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金纳米棒的手性种子生长为具有等离子体光学活性的四重扭曲纳米颗粒。

Chiral Seeded Growth of Gold Nanorods Into Fourfold Twisted Nanoparticles with Plasmonic Optical Activity.

作者信息

Ni Bing, Mychinko Mikhail, Gómez-Graña Sergio, Morales-Vidal Jordi, Obelleiro-Liz Manuel, Heyvaert Wouter, Vila-Liarte David, Zhuo Xiaolu, Albrecht Wiebke, Zheng Guangchao, González-Rubio Guillermo, Taboada José M, Obelleiro Fernando, López Núria, Pérez-Juste Jorge, Pastoriza-Santos Isabel, Cölfen Helmut, Bals Sara, Liz-Marzán Luis M

机构信息

Physical Chemistry, University of Konstanz, Universitätsstrasse 10, 78457, Konstanz, Germany.

EMAT, University of Antwerp, 2020, Antwerp, Belgium.

出版信息

Adv Mater. 2023 Jan;35(1):e2208299. doi: 10.1002/adma.202208299. Epub 2022 Nov 17.

Abstract

A robust and reproducible methodology to prepare stable inorganic nanoparticles with chiral morphology may hold the key to the practical utilization of these materials. An optimized chiral growth method to prepare fourfold twisted gold nanorods is described herein, where the amino acid cysteine is used as a dissymmetry inducer. Four tilted ridges are found to develop on the surface of single-crystal nanorods upon repeated reduction of HAuCl , in the presence of cysteine as the chiral inducer and ascorbic acid as a reducing agent. From detailed electron microscopy analysis of the crystallographic structures, it is proposed that the dissymmetry results from the development of chiral facets in the form of protrusions (tilted ridges) on the initial nanorods, eventually leading to a twisted shape. The role of cysteine is attributed to assisting enantioselective facet evolution, which is supported by density functional theory simulations of the surface energies, modified upon adsorption of the chiral molecule. The development of R-type and S-type chiral structures (small facets, terraces, or kinks) would thus be non-equal, removing the mirror symmetry of the Au NR and in turn resulting in a markedly chiral morphology with high plasmonic optical activity.

摘要

一种用于制备具有手性形态的稳定无机纳米粒子的强大且可重复的方法,可能是这些材料实际应用的关键。本文描述了一种优化的手性生长方法来制备四重扭曲的金纳米棒,其中氨基酸半胱氨酸用作不对称诱导剂。在半胱氨酸作为手性诱导剂和抗坏血酸作为还原剂的情况下,当反复还原 HAuCl 时,发现单晶纳米棒表面会形成四条倾斜的脊。通过对晶体结构的详细电子显微镜分析,提出不对称性源于初始纳米棒上以突起(倾斜的脊)形式出现的手性晶面的发展,最终导致扭曲形状。半胱氨酸的作用归因于协助对映选择性晶面演化,这得到了表面能的密度泛函理论模拟的支持,在手性分子吸附后表面能发生了改变。因此,R 型和 S 型手性结构(小晶面、平台或扭结)的发展将不相等,消除了金纳米棒的镜面对称性,进而产生具有高等离子体光学活性的明显手性形态。

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