BAM Federal Institute of Materials Research and Testing, Richard-Willstatter-Strasse 11, D-12489 Berlin, Germany.
ACS Nano. 2010 Feb 23;4(2):1076-82. doi: 10.1021/nn901499c.
Gold nanoparticles (AuNP) were prepared by the homogeneous mixing of continuous flows of an aqueous tetrachloroauric acid solution and a sodium borohydride solution applying a microstructured static mixer. The online characterization and screening of this fast process ( approximately 2 s) was enabled by coupling a micromixer operating in continuous-flow mode with a conventional in-house small angle X-ray scattering (SAXS) setup. This online characterization technique enables the time-resolved investigation of the growth process of the nanoparticles from an average radius of ca. 0.8 nm to about 2 nm. To the best of our knowledge, this is the first demonstration of a continuous-flow SAXS setup for time-resolved studies of nanoparticle formation mechanisms that does not require the use of synchrotron facilities. In combination with X-ray absorption near edge structure microscopy, scanning electron microscopy, and UV-vis spectroscopy the obtained data allow the deduction of a two-step mechanism of gold nanoparticle formation. The first step is a rapid conversion of the ionic gold precursor into metallic gold nuclei, followed by particle growth via coalescence of smaller entities. Consequently it could be shown that the studied synthesis serves as a model system for growth driven only by coalescence processes.
金纳米粒子(AuNP)是通过在微结构静态混合器中连续流动的四氯金酸水溶液和硼氢化钠溶液的均匀混合制备的。通过将连续流动模式下运行的微混合器与常规的原位小角 X 射线散射(SAXS)装置相耦合,实现了对这个快速过程(约 2 秒)的在线表征和筛选。这种在线表征技术能够实时研究纳米粒子的生长过程,从平均半径约 0.8nm 增加到约 2nm。据我们所知,这是首次展示不需要使用同步加速器设施的连续流动 SAXS 装置用于实时研究纳米颗粒形成机制的应用。结合 X 射线吸收近边结构显微镜、扫描电子显微镜和紫外可见光谱,获得的数据可以推断出金纳米粒子形成的两步机制。第一步是将离子金前驱体快速转化为金属金核,然后通过较小实体的聚合并进一步生长。因此,可以证明所研究的合成可以作为仅由聚并过程驱动的生长的模型体系。