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Modeling Photopolymers for Holographic Data Storage Applications

机译:适用于全息数据存储应用的光聚合物

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The Nonlocal Polymerization Driven Diffusion model, NPDD, is can be used to describe holographic grating formation in Acrylamide-based photopolymer. The free radical chain polymerization process results in polymer being generated nonlocal both in space and time to the point of chain initiation. Temporal nonlocality can be used to describepost exposure dark effects. Nonlinear response and the effects of dye bleaching have been examined. Both primary and bimolecular chain termination mechanisms have been included and examined. Recently 3-D, and inhibition effects have also been included. In this paper we review of our recent work. It is shown that temporal effects become most notable for short exposres and the inclusion of the nonlocal temporal response function is shown to be necessary to accurately describe the process. In particular, brief post exposure self-amplification of the refractive index modulation is noted. This is attributed to continued chain growth for a brief period after exposure. Following this a slight decay in the grating amplitude also occurs. This we believe is due to the continued diffusion of monomer after exposure. Since the sinusoidal recording pattern generates a monomer concentration gradient during the recording process monomer diffusion occurs both during and after exposure. The evolution of the refractive index modulation is determined by the respective refractive index values of the recording material components. From independent measurements it is noted that the refractive index value of the monomer is slightly less than that of the background material. Therefore as monomer diffuses back into the dark regions, a reduction in overall refractive index modulation occurs. Volume changes occurring within the material also affect the nature of grating evolution. To model these effects we employ a free volume concept. Due to the fact that the covalent single carbon bond in the polymer is up to 50% shorter than the van der Waals bond in the liquid monomer state, free volume is created when monomer is converted to polymer. For each bond conversion we assume a hole is generated which then collapses at some characteristic rate constant. The Lorentz-Lorenz relation is used to determine the overall evolution refractive index modulation and the corresponding diffraction efficiency of the resulting grating is calculated using Rigorous Coupled Wave Analysis (RCWA). The Lorentz-Lorenz relation is used to determine the overall evolution refractive index modulation and the corresponding diffraction efficiency of the resulting grating is calculated using Rigorous Coupled Wave Analysis (RCWA). Inhibition is typically observed at the start of grating growth during which the formation of polymer chains is suppressed. In this paper experiments are reported, carried out with the specific aim of understanding of these processes. The results support our description of the inhibition process in an PVA/Acrylamide based photopolymer and can be used to predict behaviour under certain conditions.
机译:非定域聚合驱动扩散模型,NPDD,是可以用于描述基于丙烯酰胺的光聚合物全息光栅的形成。在聚合物中的自由基链式聚合过程的结果而产生在空间和时间到链起始点非局部。时间非局域性可以用来describepost曝光暗的效果。非线性响应和染料脱色的效果已经被检查。初级和双分子链终止机制已列入并检查。最近3-d,和抑制作用也被包括在内。在本文中,我们回顾我们最近的工作。结果表明,时间效应成为最显着的短exposres和非局部时间响应函数的夹杂物被示出为需要准确地描述该过程。特别是,短暂曝光后的折射率调制的自放大注意。这是由于持续的环比增长在接触后的短暂时期。在此之后在光栅的幅度略有衰减也会发生。我们认为,这是由于单体的暴露后持续扩散。由于正弦记录图案的记录过程单体扩散时产生单体浓度梯度期间和曝光之后发生。折射率调制的演变由记录材料部件各自的折射率值确定。从独立的测量应注意的是所述单体的折射率值比背景材料的略少是。因此作为单体扩散放回暗区,多发生在整体折射率调制的降低。在材料中发生的体积变化也影响光栅进化的本质。为了模拟这些影响,我们采用了自由体积的概念。由于这样的事实,在聚合物中的共价单一碳键比范德在液体单体状态范德华键较短高达50%,当单体转化成聚合物被创建的自由体积。对于每一个键转换我们假设产生一个孔,然后在折叠一些特性速率常数。洛伦兹洛伦茨关系被用于确定整个演化折射率调制,并使用严格耦合波分析(RCWA)计算得到的光栅的相应的衍射效率。洛伦兹洛伦茨关系被用于确定整个演化折射率调制,并使用严格耦合波分析(RCWA)计算得到的光栅的相应的衍射效率。抑制在其间的聚合物链的形成被抑制光栅生长开始通常观察到。在本文的实验报告,与这些过程的理解的特定目的进行。该结果支持我们的抑制过程的描述在PVA /丙烯酰胺的基于光聚合物,可用于在某些条件下,预测的行为。

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