The use of catechols, and more specifically of dopamine, as a specific redox mediator for scanning electrochemical microscopy (SECM) investigations was evaluated in the challenging situation of an ultrathin layer deposited on a conductive substrate (carbon materials). Experiments show that dopamine is a well-adapted redox system for SECM in feedback mode and in unbiased conditions. Used as a redox mediator, catechol permits the investigations of modified surfaces without an electrical connection of the sample thanks to fast charge transfer kinetics but with a surface selectivity that does not exist in classical outer-sphere redox mediators. The interest of catechol in SECM as a sensitive redox mediator is exemplified by monitoring several modification steps of an ultrathin (<1 nm) hierarchically porous organic monolayer deposited on carbon substrates. For quantitative analysis, the SECM approach curves using dopamine could simply be characterized with an irreversible electron transfer kinetics model in a large range of pH.

International audienceSurface functionalization with ultrathin layers exhibiting a highly robust interface is of paramount importance for designing materials with tailored properties or operating functions, without modifying drastically the material’s bulk structures. A fine-tuning of the surface composition obtained, for instance from binary mixed layers, is also a key issue for developing high value-added applications like efficient sensors. Herein, binary mixtures of calix[4]arene-tetra-diazonium salts generated in situ from their corresponding calix[4]tetra-anilines are electrografted to form covalently bound monolayers onto substrates for yielding versatile functionalizable molecular platforms. Wettability studies, X-ray photoelectron spectroscopy analyses, and scanning electrochemical microscopy show the formation of homogeneous mixed monolayers. The distribution of the two calixarenes on the surface is directed by their relative molar fraction in the deposition solution. The strategy allows the control of the composition of mixed monolayers in a one-step approach. Postfunctionalization of the mixed layers with ferrocene centers is performed to exemplify the benefit of a dilution procedure when functional groups are introduced at the calix[4]arene small rim. This study highlights the potential of diazonium salt electrografting as a competitive alternative to chemisorption strategies such as self-assembled monolayers of alkyl thiols in the field of surface functionalization

Charge transport through an insulating layer was probed using ferrocenyl-terminated dendrimers and scanning electrochemical microscopy. Experiments show that the passage through the layer is considerably enhanced when the transferred charges are brought globally to the surface by the ferrocenyl dendrimer instead of a single ferrocene molecule. This result shows that charge tunneling through an insulator could be promoted by a purely molecular nano-object.

Fabrication of scanning electrochemical microscopy (SECM) tips cannot always guarantee a perfect disk geometry. In the present work, the impact of these defaults is investigated both theoretically and experimentally. The situations where these defaults can accurately be taken into account by considering that the probe behaves like a microdisk with effective geometric parameters are determined. In these situations, the quantitative analysis of the experimental results is greatly simplified. The study also proposes expressions to evaluate the apparent microdisk parameters from a picture of the probe.

No abstract

The use of a chemically irreversible redox probe in scanning electrochemical microscopy (SECM) was evaluated for the determination of the absolute tip-substrate distance. This data is required for a quantitative use of the method in the analysis of functional surfaces with an unknown redox response. Associated with the relevant model curves, the electrochemical response allows an easy positioning of the tip versus the substrate that is independent of the nature of the materials under investigation. The irreversible oxidation of polyaromatic compounds was found to be well adapted for such investigations in organic media. Anthracene oxidation in acetonitrile was chosen as a demonstrative example for evaluating the errors and limits of the procedure. Interest in the procedure was exemplified for the local investigations of surfaces modified by redox entities. This permits discrimination between the different processes occurring at the sample surface as the permeability of the probe through the layer or the charge transfer pathways. It was possible to observe small differences with simple kinetic models (irreversible charge transfer) that are related to permeation: charge transport steps through a permeable redox layer.

International audienceAnthracene-appended receptor monolayers covalently bound to hydrogen-terminated Si(111) surfaces have been prepared from attachment of an aminoalkane-substituted receptor to a preassembled acid-terminated alkyl monolayer using carbodiimide coupling. Subsequent irradiation at 350 nm of the receptor-modified surface yielded the open → closed conversion of the grafted anthracene-appended receptor, as clearly supported by IR spectroscopy data. Grafting of the open receptor and its subsequent closing did not change significantly the surface topography, and atomic force microscopy (AFM) images showed formation of perfectly dense and homogeneous molecular films without adventitious contamination or aggregated islands. Scanning electrochemical microscopy (SECM) measurements in feedback mode using an appropriate redox mediator (i.e., 9,10-diethoxyanthracene DEA) provided clear evidence for an efficient charge transport process between grafted receptors. However, the kinetics of the mediator regeneration was faster when the receptors were under their closed form. Interestingly, light-activated switching of the anthracene-appended receptor offered the unique opportunity to pattern the surface using UV photolithography through an optical mask. After the lithographic step, the SECM image clearly showed the expected current regeneration contrast between the open and produced closed receptor micropatterns

Localized "electroclick" was achieved on azido-terminated self-assembled monolayers using Scanning Electrochemical Microscopy (SECM) in feedback mode, in which the substrate is not electrically connected (unbiased conditions). The method allows both the local immobilization of diverse functional moieties and the monitoring of each modification step at a micrometer scale. Conditions of the "click" coupling reaction were optimized especially to avoid the deposit of metallic copper by the choice of a specific ligand to stabilize the Cu(I) species. The catalytic efficiency in localized "electroclick" reaction of Cu(II)TMPA (TMPA: tris(2-pyridylmethyl)amine) as the "click" catalyst was compared with a derivative containing an alkyne group Cu(II)6eTMPA, the same molecule playing the role of the catalyst and the substrate. Evidences for surface self-catalysis propagation are demonstrated through SECM imaging showing a random 2D progression of the catalytic modification.