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Physics and Astronomy Condensed Matter Seminar

Tuning Transport and Magnetism at Polar Oxide Interfaces

Prof. Divine Kumah

Department of Physics

North Carolina State University

Host: Gannon

Title: Tuning Transport and Magnetism at Polar Oxide Interfaces

Abstract: Atomic-scale interactions at the interfaces between polar and non-polar transition metal oxides have led to the realization of exciting phenomena including two-dimensional electron gases, superconductivity and interfacial magnetism. However, these interactions may lead to the suppression of electronic and magnetic ordering at interfaces with strong structure-property relationships. By imaging the atomic structure of the interface between polar LaSrMnO3 (LSMO) and non-polar SrTiO3, we identify interfacial structural distortions which are correlated with thickness-dependent metal-insulator and ferromagnetic-paramagnetic transitions in the rare-earth manganites. We show that these structural distortions can be tuned by inserting polarity-matched spacer layers at the LSMO interfaces leading to a stabilization of ferromagnetism in LSMO layers as thin as two unit cells. The stabilized magnetism is found to be independent of strain. We employ a combination of synchrotron X-ray diffraction, temperature-dependent magnetization measurements and X-ray magnetic circular dichroism to elucidate the interplay between structural and spin degrees of freedom in the rare-earth manganites.[1,2] Additionally, we find that by tuning growth and post-growth processing conditions, a two-dimensional electron gas (2DEG) forms at the interface between antiferromagnetic LaCrO3 and SrTiO3 providing a route to design all-oxide heterostructures which couple magnetic ordering with the mobile carriers within the 2DEG.[3] These results demonstrate the intimate role of picometer-scale structural distortions on the physical properties of transition metal oxides and have important implications for designing novel quantum materials.



References



[1] Koohfar et. al., npj Quantum Materials 4 (1), 25 (2019)

[2] Koohfar et. al., Physical Review B 101 (6), 064420 (2020)

[3] Al-Tawhid et. al., AIP Advances 10 (4), 045132 (2020)

Date:
-
Location:
Zoom

Tuning Transport and Magnetism at Polar Oxide Interfaces

Prof. Divine Kumah

Department of Physics

North Carolina State University

Host: Gannon

Title: Tuning Transport and Magnetism at Polar Oxide Interfaces

Abstract: Atomic-scale interactions at the interfaces between polar and non-polar transition metal oxides have led to the realization of exciting phenomena including two-dimensional electron gases, superconductivity and interfacial magnetism. However, these interactions may lead to the suppression of electronic and magnetic ordering at interfaces with strong structure-property relationships. By imaging the atomic structure of the interface between polar LaSrMnO3 (LSMO) and non-polar SrTiO3, we identify interfacial structural distortions which are correlated with thickness-dependent metal-insulator and ferromagnetic-paramagnetic transitions in the rare-earth manganites. We show that these structural distortions can be tuned by inserting polarity-matched spacer layers at the LSMO interfaces leading to a stabilization of ferromagnetism in LSMO layers as thin as two unit cells. The stabilized magnetism is found to be independent of strain. We employ a combination of synchrotron X-ray diffraction, temperature-dependent magnetization measurements and X-ray magnetic circular dichroism to elucidate the interplay between structural and spin degrees of freedom in the rare-earth manganites.[1,2] Additionally, we find that by tuning growth and post-growth processing conditions, a two-dimensional electron gas (2DEG) forms at the interface between antiferromagnetic LaCrO3 and SrTiO3 providing a route to design all-oxide heterostructures which couple magnetic ordering with the mobile carriers within the 2DEG.[3] These results demonstrate the intimate role of picometer-scale structural distortions on the physical properties of transition metal oxides and have important implications for designing novel quantum materials.



References



[1] Koohfar et. al., npj Quantum Materials 4 (1), 25 (2019)

[2] Koohfar et. al., Physical Review B 101 (6), 064420 (2020)

[3] Al-Tawhid et. al., AIP Advances 10 (4), 045132 (2020)

Date:
-
Location:
Zoom

Nanoscale Magnetometry Using Nitrogen Vacancies in Diamond

Dr. Andrew Mounce

Center For Integrated Nanotechnologies

Sandia National Laboratory

Host: Gannon

Title:  Nanoscale Magnetometry Using Nitrogen Vacancies in Diamond

Abstract: The properties that make nitrogen vacancies in diamond (NVs) good qubits, for example long coherence times at room temperature, also make them excellent sensors for magnetic fields. In this presentation, I will discuss the properties of nitrogen vacancies and how to utilize them for magnetometry of devices and materials with DC magnetic fields and fluctuating fields up to GHz frequencies. To be useful as sensors, NVs must be activated close to the surface of diamond but near the surface nitrogen has a low probability of incorporating with a vacancy to create a magnetically sensitive NV defect. With this in mind, I will present our efforts toward improving NV activation yield to optimize sensitivity.  Finally, I will discuss our recent results as examples of the utility of using nitrogen vacancies for wide-field magnetic imaging for applied physics problems and NV detected nuclear magnetic resonance toward fundamental physics problems.

