Yakov Kopelevich
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The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
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Yakov Kopelevich has a total of 271 co-authors. Here are the top co-authors by number of shared publications:
- Pablo Esquinazi
Division of Quantum Magnetism and Superconductivity, Felix-Bloch-Institute for Solid State Physics, University of Leipzig, 04103 Leipzig, Germany
34 shared publications - Robson Ricardo da Silva
Univ Estadual Campinas, UNICAMP, Inst Fis Gleb Wataghin, BR-13083859 Campinas, SP, Brazil
32 shared publications S. Moehlecke
Instituto de Física "Gleb Wataghin" Universidade Estadual de Campinas 13083-859 Campinas São Paulo Unicamp Brasil
28 shared publicationsJ. H. S. Torres
Instituto de Física, Universidade Estadual de Campinas, Unicamp 13083-970, Campinas, São Paulo, Brazil
9 shared publications- Bruno Cury Camargo
University of Warsaw, Faculty of Physics, Pasteura 5, 02-093 Warsaw, Poland
6 shared publications A. Gupta
Physikalisches Institut, Universität Bayreuth, 95440 Bayreuth, Germany
5 shared publications
Latest Publications
- 28 August 2026
- Published by American Physical Society (APS) in Physical Review Materials
- Vol. 10 (8) , 084410
Role of defects in the paramagnetism of Fe-doped Cs 2 AgBiBr 6 double perovskite
Transition-metal doping enables the introduction of spin functionality into halide double perovskites, while simultaneously modifying optical properties. Here, we combine controlled single-crystal growth, optical characterization, comprehensive electron paramagnetic resonance (EPR) spectroscopy, and first-principles modeling to identify the microscopic nature of Fe-related centers in Fe-doped ${\mathrm{Cs}}_{2}{\mathrm{AgBiBr}}_{6}$. Single crystals with nominal $\mathrm{F}{\mathrm{e}}^{3+}$ concentrations up to 15% in the precursor stage were grown using a controlled-cooling method, yielding reproducible Fe incorporation up to 0.1% with respect to Bi, without secondary phases. Despite this low concentration, Fe doping introduces electronic states that influence optical absorption and photoluminescence. EPR measurements reveal an S = 5/2 $\mathrm{F}{\mathrm{e}}^{3+}$-related center whose anisotropy follows the cubic-to-tetragonal phase transition below 120 K. Angular-dependent EPR resolves two configurations of this nearly axial spin center, with principal axes rotated by 90\ifmmode^\circ\else\textdegree\fi{} and aligned with the a/b plane of the tetragonal lattice. Density-functional calculations attribute these centers to impurity-vacancy complexes, most likely ${\mathrm{Fe}}_{\mathrm{Bi}}\text{\ensuremath{-}}{\mathrm{V}}_{\mathrm{Br}}$, that stabilize in a basal configuration of the low-temperature phase. This approach resolves vacancy-coupled defect orientations, narrowing possible models to $\mathrm{F}{\mathrm{e}}^{3+}$-vacancy complexes and establishing them as stable, orientation-sensitive spin probes of structural symmetry in halide double perovskites, while providing a microscopic basis for tuning their magnetic and optical responses.- 28 August 2026
- Published by American Physical Society (APS) in Physical Review Materials
- Vol. 10 (8) , 084410
Role of defects in the paramagnetism of Fe-doped Cs 2 AgBiBr 6 double perovskite
Transition-metal doping enables the introduction of spin functionality into halide double perovskites, while simultaneously modifying optical properties. Here, we combine controlled single-crystal growth, optical characterization, comprehensive electron paramagnetic resonance (EPR) spectroscopy, and first-principles modeling to identify the microscopic nature of Fe-related centers in Fe-doped ${\mathrm{Cs}}_{2}{\mathrm{AgBiBr}}_{6}$. Single crystals with nominal $\mathrm{F}{\mathrm{e}}^{3+}$ concentrations up to 15% in the precursor stage were grown using a controlled-cooling method, yielding reproducible Fe incorporation up to 0.1% with respect to Bi, without secondary phases. Despite this low concentration, Fe doping introduces electronic states that influence optical absorption and photoluminescence. EPR measurements reveal an S = 5/2 $\mathrm{F}{\mathrm{e}}^{3+}$-related center whose anisotropy follows the cubic-to-tetragonal phase transition below 120 K. Angular-dependent EPR resolves two configurations of this nearly axial spin center, with principal axes rotated by 90\ifmmode^\circ\else\textdegree\fi{} and aligned with the a/b plane of the tetragonal lattice. Density-functional calculations attribute these centers to impurity-vacancy complexes, most likely ${\mathrm{Fe}}_{\mathrm{Bi}}\text{\ensuremath{-}}{\mathrm{V}}_{\mathrm{Br}}$, that stabilize in a basal configuration of the low-temperature phase. This approach resolves vacancy-coupled defect orientations, narrowing possible models to $\mathrm{F}{\mathrm{e}}^{3+}$-vacancy complexes and establishing them as stable, orientation-sensitive spin probes of structural symmetry in halide double perovskites, while providing a microscopic basis for tuning their magnetic and optical responses.- 7 April 2025
