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We predict the existence of Einstein-de Haas effect in topological magnon insulators. Temperature variation of angular momentum in the topological state shows a sign change behavior, akin to the low temperature thermal Hall conductance response. This manifests itself as a macroscopic mechanical rotation of the material hosting topological magnons. We show that an experimentally observable Einstein-de Haas effect can be measured in the square-octagon, the kagome, and the honeycomb lattices. Albeit, the effect is the strongest in the square-octagon lattice. We treat both the low and the high temperature phases using spin wave and Schwinger boson theory, respectively. We propose an experimental set up to detect our theoretical predictions. We suggest candidate square-octagon materials where our theory can be tested.
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The Einstein-de Haas (EdH) effect, where the spin angular momentum of electrons is transferred to the mechanical angular momentum of atoms, was established experimentally in 1915. While a semi-classical explanation of the effect exists, modern electronic structure methods have not yet been applied to modelling the phenomenon. In this paper we investigate its microscopic origins by means of a non-collinear tight-binding model of an $textrm{O}_2$ dimer, which includes the effects of spin-orbit coupling, coupling to an external magnetic field, and vector Stoner exchange. By varying an external magnetic field in the presence of spin-orbit coupling, a torque can be generated on the dimer, validating the presence of the EdH effect. Avoided energy level crossings and the rate of change of magnetic field determine the evolution of the spin. We find also that the torque exerted on the nuclei by the electrons in a time-varying $B$ field is not only due to the EdH effect. Other contributions arise from field-induced changes in the electronic orbital angular momentum and from the direct action of the Faraday electric field associated with the time-varying magnetic field.
The original observation of the Einstein-de Haas effect was a landmark experiment in the early history of modern physics that illustrates the relationship between magnetism and angular momentum. Today the effect is still discussed in elementary physics courses to demonstrate that the angular momentum associated with the aligned electron spins in a ferromagnet can be converted to mechanical angular momentum by reversing the direction of magnetisation using an external magnetic field. In recent times, a related problem in magnetism concerns the time-scale over which this angular momentum transfer can occur. It is known experimentally for several metallic ferromagnets that intense photoexcitation leads to a drop in the magnetisation on a time scale shorter than 100 fs, a phenomenon called ultrafast demagnetisation. The microscopic mechanism for this process has been hotly debated, with one key question still unanswered: where does the angular momentum go on these sub-picosecond time scales? Here we show using femtosecond time-resolved x-ray diffraction that a large fraction of the angular momentum lost from the spin system on the laserinduced demagnetisation of ferromagnetic iron is transferred to the lattice on sub-picosecond timescales, manifesting as a transverse strain wave that propagates from the surface into the bulk. By fitting a simple model of the x-ray data to simulations and optical data, we roughly estimate that the angular momentum occurs on a time scale of 200 fs and corresponds to 80% of the angular momentum lost from the spin system. Our results show that interaction with the lattice plays an essential role in the process of ultrafast demagnetisation in this system.
Layered three-dimensional (3D) topological semimetals have attracted intensively attention due to the exotic phenomena and abundantly tunable properties. Here we report the experimental evidence for the 3D topological semimetal phase in layered material TaNiTe5 single crystals through quantum oscillations. Strong quantum oscillations have been observed with diamagnetism background in TaNiTe5. By analyzing the de Haas-van Alphen oscillations, multi-periodic oscillations were extracted, in content with magnetotransport measurements. Moreover, nontrivial {pi} Berry phase with 3D Fermi surface is identified, indicating the topologically nontrivial feature in TaNiTe5. Additionally, we demonstrated the thin-layer of TaNiTe5 crystals is highly feasible by the mechanical exfoliation, which offers a platform to explore exotic properties in low dimensional topological semimetal and paves the way for potential applications in nanodevices.
The field of topological electronic materials has seen rapid growth in recent years, in particular with the increasing number of weakly interacting systems predicted and observed to host topologically non-trivial bands. Given the broad appearance of topology in such systems, it is expected that correlated electronic systems should also be capable of hosting topologically non-trivial states. Interest in correlated platforms is heightened by the prospect that collective behavior therein may give rise to new types of topological states and phenomena not possible in non-interacting systems. However, to date only a limited number of correlated topological materials have been definitively reported due to both the challenge in calculation of their electronic properties and the experimental complexity of correlation effects imposed on the topological aspects of their electronic structure. Here, we report a de Haas-van Alphen (dHvA) study of the recently discovered kagome metal Fe$_3$Sn$_2$ mapping the massive Dirac states strongly coupled to the intrinsic ferromagnetic order. We observe a pair of quasi-two-dimensional Fermi surfaces arising from the massive Dirac states previously detected by spectroscopic probes and show that these band areas and effective masses are systematically modulated by the rotation of the ferromagnetic moment. Combined with measurements of Berry curvature induced Hall conductivity, we find that along with the Dirac fermion mass, velocity, and energy are suppressed with rotation of the moment towards the kagome plane. These observations demonstrate that strong coupling of magnetic order to electronic structure similar to that observed in elemental ferromagnets can be extended to topologically non-trivial electronic systems, suggesting pathways for connecting topological states to robust spintronic technologies.
In 1915, Einstein and de Haas and Barnett demonstrated that changing the magnetization of a magnetic material results in mechanical rotation, and vice versa. At the microscopic level, this effect governs the transfer between electron spin and orbital angular momentum, and lattice degrees of freedom, understanding which is key for molecular magnets, nano-magneto-mechanics, spintronics, and ultrafast magnetism. Until now, the timescales of electron-to-lattice angular momentum transfer remain unclear, since modeling this process on a microscopic level requires addition of an infinite amount of quantum angular momenta. We show that this problem can be solved by reformulating it in terms of the recently discovered angulon quasiparticles, which results in a rotationally invariant quantum many-body theory. In particular, we demonstrate that non-perturbative effects take place even if the electron--phonon coupling is weak and give rise to angular momentum transfer on femtosecond timescales.
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