Hostname: page-component-54dcc4c588-scsgl Total loading time: 0 Render date: 2025-09-29T00:09:08.534Z Has data issue: false hasContentIssue false

Real Time Probes of Dye Doped Polymer Systems

Published online by Cambridge University Press:  21 February 2011

J. B. Halpern
Affiliation:
Department of Chemistry & Materials Research Center of Excellence, Howard University, Washington, DC 20059.
P. Amuzu-Williams
Affiliation:
Department of Chemistry & Materials Research Center of Excellence, Howard University, Washington, DC 20059.
L. House
Affiliation:
Department of Chemistry & Materials Research Center of Excellence, Howard University, Washington, DC 20059.
L. A. Lee
Affiliation:
Lester A. Lee Associates, Ft. Washington, MD.
Get access

Extract

Recently, advanced photonic devices have been fabricated in the laboratoryand are becoming commercially available. Thus, there is considerableinterest in inexpensive but efficient non-linear optical (NLO) materialsthat are simple to make and work with. In the last three years a largenumber of publications and patents have appeared describing NLO propertiesof organic materials, usually dyes, incorporated into or syntheticallyattached to polymers [1]. Such materials must be oriented before they havesecond-order NLO activity. Two methods have been used. In one, contactpoling [2–5], two electrodes are formed on or in the material and anelectric field is placed between them. In the other, corona poling, adischarge deposits charge on the polymer, which creates a strong orientingfield [6–8]. One could generalize that contact poling is (more) difficult todo, but the results are easy to understand, while corona poling is simple todo, but the results are (more) difficult to understand. This paper describesa set of corona poling experiments.

Information

Type
Research Article
Copyright
Copyright © Materials Research Society 1992

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.)

Article purchase

Temporarily unavailable

References

REFERENCES

1. A Chemical Abstracts search finds: 1985 - 4 items); 1986 13; 1987 - 23; 1988, 57; 1989 - 70; 1990 - 50 part year.Google Scholar
2. Krongauz, V.A., Fishman, S.N. and Goldburt, E.S., J. Phys. Chem., 82, 2469 (1978).CrossRefGoogle Scholar
3. Meredith, G.R., VanDusen, J.G. and Williams, D.J., Macrolmol. 15, 1385, (1982).CrossRefGoogle Scholar
4. Singer, K.D., Sohn, J.E. and Lalama, S.T., Appl. Phys. Lett., 49, 248 (1986).CrossRefGoogle Scholar
5. Boyd, G.T., Thin Solid Films, 152, 295 (1987).CrossRefGoogle Scholar
6. Bergman, J.G. Jr. McFee, J.H. and Crane, G.R., Appl. Phys. Lett. 18, 203 (1971).CrossRefGoogle Scholar
7. Hill, J.R., Dunn, P.L., Davies, G.J., Oliver, S.N., Pantelis, P. and Rush, J.D., Electronics Letters, 23, 700 (1987)CrossRefGoogle Scholar
8. Mortazavi, M.A., Knoesen, A., Kowel, S.T., Higgins, B.G. and Dines, A., J. Opt. Soc. Am. B, 6, 742 (1989).CrossRefGoogle Scholar
9. Daigo, H., Okamoto, N. and Fujimura, H., Opt. Comm., 69, 177, (1988).CrossRefGoogle Scholar
10. Hampsch, H.L., Yang, J., Wong, G.K. and Torkelson, J.M., Macromol. 23, 3640 (1990).CrossRefGoogle Scholar
11. Hampsch, H.L., Yang, J., Wong, G.K. and Torkelson, J.M., Macromol. 23, 3648 (1990).CrossRefGoogle Scholar
12. Hampsch, H.L., Torkelson, J.M., Bethke, S.J. and Grubb, S.G., J. Appl. Phys., 67, 1037 (1990).CrossRefGoogle Scholar
13. Eich, M., Looser, H., Yoon, D.Y., Tweig, R., Bjorklund, G.C., and Baumert, J.C., J. Opt. Soc. Am. B, 6, 1590 (1989).CrossRefGoogle Scholar