arXiv subjects

Klaus Zollner

Publications and source records attributed to Klaus Zollner.

36 records · Page 2Linked to original sources

arXiv2022

Proximity spin-orbit and exchange coupling in ABA and ABC trilayer graphene van der Waals heterostructures

We investigate the proximity spin-orbit and exchange couplings in ABA and ABC trilayer graphene encapsulated within monolayers of semiconducting transition-metal dichalcogenides and the ferromagnetic semiconductor Cr$_2$Ge$_2$Te$_6$. Employing first-principles calculations we obtain the electronic structures of the multilayer stacks and extract the relevant proximity-induced orbital and spin interaction parameters by fitting the low-energy bands to model Hamiltonians. We also demonstrate the tunability of the proximity effects by a transverse electric field. Using the model Hamiltonians we also study mixed spin-orbit/exchange coupling encapsulation, which allows to tailor the spin interactions very efficiently by the applied field. We also summarize the spin-orbit physics of bare ABA, ABC, and ABB trilayers, and provide, along with the first-principles results of the electronic band structures, density of states, spin splittings, and electric-field tunabilities of the bands, qualitative understanding of the observed behavior and realistic model parameters as a resource for model simulations of transport and correlation physics in trilayer graphene.

cond-mat.mes-hall↗

arXiv2021

Bilayer graphene encapsulated within monolayers of WS$_2$ or Cr$_2$Ge$_2$Te$_6$: Tunable proximity spin-orbit or exchange coupling

Van der Waals (vdW) heterostructures consisting of bilayer graphene (BLG) encapsulated within monolayers of strong spin-orbit semiconductor WS$_2$ or ferromagnetic semiconductor Cr$_2$Ge$_2$Te$_6$ (CGT), are investigated. By performing realistic first-principles calculations we capture the essential BLG band structure features, including layer- and sublattice-resolved proximity spin-orbit or exchange couplings. For different relative twist angles (0 or 60$^{\circ}$) of the WS$_2$ layers, and the magnetizations (parallel or antiparallel) of the CGT layers, with respect to BLG, the low energy bands are found and characterized by a series of fit parameters of model Hamiltonians. These effective models are then employed to investigate the tunability of the relevant energy dispersions by a gate field. For WS$_2$/BLG/WS$_2$ encapsulation we find that twisting allows to turn off the spin splittings away from the $K$ points, due to opposite proximity-induced valley-Zeeman couplings in the two sheets of BLG. Close to the $K$ points the electron spins are polarized out of the plane. This polarization can be flipped by applying a gate field. As for magnetic CGT/BLG/CGT structures, we realize the recently proposed spin-valve effect, whereby a gap opens for antiparallel magnetizations of the CGT layers. Furthermore, we find that for the antiferromagnetic orientation the electron states away from $K$ have vanishingly weak proximity exchange, while the states close to $K$ remain spin polarized in the presence of an electric field. The induced magnetization can be flipped by changing the gate field. These findings should be useful for spin transport, spin filtering, and spin relaxation anisotropy studies of BLG-based vdW heterostructures.

cond-mat.mes-hall↗

arXiv2021

Graphene on two-dimensional hexagonal BN, AlN, and GaN: Electronic, spin-orbit, and spin relaxation properties

We investigate the electronic structure of graphene on a series of 2D hexagonal nitride insulators hXN, X = B, Al, and Ga, with DFT calculations. A symmetry-based model Hamiltonian is employed to extract orbital parameters and spin-orbit coupling (SOC) from the low-energy Dirac bands of proximitized graphene. While commensurate hBN induces a staggered potential of about 10 meV into the Dirac bands, less lattice-matched hAlN and hGaN disrupt the Dirac point much less, giving a staggered gap below 100 $μ$eV. Proximitized intrinsic SOC surprisingly does not increase much above the pristine graphene value of 12 $μ$eV; it stays in the window of (1-16) $μ$eV, depending strongly on stacking. However, Rashba SOC increases sharply when increasing the atomic number of the boron group, with calculated maximal values of 8, 15, and 65 $μ$eV for B, Al, and Ga-based nitrides, respectively. The individual Rashba couplings also depend strongly on stacking, vanishing in symmetrically-sandwiched structures, and can be tuned by a transverse electric field. The extracted spin-orbit parameters were used as input for spin transport simulations based on Chebyshev expansion of the time-evolution of the spin expectation values, yielding interesting predictions for the electron spin relaxation. Spin lifetime magnitudes and anisotropies depend strongly on the specific (hXN)/graphene/hXN system, and they can be efficiently tuned by an applied external electric field as well as the carrier density in the graphene layer. A particularly interesting case for experiments is graphene/hGaN, in which the giant Rashba coupling is predicted to induce spin lifetimes of 1-10 ns, short enough to dominate over other mechanisms, and lead to the same spin relaxation anisotropy as observed in conventional semiconductor heterostructures: 50\%, meaning that out-of-plane spins relax twice as fast as in-plane spins.

