Formation Mechanisms of Co-existence of α-Fe and Iron Oxides Nanoparticles Decorated on Carbon Nanofibers by a Simple Liquid Phase Adsorption-Thermal Oxidation
A. Alimin, L. Kadidae, L. Agusu, L. Ahmad, S. J. Santosa, A. Asria
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引用次数: 0
Abstract
We propose formation mechanisms of co-existence of α-Fe and iron oxides nanoparticles decorated on CNFs. The α-Fe nanoparticles are produced via oxidation-reduction mechanisms, which occur in liquid phase adsorption (LPA) assisted by ultrasonic energy, while α-Fe2O3 nanoparticles are thermally formed through mechanisms of Lewis acidbase. In addition, Fe3O4 is thermally formed by reducing Fe2O3 by CNFs. Liquid phase adsorption assisted by ultrasonic energy under ambient temperature using Fe(NO3)3•9H2O as a precursor of iron oxides and α-Fe has been applied. Then, as prepared, Fe(III)@CNFs were thermally calcined at 573 K under air atmosphere in various holding times ranging from 0.5 to 2 h. XRD data confirmed that α- Fe2O3 and Fe3O4 had been successfully grown onto CNFs. Moreover, the presence of the iron oxides and iron nanoparticles was studied by the SEMEDX technique. The iron oxide nanoparticles appeared after a heating period of 0.5h. However, at a holding time of 0.5 h, we found an exciting and unexpected phenomenon where oxygen content is zero percent while Fe is 0.23 wt %. It implies that α-Fe nanoparticles were formed earlier than α-Fe2O3 and Fe3O4 as the proposed mechanisms. Formation mechanisms of iron and its oxides such as α-Fe2O3 and Fe3O4 decorated on CNFs through liquid-phase adsorption followed by thermally treatment technique in this work is expected to give significant contribution in the field of nanocomposite materials, especially for anode materials based on iron oxides.
期刊介绍:
This international Journal is intended for the publication of original work, both analytical and experimental, and of reviews and commercial aspects related to the field of New Materials for Electrochemical Systems. The emphasis will be on research both of a fundamental and an applied nature in various aspects of the development of new materials in electrochemical systems.