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Register a new userDriving spin chirality by electron dynamics in laser-excited antiferromagnets
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Optical generation of complex spin textures is one of the most exciting challenges of modern spintronics. Here, we uncover a distinct physical mechanism for imprinting spin chirality into collinear magnets with short laser pulses. By simultaneously treating the laser-ignited evolution of electronic structure and magnetic order, we show that their intertwined dynamics can result in an emergence of quasi-stable chiral states. We find that laser-driven chirality does not require any auxiliary external fields or intrinsic spin-orbit interaction to exist, and it can survive on the time scale of nanoseconds even in the presence of thermal fluctuations, which makes the uncovered mechanism relevant for understanding various optical experiments on magnetic materials. Our findings open a new perspective at the interaction of complex chiral magnetism with light.
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An ultrafast spin current can be induced by femtosecond laser excitation in a ferromagnetic (FM) thin film in contact with a nonmagnetic (NM) metal. The propagation of an ultrafast spin current into NM metal has recently been found in experiments to generate transient spin accumulation. Unlike spin accumulation in equilibrium NM metals that occurs due to spin transport at the Fermi energy, transient spin accumulation involves highly nonequilibrium hot electrons well above the Fermi level. To date, the diffusion and dissipation of this transient spin accumulation has not been well studied. Using the superdiffusive spin transport model, we demonstrate how spin accumulation is generated in NM metals after laser excitation in an FM|NM bilayer. The spin accumulation shows an exponential decay from the FM|NM interface, with the decay length increasing to the maximum value and then decreasing until saturation. By analyzing the ultrafast dynamics of laser-excited hot electrons, the effective mean free path, which can be characterized by the averaged product of the group velocity and lifetime of hot electrons, is found to play a key role. The interface reflectivity has little influence on the spin accumulation in NM metals. Our calculated results are in qualitative agreement with recent experiments.
We measure and analyze the chirality of the Dzyaloshinskii-Moriya interaction (DMI) stabilized spin textures in multilayers of Ta/Co$_{20}$Fe$_{60}$B$_{20}$/MgO. The effective DMI is measured experimentally using domain wall motion measurements, both in the presence (using spin orbit torques) and absence of driving currents (using magnetic fields). We observe that the current-induced domain wall motion yields a change in effective DMI magnitude and opposite domain wall chirality when compared to field-induced domain wall motion (without current). We explore this effect, which we refer to as current-induced DMI, by providing possible explanations for its emergence, and explore the possibilty of its manifestation in the framework of recent theoretical predictions of DMI modifications due to spin currents.
Chirality induced spin selectivity, discovered about two decades ago in helical molecules, is a non-equilibrium effect that emerges from the interplay between geometrical helicity and spin-orbit interactions. Several model Hamiltonians building on this interplay have been proposed and while these can yield spin-polarized transport properties that agrees with experimental observations, they simultaneously depend on unrealistic values of the spin-orbit interaction parameters. It is likely, however, that a common deficit originates from the fact that all these models are uncorrelated, or, single-electron theories. Therefore, chirality induced spin selectivity is, here, addressed using a many-body approach, which allows for non-equilibrium conditions and a systematic treatment of the correlated state. The intrinsic molecular spin-polarization increases by two orders of magnitudes, or more, compared to the corresponding result in the uncorrelated model. In addition, the electronic structure responds to varying external magnetic conditions which, therefore, enables comparisons of the currents provided for different spin-polarizations in one of the (or both) leads between which the molecule is mounted. Using experimentally feasible parameters and room temperature, the obtained normalized difference between such currents may be as large as 5 - 10 % for short molecular chains, clearly suggesting the vital importance of including electron correlations when searching for explanations of the phenomenon.
The quantum point contact (QPC) back-action has been found to cause non-thermal-equilibrium excitations to the electron spin states in a quantum dot (QD). Here we use back-action as an excitation source to probe the spin excited states spectroscopy for both the odd and even electron numbers under a varying parallel magnetic field. For a single electron, we observed the Zeeman splitting. For two electrons, we observed the splitting of the spin triplet states $|T^{+}>$ and $|T^{0}>$ and found that back-action drives the singlet state $|S>$ overwhelmingly to $|T^{+}>$ other than $|T^{0}>$. All these information were revealed through the real-time charge counting statistics.
Here we propose a mechanism by which spin polarization can be generated dynamically in chiral molecular systems undergoing photo-induced electron transfer. The proposed mechanism explains how spin polarization emerges in systems where charge transport is dominated by incoherent hopping, mediated by spin orbit and electronic exchange couplings through an intermediate charge transfer state. We derive a simple expression for the spin polarization that predicts a non-monotonic temperature dependence consistent with recent experiments. We validate this theory using approximate quantum master equations and the numerically exact hierarchical equations of motion. The proposed mechanism of chirality induced spin selectivity should apply to many chiral systems, and the ideas presented here have implications for the study of spin transport at temperatures relevant to biology, and provide simple principles for the molecular control of spins in fluctuating environments.
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