Acoustic nanocavities (ANCs) with resonance frequencies much above 1 GHz are prospective to be exploited in sensors and quantum operating devices. Nowadays, acoustic nanocavities fabricated from van der Waals (vdW) nanolayers allow them to exhibit resonance frequencies of the breathing acoustic mode up to f ∼ 1 THz and quality factors up to Q ∼ 103. For such high acoustic frequencies, electrical methods fail, and optical techniques are used for the generation and detection of coherent phonons. Here, we study experimentally acoustic nanocavities fabricated from WSe2 layers with thicknesses from 8 up to 130 nm deposited onto silica colloidal crystals. The substrate provides a strong mechanical support for the layers while keeping their acoustic properties the same as in membranes. We concentrate on experimental and theoretical studies of the amplitude of the optically measured acoustic signal from the breathing mode, which is the most important characteristic for acousto-optical devices. We probe the acoustic signal optically with a single wavelength in the vicinity of the exciton resonance and measure the relative changes in the reflectivity induced by coherent phonons up to 3 × 10-4 for f ∼ 100 GHz. We reveal the enhancement of photon-phonon interaction for a wide range of acoustic frequencies and show high sensitivity of the signal amplitude to the photoelastic constants governed by the deformation potential and dielectric function for photon energies near the exciton resonance. We also reveal a resonance in the photoelastic response (we call it photoelastic resonance) in the nanolayers with thickness close to the Bragg condition. The estimates show the capability of acoustic nanocavities with an exciton resonance for operations with high-frequency single phonons at an elevated temperature.

We propose and demonstrate the concept of hybrid coherent control (CC) whereby a quantum or classical harmonic oscillator is excited by two excitations: one is quasiharmonic (i.e., harmonic with a finite lifetime) and the other is a pulsed broadband excitation. Depending on the phase relation between the two excitations, controlled by the detuning of the oscillator eigenfrequencies and the wave forms of the quasiharmonic and broadband excitations, it is possible to observe Fano-like spectra of the harmonic oscillator due to the interference of the two responses to the simultaneously acting excitations. Experimentally, as an example, the hybrid CC is implemented for magnons in a ferromagnetic grating where GHz coherent phonons act as the quasiharmonic excitation and the broadband impact arises from pulsed optical excitation followed by spin dynamics in the ferromagnetic nanostructure.

Nanoscale detection and control of the magnetic order underpins a broad spectrum of fundamental research and practical device applications. The key principle involved is the breaking of time-reversal (T) symmetry, which in ferromagnets is generated by an internal magnetization. However, the presence of a net-magnetization also imposes severe limitations on compatibility with other prominent phases ranging from superconductors to topological insulators, as well as on spintronic device scalability. Recently, altermagnetism has been proposed as a solution to this restriction, since it shares the enabling T-symmetry breaking characteristic of ferromagnetism, combined with the antiferromagnetic-like vanishing net-magnetization. To date, altermagnetic ordering has been inferred from spatially averaged probes. Here, we demonstrate nanoscale imaging and control of altermagnetic ordering ranging from nanoscale vortices to domain walls to microscale single-domain states in MnTe. We combine the T-symmetry breaking sensitivity of X-ray magnetic circular dichroism with magnetic linear dichroism and photoemission electron microscopy, to achieve detailed imaging of the local altermagnetic ordering vector. A rich variety of spin configurations can be imposed using microstructure patterning or thermal cycling in magnetic fields. The demonstrated detection and control of altermagnetism paves the way for future research ranging from ultra-scalable digital and neuromorphic spintronic devices, to the interplay of altermagnetism with non-dissipative superconducting or topological phases.

Nanoscale detection and control of the magnetic order underpins a spectrum of condensed-matter research and device functionalities involving magnetism. The key principle involved is the breaking of time-reversal symmetry, which in ferromagnets is generated by an internal magnetization. However, the presence of a net magnetization limits device scalability and compatibility with phases, such as superconductors and topological insulators. Recently, altermagnetism has been proposed as a solution to these restrictions, as it shares the enabling time-reversal-symmetry-breaking characteristic of ferromagnetism, combined with the antiferromagnetic-like vanishing net magnetization1-4. So far, altermagnetic ordering has been inferred from spatially averaged probes4-19. Here we demonstrate nanoscale imaging of altermagnetic states from 100-nanometre-scale vortices and domain walls to 10-micrometre-scale single-domain states in manganese telluride (MnTe)2,7,9,14-16,18,20,21. We combine the time-reversal-symmetry-breaking sensitivity of X-ray magnetic circular dichroism12 with magnetic linear dichroism and photoemission electron microscopy to achieve maps of the local altermagnetic ordering vector. A variety of spin configurations are imposed using microstructure patterning and thermal cycling in magnetic fields. The demonstrated detection and controlled formation of altermagnetic spin configurations paves the way for future experimental studies across the theoretically predicted research landscape of altermagnetism, including unconventional spin-polarization phenomena, the interplay of altermagnetism with superconducting and topological phases, and highly scalable digital and neuromorphic spintronic devices3,14,22-24.

