Sublattice spin reversal and field induced Fe3+spin-canting across the magnetic compensation temperature in Y1.5Gd1.5Fe5O12rare-earth iron garnet.

In the present work Fe3+sublattice spin reversal and Fe3+spin-canting across the magnetic compensation temperature (TComp) are demonstrated in polycrystalline Y1.5Gd1.5Fe5O12(YGdIG) by means of in-field57FeMössbauer spectroscopy measurements. Corroborating in-field57FeMössbauer measurements, both Fe3+& Gd3+sublattice spin reversal has also been manifested in hard x-ray magnetic circular dichroism (XMCD) measurements. From in-field57FeMössbauer measurements, estimation and analysis of effective internal hyperfine field (Heff), relative intensity of absorption lines in a sextet elucidated unambiguously the signatures of Fe3+spin reversal and field induced spin-canting of Fe3+sublattices across TComp. Gd L3-edge XMCD signal is observed to consist of an additional spectral feature, identified as Fe3+magnetic contribution to XMCD spectra of Gd L3-edge, enabling us the extraction of both the sublattices (Fe3+& Gd3+) information from a single absorption edge analysis. The evolution of the XMCD amplitudes, which is proportional to magnetic moments, as a function of temperature for both magnetic sublattices extracted at the Gd L3-edge reasonably match with values that are extracted from bulk magnetization data of YGdIG and YIG (Y3Fe5O12) and corresponding Fe K-edge XMCD amplitudes for Fe contribution. These measurements pave new avenues to investigate how the magnetic behavior of such complex system acts across the compensation point.

Syntheses and magnetic properties of substituted bis-indacenyl bi-metallic complexes & application / Síntesis y propiedades magnéticas de complejos bimetálicos de bis-indacenilo sustituido y su aplicación / Sínteses e propriedades magnéticas de complexos bimetálicos bis-indaceníli-cossubstituídos e aplicação

Abstract Organometallic compounds, Bis (2,4,6,8 teramethyl-indacenyl) di Iron (1), Bis (2,4,6,8 teramethyl s-indacenyl) mono iron, mono cobalt (2), and Bis (2,6 diethyl-4,8-dimethyl-s-indacenyl) di cobalt (3) were synthesised by means of salt elimination strategy, using Fe(II) and Co(II) salts. The compounds were characterised through spectroscopic and electrochemical methods. Magnetic measurements were carried out by Physical Property Measurement System (PPMS). Mossbauer spectroscopic data reveals that in all compounds, surprisingly, Iron is in +3 oxidation state. DFT calculations have been carried out to understand the change in the oxidation state of a metal. DFT study confirms the electron transfer nature of ligand to metal. Cyclic voltametric study on these compounds shows a large separation (ΔE>800mV) between two oxidation peaks confirming the strong interaction between the metal centres. Magnetic measurements on these organometallic compounds reveals that they exhibit a ferrimagnetic behaviour at temperatures below 40 K.

Resumen En este trabajo se sintetizaron los compuestos organometálicos Bis (2,4,6,8 terametil-indacenil) férrico (1), Bis (2,4,6,8 terametil s-indacenil) ferroso, cobaltoso (2) y Bis (2,6 dietil-4,8-dimetil-s-indacenil) di cobalto (3) mediante la estrategia de eliminación de sales, utilizando sales de Fe(II) y Co(II).Los compuestos se caracterizan por métodos espectroscópicos y electroquímicos. Las mediciones magnéticas se llevaron a cabo mediante el sistema de medición de propiedades físicas (PPMS). Los datos espectroscópicos Mossbauer revelan que, en todos los compuestos, sorprendentemente, el hierro se encuentra en el estado de oxidación +3. También se realizaron cálculos DFT para comprender el cambio en el estado de oxidación de los metales. El estudio DFT confirmó la naturaleza de transferencia de electrones del ligando al metal. El estudio voltamperométrico cíclico de estos compuestos muestra una gran separación (ΔE>800mV) entre los dos picos de oxidación que confirman la fuerte interacción entre los centros metálicos. Las mediciones magnéticas de estos compuestos organometálicos revelan que presentan un comportamiento ferrimagnético a temperaturas inferiores a 40 K.

