F. Figueiras

Effect of Fe-doping on the structure and magnetoelectric properties of (Ba0.85Ca0.15)(Ti0.9Zr0.1)O3 synthesized by a chemical route

B-site Fe-doped (Ba0.85Ca0.15)(Ti0.9Zr0.1)O3 was synthesized by a facile chemical route to study the effect of doping on its physical properties. Detailed analysis of X-ray diffraction and Raman spectroscopy data revealed an increased lattice strain and thereby deviation from the morphotropic phase boundary with the progressive doping of Fe from 1 to 5 mol%. Such structural changes have resulted in the weakening of the energy band gap as well as deterioration of the ferroelectric polar nature which was evidenced by a shift of tetragonal to cubic transitions towards room temperature and hard doping effects in ferroelectric hysteresis. The doped samples exhibited room temperature ferromagnetism. Combined Mossbauer and X-ray photoelectron spectroscopic studies suggest that oxygen vacancies and defect complexes induced by Fe doping play a major role in magnetic properties. Local piezoresponse measurements illustrated imprint characteristics of ferroelectric domains in undoped and doped samples at the nanoscale. Room temperature magnetoelectric (ME) measurements revealed that 1 mol% Fe doped sample, having higher ferroelectric polarization and moderate magnetization, exhibits a strong ME response with a coefficient of 12.8 mV cm−1 Oe−1. The present study on Fe-doping effects on the structure and related ME properties of this important lead-free material is useful to tailor multiferroic applications in electronics.

Peculiar Magnetoelectric Coupling in BaTiO3:Fe113 ppm Nanoscopic Segregations

We report polycrystalline BaTiO3 with cooperative magnetization behavior associated with the scarce presence of about 113 atomic ppm of Fe ions, clearly displaying magnetoelectric coupling with significant changes in magnetization (up to ΔM/M ≈ 32%) at the ferroelectric transitions. We find that Fe ions are segregated mostly at the interfaces between grain boundaries and an Fe-rich phase, forming a self-composite with high magnetoelectric coupling above room temperature. We compare our results with ab initio calculations and other experimental results found in the literature, proposing mechanisms that could be behind the magnetoelectric coupling within the ferroelectric matrix. These findings open the way for further strategies to optimize interfacial magnetoelectric couplings.

Breaking the geometric magnetic frustration in controlled off-stoichiometric LuMn1+zO3+δ compounds

This study explores controlled off-stoichiometric LuMn1+zO3+δ (|z| < 0.1) compounds, intended to retain the utter LuMnO3 intrinsic hexagonal symmetry and ferroelectric properties. X-ray powder diffraction measurements evidenced a single phase P63cm structure. Thermo-gravimetric experiments show a narrow impact of oxygen vacancies while a distinguishable gas exchange at ∼700 K, a surprisingly lower temperature when compared to perovskite systems. A comparison of different nominal ceramics revealed pertinent structural and magnetic property variations owing to subtle self-doping effects. Deviations from the archetypal antiferromagnetic state were detected below ∼90 K suggesting local rearrangements of the nominal Mn(3+) ions matrix, breaking the ideal geometrical spin frustration, leading to a non-compensated magnetic structure.

The Effects of Ca and Mn Excess Co-Doping in CMR Manganites Solid Solution Structures

A comprehensive study of CMR manganite related phases, particularly those that develop under the effects of Ca and Mn-excess co-doping is undertaken. The relationships between phase composition, processing and observed crystalline structure are investigated for co-precipitated powders of composition La1-xCaxMn1+zO3+δ, thermally treated at 800 and 1000 °C in air for Ca contents of x=0.10 and x=0.15 and Mn content from z=0 up to z=0.88. A relevant structural transition from orthorhombic to rhombohedric symmetry is observed as a function of Mn excess near 25% A site vacancies. This solid solution is in equilibrium with the conjugated phases, either LaMn7O12 at 800°C, or Mn3O4 at 1000°C, respectively. Results suggest that at the polymorphic phase transition the solid solution is stable enough to slow down Mn diffusion into the perovskite cell. Ca-doping introduces stability in the perovskite structure and broadens the domain for phase formation reaction. The solid solution limit of the Ca-manganite solid solution is set above 50% Mn excess.

Unravelling the effect of SrTiO3 antiferrodistortive phase transition on the magnetic properties of La0.7Sr0.3MnO3 thin films

Abstract Epitaxial La 0.7 Sr 0.3 MnO 3 (LSMO) thin films, with different thicknesses ranging from 20 to 330 nm, were deposited on (1 0 0)-oriented strontium titanate (STO) substrates by pulsed laser deposition, with their structure and morphology characterized at room temperature. The magnetic and electric transport properties of the as-processed thin films reveal an abnormal behaviour in the temperature dependent magnetization M ( T ) below the antiferrodistortive STO phase transition ( T STO ), and also an anomaly in the magnetoresistance and electrical resistivity close to the same temperature. Films with thickness ≤100 nm show an in-excess magnetization and pronounced changes in the coercivity due to the interface-mediated magnetoelastic coupling with antiferrodistortive domain wall movement occurring below T STO . However, in thicker LSMO thin films, an in-defect magnetization is observed. This reversed behaviour can be understood with the emergence in the upper layer of the film, of a columnar structure needed to relax the elastic energy stored in the film, which leads to randomly oriented magnetic domain reconstructions. For enough high-applied magnetic fields, as thermodynamic equilibrium is reached, a full suppression of the anomalous magnetization occurs, wherein the temperature dependence of the magnetization starts to follow the expected Brillouin behaviour.Keywords: thin films, magnetic domain reconstruction, interface-mediated coupling, magnetoelasticity(Some figures may appear in colour only in the online journal)

Dielectric Relaxation and Optical Transmittance of PVC Membranes Modified by Nematic Liquid Crystal

This study intends to present some further research in polymer-dispersed liquid crystal (PDLC) systems [1]. These PDLC type cells were produced based on a low-cost commercial polymer (PVC) and liquid crystal E48 (Merck), using a modified solvent preparation method (SIPS). These cells were characterized electro-optically and by low frequency dielectric relaxation (20 Hz to 1 MHz) experiments. Results are encouraging; the prepared composites show regular microstructures and optical transmittance changes induced by the electric field, introducing an alternative way of producing low-cost PDLC electro-optical cells.