Comparison of O2 and H2O as oxygen source for homoepitaxial growth of β-Ga2O3 layers by halide vapor phase epitaxy

被引:25
作者
Konishi, Keita [1 ]
Goto, Ken [1 ,3 ]
Togashi, Rie [1 ,4 ]
Murakami, Hisashi [1 ,4 ]
Higashiwaki, Masataka [5 ]
Kuramata, Akito [2 ,3 ]
Yamakoshi, Shigenobu [2 ,3 ]
Monemar, Bo [4 ,6 ]
Kumagai, Yoshinao [1 ,4 ]
机构
[1] Tokyo Univ Agr & Technol, Dept Appl Chem, 2-24-16 Naka Cho, Koganei, Tokyo 1848588, Japan
[2] Tamura Corp, 2-3-1 Hirosedai, Sayama, Saitama 3501328, Japan
[3] Novel Crystal Technol Inc, 2-3-1 Hirosedai, Sayama, Saitama 3501328, Japan
[4] Tokyo Univ Agr & Technol, Inst Global Innovat Res, 2-24-16 Naka Cho, Koganei, Tokyo 1848588, Japan
[5] Natl Inst Informat & Commun Technol, 4-2-1 Nukui Kitamachi, Koganei, Tokyo 1848795, Japan
[6] Linkoping Univ, Dept Phys Chem & Biol IFM, SE-58183 Linkoping, Sweden
基金
日本学术振兴会;
关键词
Thermodynamic analysis; Halide vapor phase epitaxy; Oxides; Gallium compounds; Semiconducting III-VI materials; FILMS;
D O I
10.1016/j.jcrysgro.2018.04.009
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
Homoepitaxial growth of p-Ga2O3 layers by halide vapor phase epitaxy (HVPE) using O-2 or H2O as an oxygen source was investigated by thermodynamic analysis, and compared with measured properties after growth. The thermodynamic analysis revealed that Ga2O3 growth is expected even at 1000 C-degrees using both oxygen sources due to positive driving forces for Ga2O3 deposition. The experimental results for homoepitaxial growth on (0 0 1) beta-Ga2O3 substrates showed that the surfaces of the layers grown with H2O were smoother than those grown with O-2, although the growth rate with H2O was approximately half that with O-2. However, in the homoepitaxial layer grown using H2O, incorporation of Si impurities with a concentration almost equal to the effective donor concentration (2 x 10(16)cm (3)) was confirmed, which was caused by decomposition of the quartz glass reactor due to the presence of hydrogen in the system. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:39 / 44
页数:6
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