Investigation of ultrafast demagnetization and Gilbert damping and their correlation in different ferromagnetic thin films grown under identical conditions.

Following the demonstration of laser-induced ultrafast demagnetization in ferromagnetic nickel, several theoretical and phenomenological propositions have sought to uncover its underlying physics. In this work we revisit the three temperature model (3TM) and the microscopic three temperature model (M3TM) to perform a comparative analysis of ultrafast demagnetization in 20 nm thick cobalt, nickel and permalloy thin films measured using an all-optical pump-probe technique. In addition to the ultrafast dynamics at the femtosecond timescales, the nanosecond magnetization precession and damping are recorded at various pump excitation fluences revealing a fluence-dependent enhancement in both the demagnetization times and the damping factors. We confirm that the Curie temperature to magnetic moment ratio of a given system acts as a figure of merit for the demagnetization time, while the demagnetization times and damping factors show an apparent sensitivity to the density of states at the Fermi level for a given system. Further, from numerical simulations of the ultrafast demagnetization based on both the 3TM and the M3TM, we extract the reservoir coupling parameters that best reproduce the experimental data and estimate the value of the spin flip scattering probability for each system. We discuss how the fluence-dependence of inter-reservoir coupling parameters so extracted may reflect a role played by nonthermal electrons in the magnetization dynamics at low laser fluences.

Bias field orientation driven reconfigurable magnonics and magnon-magnon coupling in triangular shaped Ni80Fe20nanodot arrays.

Reconfigurable magnonics have attracted intense interest due to their myriad advantages including energy efficiency, easy tunability and miniaturization of on-chip data communication and processing devices. Here, we demonstrate efficient reconfigurability of spin-wave (SW) dynamics as well as SW avoided crossing by varying bias magnetic field orientation in triangular shaped Ni80Fe20nanodot arrays. In particular, for a range of in-plane angles of bias field, we achieve mutual coherence between two lower frequency modes leading to a drastic modification in the ferromagnetic resonance frequency. Significant modification in magnetic stray field distribution is observed at the avoided crossing regime due to anisotropic dipolar interaction between two neighbouring dots. Furthermore, using micromagnetic simulations we demonstrate that the hybrid SW modes propagate longer through an array as opposed to the non-interacting modes present in this system, indicating the possibility of coherent energy transfer of hybrid magnon modes. This result paves the way for the development of integrated on-chip magnonic devices operating in the gigahertz frequency regime.

Strain and crystallite size controlled ordering of Heusler nanoparticles having high heating rate for magneto-thermal application.

Heusler compound nanoparticles with good structural ordering need to be investigated as a potential material class for magneto-thermal applications requiring heat generation in presence of an oscillating magnetic field. Here, we report an important finding of a structural parameter related to the product of the strain and the coherent crystallite size, that can be used to efficiently control the structural ordering and the magnetic property of the Heulser compound nanoparticles. The optimization of this product parameter is found to enhance both the structural ordering and magnetic transition temperature in Co2FeSn Heusler nanoparticles. Furthermore, using magnetic hyperthermia measurements we demonstrate the possibility of heat generation using Heusler compound nanoparticles comparable to that of conventional magnetic nanoparticles. This shall lead to the development of Heulser compounds for similar applications.

Observation of Coherent Spin Waves in a Three-Dimensional Artificial Spin Ice Structure.

Harnessing high-frequency spin dynamics in three-dimensional (3D) nanostructures may lead to paradigm-shifting, next-generation devices including high density spintronics and neuromorphic systems. Despite remarkable progress in fabrication, the measurement and interpretation of spin dynamics in complex 3D structures remain exceptionally challenging. Here, we take a first step and measure coherent spin waves within a 3D artificial spin ice (ASI) structure using Brillouin light scattering. The 3D-ASI was fabricated by using a combination of two-photon lithography and thermal evaporation. Two spin-wave modes were observed in the experiment whose frequencies showed nearly monotonic variation with the applied field strength. Numerical simulations qualitatively reproduced the observed modes. The simulated mode profiles revealed the collective nature of the modes extending throughout the complex network of nanowires while showing spatial quantization with varying mode quantization numbers. The study shows a well-defined means to explore high-frequency spin dynamics in complex 3D spintronic and magnonic structures.

Applications of nanomagnets as dynamical systems: I.

When magnets are fashioned into nanoscale elements, they exhibit a wide variety of phenomena replete with rich physics and the lure of tantalizing applications. In this topical review, we discuss some of these phenomena, especially those that have come to light recently, and highlight their potential applications. We emphasize what drives a phenomenon, what undergirds the dynamics of the system that exhibits the phenomenon, how the dynamics can be manipulated, and what specific features can be harnessed for technological advances. For the sake of balance, we point out both advantages and shortcomings of nanomagnet based devices and systems predicated on the phenomena we discuss. Where possible, we chart out paths for future investigations that can shed new light on an intriguing phenomenon and/or facilitate both traditional and non-traditional applications.

Applications of nanomagnets as dynamical systems: II.

