Hostname: page-component-848d4c4894-nr4z6 Total loading time: 0 Render date: 2024-05-16T22:28:25.105Z Has data issue: false hasContentIssue false

A conductive composite film by permeation method

Published online by Cambridge University Press:  10 February 2011

Jin Wei Wang
Affiliation:
Department of Chemical & Environmental Engineering, National University of Singapore, 10 Kent Ridge Crescent, Singapore 119260, Singapore
M. P. Srinivasan
Affiliation:
Department of Chemical & Environmental Engineering, National University of Singapore, 10 Kent Ridge Crescent, Singapore 119260, Singapore
Get access

Abstract

A new method of making conductive composite films by permeation of the conducting guest species into the host is reported. A layer of poly(3-n-dodecyl thiophene) (P3ddt) is embedded at the surface of polyimide by permeation of the monomer or polymer (in solution in tetrahydrofuran or chloroform) into a solution of polyamic acid in n-methyl pyrrolidinone or dimethyl acetamide. The resulting composites were imidised and polymerized (if necessary). Chemical imidisation yielded composite -films that retained the conducting polymer even when the composite was subjected to solvent extraction. The films were conductive upon doping with iodine and recovered conductivity when they were exposed to iodine vapor subsequent to thermal de-doping. Thermogravimetry showed that the amount of thiophene incorporated into the polyimide was higher for permeation of the polymer than that of the monomer; however, the amount of p3ddt incorporated by the latter method was still higher than the amount that could be incorporated by blending polyamic acid with p3ddt. The levels of conductivity and speed of recovery for doped films were also higher for the permeated films. Results of scanning electron microscopy suggested that the higher mobility afforded by contact in the liquid state have contributed greater entanglement between the constituents leading to higher thermal and solvent resistance of the conducting constituent. The permeation method could be adopted to form composite films in solvent systems that are not completely miscible.

Type
Research Article
Copyright
Copyright © Materials Research Society 2000

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. Sugimoto, R., Takeda, S., Gu, H. B., and Yoshino, K., Chem. Express 11, 635638 (1986).Google Scholar
2. Hotta, S., Rughooputh, S. D. D. V., and Heeger, A. J., Synth. Met. 22, 7987 (1987).Google Scholar
3. Ruckenstein, E., and Park, J. S., J. Appl. Polym. Sci. 42, 925 (1991).Google Scholar
4. Osterholm, J. E., Laakso, J., and Nyholm, P., Synth. Met. 28, C435–C444 (1989).Google Scholar
5. Ho, K. S., Levon, K., Mao, J., and Zheng, W. Y., Synth. Met. 55–57, 35913596 (1993).Google Scholar
6. Dao, L. H., Zhong, X. F., Menikh, A., Paynter, R. and F, Martim, Annu. Tech. Conf. Soc., Plast. Eng. 49, 783 (1991).Google Scholar
7. Tieke, B., and Gabriel, W., Polymer 31, 20 (1990).Google Scholar
8. Meador, M. B., Green, D. H., Auping, J. V., Gaier, J. R., Ferrara, L. A., Paradopoulos, D. S., Smith, J. W., Keller, D. J., J. Appl. Polym. Sci. 63, 7, 821834 (1997).Google Scholar
9. Sun, Y., Ruckenstein, E., Synth. Met., 74, 145150 (1995).Google Scholar
10. Sroog, C. E.; Engrey, A. L.; Abramo, S. V.; Berr, C. E.; Edwards, W. M.; and Olivier, K. L., Journal of Polymer Science: Part A, 3, 13731390 (1965).Google Scholar
11. Sugimoto, E., Takeda, S., Gu, H. B., Yoshino, K., Chem. Express 1, 11, 635638 (1986).Google Scholar
12. Endrey, A. L., U. S. Patent 3,179,633, 5pp (1965).Google Scholar
13. Wang, J. W., Srinivasan, M. P., Synthetic Metals 105, 17 (1999).Google Scholar
14. Chen, S. A., and Ni, J. M., Polymer Bulletin 26, 673680 (1991).Google Scholar