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Jurij Koruza

Publications and source records attributed to Jurij Koruza.

8 recordsLinked to original sources

How semiconducting are ferroelectrics: The fundamental, optical and transport gaps of Na$_{0.5}$Bi$_{0.5}$TiO$_3$-BaTiO$_3$ and NaNbO$_{3}$

The energy gap is a fundamental property of materials, directly related to their optical and electronic properties. The energy gap of ferroelectric compounds and its adjustment by compositional variation has particularly attracted attention in recent years due to potential application in energy conversion and/or catalytic devices. It is demonstrated that it is necessary to distinguish between the fundamental gap, $E_{\rm g}^{0}$, the optical gap, $E_{\rm g}^{\rm opt}$, and the transport gap, $E_{\rm g}^{\rm tr}$, of ferroelectrics, which can differ significantly. The situation is comparable to those in organic semiconductors and emerges from the presence of localized charges. The fundamental gap is a ground state property, i.e.\ the energy difference between the maximum of the fully occupied valence band and the minimum of the completely empty conduction band. In contrast, the optical and transport gaps are excited state properties involving localized (polaronic) electrons and/or holes at energies considerably different from the band edges. This work illustrates how the different energy gaps of ferroelectrics can be determined by combining optical measurements, X-ray photoelectron spectroscopy and temperature and oxygen partial pressure dependent electrical conductivity measurements. We determine fundamental gaps of $\approx 4.5\,$eV for both materials, optical gaps of $3.25-3.45\,$eV/$3.5\,$eV and electrical gaps of $\approx 1.4\,$eV/$3.3\,$eV for Na$_{0.5}$Bi$_{0.5}$TiO$_3$-BaTiO$_3$/NaNbO$_{3}$, respectively.

cond-mat.mtrl-sci

Towards understanding the defect properties in the multivalent A-site Na$_{0.5}$Bi$_{0.5}$TiO$_3$-based perovskite ceramics

A defect model involving cation and anion vacancies and anti-site defects is proposed that accounts for the non-stoichiometry of multi-valent $A$-site Na$_{0.5}$Bi$_{0.5}$TiO$_3$ based perovskite oxides with $ABO_3$ composition. A series of samples with varying $A$-site non-stoichiometry and $A$:$B$ ratios were prepared to investigate their electrical conductivity. The oxygen partial pressure and temperature dependent conductivities where studied with direct current (dc) and alternating current (ac) techniques, enabling to separate between ionic and electronic conduction. The Na-excess samples, regardless of the $A$:$B$ ratio, exhibit dominant ionic conductivity and $p$-type electronic conduction, with the highest total conductivity reaching $4 \times 10^{-4}$ S/cm at 450$^\circ$C. In contrast, the Bi-excess samples display more insulating characteristics and $n$-type electronic conductivity, with conductivity values within the 10$^{-8}$ S/cm range at 450$^\circ$C. These conductivity results strongly support the proposed defect model, which offers a straightforward description of defect chemistry in NBT-based ceramics and serves as a valuable guide for optimizing sample processing to achieve tailored properties.

cond-mat.mtrl-sci

Heterogeneous antiferroelectric ordering in NaNbO3-SrSnO3 ceramics revealed by direct superstructure imaging

NaNbO3-based antiferroelectric materials offer a promising pathway towards greener and more cost-effective energy storage devices. However, their intrinsic structural instabilities often lead to reduced energy density that compromises their performance and longevity. In this brief communication, we demonstrate how Dark-Field X-ray Microscopy, when carried out on the characteristically weak 1/4{843}pc superstructure reflection, can map the antiferroelectric phase and its strain heterogeneity in typically small, deeply-embedded grains of a NaNbO3 and 0.95NaNbO3-0.05SrSnO3 ceramics, representative of different phase transition behavior. Our results clearly evidences the stabilizing effect of SrSnO3 on the antiferroelectric phase by enhancing the degree of mesostructural order. In doing so, our method establishes a new platform for exploring the impact of disorder on the long-range strain heterogeneity within antiferroelectrics and other materials with modulated crystal structures.

