Spin-flip Excitations Research Articles

Spin-Conserved and Spin-Flip Optical Excitations from the Bethe-Salpeter Equation Formalism.

Like adiabatic time-dependent density-functional theory (TD-DFT), the Bethe–Salpeter equation (BSE) formalism of many-body perturbation theory, in its static approximation, is “blind” to double (and higher) excitations, which are ubiquitous, for example, in conjugated molecules like polyenes. Here, we apply the spin-flip ansatz (which considers the lowest triplet state as the reference configuration instead of the singlet ground state) to the BSE formalism in order to access, in particular, double excitations. The present scheme is based on a spin-unrestricted version of the GW approximation employed to compute the charged excitations and screened Coulomb potential required for the BSE calculations. Dynamical corrections to the static BSE optical excitations are taken into account via an unrestricted generalization of our recently developed (renormalized) perturbative treatment. The performance of the present spin-flip BSE formalism is illustrated by computing excited-state energies of the beryllium atom, the hydrogen molecule at various bond lengths, and cyclobutadiene in its rectangular and square-planar geometries.

Coulomb Correlations as the Root Cause of the Ferromagnetic Transition in a Quantum Hall State with Filling Factor v = 2

A study is preformed of the relationship between the spectrum of low-energy collective excitations in two-dimensional Fermi liquids and the paramagnet/ferromagnet phase transition in the quantum Hall state with filling factor v = 2. It is shown theoretically and experimentally that the softening of the energy of collective spin–flip excitations accompanies the spontaneous switching of the spin configuration of the system from the paramagnetic to the ferromagnetic phase.

Half-Metal–Spin-Gapless-Semiconductor Junctions as a Route to the Ideal Diode

The ideal diode is a theoretical concept that completely conducts the electric current under forward bias without any loss and that behaves like a perfect insulator under reverse bias. However, real diodes have a junction barrier that electrons have to overcome and thus they have a threshold voltage $V_T$, which must be supplied to the diode to turn it on. This threshold voltage gives rise to power dissipation in the form of heat and hence is an undesirable feature. In this work, based on half-metallic magnets and spin-gapless semiconductors we propose a diode concept that does not have a junction barrier and the operation principle of which relies on the spin-dependent transport properties of the HMM and SGS materials. We show that the HMM and SGS materials form an Ohmic contact under any finite forward bias, while for a reverse bias the current is blocked due to spin-dependent filtering of the electrons. Thus, the HMM-SGS junctions act as a diode with zero threshold voltage $V_T$, and linear $I-V$ characteristics as well as an infinite on:off ratio at zero temperature. However, at finite temperatures, non-spin-flip thermally excited high-energy electrons as well as low-energy spin-flip excitations can give rise to a leakage current and thus reduce the on:off ratio under a reverse bias. Furthermore, a zero threshold voltage allows one to detect extremely weak signals and due to the Ohmic HMM-SGS contact, the proposed diode has a much higher current drive capability and low resistance, which is advantageous compared to conventional semiconductor diodes. We employ the NEGF method combined with DFT to demonstrate the linear $I-V$ characteristics of the proposed diode based on two-dimensional half-metallic Fe/MoS$_2$ and spin-gapless semiconducting VS$_2$ planar heterojunctions.

Spin-flip excitations and Stoner ferromagnetism in a strongly correlated quantum Hall system

Spin-flip excitations in a quantum Hall electron system at fixed filling factor $\ensuremath{\nu}=2$ are modeled and studied under conditions of a strong Coulomb interaction when the ``Landau level mixing'' is a dominant factor determining the excitation energy. The ``one-exciton'' approach used for the purely electronic excitations in question allows us to describe the Stoner transition from the unpolarized/paramagnet state to the polarized/ferromagnet one. The theoretical results are compared with the available experimental data.

