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D. Prabhakaran

Publications and source records attributed to D. Prabhakaran.

At least 127 records · Page 7Linked to original sources

Nature of the magnetic order and origin of induced ferroelectricity in TbMnO$_3$

The magnetic structures which endow TbMnO$_3$ with its multiferroic properties have been reassessed on the basis of a comprehensive soft x-ray resonant scattering (XRS) study. The selectivity of XRS facilitated separation of the various contributions (Mn $L_2$ edge, Mn 3d moments; Tb M$_4$ edge, Tb 4f moments), while its variation with azimuth provided information on the moment direction of distinct Fourier components. When the data are combined with a detailed group theory analysis, a new picture emerges of the ferroelectric transition at 28 K. Instead of being driven by the transition from a collinear to a non-collinear magnetic structure, as has previously been supposed, it is shown to occur between two non-collinear structures.

cond-mat.str-el↗

Inward dispersion of the spin excitation spectrum of stripe-ordered La2NiO4+d

Polarized- and unpolarized-neutron scattering measurements of the spin excitation spectrum in the stripe-ordered phase of La2NiO4+d (d = 0.11) are presented. At low energies, the magnetic spectral weight is found to shift anomalously towards the two-dimensional antiferromagnetic wave vector, similar to the low-energy dispersions observed in cuprate superconductors. While spin-wave spectra in stripe phases can exhibit an apparent inward dispersion, we find that the peak shifts measured here cannot be accounted for by this effect. Possible extensions of the model are discussed.

cond-mat.str-el↗

Experimental study of the interfacial cobalt oxide in Co3O4/a-Al2O3(0001) epitaxial films

A detailed spectroscopic and structural characterization of ultrathin cobalt oxide films grown by O-assisted molecular beam epitaxy on a-Al2O3(0001) single crystals is reported. The experimental results show that the cobalt oxide films become progressively more disordered with increasing thickness, starting from the early stages of deposition. Low energy electron diffraction patterns suggest that the unit cell remains similar to that of a-Al2O3(0001) up to a thickness of 17 A, while at larger thicknesses a pattern identified with that of Co3O4(111) becomes visible. X-ray photoelectron spectroscopy reveals sudden changes in the shape of the Co 2p lines from 3.4 to 17 A cobalt oxide thickness, indicating the transition from an interfacial cobalt oxide layer towards [111]-oriented Co3O4. In particular, the absence of characteristic satellite peaks in the Co 2p lines indicates the formation of a trivalent, octahedrally coordinated, interfacial cobalt oxide layer during the early stages of growth, identified as the Co2O3 corundum phase.

cond-mat.mtrl-sci↗

Magnetic order and dynamics of the charge-ordered antiferromagnet La1.5Sr0.5CoO4

We describe neutron scattering experiments performed to investigate the magnetic order and dynamics of half-doped La1.5Sr0.5CoO4. This layered perovskite exhibits a near-ideal checkerboard pattern of Co2+/Co3+ charge order at temperatures below ~ 800 K. Magnetic correlations are observed at temperatures below ~ 60 K but static magnetic order only becomes established at 31 K, a temperature at which a kink is observed in the susceptibility. On warming above 31 K we observed a change in the magnetic correlations which we attribute either to a spin canting or to a change in the proportion of inequivalent magnetic domains. The magnetic excitation spectrum is dominated by an intense band extending above a gap of approximately 3 meV up to a maximum energy of 16 meV. A weaker band exists in the energy range 20-30 meV. We show that the excitation spectrum is in excellent quantitative agreement with the predictions of a spin-wave theory generalized to include the full magnetic degrees of freedom of high-spin Co2+ ions in an axially distorted crystal field, coupled by Heisenberg exchange interactions. The magnetic order is found to be stabilized by dominant antiferromagnetic Co2+ -- Co2+ interactions acting in a straight line through Co3+. No evidence is found for magnetic scattering from the Co3+ ions, supporting the view that Co3+ is in the S = 0 state in this material.

