Blagoeva Blaga, Nedelchev Lian, Nazarova Dimana, Stoykova Elena, Park Joongki
Appl Opt. 2022 Feb 10;61(5):B147-B155. doi: 10.1364/AO.444159.
Photoinduced supramolecular chiral structures in azo materials have been extensively studied for the development of all-optical switches and because of their influence on the properties of certain types of polarization holographic gratings. Here, we investigate chiral structures induced by irradiation with elliptically polarized light in thin films of four azopolymers denoted as PAZO, , , which are amorphous, and , which is liquid crystalline. Their formation is characterized in real time by the kinetics of azimuth rotation. The influence of the irradiation wavelength and intensity is also analyzed. The largest azimuth rotation per unit thickness is achieved in PAZO (33°/µm) and (25°/µm). Reversibility of the chiral structures is demonstrated by a tenfold change in the direction of rotation. Our results also indicate that chiral structures formation occurs significantly faster than the induction of linear birefringence.
由于偶氮材料中的光致超分子手性结构对全光开关的发展具有重要意义,并且对某些类型的偏振全息光栅的性质有影响,因此对其进行了广泛的研究。在此,我们研究了椭圆偏振光照射在四种偶氮聚合物薄膜中诱导产生的手性结构,这四种聚合物分别为非晶态的PAZO、 、 以及液晶态的 。通过方位角旋转动力学实时表征它们的形成过程。还分析了照射波长和强度的影响。在PAZO(33°/µm)和 (25°/µm)中实现了每单位厚度最大的方位角旋转。手性结构的可逆性通过旋转方向的十倍变化得到证明。我们的结果还表明,手性结构的形成比线性双折射的诱导要快得多。