38 research outputs found

    Multiferroic properties of an \aa kermanite Sr2_2CoSi2_2O7_7 single crystal in high magnetic fields

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    The magnetic and dielectric properties of \aa kermanite Sr2_2CoSi2_2O7_7 single crystals in high magnetic fields were investigated. We have observed finite induced electric polarization along the c axis in high fields, wherein all Co spins were forcibly aligned to the magnetic field direction. Existence of the induced polarization in the spin-polarized state accompanied with the finite slope in the magnetization curve suggests the possible role of the orbital angular momenta in the excited states as its microscopic origin. The emergence of the field-induced polarization without particular magnetic order can be regarded as the magnetoelectric effects of the second order from the symmetry point of view. A low magnetic field-driven electric polarization flip induced by a rotating field, even at room temperature, has been successfully demonstrated.Comment: 12 pages, 4 figure

    Landau Theory of the Phase Transitions in Half Doped Manganites: Interplay of Magnetic, Charge and Structural Orders

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    The order parameters of the magnetic, charge and structural orders at half-doped manganites are identified. A corresponding Landau theory of the phase transitions is formulated. Many structural and thermodynamical behaviors are accounted for and clarified within the framework. In particular, the theory provides a unified picture for the scenario of the phase transitions and their nature with respect to the variation of the tolerance factor of the manganites. It also accounts for the origin of the incommensurate nature of the orbital order and its subsequently accompanying antiferromagnetic order.Comment: 4 pages, 3 eps figures, Revtex, Phys. Rev. B61, 200

    Thickness dependence of the stability of the charge-ordered state in Pr0.5_{0.5}Ca0.5_{0.5}MnO3_{3} thin films

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    Thin films of the charge-ordered (CO) compound Pr0.5_{0.5}Ca0.5_{0.5}MnO3_{3} have been deposited onto (100)-oriented SrTiO3_{3} substrates using the Pulsed Laser Deposition technique. Magnetization and transport properties are measured when the thickness of the film is varied. While the thinner films do not exhibit any temperature induced insulator-metal transition under an applied magnetic field up to 9T, for thickness larger than 1100\UNICODE{0xc5} a 5T magnetic field is sufficient to melt the CO state. For this latest film, we have measured the temperature-field phase diagram. Compared to the bulk material, it indicates that the robustness of the CO state in thin films is strongly depending on the strains and the thickness. We proposed an explanation based on the distortion of the cell of the film.Comment: 9 pages, 6 figures, submitted to Phys. Rev.

    Studies on Fabrication of Ag/HgBaCaCuO/CdSe Heterostructures by Pulse-Electrodeposition Route

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    Metal/superconductor/semiconductor (Ag/HgBaCaCuO/CdSe) heterostructures have been successfully fabricated using pulse-electrodeposition technique. The electrochemical parameters are optimized and diffusion free growth of CdSe onto Ag/HgBaCaCuO was obtained by employing under-potential deposition and by studying nucleation and growth mechanism during deposition. The heterostructures are characterized by X-ray diffraction (XRD), full-width at half-maximum (FWHM), scanning electron microscopy (SEM) studies and low temperature four probe electrical resistivity measurements. After the deposition of CdSe the critical transition temperature of HgBaCaCuO films was found be increased from 115 K with Jc = 1.7 x 103 A/cm2 to 117.2 K with Jc = 1.91 x 103 A/cm2. When the heterostructure was irradiated with red He-Ne laser (2 mW), the Tc was further enhanced to 120.3 K with Jc = 3.7 x 103 A/cm2. This increase in superconducting parameters of HgBaCaCuO in Ag/ HgBaCaCuO/CdSe heterostructure has been explained at length in this paper. Keywords. Electrodeposition; Hg-based cuprate; semiconductor; heterostructures; electrical properties. PACS Nos 81.15.Pq; 74.72.Gr; 78.40.Fy; 84.37; 73.40 *E-mail: [email protected], [email protected]: 22 Pages, 12 Figures. Submitted to Semiconductor Science and Technology. Submitted to Semiconductor Science and Technolog

    Anomalous field-dependent specific heat in charge-ordered Pr1−x_{1-x}Cax_xMnO3_3 and La0.5_{0.5}Ca0.5_{0.5}MnO3_3

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    We report low temperature specific heat measurements of Pr1−x_{1-x}Cax_{x}MnO3_{3} (0.3≀x≀0.50.3\leq x \leq 0.5) and La0.5_{0.5}Ca0.5_{0.5}MnO3_{3} with and without applied magnetic field. An excess specific heat, Câ€Č(T)C^{\prime}(T), of non-magnetic origin associated with charge ordering is found for all the samples. A magnetic field sufficient to induce the transition from the charge-ordered state to the ferromagnetic metallic state does not completely remove the Câ€ČC^{\prime} contribution. This suggests that the charge ordering is not completely destroyed by a "melting" magnetic field. In addition, the specific heat of the Pr1−x_{1-x}Cax_{x}MnO3_{3} compounds exhibit a large contribution linear in temperature (ÎłT\gamma T) originating from magnetic and charge disorder.Comment: submitted to PRL 5 pages, 3 figures include

