No Arabic abstract
Femtosecond laser excitation of FeRh/Pt bilayers launches an ultrafast pulse of electric photocurrent in the Pt-layer and thus results in emission of electromagnetic radiation in the THz spectral range. Analysis of the THz emission as a function of polarization of the femtosecond laser pulse, external magnetic field, sample temperature and sample orientation shows that photocurrent can emerge due to vertical spin pumping and photo-induced inverse spin-orbit torque at the FeRh/Pt interface. The vertical spin pumping from FeRh to Pt does not depend on the polarization of light and originates from ultrafast laser-induced demagnetization of the ferromagnetic phase of FeRh. The photo-induced inverse spin-orbit torque at the FeRh/Pt interface can be described in terms of a helicity-dependent effect of circularly polarized light on the magnetization of the ferromagnetic FeRh and subsequent generation of a photocurrent.
The ultrashort laser excitation of Co/Pt magnetic heterostructures can effectively generate spin and charge currents at the interfaces between magnetic and nonmagnetic layers. The direction of these photocurrents can be controlled by the helicity of the circularly polarized laser light and an external magnetic field. Here, we employ THz time-domain spectroscopy to investigate further the role of interfaces in these photo-galvanic phenomena. In particular, the effects of either Cu or ZnO interlayers on the photocurrents in Co/X/Pt (X = Cu, ZnO) have been studied by varying the thickness of the interlayers up to 5 nm. The results are discussed in terms of spin-diffusion phenomena and interfacial spin-orbit torque.
The possibility of hybridizing collective electronic motion with mid-infrared (mid-IR) light to form surface polaritons has made van der Waals layered materials a versatile platform for extreme light confinement and tailored nanophotonics. Graphene and its heterostructures have attracted particular attention because the absence of an energy gap allows for plasmon polaritons to be continuously tuned. Here, we introduce black phosphorus (BP) as a promising new material in surface polaritonics that features key advantages for ultrafast switching. Unlike graphene, BP is a van der Waals bonded semiconductor, which enables high-contrast interband excitation of electron-hole pairs by ultrashort near-infrared (near-IR) pulses. We design a SiO$_2$/BP/SiO$_2$ heterostructure in which the surface phonon modes of the SiO$_2$ layers hybridize with surface plasmon modes in BP that can be activated by photo-induced interband excitation. Within the Reststrahlen band of SiO$_2$, the hybrid interface polariton assumes surface-phonon-like properties, with a well-defined frequency and momentum and excellent coherence. During the lifetime of the photogenerated electron-hole plasma, coherent polariton waves can be launched by a broadband mid-IR pulse coupled to the tip of a scattering-type scanning near-field optical microscopy (s-SNOM) setup. The scattered radiation allows us to trace the new hybrid mode in time, energy, and space. We find that the surface mode can be activated within ~50 fs and disappears within 5 ps, as the electron-hole pairs in BP recombine. The excellent switching contrast and switching speed, the coherence properties, and the constant wavelength of this transient mode make it a promising candidate for ultrafast nanophotonic devices.
We consider the role of non-triviality resulting from a non-Hermitian Hamiltonian that conserves twofold PT-symmetry assembled by interconnections between a PT-symmetric lattice and its time reversal partner. Twofold PT-symmetry in the lattice produces additional surface exceptional points that play the role of new critical points, along with the bulk exceptional point. We show that there are two distinct regimes possessing symmetry-protected localized states, of which localization lengths are robust against external gain and loss. The states are demonstrated by numerical calculation of a quasi-1D ladder lattice and a 2D bilayered square lattice.
We have studied spin-orbit (SO) field in Ni$_{80}$Fe$_{20}$(Py)/W/Pt trilayer by means of spin-torque ferromagnetic resonance, and demonstrated that the W/Pt interface generates an extra SO field acting on the Py layer. This unprecedented field originates from the following three processes, 1) spin accumulation at W/Pt interface via the Rashba-Edelstein effect, 2) diffusive spin transport in the W layer, and 3) spin absorption into the Py layer through accumulation at the Py/W interface. Our result means that we can create extra SO field away from the ferromagnet/ metal interface and control its strength by a combination of two different metals.
Topological phononic crystals (PCs) are periodic artificial structures which can support nontrivial acoustic topological bands, and their topological properties are linked to the existence of topological edge modes. Most previous studies focused on the topological edge modes in Bragg gaps which are induced by lattice scatterings. While local resonant gaps would be of great use in subwavelength control of acoustic waves, whether it is possible to achieve topological interface states in local resonant gaps is a question. In this article, we study the topological bands near local resonant gaps in a time-reversal symmetric acoustic systems and elaborate the evolution of band structure using a spring-mass model. Our acoustic structure can produce three band gaps in subwavelength region: one originates from local resonance of unit cell and the other two stem from band folding. It is found that the topological interface states can only exist in the band folding induced band gaps but never appear in the local resonant band gap. The numerical simulation perfectly agrees with theoretical results. Our study provides an approach of localizing the subwavelength acoustic wave.