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The kinetics of homogeneous nucleation of silver nanoparticles stabilized by polymers

机译:聚合物稳定的银纳米颗粒的均匀成核动力学

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The formation of Ag nanoparticles synthesized by homogeneous nucleation, stabilized by polymers (PVA and PVP) was monitored by UV–Vis spectrophotometry and transmission electron microscopy. Our aim was to differentiate between the two main phases of particle formation, i.e. nucleation and growth and to characterize their rates with the help of appropriate kinetic equations. Time resolved spectrophotometric measurements revealed that particle formation is an autocatalytic process: a slow, continuous nucleation phase (3–5 min) is followed by a rapid, autocatalytic growth phase where the maximal particle size is 5–7 nm. By freezing the reaction mixture, the process of particle growth can be followed from 5 to 40 min on TEM pictures. The first order rate constants were calculated and they are strongly depend on the polymer concentration. If the growing particles are attached by PEI to the surface of a solid support, the formation of silver nanoparticles can also be followed by atomic force microscopy (AFM) and we can control the particle growth on mica surface. The cross section analysis of the pictures show, that the particle growing process can be also monitored at solid–liquid interface.
机译:通过紫外可见分光光度法和透射电子显微镜监测通过均相成核合成的,由聚合物(PVA和PVP)稳定的Ag纳米颗粒的形成。我们的目的是区分颗粒形成的两个主要阶段,即成核和生长,并借助适当的动力学方程来表征其速率。时间分辨分光光度法测量表明,颗粒形成是一种自催化过程:缓慢的,连续的成核阶段(3-5分钟),然后是快速的自催化生长阶段,最大粒径为5-7 nm。通过冻结反应混合物,可以在TEM图片上跟踪颗粒生长的过程5到40分钟。计算出一级速率常数,它们很大程度上取决于聚合物的浓度。如果通过PEI将生长的颗粒附着到固体支持物的表面,则还可以通过原子力显微镜(AFM)跟踪银纳米颗粒的形成,并且我们可以控制云母表面上的颗粒生长。图片的横截面分析表明,还可以在固液界面处监控颗粒的生长过程。

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