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11.
Photorefractive materials exhibit a spatial modulation of the refractive index due to redistribution of photogenerated charges in an optically nonlinear medium. As such, they have the ability to manipulate light and are potentially important for optical applications including image processing, optical storage, programmable optical interconnects and simulation of neural networks. Photorefractive materials are generally crystals, polymers and glasses with electro-optic or birefringent properties and noncentrosymmetric structure. Here we report the photorefractive effect in both non-centrosymmetric and centrosymmetric azo-dye-doped silica glasses, in which refractive index gratings that are spatially phase-shifted with respect to the incident light intensity pattern are observed. The effect results from a nonlocal response of the material to optical illumination, and enables the transfer of energy between two interfering light beams (asymmetric two-beam coupling). Although the writing time for the present grating is relatively slow, we have achieved a two-beam coupling optical gain of 188 cm(-1) in the centrosymmetric glasses, and a gain of 444 cm(-1) in the non-centrosymmetric structures. The latter are fabricated using a corona discharge process to induce a permanent arrangement of azo-dye chromophores. 相似文献
12.
Peng Liang Bo Chen Xiaoping Yang Qianqian Liu Airui Li Lydia Mackenzie Deguo Zhang 《科学通报(英文版)》2022,(1):21-24
The dust cycle is an important component of the Earth system,and dust storms are a severe environmental issue affecting many countries around the world [1].East... 相似文献
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Bicknell LS Bongers EM Leitch A Brown S Schoots J Harley ME Aftimos S Al-Aama JY Bober M Brown PA van Bokhoven H Dean J Edrees AY Feingold M Fryer A Hoefsloot LH Kau N Knoers NV Mackenzie J Opitz JM Sarda P Ross A Temple IK Toutain A Wise CA Wright M Jackson AP 《Nature genetics》2011,43(4):356-359
Meier-Gorlin syndrome (ear, patella and short-stature syndrome) is an autosomal recessive primordial dwarfism syndrome characterized by absent or hypoplastic patellae and markedly small ears1?3. Both pre- and post-natal growth are impaired in this disorder, and although microcephaly is often evident, intellect is usually normal in this syndrome. We report here that individuals with this disorder show marked locus heterogeneity, and we identify mutations in five separate genes: ORC1, ORC4, ORC6, CDT1 and CDC6. All of these genes encode components of the pre-replication complex, implicating defects in replication licensing as the cause of a genetic syndrome with distinct developmental abnormalities. 相似文献