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Controlled synthesis and self-assembly of dendrite patterns of Fe3O4 nanoparticles

机译:Fe3O4纳米粒子的可控合成和自组装枝晶图案

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摘要

A method for the growth and self-assembly of Fe3O4 nanoparticles that is template assisted, as well as gas diffusion and surface tension controlled, has been developed at room temperature. Well-defined dendrite patterns of Fe3O4 nanoparticles were obtained upon ion (Fe3+/Fe2+) entrapment in a polyethylene glycol solution followed by NH3 gas exposure on the surface of an aqueous solution on the glass substrate. During the formation of Fe3O4 nanoparticles, the diffusion of volatile NH3 limits the hydrolysis rate of the molecular precursor and catalyzes slow formation. The template and surface tension also provided significant driving forces to promote the formation of dendrite patterns and influence the nature of the pattern. The Fe3+/Fe2+ concentration was varied in order to see the affects on the template molecular weight. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), x-ray diffraction (XRD), and SQUID measurements were used to characterize the final product. The derived patterned structure can be tailored by a simple combination of the physical and chemical procedure, which provides a new opportunity for obtaining a controllable pattern of nanoparticles.
机译:已经在室温下开发了一种模板辅助的Fe3O4纳米粒子的生长和自组装方法,以及气体扩散和表面张力控制方法。通过将离子(Fe3 + / Fe2 +)截留在聚乙二醇溶液中,然后将NH3气体暴露在玻璃基板上的水溶液表面上,可以得到Fe3O4纳米粒子的明确的枝晶图案。在Fe3O4纳米颗粒的形成过程中,挥发性NH3的扩散限制了分子前体的水解速率,并催化了缓慢的形成过程。模板和表面张力还提供了显着的驱动力,以促进枝晶图案的形成并影响图案的性质。为了观察对模板分子量的影响,改变了Fe 3+ / Fe 2+的浓度。使用扫描电子显微镜(SEM),透射电子显微镜(TEM),X射线衍射(XRD)和SQUID测量来表征最终产品。可以通过物理和化学过程的简单组合来定制派生的图案化结构,这为获得可控制的纳米粒子图案提供了新的机会。

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