Magnetic Fe@FeO, Fe@C and α-Fe₂O₃ Single-Crystal Nanoblends Synthesized by Femtosecond Laser Ablation of Fe in Acetone.

There are few reports on zero-field-cooled (ZFC) magnetization measurements for Fe@FeO or FeO particles synthesized by laser ablation in liquids (LAL) of Fe, and the minimum blocking temperature (T) of 120 K reported so far is still much higher than those of their counterparts synthesized by chemical methods. In this work, the minimum blocking temperature was lowered to 52 K for 4⁻5 nm α-Fe₂O₃ particles synthesized by femtosecond laser ablation of Fe in acetone. The effective magnetic anisotropy energy density (K) is calculated to be 2.7⁻5.4 × 10⁵ J/m³, further extending the K values for smaller hematite particles synthesized by different methods. Large amorphous-Fe@α-Fe₂O₃ and amorphous-Fe@C particles of 10⁻100 nm in diameter display a soft magnetic behavior with saturation magnetization (M) and coercivities (H) values of 72.5 emu/g and 160 Oe at 5 K and 61.9 emu/g and 70 Oe at 300 K, respectively, which mainly stem from the magnetism of amorphous Fe cores. Generally, the nanoparticles obtained by LAL are either amorphous or polycrystalline, seldom in a single-crystalline state. This work also demonstrates the possibility of synthesizing single-crystalline α-Fe₂O₃ hematite crystals of several nanometers with (104), (113), (116) or (214) crystallographic orientations, which were produced simultaneously with other products including carbon encapsulated amorphous Fe (a-Fe@C) and Fe@FeO core-shell particles by LAL in one step. Finally, the formation mechanisms for these nanomaterials are proposed and the key factors in series events of LAL are discussed.