    Charge and orbital order in half-doped manganites

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    An explanation is given for the charge order, orbital order and insulating state observed in half-doped manganese oxides, such as Nd1/2_{1/2}Sr1/2_{1/2}MnO3_{3}. The competition between the kinetic energy of the electrons and the magnetic exchange energy drives the formation of effectively one-dimensional ferromagnetic zig-zag chains. Due to a topological phase factor in the hopping, the chains are intrinsically insulating and orbital-ordered. Most surprisingly, the strong Coulomb interaction between electrons on the same Mn-ion leads to the experimentally observed charge ordering. For doping less than 1/2 the system is unstable towards phase separation into a ferromagnetic metallic and charge-ordered insulating phase.Comment: To appear in Phys. Rev. Lett., 4 pages, 4 figure

    High magnetic field transport measurement of charge-ordered Pr0.5_{0.5}Ca0.5_{0.5}MnO3_3 strained thin films

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    We have investigated the magnetic-field-induced phase transition of charge-ordered (CO) Pr0.5_{0.5}Ca0.5_{0.5}MnO3_3 thin films, deposited onto (100)-oriented LaAlO3_3 and (100)-oriented SrTiO3_3 substrates using the pulsed laser deposition technique, by measuring the transport properties with magnetic fields up to 22T. The transition to a metallic state is observed on both substrates by application of a critical magnetic field (HC>10TH_C>10T at 60K). The value of the field required to destroy the charge-ordered insulating state, lower than the bulk compound, depends on both the substrate and the thickness of the film. The difference of the critical magnetic field between the films and the bulk material is explained by the difference of in-plane parameters at low temperature (below the CO transition). Finally, these results confirm that the robustness of the CO state, depends mainly on the stress induced by the difference in the thermal dilatations between the film and the substrate.Comment: 10 pages, 6 figures. To be published in Phys. Rev.

    Multipole Ordering and Fluctuations in f-Electron Systems

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    We investigate effects of multipole moments in f-electron systems both from phenomenological and microscopic viewpoints. First, we discuss significant effects of octupole moment on the magnetic susceptibility in a paramagnetic phase. It is found that even within mean-field approximation, the magnetic susceptibility deviates from the Curie-Weiss law due to interactions between dipole and octupole moments. Next, we proceed to a microscopic theory for multipole ordering on the basis of a j-j coupling scheme. After brief explanation of a method to derive multipole interactions from the ff-electron model, we discuss several multipole ordered phases depending on lattice structure. Finally, we show our new development of the microscopic approach to the evaluation of multipole response functions. We apply fluctuation exchange approximation to the f-electron model, and evaluate multipole response functions.Comment: 7 pages, 4 figures, Proceedings of ASR-WYP-200

    A Real Space Description of Magnetic Field Induced Melting in the Charge Ordered Manganites: I. The Clean Limit

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    We study the melting of charge order in the half doped manganites using a model that incorporates double exchange, antiferromagnetic superexchange, and Jahn-Teller coupling between electrons and phonons. We primarily use a real space Monte Carlo technique to study the phase diagram in terms of applied field (h)(h) and temperature (T)(T), exploring the melting of charge order with increasing hh and its recovery on decreasing hh. We observe hysteresis in this response, and discover that the `field melted' high conductance state can be spatially inhomogeneous even without extrinsic disorder. The hysteretic response plays out in the background of field driven equilibrium phase separation. Our results, exploring hh, TT, and the electronic parameter space, are backed up by analysis of simpler limiting cases and a Landau framework for the field response. This paper focuses on our results in the `clean' systems, a companion paper studies the effect of cation disorder on the melting phenomena.Comment: 16 pages, pdflatex, 11 png fig

    Hole-doping dependence of percolative phase separation in Pr_(0.5-delta)Ca_(0.2+delta)Sr_(0.3)MnO_(3) around half doping

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    We address the problem of the percolative phase separation in polycrystalline samples of Pr0.5−ή_{0.5-\delta}Ca0.2+ÎŽ_{0.2+\delta}Sr0.3_{0.3}MnO3_3 for −0.04≀Ύ≀0.04-0.04\leq \delta \leq 0.04 (hole doping nn between 0.46 and 0.54). We perform measurements of X-ray diffraction, dc magnetization, ESR, and electrical resistivity. These samples show at TCT_C a paramagnetic (PM) to ferromagnetic (FM) transition, however, we found that for n>0.50n>0.50 there is a coexistence of both of these phases below TCT_C. On lowering TT below the charge-ordering (CO) temperature TCOT_{CO} all the samples exhibit a coexistence between the FM metallic and CO (antiferromagnetic) phases. In the whole TT range the FM phase fraction (XX) decreases with increasing nn. Furthermore, we show that only for n≀0.50n\leq 0.50 the metallic fraction is above the critical percolation threshold XC≃15.5X_C\simeq 15.5%. As a consequence, these samples show very different magnetoresistance properties. In addition, for n≀0.50n\leq 0.50 we observe a percolative metal-insulator transition at TMIT_{MI}, and for TMI<T<TCOT_{MI}<T<T_{CO} the insulating-like behavior generated by the enlargement of XX with increasing TT is well described by the percolation law ρ−1=σ∌(X−XC)t\rho ^{-1}=\sigma \sim (X-X_C)^t, where tt is a critical exponent. On the basis of the values obtained for this exponent we discuss different possible percolation mechanisms, and suggest that a more deep understanding of geometric and dimensionality effects is needed in phase separated manganites. We present a complete TT vs nn phase diagram showing the magnetic and electric properties of the studied compound around half doping.Comment: 9 text pages + 12 figures, submitted to Phys. Rev.
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