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Iron oxide film growth under ultrathin polysiloxane networks
Authors:Patrick Degen  D. C. Florian Wieland  Michael Paulus  Martin A. Schroer  Metin Tolan  Heinz Rehage
Affiliation:1. Physical Chemistry II, TU Dortmund, Otto Hahn Stra?e 6, 44227, Dortmund, Germany
2. Fakult?t Physik/DELTA, TU Dortmund, Maria-Goeppert-Mayer Str.2, 44227, Dortmund, Germany
Abstract:This study focuses on the preparation and characterization of magnetic switchable thin iron oxide–polymer films. In a series of experiments, the formation and growth of iron oxide under ultrathin polysiloxane layers was controlled by changing the concentration of iron ions in the aqueous subphase or by varying the residence time of ammonia in the gas phase above the liquid sample. The growth of the combined film structures is studied in situ by interfacial rheology, optical microscopy, and x-ray scattering experiments and ex situ by scanning electron microscopy. Different stages of iron oxide aggregation, from a very thin layer of amorphous iron oxide with thickness of a few nanometers up to micrometer thick coatings of crystalline maghemite (γ-Fe2O3) were investigated. The specific interactions between the inorganic iron oxide and the polymer membranes cause the creation of new composite materials which are sensitive to magnetic forces.
Figure
Magnetic switchable membranes should be achieved by the combination of an ultrathin polymer network with the in-situ formation of iron oxide at the interface. (Left) After completing the polymerization the creation of iron oxide was induced by adding NH3 gas. (Right) SEM investigations clearly approve the formation of a thin composite layer as well as the growth of iron-oxide under this layer
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