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Register a new userNegative magnetostrictive magnetoelectric coupling of BiFeO3
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How the magnetoelectric coupling actually occurs on a microscopic level in multiferroic BiFeO3 is not well known. By using the high-resolution single crystal neutron diffraction techniques, we have determined the electric polarization of each individual elements of BiFeO3, and concluded that the magnetostrictive coupling suppresses the electric polarization at the Fe site below TN. This negative magnetoelectric coupling appears to outweigh the spin current contributions arising from the cycloid spin structure, which should produce a positive magnetoelectric coupling.
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The Loewdin orthogonalization procedure being the well-known technique, particularly in quantum chemistry, however, gives rise to novel effects missed in earlier studies. Making use of the technique of irreducible tensorial operators we have developed a regular procedure for account of the orthogonalization effects. For illustration we address the emergence of a specific magnetoelectric coupling for noncentrosymmetric 3d or 4f ions.
Raman scattering measurements on BiFeO3 single crystals show an important coupling between the magnetic order and lattice vibrations. The temperature evolution of phonons shows that the lowest energy E and A1 phonon modes are coupled to the spin order up to the Neel temperature. Furthermore, low temperature anomalies associated with the spin re-orientation are observed simultaneously in both the E phonon and the magnon. These results suggest that magnetostriction plays an important role in BiFeO3.
We report the results of direct measurement of remanent hysteresis loops on nanochains of BiFeO$_3$ at room temperature under zero and $sim$20 kOe magnetic field. We noticed a suppression of remanent polarization by nearly $sim$40% under the magnetic field. The powder neutron diffraction data reveal significant ion displacements under a magnetic field which seems to be the origin of the suppression of polarization. The isolated nanoparticles, comprising the chains, exhibit evolution of ferroelectric domains under dc electric field and complete 180$^o$ switching in switching-spectroscopy piezoresponse force microscopy. They also exhibit stronger ferromagnetism with nearly an order of magnitude higher saturation magnetization than that of the bulk sample. These results show that the nanoscale BiFeO$_3$ exhibits coexistence of ferroelectric and ferromagnetic order and a strong magnetoelectric multiferroic coupling at room temperature comparable to what some of the type-II multiferroics show at a very low temperature.
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 transverse and longitudinal magnetoelectric susceptibilities (MES) were quantitatively determined for (001) heteroepitaxial BiFeO$_{3}$-CoFe$_{2}$O$_{4}$ nanostructures. Both of these MES values were sharply enhanced at magnetic fields below 6 kOe and revealed asymmetric lineshapes with respect to the dc magnetic field, demonstrating the strain-induced magnetoelectric effect. The maximum transverse MES, which reached as high as $sim$60 mV/cm Oe, was about five times larger than the longitudinal MES. This observation signifies that transverse magnetostriction of the CoFe$_{2}$O$_{4}$ nanopillars is enhanced more than the bulk value due to preferred magnetic domain alignment along the [001] direction coming from compressive, heteroepitaxial strain.
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