43 research outputs found

    Intrinsic interface exchange coupling of ferromagnetic nanodomains in a charge ordered manganite

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    We present a detailed magnetic study of the Pr1/3Ca2/3MnO3 manganite, where we observe the presence of small ferromagnetic (FM) domains (diameter ~ 10A) immersed within the charge-ordered antiferromagnetic (AFM) host. Due to the interaction of the FM nanodroplets with a disordered AFM shell, the low-temperature magnetization loops present exchange bias (EB) under cooling in an applied magnetic field. Our analysis of the cooling field dependence of the EB yields an antiferromagnetic interface exchange coupling comparable to the bulk exchange constant of the AFM phase. We also observe training effect of the EB, which is successfully described in terms of a preexisting relaxation model developed for other classical EB systems. This work provides the first evidence of intrinsic interface exchange coupling in phase separated manganites.Comment: 7 pages, 6 figure

    Lamellar phase separation and dynamic competition in La0.23Ca0.77MnO3

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    We report the coexistence of lamellar charge-ordered (CO) and charge-disordered (CD) domains, and their dynamical behavior, in La0.23Ca0.77MnO3. Using high resolution transmission electron microscopy (TEM), we show that below Tcd~170K a CD-monoclinic phase forms within the established CO-orthorhombic matrix. The CD phase has a sheet-like morphology, perpendicular to the q vector of the CO superlattice (a axis of the Pnma structure). For temperatures between 64K and 130K, both the TEM and resistivity experiments show a dynamic competition between the two phases: at constant T, the CD phase slowly advances over the CO one. This slow dynamics appears to be linked to the magnetic transitions occurring in this compound, suggesting important magnetoelastic effects.Comment: 4 pages, 4 figure

    Nanoscale magnetic structure of ferromagnet/antiferromagnet manganite multilayers

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    Polarized Neutron Reflectometry and magnetometry measurements have been used to obtain a comprehensive picture of the magnetic structure of a series of La{2/3}Sr{1/3}MnO{3}/Pr{2/3}Ca{1/3}MnO{3} (LSMO/PCMO) superlattices, with varying thickness of the antiferromagnetic (AFM) PCMO layers (0<=t_A<=7.6 nm). While LSMO presents a few magnetically frustrated monolayers at the interfaces with PCMO, in the latter a magnetic contribution due to FM inclusions within the AFM matrix was found to be maximized at t_A~3 nm. This enhancement of the FM moment occurs at the matching between layer thickness and cluster size, where the FM clusters would find the optimal strain conditions to be accommodated within the "non-FM" material. These results have important implications for tuning phase separation via the explicit control of strain.Comment: 4 pages, submitted to PR

    Disorder effects in the S1⁄41 antiferromagnetic spin ladder CaV2O4

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    We study the physical properties of the antiferromagnetic spin ladder CaV2O4 (CVO) and the Y-doped related compound Ca0.9Y0.1V2O4. In the latter, X-ray diffraction demonstrates the segregation of a small amount of a vanadium?perovskite impurity phase, leading to the formation of V vacancies within the main CVO-type structure. The 1D character of this calcium?vanadite enhances the influence of the va- cancies on the electric and magnetic properties of Ca0.9Y0.1V2O4. Electrical transport is characterized by a variable-range hopping mechanism determined by the charging energy of nm-sized segments of V chains delimited by V vacancies, i.e. a Coulomb gap is formed at the Fermi level. These vacancies also locally affect the magnetic correlations, breaking the long-range AFM order observed in CaV2O4 and producing exchange bias when the Y-doped sample is cooled with an applied magnetic field.Fil: Guitarra, S.R.. Universidad San Francisco de Quito; EcuadorFil: Caneiro, Alberto. Comisión Nacional de Energía Atómica. Gerencia del Area de Energía Nuclear. Instituto Balseiro; ArgentinaFil: Niebieskikwiat, D.. Universidad San Francisco de Quito; Ecuado

    Evidence of strong antiferromagnetic coupling between localized and itinerant electrons in ferromagnetic Sr2FeMoO6

