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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Vancso, Gyula Julius
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Topics
Publications (10/10 displayed)
- 2023Designer Adhesives for Tough and Durable Interfaces in High-Performance Ti-Carbon PEKK Hybrid Jointscitations
- 2019Oscillating surfaces fueled by a continuous AC electric fieldcitations
- 2019Printing "smart" Inks of Redox-Responsive Organometallic Polymers on Microelectrode Arrays for Molecular Sensingcitations
- 2019Brush Swelling and Attachment Strength of Barnacle Adhesion Protein on Zwitterionic Polymer Films as a Function of Macromolecular Structurecitations
- 2017Synchrotron SAXS and Impedance Spectroscopy Unveil Nanostructure Variations in Redox-Responsive Porous Membranes from Poly(ferrocenylsilane) Poly(ionic liquid)scitations
- 2017Ion-Selective Ionic Polymer Metal Composite (IPMC) Actuator Based on Crown Ether Containing Sulfonated Poly(Arylene Ether Ketone)citations
- 2016Development of multifunctional complex fluids for coating of semi-porous surfaces
- 2010An overview on 12-polyurethane:Synthesis, structure and crystallizationcitations
- 2005Electrochemistry of Surface-Grafted Stimulus-Responsive Monolayers of Poly(ferrocenyldimethylsilane) on Goldcitations
- 2004Electrochemically Induced Morphology and Volume Changes in Surface-Grafted Poly(ferrocenyldimethylsilane) Monolayerscitations
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article
Electrochemistry of Surface-Grafted Stimulus-Responsive Monolayers of Poly(ferrocenyldimethylsilane) on Gold
Abstract
Poly(ferrocenyldimethylsilane)s with various degrees of polymerization and featuring a thiol end group were chemically end-grafted onto gold substrates by self-assembly, forming redox-active monolayers. The monolayers were characterized by contact angle measurements, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy. Layer thickness values were determined by surface plasmon resonance spectroscopy and ellipsometry. The electrochemical properties of these films in aqueous NaClO4 were studied using cyclic voltammetry (CV), differential pulse voltammetry, chronoamperometry, and chronocoulometry. Cyclic voltammograms showed two reversible redox peaks, indicating a stepwise oxidation of the electroactive sites. The first oxidation step showed reversible behavior at low scan rates and quasi-reversible behavior at higher scan rates. Peak currents (ip) plotted against the square root of scan rates (v1/2) for the first oxidation peak and for the corresponding reduction peak exhibited a linear dependence, indicating that the oxidation process in the first step is controlled by the diffusion of counterions into the polymer film. For the second oxidation peak and the corresponding reduction peak, ip varied linearly with v. This redox behavior is characteristic of surface-immobilized electroactive layers. The higher reversibility of the second oxidation and reduction waves in the CV experiments was explained from the solvation of the surface-grafted poly(ferrocenylsilane) (PFS) chains, which depends on the degree of oxidation. Oxidized PFS films are swollen in the aqueous electrolyte solutions, leading to a higher segmental mobility of the polymer chains and a much increased counterion mobility within the film. Kinetic parameters for the redox processes were obtained from chronocoulometry experiments.