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Condensed Matter Seminar

Magnetic order and spin excitations in two-dimensional honeycomb lattice van der Waals ferromagnetic CrI3

Professor Pengcheng Dai

Department of Physics and Astronomy

Rice University

Host: Gannon

Title:  Magnetic order and spin excitations in two-dimensional honeycomb lattice van der Waals ferromagnetic CrI3

Abstract:  We use neutron scattering to study magnetic order and spin excitations in honeycomb lattice van der Waals ferromagnet CrI3. We show that ferromagnetic phase transition is first order in nature, and controlled by spin-orbit coupling (SOC) induced magnetic anisotropy, instead of magnetic exchange coupling as in a conventional ferromagnet. We discuss the role of the next-nearest-neighbor Dzyaloshinskii-Moriya interaction and Kitaev’s interaction plays on the spin-wave spectra and the possible presence of topological spin excitations in CrI3.

Date:
-
Location:
Zoom

Magnetic order and spin excitations in two-dimensional honeycomb lattice van der Waals ferromagnetic CrI3

Professor Pengcheng Dai

Department of Physics and Astronomy

Rice University

Host: Gannon

Title:  Magnetic order and spin excitations in two-dimensional honeycomb lattice van der Waals ferromagnetic CrI3

Abstract:  We use neutron scattering to study magnetic order and spin excitations in honeycomb lattice van der Waals ferromagnet CrI3. We show that ferromagnetic phase transition is first order in nature, and controlled by spin-orbit coupling (SOC) induced magnetic anisotropy, instead of magnetic exchange coupling as in a conventional ferromagnet. We discuss the role of the next-nearest-neighbor Dzyaloshinskii-Moriya interaction and Kitaev’s interaction plays on the spin-wave spectra and the possible presence of topological spin excitations in CrI3.

Date:
-
Location:
Zoom

a-RuCl3 as a 2d crystalline acceptor: modulation doping, pn junctions, and the pursuit of Veselago's lens

Professor Erik Henriksen

Department of Physics

Washington University in St. Louis

Host: Kaul

Title:  a-RuCl3 as a 2d crystalline acceptor: modulation doping, pn junctions, and the pursuit of Veselago's lens

Abstract: a-RuCl3 is a layered antiferromagnetic Mott insulator widely thought to host a quantum spin liquid state related to the Kitaev QSL. It can be exfoliated down to monolayer thicknesses and incorporated into van der Waals heterostructures along with graphene and myriad other atomically thin materials. Proximity of a-RuCl3 to graphene leads to a significant charge transfer between the two that, surprisingly, persists even when a thin insulating layer is inserted between them, a phenomenon analogous to modulation doping in epitaxially-grown semiconductors. In addition to constituting a new method of charge control in van der Waals stacks, we are using this to generate near-atomically-sharp pn junctions in graphene that may enable a realization of the electron-optic version of Veselago's lens. 

 
Date:
-
Location:
Zoom

a-RuCl3 as a 2d crystalline acceptor: modulation doping, pn junctions, and the pursuit of Veselago's lens

Professor Erik Henriksen

Department of Physics

Washington University in St. Louis

Host: Kaul

Title:  a-RuCl3 as a 2d crystalline acceptor: modulation doping, pn junctions, and the pursuit of Veselago's lens

Abstract: a-RuCl3 is a layered antiferromagnetic Mott insulator widely thought to host a quantum spin liquid state related to the Kitaev QSL. It can be exfoliated down to monolayer thicknesses and incorporated into van der Waals heterostructures along with graphene and myriad other atomically thin materials. Proximity of a-RuCl3 to graphene leads to a significant charge transfer between the two that, surprisingly, persists even when a thin insulating layer is inserted between them, a phenomenon analogous to modulation doping in epitaxially-grown semiconductors. In addition to constituting a new method of charge control in van der Waals stacks, we are using this to generate near-atomically-sharp pn junctions in graphene that may enable a realization of the electron-optic version of Veselago's lens. 

