扩展X射线吸收精细结构
纳米颗粒
纳米团簇
材料科学
胶体金
相(物质)
协调数
纳米材料
表征(材料科学)
纳米
纳米技术
结晶学
分析化学(期刊)
化学物理
化学工程
吸收光谱法
化学
物理
色谱法
有机化学
光学
离子
工程类
复合材料
作者
Anatoly I. Frenkel,S. Nemzer,I. Pister,Laurence Soussan,Tanisha L Harris,Yao Sun,Miriam Rafailovich
摘要
Size-controlled synthesis of nanoparticles of less than a few nanometers in size is a challenge due to the spatial resolution limit of most scattering and imaging techniques used for their structural characterization. We present the self-consistent analysis of the extended x-ray absorption fine-structure (EXAFS) spectroscopy data of ligand-stabilized metal nanoclusters. Our method employs the coordination number truncation and the surface-tension models in order to measure the average diameter and analyze the structure of the nanoparticles. EXAFS analysis was performed on the two series of dodecanethiol-stabilized gold nanoparticles prepared by one-phase and two-phase syntheses where the only control parameter was the gold/thiol ratio xi, varied between 6:1 and 1:6. The two-phase synthesis resulted in the smaller particles whose size decreased monotonically and stabilized at 16 A when xi was lowered below 1:1. This behavior is consistent with the theoretically predicted thermodynamic limit obtained previously in the framework of the spherical drop model of Au nanoparticles.
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