arXiv subjects

N. Pavlenko

Publications and source records attributed to N. Pavlenko.

12 recordsLinked to original sources

arXiv2016

Hydrostatic pressure response of an oxide two-dimensional electron system

Two-dimensional electron systems with fascinating properties exist in multilayers of standard semiconductors, on helium surfaces, and in oxides. Compared to the two-dimensional (2D) electron gases of semiconductors, the 2D electron systems in oxides are typically more strongly correlated and more sensitive to the microscopic structure of the hosting lattice. This sensitivity suggests that the oxide 2D systems are highly tunable by hydrostatic pressure. Here we explore the effects of hydrostatic pressure on the well-characterized 2D electron system formed at LaAlO$_{3}$ -SrTiO$_{3}$ interfaces[1] and measure a pronounced, unexpected response. Pressure of $\sim$2 GPa reversibly doubles the 2D carrier density $n_{s}$ at 4 K. Along with the increase of $n_{s}$, the conductivity and mobility are reduced under pressure. First-principles pressure simulations reveal the same behavior of the carrier density and suggest a possible mechanism of the mobility reduction, based on the dielectric properties of both materials and their variation under external pressure.

cond-mat.str-el↗

arXiv2013

Emerging magnetism and electronic phase separation at titanate interfaces

The emergence of magnetism in otherwise nonmagnetic compounds and its underlying mechanisms have become the subject of intense research. Here we demonstrate that the nonmagnetic oxygen vacancies are responsible for an unconventional magnetic state common for titanate interfaces and surfaces. Using an effective multiorbital modelling, we find that the presence of localized vacancies leads to an interplay of ferromagnetic order in the itinerant t2g band and complex magnetic oscillations in the orbitally-reconstructed eg-band, which can be tuned by gate fields at oxide interfaces. The magnetic phase diagram includes highly fragmented regions of stable and phase-separated magnetic states forming beyond nonzero critical defect concentrations.

cond-mat.mes-hall↗

arXiv2013

Direct k-space mapping of the electronic structure in an oxide-oxide interface

The interface between LaAlO3 and SrTiO3 hosts a two-dimensional electron system of itinerant carriers, although both oxides are band insulators. Interface ferromagnetism coexisting with superconductivity has been found and attributed to local moments. Experimentally, it has been established that Ti 3d electrons are confined to the interface. Using soft x-ray angle-resolved resonant photoelectron spectroscopy we have directly mapped the interface states in k-space. Our data demonstrate a charge dichotomy. A mobile fraction contributes to Fermi surface sheets, whereas a localized portion at higher binding energies is tentatively attributed to electrons trapped by O-vacancies in the SrTiO3. While photovoltage effects in the polar LaAlO3 layers cannot be excluded, the apparent absence of surface-related Fermi surface sheets could also be fully reconciled in a recently proposed electronic reconstruction picture where the built-in potential in the LaAlO3 is compensated by surface O-vacancies serving also as charge reservoir.

cond-mat.str-el↗

arXiv2012

Oxygen vacancies at titanate interfaces: two-dimensional magnetism and orbital reconstruction

We show that oxygen vacancies at titanate interfaces induce a complex multiorbital reconstruction which involves a lowering of the local symmetry and an inversion of t2g and eg orbitals resulting in the occupation of the eg orbitals of Ti atoms neighboring the O vacancy. The orbital reconstruction depends strongly on the clustering of O vacancies and can be accompanied by a magnetic splitting between the local eg orbitals with lobes directed towards the vacancy and interface dxy orbitals. The reconstruction generates a two-dimensional interface magnetic state not observed in bulk SrTiO3. Using generalized gradient approximation (LSDA) with intra-atomic Coulomb repulsion (GGA+U), we find that this magnetic state is common for titanate surfaces and interfaces.

cond-mat.str-el↗

arXiv2012

Magnetism and superconductivity at LAO/STO-interfaces: the role of Ti 3d interface electrons

Ferromagnetism and superconductivity are in most cases adverse. However, recent experiments reveal that they coexist at interfaces of LaAlO3 and SrTiO3. We analyze the magnetic state within density functional theory and provide evidence that magnetism is not an intrinsic property of the two-dimensional electron liquid at the interface. We demonstrate that the robust ferromagnetic state is induced by the oxygen vacancies in SrTiO3- or in the LaAlO3-layer. This allows for the notion that areas with increased density of oxygen vacancies produce ferromagnetic puddles and account for the previous observation of a superparamagnetic behavior in the superconducting state.

cond-mat.str-el↗

arXiv2011

Interstitial Fe-Cr alloys: Tuning of magnetism by nanoscale structural control and by implantation of nonmagnetic atoms

Using the density functional theory, we perform a full atomic relaxation of the bulk ferrite with 12.5%-concentration of monoatomic interstitial Cr periodically located at the edges of the bcc Fe$_α$ cell. We show that structural relaxation in such artificially engineered alloys leads to significant atomic displacements and results in the formation of novel highly stable configurations with parallel chains of octahedrically arranged Fe. The enhanced magnetic polarization in the low-symmetry metallic state of this type of alloys can be externally controlled by additional inclusion of nonmagnetic impurities like nitrogen. We discuss possible applications of generated interstitial alloys in spintronic devices and propose to consider them as a basis of novel durable types of stainless steels.

