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金纳米粒子柠檬酸合成中的亚微米中间体:成核和晶体生长机制的新见解。

Submicrometer intermediates in the citrate synthesis of gold nanoparticles: new insights into the nucleation and crystal growth mechanisms.

机构信息

Institute of Chemistry and Chemical Technology of Siberian Branch of Russian Academy of Sciences, K. Marx Street, 42, Krasnoyarsk 660049, Russia.

出版信息

J Colloid Interface Sci. 2011 Oct 15;362(2):330-6. doi: 10.1016/j.jcis.2011.06.077. Epub 2011 Jul 7.

Abstract

The reduction of tetrachloroaurate by citrate ions in aqueous solutions yielding gold nanoparticles (GNPs) has been studied using in situ tapping mode atomic force microscopy (AFM), UV-vis absorption and dynamic light scattering (DLS) spectroscopies, small-angle X-ray scattering (SAXS) along with ex situ TEM, EDX and XPS. Special attention is given to mesoscale intermediates responsible for the intense coloring of the transient solutions and their role in nucleation and crystal growth. AFM detects liquid droplet-like domains, globules 30-50 nm in diameter arranged in submicrometer aggregates in the gray and blue solutions, and well separated individual particles in the final red sols. DLS shows abrupt appearance of species about 30 nm and larger but not growing Au nanoparticles, while SAXS reveals gradually increasing nanoparticles and no aggregates. The mesoscale structures observed in TEM become looser as the reaction proceeds; they contain signatures of oxidized Au and other solutes. The results are interpreted in terms of decomposition of supersaturated solutions to afford domains ("dense droplets") enriched by gold, and then, after nucleation and coalescence of Au nuclei inside them, rather slow growth of gold nanoparticles within the associated globules; the color changes of the transient solutions are due to increasing interparticle distances.

摘要

在水溶液中,柠檬酸根离子将四氯金酸还原为金纳米粒子(GNPs),本研究使用了原位敲击模式原子力显微镜(AFM)、紫外-可见吸收和动态光散射(DLS)光谱、小角 X 射线散射(SAXS)以及透射电子显微镜(TEM)、能量色散 X 射线光谱(EDX)和 X 射线光电子能谱(XPS)。特别关注了介观中间体,它们是瞬态溶液强烈着色的原因,也是成核和晶体生长的关键。AFM 检测到液滴状畴,直径 30-50nm 的小球在灰色和蓝色溶液中排列成亚微米级聚集体,而在最终的红色溶胶中则是很好分离的单个颗粒。DLS 显示出约 30nm 及更大的物种的突然出现,但不是生长的 Au 纳米颗粒,而 SAXS 则揭示了逐渐增加的纳米颗粒,没有聚集体。在 TEM 中观察到的介观结构随着反应的进行变得更加松散;它们包含氧化金和其他溶质的特征。研究结果从过饱和溶液的分解来解释,从而提供富含金的畴(“密集液滴”),然后在其中进行 Au 核的成核和聚合并形成金纳米核,随后在相关小球内进行相对缓慢的金纳米颗粒生长;瞬态溶液颜色的变化归因于颗粒间距离的增加。

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