Date:
-
Location:
Zoom

Nanoscale Magnetometry Using Nitrogen Vacancies in Diamond

Dr. Andrew Mounce

Center For Integrated Nanotechnologies

Sandia National Laboratory

Host: Gannon

Title:  Nanoscale Magnetometry Using Nitrogen Vacancies in Diamond

Abstract: The properties that make nitrogen vacancies in diamond (NVs) good qubits, for example long coherence times at room temperature, also make them excellent sensors for magnetic fields. In this presentation, I will discuss the properties of nitrogen vacancies and how to utilize them for magnetometry of devices and materials with DC magnetic fields and fluctuating fields up to GHz frequencies. To be useful as sensors, NVs must be activated close to the surface of diamond but near the surface nitrogen has a low probability of incorporating with a vacancy to create a magnetically sensitive NV defect. With this in mind, I will present our efforts toward improving NV activation yield to optimize sensitivity.  Finally, I will discuss our recent results as examples of the utility of using nitrogen vacancies for wide-field magnetic imaging for applied physics problems and NV detected nuclear magnetic resonance toward fundamental physics problems.

Date:
-
Location:
Zoom

Fission induced vortex lattice disordering in UPt3

Prof. Morten Eskildsen

Department of Physics

University of Notre Dame

Host: Gannon

Title: Fission induced vortex lattice disordering in UPt3

Abstract:  Subjecting a type-II superconductor to a magnetic field will cause the formations of quantized vortices.  Due to their repulsive interaction the vortices will, in an ideal situation, arrange themselves into a perfectly order vortex lattice (VL).  In reality, however, thermal effects and/or pinning to material defects are present, and the balance between these competing factors determine both the structural and dynamic properties of vortex matter.  This leads to a rich phase diagram comprised of both ordered and disordered solid phases and vortex liquids.  While transitions between the different phases are driven by changes of intensive quantities such as the magnetic field or temperature, their locations in the phase diagram are sensitive to the amount of defects in the host superconductor.  This provides an experimental handle with which one can tune the vortex matter phase diagram, e.g by introducing impurities during the material synthesis or by bombardment with heavy ions to create columnar defects post growth.

Here we report on small-angle neutron scattering (SANS) studies of vortices in the topological superconductor UPt3, and specifically how the VL in this material undergoes a gradual disordering as it is subjected to a beam of cold neutrons.  The disordering occurs on a time scale of tens of minutes, and is attributed to local heating events caused by neutron induced fission of 235U, which temporarily heat regions of the sample above the critical temperature.  Vortices in the affected regions remain in a disordered configuration after re-cooling, which is most likely a quenched vortex glass.  Moreover, the rate of disordering is proportional to the magnetic field, suggesting a direct relation to collective VL properties such as the elastic moduli.  While the VL does not spontaneously re-order once the local heating has been dissipated it is possible to re-anneal the VL by the application of a damped field oscillation, indicating that no permanent radiation damage of the UPt3 crystal occur within experimental time scales.  The results demonstrate a novel avenue for vortex matter studies, allowing an introduction of localized and reversible quenched disorder.


Date:
-
Location:
Zoom

Fission induced vortex lattice disordering in UPt3

Prof. Morten Eskildsen

Department of Physics

University of Notre Dame

Host: Gannon

Title: Fission induced vortex lattice disordering in UPt3

Abstract:  Subjecting a type-II superconductor to a magnetic field will cause the formations of quantized vortices.  Due to their repulsive interaction the vortices will, in an ideal situation, arrange themselves into a perfectly order vortex lattice (VL).  In reality, however, thermal effects and/or pinning to material defects are present, and the balance between these competing factors determine both the structural and dynamic properties of vortex matter.  This leads to a rich phase diagram comprised of both ordered and disordered solid phases and vortex liquids.  While transitions between the different phases are driven by changes of intensive quantities such as the magnetic field or temperature, their locations in the phase diagram are sensitive to the amount of defects in the host superconductor.  This provides an experimental handle with which one can tune the vortex matter phase diagram, e.g by introducing impurities during the material synthesis or by bombardment with heavy ions to create columnar defects post growth.

Here we report on small-angle neutron scattering (SANS) studies of vortices in the topological superconductor UPt3, and specifically how the VL in this material undergoes a gradual disordering as it is subjected to a beam of cold neutrons.  The disordering occurs on a time scale of tens of minutes, and is attributed to local heating events caused by neutron induced fission of 235U, which temporarily heat regions of the sample above the critical temperature.  Vortices in the affected regions remain in a disordered configuration after re-cooling, which is most likely a quenched vortex glass.  Moreover, the rate of disordering is proportional to the magnetic field, suggesting a direct relation to collective VL properties such as the elastic moduli.  While the VL does not spontaneously re-order once the local heating has been dissipated it is possible to re-anneal the VL by the application of a damped field oscillation, indicating that no permanent radiation damage of the UPt3 crystal occur within experimental time scales.  The results demonstrate a novel avenue for vortex matter studies, allowing an introduction of localized and reversible quenched disorder.


