SearcharxivSearch

arXiv subjects

N. Aliouane

Publications and source records attributed to N. Aliouane.

At least 19 recordsLinked to original sources

Magnetic phase diagram of $Sr_3 Fe_2 O_{7-x}$

Magnetometry, electrical transport, and neutron scattering measurements were performed on single crystals of the Fe^{4+}-containing perovskite-related phase Sr_3Fe_2O_7-x as a function of oxygen content. Although both the crystal structure and electron configuration of this compound are closely similar to those of well-studied ruthenates and manganates, it exhibits very different physical properties. The fully-oxygenated compound (x=0) exhibits a charge-disproportionation transition at T_D = 340 K, and an antiferromagnetic transition at T_N = 115 K. For temperatures T \leq T_D, the material is a small-gap insulator; the antiferromagnetic order is incommensurate, which implies competing exchange interactions between the Fe^{4+} moments. The fully-deoxygenated compound (x=1) is highly insulating, and its Fe^{3+} moments exhibit commensurate antiferromagnetic order below T_N ~ 600 K. Compounds with intermediate x exhibit different order with lower T_N, likely as a consequence of frustrated exchange interactions between Fe^{3+} and Fe^{4+} sublattices. A previous proposal that the magnetic transition temperature reaches zero is not supported.

cond-mat.str-el

Magnetic structure of CuCrO2: a single crystal neutron diffraction study

This paper presents results of a recent study of multiferroic \CCO\ by means of single crystal neutron diffraction. This system has two close magnetic phase transitions at $T\nsub{N1}=24.2$ K and $T\nsub{N2}=23.6$ K. The low temperature magnetic structure below $T\nsub{N2}$ is unambiguously determined to be a fully 3-dimensional proper screw. Between $T\nsub{N1}$ and $T\nsub{N2}$ antiferromagnetic order is found that is essentially 2-dimensional. In this narrow temperature range, magnetic near neighbor correlations are still long range in the ($H,K$) plane, whereas nearest neighbors along the $L$-direction are uncorrelated. Thus, the multiferroic state is realized only in the low-temperature 3-dimensional state and not in the 2-dimensional state.

cond-mat.mtrl-sci

Incompatible Magnetic Order in Multiferroic Hexagonal DyMnO3

Magnetic order of the manganese and rare-earth lattices according to different symmetry representations is observed in multiferroic hexagonal (h-) DyMnO$_3$ by optical second harmonic generation and neutron diffraction. The incompatibility reveals that the 3d-4f coupling in the h-$R$MnO$_3$ system ($R$ = Sc, Y, In, Dy - Lu) is substantially less developed than commonly expected. As a consequence, magnetoelectric coupling effects in this type of split-order parameter multiferroic that were previously assigned to a pronounced 3d-4f coupling have now to be scrutinized with respect to their origin.

cond-mat.str-el

Signature of checkerboard fluctuations in the phonon spectra of a possible polaronic metal La1.2Sr1.8Mn2O7

Charge carriers in low-doped semiconductors may distort the atomic lattice and trap themselves forming so-called small polarons. High carrier concentrations can lead to short range ordered polarons (large polarons) and even to long range charge and orbital order. Both systems should be insulating with a large electrical resistivity, which decreases with increasing temperature. However, photoemission measurements recently found a polaronic pseudogap, in a metallic phase of La2-2xSr1+2xMn2O7. This layered manganite is famous for colossal magnetoresistance (CMR) associated with a phase transition from this low-temperature metallic phase to a high temperature insulating phase. Broad charge order peaks due to large polarons observed by neutron and x-ray scattering in the insulating phase disappear when La2-2xSr1+2xMn2O7 becomes metallic. We report results of inelastic neutron scattering measurements showing that polarons remain inside the metallic phase as fluctuations that strongly broaden and soften certain phonons near the wave vectors where the charge order peaks appeared in the insulating phase. Our findings imply that polaronic signatures in metals may generally come from a competing insulating charge-ordered phase. It is highly relevant to cuprate superconductors with both a pseudogap, and a similar phonon effect associated with a competing stripe order.

cond-mat.str-el

Ga substitution as an effective variation of Mn-Tb coupling in multiferroic TbMnO3

Ga for Mn substitution in multiferroic TbMnO$_{3}$ has been performed in order to study the influence of Mn-magnetic ordering on the Tb-magnetic sublattice. Complete characterization of TbMn$_{1-x}$Ga$_x$O$_{3}$ ($x$ = 0, 0.04, 0.1) samples, including magnetization, impedance spectroscopy, and x-ray resonant scattering and neutron diffraction on powder and single crystals has been carried out. We found that keeping the same crystal structure for all compositions, Ga for Mn substitution leads to the linear decrease of $T_{\rm N}^{\rm Mn}$ and $τ^{\rm Mn}$, reflecting the reduction of the exchange interactions strength $J_{\rm Mn-Mn}$ and the change of the Mn-O-Mn bond angles. At the same time, a strong suppression of both the induced and the separate Tb-magnetic ordering has been observed. This behavior unambiguously prove that the exchange fields $J_{\rm Mn-Tb}$ have a strong influence on the Tb-magnetic ordering in the full temperature range below $T_{\rm N}^{\rm Mn}$ and actually stabilize the Tb-magnetic ground state.

cond-mat.str-el

Magnetic-field induced effects on the electric polarization in RMnO3 (R = Dy, Gd)

X-ray resonant magnetic scattering studies of rare earth magnetic ordering were performed on perovskite manganites RMnO3 (R = Dy, Gd) in an applied magnetic field. The data reveal that the field-induced three-fold polarization enhancement for H || a (H approx. 20 kOe) observed in DyMnO3 below 6.5 K is due to a re-emergence of the Mn-induced Dy spin order with propagation vector k(Dy) = k(Mn) = 0.385 b*, which accompanies the suppression of the independent Dy magnetic ordering, k(Dy) = 1/2 b*. For GdMnO3, the Mn-induced ordering of Gd spins is used to track the Mn-ordering propagation vector. The data confirm the incommensurate ordering reported previously, with k(Mn) varying from 0.245 to 0.16 b* on cooling from T_N(Mn) down to a transition temperature T'. New superstructure reflections which appear below T' suggest a propagation vector k(Mn) = 1/4 b* in zero magnetic field, which may coexist with the previously reported A-type ordering of Mn. The Gd spins order with the same propagation vector below 7 K. Within the ordered state of Gd at T = 1.8 K we find a phase boundary for an applied magnetic field H || b, H = 10 kOe, which coincides with the previously reported transition between the ground state paraelectric and the ferroelectric phase of GdMnO3. Our results suggest that the magnetic ordering of Gd in magnetic field may stabilize a cycloidal ordering of Mn that, in turn, produces ferroelectricity.

cond-mat.str-el

Magnetic field induced flop of cycloidal spin order in multiferroic TbMnO3: The magnetic structure of the P||a phase

Using in-field single crystal neutron diffraction we have determined the magnetic structure of TbMnO3 in the high field P||a phase. We unambiguously establish that the ferroelectric polarization arises from a cycloidal Mn spins ordering, with spins rotating in the ab plane. Our results demonstrate directly that the flop of the ferroelectric polarization in TbMnO3 with applied magnetic field is caused from the flop of the Mn cycloidal plane.

cond-mat.str-el

Magnetic field induced transitions in multiferroic TbMnO3 probed by resonant and non-resonant X-ray diffraction

Multiferroic TbMnO3 is investigated using x-ray diffraction in high magnetic fields. Measurements on first and second harmonic structural reflections due to modulations induced by the Mn and Tb magnetic order are presented as function of temperature and field oriented along the a and b-directions of the crystal. The relation to changes in ordering of the rare earth moments in applied field is discussed. Observations below T_N(Tb) without and with applied magnetic field point to a strong interaction of the rare earth order, the Mn moments and the lattice. Also, the incommensurate to commensurate transition of the wave vector at the critical fields is discussed with respect to the Tb and Mn magnetic order and a phase diagram on basis of these observations for magnetic fields H||a and H||b is presented. The observations point to a complicated and delicate magneto-elastic interaction as function of temperature and field.

