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金螺旋体:具有可控形态和强手性光学性能的金纳米粒子形成三维螺旋超结构。

GoldHelix: Gold Nanoparticles Forming 3D Helical Superstructures with Controlled Morphology and Strong Chiroptical Property.

机构信息

Chimie et Biologie des Membranes et des Nanoobjets (CBMN), CNRS - Université Bordeaux - Bordeaux INP, UMR 5248 , Allée St Hilaire, Bat B14, 33607 Pessac, France.

Institut des Sciences Moléculaires (ISM), Université Bordeaux-CNRS, UMR 5255 , 351 Cours de la Libération, 33405 Talence, France.

出版信息

ACS Nano. 2017 Apr 25;11(4):3806-3818. doi: 10.1021/acsnano.6b08723. Epub 2017 Apr 3.

Abstract

Plasmonic nanoparticles, particularly gold nanoparticles (GNPs) hold a great potential as structural and functional building blocks for three-dimensional (3D) nanoarchitectures with specific optical applications. However, a rational control of their assembly into nanoscale superstructures with defined positioning and overall arrangement still remains challenging. Herein, we propose a solution to this challenge by using as building blocks: (1) nanometric silica helices with tunable handedness and sizes as a matrix and (2) GNPs with diameter varying from 4 to 10 nm to prepare a collection of helical GNPs superstructures (called Goldhelices hereafter). These nanomaterials exhibit well-defined arrangement of GNPs following the helicity of the silica template. Strong chiroptical activity is evidenced by circular dichroism (CD) spectroscopy at the wavelength of the surface plasmon resonance (SPR) of the GNPs with a anisotropy factor (g-factor) of the order of 1 × 10, i.e., 10-fold larger than what is typically reported in the literature. Such CD signals were simulated using a coupled dipole method which fit very well the experimental data. The measured signals are 1-2 orders of magnitude lower than the simulated signals, which is explained by the disordered GNPs grafting, the polydispersity of the GNPs, and the dimension of the nanohelices. These Goldhelices based on inorganic templates are much more robust than previously reported organic-based chiroptical nanostructures, making them good candidates for complex hierarchical organization, providing a promising approach for light management and benefits in applications such as circular polarizers, chiral metamaterials, or chiral sensing in the visible range.

摘要

等离子体纳米粒子,尤其是金纳米粒子(GNPs),作为具有特定光学应用的三维(3D)纳米结构的结构和功能构建块,具有巨大的潜力。然而,将它们组装成具有明确定位和整体排列的纳米级超结构仍然具有挑战性。在此,我们提出了一个解决方案,使用以下构建块:(1)具有可调手性和尺寸的纳米级二氧化硅螺旋作为基质;(2)直径从 4nm 到 10nm 变化的 GNPs,以制备一系列螺旋 GNPs 超结构(以下称为 Goldhelices)。这些纳米材料表现出 GNPs 沿着二氧化硅模板的螺旋性的明确定位排列。圆二色性(CD)光谱在 GNPs 的表面等离子体共振(SPR)波长处证实了强手性活性,其各向异性因子(g 因子)约为 1×10,即比文献中通常报道的大 10 倍。使用偶极子耦合方法模拟了这种 CD 信号,该方法非常适合实验数据。测量的信号比模拟信号低 1-2 个数量级,这是由于 GNPs 的无规接枝、GNPs 的多分散性和纳米螺旋的尺寸引起的。与以前报道的基于有机的手性纳米结构相比,基于无机模板的这些 Goldhelices 更加坚固,这使得它们成为复杂的层次组织的良好候选者,为光管理提供了一种有前途的方法,并在圆偏振器、手性超材料或可见光范围内的手性传感等应用中带来了益处。

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