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Facile Synthesis of Branched Au Nanostructures by Templating against a Self-Destructive Lattice of Magnetic Fe Nanoparticles

机译:通过对磁性铁纳米粒子的自毁晶格进行模板化轻松合成支化金纳米结构

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摘要

This paper reports the demonstration of a reactive, self-destructive template for the facile synthesis of branched Au nanostructures. The template is a three-dimensionally porous lattice of uniform, magnetic Fe nanoparticles self-assembled in situ on the surface of a magnetic stir bar. Upon introduction of AuCl, Au atoms are formed in the voids among Fe nanoparticles due to the galvanic replacement reaction between Fe and Au+. The Au atoms then nucleate and grow into branched nanostructures under the confinement of Fe nanoparticles. As the replacement proceeds, Fe is consumed to gradually reduce the sizes and magnetic moments of the Fe nanoparticles. At a certain stage of the reaction, the template starts to fall apart to automatically release the branched Au nanostructures. We can routinely obtain Au multipods as pure samples via selective dissolution of the remaining Fe nanoparticles with sulfuric acid. The as-prepared Au multipods show strong absorption in the near infrared region and exhibit distinctive oxidative etching behaviors in different acidic solutions due to the presence of crystal defects and lattice distortions.
机译:本文报道了一种反应性,自破坏模板的演示,该模板可轻松合成支链金纳米结构。模板是在磁性搅拌棒表面上就地自组装的,均匀的磁性Fe纳米粒子的三维多孔晶格。引入AuCl后,由于Fe和Au + 之间的电流置换反应,在Fe纳米颗粒之间的空隙中形成了Au原子。然后,在Fe纳米颗粒的限制下,Au原子成核并生长为分支的纳米结构。随着置换的进行,Fe被消耗,从而逐渐减小了Fe纳米颗粒的尺寸和磁矩。在反应的某个阶段,模板开始崩解以自动释放分支的Au纳米结构。我们可以通过用硫酸选择性溶解剩余的Fe纳米颗粒来常规获得纯金样品的Au多足动物。所制备的Au多脚架由于晶体缺陷和晶格畸变的存在而在近红外区显示出强吸收性,并且在不同的酸性溶液中表现出独特的氧化蚀刻行为。

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