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Nanometer precise adjustment of the silver shell thickness during automated Au-Ag core-shell nanoparticle synthesis in micro fluid segment sequences

机译:在微流体片段序列中自动Au-Ag核壳纳米粒子合成过程中,纳米级银壳厚度的精确调节

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摘要

In this work, a wet-chemical synthesis method for gold–silver core–shell particles with nanometer precise adjustable silver shell thicknesses is presented. Typically wet-chemical syntheses lead to relatively large diameter size distributions and losses in the yield of the desired particle structure due to thermodynamical effects. With the here explained synthesis method in micro fluidic segment sequences, a combinatorial in situ parameter screening of the reactant concentration ratios by programmed flow rate shifts in conjunction with efficient segment internal mixing conditions is possible. The highly increased mixing rates ensure a homogeneous shell deposition on all presented gold core particles while the amount of available silver ions was adjusted by automated flow rate courses, from which the synthesis conditions for exactly tunable shell thicknesses between 1.1 and 6.1 nm could be derived. The findings according to the homogeneity of size and particle structure were confirmed by differential centrifugal sedimentation (DCS), scanning and transmission electron microscopy (SEM, TEM) and X-ray photoelectron spectroscopy (XPS) measurements. In UV-Vis measurements, a significant contribution of the core metal was found in the shape of the extinction spectra in the case of thin shells. These results were confirmed by theoretical calculations.
机译:在这项工作中,提出了一种湿化学合成方法,用于纳米级可精确调节银壳厚度的金-银核-壳颗粒。通常,湿化学合成导致相对较大的直径尺寸分布,并且由于热力学效应而导致所需颗粒结构的产率损失。使用此处解释的微流体段序列合成方法,可以结合有效的段内部混合条件,通过程序设计的流量偏移对反应物浓度比进行组合式原位参数筛选。高度增加的混合速率确保了在所有存在的金核颗粒上均一的壳层沉积,而可用的银离子量通过自动流速过程进行了调整,由此可以得出精确可调壳层厚度在1.1至6.1 nm之间的合成条件。根据尺寸和颗粒结构均一性的发现已通过差速离心沉降(DCS),扫描和透射电子显微镜(SEM,TEM)和X射线光电子能谱(XPS)测量得到证实。在紫外线-可见光测量中,对于薄壳,在消光光谱的形状中发现了核心金属的重要贡献。这些结果通过理论计算得到了证实。

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