Phonons and magnons are prospective information carriers to substitute the transfer of charge in nanoscale communication devices. Our ability to manipulate them at the nanoscale and with ultimate speed is examined by ultrafast acoustics and femtosecond optomagnetism, which use ultrashort laser pulses for generation and detection of the corresponding coherent excitations. Ultrafast magnetoacoustics merges these research directions and focuses on the interaction of optically generated coherent phonons and magnons. In this review, we present ultrafast magnetoacoustic experiments with nanostructures based on the alloy (Fe,Ga) known as Galfenol. We demonstrate how broad we can manipulate the magnetic response on an optical excitation by controlling the spectrum of generated coherent phonons and their interaction with magnons. Resonant phonon pumping of magnons, formation of magnon polarons, driving of a magnetization wave by a guided phonon wavepacket are demonstrated. The presented experimental results have great application potential in emerging areas of modern nanoelectronics.

In this work, we present a method to enhance the longitudinal spin Seebeck effect at platinum/yttrium iron garnet (Pt/YIG) interfaces. The introduction of a partial interlayer of bismuth selenide (Bi2Se3, 2.5% surface coverage) interfaces significantly increases (by ∼380%–690%) the spin Seebeck coefficient over equivalent Pt/YIG control devices. Optimal devices are prepared by transferring Bi2Se3 nanoribbons, prepared under anaerobic conditions, onto the YIG (111) chips followed by rapid over-coating with Pt. The deposited Pt/Bi2Se3 nanoribbon/YIG assembly is characterized by scanning electron microscope. The expected elemental compositions of Bi2Se3 and YIG are confirmed by energy dispersive x-ray analysis. A spin Seebeck coefficient of 0.34–0.62 μV/K for Pt/Bi2Se3/YIG is attained for our devices, compared to just 0.09 μV/K for Pt/YIG controls at a 12 K thermal gradient and a magnetic field swept from −50 to +50 mT. Superconducting quantum interference device magnetometer studies indicate that the magnetic moment of Pt/Bi2Se3/YIG treated chips is increased by ∼4% vs control Pt/YIG chips (i.e., a significant increase vs the ±0.06% chip mass reproducibility). Increased surface magnetization is also detected in magnetic force microscope studies of Pt/Bi2Se3/YIG, suggesting that the enhancement of spin injection is associated with the presence of Bi2Se3 nanoribbons.

Topologically protected magnetic textures are promising candidates for information carriers in future memory devices, as they can be efficiently propelled at very high velocities using current-induced spin torques. These textures—nanoscale whirls in the magnetic order—include skyrmions, half-skyrmions (merons) and their antiparticles. Antiferromagnets have been shown to host versions of these textures that have high potential for terahertz dynamics, deflection-free motion and improved size scaling due to the absence of stray field. Here we show that topological spin textures, merons and antimerons, can be generated at room temperature and reversibly moved using electrical pulses in thin-film CuMnAs, a semimetallic antiferromagnet that is a testbed system for spintronic applications. The merons and antimerons are localized on 180° domain walls, and move in the direction of the current pulses. The electrical generation and manipulation of antiferromagnetic merons is a crucial step towards realizing the full potential of antiferromagnetic thin films as active components in high-density, high-speed magnetic memory devices.

This work presents micromagnetic simulations in ferromagnetic nanogratings for the full range of directions of an applied in-plane external magnetic field. We focus on the modification of the magnon mode characteristics when the magnetic field orientation is gradually changed between the classical Damon-Eshbach (DE) and backward-volume (BV) geometries. We found that in a specific range of field directions, the magnon mode parameters differ significantly from the parameters in the classical cases, namely, the modes are characterized by complex spatial distributions and have low group velocities. The center of this range corresponds to the direction of the external magnetic field, which gives the maximal nonuniform distribution of the static magnetization in the nanogratings.

We present an experimental study of ultrafast optical excitation of magnetostatic surface spin wave (MSSW) packets and their spectral properties in thin films of pure iron. As the packets leave the excitation area and propagate in space, their spectra evolve non-trivially. Particularly, low or high frequency components are suppressed at the border of the excitation area depending on the orientation of the external magnetic field with respect to the magnetocrystalline anisotropy axes of the film. The effect is ascribed to the ultrafast local heating of the film. Furthermore, the time resolution of the implemented all-optical technique allows us to extract the chirp of the MSSW packet in the time domain via wavelet analysis. The chirp is a result of the group velocity dispersion of the MSSW and, thus, is controlled by the film's magnetic parameters, magnetization and anisotropy, and external field orientation. The demonstrated tunable modulation of MSSW wave packets with femtosecond laser pulses may find application in future magnonic-photonic hybrid devices for wave-based data processing.