Resumo Compostos organometálicos, Bis (2,4,6,8 terametil-indacenil) di ferro (1), Bis (2,4,6,8 terametil s-indacenil) mono ferro, mono cobalto (2) e Bis (2,6 dietil-4,8-dimetil-s-indacenil) di cobalto (3) foram sintetizados por estratégia de eliminação de sal, utilizando sais de Fe(II) e Co(II). Os compostossão caracterizados por métodos espectroscópicos e eletroquímicos. As medições magnéticas foram realizadas pelo Sistema de Medição de Propriedades Físicas (PPMS). Os dados espectroscópicos Mossbauerrevelam que em todos os compostos, surpreendentemente, o ferro está em +3 estado de oxidação.Os cálculos do DFT foram realizados para entender a mudança no estado de oxidação de um metal. O estudo DFT confirma a natureza da transferência de elétrons do ligante para o metal. O estudovoltamétrico cíclico dessescompostosmostrauma grande separação (ΔE>800mV) entre dois picos de oxidação confirmando a forteinteração entre os centros metálicos. As medições magnéticas nestescompostos organometálicos revelam que eles apresentam um comportamento ferrimagnético a uma temperatura abaixo de 40 K.

Polar state in polycrystalline BaSn0.3Ti0.7O3thin film determined from ac- & dc-field studies.

The present work reports polarization response and the effects ofac- &dc-fields on 30% Sn doped BaTiO3polycrystalline relaxor thin films as a function of temperature. Apart from the low temperature frequency dispersion in dielectric data, a frequency independent local maxima in dielectric constant and a concomitant peak in dielectric loss atT* ∼ 245 K is observed, which is unusual of bulk relaxor systems. BelowT*, dispersion in dielectric constant becomes quite evident showing signatures of non-ergodic behavior. Subsequently, the dielectric and polarization responses in ergodic (>T*) and non-ergodic (

Lattice assisted dielectric relaxation in four-layer Aurivillius Bi5FeTi3O15ceramic at low temperatures.

We have investigated magnetic, structural and dielectric properties of Bi5FeTi3O15(BFTO) in the temperature range 5K-300 K. Using diffraction, Raman spectroscopy and x-ray absorption fine structure measurements, iso-structural modifications are observed at low temperatures (≈100 K). The analysis of dielectric constant data revealed signatures of dielectric relaxation, concomitant with these structural modifications in BFTO at the same temperatures. Further, employing complementary experimental methods, it is shown that the distribution of Fe/Ti ions in BFTO is random. With the help of techniques that probe magnetism at various length and time scales, it is shown that the phase-pure BFTO is non-magnetic down to the lowest temperatures.

Unconventional domain wall magnetoresistance of patterned Ni/Nb bilayer structures below superconducting transition temperature of Nb.

Scattering of spin-up and spin-down electrons while passing through a ferromagnetic domain wall (DW) leads to an additional resistance for transport current, usually observed prominently in constricted magnetic structures. In this report we use the resistance of the DW as a probe to find an indirect signatures of the theoretically predicted spin-singlet supercurrent to spin-triplet supercurrent conversion effect of ferromagnetic DWs. Here we examine the DW induced resistance in Ni stripe in a bilayer Ni/Nb geometry in the normal state and in the superconducting state of Nb. By making a 3µm wide gap in the top Nb layer we routed the transport current through the Ni layer in the normal state and in the superconducting state of Nb. In the normal state of Nb, in-field transport measurements showed a clear domain wall magneto-resistance (DWMR) peak of amplitude ∼5.9 mΩ near the coercive field, where the DW density is expected to be maximum. Interestingly, however, below the superconducting transition temperature of Nb, the DWMR peak of the Ni layer showed a sharp drop in the field range where the number of DWs become maximum. This observation may be a possible signature of magnetic DW induced spin-triplet correlations in the Ni layer due to the direct injection of spin-singlet Cooper pairs from Nb into the magnetic DWs.

