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Aggregation kinetics and cluster structure of amino-PEG covered gold nanoparticles

机译:氨基 - PEG覆盖金纳米粒子的聚集动力学和簇结构

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In this study controlled clustering kinetics is demonstrated for PEG grafted gold nanoparticles, in response to applied environmental stimuli; the temperature and ionic strength of the medium. It is also found that the rate of assembly determines the structure of the prepared clusters. After the system is brought out of equilibrium, time-dependent extinction and dynamic light scattering data are used to follow the evolution of nanoparticle cluster formation in real time. The results show that the rate of assembly increases with increasing ionic strength or temperature of the medium. As a result the nanoparticle cluster size scales with ionic strength and temperature, over a cluster size range from a few particle sizes up to the micron-scale. It is found that, even at the lowest ionic strength, the electric double layer repulsion is eliminated; hence the observed differences in kinetics and in cluster structure arise from modulation of the repulsive steric interactions between nanoparticles. The approach should be extendable to suspensions of other nanoparticle types, where the nanoparticle stability is determined by surface-grafted responsive macromolecules.
机译:在该研究中,控制聚类动力学是针对佩格接枝金纳米颗粒的证明,响应于应用环境刺激;培养基的温度和离子强度。还发现组装速率决定了制备的簇的结构。在均衡的系统被带出平衡之后,使用时间依赖性灭绝和动态光散射数据实时追踪纳米粒子簇形成的演变。结果表明,随着介质的离子强度或温度的增加,组装速率增加。结果,纳米粒子簇尺寸的尺寸与离子强度和温度,在簇尺寸范围内,从几个颗粒尺寸直到微米尺寸。结果发现,即使在离子强度最低,也消除了电双层排斥;因此,从纳米颗粒之间的排斥空间相互作用的调节产生了观察到的动力学和簇结构的差异。该方法应伸展到其他纳米颗粒类型的悬浮液中,其中纳米颗粒稳定性由表面接枝响应性大分子测定。

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