cond-mat.str-el

Field dependence of magnetic correlations through the polarization flop transition in multiferroic TbMnO3 : evidence for a magnetic memory effect

The field-induced multiferroic transition in TbMnO3 has been studied by neutron scattering. Apart strong hysteresis, the magnetic transition associated with the flop of electronic polarization exhibits a memory effect: after a field sweep, TbMnO3 does not exhibit the same phase as that obtained by zero-field cooling. The strong changes in the magnetic excitations across the transition perfectly agree with a rotation of the cycloidal spiral plane indicating that the inverse Dzyaloshinski-Moriya coupling causes the giant magnetoelectric effect at the field-induced transition. The analysis of the zone-center magnetic excitations identifies the electromagnon of the multiferroic high-field phase.

cond-mat.str-el

Coupling of frustrated Ising spins to magnetic cycloid in multiferroic TbMnO3

We report on diffraction measurements on multiferroic TbMnO3 which demonstrate that the Tb- and Mn-magnetic orders are coupled below the ferroelectric transition TFE = 28 K. For T < TFE the magnetic propagation vectors (tau) for Tb and Mn are locked so that tauTb = tauMn, while below TNTb = 7 K we find that tauTb and tauMn lock-in to rational values of 3/7 b* and 2/7 b*, respectively, and obey the relation 3tauTb - tauMn = 1. We explain this novel matching of wave vectors within the frustrated ANNNI model coupled to a periodic external field produced by the Mn-spin order. The tauTb = tauMn behavior is recovered when Tb magnetization is small, while the tauTb = 3/7 regime is stabilized at low temperatures by a peculiar arrangement of domain walls in the ordered state of Ising-like Tb spins.

cond-mat.str-el

Absence of commensurate ordering at the polarization flop transition in multiferroic DyMnO3

Ferroelectric spiral magnets DyMnO3 and TbMnO3 show similar behavior of electric polarization in applied magnetic fields. Studies of the field dependence of lattice modulations on the contrary show a completely different picture. Whereas in TbMnO3 the polarization flop from P||c to P||a is accompanied by a sudden change from incommensurate to commensurate wave vector modulation, in DyMnO3 the wave vector varies continuously through the flop transition. This smooth behavior may be related to the giant magnetocapacitive effect observed in DyMnO3.

cond-mat.str-el

Anomalous thermal expansion and strong damping of the thermal conductivity of NdMnO$_3$ and TbMnO$_3$ due to 4f crystal-field excitations

We present measurements of the thermal conductivity $κ$ and the thermal expansion $α$ of NdMnO$_3$ and TbMnO$_3$. In both compounds a splitting of the $4f$ multiplet of the $R^{3+}$ ion causes Schottky contributions to $α$. In TbMnO$_3$ this contribution arises from a crystal-field splitting, while in NdMnO$_3$ it is due to the Nd-Mn exchange coupling. Another consequence of this coupling is a strongly enhanced canting of the Mn moments. The thermal conductivity is greatly suppressed in both compounds. The main scattering process at low temperatures is resonant scattering of phonons between different energy levels of the $4f$ multiplets, whereas the complex 3d magnetism of the Mn ions is of minor importance.

cond-mat.str-el

New features in the phase diagram of TbMnO$_3$

The (H,T)-phase diagram of the multiferroic perovskite TbMnO$_3$ was studied by high-resolution thermal expansion $α(T)$ and magnetostriction $ΔL(H)/L$ measurements. Below $T_{N}\simeq 42$ K, TbMnO$_3$ shows antiferromagnetic order, which changes at $T_{FE}\simeq 28$ K where simultaneously a spontaneous polarization $P||c$ develops. Sufficiently high magnetic fields applied along $a$ or $b$ induce a polarization flop to $P||a$. We find that all of these transitions are strongly coupled to the lattice parameters. Thus, our data allow for a precise determination of the phase boundaries and also yield information about their uniaxial pressure dependencies. The strongly hysteretic phase boundary to the ferroelectric phase with $P||a$ is derived in detail. Contrary to previous reports, we find that even in high magnetic fields there are no direct transitions from this phase to the paraelectric phase. We also determine the various phase boundaries in the low-temperature region related to complex reordering transitions of the Tb moments.