Studying the onset of galvanic steel corrosionin situusing thin films: film preparation, characterization and application to pitting.

This work reports about a novel approach for investigating surface processes during the early stages of galvanic corrosion of stainless steelin situby employing ultra-thin films and synchrotron x-radiation. Characterized by x-ray techniques and voltammetry, such films, sputter deposited from austenitic steel, were found representing useful replicas of the target material. Typical for stainless steel, the surface consists of a passivation layer of Fe- and Cr-oxides, a couple of nm thick, that is depleted of Ni. Films of ≈4 nm thickness were studiedin situin an electrochemical cell under potential control (-0.6 to +0.8 V vs Ag/AgCl) during exposure to 0.1 M KCl. Material transport was recorded with better than 1/10 monolayer sensitivity by x-ray spectroscopy. Leaching of Fe was observed in the cathodic range and the therefor necessary reduction of Fe-oxide appears to be accelerated by atomic hydrogen. Except for minor leaching, reduction of Ni, while expected from Pourbaix diagram, was not observed until at a potential of about +0.8 V Cr-oxide was removed from the steel film. After couple of minutes exposure at +0.8 V, the current in the electrochemical cell revealed a rapid pitting event that was simultaneously monitored by x-ray spectroscopy. Continuous loss of Cr and Ni was observed during the induction time leading to the pitting, suggesting a causal connection with the event. Finally, a spectroscopic image of a pit was recordedex situwith 50 nm lateral and 1 nm depth resolution by soft x-ray scanning absorption microscopy at the Fe L2,3-edges by using a 80 nm film on a SiN membrane, which is further demonstrating the usefulness of thin films for corrosion studies.

Antiphase boundary in antiferromagnetic multiferroic LuMn0.5Fe0.5O3: anomalous ferromagnetism, exchange bias effect and large vertical hysteretic shift.

The emergence of exchange bias effect in Fe3O4 thin films has been since attributed to the presence of anti phase boundary (APB) growth defects despite lack of direct experimental evidence. In the present report, APB induced anomalous weak ferromagnetism and exchange bias property of single-phase antiferromagnetic (AFM) system LuMn0.5Fe0.5O3 (LMFO) is discussed and 57Fe Mössbauer spectroscopy and high resolution transmission electron microscopy (HRTEM) measurements are used to probe the origin of the observed effect. In addition to the sextet component corresponding to the long range AFM ordering, the measured Mössbauer spectra reveal the presence of a small component (10%-12%) near zero velocity with unusually small internal field. This indicates the presence of APB defects. From micro structural investigations using HRTEM, presence of APB type defects and dislocations are confirmed. In addition to the exchange bias effect, upon field cooling, hysteresis loop exhibits large vertical shift due to strong pinning effect of the APB. Finally we further annealed the optimally sintered sample LMFO and studied the evolution of defects, and their influence on weak ferromagnetism and exchange bias properties. Our present experimental findings may pave the way in creating new functionalities in materials using APB-type growth defects.

Pr2FeCrO6: A Type I Multiferroic.

We synthesized double perovskite Pr2FeCrO6 by solid-state method. Analysis of its X-ray powder diffraction shows that the compound crystallizes in a centrosymmetric structure with space group Pbnm. Our X-ray photoelectron spectroscopy (XPS) studies show that all the cations are present in +3 oxidation state. Magnetization studies of Pr2FeCrO6 show that the material is paramagnetic at room temperature and undergoes a magnetic transition below TCM = 250 K. We observe clear magnetic hysteresis loop, for example, below 150 K. A low remnant magnetization Mr, ∼0.05 µB/f. u., is inferred from the observed magnetic hysteresis loop. 57Fe Mössbauer study at 25 K shows a high hyperfine magnetic field of ∼53 T at the Fe nucleus, which corresponds to a magnetic moment of ∼6-7 µB/Fe. These two results together suggest a ferrimagnetic (nearly compensated or canted) ordering of the Fe moments. Mössbauer studies close to the ferrimagnetic ordering temperature suggest interesting magnetic relaxation effects. A dielectric anomaly observed at TCE = 453 K signals a ferroelectric ↔ paraelectric phase transition. We observe at room temperature a clear and well-defined ferroelectric hysteresis loop, PS = 1.04 µC/cm2, establishing ferroelectricity in the material. From these results, we conclude that Pr2FeCrO6 is a type I multiferroic (TCE > TCM).

