ترغب بنشر مسار تعليمي؟ اضغط هنا

Ferroelectricity induced by ferriaxial crystal rotation and spin helicity in a B-site-ordered double-perovskite multiferroic In2NiMnO6

64   0   0.0 ( 0 )
 نشر من قبل Dmitry Khalyavin
 تاريخ النشر 2019
  مجال البحث فيزياء
والبحث باللغة English




اسأل ChatGPT حول البحث

We have performed dielectric measurements and neutron diffraction experiments on the double perovskite In2NiMnO6. A ferroelectric polarization, P ~ 30 {mu}C/m2, is observed in a polycrystalline sample below TN = 26 K where a magnetic phase ransition occurs. The neutron diffraction experiment demonstrates that a complex noncollinear magnetic structure with cycloidal and proper screw components appears below TN, which has the incommensurate propagation vector k = (ka,0,ks; ka ~ 0.274, ks ~ -0.0893). The established magnetic point group 21 implies that the macroscopic ferroelectric polarization is along the monoclinic b axis. Recent theories based on the inverse Dzyaloshinskii-Moriya effect allow us to specify two distinct contributions to the polarization of In2NiMnO6. One of them is associated with the cycloidal component, p1 ~ rij x (Si x Sj), and the other with the proper screw component, p2 ~ [rij (Si x Sj )]A. The latter is explained by coupling between spin helicity and ferriaxial crystal rotation with macroscopic ferroaxial vector A, characteristic of the B-site ordered perovskite systems with out-of-plane octahedral tilting.



قيم البحث

اقرأ أيضاً

The magnetic ground state of double perovskite Sr2DyRuO6 has been investigated using muon spin rotation and relaxation (muSR), neutron powder diffraction (NPD) and inelastic neutron scattering (INS), in addition to heat capacity and magnetic suscepti bility (ac and dc) measurements. A clear signature of a long-range ordered magnetic ground state has been observed in the heat capacity data, which exhibit two sharp anomalies at 39.5 and 36 K found as well in the magnetic data. Further confirmation of long-range magnetic ordering comes from a sharp drop in the muon initial asymmetry and a peak in the relaxation rate at 40 K, along with a weak anomaly near 36 K. Based on temperature dependent NPD, the low temperature magnetic structure contains two interpenetrating lattices of Dy and Ru5, forming an antiferromagnetic ground state below 39.5 K with magnetic propagation vector k = (0,0,0). The magnetic moments of Dy and Ru at 3.5 K are pointing along the crystallographic b-axis with values of muDy = 4.92(10) muB and muRu = 1.94(7) muB, respectively. The temperature dependence of the Ru moments follows a mean field type behaviour, while that of the Dy moments exhibits a deviation indicating that the primary magnetic ordering is induced by the order of the 4d electrons of Ru rather than that of its proper 4f Dy electrons. The origin of the second anomaly observed in the heat capacity data at 36.5 K must be connected to a very small spin reorientation as the NPD studies do not reveal any clear change in the observed magnetic Bragg peaks positions or intensities between these two transitions. INS measurements reveal the presence of crystal field excitations (CEF) in the paramagnetic state with overall CEF splitting of 73.8 meV, in agreement with the point change model calculations.
186 - S. Esser , C.F. Chang , C.-Y. Kuo 2018
B-site ordered thin films of double perovskite Sr$_2$CoIrO$_6$ were epitaxially grown by a metal-organic aerosol deposition technique on various substrates, actuating different strain states. X-ray diffraction, transmission electron microscopy and po larized far-field Raman spectroscopy confirm the strained epitaxial growth on all used substrates. Polarization dependent Co $L_{2,3}$ X-ray absorption spectroscopy reveals a change of the magnetic easy axis of the antiferromagnetically ordered (high-spin) Co$^{3+}$ sublattice within the strain series. By reversing the applied strain direction from tensile to compressive, the easy axis changes abruptly from in-plane to out-of-plane orientation. The low-temperature magnetoresistance changes its sign respectively and is described by a combination of weak anti-localization and anisotropic magnetoresistance effects.
Magnetic structures and the relationship between spin and charge-orbital orderings of an A-site ordered double-perovskite manganite SmBaMn2O6, an anticipated multiferroic material, were investigated by means of neutron diffraction. The spin arrangeme nt in MnO2 planes perpendicular to the c axis is revealed to be the same as that in the A-site disordered half-doped manganites CE-type but the stacking pattern is found to be different displaying a unique twofold period. The temperature dependence of the superlattice magnetic and nuclear reflections clarifies that the antiferromagnetic spin ordering occurs at a temperature slightly lower than the temperature at which a rearrangement of the charge-orbital orderings occurs. The result evidences that the rearrangement leads the spin ordering. The intensities of the magnetic reflections are found to change across Tf = 10 K, suggesting a spin-flop by 90 [deg.] while keeping the Mn spin ordering pattern unchanged.
We construct and analyze a microscopic model for insulating rock salt ordered double perovskites, with the chemical formula A$_2$BBO$_6$, where the B atom has a 4d$^1$ or 5d$^1$ electronic configuration and forms a face centered cubic (fcc) lattice. The combination of the triply-degenerate $t_{2g}$ orbital and strong spin-orbit coupling forms local quadruplets with an effective spin moment $j=3/2$. Moreover, due to strongly orbital-dependent exchange, the effective spins have substantial biquadratic and bicubic interactions (fourth and sixth order in the spins, respectively). This leads, at the mean field level, to three main phases: an unusual antiferromagnet with dominant octupolar order, a ferromagnetic phase with magnetization along the $[110]$ direction, and a non-magnetic but quadrupolar ordered phase, which is stabilized by thermal fluctuations and intermediate temperatures. All these phases have a two sublattice structure described by the ordering wavevector ${boldsymbol Q} =2pi (001)$. We consider quantum fluctuations and argue that in the regime of dominant antiferromagnetic exchange, a non-magnetic valence bond solid or quantum spin liquid state may be favored instead. Candidate quantum spin liquid states and their basic properties are described. We also address the effect of single-site anisotropy driven by lattice distortions. Existing and possible future experiments are discussed in light of these results.
We present the magnetic structure of $mathrm{TmMn_3O_6}$, solved via neutron powder diffraction - the first such study of any $Rmathrm{Mn_3O_6}$ A-site columnar-ordered quadruple perovskite to be reported. We demonstrate that long range magnetic orde r develops below 74 K, and at 28 K a spin-flop transition occurs driven by $f$-$d$ exchange and rare earth single ion anisotropy. In both magnetic phases the magnetic structure may be described as a collinear ferrimagnet, contrary to conventional theories of magnetic order in the manganite perovskites. Instead, we show that these magnetic structures can be understood to arise due to ferro-orbital order, the A, A$$ and A$$ site point symmetry, $mm2$, and the dominance of A-B exchange over both A-A and B-B exchange, which together are unique to the $Rmathrm{Mn_3O_6}$ perovskites.
التعليقات
جاري جلب التعليقات جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا