Materials Science (cond-mat.mtrl-sci)

Abstract: Spin-orbit torque (SOT) is receiving tremendous attention from both fundamental and application-oriented aspects. Co2MnGa, a Weyl ferromagnet that is in a class of topological quantum materials, possesses cubic-based high structural symmetry, the L21 crystal ordering, which should be incapable of hosting anisotropic SOT in conventional understanding. Here we show the discovery of a gigantic anisotropy of self-induced SOT in Co2MnGa. The magnitude of the SOT is comparable to that of heavy metal/ferromagnet bilayer systems despite the high inversion symmetry of the Co2MnGa structure. More surprisingly, a sign inversion of the self-induced SOT is observed for different crystal axes. This finding stems from the interplay of the topological nature of the electronic states and their strong modulation by external strain. Our research enriches the understanding of the physics of self-induced SOT and demonstrates a versatile method for tuning SOT efficiencies in a wide range of materials for topological and spintronic devices.

Abstract: $1T$-TiSe$_2$ is believed to posses a soft electronic mode, i.e., plasmon or exciton, that might be responsible for the exciton condensation and charge-density-wave (CDW) transition. Here, we explore collective electronic excitations in single-layer $1T$-TiSe$_2$ by using the ab-initio electromagnetic linear response and unveil intricate scattering pathways of two-dimensional (2D) plasmon mode. We found the dominant role of plasmon-phonon scattering, which in combination with the CDW gap excitations leads to the anomalous temperature dependence of the plasmon linewidth across the CDW transition. Below the transition temperature $T_{\rm CDW}$ a strong hybridization between 2D plasmon and CDW excitations is obtained. These optical features are highly tunable due to temperature-dependent CDW gap modifications and are argued to be universal for the CDW-bearing 2D materials.

Abstract: As a topological Dirac semimetal with controllable spin-orbit coupling and conductivity, PtSe$_2$, a transition-metal dichalcogenide, is a promising material for several applications from optoelectric to sensors. However, its potential for spintronics applications is yet to be explored. In this work, we demonstrate that PtSe$_{2}$/Ni$_{80}$Fe$_{20}$ heterostructure can generate a large damping-like current-induced spin-orbit torques (SOT), despite the absence of spin-splitting in bulk PtSe$_{2}$. The efficiency of charge-to-spin conversion is found to be $(-0.1 \pm 0.02)$~nm$^{-1}$ in PtSe$_{2}$/Ni$_{80}$Fe$_{20}$, which is three times that of the control sample, Ni$_{80}$Fe$_{20}$/Pt. Our band structure calculations show that the SOT due to the PtSe$_2$ arises from an unexpectedly large spin splitting in the interfacial region of PtSe$_2$ introduced by the proximity magnetic field of the Ni$_{80}$Fe$_{20}$ layer. Our results open up the possibilities of using large-area PtSe$_{2}$ for energy-efficient nanoscale devices by utilizing the proximity-induced SOT.

Abstract: We present the experimental study of the primary, $\alpha$, and secondary, $\beta^*$, relaxations of the glassy polymer polyethylene naphthalate (PEN), by Modulated Differential Scanning Calorimetry (MDSC), Thermally Stimulated Discharge Currents (TSDC) and Broadband Dielectric Spectroscopy (BDS). Results show how the $\alpha$ and $\beta^*$ relaxations can be considered part of a very broad and distributed relaxation. The $\beta^*$ relaxation is composed of a main contribution ($\beta_3^*$) and two additional ones ($\beta_1^*$ and $\beta_2^*$) and each elementary mode of the relaxation has its own glass transition temperature. This scenario gives rise to an extended glass transition mainly centered in $T_{g\beta^*} \sim 305$ K and $T_{g\alpha} \sim 387$ K.

