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Photo and Scanning Probe Lithography Using Alkylsilane Self-Assembled Monolayers

Published online by Cambridge University Press:  10 February 2011

H. Sugimura
Affiliation:
Department of Materials Processing Engineering, Graduate School of Engineering, Nagoya University, Chikusa Nagoya 464–8603, JAPAN, [email protected]
T. Hanji
Affiliation:
Department of Materials Processing Engineering, Graduate School of Engineering, Nagoya University, Chikusa Nagoya 464–8603, JAPAN, [email protected]
O. Takai
Affiliation:
Department of Materials Processing Engineering, Graduate School of Engineering, Nagoya University, Chikusa Nagoya 464–8603, JAPAN, [email protected]
K. Fukuda
Affiliation:
Department of Ecosystem Engineering, Graduate School of Engineering, The University of Tokushima, 2-1 Minamijosanjima, Tokushima 770–8506, JAPAN
H. Misawa
Affiliation:
Department of Ecosystem Engineering, Graduate School of Engineering, The University of Tokushima, 2-1 Minamijosanjima, Tokushima 770–8506, JAPAN
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Abstract

An organic film of a few nm in thickness was applied as a resist for photolithography and scanning probe lithography. This resist film was prepared on an oxide-covered Si substrate through chemisorption and spontaneous organization of organosilane molecules, e.g., n-octadecyltrimethoxysilane. The film belongs to a class of materials referred to as self-assembled monolayer (SAM). A SAM/Si sample was irradiated through a photomask with vacuum ultraviolet (VUV) light at a wavelength of 172 nm. The photomask image was transferred to the SAM through the decomposition of the SAM. Furthermore, we demonstrate nano-scale patterning of the SAM using an atomic force microscope (AFM) with an electrically conductive probe. The SAM was electrochemically degraded in the region where the AFM probe had been scanned. Both the photo-printed and AFM-genereated patterns were successfully transferred into the Si substrates based on wet chemical etching or on dry plasma etching. At present, using these VUV and AFM-based lithographies, we have succeeded in fabricating minute features of 2 μm and 20 nm in width, respectively.

Type
Research Article
Copyright
Copyright © Materials Research Society 2000

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References

1.Plueddemann, E. P., Silane Coupling Reagents (Plenum Press: New York, 1991)Google Scholar
2.Sagiv, J., J. Am. Chem. Soc. 102, 92 (1980).Google Scholar
3.Wasserman, S. R., Tao, Y.-T. and Whitesides, G. M., Langmuir 5, 1,074 (1989).Google Scholar
4.Dressick, W. J. and Calvert, J. M., Jpn. J. Appl. Phys. 32, 5829 (1993).Google Scholar
5.Lercel, M. J., Tiberio, R. C., Chapman, P. F., Craighead, H. G., Sheen, C. W., Parikh, A. N. and Allara, D. L., J. Vac. Sci. Technol. B 11, 2823 (1993).Google Scholar
6.Marrian, C. R. K., Perkins, F. K., Brandow, S. L., Koloski, T. S., Dobisz, E. A., and Calvert, J. M., Appl. Phys. Lett. 64, 390 (1994).Google Scholar
7.Sugimura, H. and Nakagiri, N., Langmuir 11, 3623 (1995).Google Scholar
8.Sugimura, H. and Nakagiri, N., J. Photopolym. Sci. Technol. 10, 661 (1997).Google Scholar
9.Hozumi, A., Ushiyama, K., Sugimura, H. and Takai, Osamu, Langmuir 15, 7600 (1999).Google Scholar
10.Lee, B. and Clark, N. A., Langmuir 14, 5498 (1998).Google Scholar
11.Sugimura, H. and Nakagiri, N., Appl. Phys. A 66, S427 (1998).Google Scholar
12.Suzuki, Y. and Shin-Ogi, M.Jpn. J. Appl. Phys. 29, L1517 (1990).Google Scholar
13.Brunner, H., Vallant, T., Mayer, U. and Hoffmann, H., Langmuir 12, 4614 (1996).Google Scholar
14.Sugimura, H.Takai, O. and Nakagiri, N., J. Vac. Sci. Technol. B 17, p. 1605 (1999).Google Scholar
15.Sugimura, H.Ushiyama, K., Hozumi, A. and Takai, Osamu, Langmuir, in press.Google Scholar
16.Sugimura, H.Uchida, T., Kitamura, N. and Masuhara, H., J. Phys. Chem. 98, 4352 (1994).Google Scholar
17.Sugimura, H. and Nakagiri, N., Nanotechnology 8, A 15 (1997).Google Scholar