手性纳米结构的光诱导组装与重构

Jiyoung Kim, Jihyeon Yeom, Heather A. Calcaterra, Gongpu Zhao, Peijun Zhang, Jiyoun Munn, N. Kotov
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摘要

如今,无机纳米胶体的成熟合成已经允许生产各种不对称纳米颗粒(NP)甚至更复杂的组件,引入了各种具有独特性能的纳米材料。由于手性物质具有旋光能力,手性是材料科学领域中最引人注目的对称群之一。无机纳米粒子(NPs)的强光学活性为利用圆偏振光子进行手性超结构的光合作用提供了途径(1)。尽管由于高度离域等离子体态的强旋转能力,等离子体纳米粒子是这种合成途径的有希望的候选物(2),但由于等离子体纳米粒子的寿命较短,实现光驱动合成手性纳米结构对等离子体纳米粒子来说比半导体更具挑战性。这个过程也很难识别,因此需要非常规的方法来量化手性产物。在这里,我们证明了在柠檬酸存在下,用右手(左手)圆偏振光(CPL)照射金前驱体可诱导手性金纳米结构的形成。尽管颗粒形状看似不规则,但所得到的胶体根据光照cpld的手性显示出独特的镜像相反的圆二色性(CD)带。通过将三维电子断层扫描(e-tomo)应用于计算模型,成功地证明了这些看似非手性结构的圆二色性响应和几何手性。光驱动手性纳米结构组装的机制是基于等离子体场在动态组装中NPs的不对称位移,然后是粒子间的附着。金纳米结构保留入射光子偏振信息的能力可应用于光吸收材料,从而制造出多种手性纳米材料。通过建议的手性测量对看似不规则的NP进行类似的检查,也可以解释以前令人困惑的纳米材料几何不对称的光学响应。
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Light-Induced Assembly and Reconfiguration of Chiral Nanostructures
Matured syntheses of inorganic nanocolloids today have allowed production of diverse asymmertic nanoparticles (NP) and even more complex assemblies, introducing a variety of nanomaterials with unique properties. Chirality is one of most intriguing symmetry groups in field of material science due to the optical rotatory power of chiral substances. Strong optical activity of inorganic nanoparticles (NPs) afford photosynthetic routes to chiral superstructures using circularly polarized photons (1). Although plasmonic NPs are promising candidates for such synthetic routes due to the strong rotatory power of highly delocalized plasmonic states (2), realization of light- driven synthesis of chiral nanostructures has been more challenging for plasmonic NPs than for the semiconductor due to the short lifetime of the plasmonic states. The process also can be difficult to recognize, and therefore requires unconventional approaches for the quantification of chiral products. Here, we demonstrate that illumination of Au precursors in the presence of citric acid with right- (left-) handed circularly polarized light (CPL) induces the formation of chiral Au nanostructures. Despite seemingly irregular shape of the particles, the resulted colloids showed distinctive mirror-imaged opposite circular dichroism (CD) bands according to the handedness of illuminated CPL. Circular dichroic response and geometric chirality from these seemingly achiral structures were successfully demonstrated and quantified by implementing three-dimensional (3D) electron tomography (e-tomo) into computational model. The mechanism of the light-driven assembly of chiral nanostructures is based on the asymmetric displacement of NPs in dynamic assemblies by plasmonic fields fol-lowed by particle-to-particle attachment. The ability of Au nanostructures to retain the polarization information of incident photons can be applicable to light absorbing materials, thus to create a variety of chiral nanomaterials. Similar examination of seemingly irregular NP through suggested chirality measure can also elucidate previously puzzling optical response from unclear geometric asymmetry of nanomaterials.
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