Date:
-
Location:
Zoom

Unbounded hydrodynamics in nodal-line semimetals

Prof. Bruno Uchoa

Department of Physics and Astronomy

University of Oklahoma

Host: Kaul

 

Title: Unbounded hydrodynamics in nodal-line semimetals

Abstract: The ratio between the shear viscosity and the entropy η/s is considered a universal measure of the strength of interactions in quantum systems. This quantity was conjectured to have a universal lower bound (1/4π)h/kB, which indicates a very strongly correlated quantum fluid. After a general overview on quantum hydrodynamics, which describes the long wavelength deviations of local thermal equilibrium, I will address the quantum kinetic theory for a nodal-line semimetal in the hydrodynamic regime. I will show that the ratio between the shear viscosity and the entropy is unbounded, scaling towards zero with decreasing temperature in the perturbative limit. Due to the large unscreened Fermi surface represented by the nodal-line, the phase space for collisions is greatly enhanced compared to either conventional relativistic systems and metals, resulting in a short hydrodynamic scattering time that is nearly temperature independent (up to logarithmic scaling corrections) and set by the radius of the nodal line. I suggest that the lower bound criteria should be modified to account for unscreened relativistic systems with a Fermi surface.

Date:
Location:
Zoom

Unbounded hydrodynamics in nodal-line semimetals

Prof. Bruno Uchoa

Department of Physics and Astronomy

University of Oklahoma

Host: Kaul

 

Title: Unbounded hydrodynamics in nodal-line semimetals

Abstract: The ratio between the shear viscosity and the entropy η/s is considered a universal measure of the strength of interactions in quantum systems. This quantity was conjectured to have a universal lower bound (1/4π)h/kB, which indicates a very strongly correlated quantum fluid. After a general overview on quantum hydrodynamics, which describes the long wavelength deviations of local thermal equilibrium, I will address the quantum kinetic theory for a nodal-line semimetal in the hydrodynamic regime. I will show that the ratio between the shear viscosity and the entropy is unbounded, scaling towards zero with decreasing temperature in the perturbative limit. Due to the large unscreened Fermi surface represented by the nodal-line, the phase space for collisions is greatly enhanced compared to either conventional relativistic systems and metals, resulting in a short hydrodynamic scattering time that is nearly temperature independent (up to logarithmic scaling corrections) and set by the radius of the nodal line. I suggest that the lower bound criteria should be modified to account for unscreened relativistic systems with a Fermi surface.

Date:
Location:
Zoom

Exciton Drift from Quantum Geometry

Professor Herb Fertig

Department of Physics

Indiana University

Host: Kaul

 

Title:

Exciton Drift from Quantum Geometry

Abstract:

In some situations, excitons – bound particle-hole pairs above an insulating ground state – carry an electric dipole moment, allowing them to be manipulated via coupling to an electric field. Excitons in two-dimensional systems turn out to be fully determined by the quantum geometry of its eigenstates, through a quantity which we call the dipole curvature.  The dipole curvature arises naturally in the semiclassical equations of motion of an exciton in an electric field, yielding a drift velocity akin to that expected for excitons in crossed electric and magnetic fields, even in the absence of a real magnetic field.  In real magnetic fields it yields corrections to the drift velocity expected based on Lorentz invariance.  The effect arises naturally in systems where the environments of the electron and hole are sufficiently different, and is particularly relevant for interlayer excitons in heterostructures -- bilayers of different materials.  We discuss estimates of these effects for simple heterostructure models, including graphene and transition-metal dichalcogenide layers, both with and without magnetic fields.  The last of these turn out to be particularly promising platforms for observing these effects.   We discuss how this quantum geometric drift velocity might be observed in experiment, and possible further consequences that follow from the semiclassical dynamics.

Date:
-
Location:
Zoom

Exciton Drift from Quantum Geometry

Professor Herb Fertig

Department of Physics

Indiana University

Host: Kaul

 

Title:

Exciton Drift from Quantum Geometry

Abstract:

In some situations, excitons – bound particle-hole pairs above an insulating ground state – carry an electric dipole moment, allowing them to be manipulated via coupling to an electric field. Excitons in two-dimensional systems turn out to be fully determined by the quantum geometry of its eigenstates, through a quantity which we call the dipole curvature.  The dipole curvature arises naturally in the semiclassical equations of motion of an exciton in an electric field, yielding a drift velocity akin to that expected for excitons in crossed electric and magnetic fields, even in the absence of a real magnetic field.  In real magnetic fields it yields corrections to the drift velocity expected based on Lorentz invariance.  The effect arises naturally in systems where the environments of the electron and hole are sufficiently different, and is particularly relevant for interlayer excitons in heterostructures -- bilayers of different materials.  We discuss estimates of these effects for simple heterostructure models, including graphene and transition-metal dichalcogenide layers, both with and without magnetic fields.  The last of these turn out to be particularly promising platforms for observing these effects.   We discuss how this quantum geometric drift velocity might be observed in experiment, and possible further consequences that follow from the semiclassical dynamics.

Date:
-
Location:
Zoom