cond-mat.str-el↗

Local magnetism and magnetoelectric effect in HoMnO3 studied with muon-spin relaxation

We present the results of muon-spin relaxation (muSR) measurements on the hexagonal manganite HoMnO3. Features in the temperature-dependent relaxation rate, lambda, correlate with the magnetic transitions at 76 K, 38 K and 34 K. The highest temperature transition, associated with the ordering of Mn3+ moments has the largest effect on lambda. The application of a static electric field of E=10^4 Vm^-1 below T=50 K causes a small reduction in lambda which is suggestive of coupling between ferroelectric and magnetic domain walls in the ordered state of the material.

cond-mat.str-el↗

The Temperature Evolution of the Out-of-Plane Correlation Lengths of Charge-Stripe Ordered La(1.725)Sr(0.275)NiO(4)

The temperature dependence of the magnetic order of stripe-ordered La(1.725)Sr(0.275)NiO(4) is investigated by neutron diffraction. Upon cooling, the widths if the magnetic Bragg peaks are observed to broaden. The degree of broadening is found to be very different for l = odd-integer and l = even-integer magnetic peaks. We argue that the observed behaviour is a result of competition between magnetic and charge order.

cond-mat.str-el↗

Crystal-to-stripe reordering of sodium ions in NaxCoO2 (x>=0.75)

The sodium reordering in NaxCoO2 in the vicinity of room temperature is rationalized at high x in terms of phase transitions between square and striped phases. A striking hexagon-of-hexagons diffraction pattern observed for x=0.78 can be reproduced using coexisting square and striped phases that are related by simple shear deformations. All compositions exhibit a partial melting transition to a disordered stripe phase just below room temperature, which alters the topology of the electrical conduction pathways.

cond-mat.str-el↗

Magnetic Charge Transport

It has recently been predicted that certain magnetic materials contain mobile magnetic charges or `monopoles'. Here we address the question of whether these magnetic charges and their associated currents (`magnetricity') can be directly measured in experiment, without recourse to any material-specific theory. By mapping the problem onto Onsager's theory of weak electrolytes, we show that this is possible, and devise an appropriate method. Then, using muon spin rotation as a convenient local probe, we apply the method to a real material: the spin ice Dy2Ti2O7. Our experimental measurements prove that magnetic charges exist in this material, interact via a Coulomb interaction, and have measurable currents. We further characterise deviations from Ohm's Law, and determine the elementary unit of magnetic charge to be 5 muB per Angstrom, which is equal to that predicted by Castelnovo, Moessner and Sondhi using the microscopic theory of spin ice. Our demonstration of magnetic charge transport has both conceptual and technological implications.

cond-mat.other↗

Experimental Proof of a Magnetic Coulomb Phase

Spin ice materials are magnetic substances in which the spin directions map onto hydrogen positions in water ice. Recently this analogy has been elevated to an electromagnetic equivalence, indicating that the spin ice state is a Coulomb phase, with magnetic monopole excitations analogous to ice's mobile ionic defects. No Coulomb phase has yet been proved in a real magnetic material, as the key experimental signature is difficult to resolve in most systems. Here we measure the scattering of polarised neutrons from the prototypical spin ice Ho2Ti2O7. This enables us to separate different contributions to the magnetic correlations to clearly demonstrate the existence of an almost perfect Coulomb phase in this material. The temperature dependence of the scattering is consistent with the existence of deconfined magnetic monopoles connected by Dirac strings of divergent length.

cond-mat.mtrl-sci↗

Circularly polarised X-rays as a probe of non-collinear magnetic order in multiferroic TbMnO3

