Abstract

Copper ferrite, belonging to the wide and technologically relevant class of spinel ferrites, was grown in the form of t-CuFe2O4 nanocrystals within a porous matrix of silica in the form of either an aerogel or a xerogel, and compared to a bulk sample. Extended X-ray absorption fine structure (EXAFS) spectroscopy revealed the presence of two different sub-lattices within the crystal structure of t-CuFe2O4, one tetragonal and one cubic, defined by the Cu2+ and Fe3+ ions respectively. Our investigation provides evidence that the Jahn-Teller distortion, which occurs on the Cu2+ ions located in octahedral sites, does not affect the coordination geometry of the Fe3+ ions, regardless of their location in octahedral or tetrahedral sites.

Highlights

  • Copper ferrite is a ceramic material belonging to a class of metal-oxides of generic formula MFe2O4 where M represents a bi-valent transition metal ion, e.g. Mn2+, Ni2+, Co2+, Cu2+ 1, possessing the spinel structure

  • The sol-gel autocombustion process proposed by Ansari et al for the synthesis of lead and copper hexaferrite (PbFe12O19 and CuFe12O19 respectively) using maltose as reducing agent[19,20] enables to tune the size and shape of the produced nanoparticles by control of the calcination temperatures and the maltose content

  • The structural and textural features as assessed by Transmission electron microscopy (TEM), X-ray diffraction (XRD) and N2-physisorption point out to the formation of t-CuFe2O4 nanophase with crystals sizes in the region of 6–7 nm and high size homogeneity, both in a relatively dense xerogel and in a highly porous aerogel

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Summary

Introduction

Copper ferrite is a ceramic material belonging to a class of metal-oxides of generic formula MFe2O4 where M represents a bi-valent transition metal ion, e.g. Mn2+, Ni2+, Co2+, Cu2+ 1, possessing the spinel structure. Many methods for the synthesis of copper ferrite nanoparticles have been proposed so far, the most common include high temperature solution phase approaches[13], thermal decomposition of nitrates[14], co-precipitation[15], combustion process[16] and sol-gel auto-combustion[17,18]. These methods yield nanoparticles with average dimensions of several tens of nanometres and a poor degree of size and shape homogeneity. The control of the particle size has a major technological importance, because the magnetic and catalytic properties of nanoparticles are highly size dependent[16]

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