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Lesya Demchenko

Publications and source records attributed to Lesya Demchenko.

5 recordsLinked to original sources

Electric Charge Transport and Dielectric Properties of the Barium Titanate Ceramics Obtained by Spark-Plasma Sintering with Different Carbon Content

Barium titanate (BaTiO3) ceramics with a different content of carbon were synthesized by spark-plasma sintering (SPS) at the temperature of 1100 C in vacuum under pressure. The concentration and distribution of carbon impurity inside the samples is estimated by scanning electron microscopy (SEM). The resistivity vs temperature and electric field dependences of the SPS ceramics with different carbon concentration have been studied. It is shown that their conduction is determined by the variable range hopping mechanism and obeys the Mott law. The density of localized states and localization radius of the electron wave function are determined. The difference in low-temperature resistivity of the SPS ceramics is caused by carbon concentration and connected with it variation of the dielectric permittivity. The relative dielectric permittivity of the SPS ceramics is colossal and reaches the values of 10^5 - 10^6 order. The larger carbon concentration is, the smaller the permittivity and resistivity are within the Mott hopping conduction temperature range. In the range from 250 K to 408 K one observes that the dielectric permittivity strongly increases forming a maximum in all samples, which may be related to the phase transition. Along with this, resistivity manifests a simultaneous sharp decrease. The decrease of resistivity along with the characteristic dependence of resistivity vs dielectric permittivity in the Mott conduction temperature range, evidences the validity of Heywang model for the description of SPS ceramics conduction mechanisms. The resistivity strongly decreases with increasing frequency in the AC regime, which agrees both with models of hopping conduction and effects based on the Maxwell-Wagner model. The studied SPS BaTiO3 ceramics are attractive for applications in energy storage and sensorics.

cond-mat.mtrl-sci

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

Colossal dielectric response of HfxZr1-xO2 nanoparticles

We reveal a colossal dielectric response of small (5 - 10 nm) oxygen-deficient HfxZr1-xO2 nanoparticles (x = 1 - 0.4), prepared by the solid-state organonitrate synthesis. The effective dielectric permittivity of the pressed HfxZr1-xO2 nanopowders has a pronounced maximum at 38 - 88 C, which shape can be fitted by the Curie-Weiss type dependence modified for the diffuse ferroelectric-paraelectric phase transition. The maximal value of the dielectric permittivity increases from 1.5*10^3 (for x = 1) to 1.5*10^5 (for x= 0.4) at low frequencies (~4 Hz); being much smaller, namely changing from 7 (for x = 1) to 20 (for x = 0.4) at high frequencies (~500 kHz). The frequency dispersion of the dielectric permittivity maximum position is almost absent, meanwhile the shape and width of the maximum changes in a complex way with increase in frequency. The temperature dependencies of the dielectric permittivity and resistivity are almost mirror-like turned over in respect to each other, which means that all their features, such as position and shape of maxima, plateau, minima and inflexions, almost coincide after the mirror reflection in respect to the temperature axis. These correlations of resistivity and dielectric permittivity are well-described in the Heywang barrier model applied together with the variable range hopping conduction model in semiconducting ferroelectrics. The ferroelectric-like behavior of the small oxygen-deficient HfxZr1-xO2 nanoparticles is expected from the Landau-Ginzburg-Devonshire approach and density functional theory calculations. Obtained results may be useful for developing silicon-compatible functional nanomaterials based on HfxZr1-xO2 nanoparticles.

cond-mat.mtrl-sci

Strain-Gradient and Curvature-Induced Changes in Domain Morphology of BaTiO3 Nanorods: Experimental and Theoretical Studies

We investigate the impact of OH- ions incorporation on the lattice strain and spontaneous polarization of BaTiO3 nanorods synthesized under different conditions. It was confirmed that the lattice strain depends directly on Ba supersaturation, with higher supersaturation leading to an increase in the lattice strain. However, it was shown that crystal growth and observed lattice distortion are not primarily influenced by external strain; rather, OH- ions incorporation plays a key role in generating internal chemical strains and driving these processes. By using the less reactive TiO2 precursor instead of TiOCl2 and controlling Ba supersaturation, the slower nucleation rate enables more effective regulation of OH- ions incorporation and crystal growth. This in turn effects both particle size and lattice distortion, leading to c/a ratio of 1.013 - 1.014. The incorporation of OH- ions induces lattice elongation along the c-axis, contributing to anisotropic growth, increasing of the rod diameter and their growth-induced bending. However, the possibility of the curvature-induced changes in domain morphology of BaTiO3 nanorods remains almost unexplored. To study the possibility, we perform analytical calculations and finite element modeling, which provide insights into the curvature-induced changes in the strain-gradient, polarization distribution, and domain morphology in BaTiO3 nanorods. Theoretical results reveal the appearance of the domain stripes in BaTiO3 nanorod when the curvature exceeds a critical angle. The physical origin of the domain stripes emergence is the tendency to minimize its elastic energy of the nanorod by the domain splitting. These findings suggest that BaTiO3 nanorods, with curvature-controllable amount of domain stripes, could serve as flexible race-track memory elements for flexo-tronics and domain-wall electronics.

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