Selective Etching of Silicon in Preference to Germanium and Si0.5Ge0.5
Source abstract
Abstract
The selective etching characteristics of silicon, germanium, and Si 0.5 Ge 0.5 subjected to a downstream H 2 /CF 4 /Ar plasma have been studied using a pair of in situ quartz crystal microbalances (QCMs) and X-ray photoelectron spectroscopy (XPS). At 50 °C and 760 mTorr, Si can be etched in preference to Ge and Si 0.5 Ge 0.5, with an essentially infinite Si/Ge etch-rate ratio (ERR), whereas for Si/Si 0.5 Ge 0.5, the ERR is infinite at 22 °C and 760 mTorr. XPS data showed that the selectivity is due to the differential suppression of etching by a ∼2 ML thick C x H y F z layer formed by the H 2 /CF 4 /Ar plasma on Si, Ge, and Si 0.5 Ge 0.5 . The data are consistent with the less exothermic reaction of fluorine radicals with Ge or Si 0.5 Ge 0.5 being strongly suppressed by the C x H y F z layer, whereas, on Si, the C x H y F z layer is not sufficient to completely suppress etching. Replacing H 2 with D 2 in the feed gas resulted in an inverse kinetic isotope effect (IKIE) where the Si and Si 0.5 Ge 0.5 etch rates were increased by ∼30 times with retention of significant etch selectivity. The use of D 2 /CF 4 /Ar instead of H 2 /CF 4 /Ar resulted in less total carbon deposition on Si and Si 0.5 Ge 0.5 and gave less Ge enrichment of Si 0.5 Ge 0.5 . These results are consistent with the selectivity being due to the differential suppression of etching by an angstrom-scale carbon layer.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Plasma Diagnostics and Applications · Semiconductor materials and devices · Metal and Thin Film Mechanics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Materials Science and Engineering Program and ‡Department of Chemistry and Biochemistry, University of California-San Diego, La Jolla, California 92093, United States
Funding
Lam Research Corporation
References (21)
Show source-provided references
1. 10.1186/s11671-016-1396-710.1186/s11671-016-1396-7 ↗
2. 10.1116/1.481931610.1116/1.4819316 ↗
3. 10.1116/1.163878010.1116/1.1638780 ↗
4. 10.1116/1.484357510.1116/1.4843575 ↗
5. 10.1016/S0039-6028(97)00304-X10.1016/S0039-6028(97)00304-X ↗
6. 10.1149/1.134826010.1149/1.1348260 ↗
7. 10.1063/1.10026910.1063/1.100269 ↗
8. 10.1116/1.58442410.1116/1.584424 ↗
9. 10.1063/1.10249010.1063/1.102490 ↗
10. 10.1149/1.205475510.1149/1.2054755 ↗
11. 10.1109/JMEMS.2013.226967310.1109/JMEMS.2013.2269673 ↗
12. 10.1116/1.239324410.1116/1.2393244 ↗
13. 10.7567/JJAP.51.01620110.7567/JJAP.51.016201 ↗
14. 10.1143/JJAP.33.220710.1143/JJAP.33.2207 ↗
15. 10.1116/1.302136110.1116/1.3021361 ↗
16. King R. B. · 2006 · 310.1002/0470862106 ↗
17. 10.1021/cr60211a00410.1021/cr60211a004 ↗
18. Hulett J. R. · J. Chem. Soc. · 1960 · 468
19. 10.1116/1.162664210.1116/1.1626642 ↗
20. 10.1116/1.58916010.1116/1.589160 ↗
21. 10.1016/0009-2614(93)80144-E10.1016/0009-2614(93)80144-E ↗