- Published by IOP Publishing in Engineering Research Express
- Vol. 7 (2) , 025307
A versatile custom-built contact switching device for multi-purpose electrical transport measurements
This work outlines the assembly of a cost-effective and straightforward apparatus designed to automate contact switching for electrical transport measurements. We report example of applications for this custom device and showcase its versatility by employing it for electrical resistivity and Hall effect measurements following the van der Pauw method on oxygen-deficient strontium titanate single crystals, measurements on compressed bismuth using the Montgomery method, and measurements on fresh cleaved Highly Oriented Pyrolytic Graphite using a multi-line electrode configuration.
- 7 April 2025
- Published by IOP Publishing in Engineering Research Express
- Vol. 7 (2) , 025307
A versatile custom-built contact switching device for multi-purpose electrical transport measurements
This work outlines the assembly of a cost-effective and straightforward apparatus designed to automate contact switching for electrical transport measurements. We report example of applications for this custom device and showcase its versatility by employing it for electrical resistivity and Hall effect measurements following the van der Pauw method on oxygen-deficient strontium titanate single crystals, measurements on compressed bismuth using the Montgomery method, and measurements on fresh cleaved Highly Oriented Pyrolytic Graphite using a multi-line electrode configuration.
- 22 July 2024
- Published by Wiley in Physica Status Solidi (RRL) – Rapid Research Letters
- Vol. 18 (12) , 2400122
Ferroelectricity‐Induced Surface Ferromagnetism in Core–Shell Magnetoelectric Nanoparticles
Magnetoelectric nanoparticles (NPs) present an important class of nanomaterials with a wide interest in piezocatalytic and biomedical applications. Herein, the results of magnetoelectric and magnetization measurements performed on core–shell NPs having magnetic core (MnFe2O4, MFO) and ferroelectric shell (Ba0.85Ca0.15Ti0.5Zr0.5O3, BCZT) synthesized by the microwave hydrothermal method are reported. Magnetic results are compared with the measurements on reference MFO NPs prepared under identical conditions. Detailed SQUID magnetometer measurements of the magnetization hysteresis loops M(H) down to 2 K reveal the existence of a clear exchange bias effect in pure MFO NPs attributed to the coexistence of ferromagnetic and antiferromagnetic short‐range interactions. When the magnetic core is covered by the thin ferroelectric BCZT shell, it is observed that 1) the shell suppresses the apparent bias effect and 2) induces an “extra” ferromagnetic magnetization at T < 20 K. The results indicate that this “extra” ferromagnetism has a 2D character and it is most likely related to the interface interactions between the MFO core and BCZT shell. Ferroelectric properties and strong magnetoelectric effect in core–shell NPs are revealed via piezoresponse force microscopy under magnetic field. The mechanisms of the observed effects are discussed.
- 22 July 2024
- Published by Wiley in Physica Status Solidi (RRL) – Rapid Research Letters
- Vol. 18 (12) , 2400122
Ferroelectricity‐Induced Surface Ferromagnetism in Core–Shell Magnetoelectric Nanoparticles
Magnetoelectric nanoparticles (NPs) present an important class of nanomaterials with a wide interest in piezocatalytic and biomedical applications. Herein, the results of magnetoelectric and magnetization measurements performed on core–shell NPs having magnetic core (MnFe2O4, MFO) and ferroelectric shell (Ba0.85Ca0.15Ti0.5Zr0.5O3, BCZT) synthesized by the microwave hydrothermal method are reported. Magnetic results are compared with the measurements on reference MFO NPs prepared under identical conditions. Detailed SQUID magnetometer measurements of the magnetization hysteresis loops M(H) down to 2 K reveal the existence of a clear exchange bias effect in pure MFO NPs attributed to the coexistence of ferromagnetic and antiferromagnetic short‐range interactions. When the magnetic core is covered by the thin ferroelectric BCZT shell, it is observed that 1) the shell suppresses the apparent bias effect and 2) induces an “extra” ferromagnetic magnetization at T < 20 K. The results indicate that this “extra” ferromagnetism has a 2D character and it is most likely related to the interface interactions between the MFO core and BCZT shell. Ferroelectric properties and strong magnetoelectric effect in core–shell NPs are revealed via piezoresponse force microscopy under magnetic field. The mechanisms of the observed effects are discussed.
