ترغب بنشر مسار تعليمي؟ اضغط هنا

Magnetic order in YbMnO$_3$ studied by Neutron Diffraction and Mossbauer Spectroscopy

269   0   0.0 ( 0 )
 نشر من قبل Xavier Fabreges
 تاريخ النشر 2008
  مجال البحث فيزياء
والبحث باللغة English




اسأل ChatGPT حول البحث

The magnetic ordering of the hexagonal multiferroic compound YbMnO$_3$ has been studied between 100 K and 1.5 K by combining neutron powder diffraction, $^{170}$Yb Mossbauer spectroscopy and magnetization measurements. The Yb moments of the two crystallographic sites order at two different temperatures, the $4b$ site together with the Mn moments (at $T_N simeq$85 K) and the $2a$ site well below (at 3.5 K). The temperature dependences of the Mn and Yb moments are explained within a molecular field model, showing that the $4b$ and $2a$ sites order via Yb-Mn and Yb-Yb interactions respectively. A simple picture taking into account the local Mn environment of the Rare earth R ($4b$) ion is proposed to couple R and Mn orders in hexagonal RMnO$_3$ manganites. The nature and symmetry of the R-Mn interactions yielding the R order are discussed.



قيم البحث

اقرأ أيضاً

The Fe(1+x)Sb compound has been synthesized close to stoichiometry with x = 0.023(8). The compound was investigated by 57Fe Mossbauer spectroscopy in the temperature range 4.2 - 300 K. The antiferromagnetic ordering temperature was found as 232 K i.e . much higher than for the less stoichiometric material. Regular iron was found to occupy two different positions in proportion 2:1. They differ by the electric quadrupole coupling constants and both of them exhibit extremely anisotropic electric field gradient tensor (EFG) with the asymmetry parameter equal one. The negative component of both EFGs is aligned with the c-axis of the hexagonal unit cell, while the positive component is aligned with the <120> direction. Hence, a model describing deviation from the NiAs P63/mmc symmetry group within Fe-planes has been proposed. Spectra in the magnetically ordered state could be explained by introduction of the incommensurate spin spirals propagating through the iron atoms in the direction of the c-axis with a complex pattern of the hyperfine magnetic fields distributed within a-b plane. Hyperfine magnetic field pattern of spirals due to major regular iron is smoothed by the spin polarized itinerant electrons, while the minor regular iron exhibits hyperfine field pattern characteristic of the highly covalent bonds to the adjacent antimony atoms. The excess interstitial iron orders magnetically at the same temperature as the regular iron, and magnetic moments of these atoms are likely to form two-dimensional spin glass with moments lying in the a-b plane. The upturn of the hyperfine field for minor regular iron and interstitial iron is observed below 80 K. Magneto-elastic effects are smaller than for FeAs, however the recoilless fraction increases significantly upon transition to the magnetically ordered state.
We report single-crystal neutron diffraction study of the magnetic structure of the multiferroic compound YbMnO$_3$, a member of the hexagonal manganite family, in zero-field and under a magnetic field applied along the $c$-axis. We propose a scenari o for the zero-field magnetic ordering and for the field-induced magnetic reorientation of the Mn and of the two Yb on distinct crystallographic sites, compatible with the macroscopic measurements, as well as with previous powder neutron diffraction experiment and results from other techniques (optical second harmonic generation, Mossbauer spectroscopy). Our study should contribute in settling some debated issues about the magnetic properties of this material, as part of a broader investigation of the entire hexagonal RMnO$_3$ (R = Dy, Ho, Er, Tm, Yb, Lu, Y) family.
Neutron diffraction measurements on a single crystal of CeGe1.76 reveal a complex series of magnetic transitions at low temperature. At T_N = 7 K, there is a transition from a paramagnetic state at higher temperature to an incommensurate magnetic str ucture characterized by a magnetic propagation vector (0 0 tau) with tau approx. 1/4 and the magnetic moment along the a axis of the orthorhombic unit cell. Below T_LI = 5 K, the magnetic structure locks in to a commensurate structure with tau = 1/4 and the magnetic moment remains along the a axis. Below T* = 4 K, we find additional half-integer and integer indexed magnetic Bragg peaks consistent with a second commensurately ordered antiferromagnetic state.
The compound BaFe2Se3 (Pnma) has been synthesized in the form of single crystals with the average composition Ba0.992Fe1.998Se3. The Moessbauer spectroscopy used for investigation of the valence states of Fe in this compound at temperature ranging fr om 4.2 K till room temperature revealed the occurrence of mixed-valence state for iron. The spectrum is characterized by sharply defined electric quadrupole doublet above magnetic ordering at about 250 K. For the magnetically ordered state one sees four iron sites at least and each of them is described by separate axially symmetric electric field gradient tensor with the principal component making some angle with the hyperfine magnetic field. They form two groups occurring in equal abundances. It is likely that each group belongs to separate spin ladder with various tilts of the FeSe4 tetrahedral units along the ladder. Two impurity phases are found, i.e., superconducting FeSe and some other unidentified iron-bearing phase being magnetically disordered above 80 K. Powder form of BaFe2Se3 is unstable in contact with the air and decomposes slowly to this unidentified phase exhibiting almost the same quadrupole doublet as BaFe2Se3 above magnetic transition temperature.
The magnetic structures and the magnetic phase transitions in the Mn-doped orthoferrite TbFeO$_3$ studied using neutron powder diffraction are reported. Magnetic phase transitions are identified at $T^mathrm{Fe/Mn}_N approx$ 295~K where a paramagneti c-to-antiferromagnetic transition occurs in the Fe/Mn sublattice, $T^mathrm{Fe/Mn}_{SR} approx$ 26~K where a spin-reorientation transition occurs in the Fe/Mn sublattice and $T^mathrm{R}_N approx$ 2~K where Tb-ordering starts to manifest. At 295~K, the magnetic structure of the Fe/Mn sublattice in TbFe$_{0.5}$Mn$_{0.5}$O$_3$ belongs to the irreducible representation $Gamma_4$ ($G_xA_yF_z$ or $Pbnm$). A mixed-domain structure of ($Gamma_1 + Gamma_4$) is found at 250~K which remains stable down to the spin re-orientation transition at $T^mathrm{Fe/Mn}_{SR}approx$ 26~K. Below 26~K and above 250~K, the majority phase ($> 80%$) is that of $Gamma_4$. Below 10~K the high-temperature phase $Gamma_4$ remains stable till 2~K. At 2~K, Tb develops a magnetic moment value of 0.6(2)~$mu_mathrm{B}/$f.u. and orders long-range in $F_z$ compatible with the $Gamma_4$ representation. Our study confirms the magnetic phase transitions reported already in a single crystal of TbFe$_{0.5}$Mn$_{0.5}$O$_3$ and, in addition, reveals the presence of mixed magnetic domains. The ratio of these magnetic domains as a function of temperature is estimated from Rietveld refinement of neutron diffraction data. Indications of short-range magnetic correlations are present in the low-$Q$ region of the neutron diffraction patterns at $T < T^mathrm{Fe/Mn}_{SR}$. These results should motivate further experimental work devoted to measure electric polarization and magnetocapacitance of TbFe$_{0.5}$Mn$_{0.5}$O$_3$.
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