journal article·2011-01

Chemical bonding structures of silicon oxynitride films grown by ionised N 2 and pure O 2 gas mixtures at low temperature

H‐J Yun, J Lee, M‐C Jung, M‐S Han, K Park, K‐S Ahn, C‐J Choi

Advances in Applied Ceramics· Volume 110· Issue 1
Publisher page

Abstract

AbstractThe ultrathin silicon oxynitride (SiOxNy) films were formed using the direct oxynitridation of Si using ionised N2 and pure O2 gas mixtures at the relatively low temperature (600°C). The in situ X‐ray photoelectron spectroscopy (XPS) was used to assess the chemical composition and chemical state of the SiOxNy films. N 1s XPS spectra reveals that at least three characteristic N bonding states such as N≡Si3, N–(SiOx)3 and N = Si2–O bonds are formed in the SiOxNy films. As growth time increases, the N–(SiOx)3 bond is dominant in SiOxNy films, although N≡Si3 bonds are mainly formed in the initial growth stage at the temperature of 600°C. As considering the absence of direct bonding between N and O atoms, the nitridation and oxidation processes are believed to proceed independently. The increase in the growth temperature leads to the breakdown of both N–(SiOx)3 and N≡ = Si3 bonds and transformation into N = Si2–O bonding structure.
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Research context

OpenAlex topics: Semiconductor materials and devices · Metal and Thin Film Mechanics · Ga2O3 and related materials

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References (24)

Show source-provided references
1. 10.1063/1.138580310.1063/1.1385803 ↗
2. 10.1063/1.11195110.1063/1.111951 ↗
3. 10.1063/1.11346110.1063/1.113461 ↗
4. 10.1063/1.10974910.1063/1.109749 ↗
5. 10.1109/16.1993510.1109/16.19935 ↗
6. Fischer D · Phys. Rev. Lett · 2004 · 92 · 236405‐1
7. 10.1016/S0040-6090(99)00650-110.1016/S0040-6090(99)00650-1 ↗
8. 10.1016/j.tsf.2004.05.04310.1016/j.tsf.2004.05.043 ↗
9. 10.1016/S0167-577X(03)00284-210.1016/S0167-577X(03)00284-2 ↗
10. 10.1016/j.mee.2005.04.04910.1016/j.mee.2005.04.049 ↗
11. 10.1016/S0955-2219(97)00051-410.1016/S0955-2219(97)00051-4 ↗
12. 10.1016/S0167-5729(02)00031-610.1016/S0167-5729(02)00031-6 ↗
13. 10.1063/1.12043810.1063/1.120438 ↗
14. 10.1063/1.11692810.1063/1.116928 ↗
15. 10.1016/0368-2048(78)85047-610.1016/0368-2048(78)85047-6 ↗
16. Kim JW · Phys. Rev. B · 2002 · 66 · 035312‐1
17. Chung YD · Phys. Rev. B · 2002 · 65 · 155310‐1
18. 10.1103/PhysRevB.61.1415710.1103/PhysRevB.61.14157 ↗
19. 10.1016/S0039-6028(02)02096-410.1016/S0039-6028(02)02096-4 ↗
20. 10.1103/PhysRevLett.79.517410.1103/PhysRevLett.79.5174 ↗
21. 10.1063/1.11653710.1063/1.116537 ↗
22. 10.1063/1.11270310.1063/1.112703 ↗
23. 10.1016/S0169-4332(00)00548-110.1016/S0169-4332(00)00548-1 ↗
24. Moulder JF, Stickle WF, Sobol PE, Bomben KD: in ‘Handbook of X‐ray photoelectron spectroscopy’, 253; 1995, Eden Prairie, MN, Physical Electronics Inc.