cond-mat.mtrl-sci↗

arXiv2011

Hydrogen transport in superionic system Rb3H(SeO4)2: a revised cooperative migration mechanism

We performed density functional studies of electronic properties and mechanisms of hydrogen transport in Rb3H(SeO4)2 crystal which represents technologically promising class M3H(XO4)2 of proton conductors (M=Rb,Cs, NH4; X=S,Se). The electronic structure calculations show a decisive role of lattice dynamics in the process of proton migration. In the obtained revised mechanism of proton transport, the strong displacements of the vertex oxygens play a key role in the establishing the continuous hydrogen transport and in the achieving low activation energies of proton conduction which is in contrast to the standard two-stage Grotthuss mechanism of proton transport. Consequently, any realistic model description of proton transport should inevitably involve the interactions with the sublattice of the XO4 groups.

cond-mat.stat-mech↗

arXiv2010

Two-dimensional electron liquid state at LaAlO3-SrTiO3 interfaces

Using tunneling spectroscopy we have measured the spectral density of states of the mobile, two-dimensional electron system generated at the LaAlO3-SrTiO3 interface. As shown by the density of states the interface electron system differs qualitatively, first, from the electron systems of the materials defining the interface and, second, from the two-dimensional electron gases formed at interfaces between conventional semiconductors.

cond-mat.mtrl-sci↗

arXiv2006

Interface hole-doping in cuprate-titanate superlattices

The electronic structure of interfaces between YBa$_2$Cu$_3$O$_6$ and SrTiO$_3$ is studied using local spin density approximation (LSDA) with intra-atomic Coulomb repulsion (LSDA+U). We find a metallic state in cuprate/titanate heterostructures with the hole carriers concentrated substantially in the CuO$_2$-layers and in the first interface TiO$_2$ and SrO planes. This effective interface doping appears due to the polarity of interfaces, caused by the first incomplete copper oxide unit cell. Interface-induced high pre-doping of CuO$_2$-layers is a key mechanism controlling the superconducting properties in engineered field-effect devices realized on the basis of cuprate/titanate superlattices.

cond-mat.str-el↗

arXiv2003

Electron-Polarization Coupling in Superconductor-Ferroelectric Superlattices

We present a phenomenological model of periodic ferroelectric-superconductor (FE-S) heterostructures containing two alternating ferroelectric and superconducting layers. The interaction at the FE-S contacts is described as a coupling of the local carrier density of the superconductor with the spontaneous ferroelectric polarization near the FE-S interface. We obtain a stable symmetric domain-type phase exhibiting a contact-induced polarization and the ferroelectric domain structure at temperatures above the bulk ferroelectric transition temperature. With an increasing coupling energy, we find the appearance of the ferroelectric phase coexisting with the suppressed superconductivity in the S-film. The system is analyzed for different thicknesses of the FE- and S-films demonstrating the dramatic change of the topology of the phase diagrams with a variation of the layers thickness. The results are expected to shed light on the processes occurring in high-temperature superconducting films grown on perovskite alloy-substrates exhibiting ferroelectric properties at lower temperatures.

cond-mat.stat-mech↗

arXiv2003

Crossover between mean-field and Ising critical behavior in a lattice-gas reaction-diffusion model

Lattice-gas models for CO oxidation can exhibit a discontinuous nonequilibrium transition between reactive and inactive states, which disappears above a critical CO-desorption rate. Using finite-size-scaling analysis, we demonstrate a crossover from Ising to mean-field behavior at the critical point, with increasing surface mobility of adsorbed CO or with decreasing system size. This behavior is elucidated by analogy with that of equilibrium Ising-type systems with long-range interactions.

cond-mat.stat-mech↗

arXiv2001

Catalytic CO Oxidation on Nanoscale Pt Facets: Effect of Inter-Facet CO Diffusion on Bifurcation and Fluctuation Behavior

We present lattice-gas modeling of the steady-state behavior in CO oxidation on the facets of nanoscale metal clusters, with coupling via inter-facet CO diffusion. The model incorporates the key aspects of reaction process, such as rapid CO mobility within each facet, and strong nearest-neighbor repulsion between adsorbed O. The former justifies our use a "hybrid" simulation approach treating the CO coverage as a mean-field parameter. For an isolated facet, there is one bistable region where the system can exist in either a reactive state (with high oxygen coverage) or a (nearly CO-poisoned) inactive state. Diffusion between two facets is shown to induce complex multistability in the steady states of the system. The bifurcation diagram exhibits two regions with bistabilities due to the difference between adsorption properties of the facets. We explore the role of enhanced fluctuations in the proximity of a cusp bifurcation point associated with one facet in producing transitions between stable states on that facet, as well as their influence on fluctuations on the other facet. The results are expected to shed more light on the reaction kinetics for supported catalysts.

cond-mat.stat-mech↗