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具有非受挫ABC瓶刷嵌段聚合物的完全光子带隙

Complete Photonic Band Gaps with Nonfrustrated ABC Bottlebrush Block Polymers.

作者信息

Lequieu Joshua, Quah Timothy, Delaney Kris T, Fredrickson Glenn H

机构信息

Department of Chemical and Biological Engineering, Drexel University, Philadelphia, Pennsylvania 19104, United States.

出版信息

ACS Macro Lett. 2020 Jul 21;9(7):1074-1080. doi: 10.1021/acsmacrolett.0c00380. Epub 2020 Jul 13.

Abstract

Bottlebrush block polymers are a promising platform for self-assembled photonic materials, yet most work has been limited to one-dimensional photonic crystals based on the lamellar phase. Here we demonstrate with simulation that nonfrustrated ABC bottlebrush block polymers can be used to self-assemble three-dimensional photonic crystals with complete photonic band gaps. To show this, we have developed a computational approach that couples self-consistent field theory (SCFT) simulations to Maxwell's equations, thereby permitting a direct link between molecular design, self-assembly, and photonic band structures. Using this approach, we calculate the phase diagram of nonfrustrated ABC bottlebrush block polymers and identify regions where the alternating gyroid and alternating diamond phases are stable. By computing the photonic band structures of these phases, we demonstrate that complete band gaps can be found in regions of thermodynamic stability, thereby suggesting a route to realize these photonic materials experimentally. Furthermore, we demonstrate that gap size depends on volume fraction, segregation strength, and polymer architecture, and we identify a design strategy based on symmetry breaking that can achieve band gaps for lower values of refractive index contrast. Taken together, the approach presented here provides a powerful and flexible tool for predicting both the self-assembly and photonic band structures of polymeric materials.

摘要

刷状嵌段聚合物是自组装光子材料的一个有前途的平台,但大多数工作仅限于基于层状相的一维光子晶体。在此,我们通过模拟证明,无挫ABC刷状嵌段聚合物可用于自组装具有完整光子带隙的三维光子晶体。为了证明这一点,我们开发了一种计算方法,将自洽场理论(SCFT)模拟与麦克斯韦方程相结合,从而在分子设计、自组装和光子能带结构之间建立直接联系。使用这种方法,我们计算了无挫ABC刷状嵌段聚合物的相图,并确定了交替螺旋状相和交替菱形相稳定的区域。通过计算这些相的光子能带结构,我们证明在热力学稳定区域可以找到完整的带隙,从而为通过实验实现这些光子材料提供了一条途径。此外,我们证明带隙大小取决于体积分数、偏析强度和聚合物结构,并且我们确定了一种基于对称破缺的设计策略,该策略可以在较低的折射率对比度值下实现带隙。综上所述,本文提出的方法为预测聚合物材料的自组装和光子能带结构提供了一个强大而灵活的工具。

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