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Magnetoelectric (ME) properties under rotating magnetic field H are comparatively investigated in two representative hexaferrites Y-type Ba0.5Sr1.5Zn2(Fe0.92Al0.08)12O22 and Z-type Ba0.52Sr2.48Co2Fe24O41, both of which have exhibited a similar transverse conical spin structure and giant ME coupling near room temperature. When the external H is rotated clockwise by 2pi, in-plane P vector is rotated clockwise by 2pi in the Y-type hexaferrite and counterclockwise by 4pi in the Z-type hexaferrite. A symmetry-based analysis reveals that the faster and opposite rotation of P vector in the Z-type hexaferrite is associated with the existence of a mirror plane perpendicular to c-axis. Moreover, such a peculiar crystal symmetry also results in contrasting microscopic origins for the spin-driven ferroelectricity; only the inverse DM interaction is responsible for the Y-type hexaferrite while additional p-d hybridization becomes more important in the Z-type hexaferrite. This work demonstrates the importance of the crystal symmetry in the determination of ME properties in the hexaferrites and provides a fundamental framework for understanding and applying the giant ME coupling in various ferrites with hexagonal crystal structure.
We have elucidated the spin, lattice, charge and orbital coupling mechanism underlying the multiferroic character in tensile strained EuTiO3 films. Symmetry determined by oxygen octahedral tilting shapes the hybridization between the Eu 4f and Ti 3d
The quantitative understanding of converse magnetoelectric effects, i.e., the variation of the magnetization as a function of an applied electric field, in extrinsic multiferroic hybrids is a key prerequisite for the development of future spintronic
Multiferroics are those materials with more than one ferroic order, and magnetoelectricity refers to the mutual coupling between magnetism and electricity. The discipline of multiferroicity has never been so highly active as that in the first decade
Pb(Fe$_{0.5}$Nb$_{0.5}$)O$_3$ (PFN), one of the few relaxor multiferroic systems, has a $G$-type antiferromagnetic transition at $T_N$ = 143 K and a ferroelectric transition at $T_C$ = 385 K. By using high-resolution neutron-diffraction experiments a
Magnetic, dielectric and calorimetric studies on 0.9BiFeO3-0.1BaTiO3 indicate strong magnetoelectric coupling. XRD studies reveal a very remarkable change in the rhombohedral distortion angle and a significant shift in the atomic positions at the mag