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Register a new userMagnetization and magneto-electric effect in La-doped BiFeO3
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Guenaelle Le Bras Jasmin
Publication date
2009
fields
Physics
and research's language is
English
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We report on magnetisation and magneto-capacitance measurements in the Bi1-xLaxFeO3 series for 0 < x < 0.15. We confirm that doping with La reduces the threshold magnetic field Hc for cancelling the magnetic spiral phase, and we show that Hc decreases as the La content increases up to x=0.15, which is the highest concentration for maintaining the non-centrosymmetric rhombohedral structure of BiFeO3. Measurements of the dielectric constant as a function of magnetic field in the series also show a maximum magneto-capacitance for x=0.15.
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We consider phase separated states in magnetic oxides (MO) thin films. We show that these states have a non-zero electric polarization. Moreover, the polarization is intimately related to a spatial distribution of magnetization in the film. Polarized states with opposite polarization and opposite magnetic configuration are degenerate. An external electric field removes the degeneracy and allows to switch between the two states. So, one can control electric polarization and magnetic configuration of the phase separated MO thin film with the external electric field.
We propose a model of magneto-electric effect in doped magnetic ferroelectrics. This magneto-electric effect does not involve the spin-orbit coupling and is based purely on the Coulomb interaction. We calculate magnetic phase diagram of doped magnetic ferroelectrics. We show that magneto-electric coupling is pronounced only for ferroelectrics with low dielectric constant. We find that magneto-electric coupling leads to modification of magnetization temperature dependence in the vicinity of ferroelectric phase transition. A peak of magnetization appears. We find that magnetization of doped magnetic ferroelectrics strongly depends on applied electric field.
We report the observation of field-induced magnetization of BiFeO3 (BFO) in an ultrathin BFO/La0.7Sr0.3MnO3 (LSMO) superlattice using polarized neutron reflectivity (PNR). Our PNR results indicate parallel alignment of magnetization across BFO/LSMO interfaces. The study showed an increase in average magnetization on increasing applied magnetic field at 10K. We observed a saturation magnetization of 110 pm 15 kA/m (~0.8 {mu}B/Fe) for ultrathin BFO layer (~2 unit cell) sandwiched between ultrathin LSMO layers (~ 2 unit cell), which is much higher than the canted moment (0.03 {mu}B/Fe) in the bulk BFO. The macroscopic VSM results on superlattice clearly indicate superparamagnetic behavior typically observed in nanoparticles of manganites.
The dynamic coercivity cannot be measured rigorously by the conventional time-resolved magneto-optical Kerr effect technique because the irreversible deviation of the transient magnetization is accumulated. In order to remove the accumulation effect, the alternating magnetic field is employed and synchronized with the femtosecond laser pulse. Since the sample is reset before each single laser pulse, the accumulation effect of the irreversible deviation of the transient magnetization is removed. For perpendicularly magnetized $L1_{mathrm{0}}$ FePt films, the dynamic magnetization reversal process is accomplished by the nucleation of reversed domains and the pinned domain wall motion.
The physical properties of epitaxial films can fundamentally differ from those of bulk single crystals even above the critical thickness. By a combination of non-resonant x-ray magnetic scattering, neutron diffraction and vector-mapped x-ray magnetic linear dichroism photoemission electron microscopy, we show that epitaxial (111)-BiFeO3 films support sub-micron antiferromagnetic domains, which are magneto-elastically coupled to a coherent crystallographic monoclinic twin structure. This unique texture, which is absent in bulk single crystals, should enable control of magnetism in BiFeO3 film devices via epitaxial strain.
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