- Open Access
Global room-temperature superconductivity in graphite
Room temperature superconductivity under normal conditions has been a major challenge of physics and material science since its very discovery. Here we report the global room-temperature superconductivity observed in cleaved highly oriented pyrolytic graphite carrying dense arrays of nearly parallel surface line defects. The multiterminal measurements performed at the ambient pressure in the temperature interval 4.5 K < T < 300 K and at magnetic fields 0 < B < 9 T applied perpendicular to the basal graphitic planes reveal that the superconducting critical current I_c(T,B) is governed by the normal state resistance RN(T, B) so that I_c(T,B) is proportional to 1/R_N(T, B). Magnetization M(T, B) measurements of superconducting screening and hysteresis loops together with the critical current oscillations with temperature that are characteristic for superconductor-ferromagnet-superconductor Josephson chains, provide strong support for occurrence of superconductivity at T > 300 K. We develop a theory of global superconductivity emerging in the array of linear structural defects which well describes the experimental findings and demonstrate that global superconductivity arises as a global phase coherence of superconducting granules in linear defects promoted by the stabilizing effect of underlying Bernal graphite via tunneling coupling to the three dimensional (3D) material.
Open AccessGlobal room-temperature superconductivity in graphite
Room temperature superconductivity under normal conditions has been a major challenge of physics and material science since its very discovery. Here we report the global room-temperature superconductivity observed in cleaved highly oriented pyrolytic graphite carrying dense arrays of nearly parallel surface line defects. The multiterminal measurements performed at the ambient pressure in the temperature interval 4.5 K < T < 300 K and at magnetic fields 0 < B < 9 T applied perpendicular to the basal graphitic planes reveal that the superconducting critical current I_c(T,B) is governed by the normal state resistance RN(T, B) so that I_c(T,B) is proportional to 1/R_N(T, B). Magnetization M(T, B) measurements of superconducting screening and hysteresis loops together with the critical current oscillations with temperature that are characteristic for superconductor-ferromagnet-superconductor Josephson chains, provide strong support for occurrence of superconductivity at T > 300 K. We develop a theory of global superconductivity emerging in the array of linear structural defects which well describes the experimental findings and demonstrate that global superconductivity arises as a global phase coherence of superconducting granules in linear defects promoted by the stabilizing effect of underlying Bernal graphite via tunneling coupling to the three dimensional (3D) material.
