Tunable magnetic properties in compositionally graded L1 0 -FePt thin films

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Authors: Isaak G. Vasileiadis, Dimitrios Karfaridis, Nikolaos Maniotis, Kristina Ignatova, Unnar B. Arnalds, G. Vourlias, George P. Dimitrakopulos, Evangelos Th. Papaioannou, Th. Kehagias
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References: 57

Abstract

Abstract The tetragonally ordered L1 0 -FePt alloy exhibits strong magnetocrystalline anisotropy and high coercivity values, making it a model platform for high-density data storage and magnetic nanoparticles applications. However, the tunability of its magnetic properties through structural and compositional design remains a challenge. Here, we present a novel approach of fabricating compositionally graded L1 0 -FePt thin films via thermally activated solid-state reactions of Fe/Pt bilayers grown on MgO(001). Upon annealing, vacancy-mediated migration and grain boundary diffusion drive the transformation into a structurally coherent columnar grain structure, consisting of epitaxial domains and misoriented regions. Nanoscale compositional analysis reveals a Pt concentration gradient, with near-stoichiometric L1 0 -FePt in the upper film and a progressively Fe-rich profile near the FePt/MgO interface, while maintaining chemical ordering and tetragonality. This self-organized gradient has profound consequences, as the Fe-enriched interfacial region enhances Fe–Fe exchange stiffness, suppressing out-of-plane anisotropy and coercivity while promoting in-plane magnetization at room temperature. Magnetization reversal occurs through softened hysteresis and complex domain configurations, as confirmed by micromagnetic simulations. These results establish chemical grading as a powerful design strategy to modulate anisotropy, coercivity and domain behavior in L1 0 -FePt, unlocking new opportunities for materials tailored for advanced spintronic and data storage applications.

Fields of Study & Subjects

Magnetic properties of thin films Metallic Glasses and Amorphous Alloys Magnetic Properties of Alloys

Publication details

Journal / source
Journal of Physics D Applied Physics
Volume
59
Issue
2
Pages
025008–025008
Publication date
2 January 2026