journal article·2019-10-09

In Situ Monitoring of Surface Reactions during Atomic Layer Etching of Silicon Nitride Using Hydrogen Plasma and Fluorine Radicals

Kazuya Nakane, René H. J. Vervuurt, Takayoshi Tsutsumi, Nobuyoshi Kobayashi, Masaru Hori

ACS Applied Materials & Interfaces· Volume 11· Issue 40
Publisher page

Abstract

The atomic layer etching (ALE) of silicon nitride (SiN) via a hydrogen plasma followed by exposure to fluorine radicals was investigated by using in situ spectroscopic ellipsometry and attenuated total reflectance Fourier transform infrared (FTIR) spectroscopy to examine the surface reactions and etching mechanism. FTIR spectra of the surface following exposure to the hydrogen plasma showed an increase in the concentration of Si-H and N-H bonds, although the N-H bond concentration plateaued more quickly. In contrast, during fluorine radical exposure, the Si-H bond concentration decreased more rapidly. Secondary ion mass spectrometry demonstrated that the nitrogen atom concentration was decreased to a depth of 4 nm from the surface after the hydrogen plasma treatment and indicated a structure consisting of N-H rich, Si-H rich, and mixed layers. This indicated that Si-H bonds were primarily present near the surface, while N-H bonds were mainly located deeper into the film. The formations of the N-H and Si-H rich layers are important phenomena associated with modification by hydrogen plasma and fluorine radical etching, respectively.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Semiconductor materials and devices · Diamond and Carbon-based Materials Research · Metal and Thin Film Mechanics

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

ASM Japan K.K., 23-1, 6-chome Nagayama, Tama, Tokyo 206-0025, Japan

References (39)

Show source-provided references
1. 10.1166/jnn.2012.665010.1166/jnn.2012.6650 ↗
2. 10.1109/IEDM.2012.647900110.1109/IEDM.2012.6479001 ↗
3. 10.1109/MM.2005.11010.1109/MM.2005.110 ↗
4. 10.1109/TED.2011.212191310.1109/TED.2011.2121913 ↗
5. 10.1116/1.481931610.1116/1.4819316 ↗
6. 10.1116/1.491337910.1116/1.4913379 ↗
7. 10.1021/acsami.7b0823410.1021/acsami.7b08234 ↗
8. 10.1116/1.494485010.1116/1.4944850 ↗
9. 10.1116/1.497966110.1116/1.4979661 ↗
10. 10.1149/2.0021506jss10.1149/2.0021506jss ↗
11. 10.1116/1.497901910.1116/1.4979019 ↗
12. 10.1116/1.302136110.1116/1.3021361 ↗
13. 10.1116/1.497117110.1116/1.4971171 ↗
14. 10.1016/j.mee.2013.03.17010.1016/j.mee.2013.03.170 ↗
15. 10.1088/0022-3727/42/5/05520210.1088/0022-3727/42/5/055202 ↗
16. 10.1166/jnn.2009.174810.1166/jnn.2009.1748 ↗
17. 10.1116/1.499399610.1116/1.4993996 ↗
18. 10.1111/j.1151-2916.2000.tb01182.x10.1111/j.1151-2916.2000.tb01182.x ↗
19. 10.1116/1.496307210.1116/1.4963072 ↗
20. 10.1063/1.12416510.1063/1.124165 ↗
21. 10.7567/JJAP.56.06HB0710.7567/JJAP.56.06HB07 ↗
22. 10.1116/1.500327110.1116/1.5003271 ↗
23. 10.7567/APEX.9.10620110.7567/APEX.9.106201 ↗
24. 10.1116/1.496723610.1116/1.4967236 ↗
25. 10.1116/1.499313310.1116/1.4993133 ↗
26. 10.1002/pssb.1966015022410.1002/pssb.19660150224 ↗
27. 10.1063/1.11806410.1063/1.118064 ↗
28. Lohner T. · Int. J. New. Hor. Phys. · 2016 · 3 · 7
29. 10.7567/1347-4065/ab17c710.7567/1347-4065/ab17c7 ↗
30. 10.1016/j.diamond.2015.02.00110.1016/j.diamond.2015.02.001 ↗
31. 10.1016/S0022-3093(05)80258-310.1016/S0022-3093(05)80258-3 ↗
32. 10.1002/pssa.20170065810.1002/pssa.201700658 ↗
33. 10.1088/0022-3727/30/7/00210.1088/0022-3727/30/7/002 ↗
34. 10.1186/1556-276X-8-3110.1186/1556-276X-8-31 ↗
35. 10.1021/acs.langmuir.7b0352210.1021/acs.langmuir.7b03522 ↗
36. 10.1116/1.58219510.1116/1.582195 ↗
37. 10.1016/S0169-4332(96)01006-910.1016/S0169-4332(96)01006-9 ↗
38. 10.1103/PhysRevB.48.531510.1103/PhysRevB.48.5315 ↗
39. 10.1038/nmat251410.1038/nmat2514 ↗