Carta, D., Casula, M.F., Floris, P., Falqui, A., Mountjoy, G., Boni, A., Sangregorio, C., Corrias, A. (2010) Synthesis and microstructure of manganese ferrite colloidal nanocrystals. Physical Chemistry Chemical Physics, 12 (19). pp. 5074-5083. ISSN 1463-9076. (doi:10.1039/b922646j) (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided) (KAR id:46209)
The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided. | |
Official URL: http://dx.doi.org/10.1039/b922646j |
Abstract
The atomic level structure of a series of monodisperse single crystalline nanoparticles with a magnetic core of manganese ferrite was studied using X-ray absorption fine structure (EXAFS) and X-ray absorption near edge structure (XANES) techniques at both the Fe and Mn K-edges, and conventional and high resolution transmission electron microscopy (TEM and HRTEM). In particular, insights on the non-stoichiometry and on the inversion degree of manganese ferrite nanocrystals of different size were obtained by the use of complementary structural and spectroscopic characterization techniques. The inversion degree of the ferrite nanocrystals, i.e. the cation distribution between the octahedral and tetrahedral sites in the spinel structure, was found to be much higher (around 0.6) than the literature values reported for bulk stoichiometric manganese ferrite (around 0.2). The high inversion degree of the nanoparticles is ascribed to the partial oxidation of Mn2+ to Mn3+ which was evidenced by XANES, leading to non-stoichiometric manganese ferrite.
Item Type: | Article |
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DOI/Identification number: | 10.1039/b922646j |
Subjects: | Q Science > QC Physics > QC176.8.N35 Nanoscience, nanotechnology |
Divisions: | Divisions > Division of Natural Sciences > Physics and Astronomy |
Depositing User: | Anna Corrias |
Date Deposited: | 17 Dec 2014 11:44 UTC |
Last Modified: | 05 Nov 2024 10:29 UTC |
Resource URI: | https://kar.kent.ac.uk/id/eprint/46209 (The current URI for this page, for reference purposes) |
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