- Open Access
Enhanced RCP and large inverse magnetocaloric effect of CoFe$_2$O$_4$ nanoparticles synthesized by auto-combustion method
This work focuses on the microstructure, magnetic properties and magnetocaloric effect of CoFe$_2$O$_4$ (CFO) nanoparticles elaborated by sol-gel auto combustion method. The XRD investigation indicates that CFO is crystallized in a cubic spinel structure and the SEM micrograph shows a fine quasi-spherical with an average grain sizes of 160 nm. The temperature dependence of the Raman spectra reveals the ferromagnetic to paramagnetic (FM-PM) transition started from 723 K and the magnetization versus temperature measurements shows the Curie temperature located at T$_{\rm C}$ = 785 K. Large value of magnetocaloric temperature change of $\Delta$T =11.2 K with a high RCP of 687.56 J Kg$^{-1}$ are achieved indirectly via the Maxwell approach making our CFO nanopowder suitable candidate for both environmentally friendly magnetic refrigeration and medical applications at ambient temperature.Open AccessEnhanced RCP and large inverse magnetocaloric effect of CoFe$_2$O$_4$ nanoparticles synthesized by auto-combustion method
This work focuses on the microstructure, magnetic properties and magnetocaloric effect of CoFe$_2$O$_4$ (CFO) nanoparticles elaborated by sol-gel auto combustion method. The XRD investigation indicates that CFO is crystallized in a cubic spinel structure and the SEM micrograph shows a fine quasi-spherical with an average grain sizes of 160 nm. The temperature dependence of the Raman spectra reveals the ferromagnetic to paramagnetic (FM-PM) transition started from 723 K and the magnetization versus temperature measurements shows the Curie temperature located at T$_{\rm C}$ = 785 K. Large value of magnetocaloric temperature change of $\Delta$T =11.2 K with a high RCP of 687.56 J Kg$^{-1}$ are achieved indirectly via the Maxwell approach making our CFO nanopowder suitable candidate for both environmentally friendly magnetic refrigeration and medical applications at ambient temperature. - Open Access
- 3 June 2020
- Published by Institute of Electrical and Electronics Engineers (IEEE) in IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control
- Vol. 67 (10) , 2142-2147
Piezoelectric Actuation of Graphene-Coated Polar Structures
Ferroelectric materials based on lead zirconate titanate (PZT) are widely used as sensors and actuators because of their strong piezoelectric activity. However, their application is limited because of the high processing temperature, brittleness, lack of conformal deposition, and a limited possibility to be integrated with the microelectromechanical systems (MEMS). Recent studies on the piezoelectricity in the 2-D materials have demonstrated their potential in these applications, essentially due to their flexibility and integrability with the MEMS. In this work, we deposited a few layer graphene (FLG) on the amorphous oxidized Si 3 N 4 membranes and studied their piezoelectric response by sensitive laser interferometry and rigorous finite-element modeling (FEM) analysis. Modal analysis by FEM and comparison with the experimental results show that the driving force for the piezoelectric-like response can be a polar interface layer formed between the residual oxygen in Si 3 N 4 and the FLG. The response was about 14 nm/V at resonance and could be further enhanced by adjusting the geometry of the device. These phenomena are fully consistent with the earlier piezoresponse force microscopy (PFM) observations of the piezoelectricity of the graphene on SiO 2 and open up an avenue for using graphene-coated structures in the MEMS.
- 3 June 2020
- Published by Institute of Electrical and Electronics Engineers (IEEE) in IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control
- Vol. 67 (10) , 2142-2147
Open AccessPiezoelectric Actuation of Graphene-Coated Polar Structures
Ferroelectric materials based on lead zirconate titanate (PZT) are widely used as sensors and actuators because of their strong piezoelectric activity. However, their application is limited because of the high processing temperature, brittleness, lack of conformal deposition, and a limited possibility to be integrated with the microelectromechanical systems (MEMS). Recent studies on the piezoelectricity in the 2-D materials have demonstrated their potential in these applications, essentially due to their flexibility and integrability with the MEMS. In this work, we deposited a few layer graphene (FLG) on the amorphous oxidized Si 3 N 4 membranes and studied their piezoelectric response by sensitive laser interferometry and rigorous finite-element modeling (FEM) analysis. Modal analysis by FEM and comparison with the experimental results show that the driving force for the piezoelectric-like response can be a polar interface layer formed between the residual oxygen in Si 3 N 4 and the FLG. The response was about 14 nm/V at resonance and could be further enhanced by adjusting the geometry of the device. These phenomena are fully consistent with the earlier piezoresponse force microscopy (PFM) observations of the piezoelectricity of the graphene on SiO 2 and open up an avenue for using graphene-coated structures in the MEMS.
- 1 December 2019
- Published by Elsevier in Journal of Magnetism and Magnetic Materials
- Vol. 491
Unconventional spin-glass-like state in AgCo2V3O10, the novel magnetically frustrated material
- 1 December 2019
- Published by Elsevier in Journal of Magnetism and Magnetic Materials
- Vol. 491
Unconventional spin-glass-like state in AgCo2V3O10, the novel magnetically frustrated material
- Open Access
Unconventional Spin-Glass-Like State in AgCo2V3O10, the Novel Magnetically Frustrated Material
Single crystals of a new silver and-cobalt based vanadate AgCo2V3O10 were grown from a melted mixture. The crystal structure determination reveals that this new vanadate crystallizes in triclinic system with space group P-1. The structure of the titled compound is constructed from CoO6octahedra and VO4 tetrahedra sharing edges and vertices leading to an open three-dimensional framework delimiting tunnels along [001], where the Ag cations are located. The bands observed in Raman spectrum were assigned to corresponding vibrations of the VO4 groups. DC and AC magnetization (susceptibility) measurements revealed the spin-glass (SG) -type transition below a frequency-independent temperature Tf(H) that is nearly independent on the applied magnetic field. Magnetic field H> 10 kOe induces the spin glass antiferromagnet. These observations brings AgCo2V3O10 into the class of geometrically frustrated magnetic systems.
