Fine tuning of magnetite nanoparticle size distribution using dissymmetric potential pulses in the presence of biocompatible surfactants and the electrochemical characterization of the nanoparticles
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The effects of varying the surfactant concentration and the anodic pulse potential on the properties and electrochemical behaviors of magnetite nanoparticles were investigated. The nanoparticles were synthesized with an electrochemical method based on applying dissymmetric potential pulses, which offers the advantage that can be used to tune the particle size distribution very precisely in the range of 10 to 50 nm. Under the conditions studied, the surfactant concentration directly affects the size distribution, with higher concentrations producing narrower distributions. Linear voltammetrywas used to characterize the electrochemical behavior of the synthesized nanoparticles in both the anodic and cathodic regions,which are attributed to the oxidation of Fe2 and the reduction of Fe3 ; these species are part of the spinel structure of magnetite. Electrochemical impedance spectroscopy data indicated that the reduction and oxidation reactions of the nanoparticles are not controlled by the mass transport step, but by the charge transfer step. The sample with the highest saturation magnetization was that synthesized in the presence of polyethylene glycol. © 2014 Elsevier B.V. All rights reserved.
The effects of varying the surfactant concentration and the anodic pulse potential on the properties and electrochemical behaviors of magnetite nanoparticles were investigated. The nanoparticles were synthesized with an electrochemical method based on applying dissymmetric potential pulses, which offers the advantage that can be used to tune the particle size distribution very precisely in the range of 10 to 50 nm. Under the conditions studied, the surfactant concentration directly affects the size distribution, with higher concentrations producing narrower distributions. Linear voltammetrywas used to characterize the electrochemical behavior of the synthesized nanoparticles in both the anodic and cathodic regions,which are attributed to the oxidation of Fe2%2b and the reduction of Fe3%2b; these species are part of the spinel structure of magnetite. Electrochemical impedance spectroscopy data indicated that the reduction and oxidation reactions of the nanoparticles are not controlled by the mass transport step, but by the charge transfer step. The sample with the highest saturation magnetization was that synthesized in the presence of polyethylene glycol. © 2014 Elsevier B.V. All rights reserved.
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Biocompatible surfactants; Dissymmetric pulses; Electrochemical synthesis; Magnetite nanoparticles Biocompatible surfactants; Dissymmetric pulses; Electrochemical characterizations; Electrochemical synthesis; Fine tuning; Nanoparticle size distribution; Potential pulse; Magnetite nanoparticles; biomaterial; magnetite; nanoparticle; powder; electrochemical analysis; powder; procedures; transmission electron microscopy; X ray diffraction; Biocompatible Materials; Electrochemical Techniques; Ferrosoferric Oxide; Microscopy, Electron, Transmission; Nanoparticles; Powders; X-Ray Diffraction
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