6533b859fe1ef96bd12b76c4

RESEARCH PRODUCT

Magnetic ordering in an (Fe0.2Cr0.8)1.5[Cr(CN)6] Prussian blue analogue studied with synchrotron radiation based spectroscopies

Helena Prima-garcíaDimitri ArvanitisRodolfo MirandaRodolfo MirandaFrancisco Jesús LuqueFrancisco M. RomeroEugenio CoronadoI.a. KowalikM. A. NiñoJuan José De MiguelJuan P. Prieto-ruiz

subject

Ligand field theoryPrussian blueMaterials scienceMagnetic momentAbsorption spectroscopyMagnetic circular dichroismRelaxation (NMR)Synchrotron radiation02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceschemistry.chemical_compoundCrystallographychemistryMaterials ChemistryCurie temperature0210 nano-technology

description

The appearance of magnetic order in the (Fe0.2Cr0.8)1.5[Cr(CN)6]·15H2O Prussian blue analogue at low temperature has been investigated by means of synchrotron radiation-based X-ray absorption spectroscopy and X-ray magnetic circular dichroism. With the help of ligand field multiplet analysis we have been able to identify the oxidation states of the metallic cations present in the sample and their evolution with temperature. Our experiments reveal that the appearance of ferromagnetic order is triggered by the transformation of CrIII cations to CrII high-spin caused by a transfer of electrons from the Fe to the Cr resulting in an increase of the magnetic interactions within the (Cr, Cr) sublattice. The misfit strain between the (Fe, Cr) and the (Cr, Cr) moieties that coexist within this ternary material influences the balance of oxidation states and hence the magnetic properties of the metallic ions. Misfit relaxation also plays a role in determining the differences between the surface and the bulk of the material. The measurement of the magnetic moments in those two regions suggests that the surface may have a reduced Curie temperature compared to the bulk.

http://hdl.handle.net/20.500.12614/1638