Strain engineering can be used to control the physical properties of two-dimensional van der Waals (2D-vdW) crystals. Coherent phonons, which carry dynamical strain, could push strain engineering to control classical and quantum phenomena in the unexplored picosecond temporal and nanometer spatial regimes. This intriguing approach requires the use of coherent GHz and sub-THz 2D phonons. Here, we report on nanostructures that combine nanometer thick vdW layers and nanogratings. Using an ultrafast pump–probe technique, we generate and detect in-plane coherent phonons with frequency up to 40 GHz and hybrid flexural phonons with frequency up to 10 GHz. The latter arises from the periodic modulation of the elastic coupling of the vdW layer at the grooves and ridges of the nanograting. This creates a new type of a tailorable 2D periodic phononic nanoobject, a flexural phononic crystal, offering exciting prospects for the ultrafast manipulation of states in 2D materials in emerging quantum technologies.

The rate and pathways of relaxation of a magnetic medium to its equilibrium following excitation with intense and short laser pulses are the key ingredients of ultrafast optical control of spins. Here we study experimentally the evolution of the magnetization and magnetic anisotropy of thin films of a ferromagnetic metal galfenol (Fe$_{0.81}$Ga$_{0.19}$) resulting from excitation with a femtosecond laser pulse. From the temporal evolution of the hysteresis loops we deduce that the magnetization $M_S$ and magnetic anisotropy parameters $K$ recover within a nanosecond, and the ratio between $K$ and $M_S$ satisfies the thermal equilibrium's power law in the whole time range spanning from a few picoseconds to 3 nanoseconds. We further use the experimentally obtained relaxation times of $M_S$ and $K$ to analyze the laser-induced precession and demonstrate how they contribute to its frequency evolution at the nanosecond timescale.

In nanoscale communications, high-frequency surface acoustic waves are becoming effective data carriers and encoders. On-chip communications require acoustic wave propagation along nanocorrugated surfaces which strongly scatter traditional Rayleigh waves. Here, we propose the delivery of information using subsurface acoustic waves with hypersound frequencies of ∼20 GHz, which is a nanoscale analogue of subsurface sound waves in the ocean. A bunch of subsurface hypersound modes are generated by pulsed optical excitation in a multilayer semiconductor structure with a metallic nanograting on top. The guided hypersound modes propagate coherently beneath the nanograting, retaining the surface imprinted information, at a distance of more than 50 μm which essentially exceeds the propagation length of Rayleigh waves. The concept is suitable for interfacing single photon emitters, such as buried quantum dots, carrying coherent spin excitations in magnonic devices and encoding the signals for optical communications at the nanoscale.

We present detailed experimental measurements and simulations of the field-dependent magnetization and magnetoresistance in the vicinity of the Curie temperature in the highly disordered dilute ferromagnetic semiconductor (Ga,Mn)As. The observed dependence of the magnetization on external magnetic field and temperature is consistent with three-dimensional Heisenberg equation of state calculations including a narrow distribution of critical temperatures. The magnetoresistance shows a peak at the Curie temperature due to the suppression of magnetic scattering in an applied magnetic field, which is well-described by considering changes in the square of the magnetization induced by the magnetic field.

The recently discovered electrical-induced switching of antiferromagnetic (AF) materials that have spatial inversion asymmetry has enriched the field of spintronics immensely and opened the door for the concept of antiferromagnetic memory devices. CuMnAs is one promising AF material that exhibits such electrical switching ability and has been studied to switch using electrical pulses of length millisecond down to picosecond but with little focus on the nanosecond regime. We demonstrate here the switching of CuMnAs/GaP using nanosecond pulses. Our results showed that in the nanosecond regime, low-energy switching and a high readout signal with highly reproducible behavior down to a single pulse can be achieved. Moreover, a comparison of the two switching methods of orthogonal switching and polarity switching was made on the same device, and it showed distinct behaviors that can be exploited selectively for different future memory/processing applications.