Low temperature high magnetic field 57Fe Mössbauer study of kinetic arrest in Ta doped HfFe2.

Low temperature high magnetic field (57)Fe Mössbauer measurements were carried out on the inter-metallic compound Hf0.77Ta0.23Fe2 by following novel paths in H-T space. The ferromagnetic (FM) fraction at 5 K and zero magnetic field is shown to depend on the cooling field, i.e., the higher the field is, the higher the FM fraction is. Mössbauer spectra collected in the presence of a 4 T magnetic field show that the antiferromagnetic (AFM) spins are canted with respect to the applied magnetic field and hence contribute to the total bulk magnetization in this compound. The data also show an induced magnetic moment even at the 2a site of the AFM phase. Mössbauer spectra collected using the CHUF (cooling and heating in un-equal magnetic fields) protocol show a reentrant transition when the sample is cooled in zero field and measured during warming in 4 T, showing the FM state as the equilibrium state. This work is the first microscopic experimental evidence for the de-vitrification of the kinetically arrested magnetic state.

Anomalous variation of the Lamb-Mössbauer factor at the magnetic transition temperature in magnetoelectric GaFeO3.

Temperature-dependent (57)Fe Mössbauer spectroscopy (5-723 K) and neutron diffraction (2-290 K) measurements are carried out on polycrystalline magnetoelectric GaFeO(3). From the neutron diffraction data, evidence for the magnetostriction and increased disorder at Fe sites close to the ferrimagnetic Curie transition temperature (T(C)) is observed. From the Mössbauer data, it is observed that the Lamb-Mössbauer factor as a function of temperature f(T), which is related to the integral over the first Brillouin zone of the phonon spectrum, shows a unequivocal variation at the T(C). The observations are discussed in terms of spin-phonon coupling. The observed average hyperfine fields from (57)Fe Mössbauer spectra match with the bulk magnetization data. A critical exponent (ß) of 0.38 ± 0.02 and a Debye temperature (θ(D)) of ~350 K is estimated from the (57)Fe Mössbauer data.

High coercivity of oleic acid capped CoFe2O4 nanoparticles at room temperature.

High coercivity (9.47 kOe) has been obtained for oleic acid capped chemically synthesized CoFe(2)O(4) nanoparticles of crystallite size approximately 20 nm. X-ray diffraction analysis confirms the formation of spinel phase in these nanoparticles. Thermal annealing at various temperatures increases the particle size and ultimately shows bulk like properties at particle size approximately 56 nm. The nature of bonding of oleic acid with CoFe(2)O(4) nanoparticles and amount of oleic acid in the sample is determined by Fourier transform infrared spectroscopy and thermogrvimetric analysis, respectively. The Raman analysis suggests that the samples are under strain due to capping molecules. Cation distribution in the sample is studied using Mossbauer spectroscopy. Oleic acid concentration dependent studies show that the amount of capping molecules plays an important role in achieving such a high coercivity. On the basis of above observations, it has been proposed that very high coercivity (9.47 kOe) is the result of the magnetic anisotropy, strain, and disorder of the surface spins developed by covalently bonded oleic acid to the surface of CoFe(2)O(4) nanoparticles.

Si(+) ion irradiation in a Co/Pt multilayer system.

This paper deals with a study of the effect of Si(+) ion irradiation on a Co/Pt multilayer system irradiated at different temperatures. The as-deposited and irradiated samples have been characterized using x-ray reflectivity (XRR), x-ray diffraction (XRD) and the magneto-optical Kerr effect (MOKE). X-ray reflectivity shows clear intermixing at the interfaces. The x-ray diffraction pattern shows that Si(+) ion irradiation at higher temperatures results in the formation of the CoPt(3) fcc phase with a small fraction of L1(0) phase. The mixing process is discussed in terms of recoil displacements induced by energy transfers from ions.