First-principles perspective on magnetic second sound

The fluctuations of the magnetic order parameter, or longitudinal spin excitations, are investigated theoretically in the ferromagnetic Fe and Ni as well as in the antiferromagnetic phase of the pnictide superconductor FeSe. The charge and spin dynamics of these systems is described by evaluating the generalized charge and spin density response function calculated from first-principles linear response time dependent density functional theory within adiabatic local spin density approximation. We observe that the formally non-interacting Kohn-Sham system features strong coupling between the magnetization and charge dynamics in the longitudinal channel and that the coupling is effectively removed upon the inclusion of the Coulomb interaction in the charge channel and the resulting appearance of plasmons. The longitudinal spin fluctuations acquire a collective character without the emergence of the Goldstone boson, similar to the case of paramagnon excitations in non-magnetic metals like Pd. In ferromagnetic Fe and Ni the longitudinal spin dynamics is governed by interactions between low-energy intraband electron-hole pairs while in quasi two dimensional antiferromagnet FeSe it is dominated by the interband transitions with energies of the order of exchange splitting. In the later material, the collective longitudinal magnetization fluctuations feature well defined energies and long life times for small momenta and appear below the particle-hole continuum. The modes become strongly Landau-damped for growing wave-vectors. We relate our theoretical findings to existing experimental spin-polarized electron energy loss spectroscopy results. In bulk bcc Fe, the longitudinal magnetic modes appear above the typical energies of transverse spin-waves, have energies comparable with the Stoner spin-flip excitation continuum, and are order of magnitude less energetic than the charge dynamics.

Engineering of Magnetic Coupling in Nanographene.

Nanographenes with sublattice imbalance host a net spin according to Lieb's theorem for bipartite lattices. Here, we report the on-surface synthesis of atomically precise nanographenes and their atomic-scale characterization on a gold substrate by using low-temperature noncontact atomic force microscopy and scanning tunneling spectroscopy. Our results clearly confirm individual nanographenes host a single spin of S=1/2 via the Kondo effect. In covalently linked nanographene dimers, two spins are antiferromagnetically coupled with each other as revealed by inelastic spin-flip excitation spectroscopy. The magnetic exchange interaction in dimers can be well engineered by tuning the local spin density distribution near the connection region, consistent with mean-field Hubbard model calculations. Our work clearly reveals the emergence of magnetism in nanographenes and provides an efficient way to further explore the carbon-based magnetism.

Many-Body Physics of Single and Double Spin-Flip Excitations in NiO.

Understanding many-body physics of elementary excitations has advanced our control over material properties. Here, we study spin-flip excitations in NiO using Ni L_{3}-edge resonant inelastic x-ray scattering (RIXS) and present a strikingly different resonant energy behavior between single and double spin-flip excitations. Comparing our results with single-site full-multiplet ligand field theory calculations we find that the spectral weight of the double-magnon excitations originates primarily from the double spin-flip transition of the quadrupolar RIXS process within a single magnetic site. Quadrupolar spin-flip processes are among the least studied excitations, despite being important for multiferroic or spin-nematic materials due to their difficult detection. We identify intermediate state multiplets and intra-atomic core-valence exchange interactions as the key many-body factors determining the fate of such excitations. RIXS resonant energy dependence can act as a convincing proof of existence of nondipolar higher-ranked magnetic orders in systems for which, only theoretical predictions are available.

Spin-flip excitations induced by dehydrogenation in a magnetic single-molecule junction.

Recent scanning tunneling microscopy experiments on electron transport through iron(ii) phthalocyanine (FePc) molecules adsorbed on Au(111) surfaces have revealed that the measured differential conductance signals can be modulated through a selective dehydrogenation process [R. Li et al., Chem. Commun. 54, 9135 (2018)]. To understand the physical origin of the variation of line shapes in the measured dI/dV spectra, we employ a first-principles-based quantum transport simulation to calculate the electronic structures and transport properties in the dehydrogenated FePc/Au(111) composite system. Theoretical results indicate that the removal of eight outermost hydrogen atoms in the FePc molecule distorts the planar molecular conformation by increasing the distance between the Fe center and substrate and thus breaks the ligand field exerted on the Fe 3d orbitals. Such variations lead to a weaker coupling with the substrate along with a different local electronic configuration of the Fe center compared with that of the intact case, which is responsible for the suppression of Kondo resonance and the appearance of spin-flip excitation in the system. The simulated dI/dV plots are consistent with the experimental observations, showing the typical step features at finite bias associated with spin-flip excitations of a spin-1 quantum magnet. These findings provide important insights into the electron correlation effects modulated by the structural and chemical environment of the molecular spin center.

