopentadienylethyl(dicarbonyl)ruthenium [RuCpEt(CO)2], which demonstrated promising results in terms of reduced nucleation delay and increased film continuity. Ru ALD was performed on silicon substrates with native oxide, using RuCpEt(CO)2 and O2 as coreactants. Our findings reveal that surface pretreatment significantly improves nucleation density and film thickness within the initial 60 ALD cycles, achieving up to a 3.2-fold increase in Ru surface coverage compared to nonpretreated substrates. Supported by density functional theory calculations, we propose that the enhanced nucleation observed with RuCpEt(CO)2 compared to previously-studied Ru(Cp)2 is due to two key mechanisms: the facilitated removal of CO ligands during deposition, which enhances the reactivity of the precursor, and a hydrogen-abstraction reaction involving the ethyl ligand of RuCpEt(CO)2 and the metal-alkyl groups on the surface. This study not only advances our understanding of Ru ALD processes but also highlights the significant impact of precursor chemistry and surface treatments in optimizing ALD for advanced microelectronic applications.
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September 2024
Research Article|
August 16 2024
Enhanced nucleation mechanism in ruthenium atomic layer deposition: Exploring surface termination and precursor ligand effects with RuCpEt(CO)2
Amnon Rothman
;
Amnon Rothman
(Conceptualization, Data curation, Formal analysis, Writing – original draft)
1
Department of Chemical Engineering, Stanford University
, Stanford, California 94305
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Seunggi Seo
;
Seunggi Seo
(Formal analysis, Writing – review & editing)
1
Department of Chemical Engineering, Stanford University
, Stanford, California 943052
School of Electrical and Electronic Engineering, Yonsei University
, Seoul 03722, Republic of Korea
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Jacob Woodruff;
Jacob Woodruff
(Resources, Writing – review & editing)
3
EMD Electronics
, Burlington, Massachusetts 01803
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Hyungjun Kim
;
Hyungjun Kim
(Writing – review & editing)
2
School of Electrical and Electronic Engineering, Yonsei University
, Seoul 03722, Republic of Korea
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Stacey F. Bent
Stacey F. Bent
a)
(Conceptualization, Funding acquisition, Resources, Supervision, Writing – review & editing)
1
Department of Chemical Engineering, Stanford University
, Stanford, California 943054
Department of Energy Science and Engineering
, Stanford University, Stanford, California 94305a)Author to whom correspondence should be addressed: sbent@stanford.edu
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a)Author to whom correspondence should be addressed: sbent@stanford.edu
J. Vac. Sci. Technol. A 42, 052402 (2024)
Article history
Received:
May 22 2024
Accepted:
July 12 2024
Citation
Amnon Rothman, Seunggi Seo, Jacob Woodruff, Hyungjun Kim, Stacey F. Bent; Enhanced nucleation mechanism in ruthenium atomic layer deposition: Exploring surface termination and precursor ligand effects with RuCpEt(CO)2. J. Vac. Sci. Technol. A 1 September 2024; 42 (5): 052402. https://doi.org/10.1116/6.0003775
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