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Olena M. Fesenko

Publications and source records attributed to Olena M. Fesenko.

7 recordsLinked to original sources

Magnetic properties and charge transport mechanisms in oxygen-deficient HfxZr1-xO2-y nanoparticles

Study of nanoscale hafnia-zirconia physical properties is the key topic in fundamental and applied science. However, charge transport mechanisms and magnetic properties of hafnia-zirconia nanoparticles are very poorly studied both theoretically and experimentally. In this work we observed a superparamagnetic-like and superparaelectric-like response of ultra-small hafnia-zirconia nanoparticles prepared by the solid-state organonitrate synthesis. The EPR spectra of hafnia-zirconia nanopowders reveal the presence of paramagnetic defect centers, which may be hafnium and/or zirconium ions, which trapped an electron near an oxygen vacancy and changed their valence state from the non-paramagnetic +4 to the paramagnetic +3 state. The Raman spectra indicate the decisive role of surface defects, presumably oxygen vacancies, for all studied Zr compositions.At the same time the EELS analysis does not reveal any noticeable concentration of magnetic impurities in the hafnia-zirconia nanopowders, and the X-ray diffraction analysis reveals the dominant presence of the orthorhombic phase. We observed that the quasi-static relative dielectric permittivity of the hafnia-zirconia nanopowders overcomes 10^6 - 10^7 and related the colossal values with the superparaelectric state of the nanoparticles cores induced by the flexo-electro-chemical strains. It has been found that ultra-small hafnia-zirconia nanoparticles reveal posistor effect and relatively large values of accumulated charge. Thus, obtained results open the way for creation of silicon-compatible ferroics oxygen-deficient hafnia-zirconia nanoparticles with superparamagnetic and superparaelectric properties, which may be used in advanced FETs and electronic logic elements.

cond-mat.mtrl-sci

Reentrant polar phase induced by the ferro-ionic coupling in Bi$_{1-x}$Sm$_x$FeO$_3$ nanoparticles

Using the model of four sublattices, the Landau-Ginzburg-Devonshire-Kittel phenomenological approach and the Stephenson-Highland ionic adsorption model for the description of coupled polar and antipolar long-range orders in ferroics, we calculated analytically the phase diagrams and polar properties of Bi$_{1-x}$Sm$_x$FeO$_3$ nanoparticles covered by surface ions in dependence on their size, surface ions density, samarium content "x" and temperature. The size effects and ferro-ionic coupling govern the appearance and stability conditions of the long-range ordered ferroelectric, reentrant ferrielectric and antiferroelectric phases in the Bi1-xSmxFeO3 nanoparticles. Calculated phase diagrams are in a qualitative agreement with the X-ray diffraction phase analysis, electron paramagnetic resonance, infra-red spectroscopy and electrophysical measurements of the Bi$_{1-x}$Sm$_x$FeO$_3$ nanopowders sintered by the solution combustion method. The combined theoretical-experimental approach allows to establish the influence of the ferro-ionic coupling and size effects in Bi$_{1-x}$Sm$_x$FeO$_3$ nanoparticles on their polar properties.

cond-mat.mtrl-sci

Temperature-Induced Hexagonal-Orthorhombic Phase Transition in Lutetium Ferrite Nanoparticles

The X-ray diffraction, Raman and infrared spectroscopies and magnetic measurements were used to explore the correlated changes of the structure, lattice dynamics and magnetic properties of the LuFeO3 nanoparticles, which appear in dependence on their sintering temperature. We revealed a gradual substitution of the hexagonal phase by the orthorhombic phase in the nanoparticles, which sintering temperature increases from 700 C to 1100 C. The origin and stability of the hexagonal phase in the LuFeO3 nanoparticles is of the special interest, because the nanoparticle in the phase can be a room-temperature multiferroic with a weak ferromagnetic and pronounced structural and ferroelectric long-range ordering, while the antiferromagnetic and nonpolar orthorhombic phase is more stable in the bulk LuFeO3. To define the ranges of the hexagonal phase stability, we determine the bulk and interface energy densities of different phases from the comparison of the Gibbs model with experimental results. Using the Gibbs model parameters, we predict the influence of size effects and temperature on the structural and polar properties of the LuFeO3 nanoparticles. Analysis of the obtained results shows that the combination of the X-ray diffraction, Raman and infrared spectroscopy, magnetic measurements and theoretical modelling of structural and polar properties allows to establish the interplay between the phase composition, lattice dynamics and multiferroic properties of the LuFeO3 nanoparticles prepared in different conditions.