Magnetic Contrast at Spin-Flip Excitations: An Advanced X-Ray Spectroscopy Tool to Study Magnetic-Ordering.

The determination of the local orientation and magnitude of the magnetization in spin textures plays a pivotal role in understanding and harnessing magnetic properties for technological applications. Here, we show that by employing the polarization dependence of resonant inelastic X-ray scattering (RIXS), we can directly probe the spin ordering with chemical and site selectivity. Applied on the prototypical ferrimagnetic mixed-valence system, magnetite ([Fe3+]A[Fe3+,Fe2+]BO4), we can distinguish spin-flip excitations at the A and B antiferromagnetically coupled Fe3+ sublattices and quantify the exchange field. Furthermore, it is possible to determine the orbital contribution to the magnetic moment from detailed angular dependence measurements. RIXS dichroism measurements performed at spin-flip excitations with nanometer spatial resolution will offer a powerful mapping contrast suitable for the characterization of magnetic ordering at interfaces and engineered spin textures.

Observation of Coexistence of Yu-Shiba-Rusinov States and Spin-Flip Excitations.

We investigate the spectral evolution in different metal phthalocyanine molecules on NbSe2 surface using scanning tunnelling microscopy (STM) as a function of the coupling with the substrate. For manganese phthalocyanine (MnPc), we demonstrate a smooth spectral crossover from Yu-Shiba-Rusinov (YSR) bound states to spin-flip excitations. This has not been observed previously and it is in contrast to simple theoretical expectations. We corroborate the experimental findings using numerical renormalization group calculations. Our results provide fundamental new insight on the behavior of atomic scale magnetic/SC hybrid systems, which is important, for example, for engineered topological superconductors and spin logic devices.

Kink far below the Fermi level reveals new electron-magnon scattering channel in Fe

Many properties of real materials can be modeled using ab initio methods within a single-particle picture. However, for an accurate theoretical treatment of excited states, it is necessary to describe electron-electron correlations including interactions with bosons: phonons, plasmons, or magnons. In this work, by comparing spin- and momentum-resolved photoemission spectroscopy measurements to many-body calculations carried out with a newly developed first-principles method, we show that a kink in the electronic band dispersion of a ferromagnetic material can occur at much deeper binding energies than expected (Eb = 1.5 eV). We demonstrate that the observed spectral signature reflects the formation of a many-body state that includes a photohole bound to a coherent superposition of renormalized spin-flip excitations. The existence of such a many-body state sheds new light on the physics of the electron-magnon interaction which is essential in fields such as spintronics and Fe-based superconductivity.

Signatures of low-energy fractionalized excitations in α−RuCl3 from field-dependent microwave absorption

Topologically ordered states of matter are generically characterized by excitations with quantum number fractionalization. A prime example is the spin liquid realized in Kitaev's honeycomb-lattice compass model where spin-flip excitations fractionalize into Majorana fermions and Ising gauge fluxes. While numerous compounds have been proposed to be proximate to such a spin-liquid phase, clear-cut evidence for fractionalized excitations is lacking. Here we employ microwave absorption measurements to study the low-energy excitations in $\alpha$-RuCl$_3$ over a wide range of frequencies, magnetic fields, and temperatures, covering in particular the vicinity of the field-driven quantum phase transition where long-range magnetic order disappears. In addition to conventional gapped magnon modes we find a highly unusual broad continuum characteristic of fractionalization which -- most remarkably -- extends to energies below the lowest sharp mode and to temperatures significantly higher than the ordering temperature, and develops a gap of a nontrivial origin in strong magnetic fields. Our results unravel the signatures of fractionalized excitations in $\alpha$-RuCl$_3$ and pave the way to a more complete understanding of the Kitaev spin liquid and its instabilities.