 
Date:
-
Location:
Zoom

Intertwined Dipolar and Quadrupolar Correlations in the Pyrochlore Tb2Ge2O7

Professor Alannah Hallas

Department of Physics and Astronomy

Stewart Blusson Quantum Matter Institute

University of British Columbia

Host:  Gannon

Title: Intertwined Dipolar and Quadrupolar Correlations in the Pyrochlore Tb2Ge2O7

Abstract:  Rare earth pyrochlores are model systems for the study of highly frustrated magnetism, in large part, because the majority of these materials have a clean separation of energy scales between their single-ion properties and their collective interactions. Terbium pyrochlores represent the exception, where a low energy crystal field excitation profoundly affects the spin interactions and imbues these materials with especially complex phase behavior. We find that the magnetic states of the terbium pyrochlores evolve over three distinct temperature regimes, strongly suggesting a universality to their low temperature phase behavior. In this talk, I will present a comprehensive heat capacity and neutron scattering study of Tb2Ge2O7 where, for the first time, we have been able to elucidate the nature of each of these three regimes. We find that the complex phase behavior of the terbium pyrochlores originates from not only the usual geometric frustration but also frustration due to the competition between magnetic dipoles and electric quadrupoles.

Date:
-
Location:
Zoom

Intertwined Dipolar and Quadrupolar Correlations in the Pyrochlore Tb2Ge2O7

Professor Alannah Hallas

Department of Physics and Astronomy

Stewart Blusson Quantum Matter Institute

University of British Columbia

Host:  Gannon

Title: Intertwined Dipolar and Quadrupolar Correlations in the Pyrochlore Tb2Ge2O7

Abstract:  Rare earth pyrochlores are model systems for the study of highly frustrated magnetism, in large part, because the majority of these materials have a clean separation of energy scales between their single-ion properties and their collective interactions. Terbium pyrochlores represent the exception, where a low energy crystal field excitation profoundly affects the spin interactions and imbues these materials with especially complex phase behavior. We find that the magnetic states of the terbium pyrochlores evolve over three distinct temperature regimes, strongly suggesting a universality to their low temperature phase behavior. In this talk, I will present a comprehensive heat capacity and neutron scattering study of Tb2Ge2O7 where, for the first time, we have been able to elucidate the nature of each of these three regimes. We find that the complex phase behavior of the terbium pyrochlores originates from not only the usual geometric frustration but also frustration due to the competition between magnetic dipoles and electric quadrupoles.

Date:
-
Location:
Zoom

Equilibrium and non-equilibrium dynamics of highly frustrated quantum magnets

Professor Hitesh Changlani

Department of Physics 

Florida State University

and The National High Magnetic Field Laboratory

Host:  Kaul

 

Abstract:

Geometrically frustrated magnets harbor novel phases of strongly interacting quantum matter, including those with fractionalized excitations, such as quantum spin liquids.  While there is tremendous progress on understanding their ground state properties, I will primarily focus on their dynamics by highlighting two directions that my group is pursuing. First, I will present our work (done in collaboration with experimentalists) on a newly synthesized pyrochlore, NaCaNi2F7, which we find to be an almost ideal realization of a spin-1 three-dimensional highly frustrated antiferromagnet with no magnetic order and a continuum of excitations, as seen in inelastic neutron scattering [1]. We determine its effective Hamiltonian and show the presence of characteristic "pinch points”, along with good quantitative agreement at intermediate energy scales, from three different theoretical techniques [2]. In the second part of my talk, I switch my focus to the dynamical non-equilibrium effect of ``quantum scarring” which was first reported in a one dimensional Rydberg atom setup [3], with no known real material analog. I demonstrate that this effect is not restricted to 1D, and can be realized in higher dimensional systems [4], which I explain with the help of an exactly solvable point (that we recently discovered) in the XXZ-Heisenberg model on the frustrated kagome lattice [5]. Within the framework of this proposal, I suggest what would be needed to realize scarring in real materials.