cond-mat.mtrl-sci

Dynamic scaling properties of multistep polarization response in ferroelectrics

Ferroelectrics are multifunctional smart materials finding applications in sensor technology, micromechanical actuation, digital information storage etc. Their most fundamental property is the ability of polarization switching under applied electric field. In particular, understanding of switching kinetics is essential for digital information storage. In this regard, scaling properties of the temporal polarization response are well-known for 180°-switching processes in ferroelectrics characterized by a unique field-dependent local switching time. Unexpectedly, these properties were now observed in multiaxial polycrystalline ferroelectrics, exhibiting a number of parallel and sequential non-180°-switching processes with distinct switching times. This behaviour can be explained by a combination of the multistep stochastic mechanism and the inhomogeneous field mechanism models of polarization reversal. Scaling properties are predicted for polycrystalline ferroelectrics of tetragonal, rhombohedral and orthorhombic symmetries and exemplarily demonstrated by measurements of polarization kinetics in (K,Na)NbO3-based ferroelectric ceramic over a timescale of 7 orders of magnitude. Dynamic scaling properties allow insight into the microscopic switching mechanisms, on the one hand, and into statistical material characteristics, on the other hand, providing thereby the description of temporal polarization with high accuracy. The gained deeper insight into the mechanisms of multistep polarization switching is crucial for future ultrafast and multilevel digital information storage.

cond-mat.mtrl-sci

Multi-step stochastic mechanism of polarization reversal in orthorhombic ferroelectrics

A stochastic model of electric field-driven polarization reversal in orthorhombic ferroelectrics is advanced, providing a description of their temporal electromechanical response. The theory accounts for all possible parallel and sequential switching events. Application of the model to the simultaneous measurements of polarization and strain kinetics in a lead-free orthorhombic (K,Na)NbO3-based ferroelectric ceramic over a wide timescale of 7 orders of magnitude allowed identification of preferable polarization switching paths, fractions of individual switching processes, and their activation fields. Particularly, the analysis revealed substantial contributions of coherent non-180° switching events, which do not cause macroscopic strain and thus mimic 180° switching processes.

cond-mat.mtrl-sci

Multi-step stochastic mechanism of polarization reversal in rhombohedral ferroelectrics

A stochastic model for the field-driven polarization reversal in rhombohedral ferroelectrics is developed, providing a description of their temporal electromechanical response. Application of the model to simultaneous measurements of polarization and strain kinetics in a rhombohedral Pb(Zr,Ti)O3 ceramic over a wide time window allows identification of preferable switching paths, fractions of individual switching processes, and their activation fields. Complementary, the phenomenological Landau-Ginzburg-Devenshire theory is used to analyze the impact of external field and stress on switching barriers showing that residual mechanical stress may promote the fast switching.

cond-mat.mtrl-sci

Stochastic model of dispersive multi-step polarization switching in ferroelectrics due to spatial electric field distribution

A stochastic model for polarization switching in tetragonal ferroelectric ceramics is introduced, which includes sequential 90°- and parallel 180°-switching processes and accounts for the dispersion of characteristic switching times due to a nonuniform spatial distribution of the applied field. It presents merging of the recent multistep stochastic mechanism (MSM) with the earlier nucleation limited switching (NLS) and inhomogeneous field mechanism (IFM) models. The new model provides a much better description of simultaneous polarization and strain responses over a wide time window and a deeper insight into the microscopic switching mechanisms, as is exemplarily shown by comparison with measurements on lead zirconate titanate.

cond-mat.mtrl-sci

Enhancement of the electrocaloric cooling by electric field reversal: simulation and experiment

An improved thermodynamic cycle is proposed, where the cooling effect of an electrocaloric refrigerant is enhanced by applying a reversed electric field. In contrast to conventional adiabatic heating or cooling by on-off cycles of the external electric field, applying a reversed field is significantly improving the cooling efficiency, since the variation in configurational entropy is increased. By comparing results from computer simulations using Monte-Carlo algorithms and experiments using direct electrocaloric measurements, we show that the electrocaloric cooling efficiency can be enhanced by more than 20\% in standard ferroelectrics and also relaxor ferroelectrics, like Pb(Mg$_{1/3}$/Nb$_{2/3}$)$_{0.71}$Ti$_{0.29}$O$_3$.

physics.comp-ph