X-ray diffraction (XRD) and Mossbauer spectroscopy techniques combined with theoretical calculations based on the Korringa-Kohn-Rostoker (KKR) electronic structure calculation method were used to investigate sigma-phase Fe_{100-x}Re_{x} alloys (x = 4
3, 45, 47, 49 and 53). Structural data such as site occupancies and lattice constants were derived from the XRD patters, while the average isomer shift and distribution curves of the quadrupole splitting were obtained from the Mossbauer spectra. Fe-site charge-densities and the quadrupole splittings were computed with the KKR method for each lattice site. The calculated quantities combined with the experimentally determined site occupancies were successfully used to decompose the measured Mossbauer spectra into five components corresponding to the five sublattices.
The compound EuFe(2-x)Co(x)As2 was investigated by means of the 57Fe and 151Eu Moessbauer spectroscopy versus temperature (4.2 - 300 K) for x=0 (parent), x=0.34 - 0.39 (superconductor) and x=0.58 (overdoped). It was found that spin density wave (SDW)
is suppressed by Co-substitution, however it survives in the region of superconductivity, but iron spectra exhibit some non-magnetic component in the superconducting region. Europium orders anti-ferromagnetically regardless of the Co concentration with the spin re-orientation from the a-axis in the parent compound toward c-axis with the increasing replacement of iron by cobalt. The re-orientation takes place close to the a-c plane. Some trivalent europium appears in EuFe(2-x)Co(x)As2 versus substitution due to the chemical pressure induced by Co-atoms and it experiences some transferred hyperfine field from Eu2+. Iron experiences some transferred field due to the europium ordering for substituted samples in the SDW and non-magnetic state both, while the transferred field is undetectable in the parent compound. Superconductivity coexists with the 4f-europium magnetic order within the same volume. It seems that superconductivity has some filamentary character in EuFe(2-x)Co(x)As2 and it is confined to the non-magnetic component seen by the iron Moessbauer spectroscopy.
