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首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Monodisperse Colloidal Metal Nanoparticles to Core-Shell Structures and Alloy Nanosystems via Digestive Ripening in Conjunction with Solvated Metal Atom Dispersion: A Mechanistic Study
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Monodisperse Colloidal Metal Nanoparticles to Core-Shell Structures and Alloy Nanosystems via Digestive Ripening in Conjunction with Solvated Metal Atom Dispersion: A Mechanistic Study

机译:通过消化熟化与溶剂化金属原子分散的消化成熟,单分散胶体金属纳米颗粒和合金纳米系统:机械研究

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摘要

Co-digestive ripening of two distinct metal nanoparticles is an exceptional method for the colloidal synthesis of Core-shell heterostructures. In this report, a detailed investigation of the underlying mechanism by which surfactant molecule assisted interatomic transfer between two metal nanoparticles occurs has been described using gold/silver as a model system. Core-shell nanoparticles with gold in the core and silver in the shell in the size regime of 6.9 +/- 1.8 nm were obtained by conducting the codigestive ripening of polydispersed particles of Au-pentanone and Ag-pentanone colloids in the presence of hexadecylamine as a capping agent used in the molar ratio of 1:30 with respect to metal. The progress of the formation of Core-shell nanoparticles has been monitored using UV-visible spectroscopy and transmission electron microscopy. Detailed analysis of the nature of Au@Ag Core-shell nanoparticles has been done with the help of HAADF-STEM technique, point-EDS analysis, elemental line scanning technique, and X-ray photoelectron spectroscopy. Variation of experimental conditions such as concentration of capping agent, molar ratio of Au and Ag, and temperature in the codigestive ripening process led to the realization that core-shell nanoparticles with thicker shell of silver can be obtained under certain reaction conditions. Alteration of the reaction conditions was also noted to affect the final Au-Ag nanoparticles with respect to average particle size and polydispersity. The as-prepared Au@Ag nanoparticles could be transformed to Au Ag nanoalloys on being exposed to ultraviolet radiation of 254 nm. We have also attempted to elucidate the factors which dictate the formation of Core-shell nanoparticles by comparing with the findings of theoretical studies from the literature with our experimental results.
机译:两个不同的金属纳米颗粒的共消化成熟是芯壳异质结构的胶体合成的特殊方法。在本报告中,通过作为模型系统描述了两种金属纳米颗粒之间的表面活性剂分子辅助外部转移的潜在机制的详细研究。核 - 壳纳米粒子在壳中的核心和银中的圆形制度,在六癸胺的存在下进行多分散的颗粒的多分散颗粒的分解粒子,获得了6.9 +/- 1.8nm。相对于金属,以1:30的摩尔比使用的覆盖剂。使用UV可见光谱和透射电子显微镜监测核 - 壳纳米粒子的形成的进展。借助于HAADF-STEM技术,点EDS分析,元素线扫描技术和X射线光电子体光谱,对AU @ AG核 - 壳纳米粒子的性质进行了详细分析。实验条件如封端剂浓度,Au和Ag的摩尔比的实验条件的变化,以及Codigigeive熟练过程中的温度导致了实现具有较厚银壳的核 - 壳纳米颗粒可以在某些反应条件下获得。还注意到反应条件的改变以影响相对于平均粒度和多分散性的最终Au-Ag纳米颗粒。可以将AS制备的Au @ Ag纳米颗粒转化为Au Ag纳米合金,接受254nm的紫外线辐射。我们还试图通过与我们的实验结果与文献的理论研究结果相比,阐明决定核壳纳米粒子的形成的因素。

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