Open AccessUnconventional Spin-Glass-Like State in AgCo2V3O10, the Novel Magnetically Frustrated Material
Single crystals of a new silver and-cobalt based vanadate AgCo2V3O10 were grown from a melted mixture. The crystal structure determination reveals that this new vanadate crystallizes in triclinic system with space group P-1. The structure of the titled compound is constructed from CoO6octahedra and VO4 tetrahedra sharing edges and vertices leading to an open three-dimensional framework delimiting tunnels along [001], where the Ag cations are located. The bands observed in Raman spectrum were assigned to corresponding vibrations of the VO4 groups. DC and AC magnetization (susceptibility) measurements revealed the spin-glass (SG) -type transition below a frequency-independent temperature Tf(H) that is nearly independent on the applied magnetic field. Magnetic field H> 10 kOe induces the spin glass antiferromagnet. These observations brings AgCo2V3O10 into the class of geometrically frustrated magnetic systems.
- 15 August 2019
- Published by Institute of Electrical and Electronics Engineers (IEEE) in IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control
- Vol. 66 (12) , 1935-1941
Structural, Dielectric, and Magnetic Properties of Multiferroic ($1 - x$ ) La0.5Ca0.5MnO3-($x$ ) BaTi0.8Sn0.2O3 Laminated Composites
High performance lead-free multiferroic composites are desired to replace the lead-based ceramics in multifunctional devices applications. Laminated compounds were prepared from ferroelectric and ferromagnetic materials. In this work, we present laminated ceramics compound by considering the ferromagnetic La0.5Ca0.5MnO3 (LCMO) and the ferroelectric BaTi0.8Sn0.2O3 (BTSO) in two different proportions. Compounds (1-x) LCMO-(x) BTSO with x=1 and 0 (pure materials) were synthesized by the sol gel method and x=0.7 and 0.5 (laminated) compounds were elaborated by welding appropriate mass ratios of each pure material by using the silver paste technique. Structural, dielectric, ferroelectric, microstructure and magnetic characterization were conducted on these samples. X-ray scattering results showed pure perovskite phases confirming the successful formation of both LCMO and BTSO. SEM images evidenced the laminated structure and good quality of the interfaces. The laminated composite materials have demonstrated a multiferroic behavior characterized by the ferroelectric and the ferromagnetic hysteresis loops. Furthermore, the enhancement of the dielectric constant in the laminated composite samples is mainly attributed to the Maxwell-Wagner polarization.
- 15 August 2019
- Published by Institute of Electrical and Electronics Engineers (IEEE) in IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control
- Vol. 66 (12) , 1935-1941
Structural, Dielectric, and Magnetic Properties of Multiferroic ($1 - x$ ) La0.5Ca0.5MnO3-($x$ ) BaTi0.8Sn0.2O3 Laminated Composites
High performance lead-free multiferroic composites are desired to replace the lead-based ceramics in multifunctional devices applications. Laminated compounds were prepared from ferroelectric and ferromagnetic materials. In this work, we present laminated ceramics compound by considering the ferromagnetic La0.5Ca0.5MnO3 (LCMO) and the ferroelectric BaTi0.8Sn0.2O3 (BTSO) in two different proportions. Compounds (1-x) LCMO-(x) BTSO with x=1 and 0 (pure materials) were synthesized by the sol gel method and x=0.7 and 0.5 (laminated) compounds were elaborated by welding appropriate mass ratios of each pure material by using the silver paste technique. Structural, dielectric, ferroelectric, microstructure and magnetic characterization were conducted on these samples. X-ray scattering results showed pure perovskite phases confirming the successful formation of both LCMO and BTSO. SEM images evidenced the laminated structure and good quality of the interfaces. The laminated composite materials have demonstrated a multiferroic behavior characterized by the ferroelectric and the ferromagnetic hysteresis loops. Furthermore, the enhancement of the dielectric constant in the laminated composite samples is mainly attributed to the Maxwell-Wagner polarization.