Hostname: page-component-848d4c4894-xfwgj Total loading time: 0 Render date: 2024-06-21T22:43:43.912Z Has data issue: false hasContentIssue false

A Structural Investigation of Polypyrrole as a Function of Oxidation State

Published online by Cambridge University Press:  01 February 2011

Mya R. Warren
Affiliation:
University of British Columbia
John D. Madden
Affiliation:
University of British Columbia
Get access

Abstract

Polypyrrole exhibits actuation under electrochemical doping and undoping of the polymer matrix. Active strain and x-ray diffraction measurements are performed in order to correlate the microscopic and macroscopic structural changes occurring during actuation. Under galvanostatic reduction, the film shows first a linear contraction with oxidation state due to expulsion of small anions. At 50% of the as-grown doping level, the film reverses direction and begins to expand, possibly due to incorporation of the larger cations. X-ray diffraction, however, does not show a linear contraction or expansion in the crystalline portions of the polymer. The polymer crystallites go through a sudden contraction in one dimension of approximately 14%, and otherwise remain constant. The contraction in the polypyrrole crystals occurs at the 50% doping level, and may be correlated with the reversal of macroscopic actuation.

Type
Research Article
Copyright
Copyright © Materials Research Society 2005

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

[1] Smela, E., Adv. Mater. 15, 481 (2003).Google Scholar
[2] Madden, J.D., Wandesteeg, N., Anquetil, P., Madden, P., Takshi, A., Pytel, R., Lafontaine, S., Wieringa, P., Hunter, I., IEEE J. Ocean. Eng. 29, 706 (2004).Google Scholar
[3] Pei, Q. and Inganäs, O., Solid State Ionics 60, 161 (1993).Google Scholar
[4] Kohlman, R.S. and Epstein, A., “Insulator-Metal Transition and Inhomogeneous Metallic State in Conducting Polymers,” Handbook of Conducting Polymers 2nd ed., ed. Skotheim, T., Elsenbaumer, R. and Reynolds, J. (Marcel Dekker, Inc., 1998) pp. 85121.Google Scholar
[5] Buckley, L.J., Roylance, D.K., and Wnek, G.E., J. Polym. Sci. B: Poly. Phys. 25, 2179 (1987).Google Scholar
[6] Pruneau, S., Graupner, W., Oniciu, L., Brie, M., and Turcu, R., Mat. Chem. Phys. 46, 55 (1996).Google Scholar
[7] Yamaura, M., Sato, K., and Hagiwara, T., Synth. Met. 39, 43 (1990).Google Scholar
[8] Yamaura, M., Hagiwara, T., and Iwata, K., Synth. Met. 26, 209 (1988).Google Scholar
[9] Yoon, C., Sung, H., Kim, J., Barsoukov, E., Kim, J., Lee, H., Synth. Met. 99, 201 (1999).Google Scholar
[10] Madden, J.D., Madden, P.G., Anquetil, P. and Hunter, I., Mat. Res. Soc. Symp. 698, 137 (2002).Google Scholar
[11] Otero, T.F., Grande, H., and Rodríguez, T., Electrochimica Acta. 41, 1863 (1996).Google Scholar
[12] Nogami, Y., Pouget, J.P., and Ishiguro, T., Synth. Met. 62, 257 (1994).Google Scholar
[13] Pei, Q. and Inganäs, O., Synth. Met. 55-57, 3724 (1993).Google Scholar