Non-resonant X-ray magnetic scattering has been used to study the magnetic structure of multiferroic TbMnO3 in its ferroelectric phase. Circularly polarized X-rays were combined with a full polarization analysis of the scattered beam to reveal important new information on the magnetic structure of this canonical multiferroic. An applied electric field is shown to create a magnetic nearly mono-domain state in which the cylcoidal order on the Mn sublattice rotates either clockwise or counter-clockwise depending on the sign of the field. It is demonstrated how this technique provides sensitivity to the absolute sense of rotation of the Mn moments, and to components of the ordering on the Tb sublattice and phase shifts that earlier neutron diffraction experiments could not resolve.

cond-mat.str-el↗

A high resolution, hard x-ray photoemission investigation of La_(2-2x)Sr_(1+2x)Mn_2O_7 (0.30<x<0.50): on microscopic phase separation and the surface electronic structure of a bilayered CMR manganite

Photoemission data taken with hard x-ray radiation on cleaved single crystals of the bilayered, colossal magnetoresistant manganite La_(2-2x)Sr_(1+2x)Mn_2O_7 (LSMO) with 0.30<x<0.50 are presented. Making use of the increased bulk-sensitivity upon hard x-ray excitation it is shown that the core level footprint of the electronic structure of the LSMO cleavage surface is identical to that of the bulk. Furthermore, by comparing the core level shift of the different elements as a function of doping level x, it is shown that microscopic phase separation is unlikely to occur for this particular manganite well above the Curie temperature.

cond-mat.str-el↗

Ordering of localized electronic states in multiferroic TbMnO3: a soft X-ray resonant scattering study

Soft X-ray resonant scattering (XRS) has been used to observe directly, for the first time, the ordering of localized electronic states on both the Mn and Tb sites in multiferroic TbMnO$_3$. Large resonant enhancement of the X-ray scattering cross-section were observed when the incident photon energy was tuned to either the Mn $L$ or Tb $M$ edges which provide information on the Mn 3d and Tb $4f$ electronic states, respectively. The temperature dependence of the XRS signal establishes, in a model independent way, that in the high-temperature phase (28 K $\leq$ T $\leq$ 42 K) the Mn 3d sublattices displays long-range order. The Tb $4f$ sublattices are found to order only on entering the combined ferroelectric/magnetic state below 28 K. Our results are discussed with respect to recent hard XRS experiments (sensitive to spatially extended orbitals) and neutron scattering.

cond-mat.str-el↗

X-ray Resonant Scattering Study of the Order Parameters in Multiferroic TbMnO$_3$

We report on an extensive investigation of the multiferroic compound TbMnO$_3$. Non-resonant x-ray magnetic scattering (NRXMS) revealed a dominant $A$-type domain. The temperature dependence of the intensity and wavevector associated with the incommensurate magnetic order was found to be in good agreement with neutron scattering data. XRS experiments were performed in the vicinity of the Mn $K$ and Tb $L_3$ edges in the high-temperature collinear phase, the intermediate temperature cycloidal/ferroelectric phase, and the low-temperature phase. In the collinear phase resonant $E1-E1$ satellites were found at the Mn $K$ edge associated with $A$-type but also $F$-type peaks. The azimuthal dependence of the $F$-type satellites (and their absence in the NRXMS experiments) indicates that they are most likely non-magnetic in origin. We suggest instead that they may be associated with an induced charge multipole. At the Tb $L_3$ edge resonant $A$- and $F$-type satellites ($E1-E1$) were observed in the collinear phase. These we attribute to a polarisation of the Tb 5$d$ states by the ordering of the Mn sublattice. In the cycloidal/ferroelectric phase a new set of resonant satellites appear corresponding to $C$-type order. These appear at the Tb $L_3$ edge only. In addition to a dominant $E1-E1$ component in the $σ-π^\prime$ channel, a weaker component is found in the pre-edge with $σ-σ^\prime$ polarization. Calculations of the XRS were performed using the $FDMNES$ code showing that the unrotated $σ-σ^\prime$ component of the Tb $L_3$ $C$-type peaks appearing in the ferroelectric phase contains a contribution from a multipole that is odd with respect to both space and time, known in various contexts as the anapole.

