| Literature DB >> 29111636 |
Seunggi Seo, Byung Chul Yeo1, Sang Soo Han1, Chang Mo Yoon, Joon Young Yang2, Jonggeun Yoon2, Choongkeun Yoo2, Ho-Jin Kim2, Yong-Baek Lee2, Su Jeong Lee, Jae-Min Myoung, Han-Bo-Ram Lee3, Woo-Hee Kim4, Il-Kwon Oh, Hyungjun Kim.
Abstract
The reaction mechanism of area-selective atomic layer deposition (AS-ALD) of Al2O3 thin films using self-assembled monolayers (SAMs) was systematically investigated by theoretical and experimental studies. Trimethylaluminum (TMA) and H2O were used as the precursor and oxidant, respectively, with octadecylphosphonic acid (ODPA) as an SAM to block Al2O3 film formation. However, Al2O3 layers began to form on the ODPA SAMs after several cycles, despite reports that CH3-terminated SAMs cannot react with TMA. We showed that TMA does not react chemically with the SAM but is physically adsorbed, acting as a nucleation site for Al2O3 film growth. Moreover, the amount of physisorbed TMA was affected by the partial pressure. By controlling it, we developed a new AS-ALD Al2O3 process with high selectivity, which produces films of ∼60 nm thickness over 370 cycles. The successful deposition of Al2O3 thin film patterns using this process is a breakthrough technique in the field of nanotechnology.Entities:
Keywords: Al2O3; area-selective ALD; atomic layer deposition; nanopattern; self-assembled monolayer
Year: 2017 PMID: 29111636 DOI: 10.1021/acsami.7b13365
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229