[1] K. W. Plumb, H.J. Changlani, A. Scheie, S. Zhang, J. Krizan, J. A. Rodriguez-Rivera, Y.Qiu, B.Winn, R.J. Cava, C.L. Broholm, Nature Physics, 15, 54-59 (2019)

[2] S. Zhang, H.J. Changlani, K. Plumb, O. Tchernyshyov, R. Moessner, Phys. Rev. Lett. 122, 167203 (2019)

[3] H. Bernien et al., Nature 551, 579–584 (2017); C. Turner et al., Nature Physics 14, 745-749 (2018)

[4] K. Lee, R. Melendrez, A. Pal, H.J. Changlani, Phys. Rev. B 101, 241111(R) (2020)

[5] H.J. Changlani, D. Kochkov, K. Kumar, B. Clark, E. Fradkin, Phys. Rev. Lett. 120, 117202 (2018)

 

 

 

Date:
-
Location:
Zoom

Equilibrium and non-equilibrium dynamics of highly frustrated quantum magnets

Professor Hitesh Changlani

Department of Physics 

Florida State University

and The National High Magnetic Field Laboratory

Host:  Kaul

 

Abstract:

Geometrically frustrated magnets harbor novel phases of strongly interacting quantum matter, including those with fractionalized excitations, such as quantum spin liquids.  While there is tremendous progress on understanding their ground state properties, I will primarily focus on their dynamics by highlighting two directions that my group is pursuing. First, I will present our work (done in collaboration with experimentalists) on a newly synthesized pyrochlore, NaCaNi2F7, which we find to be an almost ideal realization of a spin-1 three-dimensional highly frustrated antiferromagnet with no magnetic order and a continuum of excitations, as seen in inelastic neutron scattering [1]. We determine its effective Hamiltonian and show the presence of characteristic "pinch points”, along with good quantitative agreement at intermediate energy scales, from three different theoretical techniques [2]. In the second part of my talk, I switch my focus to the dynamical non-equilibrium effect of ``quantum scarring” which was first reported in a one dimensional Rydberg atom setup [3], with no known real material analog. I demonstrate that this effect is not restricted to 1D, and can be realized in higher dimensional systems [4], which I explain with the help of an exactly solvable point (that we recently discovered) in the XXZ-Heisenberg model on the frustrated kagome lattice [5]. Within the framework of this proposal, I suggest what would be needed to realize scarring in real materials.

[1] K. W. Plumb, H.J. Changlani, A. Scheie, S. Zhang, J. Krizan, J. A. Rodriguez-Rivera, Y.Qiu, B.Winn, R.J. Cava, C.L. Broholm, Nature Physics, 15, 54-59 (2019)

[2] S. Zhang, H.J. Changlani, K. Plumb, O. Tchernyshyov, R. Moessner, Phys. Rev. Lett. 122, 167203 (2019)

[3] H. Bernien et al., Nature 551, 579–584 (2017); C. Turner et al., Nature Physics 14, 745-749 (2018)

[4] K. Lee, R. Melendrez, A. Pal, H.J. Changlani, Phys. Rev. B 101, 241111(R) (2020)

[5] H.J. Changlani, D. Kochkov, K. Kumar, B. Clark, E. Fradkin, Phys. Rev. Lett. 120, 117202 (2018)

 

 

 

Date:
-
Location:
Zoom

From Molecules to Organic Semiconductors: The Challenges of Processing and Polymorphs from the Perspective of Modeling

Professor Chad Risko

Department of Chemistry

University of Kentucky

Host:  Brill

 

Abstract:

Organic semiconductors are derived from π-conjugated molecules or polymers, whose chemical composition and structure are only limited by the imagination of the synthetic chemist – or, perhaps in the future, are determined through machine-learned paradigms. The structure of organic semiconductors are also determined by their processing environment. Currently, how molecular design and processing are interwoven to result in semiconducting materials with optimal performance remains a mixture of art and science. Here we will discuss the development of atomistic-scale models that bring together molecular topology and processing conditions to provide first-principles insight into the physicochemical connections that are required to be controlled.

Date:
-
Location:
Zoom

From Molecules to Organic Semiconductors: The Challenges of Processing and Polymorphs from the Perspective of Modeling

Professor Chad Risko

Department of Chemistry

University of Kentucky

Host:  Brill

 

Abstract:

Organic semiconductors are derived from π-conjugated molecules or polymers, whose chemical composition and structure are only limited by the imagination of the synthetic chemist – or, perhaps in the future, are determined through machine-learned paradigms. The structure of organic semiconductors are also determined by their processing environment. Currently, how molecular design and processing are interwoven to result in semiconducting materials with optimal performance remains a mixture of art and science. Here we will discuss the development of atomistic-scale models that bring together molecular topology and processing conditions to provide first-principles insight into the physicochemical connections that are required to be controlled.

Date:
-
Location:
Zoom