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    Magnetic dc susceptibility (χ\chi) and electron spin resonance (ESR) measurements in the paramagnetic regime, are presented. We found a Curie-Weiss (CW) behavior for χ\chi(T) with a ferromagnetic Θ=446(5)\Theta = 446(5) K and μeff=4.72(9)μB/f.u.\mu_{eff} = 4.72(9) \mu_{B}/f.u., this being lower than that expected for either Fe3+(5.9μB)Fe^{3+}(5.9\mu_{B}) or Fe2+(4.9μB)Fe^{2+}(4.9\mu_{B}) ions. The ESR g-factor g=2.01(2)g = 2.01(2), is associated with Fe3+Fe^{3+}. We obtained an excellent description of the experiments in terms of two interacting sublattices: the localized Fe3+Fe^{3+} (3d53d^{5}) cores and the delocalized electrons. The coupled equations were solved in a mean-field approximation, assuming for the itinerant electrons a bare susceptibility independent on TT. We obtained χe0=3.7\chi_{e}^{0} = 3.7 10410^{-4} emu/mol. We show that the reduction of μeff\mu_{eff} for Fe3+Fe^{3+} arises from the strong antiferromagnetic (AFM) interaction between the two sublattices. At variance with classical ferrimagnets, we found that Θ\Theta is ferromagnetic. Within the same model, we show that the ESR spectrum can be described by Bloch-Hasegawa type equations. Bottleneck is evidenced by the absence of a gg-shift. Surprisingly, as observed in CMR manganites, no narrowing effects of the ESR linewidth is detected in spite of the presence of the strong magnetic coupling. These results provide evidence that the magnetic order in Sr2FeMoO6Sr_{2}FeMoO_{6} does not originates in superexchange interactions, but from a novel mechanism recently proposed for double perovskites

    Tailoring transport properties of phase-separated manganite films with ordered magnetic nanostructures

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    International audienceThe magnetotransport properties of thin manganite films (La 0.7 Ca 0.3 MnO 3) coupled with arrays of permalloy (Py) nanodots deposited on the surface of the film is studied as a function of temperature , magnetic field and size of the dots. In the presence of the magnetic dots, a reduction of the electrical resistivity is observed, especially at the insulator-to-metal transition, as well as a shift of the transition peak towards higher temperature. This indicates that, due to the local interface exchange coupling, highly conductive ferromagnetic domains are nucleated in the manganite film underneath the Py nanodots. The use of a simplified resistor network model allows us to estimate the size of the metallic regions induced by the exchange coupling. At low temperatures, these regions extend ∼ 70 nm beyond the edge of the nanodots, a lengthscale comparable to the correlation length of the ferromagnetic clusters in the phase-separated state of La 0.7 Ca 0.3 MnO 3

    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 Pr0.5δ_{0.5-\delta}Ca0.2+δ_{0.2+\delta}Sr0.3_{0.3}MnO3_3 for 0.04δ0.04-0.04\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 n0.50n\leq 0.50 the metallic fraction is above the critical percolation threshold XC15.5X_C\simeq 15.5%. As a consequence, these samples show very different magnetoresistance properties. In addition, for n0.50n\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 ρ1=σ(XXC)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.

    Anclaje de paredes de dominio de interfaces ferromagneto/antiferromagneto

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    Aquí presentamos un estudio de las propiedades magnéticas de la manganita Pr0.5Sr0.5-xCaxMnO3 para x=0.1 y 0.2, donde se presenta la coexistencia entre las fases ferromagnética (FM) y antiferromagnética (AFM). Este estado está caracterizado por la presencia de inclusiones FM dentro de una matriz AFM. La evolución de la magnetización (M) con el campo magnético aplicado (H) muestra la existencia de un campo crítico HC, por encima del cual M crece rápidamente, indicando una expansión repentina del volumen de la fase FM en detrimento del volumen de la fase AFM. Analizamos este comportamiento y la respuesta de la susceptibilidad magnética a bajos campos (H&lt;HC) en términos de un modelo simplificado que considera el anclaje de las paredes de dominio FM/AFM (las interfaces entre las fases FM y AFM). A partir de este análisis podemos estimar algunos parámetros relevantes, incluyendo la energía y longitud característica de anclaje y el tamaño característico de los dominios ferromagnéticos, el cual coincide con otras observaciones experimentales

    Inhomogeneous ferrimagnetic-like behavior in Gd2/3Ca1/3MnO3 single crystals

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    We present a study of the magnetic properties of Gd2/3Ca1/3MnO3 single crystals at low temperatures. We show that this material behave as an inhomogeneous ferrimagnet. In addition to small saturation magnetization at 5 K, we have found history dependent effects in the magnetization and the presence of exchange bias. These features are compatible with microscopic phase separation in the clean Gd2/3Ca1/3MnO3 system studied.Comment: 7 pages, 6 figures, submitted Journal of Magnetism and Magnetic Material

    Suppression of matching field effects by splay and pinning energy dispersion in YBa_2Cu_3O_7 with columnar defects

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    We report measurements of the irreversible magnetization M_i of a large number of YBa_2Cu_3O_7 single crystals with columnar defects (CD). Some of them exhibit a maximum in M_i when the density of vortices equals the density of tracks, at temperatures above 40K. We show that the observation of these matching field effects is constrained to those crystals where the orientational and pinning energy dispersion of the CD system lies below a certain threshold. The amount of such dispersion is determined by the mass and energy of the irradiation ions, and by the crystal thickness. Time relaxation measurements show that the matching effects are associated with a reduction of the creep rate, and occur deep into the collective pinning regime.Comment: 7 pages, 5 figures, submitted to Phys. Rev.
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