Abstract: Recent studies identified spin-order-driven phenomena such as spin-charge interconversion without relying on the relativistic spin-orbit interaction. Those physical properties can be prominent in systems containing light magnetic atoms due to sizable exchange splitting and may pave the way for realizations of giant responses correlated with the spin degree of freedom. In this paper, we present a systematic symmetry analysis based on the spin crystallographic groups and identify physical property of a vast number of magnetic materials up to 1500 in total. Absence of spin-orbital entanglement leads to the spin crystallographic symmetry having richer property compared to the well-known magnetic space group symmetry. By decoupling the spin and orbital degrees of freedom, our analysis enables us to take a closer look into the relation between the dimensionality of spin structures and the resultant physical properties and to identify the spin and orbital contributions separately. In stark contrast to the established analysis with magnetic space groups, the spin crystallographic group manifests richer symmetry including spin translation symmetry and leads to nontrivial emergent responses. For representative examples, we discuss geometrical nature of the anomalous Hall effect and magnetoelectric effect, and classify the spin Hall effect arising from the spontaneous spin-charge coupling. Using the power of computational analysis, we apply our symmetry analysis to a wide range of magnets, encompassing complex magnets such as those with noncoplanar spin structures as well as collinear and coplanar magnets. We identify emergent multipoles relevant to physical responses and argue that our method provides a systematic tool for exploring sizable electromagnetic responses driven by spin ordering.

Abstract: Degenerate states in condensed matter are frequently the cause of unwanted fluctuations, which prevent the formation of ordered phases and reduce their functionalities. Removing these degeneracies has been a common theme in materials design, pursued for example by strain engineering at interfaces. Here, we explore a non-equilibrium approach to lift degeneracies in solids. We show that coherent driving of the crystal lattice in bi- and multilayer graphene, boosts the coupling between two doubly-degenerate modes of E1u and E2g symmetry, which are virtually uncoupled at equilibrium. New vibronic states result from anharmonic driving of the E1u mode to large amplitdues, boosting its coupling to the E2g mode. The vibrational structure of the driven state is probed with time-resolved Raman scattering, which reveals laser-field dependent mode splitting and enhanced lifetimes. We expect this phenomenon to be generally observable in many materials systems, affecting the non-equilibrium emergent phases in matter.

Abstract: The occurrence of a noncollinear magnetic structure at a Mn monolayer grown epitaxially on Fe(100) is predicted theoretically, using spinor density-functional theory, and observed experimentally, using x-ray magnetic circular dichroism (XMCD) and linear dichroism (XMLD) spectroscopies. The combined use of XMCD and XMLD at the Mn-absorption edge allows us to assess the existence of ferromagnetic and antiferromagnetic order at the interface, and also to determine the moment orientations with element specificity. The experimental results thus obtained are in excellent agreement with the magnetic structure determined theoretically.

Abstract: The electronic structure of short-chain thiophenes (thiophene, 2,2'-bithiophene and 2,2':5',2'-terthiophene) in the gas phase has been investigated by combining the outcomes of Near-Edge X-ray-Absorption Fine-Structure (NEXAFS) and X-ray Photoemission Spectroscopy (XPS) at the C K-edge with those of density functional theory (DFT) calculations. The calculated NEXAFS spectra provide a comprehensive description of the main experimental features and allow their attribution. The evolution of the C1s NEXAFS spectral features is analyzed as a function of the number of thiophene rings; a tendency to a stabilization for increasing chain length is found. The computation of the binding energy allows to assign the experimental XPS peaks to the different carbon sites on the basis of both the inductive effects generated by the presence of the S atom as well as of the differential aromaticity effects.

Abstract: We theoretically investigate the optically-induced demagnetization of ferromagnetic FePt using the time-dependent density functional theory (TDDFT). We compare the demagnetization mechanism in the perturbative and nonperturbative limits of light-matter interaction and show how the underlying mechanism of the ultrafast demagnetization depends on the driving laser intensity. Our calculations show that the femtosecond demagnetization in TDDFT is a longitudinal magnetization reduction and results from a nonlinear optomagnetic effect, akin to the inverse Faraday effect. The demagnetization scales quadratically with the electric field $E$ in the perturbative limit, i.e., $\Delta M_z \propto E^{2}$. Moreover, the magnetization dynamics happens dominantly at even multiples $n\omega_0$, ($n = 0, 2, \cdots$) of the pump-laser frequency $\omega_0$, whereas odd multiples of $\omega_0$ do not contribute. We further investigate the demagnetization in conjunction to the optically-induced change of electron occupations and electron correlations. Correlations within the Kohn-Sham local-density framework are shown to have an appreciable yet distinct effect on the amount of demagnetization depending on the laser intensity. Comparing the ${ab~initio}$ computed demagnetizations with those calculated from spin occupations, we show that electronic coherence plays a dominant role in the demagnetization process, whereas interpretations based on the time-dependent occupation numbers poorly describe the ultrafast demagnetization.