cond-mat.mtrl-sci

Phase diagrams and polarization reversal in nanosized Hf$_x$Zr$_{1-x}$O$_{2-y}$

To describe the polar properties of the nanosized HfxZr1-xO2-y, we evolve the "effective" Landau-Ginzburg-Devonshire (LGD) model based on the parametrization of the Landau expansion coefficients for the polar and antipolar orderings. We have shown that the effective LGD model can predict the influence of screening conditions and size effects on phase diagrams, polarization reversal and structural properties of the nanosized HfxZr1-xO2-y of various shape and sizes. To verify the model, we use available experimental results for HfxZr1-xO2 thin films and oxygen-deficient HfO2-y nanoparticles prepared at different annealing conditions. X-ray diffraction, which was used to determine the phase composition of the HfO2-y nanoparticles, revealed the formation of the ferroelectric orthorhombic phase in them. Micro-Raman spectroscopy was used to explore the correlation of lattice dynamics and structural changes appearing in dependence on the oxygen vacancies concentration in the HfO2-y nanoparticles. Since our approach allows to determine the conditions (shape, sizes, Zr content and/or oxygen vacancies amount) for which the nanosized HfxZr1-xO2-y are ferroelectrics or antiferroelectrics, we hope that obtained results are useful for creation of next generation of Si-compatible ferroelectric gate oxide nanomaterials.

cond-mat.mes-hall

A Combined Theoretical and Experimental Study of the Phase Coexistence and Morphotropic Boundaries in Ferroelectric-Antiferroelectric-Antiferrodistortive Multiferroics

The physical nature of the ferroelectric (FE), ferrielectric (FEI) and antiferroelectric (AFE) phases, their coexistence and spatial distributions underpin the functionality of antiferrodistortive (AFD) multiferroics in the vicinity of morphotropic phase transitions. Using Landau-Ginzburg-Devonshire (LGD) phenomenology and a semi-microscopic four sublattice model (FSM), we explore the behavior of different AFE, FEI and FE long-range orderings and their coexistence at the morphotropic phase boundaries in FE-AFE-AFD multiferroics. These theoretical predictions are compared with the experimental observations for dense Bi1-yRyFeO3 ceramics, where R is Sm or La atoms with the fraction 0 < y< 0.25, as confirmed by the X-ray diffraction (XRD) and Piezoresponse Force Microscopy (PFM). These complementary measurements were used to study the macroscopic and nanoscopic transformation of the crystal structure with the doping. The comparison of the measured and calculated AFE/FE phase fractions demonstrate that the LGD-FSM approach well describes the experimental results obtained by XRD and PFM for Bi1-yRyFeO3. Hence, this combined theoretical and experimental approach provides further insight into the origin of the morphotropic boundaries and coexisting FE and AFE states in model rare-earth doped multiferroics.

cond-mat.mtrl-sci

Ferromagnetic-like behavior of Bi0.9La0.1FeO3-KBr nanocomposites

We studied magnetostatic response of the Bi0.9La0.1FeO3-KBr composites (BLFO-KBr) consisting of nanosized (about 100 nm) ferrite Bi0.9La0.1FeO3 (BLFO) conjugated with fine grinded ionic conducting KBr. When the fraction of KBr is rather small (less than 15 wt percent) the magnetic response of the composite is very weak and similar to that observed for the BLFO (pure KBr matrix without Bi1-xLaxFeO3 has no magnetic response as anticipated). However, when the fraction of KBr increases above 15percent, the magnetic response of the composite changes substantially and the field dependence of magnetization reveals ferromagnetic-like hysteresis loop with a remanent magnetization about 0.14 emu/g and coercive field about 1.8 Tesla (at room temperature). Nothing similar to the ferromagnetic-like hysteresis loop can be observed in BLFO ceramics, which magnetization quasi linearly increases with magnetic field. Different physical mechanisms were considered to explain the unusual experimental results for BLFO-KBr nanocomposites, but only those among them, which are highly sensitive to the interaction of antiferromagnetic Bi0.9La0.1FeO3 with ionic conductor KBr, can be relevant. An appropriate mechanism turned out to be ferro-magneto-ionic coupling.

cond-mat.mtrl-sci

Rotomagnetic coupling in fine grained multiferroic BiFeO3: Theory and experiment

Using Landau-Ginzburg-Devonshire (LGD) theory for BiFeO3 dense fine grained ceramics with quasi spherical grains and nanosized inter grain spaces enriched by elastic defects, we calculated a surprisingly strong size-induced increase of the AFM temperature caused by the joint action of rotomagnetic and magnetostrictive coupling. Notably that all parameters included in the LGD functional have been extracted from experiments, not assumed. Complementary we performed experiments for dense BiFeO3 ceramics, which revealed that the shift of antiferromagnetic transition to 690 K instead of 645 K for a single crystal. To explain theoretically the result, we consider the possibility to control antiferromagnetic state of multiferroic BiFeO3 via biquadratic antiferrodistortive rotomagnetic, rotoelectric, magnetostrictive and magnetoelectric couplings. According to our calculations the highest is the rotostriction contribution, the magnetostrictive and electrostriction contributions appeared smaller.

cond-mat.mtrl-sci