cond-mat.str-el↗

Investigation of the spin state of Co in LaCoO3 at room temperature

We investigate the spin state of LaCoO3 using state-of-the-art photoemission spectroscopy and ab initio band structure calculations. The GGA+U calculations provide a good description of the ground state for the experimentally estimated value of electron correlation strength, U. In addition to the correlation effect, spin-orbit interaction is observed to play a significant role in the case of intermediate spin and high spin configurations. The comparison of the calculated Co 3d and O 2p partial density of states with the experimental valence band spectra indicates that at room temperature, Co has dominant intermediate spin state configuration and that the high spin configuration may not be significant at this temperature. The lineshape of the La 5p and O 2s core level spectra could be reproduced well within these ab initio calculations.

cond-mat.str-el↗

Orbital and Spin Excitations in Cobalt Oxide

By means of neutron scattering we have determined new branches of magnetic excitations in orbitally active CoO (TN=290 K) up to 15 THz and for temperatures from 6 K to 450 K. Data were taken in the (111) direction in six single-crystal zones. From the dependence on temperature and Q we have identified several branches of magnetic excitation. We describe a model for the coupled orbital and spin states of Co2+ subject to a crystal field and tetragonal distortion.

cond-mat.str-el↗

Magnetism in Geometrically Frustrated YMnO3 Under Hydrostatic Pressure Studied with Implanted Muons

The rare-earth ferroelectromagnet YMnO3 consists of weakly coupled triangular layers of S=2 spins. Below T_N ~ 70 K muon-spin relaxation data show two oscillatory relaxing signals due to magnetic order, with no relaxing signal resolvable (which would be expected for different coexisting spin distributions). The transition temperature T_N increases with applied hydrostatic pressure, even though the ordered moment decreases. These results suggest that pressure increases both the exchange coupling between the layers and the frustration within the layers.

cond-mat.str-el↗

Patterning of sodium ions and the control of electrons in sodium cobaltate

NaxCoO2 has emerged as a material of exceptional scientific interest due to the potential for thermoelectric applications, and because the strong interplay between the magnetic and superconducting properties has led to close comparisons with the physics of the high-Tc cuprates. The density, x, of the sodium in the intercalation layers can be altered electrochemically, directly changing the number of conduction electrons on triangular Co layers. Recent electron diffraction measurements reveal a kaleidoscope of Na+ ion patterns as a function of concentration. Here we use single-crystal neutron diffraction supported by numerical simulations to determine the long-range three-dimensional superstructures of these ions. We show that the sodium ordering and its associated distortion field are governed by pure electrostatics, and the organizational principle is the stabilization of charge droplets that order long range at some simple fractional fillings. Our results provide a good starting point to understand the electronic properties in terms of a Hubbard Hamiltonian taking into account the electrostatic potential from the Na superstructures. The resulting depth of potential wells in the Co layer is greater than the single-particle hopping kinetic energy. As a consequence, holes occupy preferentially the lowest potential regions and, therefore, the Na+ ion patterning plays a decisive role in the transport and magnetic properties.

cond-mat.str-el↗

The kagome staircase compounds Ni$_{3}$V$_{2}$O$_{8}$ and Co$_{3}$V$_{2}$O$_{8}$ studied with implanted muons

We present the results of muon-spin relaxation ($μ^{+}$SR) measurements on the kagome staircase compounds Ni$_{3}$V$_{2}$O$_{8}$ and Co$_{3}$V$_{2}$O$_{8}$. The magnetic behavior of these materials may be described in terms of two inequivalent magnetic ion sites, known as spine sites and cross-tie sites. Our $μ^{+}$SR results allow us to probe each of these sites individually, revealing the distribution of the local magnetic fields near these positions. We are able not only to confirm the magnetic structures of the various phases proposed on the basis of bulk measurements but also to give an insight into the temperature evolution of the local field distribution in each phase.

cond-mat.str-el↗