arXiv subjects

Victor I. Styopkin

Publications and source records attributed to Victor I. Styopkin.

5 recordsLinked to original sources

arXiv2026

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↗

arXiv2026

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↗

arXiv2025

Resistive switching and charge accumulation in Hf0.5Zr0.5O2 nanoparticles

We revealed the resistive switching, negative differential resistance and charge accumulation effects in Hf0.5Zr0.5O2 nanopowders sintered by the auto-combustion sol-gel method and annealed at temperatures from 500°C to 800°C. The fraction of the orthorhombic phase, determined by the X-ray diffraction (XRD), decreases from 91 vol.% to 7 vol.% with an increase in the annealing temperature from 600°C to 800°C. The electron paramagnetic resonance (EPR) spectra reveal the great amount of oxygen vacancies in the annealed samples, at that the decrease of the orthorhombic phase fraction (observed with an increase in the annealing temperature) correlates with a decrease in the intensity of EPR spectral lines associated with the oxygen vacancies and impurities. This indicates the participation of oxygen vacancies and other defects in the formation of the orthorhombic phase in the Hf0.5Zr0.5O2 powders. To explain the results of electrophysical measurements, we compare the features of the current-voltage characteristics with the phase composition of the Hf0.5Zr0.5O2 powders and with the peculiarities of their EPR spectra. The analysis allows us to relate the resistive switching and charge accumulation observed in Hf0.5Zr0.5O2 nanopowders with the appearance of the ferroelectric-like polar regions in the orthorhombic phase of the nanoparticles, which agrees with the calculations performed in the framework of Landau-Ginzburg-Devonshire approach and density functional theory.

cond-mat.mtrl-sci↗

arXiv2025

Interfacial Effects and Negative Capacitance State in P(VDF-TrFE) Films with BaTiO3 Nanoparticles

We analyze the temperature dependences of the effective dielectric permittivity of P(VDF-TrFE) films with BaTiO3 nanoparticles (with the average size 24 nm). Transition from a weak to a strong nonlinear temperature dependence of the dielectric permittivity is observed near the freezing temperature (near -50 °C) of P(VDF-TrFE). The transition is followed by a diffuse step-like change in the temperature range (0 - 40)°C, and a subsequent maximum of the dielectric permittivity in the P(VDF-TrFE) films with a lower content (~20-40 vol.%) of BaTiO3 nanoparticles; or by a quasi-plateau of the dielectric permittivity in the P(VDF-TrFE) films with a higher content (~ 50-70 vol.%) of BaTiO3 nanoparticles. The frequency dispersion of the dielectric permittivity is significant in the vicinity of its maxima. The temperature-frequency shift of the permittivity region with a strong temperature dependence is positive. The temperature-frequency shift of the maxima is insignificant (or negative) for the P(VDF-TrFE) films with lower content of BaTiO3 nanoparticles. Increasing the content of BaTiO3 nanoparticles leads to a significant increase in the relative dielectric permittivity of the P(VDF-TrFE)-BaTiO3 films compared to pure P(VDF-TrFE) films (from 8 to 50 at 25 °C). At the same time, the voltage response of the studied P(VDF-TrFE)/BaTiO3 films to the frequency-modulated IR radiation flux has rather photoelectric than pyroelectric nature. A phenomenological model, which considers the screening charges at the interfaces, as well as dipole-dipole cross-interaction effects between the ferroelectric nanoparticles, is proposed to describe the temperature and frequency behavior of the effective dielectric permittivity. The negative capacitance state, which originates due to the interfacial effects, is predicted in the P(VDF-TrFE) films with a high content of BaTiO3 nanoparticles.

cond-mat.mtrl-sci↗

arXiv2024

Anomalous Behavior of the Dielectric and Pyroelectric Responses of Ferroelectric Fine-Grained Ceramics

We revealed the anomalous temperature behavior of the giant dielectric permittivity and unusual frequency dependences of the pyroelectric response of the fine-grained ceramics prepared by the spark plasma sintering of the ferroelectric BaTiO3 nanoparticles. The temperature dependences of the electro-resistivity indicate the frequency-dependent transition in the electro-transport mechanisms between the lower and higher conductivity states accompanied by the maximum in the temperature dependence of the loss angle tangent. The pyroelectric thermal-wave probing revealed the existence of the spatially inhomogeneous counter-polarized ferroelectric state at the opposite surfaces of the ceramic sample. We described the temperature behavior of the giant dielectric response and losses using the core-shell model for ceramic grains, effective medium approach and Maxwell-Wagner approach. The superparaelectric-like state with a giant dielectric response may appear due to the internal barrier-layer capacitance effect, while the step-like thermal activation of localized polarons in the semiconducting grains is not excluded. The elucidation of the state microscopic origin requires measurements in the frequency range above 1 MHz.

cond-mat.mtrl-sci↗