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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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Hyde, Michael
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article
Nanoporous iron oxide membranes
Abstract
<p>A versatile procedure for the formation of nanoporous metal oxide membranes is reported, based on a layer-by-layer deposition procedure ('directed assembly') of metal oxide nanoparticles with appropriate 'linker' molecules; here Fe<sub>2</sub>O<sub>3</sub> particles and phytic acid. Two types of nanoporous Fe<sub>2</sub>O<sub>3</sub> membranes have been prepared and characterised: (A) a nanofilm deposit composed of 4-5 nm diameter Fe<sub>2</sub>O<sub>3</sub> particles linked by phytic acid and (B) a nanoporous film formed after calcination of the type A deposit at 500°C in air. The nanofilm deposits are characterised by microscopy (SEM and AFM) and by electrochemical methods. Mechanically stable and homogeneous nanofilm deposits with controlled thickness (ca. 3 nm per layer deposited) were obtained. Transport of small molecules or ions through the nanoporous structure and their electrochemical conversion are shown to be fast in the presence of a sufficiently high concentration of supporting electrolyte. During the electrochemical oxidation of ferrocyanide, Fe(CN)<sub>6</sub><sup>-4</sup>, the nanoporous structure of the type A deposit is shown to act as an 'active' membrane, which changes the electrode kinetics by 'double-layer superposition' effects. For the second type of nanofilm, type B, ferrocyanide is accumulated by adsorption within the porous structure.</p>