Coupling between dynamic magnetic and charge-order correlations in the cuprate superconductor Nd2−xCexCuO4

Charge order has now been observed in several cuprate high-temperature superconductors. We report a resonant inelastic x-ray scattering experiment on the electron-doped cuprate Nd$_{2-x}$Ce$_{x}$CuO$_4$ that demonstrates the existence of dynamic correlations at the charge order wave vector. Upon cooling we observe a softening in the electronic response, which has been predicted to occur for a d-wave charge order in electron-doped cuprates. At low temperatures, the energy range of these excitations coincides with that of the dispersive magnetic modes known as paramagnons. Furthermore, measurements where the polarization of the scattered photon is resolved indicate that the dynamic response at the charge order wave vector primarily involves spin-flip excitations. Overall, our findings indicate a coupling between dynamic magnetic and charge-order correlations in the cuprates.

Finite-temperature dynamical correlations for the dimerized spin- 12 chain

We use the density matrix renormalization group method (DMRG) to compute the frequency and momentum resolved spin-spin correlation functions of a dimerized spin-1/2 chain under a magnetic field at finite temperature. The spectral features strongly depend on the regime of the magnetic field. For increasing magnetic fields, the transitions from a gapped spin liquid phase to a Tomonaga-Luttinger liquid, and then to a totally polarized phase, can be identified in the spectra. Compared to the zero temperature case, the finite temperature excitations give rise to additional spectral features that we compute numerically and identify analytically as transitions from thermally excited states. We compute quantitatively the broadening of the dispersion of a single spin-flip excitation due to the temperature and find a strong asymmetric broadening. We discuss the consequences of these findings for neutron experiments on dimerized one dimensional quantum chains.

Effects of random atomic disorder on the magnetic stability of graphene nanoribbons with zigzag edges

We investigate the effects of randomly distributed atomic defects on the magnetic properties of graphene nanoribbons with zigzag edges using an extended mean-field Hubbard model. For a balanced defect distribution among the sublattices of the honeycomb lattice in the bulk region of the ribbon, the ground state antiferromagnetism of the edge states remains unaffected. By analyzing the excitation spectrum, we show that while the antiferromagnetic ground state is susceptible to single spin flip excitations from edge states to magnetic defect states at low defect concentrations, it's overall stability is enhanced with respect to the ferromagnetic phase.

Electromagnetic modes from Stoner enhancement: Graphene as a case study

In systems with substantial spin fluctuations, dressing the polarization function by ladder diagram of Stoner (spin-flip) excitations can drastically modify the electromagnetic response. As a case study, we provide the detailed analysis of the corrections to the non-local optical conductivity of both doped and undoped graphene. While the resummation of ladder diagram of Stoner excitations does not affect the TE mode in doped graphene, it allows for a new undamped TM mode in undoped graphene. This is the sole effect of corrections arising from ladder diagrams and is dominated by Stoner excitations along the ladder rung which goes away by turning off the source of spin-flip interactions. In the case of doped graphene, the inclusion of spin-flip particle-hole fluctuations reduces the energy of plasmon mode.

Simulation of inelastic spin flip excitations and Kondo effect in STM spectroscopy of magnetic molecules on metal substrates

Single-ion magnetic anisotropy in molecular magnets leads to spin flip excitations that can be measured by inelastic scanning tunneling microscope (STM) spectroscopy. Here I present a semi ab initio scheme to compute the spectral features associated with inelastic spin flip excitations and Kondo effect of single molecular magnets. To this end density functional theory calculations of the molecule on the substrate are combined with more sophisticated many-body techniques for solving the Anderson impurity problem of the spin-carrying orbitals of the magnetic molecule coupled to the rest of the system, containing a phenomenological magnetic anisotropy term. For calculating the STM spectra an exact expression for the in the ideal STM limit, when the coupling to the STM tip becomes negligibly small, is derived. In this limit the is simply related to the spectral function of the molecule–substrate system. For the case of an Fe porphyrin molecule on the Au(1 1 1) substrate, the calculated STM spectra are in good agreement with recently measured STM spectra, showing the typical step features at finite bias associated with spin flip excitation of a spin-1 quantum magnet. For the case of Kondo effect in Mn porphyrin on Au(1 1 1), the agreement with the experimental spectra is not as good due to the neglect of quantum interference in the tunneling.

