Cation-engineered Zn Ti co-substituted BaM Hexaferrites with enhanced magnetic and Magnetocaloric performance

Tailoring the functional properties of M-type hexaferrites through controlled cation engineering has emerged as a powerful route for developing next-generation magnetic materials. In this work, Zn Ti co-substituted barium hexaferrites BaFe 12-2x Zn x Ti x O 19 (x = 0.0 and 0.2, BFZTO) were synthesized via a sol–gel auto-combustion method to examine the structural, microstructural, magnetic, and magnetocaloric effects induced by dual-cation substitution. X-ray diffraction patterns refined using the Rietveld method demonstrated that the samples crystallize solely in the magnetoplumbite structure (space group P63/mmc). Increasing the dopant level led to a marked reduction in crystallite dimensions, decreasing from about 89 nm to nearly 43 nm. SEM and TEM analyses further revealed well-defined hexagonal platelets and demonstrated that Zn Ti incorporation promotes finer grains and enhanced microstructural homogeneity.Raman spectroscopy further confirms the structural integrity and highlights Zn–Ti-induced local lattice distortions.Magnetic characterization indicated that introducing non-magnetic Zn 2+ and Ti 4+ ions weakens Fe–O–Fe superexchange interactions, resulting in a decrease in Curie temperature T C (740 → 690 K) and a moderate reduction in saturation magnetization M S (74.45 → 68.29 emu.g −1 ). In contrast, coercivity H C increased significantly (1.57 → 3.12 kOe), reflecting grain refinement and strengthened magnetocrystalline anisotropy. Law of Approach to Saturation analysis confirmed a notable enhancement in the effective anisotropy constant with higher substitution levels. Importantly, Zn Ti co-substitution considerably improved the magnetocaloric behavior: the maximum magnetic entropy change increased from −ΔS M max 1.85 to 2.18 J.kg −1 .K −1 , and the relative cooling power RCP max with rose from 158 to 247 J.kg −1 under a 10 T magnetic field. This enhancement is associated with dopant-induced lattice perturbations that broaden the magnetic transition and amplify spin-entropy variations near T C . Overall, this study shows that controlled Zn Ti co-substitution effectively tailors the magnetic properties of M hexaferrites, making them suitable for moderate-temperature magnetic refrigeration and rare-earth-free permanent magnet applications. • Zn Ti co-substituted BaM hexaferrites were successfully synthesized by sol–gel method. • Rietveld refinement confirms single-phase magnetoplumbite structure. • Zn Ti substitution refines grains and improves microstructural homogeneity. • Zn Ti co-substitution weakens Fe–O–Fe interactions, enhancing coercivity. • Magnetocaloric response is improved with higher entropy change and cooling power.

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Journal
Materials Science and Engineering B
Published
2026-03-02
DOI
https://doi.org/10.1016/j.mseb.2026.119227
Primary Topic
Magnetic Properties and Synthesis of Ferrites
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article
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article

Cation-engineered Zn Ti co-substituted BaM Hexaferrites with enhanced magnetic and Magnetocaloric performance

R. Thaljaoui, Kawther Laajimi, José Ordoñez-Miranda, Amal Homri et al.
Materials Science and Engineering B
Magnetic Properties and Synthesis of Ferrites
article

Cation-engineered Zn Ti co-substituted BaM Hexaferrites with enhanced magnetic and Magnetocaloric performance

R. Thaljaoui, Kawther Laajimi, José Ordoñez-Miranda, Amal Homri, Jemai dhahri, Abdullah Aljaafari
article en

Abstract

Tailoring the functional properties of M-type hexaferrites through controlled cation engineering has emerged as a powerful route for developing next-generation magnetic materials. In this work, Zn Ti co-substituted barium hexaferrites BaFe 12-2x Zn x Ti x O 19 (x = 0.0 and 0.2, BFZTO) were synthesized via a sol–gel auto-combustion method to examine the structural, microstructural, magnetic, and magnetocaloric effects induced by dual-cation substitution. X-ray diffraction patterns refined using the Rietveld method demonstrated that the samples crystallize solely in the magnetoplumbite structure (space group P63/mmc). Increasing the dopant level led to a marked reduction in crystallite dimensions, decreasing from about 89 nm to nearly 43 nm. SEM and TEM analyses further revealed well-defined hexagonal platelets and demonstrated that Zn Ti incorporation promotes finer grains and enhanced microstructural homogeneity.Raman spectroscopy further confirms the structural integrity and highlights Zn–Ti-induced local lattice distortions.Magnetic characterization indicated that introducing non-magnetic Zn 2+ and Ti 4+ ions weakens Fe–O–Fe superexchange interactions, resulting in a decrease in Curie temperature T C (740 → 690 K) and a moderate reduction in saturation magnetization M S (74.45 → 68.29 emu.g −1 ). In contrast, coercivity H C increased significantly (1.57 → 3.12 kOe), reflecting grain refinement and strengthened magnetocrystalline anisotropy. Law of Approach to Saturation analysis confirmed a notable enhancement in the effective anisotropy constant with higher substitution levels. Importantly, Zn Ti co-substitution considerably improved the magnetocaloric behavior: the maximum magnetic entropy change increased from −ΔS M max 1.85 to 2.18 J.kg −1 .K −1 , and the relative cooling power RCP max with rose from 158 to 247 J.kg −1 under a 10 T magnetic field. This enhancement is associated with dopant-induced lattice perturbations that broaden the magnetic transition and amplify spin-entropy variations near T C . Overall, this study shows that controlled Zn Ti co-substitution effectively tailors the magnetic properties of M hexaferrites, making them suitable for moderate-temperature magnetic refrigeration and rare-earth-free permanent magnet applications. • Zn Ti co-substituted BaM hexaferrites were successfully synthesized by sol–gel method. • Rietveld refinement confirms single-phase magnetoplumbite structure. • Zn Ti substitution refines grains and improves microstructural homogeneity. • Zn Ti co-substitution weakens Fe–O–Fe interactions, enhancing coercivity. • Magnetocaloric response is improved with higher entropy change and cooling power.

Materials Science and Engineering BVol. 328
Centre National de la Recherche Scientifique (FR), Qassim University (SA), University of Monastir (TN), Sorbonne Université (FR), Institut des NanoSciences de Paris (FR), King Faisal University (SA), Université de Caen Normandie (FR)
Openalex Percentile: Top 40%
Magnetic Properties and Synthesis of Ferrites
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