Energy harvesting is a concept which makes dissipated heat useful by transferring thermal energy to other excitations. Most of the existing principles are realized in systems which are heated continuously. We present the concept of high-frequency energy harvesting where the dissipated heat in a sample excites resonant magnons in a thin ferromagnetic metal layer. The sample is excited by femtosecond laser pulses with a repetition rate of 10 GHz, which results in temperature modulation at the same frequency with amplitude ~0.1 K. The alternating temperature excites magnons in the ferromagnetic nanolayer which are detected by measuring the net magnetization precession. When the magnon frequency is brought onto resonance with the optical excitation, a 12-fold increase of the amplitude of precession indicates efficient resonant heat transfer from the lattice to coherent magnons. The demonstrated principle may be used for energy harvesting in various nanodevices operating at GHz and sub-THz frequency ranges.

Recent research works have shown that the magnetic order in some antiferromagnetic materials can be manipulated and detected electrically, due to two physical mechanisms: Neel-order spin-orbit torques and anisotropic magnetoresistance. While these observations open up opportunities to use antiferromagnets for magnetic memory devices, different physical characterization methods are required for a better understanding of those mechanisms. Here we report a magnetic field induced rotation of the antiferromagnetic Neel vector in epitaxial tetragonal CuMnAs thin films. Using soft x-ray magnetic linear dichroism spectroscopy, x-ray photoemission electron microscopy, integral magnetometry and magneto-transport methods, we demonstrate spin-flop switching and continuous spin reorientation in antiferromagnetic films with uniaxial and biaxial magnetic anisotropies, respectively. From field-dependent measurements of the magnetization and magnetoresistance, we obtain key material parameters including the anisotropic magnetoresistance coefficients, magnetocrystalline anisotropy, spin-flop and exchange fields.

We propose a method to induce deterministic motion of a magnetic domain wall in a nanowire by inducing short strain pulses uniformly along the nanowire. Via inverse magnetostriction, a strain pulse causes the magnetic anisotropy to vary uniformly on a timescale comparable to the magnetisation dynamics. The resultant torque on the magnetic moments within the domain wall cause it to move along the nanowire. Using numerical calculations we analyse in detail the dependence of the domain wall’s motion on the material’s parameters and on the anisotropy pulse profile, and we consider the specific case of the anisotropy induced by voltage pulses applied to a hybrid piezoelectric/ferromagnet device. The method will be applicable to a range of magnetic textures including skyrmions, solitons, and domain walls in antiferromagnets, and is prospective for applications in a range of areas including ultra-energy efficient information storage and processing, communications technologies, position encoding and biomedical science.

Stochastic behavior fundamentally limits the performance and reliability of nanomagnetic devices. Typically, stochastic behavior is assumed to be the result of simple thermal activation, but it may also be "dynamically induced," i.e., a direct result of the spatial and temporal complexity of magnetization dynamics. Here, we show how materials engineering can be used to comprehensively suppress dynamically induced stochasticity. Using the dynamics of magnetic domain walls in Ni80Fe20 nanowires as a case study, we show how manipulation of the Gilbert damping constant via doping with the rare-earth-element terbium dramatically simplifies domain-wall dynamics. This allows us to obtain quasi-deterministic behaviors from systems that nominally exhibit exceptionally high levels of stochasticity.

Strong coupling between two quanta of different excitations leads to the formation of a hybridized state which paves a way for exploiting new degrees of freedom to control phenomena with high efficiency and precision. A magnon polaron is the hybridized state of a phonon and a magnon, the elementary quanta of lattice vibrations and spin waves in a magnetically-ordered material. A magnon polaron can be formed at the intersection of the magnon and phonon dispersions, where their frequencies coincide. The observation of magnon polarons in the time domain has remained extremely challenging because the weak interaction of magnons and phonons and their short lifetimes jeopardize the strong coupling required for the formation of a hybridized state. Here, we overcome these limitations by spatial matching of magnons and phonons in a metallic ferromagnet with a nanoscale periodic surface pattern. The spatial overlap of the selected phonon and magnon modes formed in the periodic ferromagnetic structure results in a high coupling strength which, in combination with their long lifetimes allows us to find clear evidence of an optically excited magnon polaron. We show that the symmetries of the localized magnon and phonon states play a crucial role in the magnon polaron formation and its manifestation in the optically excited magnetic transients.

We study experimentally the influence of the laser-induced temperature gradient on the parameters of propagating magnetostatic surface waves in thin film of the ferromagnetic metallic alloy Galfenol Fe0.81Ga0.19. The material has a pronounced magnetocrystalline anisotropy and exhibits the long-distance propagation of magnetostatic surface waves excited with femtosecond laser pulses. The excitation pulse heats up the sample locally, what leads to the spatial-temporal change of magnetization and anisotropy parameters of the film, and thus excites the magnetostatic surface waves. We show experimentally that the spectrum of the excited waves narrows as they propagate in such a gradient medium. By changing the orientation of external magnetic field with respect to anisotropy axes of the sample, we control whether the low- or high-frequency part of the spin waves spectrum is suppressed.