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Aleksandra Lindner

Publications and source records attributed to Aleksandra Lindner.

4 recordsLinked to original sources

Chiral Spinterfaces as an Overlooked Component of the Chiral-Induced Spin Selectivity Effect

The chiral-induced spin selectivity (CISS) effect is generally attributed to spin-selective transport through chiral molecules, while the role of the molecule-electrode interface remains largely unexplored. Here, we show that adsorption of chiral amino acid derived molecules on ferromagnetic Ni thin films generates a remanent chirality-dependent magneto-optical response that is localized to the molecule-Ni/NiO interface and can be reversibly switched by an external magnetic field, demonstrating its genuine magnetic character. A comprehensive series of control experiments establishes that the response originates from the interfacial region rather than from the molecular layer or the bulk ferromagnet. First-principles calculations reveal that Boc-methionine adsorption proceeds through energetically accessible sulfur- and carboxyl-bound configurations that produce distinct molecular orientations and ligand-p/Ni-d hybridization, thereby defining structurally and electronically distinct interfaces. Together, the experimental and theoretical results support the formation of chiral spinterfaces, identifying the molecule-ferromagnet interface as an active and previously overlooked component of CISS systems. These findings broaden the microscopic picture of CISS beyond the chiral molecule itself and reveals interface electronic structure as a key design parameter for spin-selective molecular devices.

cond-mat.mtrl-sci

Chiral molecule-induced contributions to ferromagnetic resonance

Despite extensive research on chirality-driven spin selectivity, most studies have focused on static magnetic properties, while the influence of chirality on the dynamic magnetic response remains largely unexplored. Here, we investigate how chiral molecular interfaces affect magnetization dynamics in thin Co/Ni multilayers with perpendicular magnetic anisotropy using broadband ferromagnetic resonance spectroscopy. A comparison between bare (reference) films and molecule-functionalized (hybrid) samples reveals no measurable changes in either the resonance field or the linewidth that could be attributed to the presence of the chiral environment. Motivated by our findings we develop a macrospin description that distinguishes equilibrium modifications of the magnetic free-energy landscape (MIPAC-type effects) from non-equilibrium, CISS-induced spin torques. Our analysis shows that equilibrium modifications primarily shift the resonance condition via changes to the free energy landscape and thereby the effective field, whereas damping-like non-equilibrium torques provide a distinct channel for varying the effective damping rate. This approach establishes clear criteria for disentangling chiral-interface-induced energy modifications from torque-driven dynamical effects in ferromagnetic resonance experiments.

cond-mat.mtrl-sci

Chiral Porphyrin Monolayers on Ferromagnetic Thin Films: Ultrafast Spectroscopy of Hybrid Interfaces

Hybrid ferromagnetic metal/organic interfaces (spinterfaces) exhibit unique properties, including spin filtering. In parallel, chiral organic molecules can themselves induce efficient spin filtering, leading to unexpectedly high spin polarizations. Here, we investigate how the proximity of gold-capped Co/Ni ferromagnetic multilayers influences the spectroscopic properties and photoinduced electron dynamics of chiral oligopeptides bearing a porphyrin chromophore. The molecules are covalently attached to the gold cap via a chiral linker, forming a self-assembled monolayer. The porphyrin macrocycles adopt an orientation parallel to the surface, resulting in the formation of J-like aggregates. Photoinduced dynamics are probed using femtosecond pump-probe transient absorption spectroscopy. Despite excitation of only a single molecular layer, a clear transient absorption signal of the porphyrin singlet excited state is observed. Adsorption on the metal surface leads to a pronounced reduction of the excited-state lifetime. However, no signatures of long-lived photoinduced charge-transfer products are detected. Furthermore, no dependence of the excited-state dynamics on either the magnetization direction of the ferromagnetic layer or the molecular chirality is observed.

cond-mat.mtrl-sci

Spin-orbit interaction driven terahertz nonlinear dynamics in transition metals

The interplay of electric charge, spin, and orbital polarizations, coherently driven by picosecond long oscillations of light fields in spin-orbit coupled systems, is the foundation of emerging terahertz spintronics and orbitronics. The essential rules for how terahertz light interacts with these systems in a nonlinear way are still not understood. In this work, we demonstrate a universally applicable electronic nonlinearity originating from spin-orbit interactions in conducting materials, wherein the interplay of light-induced spin and orbital textures manifests. We utilized terahertz harmonic generation spectroscopy to investigate the nonlinear dynamics over picosecond timescales in various transition metal films. We found that the terahertz harmonic generation efficiency scales with the spin Hall conductivity in the studied films, while the phase takes two possible values (shifted by π), depending on the d-shell filling. These findings elucidate the fundamental mechanisms governing non-equilibrium spin and orbital polarization dynamics at terahertz frequencies, which is relevant for potential applications of terahertz spin- and orbital-based devices.

physics.app-ph