Hostname: page-component-78c5997874-t5tsf Total loading time: 0 Render date: 2024-11-09T07:03:59.132Z Has data issue: false hasContentIssue false

Molecular-Level Control in The Deposition of Ultrathin Films of Highly Conductive, In-Situ Polymerized P-Doped Conjugated Polymers

Published online by Cambridge University Press:  16 February 2011

A. C. Fou
Affiliation:
Department of Materials Science & Engineering, MIT, Cambridge, MA 02139
D. L. Ellis
Affiliation:
Department of Materials Science & Engineering, MIT, Cambridge, MA 02139
M. F. Rubner
Affiliation:
Department of Materials Science & Engineering, MIT, Cambridge, MA 02139
Get access

Abstract

A novel thin film processing technique has been developed for the fabrication of ultrathin films of conducting polymers with angstrom-level control over thickness and multilayer architecture. Molecular self-assembly of in-situ polymerized conjugated polymers consists of a layer-by-layer process in which a substrate is alternately dipped into a solution of a p-doped conducting polymer (e.g. polypyrrole, polyaniline) and a solution of a polyanion. In-situ oxidative polymerization produces the more highly conductive, underivatized form of the conjugated polymer, which is deposited in a single layer of precisely controlled thickness (30 to 60 Å). The thickness of each layer can be fine-tuned by adjusting the dipping time and the solution chemistry. The surface chemistry of the substrate (e.g. hydrophobic, charged, etc.) also strongly influences the deposition, thereby making it possible to selectively deposit conducting polypyrrole onto well defined regions of the substrates. Typical multilayer films exhibit conductivities in the range of 20–50 S/cm, but samples with conductivities as high as 300 S/cm have been realized. There is no limit to the number of layers that can be built up nor to the complexity of the multilayer architecture of the film; achieved simply by alternating the sequence of dips into solutions of various polycations and polyanions. This new self-assembly process opens up vast possibilities in applications which require large area, ultrathin films of conducting polymers and, more importantly, in applications that can take advantage of the unique interactions achievable in the complex, supermolecular architectures of multilayer films.

Type
Research Article
Copyright
Copyright © Materials Research Society 1994

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

[1] Burroughes, J.H., Bradley, D.D.C., Brown, A.R., Marks, R.N., MacKay, K., Friend, R.H., Burn, P.L., Holmes, A.L., Nature, 347, 539 (1990). andCrossRefGoogle Scholar
Gustafsson, G., Cao, Y., Treacy, G.M., Klavetter, F., Colaneri, N., Heeger, A.J., Nature, 357, 477 (1992).CrossRefGoogle Scholar
[2] Ellis, D.L., PhD Thesis, Dept. of Chemistry, Harvard University, 1993.Google Scholar
[3] Weinberger, B.R., Akhtar, M., Gau, S.C., Synthetic Metals, 4 (1982), 187.CrossRefGoogle Scholar
[4] Rosner, R.B., Rubner, M.F., Chem. Comm., 1449 (1991);CrossRefGoogle Scholar
Rosner, R.B., PhD Thesis, Matl. Sci. and Engr. Dept., MIT, 1992.Google Scholar
[5] Cheung, J.H., Fou, A.C., Rubner, M.F., Thin Solid Films, 1993, in press;Google Scholar
Fou, A.C., Rubner, M.F., to be published.Google Scholar
[6] Ferreira, M., Cheung, J.H., Rubner, M.F., SPE Proceedings, New Orleans, LA, USA (1993).Google Scholar
[7] Decher, G., Hong, J.D., Makromol. Chem., Macromol. Symp., 46, 321, (1991);CrossRefGoogle Scholar
Ber. Bunsen-Ges. Phys. Chem., 95, 1430, (1991).Google Scholar
[8] Pron, A., Fabianowski, W., Brudowski, C., Synthetic Metals, 18 (1987), 49.CrossRefGoogle Scholar
[9] Dubitsky, Y.A., Zhubanov, B.A., Synthetic Metals, 53 (1993), 303.CrossRefGoogle Scholar
[10] Gregory, R.V., Kimbrell, W.C., Kuhn, H.H., Synthetic Metals, 28 (1989), C823; Journal of Coated Fabrics, vol. 20, January 1991.CrossRefGoogle Scholar
[11] Kuhn, H.H. is gratefully acknowledged for the useful discussions regarding the use of ASA to enhance the conductivity and electrical stability of PPY.Google Scholar
[12] Fou, A.C., Rozsnyai, L.F., Rubner, M.F., Wrighton, M.S., unpublished resultsGoogle Scholar
[13] Singh, R., Tandon, R.P., Panwar, V.S., Chandra, S., J. Appl. Phys., 69 (4), 1991, p.2504 CrossRefGoogle Scholar