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Relaxation Phenomena in Poled Electro-Optic Polymers

Published online by Cambridge University Press:  16 February 2011

K. D. Singer ,
R. Dureiko ,
J. Khaydarov  and
R. Fuerst
K. D. Singer
Affiliation:
Case Western Reserve University, Department of Physics, Cleveland, OH 44106–7079
R. Dureiko
Affiliation:
Case Western Reserve University, Department of Physics, Cleveland, OH 44106–7079
J. Khaydarov
Affiliation:
Case Western Reserve University, Department of Physics, Cleveland, OH 44106–7079
R. Fuerst
Affiliation:
Case Western Reserve University, Department of Physics, Cleveland, OH 44106–7079
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Abstract

The relaxation of the nonlinear optical coefficient of poled electro-optic polymers remains an important issue in the potential application of these Materials. This relaxation is due to the homogenization of the orientational distribution function of nonlinear chromophores in the polymer glass over time. We have measured the relaxation using optical second harmonic generation as a function of temperature for doped polymer materials over a range of temperatures deep in the glassy state. We relate the data to widely used physical models of the glassy state which indicate that the relaxation process occurs over a considerable range of time scales. It has been found that the decay of the nonlinear polarization exhibits two mechanisms depending on the time and temperature scales over which measurements are performed. We have carried out measurements over a range of times and show that a broad distribution of relaxation times characterizes the data. This broad distribution is an appealing model in that it not only fits the data well, but is well connected to accepted physical models of the relaxation behavior of glasses. The characteristic energy of the relaxation can be estimated from the temperature dependence and is found to be equal to or less than the energy characterizing the polymer Motion, and agrees with dielectric studies. This indicates that the chromophores are more or less coupled to the dynamics of the polymer chain. A figure of merit for the coupling of the chromophore to the polymer chain is proposed.

Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 328: Symposium Q – Electrical, Optical, and Magnetic Properties of Organic Solid State Materials , 1993 , 499
Copyright
Copyright © Materials Research Society 1994

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References

REFERENCES

[1] Ye, C., Marks, T.J., Yang, J., and Wong, G.K., Macromol. 20, 2322 (1987).Google Scholar
[2] Reck, B., Eich, M., Jungbauer, D., Twieg, R.J., Willson, C.G., Yoon, D.Y., and Bjorklund, G.C., Proc. SPIE 1147, 74 (1989).Google Scholar
[3] Hampsch, H.L., Yang, J., Wong, G.K., and Torkelson, J.M., Polym. Commun. 30, 40 (1989).Google Scholar
[4] Eich, M., Looser, H., Yoon, D.Y., Twieg, R., Bjorklund, G., and Baumert, J.C., J. Opt. Soc. Am. B 6, 1590 (1989).Google Scholar
[5] Singer, K.D. and King, L.A., J. Appl. Phys. 70, 3251 (1991).Google Scholar
[6] Wu, J.W., J. Opt. Soc. Am. B 8, 142 (1991).Google Scholar
[7] Eich, M., Sen, A., Looser, H., Bjorklund, G.C., Swalen, J.D., Twieg, R., and Yoon, D.Y., J. Appl. Phys. 66, 2559 (1989).Google Scholar
[8] Teraoka, I., Jungbauer, D., Reck, B., Yoon, D.Y., Twieg, R., and Willson, C.G., J. Appl. Phys. 69, 2569 (1991).CrossRefGoogle Scholar
[9] Lindsay, G.A., Henry, R.A., Hoover, J.M., Knoesen, A., and Mortazarvi, M.A., Macromol. 25, 4888 (1992).Google Scholar
[10] Stähelin, M., Burland, D.M., Ebert, M., Miller, R.D., Smith, B.A., Twieg, R.J., Volksen, W., and Walsh, C.A., Appl. Phys. Lett. 61, 1625 (1992).Google Scholar
[11] Sehen, M.A. and Mopsik, F.I., Proc. SPIE 1560, 315 (1991).Google Scholar
[12] Broussoux, D., Chastaing, E., Esselin, S., LeBarny, P., Robin, P., Bourbin, Y., Pocholle, J.P., and Raffy, J., Rev. Tech. Thomson-CSF 20–21, 151 (1989).Google Scholar
[13] Kuzyk, M.G., Moore, R.C., and King, L.A., J. Opt. Soc. Am. B 7, 64 (1990).CrossRefGoogle Scholar
[14] Valley, J.F., Wu, J.W., and Valencia, C.L., Appl. Phys. Lett. 57, 1084 (1990).CrossRefGoogle Scholar
[15] Köhler, W., Robello, D.R., Dao, P.T., Willand, C.S., and Williams, D.J., J. Chem. Phys. 93, 9157 (1990).Google Scholar
[16] Boyd, G.T., Francis, C.V., Trend, J.E., Ender, D.A., J. Opt. Soc. Am. B 8, 887 (1991).Google Scholar
[17] Kohlrausch, F., Pogg. Ann. Physk. 119, 352 (1863);Google Scholar
Williams, G. and Watts, D.C., Trans. Faraday. Soc. 66, 80 (1970).Google Scholar
[18] Scher, H., Shlesinger, M.F., and Bendler, J.T., Physics Today 44, 26 (1991).Google Scholar
[19] Shlesinger, M.F., Ann. Rev. Phys. Chem. 39, 269 (1988).Google Scholar
[20] Palmer, R.G., Stein, D.L., Abrahams, E., and Anderson, P.W., Phys. Rev. Lett. 53, 958 (1984).Google Scholar
[21] Dhinojwala, A., Wong, G.K., and Torkelson, J.M., Macromol. 25 7395 (1992).Google Scholar
[22] Williams, M.L., Landel, R.F., and Ferry, J.P., J. Am. Chem. Soc. 77, 3701 (1955).Google Scholar
[23] Hampsch, H.L., Yang, J., Wong, G.K., and Torkelson, J.M., Macromol. 21, 526 (1988).Google Scholar
[24] Lei, D., Runt, J., Safari, A., and Newnham, R.E., Macromol. 20, 1797 (1987).CrossRefGoogle Scholar
[25] Matsuoka, S., Williams, G., Johnson, G.E., Anderson, E.W., and Furukawa, T., Macromol. 18, 2652 (1985).Google Scholar
[26] Struik, L.C.E., Physical Aging in AMorphous Polymers and Other Materials (Elsevier, Amsterdam, 1978).Google Scholar