Multiferroic materials have attracted significant attention due to their potential to revolutionize logic and memory devices by reducing energy consumption or increasing information density. Barium monoferrite (γ-BaFe2O4 or BaFeO) is a promising lead- and bismuth-free multiferroic material with a stuffed tridymite-like structure, exhibiting both ferroelectricity and antiferromagnetism at room temperature. BaFeO thin films with engineered grain orientation, composition, elastic strain, and magnetic interlayer couplings could open new avenues for novel devices. However, synthesizing the stoichiometric "1–2–4" phase in the BaO-Fe2O3 system remains a challenge. This study focuses on the deposition of pure and crystalline γ-BaFe2O4 thin films using the Pulsed Electron Deposition (PED) method. An analysis of the plasma plume revealed that two main mechanisms govern the dynamics of BaFeO deposition: a congruent ablation process occurring far from thermodynamic equilibrium and an incongruent low-energy evaporation process. The regions of the film with maximized ablative/evaporative ratios are free from the secondary Ba2Fe2O5 phase, suggesting that the thermal evaporative contribution is the primary factor responsible for the out-of-stoichiometry composition. The influence of the substrate type on the structural properties of BaFeO films was also evaluated. It was confirmed that (h00)-oriented BaFeO tends to grow on amorphous quartz and polycrystalline Pt-coated quartz in the 700–800°C temperature range. Conversely, the growth on SiO2/Si leads to the preferential grain orientation along the (0k0) and (0kl) directions by increasing the temperature. These findings demonstrate the potential of PED for producing high-quality γ-BaFe2O4 polycrystalline thin films. A fully heteroepitaxial (h00)-BaFeO/(111)-MgO system was even achieved by depositing on a single-crystal MgO substrate. This unprecedented result paves the way for utilizing such thin films in multiferroic applications, where phase purity, structural orientation, and defect-free structures can be exploited to enhance the magnetoelectric properties of the device.
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