cond-mat.mes-hall↗

arXiv2020

Swapping Exchange and Spin-Orbit Coupling in 2D van der Waals Heterostructures

The concept of swapping the two most important spin interactions -- exchange and spin-orbit coupling -- is proposed based on two-dimensional multilayer van der Waals heterostructures. Specifically, we show by performing realistic ab initio simulations, that a single device consisting of a bilayer graphene sandwiched by a 2D ferromagnet Cr$_2$Ge$_2$Te$_6$ (CGT) and a monolayer WS$_2$, is able not only to generate, but also to swap the two interactions. The highly efficient swapping is enabled by the interplay of gate-dependent layer polarization in bilayer graphene and short-range spin-orbit and exchange proximity effects affecting only the layers in contact with the sandwiching materials. We call these structures ex-so-tic, for supplying either exchange (ex) or spin-orbit (so) coupling in a single device, by gating. Such bifunctional devices demonstrate the potential of van der Waals spintronics engineering using 2D crystal multilayers.

cond-mat.mes-hall↗

arXiv2020

Electronic and magnetic properties of $α$-FeGe$_2$ films embedded in vertical spin valve devices

We studied metastable $α$-FeGe$_2$, a novel layered tetragonal material, embedded as a spacer layer in spin valve structures with ferromagnetic Fe$_3$Si and Co$_2$FeSi electrodes. For both types of electrodes, spin valve operation is demonstrated with a metallic transport behavior of the $α$-FeGe$_2$ spacer layer. The spin valve signals are found to increase both with temperature and spacer thickness, which is discussed in terms of a decreasing magnetic coupling strength between the ferromagnetic bottom and top electrodes. The temperature-dependent resistances of the spin valve structures exhibit characteristic features, which are explained by ferromagnetic phase transitions between 55 and 110~K. The metallic transport characteristics as well as the low-temperature ferromagnetism are found to be consistent with the results of first-principles calculations.

cond-mat.mtrl-sci↗

arXiv2020

Scattering-induced and highly tunable by gate damping-like spin-orbit torque in graphene doubly proximitized by two-dimensional magnet Cr$_2$Ge$_2$Te$_6$ and WS$_2$

Graphene sandwiched between semiconducting monolayers of ferromagnet Cr$_2$Ge$_2$Te$_6$ and transition-metal dichalcogenide WS$_2$ acquires both spin-orbit (SO), of valley-Zeeman and Rashba types, and exchange couplings. Using first-principles combined with quantum transport calculations, we predict that such doubly proximitized graphene within van der Waals heterostructure will exhibit SO torque driven by unpolarized charge current. This system lacking spin Hall current, putatively considered to be necessary for efficient damping-like (DL) SO torque that plays a key role in magnetization switching, demonstrates how DL torque component can be generated solely by skew-scattering off spin-independent potential barrier or impurities in purely two-dimensional electronic transport due to the presence of proximity SO coupling and its spin texture tilted out-of-plane. This leads to current-driven nonequilibrium spin density emerging in all spatial directions, whose cross product with proximity magnetization yields DL SO torque, unlike the ballistic regime with no scatterers in which only field-like (FL) SO torque appears. In contrast to SO torque on conventional metallic ferromagnets in contact with three dimensional SO-coupled materials, the ratio of FL and DL torque can be tuned by more than an order of magnitude via combined top and back gates.