Phase diagram of the frustrated J1 − J2 transverse field Ising model on the square lattice

We study the zero-temperature phase diagram of transverse field Ising model on the J1 − J2 square lattice. In zero magnetic field, the model has a classical Néel phase for J2/J1 < 0.5 and an antiferromagnetic collinear phase for J2/J1 > 0.5. We incorporate harmonic fluctuations by using linear spin wave theory (LSWT) with single spin flip excitations above a magnetic order background and obtain the phase diagram of the model in this approximation. We find that harmonic quantum fluctuations of LSWT fail to lift the large degeneracy at J2/J1 = 0.5 and exhibit some inconsistent regions on the phase diagram. However, we show that anharmonic fluctuations of cluster operator approach (COA) resolve the inconsistency of the LSWT, which reveals a string-valence bond solid ordered phase for the highly frustrated region.

Renormalization of single-ion magnetic anisotropy in the absence of the Kondo effect

Inelastic spin flip excitations associated with single-ion magnetic anisotropy of quantum spins, can be strongly renormalized by Kondo exchange coupling to the conduction electrons in the substrate, as shown recently for the case of Co adatoms on CuN$_2$ islands. In this case differential conductance spectra show zero-bias anomalies due to a Kondo effect of the doubly degenerate ground state, and finite-bias step features due to spin flip excitations. Here I consider spin-1 quantum magnets with positive uniaxial anisotropy, where the ground state is non-degenerate and hence the Kondo effect does not take place. Nevertheless the renormalization of inelastic spin excitations due to exchange coupling by hybridization of the quantum spin with the conduction electrons still takes place despite the complete absence of the Kondo effect in the ground state. Additionally, I show that away from particle-hole symmetry, charge fluctuations have a similar effect to Kondo exchange coupling, leading to the renormalization of spin flip excitations. However, in contrast to the renormalization by Kondo exchange, charge fluctuations lead to asymmetric spectra, which for strong charge fluctuations can mimic Fano behavior.

Dzyaloshinskii-Moriya interaction in α−Fe2O3 measured by magnetic circular dichroism in resonant inelastic soft x-ray scattering

Fe ${L}_{2,3}$-edge x-ray absorption spectra (XAS) and magnetic circular dichroism (MCD) in resonant inelastic x-ray scattering (RIXS) of $\ensuremath{\alpha}\text{\ensuremath{-}}{\mathrm{Fe}}_{2}{\mathrm{O}}_{3}$ were measured to identify the electronic structure responsible for its weak ferromagnetism caused by the Dzyaloshinskii-Moriya interaction (DMI) at room temperature. In contrast to negligible MCD in XAS, MCD in RIXS (RIXS-MCD) was clearly observed in the $dd$ excitation at 1.8 eV via excitation to charge-transfer states. Furthermore, RIXS-MCD showed a crystal orientation dependence, indicating that the observed RIXS-MCD originated from DMI. The observed RIXS-MCD is well described by ab initio charge-transfer multiplet calculations, revealing that the RIXS-MCD derives from spin flip excitations at delocalized ${e}_{\mathrm{g}}$ orbitals. By the combination of the experiments and calculations, RIXS-MCD has unraveled that the origin of DMI in $\ensuremath{\alpha}\text{\ensuremath{-}}{\mathrm{Fe}}_{2}{\mathrm{O}}_{3}$ is the ${e}_{\mathrm{g}}$ orbitals, which are strongly hybridized with the $2p$ orbitals of oxygen atoms. The results demonstrate the importance of RIXS-MCD for identifying the electronic structure related to DMI.