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Register a new userComplex magnetic ordering in CeGe1.76 studied by neutron diffraction
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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 structure 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.
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We present the results of the first neutron powder and single crystal diffraction studies of the coupled spin tetrahedra systems ${CuTeX}$ (X=Cl, Br). Incommensurate antiferromagnetic order with the propagation vectors ${bf{k}_{Cl}}approx[0.150,0.422,half]$, ${bf{k}_{Br}}approx[0.158,0.354,half]$ sets in below $T_{N}$=18 K for X=Cl and 11 K for X=Br. No simple collinear antiferromagnetic or ferromagnetic arrangements of moments within Cu${}^{2+}$ tetrahedra fit these observations. Fitting the diffraction data to more complex but physically reasonable models with multiple helices leads to a moment of 0.67(1)$mu_B$/Cu${}^{2+}$ at 1.5 K for the Cl-compound. The reason for such a complex ground state may be geometrical frustration of the spins due to the intra- and inter-tetrahedral couplings having similar strengths. The magnetic moment in the Br- compound, calculated assuming it has the same magnetic structure as the Cl compound, is only 0.51(5)$mu_B$/Cu${}^{2+}$ at 1.5 K. In neither compound has any evidence for a structural transition accompanying the magnetic ordering been found.
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.
Polarized and unpolarized neutron diffraction studies have been carried out on single crystals of the coupled spin tetrahedra systems Cu2Te2O5X2 (X=Cl, Br). A model of the magnetic structure associated with the propagation vectors kCl ~ -0.150,0.422,1/2 and kBr ~ -0.172,0.356,1/2 and stable below TN=18 K for X=Cl and TN=11 K for X=Br is proposed. A feature of the model, common to both the bromide and chloride, is a canted coplanar motif for the 4 Cu2+ spins on each tetrahedron which rotates on a helix from cell to cell following the propagation vector. The Cu2+magnetic moment determined for X=Br, 0.395(5)muB, is significantly less than for X=Cl, 0.88(1)muB at 2K. The magnetic structure of the chloride associated with the wave-vector k differs from that determined previously for the wave vector k~0.150,0.422,1/2 [O. Zaharko et.al. Phys. Rev. Lett. 93, 217206 (2004)].
Element-specific x-ray resonant magnetic scattering investigations were performed to determine the magnetic structure of Eu in EuRh2As2. In the temperature range from 46 K down to 6 K, an incommensurate antiferromagnetic (ICM)structure with a temperature dependent propagation vector (0 0 0.9) coexists with a commensurate antiferromagnetic (CM) structure. Angular-dependent measurements of the magnetic intensity indicate that the magnetic moments lie in the tetragonal basal plane and are ferromagnetically aligned within the a-b plane for both magnetic structures. The ICM structure is a spiral-like magnetic structure with a turn angle of 162 deg between adjacent Eu planes. In the CM structure, this angle is 180 deg. These results are consistent with band-structure calculations which indicate a strong sensitivity of the magnetic configuration on the Eu valence.
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 paramagnetic-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$_3$.
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