cond-mat.mes-hall↗

arXiv2020

Heterostructures of graphene and topological insulators Bi$_2$Se$_3$, Bi$_2$Te$_3$, and Sb$_2$Te$_3$

Prototypical three-dimensional topological insulators of the Bi$_2$Se$_3$ family provide a beautiful example of the appearance of the surface states inside the bulk band gap caused by spin-orbit coupling-induced topology. The surface states are protected against back scattering by time reversal symmetry, and exhibit spin-momentum locking whereby the electron spin is polarized perpendicular to the momentum, typically in the plane of the surface. On the other hand, graphene is a prototypical two-dimensional material, with negligible spin-orbit coupling. When graphene is placed on the surface of a topological insulator, giant spin-orbit coupling is induced by the proximity effect, enabling interesting novel electronic properties of its Dirac electrons. We present a detailed theoretical study of the proximity effects of monolayer graphene and topological insulators Bi$_2$Se$_3$, Bi$_2$Te$_3$, and Sb$_2$Te$_3$, and elucidate the appearance of the qualitatively new spin-orbit splittings well described by a phenomenological Hamiltonian, by analyzing the orbital decomposition of the involved band structures. This should be useful for building microscopic models of the proximity effects between the surfaces of the topological insulators and graphene.

cond-mat.mes-hall↗

arXiv2020

Quantum Anomalous Hall Effects in Graphene from Proximity-Induced Uniform and Staggered Spin-Orbit and Exchange Coupling

We investigate an effective model of proximity modified graphene (or symmetrylike materials) with broken time-reversal symmetry. We predict the appearance of quantum anomalous Hall phases by computing bulk band gap and Chern numbers for benchmark combinations of system parameters. Allowing for staggered exchange field enables quantum anomalous Hall effect in flat graphene with Chern number $C=1$. We explicitly show edge states in zigzag and armchair nanoribbons and explore their localization behavior. Remarkably, the combination of staggered intrinsic spin-orbit and uniform exchange coupling gives topologically protected (unlike in time-reversal systems) pseudohelical states, whose spin is opposite in opposite zigzag edges. Rotating the magnetization from out of plane to in plane makes the system trivial, allowing to control topological phase transitions. We also propose, using density functional theory, a material platform---graphene on Ising antiferromagnet MnPSe$_3$---to realize staggered exchange (pseudospin Zeeman) coupling.

cond-mat.mes-hall↗

arXiv2020

Giant proximity exchange and valley splitting in transition metal dichalcogenide/$h\mathrm{BN}$/(Co, Ni) heterostructures

We investigate the proximity-induced exchange coupling in transition-metal dichalcogenides (TMDCs), originating from spin injector geometries composed of hexagonal boron-nitride (hBN) and ferromagnetic (FM) cobalt (Co) or nickel (Ni), from first-principles. We employ a minimal tight-binding Hamiltonian that captures the low energy bands of the TMDCs around K and K' valleys, to extract orbital, spin-orbit, and exchange parameters. The TMDC/hBN/FM heterostructure calculations show that due to the hBN buffer layer, the band structure of the TMDC is preserved, with an additional proximity-induced exchange splitting in the bands. We extract proximity exchange parameters in the 1--10 meV range, depending on the FM. The combination of proximity-induced exchange and intrinsic spin-orbit coupling (SOC) of the TMDCs, leads to a valley polarization, translating into magnetic exchange fields of tens of Tesla. The extracted parameters are useful for subsequent exciton calculations of TMDCs in the presence of a hBN/FM spin injector. Our calculated absorption spectra show large splittings for the exciton peaks; in the case of MoS$_2$/hBN/Co we find a value of about 8 meV, corresponding to about 50 Tesla external magnetic field in bare TMDCs. The reason lies in the band structure, where a hybridization with Co $d$ orbitals causes a giant valence band exchange splitting of more than 10 meV. Structures with Ni do not show any $d$ level hybridization features, but still sizeable proximity exchange and exciton peak splittings of around 2 meV are present in the TMDCs.

