journal article·2004-01

Copper chemical vapour deposition on organosilane-treated SiO2 surfaces

N.G Semaltianos, J.-L Pastol, P Doppelt

Applied Surface Science· Volume 222· Issue 1-4
Publisher page

Abstract

Abstract Copper thin films were grown on SiO2 substrates by chemical vapour deposition using the precursor (2-methyl-1-hexene-3-yne)Cu(1,1,1,5,5,5-hexafluoroacetylacetonate) ((MHY)Cu(hfac)) and were examined by scanning electron and atomic force microscopy. The affinity for copper chemical vapour deposition of the substrate surface is higher after the formation of self-assembled monolayers of organosilanes onto the substrate surface. Furthermore, the affinity is greatly enhanced by a subsequent UV light irradiation of the organosilane monolayer, in air, prior to deposition. The dependence of film morphology and statistical surface parameters on substrate temperature and amount of vapour precursor introduced during deposition, provide information for the optimisation of external parameters towards obtaining a thin yet continuous film. Self-assembled monolayers of organosilanes can be used for a selective metallization of SiO2 substrates by copper chemical vapour deposition, in addition to acting as ultrathin barriers which prevent copper diffusion into the SiO2, thus opening a route for a technology useful in microelectronic industrial applications.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Copper Interconnects and Reliability · Molecular Junctions and Nanostructures · Nanofabrication and Lithography Techniques

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

References (24)

Show source-provided references
1. Li · MRS Bull. · 1994 · 19 · 1510.1557/S0883769400047692 ↗
2. Gates · Chem. Rev. · 1996 · 96 · 151910.1021/cr950233m ↗
3. Doppelt · Coord. Chem. Rev. · 1998 · 180 · 1783
4. Doppelt · Microelctr. Eng. · 1997 · 33 · 1510.1016/S0167-9317(96)00026-3 ↗
5. Krishnamoorthy · Appl. Phys. Lett. · 2001 · 78 · 246710.1063/1.1365418 ↗
6. Kaloyeros · Annu. Rev. Mater. Sci. · 2000 · 30 · 36310.1146/annurev.matsci.30.1.363 ↗
7. P. Doppelt, French Patent 97 03 029, US Patent 6,130,345.
8. T.-Y. Chen, Ph.D. thesis, Universite de Paris 6, 2000.
9. Chen · Chem. Mater. · 2001 · 13 · 399310.1021/cm0012318 ↗
10. Krishnamoorthy · Appl. Phys. Lett. · 2001 · 78 · 246710.1063/1.1365418 ↗
11. Ramanath · Appl. Phys. Lett. · 2003 · 83 · 38310.1063/1.1591232 ↗
12. Schwartz · Surf. Sci. · 1999 · 423 · 20810.1016/S0039-6028(98)00907-8 ↗
13. Nguyen · J. Electrochem. Soc. · 1997 · 144 · 282910.1149/1.1837902 ↗
14. Venables · Rep. Prog. Phys. · 1984 · 47 · 39910.1088/0034-4885/47/4/002 ↗
15. Ekerdt · Chem. Rev. · 1996 · 96 · 149910.1021/cr950236z ↗
16. Doppelt · Lett. Sci. Chim. · 1996 · 58 · 22
17. J.H. Seinfeld, Atmospheric Chemistry and Physics of Air Pollution, Wiley, New York, 1986.10.1021/es00151a602 ↗
18. Demore · J. Chem. Phys. · 1966 · 44 · 178010.1063/1.1726939 ↗
19. Snelling · J. Chem. Phys. · 1966 · 44 · 413710.1063/1.1726595 ↗
20. Zhang · J. Am. Chem. Soc. · 1998 · 120 · 265410.1021/ja9714853 ↗
21. Huang · J. Am. Chem. Soc. · 1993 · 115 · 334210.1021/ja00061a048 ↗
22. Norrod · J. Am. Chem. Soc. · 1998 · 120 · 265610.1021/ja9738642 ↗
23. Tarlow · J. Am. Chem. Soc. · 1993 · 115 · 530510.1021/ja00065a056 ↗
24. E.S. Beck, E.J. Karwacki Jr., R.J. Ciotti, T.A.J. Norman, European Patent 1180553, US Patent 2000-638586.