分散性
成核
纳米颗粒
Zeta电位
动态光散射
氧化还原
胶体金
柠檬酸钠
材料科学
纳米技术
化学
航程(航空)
化学工程
化学物理
无机化学
高分子化学
有机化学
医学
工程类
病理
复合材料
作者
Haibing Xia,Yujiao Xiahou,Peina Zhang,Wenchao Ding,Dayang Wang
出处
期刊:Langmuir
[American Chemical Society]
日期:2016-06-06
卷期号:32 (23): 5870-5880
被引量:102
标识
DOI:10.1021/acs.langmuir.6b01312
摘要
In this work, we have successfully developed a new and consistent model to describe the growth of gold nanoparticles (Au NPs) via citrate reduction of auric acid (HAuCl4) by carefully assessing the temporal evolution of the NP sizes and surface charges by means of dynamic light scattering (DLS) and zeta-potential measurements. The new model demonstrates that the nucleation and growth of the Au NPs occur exclusively in the particles of the complexes of Au(+) ions and sodium acetone dicarboxylate (SAD) derived from the citrate/HAuCl4 redox reaction, which proceeds as described by the classic LaMer model. Concomitant with the Au NP growing therein, the Au(+)/SAD complex particles undergo reversible agglomeration with the reaction time, which may result in an abnormal color change of the reaction media but have little impact on the Au NP growth. Built on the new model, we have successfully produced monodisperse quasi-spherical Au NPs with sizes precisely regulated from 2 to 330 nm via simple citrate reduction in a one-pot manner. To date, highly uniform Au NPs with sizes spanning such a large size range could not be formed otherwise even via deliberately controlled seeded growth methods.
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