(57)Fe Mössbauer spectroscopy has been used to investigate the structural and magnetic phase transitions of CaFe₂As₂ (T(N) = 173 K) single crystals. For this compound we found that V(ZZ) is positive and parallel to the c-axis of the tetragonal structure. For CaFe₂As₂ a magnetic hyperfine field B(hf) was observed at the (57)Fe nucleus below T(N) ~173 K. Analysis of the temperature dependence of B(hf) data using the Bean-Rodbell model shows that the Fe spins undergo a first-order magnetic transition at ~173 K. A collinear antiferromagnetic structure is established below this temperature with the Fe spin lying in the (a, b) plane. Below T(N) the paramagnetic fraction of Fe decreases down to 150 K and for lower temperatures all the Fe spins are magnetically ordered.

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The design of novel nanostructured magnetic materials requires a good understanding of the variation in the magnetic properties due to different synthesis conditions. In this work, four different procedures for fabricating Co‐ferrite nanoparticles with similar sizes between 7 and 10 nm are compared by studying their structural and magnetic properties. Non‐aqueous methods based on the thermal decomposition of metal acetylacetonates at high temperatures, either with or without surfactants, provide highly crystalline nanoparticles with large saturation magnetization values and a coherent reversal of the magnetic moment. However, variations in the density of defects and in the shape of the nanocrystals determine the distribution of switching fields and the effective magnetic anisotropy, which reaches up to ≈1 × 107 erg cm−3 for oleic acid‐capped 9 nm nanoparticles. It is shown that the saturation magnetization values for nanoparticles produced by different methods are in the range between 49 and 95 emu g−1 due to differences in the stoichiometry, in the cation occupancy, in the magnetic disorder and in the spin canting of the magnetic sub‐lattices, the latter evaluated by in‐field Mössbauer spectroscopy.