Park Sung Hun, Park Haedong, Hur Kahyun, Lee Seungwoo
Materials and Life Science Research Division, Korea Institute of Science and Technology, Seoul 02792, Republic of Korea.
ACS Appl Bio Mater. 2020 Jan 21;3(1):747-756. doi: 10.1021/acsabm.9b01171. Epub 2020 Jan 7.
Self-assembled photonic crystals have proven to be a fascinating class of photonic materials for nonabsorbing structural colorizations over large areas and in diverse relevant applications, including tools for on-chip spectrometers and biosensors, platforms for reflective displays, and templates for energy devices. The most prevalent building blocks for the self-assembly of photonic crystals are spherical colloids and block copolymers (BCPs) because of the generic appeal of these materials, which can be crafted into large-area 3D lattices. However, because of the intrinsic limitations of these structures, these two building blocks are difficult to assemble into a direct rod-connected diamond lattice, which is considered to be a champion photonic crystal. Here, we present a DNA origami-route for a direct rod-connected diamond photonic crystal exhibiting a complete photonic bandgap (PBG) in the visible regime. Using a combination of electromagnetic, phononic, and mechanical numerical analyses, we identify (i) the structural constraints of the 50 megadalton-scale giant DNA origami building blocks that could self-assemble into a direct rod-connected diamond lattice with high accuracy, and (ii) the elastic moduli that are essentials for maintaining lattice integrity in a buffer solution. A solution molding process could enable the transformation of the as-assembled DNA origami lattice into a porous silicon- or germanium-coated composite crystal with enhanced refractive index contrast, in that a champion relative bandwidth for the photonic bandgap (i.e., 0.29) could become possible even for a relatively low volume fraction (i.e., 16 vol %).
自组装光子晶体已被证明是一类引人入胜的光子材料,可用于大面积的非吸收性结构着色以及各种相关应用,包括片上光谱仪和生物传感器工具、反射式显示器平台以及能量装置模板。由于这些材料具有普遍吸引力,并且可以制成大面积的三维晶格,因此用于光子晶体自组装的最常见构建块是球形胶体和嵌段共聚物(BCP)。然而,由于这些结构的固有局限性,这两种构建块很难组装成直接的棒连接金刚石晶格,而这种晶格被认为是一种理想的光子晶体。在这里,我们提出了一种DNA折纸路线,用于制备在可见光范围内具有完整光子带隙(PBG)的直接棒连接金刚石光子晶体。通过结合电磁、声子和机械数值分析,我们确定了:(i)50兆道尔顿规模的巨型DNA折纸构建块的结构限制,这些构建块可以高精度地自组装成直接的棒连接金刚石晶格;(ii)在缓冲溶液中维持晶格完整性所必需的弹性模量。溶液成型工艺可以使组装好的DNA折纸晶格转变为具有增强折射率对比度的多孔硅或锗涂层复合晶体,因为即使对于相对较低的体积分数(即16体积%),也有可能实现光子带隙的理想相对带宽(即0.29)。