4.7 Article

Electrochemistry at gold nanoparticles deposited on dendrimers assemblies adsorbed onto gold and platinum surfaces

期刊

JOURNAL OF ELECTROANALYTICAL CHEMISTRY
卷 659, 期 1, 页码 76-82

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jelechem.2011.05.004

关键词

PAMAM; Dendrimer; Nanoparticle; AFM; Ferrocene; Cyclic voltammetry

资金

  1. CNRS
  2. Ecole Normale Superieure (ENS)
  3. Universite Pierre et Marie Curie (UPMC)
  4. French Ministry of Research
  5. LIA CNRS XiamENS [UMR 8640]
  6. PCOSS State Key Laboratory
  7. China Scholarship Council

向作者/读者索取更多资源

Cyclic voltammetry and atomic force microscopy (AFM) were used to investigate the electrochemical communication between gold nanoparticles deposited onto adsorbed dendrimers of 4th generation poly(amido amine) (PAMAM) and gold or platinum electrode surfaces. Combination of these techniques evidenced that adsorption of dendrimers depends on both their chemical structures and the nature of the metallic surface. The adsorption process could be controlled as a function of either the dendrimer concentration or the time during which the electrodes were soaked in the dendrimer containing solution. Accordingly, mono- and multi-layer films of dendrimers could be obtained. The presence of dendrimer multilayer film did not prevent redox species such as ferrocene to reach the electrode surface presumably through pinholes in the dendrimers array. Interestingly, the dendrimer layer did not behave as an insulating film but was electrochemically transparent over the time ranges investigated. Thus, depositing gold nanoparticles over the dendrimer layers and constructing a self-assembled monolayer (SAM) consisting of 6-ferrocenyl hexanethiol onto the gold surfaces still allowed electrochemical communication with the ferrocene groups. This opens the future possibility of using dendrimers as anchors for gold nanoparticles so as to construct 2D-arrays of metal nanoparticles for electronic applications. (C) 2011 Elsevier B.V. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据