Correlation between polymer architecture and sub-glass-transition-temperature light-induced molecular movement in azo-polyimide polymers: Influence on linear and second- and third-order nonlinear optical processes

被引:53
作者
Sekkat, Z [1 ]
Pretre, P
Knoesen, A
Volksen, W
Lee, VY
Miller, RD
Wood, J
Knoll, W
机构
[1] Univ Calif Davis, Dept Elect & Comp Engn, Davis, CA 95616 USA
[2] IBM, Res Ctr, San Jose, CA 95120 USA
[3] Max Planck Inst Polymerforsch, D-55128 Mainz, Germany
[4] Univ Sidi Mohamed Ben Abdellah, Fac Sci, Dept Phys, Lab Opt & Spect, Atlas Fes, Morocco
[5] RIKEN, Inst Phys & Chem Res, Frontier Res Program, Wako, Saitama 35101, Japan
关键词
D O I
10.1364/JOSAB.15.000401
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
We report on light-induced linear and second-and third-order nonlinear optical effects in high-glass-transition-temperature (T-g) photosensitive nonlinear optical azo polyimides. We present evidence of light-induced orientation of azo chromophores at room temperature in very high-T-g polyimides (T-g up to 350 degrees C) even though the chromophore is firmly embedded into the polymer backbone. We show that the isomerization reaction and the light-induced polar and nonpolar orientation depend on the molecular structure of the unit building blocks of the polymer. The mechanism of the photoassisted poling process is clarified, and it is shown how the linear and second-and third-order nonlinear optical effects can be controlled by light. (C) 1998 Optical Society of America.
引用
收藏
页码:401 / 413
页数:13
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