cond-mat.mes-hall↗

arXiv2019

Strain-tunable orbital, spin-orbit, and optical properties of monolayer transition-metal dichalcogenides

When considering transition-metal dichalcogenides (TMDCs) in van der Waals (vdW) heterostructures for periodic ab-initio calculations, usually, lattice mismatch is present, and the TMDC needs to be strained. In this study we provide a systematic assessment of biaxial strain effects on the orbital, spin-orbit, and optical properties of the monolayer TMDCs using ab-initio calculations. We complement our analysis with a minimal tight-binding Hamiltonian that captures the low-energy bands of the TMDCs around K and K' valleys. We find characteristic trends of the orbital and spin-orbit parameters as a function of the biaxial strain. Specifically, the orbital gap decreases linearly, while the valence (conduction) band spin splitting increases (decreases) nonlinearly in magnitude when the lattice constant increases. Furthermore, employing the Bethe-Salpeter equation and the extracted parameters, we show the evolution of several exciton peaks, with biaxial strain, on different dielectric surroundings, which are particularly useful for interpreting experiments studying strain-tunable optical spectra of TMDCs.

cond-mat.mes-hall↗

arXiv2019

Single and bilayer graphene on the topological insulator Bi$_2$Se$_3$: Electronic and spin-orbit properties from first principles

We present a detailed study of the electronic and spin-orbit properties of single and bilayer graphene in proximity to the topological insulator Bi$_2$Se$_3$. Our approach is based on first-principles calculations, combined with symmetry derived model Hamiltonians that capture the low-energy band properties. We consider single and bilayer graphene on 1--3 quintuple layers of Bi$_2$Se$_3$ and extract orbital and proximity induced spin-orbit coupling (SOC) parameters. We find that graphene gets significantly hole doped (350 meV), but the linear dispersion is preserved. The proximity induced SOC parameters are about 1 meV in magnitude, and are of valley-Zeeman type. The induced SOC depends weakly on the number of quintuple layers of Bi$_2$Se$_3$. We also study the effect of a transverse electric field, that is applied across heterostructures of single and bilayer graphene above 1 quintuple layer of Bi$_2$Se$_3$. Our results show that band offsets, as well as proximity induced SOC parameters can be tuned by the field. Most interesting is the case of bilayer graphene, in which the band gap, originating from the intrinsic dipole of the heterostructure, can be closed and reopened again, with inverted band character. The switching of the strong proximity SOC from the conduction to the valence band realizes a spin-orbit valve. Additonally, we find a giant increase of the proximity induced SOC of about 200%, when we decrease the interlayer distance between graphene and Bi$_2$Se$_3$ by only 10%. Finally, for a different substrate material Bi$_2$Te$_2$Se, band offsets are significantly different, with the graphene Dirac point located at the Fermi level, while the induced SOC strength stays similar in magnitude compared to the Bi$_2$Se$_3$ substrate.

cond-mat.mes-hall↗

arXiv2019

Magnetic proximity in a van der Waals heterostructure of magnetic insulator and graphene

Engineering two-dimensional material heterostructures by combining the best of different materials in one ultimate unit can offer a plethora of opportunities in condensed matter physics. Here, in the van der Waals heterostructures of the ferromagnetic insulator Cr2Ge2Te6 and graphene, our observations indicate an out-of-plane proximity-induced ferromagnetic exchange interaction in graphene. The perpendicular magnetic anisotropy of Cr2Ge2Te6 results in significant modification of the spin transport and precession in graphene, which is ascribed to the proximity-induced exchange interaction. Furthermore, the observation of a larger lifetime for perpendicular spins in comparison to the in-plane counterpart suggests the creation of a proximity-induced anisotropic spin texture in graphene. Our experimental results and density functional theory calculations open up opportunities for the realization of proximity-induced magnetic interactions and spin filters in 2D material heterostructures and can form the basic building blocks for future spintronic and topological quantum devices.

cond-mat.mes-hall↗

arXiv2019

First-principles theory of proximity spin-orbit torque on a two-dimensional magnet: Current-driven antiferromagnet-to-ferromagnet reversible transition in bilayer CrI$_3$

