Surface Preparation Techniques for the Atomic Layer Deposition of Hafnium Oxide

2006 ◽  
Vol 917 ◽  
Author(s):  
Laura Nyns ◽  
Lindsey Hall ◽  
Thierry Conard ◽  
Annelies Delabie ◽  
Wim Deweerd ◽  
...  

AbstractAtomic layer deposition (ALD) has been successfully used over the years for the deposition of conformal dielectric layers with precise thickness down to the nanometer scale. Therefore, optimization of the growth behaviour of the dielectric is mandatory. Since ALD is a surface sensitive growth technique, determined by the amount of available reaction sites at the starting surface, the impact of various wet chemical and thermal Si treatments on the HfO2 growth was evaluated. Thin SiO2 starting layers, based on wet chemical processing, were prepared by using a diluted peroxide mixture and an ozone/DI-water treatment. The thermally grown oxides were gradually etched by slowly immersing the oxidized Si substrate into a diluted HF solution, creating a thickness range on a single wafer. Our results demonstrate that the HfO2 deposition is more dependent on the thickness of the SiO2 layer than on the chemistry used to grow the oxide layer. For all studied oxides, two regions can clearly be distinguished. First, a linear relationship between the oxide thickness and the amount of deposited HfO2 is seen. Because chemical oxides tend to grow in islands, this trend can be explained by an increase in density of surface OH groups when the oxide grows thicker. When an ellipsometric thickness of ~0.8 nm is reached, saturation of the HfO2 growth is obtained. We believe that, from this thickness on, the starting surface is completely covered with hydroxyl groups, leaving the HfO2 growth only dependent on the ALD process itself. Since both the wet chemical as the thermal oxides are showing the same trend in HfO2 deposition, it can be stated that surface preparations can be selected solely based on their ease of processing. However, the electrical results show that there may be a difference between the ozone based wet chemical oxides and the etched thermal oxides, since the latter seems to possess slightly more leakage current. The electrical results will be discussed in more detail during the presentation.

2006 ◽  
Vol 153 (8) ◽  
pp. F180 ◽  
Author(s):  
Annelies Delabie ◽  
Matty Caymax ◽  
Bert Brijs ◽  
David P. Brunco ◽  
Thierry Conard ◽  
...  

2008 ◽  
Vol 155 (12) ◽  
pp. H937 ◽  
Author(s):  
Annelies Delabie ◽  
David P. Brunco ◽  
Thierry Conard ◽  
Paola Favia ◽  
Hugo Bender ◽  
...  

2005 ◽  
Vol 15 (4) ◽  
pp. 275-280
Author(s):  
Hie-Chul Kim ◽  
Min-Wan Kim ◽  
Hyung-Su Kim ◽  
Hyug-Jong Kim ◽  
Woo-Keun Sohn ◽  
...  

2002 ◽  
Vol 92 (10) ◽  
pp. 5698-5703 ◽  
Author(s):  
Kaupo Kukli ◽  
Mikko Ritala ◽  
Jonas Sundqvist ◽  
Jaan Aarik ◽  
Jun Lu ◽  
...  

2018 ◽  
Vol 6 (30) ◽  
pp. 8051-8059 ◽  
Author(s):  
Ermioni Polydorou ◽  
Martha Botzakaki ◽  
Charalampos Drivas ◽  
Kostas Seintis ◽  
Ilias Sakellis ◽  
...  

Atomic layer deposition of HfO2 significantly increases the efficiency and prolongs the lifetime of organic solar cells.


Nanomaterials ◽  
2019 ◽  
Vol 9 (8) ◽  
pp. 1085 ◽  
Author(s):  
Kemelbay ◽  
Tikhonov ◽  
Aloni ◽  
Kuykendall

As one of the highest mobility semiconductor materials, carbon nanotubes (CNTs) have been extensively studied for use in field effect transistors (FETs). To fabricate surround-gate FETs— which offer the best switching performance—deposition of conformal, weakly-interacting dielectric layers is necessary. This is challenging due to the chemically inert surface of CNTs and a lack of nucleation sites—especially for defect-free CNTs. As a result, a technique that enables integration of uniform high-k dielectrics, while preserving the CNT’s exceptional properties is required. In this work, we show a method that enables conformal atomic layer deposition (ALD) of high-k dielectrics on defect-free CNTs. By depositing a thin Ti metal film, followed by oxidation to TiO2 under ambient conditions, a nucleation layer is formed for subsequent ALD deposition of Al2O3. The technique is easy to implement and is VLSI-compatible. We show that the ALD coatings are uniform, continuous and conformal, and Raman spectroscopy reveals that the technique does not induce defects in the CNT. The resulting bilayer TiO2/Al2O3 thin-film shows an improved dielectric constant of 21.7 and an equivalent oxide thickness of 2.7 nm. The electrical properties of back-gated and top-gated devices fabricated using this method are presented.


Nanomaterials ◽  
2020 ◽  
Vol 10 (8) ◽  
pp. 1496 ◽  
Author(s):  
Dominik Benz ◽  
Hao Van Bui ◽  
Hubertus T. Hintzen ◽  
Michiel T. Kreutzer ◽  
J. Ruud van Ommen

Photocatalysts for water purification typically lack efficiency for practical applications. Here we present a multi-component (Pt:SiO2:TiO2(P25)) material that was designed using knowledge of reaction mechanisms of mono-modified catalysts (SiO2:TiO2, and Pt:TiO2) combined with the potential of atomic layer deposition (ALD). The deposition of ultrathin SiO2 layers on TiO2 nanoparticles, applying ALD in a fluidized bed reactor, demonstrated in earlier studies their beneficial effects for the photocatalytic degradation of organic pollutants due to more acidic surface Si–OH groups which benefit the generation of hydroxyl radicals. Furthermore, our investigation on the role of Pt on TiO2(P25), as an improved photocatalyst, demonstrated that suppression of charge recombination by oxygen adsorbed on the Pt particles, reacting with the separated electrons to superoxide radicals, acts as an important factor for the catalytic improvement. Combining both materials into the resulting Pt:SiO2:TiO2(P25) nanopowder exceeded the dye degradation performance of both the individual SiO2:TiO2(P25) (1.5 fold) and Pt:TiO2(P25) (4-fold) catalysts by 6-fold as compared to TiO2(P25). This approach thus shows that by understanding the individual materials’ behavior and using ALD as an appropriate deposition technique enabling control on the nano-scale, new materials can be designed and developed, further improving the photocatalytic activity. Our research demonstrates that ALD is an attractive technology to synthesize multicomponent catalysts in a precise and scalable way.


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