首页> 外文会议>Conference on Photonics North 2006; 20060605-08; Quebec City(CA) >Modeling Photopolymers for Holographic Data Storage Applications
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Modeling Photopolymers for Holographic Data Storage Applications

机译:为全息数据存储应用建模光聚合物

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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:非本地聚合驱动扩散模型NPDD可用于描述基于丙烯酰胺的光敏聚合物中的全息光栅形成。自由基链聚合过程导致聚合物在空间和时间上都是非局部生成的,直至发生链引发。时间上的非局部性可以用来描述暴露后的黑暗效应。已经研究了非线性响应和染料漂白的影响。初级和双分子链终止机制均已包括在内并已进行了检查。最近还包括3-D和抑制作用。在本文中,我们回顾了我们最近的工作。结果表明,时间效应对于短时间曝光最为显着,并且非局部时间响应函数的包含对于精确描述该过程是必要的。特别地,注意到了折射率调制的简短的曝光后自放大。这归因于暴露后短时间内链的持续增长。此后,光栅振幅也会发生轻微衰减。我们认为这是由于单体在暴露后继续扩散所致。由于正弦记录图案在记录过程中会产生单体浓度梯度,因此在曝光期间和之后都会发生单体扩散。折射率调制的演变取决于记录材料组分的各自的折射率值。从独立的测量结果可以看出,单体的折射率值略小于本底材料的折射率值。因此,当单体扩散回暗区时,总折射率调制会降低。材料内发生的体积变化也会影响光栅演化的性质。为了模拟这些效果,我们采用了自由音量概念。由于聚合物中的共价单碳键比液态单体状态下的范德华键短多达50%,因此在单体转化为聚合物时会产生自由体积。对于每次键转换,我们假设都会生成一个孔,然后该孔以某个特征速率常数崩溃。洛伦兹-洛伦兹(Lorentz-Lorenz)关系用于确定总体演化折射率调制,并使用严格耦合波分析(RCWA)计算所得光栅的相应衍射效率。洛伦兹-洛伦兹(Lorentz-Lorenz)关系用于确定总体演化折射率调制,并使用严格耦合波分析(RCWA)计算所得光栅的相应衍射效率。通常在光栅生长开始时观察到抑制作用,在此期间聚合物链的形成被抑制。本文报道了一些实验,目的是为了理解这些过程。结果支持了我们对基于PVA /丙烯酰胺的光敏聚合物中抑制过程的描述,可用于预测某些条件下的行为。

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