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Strontium ferromolybdate, Sr 2 FeMoO 6 , is an important member of the family of double perovskites with the possible technological applications in the field of spintronics and solid oxide fuel cells. Its preparation  via  a multi-step ceramic route or various wet chemistry-based routes is notoriously difficult. The present work demonstrates that Sr 2 FeMoO 6  can be mechanosynthesized at ambient temperature in air directly from its precursors (SrO, α-Fe, MoO 3 ) in the form of nanostructured powders, without the need for solvents and/or calcination under controlled oxygen fugacity. The mechanically induced evolution of the Sr 2 FeMoO 6  phase and the far-from-equilibrium structural state of the reaction product are systematically monitored with XRD and a variety of spectroscopic techniques including Raman spectroscopy,  57 Fe Mössbauer spectroscopy, and X-ray photoelectron spectroscopy. The unique extensive oxidation of iron species (Fe 0  → Fe 3+ ) with simultaneous reduction of Mo cations (Mo 6+  → Mo 5+ ), occuring during the mechanosynthesis of Sr 2 FeMoO 6 , is attributed to the mechanically triggered formation of tiny metallic iron nanoparticles in superparamagnetic state with a large reaction surface and a high oxidation affinity, whose steady presence in the reaction mixture of the milled educts initiates/promotes the swift redox reaction. High-resolution transmission electron microscopy observations reveal that the mechanosynthesized Sr 2 FeMoO 6 , even after its moderate thermal treatment at 923 K for 30 min in air, exhibits the nanostructured nature with the average particle size of 21(4) nm. At the short-range scale, the nanostructure of the as-prepared Sr 2 FeMoO 6  is characterized by both, the strongly distorted geometry of the constituent FeO 6  octahedra and the extraordinarily high degree of anti-site disorder. The degree of anti-site disorder  ASD  = 0.5, derived independently from the present experimental XRD, Mössbauer, and SQUID magnetization data, corresponds to the completely random distribution of Fe 3+  and Mo 5+  cations over the sites of octahedral coordination provided by the double perovskite structure. Moreover, the fully anti-site disordered Sr 2 FeMoO 6  nanoparticles exhibit superparamagnetism with the blocking temperature  T  B  = 240 K and the deteriorated effective magnetic moment  μ  = 0.055  μ  B  per formula unit.

A Unique Mechanochemical Redox Reaction Yielding Nanostructured Double Perovskite Sr2FeMoO6 With an Extraordinarily High Degree of Anti-Site Disorder