The recently discovered two-dimensional (2D) magnetic insulator CrI$_3$ is an intriguing case for basic research and spintronic applications since it is a ferromagnet in the bulk, but an antiferromagnet in bilayer form, with its magnetic ordering amenable to external manipulations. Using first-principles quantum transport approach, we predict that injecting unpolarized charge current parallel to the interface of bilayer-CrI$_3$/monolayer-TaSe$_2$ van der Waals heterostructure will induce spin-orbit torque (SOT) and thereby driven dynamics of magnetization on the first monolayer of CrI$_3$ in direct contact with TaSe$_2$. By combining calculated complex angular dependence of SOT with the Landau-Lifshitz-Gilbert equation for classical dynamics of magnetization, we demonstrate that current pulses can switch the direction of magnetization on the first monolayer to become parallel to that of the second monolayer, thereby converting CrI$_3$ from antiferromagnet to ferromagnet while not requiring any external magnetic field. We explain the mechanism of this reversible current-driven nonequilibrium phase transition by showing that first monolayer of CrI$_3$ carries current due to evanescent wavefunctions injected by metallic transition metal dichalcogenide TaSe$_2$, while concurrently acquiring strong spin-orbit coupling (SOC) via such proximity effect, whereas the second monolayer of CrI$_3$ remains insulating. The transition can be detected by passing vertical read current through the vdW heterostructure, encapsulated by bilayer of hexagonal boron nitride and sandwiched between graphite electrodes, where we find tunneling magnetoresistance of $\simeq 240$%.

cond-mat.mes-hall↗

arXiv2019

Proximity exchange effects in MoSe$_2$ and WSe$_2$ heterostructures with CrI$_3$: twist angle, layer, and gate dependence

Proximity effects in two-dimensional (2D) van der Waals heterostructures offer controllable ways to tailor the electronic band structure of adjacent materials. Exchange proximity in particular is important for making materials magnetic without hosting magnetic ions. Such synthetic magnets could be used for studying magnetotransport in high-mobility 2D materials, or magneto-optics in highly absorptive nominally nonmagnetic semiconductors. Using first-principles calculations, we show that the proximity exchange in monolayer MoSe$_2$ and WSe$_2$ due to ferromagnetic monolayer CrI$_3$ can be tuned (even qualitatively) by twisting and gating. Remarkably, the proximity exchange remains the same when using antiferromagnetic CrI$_3$ bilayer, paving the way for optical and electrical detection of layered antiferromagnets. Interestingly, the proximity exchange is opposite to the exchange of the adjacent antiferromagnetic layer. Finally, we show that the exchange proximity is confined to the layer adjacent to CrI$_3$, and that adding a separating hBN barrier drastically reduces the proximity effect. We complement our it ab initio results with tight-binding modeling and solve the Bethe-Salpeter equation to provide experimentally verifiable optical signatures (in the exciton spectra) of the proximity exchange effects.

cond-mat.mes-hall↗

arXiv2019

Heterostructures of graphene and hBN: electronic, spin-orbit, and spin relaxation properties from first principles

We perform extensive first-principles calculations for heterostructures composed of monolayer graphene and hexagonal boron nitride (hBN). Employing a symmetry-derived minimal tight-binding model, we extract orbital and spin-orbit coupling (SOC) parameters for graphene on hBN, as well as for hBN encapsulated graphene. Our calculations show that the parameters depend on the specific stacking configuration of graphene on hBN. We also perform an interlayer distance study for the different graphene/hBN stacks to find the corresponding lowest energy distances. For very large interlayer distances, one can recover the pristine graphene properties, as we find from the dependence of the parameters on the interlayer distance. Furthermore, we find that orbital and SOC parameters, especially the Rashba one, depend strongly on an applied transverse electric field, giving a rich playground for spin physics. Armed with the model parameters, we employ the Dyakonov-Perel formalism to calculate the spin relaxation in graphene/hBN heterostructures. We find spin lifetimes in the nanosecond range, in agreement with recent measurements. The spin relaxation anisotropy, being the ratio of out-of-plane to in-plane spin lifetimes, is found to be giant close to the charge neutrality point, decreasing with increasing doping, and being highly tunable by an external transverse electric field. This is in contrast to bilayer graphene in which an external field saturates the spin relaxation anisotropy.

