Literature DB >> 16944879

Scanning electrochemical microscopy investigations of monolayers bound to p-type silicon substrates.

Jalal Ghilane1, Fanny Hauquier, Bruno Fabre, Philippe Hapiot.   

Abstract

p-Si type electrodes modified with different organic monolayers were investigated by reaction with radical anion and cation electrogenerated at a microelectrode operating in the configuration of a scanning electrochemical microscope. The method proves to be a convenient tool for investigating both the quality and the redox properties of the layer as previously demonstrated on metallic electrodes especially when the sample cannot be electrically connected. Approach curves recorded with the different mediators were used to investigate the electron-transfer rates across alkyl monolayers bound to p-type silicon substrates. Preliminary results indicate that the interfacial electron transfer occurs via electron tunneling through the organic layer as generally described for SAMs grafted on gold electrodes.

Entities:  

Year:  2006        PMID: 16944879     DOI: 10.1021/ac060058h

Source DB:  PubMed          Journal:  Anal Chem        ISSN: 0003-2700            Impact factor:   6.986


  3 in total

1.  Probing heterogeneous electron transfer at an unbiased conductor by scanning electrochemical microscopy in the feedback mode.

Authors:  Hui Xiong; Jidong Guo; Shigeru Amemiya
Journal:  Anal Chem       Date:  2007-03-07       Impact factor: 6.986

2.  Scanning Electrochemical Microscopy Study of Permeability of a Thiolated Aryl Multilayer and Imaging of Single Nanocubes Anchored to It.

Authors:  Pierre-Yves Blanchard; Tong Sun; Yun Yu; Zengyan Wei; Hiroshi Matsui; Michael V Mirkin
Journal:  Langmuir       Date:  2016-02-29       Impact factor: 3.882

3.  Scanning electrochemical microscopy studies of micropatterned copper sulfide (Cu(x)S) thin films fabricated by a wet chemistry method.

Authors:  Miao Chen; Jing Zhao; Xiaocui Zhao
Journal:  Electrochim Acta       Date:  2011-05-30       Impact factor: 6.901

  3 in total

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