Photoinduced multipolar tensorial patterning in polymer films by coherent control of molecular orientation

被引:7
作者
Brasselet, S [1 ]
Bidault, S [1 ]
Zyss, J [1 ]
机构
[1] Ecole Normale Super, Inst Alembert, Lab Photon Quant & Mol, CNRS,UMR 8537,IFR 121 FR 2357, F-94235 Cachan, France
关键词
nonlinear optics; tensorial holographic storage; multipolar molecular engineering; SHG; THG;
D O I
10.1016/S1631-0705(02)01333-6
中图分类号
P1 [天文学];
学科分类号
0704 ;
摘要
Based on an early proposition by R.J. Glauber in 1967, the possibility to break centrosymmetry in molecular media by interference between one- and two-photon absorption pathways has been implemented in polymers throughout the last decade. This effect has been more recently advantageously generalized to optically induce adjustable multipolar molecular ordering in polymer thin films for nonlinear optics. A major benefit of this approach lies in the control of the final molecular orientational distribution by pure Optical parameters such as phase or polarization of write beams. In this article. we extend a tensorial multipolar engineering experiment to encompass tensorial monitoring of photo-induced molecular orientational orders up to the 4th order. Coherent control of optical write beams, combined with real-time tensorial probing of optical properties in the material, provide access to a complete characterization of each excitation pathway contributing to the process. (C) 2002 Academie des sciences/Editions scientifiques et medicales Elsevier SAS.
引用
收藏
页码:479 / 492
页数:14
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