cond-mat.str-el

Magnetic excitations in multiferroic TbMnO3

The magnetic excitations in multiferroic TbMnO3 have been studied by inelastic neutron scattering in the spiral and sinusoidally ordered phases. At the incommensurate magnetic zone center of the spiral phase, we find three low-lying magnons whose character has been fully determined using neutron-polarization analysis. The excitation at the lowest energy is the sliding mode of the spiral, and two modes at 1.1 and 2.5meV correspond to rotations of the spiral rotation plane. These latter modes are expected to couple to the electric polarization. The 2.5meV-mode is in perfect agreement with recent infra-red-spectroscopy data giving strong support to its interpretation as an hybridized phonon-magnon excitation.

cond-mat.str-el

Enhanced ferroelectric polarization by induced Dy spin-order in multiferroic DyMnO3

Neutron powder diffraction and single crystal x-ray resonant magnetic scattering measurements suggest that Dy plays an active role in enhancing the ferroelectric polarization in multiferroic DyMnO3 above TNDy = 6.5 K. We observe the evolution of an incommensurate ordering of Dy moments with the same periodicity as the Mn spiral ordering. It closely tracks the evolution of the ferroelectric polarization which reaches a maximum value of 0.2 muC/m^2. Below TNDy, where Dy spins order commensurately, the polarization decreases to values similar for those of TbMnO3.

cond-mat.str-el

Commensurate Dy magnetic ordering associated with incommensurate lattice distortion in orthorhombic DyMnO3

Synchrotron x-ray diffraction and resonant magnetic scattering experiments on single crystal DyMnO3 have been carried out between 4 and 40 K. Below TN(Dy) = 5K, the Dy magnetic moments order in a commensurate structure with propagation vector 0.5 b*. Simultaneous with the Dy magnetic ordering, an incommensurate lattice modulation with propagation vector 0.905 b* evolves while the original Mn induced modulation is suppressed and shifts from 0.78 b* to 0.81 b*. This points to a strong interference of Mn and Dy induced structural distortions in DyMnO3 besides a magnetic coupling between the Mn and Dy magnetic moments.

cond-mat.str-el

Quasiparticle-like peaks, kinks, and electron-phonon coupling at the ($π$,0) regions in the CMR oxide La$_{2-2x}$Sr$_{1+2x}$Mn$_{2}$O$_{7}$

Using Angle-Resolved Photoemission (ARPES), we present the first observation of sharp quasiparticle-like peaks in a CMR manganite. We focus on the ($π$,0) regions of k-space and study their electronic scattering rates and dispersion kinks, uncovering the critical energy scales, momentum scales, and strengths of the interactions that renormalize the electrons. To identify these bosons we measured phonon dispersions in the energy range of the kink by inelastic neutron scattering (INS), finding a good match in both energy and momentum to the oxygen bond-stretching phonons.

cond-mat.str-el

Field induced linear magneto-elastic coupling in multiferroic TbMnO3

We have used in-field neutron and X-ray single crystal diffraction to measure the incommensurability δ of the crystal and magnetic structure of multiferroic TbMnO3 . We show that the flop in the electric polarization at the critical field HC, for field H along the a− and b−axis coincides with a 1st order transition to a commensurate phase with propagation vector κ = (0, 1/4, 0). In-field X-ray diffraction measurements show that the quadratic magneto-elastic coupling breaks down with applied field as shown by the observation of the 1st harmonic lattice reflections above and below HC . This indicates that magnetic field induces a linear magneto-elastic coupling. We argue that the commensurate phase can be described by an ordering of Mn-O-Mn bond angles.

cond-mat.str-el