cond-mat.mes-hall↗

arXiv2018

Electrically tunable exchange splitting in bilayer graphene on monolayer Cr$_2$X$_2$Te$_6$ with X=Ge, Si, and Sn

We investigate the electronic band structure and the proximity exchange effect in bilayer graphene on a family of ferromagnetic multilayers Cr$_2$X$_2$Te$_6$, X=Ge, Si, and Sn, with first principles methods. In each case the intrinsic electric field of the heterostructure induces an orbital gap on the order of 10 meV in the graphene bilayer. The proximity exchange is strongly band dependent. For example, in the case of Cr$_2$Ge$_2$Te$_6$, the low-energy valence band of bilayer graphene has exchange splitting of 8 meV, while the low energy conduction band's splitting is 30 times less (0.3 meV). This striking discrepancy stems from the layer-dependent hybridization with the ferromagnetic substrate. Remarkably, applying a vertical electric field of a few V/nm reverses the exchange, allowing us to effectively turn ON and OFF proximity magnetism in bilayer graphene. Such a field-effect should be generic for van der Waals bilayers on ferromagnetic insulators, opening new possibilities for spin-based devices.

cond-mat.mes-hall↗

arXiv2016

Theory of proximity-induced exchange coupling in graphene on hBN/(Co, Ni)

We perform systematic first-principles calculations of the proximity exchange coupling, induced by cobalt (Co) and nickel (Ni) in graphene, via a few (up to three) layers of hexagonal boron nitride (hBN). We find that the induced spin splitting of the graphene bands is of the order of 10 meV for a monolayer of hBN, decreasing in magnitude but alternating in sign by adding each new insulating layer. We find that the proximity exchange can be giant if there is a resonant $d$ level of the transition metal close to the Dirac point. Our calculations suggest that this effect could be present in Co heterostructures, in which a $d$ level strongly hybridizes with the valence-band orbitals of graphene. Since this hybridization is spin dependent, the proximity spin splitting is unusually large, about 10 meV even for two layers of hBN. An external electric field can change the offset of the graphene and transition-metal orbitals and can lead to a reversal of the sign of the exchange parameter. This we predict to happen for the case of two monolayers of hBN, enabling electrical control of proximity spin polarization (but also spin injection) in graphene/hBN/Co structures. Nickel-based heterostructures show weaker proximity effects than cobalt heterostructures. We introduce two phenomenological models to describe the first-principles data. The minimal model comprises the graphene (effective) $p_z$ orbitals and can be used to study transport in graphene with proximity exchange, while the $p_z$-$d$ model also includes hybridization with $d$ orbitals, which is important to capture the giant proximity exchange. Crucial to both models is the pseudospin-dependent exchange coupling, needed to describe the different spin splittings of the valence and conduction bands.

cond-mat.mes-hall↗

arXiv2016

Spin-orbit coupling in methyl functionalized graphene

We present first-principles calculations of the electronic band structure and spin-orbit effects in graphene functionalized with methyl molecules in dense and dilute limits. The dense limit is represented by a 2$\times$2 graphene supercell functionalized with one methyl admolecule. The calculated spin-orbit splittings are up to $0.6$ meV. The dilute limit is deduced by investigating a large, 7$\times$7, supercell with one methyl admolecule. The electronic band structure of this supercell is fitted to a symmetry-derived effective Hamiltonian, allowing us to extract specific hopping parameters including intrinsic, Rashba, and PIA (pseudospin inversion asymmetry) spin-orbit terms. These proximity-induced spin-orbit parameters have magnitudes of about 1 meV, giant compared to pristine graphene whose intrinsic spin-orbit coupling is about 10 $μ$eV. We find that the origin of this giant local enhancement is the $sp^3$ corrugation and the breaking of local pseudospin inversion symmetry, as in the case of hydrogen adatoms. Also similar to hydrogen, methyl acts as a resonant scatterer, with a narrow resonance peak near the charge neutrality point. We also calculate STM-like images showing the local charge densities at different energies around methyl on graphene.

cond-mat.mes-hall↗