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Formation of surface relief grating in polymers with pendant azobenzene chromophores as studied by AFM/UFM

机译:通过AFM / UFM研究在带有偶氮苯侧基生色团的聚合物中形成表面凹凸光栅

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摘要

We studied peculiarities of the structural reconstruction within holographically recorded gratings on the surface of several different amorphous azobenzene-containing polymers. Under illumination with a light interference pattern, two processes take place in this type of polymer. The first process is the light-induced orientation of azobenzene units perpendicular to the polarization plane of the incident light. The second one is a transfer of macromolecules along the grating vector (i.e.perpendicular to the grating lines). These two processes result in the creation of a volume orientation grating (alternating regions of different direction or degree of molecular orientation) and a surface relief grating (SRG) - i.e.modulation of film thickness. One can assume that both orientation of molecules and their movement might change the local mechanical properties of the material. Therefore, formation of the SRG is expected to result also in modulation of the local stiffness of the polymer film. To reveal and investigate these stiffness changes within the grating, spin-coated polymer films were prepared and the gratings were recorded on them in two different ways: with an orthogonal circular or orthogonal linear polarization of two recording light beams. A combination of atomic force microscopy (AFM) and ultrasonic force microscopy (UFM) techniques was applied for SRG development monitoring. We demonstrate that formation of the phase gratings depends on the chemical structure of polymers being used, polymer film thickness, and recording parameters, with the height of grating structures (depth of modulation) increasing with both the exposure time and the film thickness. UFM images suggest that the slopes of the topographic peaks in the phase gratings exhibit an increased stiffness with respect to the grating depressions.
机译:我们研究了几种不同的无定形含偶氮苯聚合物表面上全息记录的光栅中结构重建的特殊性。在具有光干涉图案的照明下,这种类型的聚合物发生两个过程。第一个过程是偶氮苯单元的光致取向垂直于入射光的偏振面。第二个是大分子沿着光栅矢量的转移(即垂直于光栅线)。这两个过程导致了体积取向光栅(分子取向或方向不同的交替区域)和表面起伏光栅(SRG)的产生,即膜厚度的调制。可以假设分子的取向及其运动都可能改变材料的局部机械性能。因此,预计SRG的形成还将导致聚合物膜的局部刚度的调节。为了揭示和研究光栅内的这些刚度变化,制备了旋涂聚合物薄膜,并以两种不同方式将光栅记录在光栅上:两个记录光束的正交圆偏振或正交线性偏振。原子力显微镜(AFM)和超声力显微镜(UFM)技术的结合被应用于SRG的发展监测。我们证明了相位光栅的形成取决于所用聚合物的化学结构,聚合物膜的厚度和记录参数,光栅结构的高度(调制深度)随曝光时间和膜厚度的增加而增加。 UFM图像表明,相对于光栅凹陷,相位光栅中形貌峰的斜率显示出更高的刚度。

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