Atomic layer deposition of Y2O3 and yttrium-doped HfO2 using a newly synthesized Y(iPrCp)2(N-iPr-amd) precursor for a high permittivity gate dielectric
- Authors
- Lee, Jae-Seung; Kim, Woo Hee; Oh, Il-Kwon; Kim, Min-Kyu; Lee, Gyeongho; Lee, Chang-Wan; Park, Jusang; Lansalot-Matras, Clement; Noh, Wontae; Kim, Hyungjun
- Issue Date
- Apr-2014
- Publisher
- Elsevier BV
- Keywords
- ALD; Atomic layer deposition; Dielectric constant; Gate oxide; High-k; Leakage current; Precursor; Rare earth; Yttrium
- Citation
- Applied Surface Science, v.297, pp.16 - 21
- Indexed
- SCIE
SCOPUS
- Journal Title
- Applied Surface Science
- Volume
- 297
- Start Page
- 16
- End Page
- 21
- URI
- https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/23340
- DOI
- 10.1016/j.apsusc.2014.01.032
- ISSN
- 0169-4332
- Abstract
- We systematically investigated the effects of Y doping in HfO 2 dielectric layer, focusing on structural phase transformation and the dielectric properties of the resultant films. Y doping was carried out using atomic layer deposition (ALD) with a novel Y(iPrCp)2(N-iPr-amd) precursor, which exhibits good thermal stability without any decomposition and clean evaporation. As a result, the ALD process of the Y 2 O 3 films showed well-saturated and linear growth characteristics of ∼0.45 Å/cycle without significant incubation delays and produced pure Y 2 O 3 films. Then, yttrium-doped HfO 2 films with various Y/(Y + Hf) compositions (yttrium content: 0.6- 4.8 mol%) were prepared by alternating Y 2 O 3 and HfO 2 growth cycles. Structural and electrical characterization revealed that the addition of yttrium to HfO 2 induced phase transformations from the monoclinic to the cubic or tetragonal phases, even at low post-annealing temperatures of 600 C, and improved leakage current densities by inducing oxygen vacancy-related complex defects. A maximum relative dielectric constant of ∼33.4 was obtained for films with a yttrium content of ∼1.2 mol%. Excellent EOT scalability was observed down to ∼1 nm without dielectric constant degradation. © 2014 Elsevier B.V. All rights reserved.
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