Atomic Layer Deposition of Iridium Thin Films Using Sequential Oxygen and Hydrogen Pulses

被引:29
|
作者
Mattinen, Miika [1 ]
Hamalainen, Jani [1 ]
Vehkamaki, Marko [1 ]
Heikkila, Mikko J. [1 ]
Mizohata, Kenichiro [2 ]
Jalkanen, Pasi [2 ]
Raisanen, Jyrki [2 ]
Ritala, Mikko [1 ]
Leskela, Markku [1 ]
机构
[1] Univ Helsinki, Inorgan Chem Lab, Dept Chem, POB 55, FI-00014 Helsinki, Finland
[2] Univ Helsinki, Div Mat Phys, Dept Phys, POB 43, FI-00014 Helsinki, Finland
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2016年 / 120卷 / 28期
关键词
NOBLE-METALS; REACTION-MECHANISM; PLATINUM; CHEMISORPTION; GROWTH; NUCLEATION; RUTHENIUM; SURFACES; IR(111); PEALD;
D O I
10.1021/acs.jpcc.6b04461
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Atomic layer deposition (ALD) is an advanced thin-film deposition method based on self-limiting surface reactions that allows for the controlled deposition of conformal, high-quality thin films of various materials. In this study, we aimed to explore how modifying the deposition chemistry affects the growth and properties of iridium films. We demonstrated a new ALD process using sequential pulses of iridium acetylacetonate [Ir(acac)(3)], oxygen (O-2), and hydrogen (H-2) and compared this to the established Ir(acac)(3) + O-2 process in the wide temperature range of 200-350 degrees C. A reaction scheme is proposed to explain how both oxygen and hydrogen affect the film growth. Comprehensive information on film properties was obtained for both processes. In particular, the strong (111) texture seen in this study has not been reported before for ALD iridium films. Changes in film properties, especially lowered resistivity, stronger (111) texture, and faster nucleation compared to the Ir(acac)(3) + O-2 process, should motivate further studies on O-2 + H-2 processes of platinum metals.
引用
收藏
页码:15235 / 15243
页数:9
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