In Part I of this topical review, we discussed dynamical phenomena in nanomagnets, focusing primarily on magnetization reversal with an eye to digital applications. In this part, we address mostly wave-like phenomena in nanomagnets, with emphasis on spin waves in myriad nanomagnetic systems and methods of controlling magnetization dynamics in nanomagnet arrays which may have analog applications. We conclude with a discussion of some interesting spintronic phenomena that undergird the rich physics exhibited by nanomagnet assemblies.

Observation of magnon-magnon coupling with high cooperativity in Ni80Fe20cross-shaped nanoring array.

We report here an experimental observation of dynamic dipolar coupling induced magnon-magnon coupling and spin wave (SW) mode splitting in Ni80Fe20cross-shaped nanoring array. Remarkably, we observe an anticrossing feature with minimum frequency gap of 0.96 GHz and the corresponding high cooperativity value of 2.25. Interestingly, splitting of the highest frequency SW mode occurs due to the anisotropic dipolar interactions between the cross nanorings. Furthermore, using micromagnetic simulations we demonstrate that the coupled SW modes propagate longer as opposed to other modes present in this system. Our work paves the way towards integrated hybrid systems-based quantum magnonics and on-chip coherent information transfer.

Hydration dynamics in aqueous Pluronic P123 solution: Concentration and temperature dependence.

Here, we report the concentration (0 ≤ wt. % ≤ 30) and temperature (293 ≤ T/K ≤ 318) dependent structural and dynamical changes in an aqueous solution of a triblock copolymer (Pluronic P123) using dielectric relaxation spectroscopy (DRS), covering a frequency regime, 0.2 ≤ ν/GHz ≤ 50. Remarkable existence of slow water molecules, ∼2 times slower than bulk type water, along with bulk-like water molecules has been detected in the present DR measurements. Differential scanning calorimetric measurements support this DR observation. The signature of the sol-gel phase transition (∼15.0 wt. %, 293 K) and temperature induced extensive dehydration (>60%) for P123 molecules, which are the other notable findings of the present work. Moreover, the rate of dehydration with temperature has been found to depend on the phase of the medium. However, dehydration follows a nonlinear pattern in both sol and gel phases. A subnanosecond (∼90 ps) component, possibly originating from the hydrogen bond relaxation dynamics of the terminal C-O-H of polymer chains, has also been observed.

Dynamics at the non-ionic micelle/water interface: Impact of linkage substitution.

The impact of atom substitution on the glycoside linkage bridging the head and the tail parts in a nonionic surfactant molecule on aqueous dynamics of the resultant micellar solutions has been explored, employing time-resolved fluorescence and dielectric relaxation (DR) measurements. We have utilized n-octyl-ß-D-glucopyranoside (OG) and n-octyl-ß-D-thioglucopyranoside (OTG) as nonionic surfactants where the oxygen atom in the glucopyranoside unit is substituted by a sulfur atom. The substitution impact is immediately reflected in the dynamic light scattering measurements of aqueous solutions where the estimated size of the OTG micelles is found to be approximately four times larger than the OG micelles. Steady state spectral features obtained by using a fluorescent probe solute, coumarin 153 (C153), in these micellar solutions are quite similar and indicate locations of the solute at the micelle/water interface for both the surfactants. Interestingly, significant differences in the rotational and solvation dynamics of C153 in these two micellar solutions have been registered. The corresponding DR measurements do not indicate any signature of relaxation typical of bound water. The absence of bound water is further supported by the differential scanning calorimetric measurements. However, the typical slow solvation time scale for aqueous micellar solutions has been observed for these surfactants. Fluctuations in the solute-interface interaction energy due to the solute motion has been argued to be the origin for this slow solvation component as DR measurements do not indicate the presence of qualitatively similar relaxation time scale in the medium.

Dielectric relaxation in acetamide + urea deep eutectics and neat molten urea: Origin of time scales via temperature dependent measurements and computer simulations.

Dielectric relaxation (DR) measurements in the frequency window 0.2 ≤ ν(GHz) ≤ 50 for deep eutectic solvents (DESs) made of acetamide (CH3CONH2) and urea (NH2CONH2) with the general composition, [f CH3CONH2 + (1 - f) NH2CONH2] at f = 0.6 and 0.7, reveal three distinct relaxation time scales-τ1 ∼ 120 ps, τ2 ∼ 40 ps, and τ3 ∼ 5 ps. Qualitatively similar time scales have been observed for DR of neat molten urea, whereas the reported DR for neat molten acetamide in the same frequency window reflects two relaxation processes with no trace of ∼100 ps time scale. This slowest DR time scale (τ1) resembles closely to the long-time constant of the simulated structural H-bond relaxation (CHB(t)) involving urea pairs. Similarity in activation energies estimated from the temperature dependent DR measurements (335 ≤ T/K ≤ 363) and structural H-bond relaxations indicates that the structural H-bond relaxation overwhelmingly dominates the slowest DR relaxation in these DESs. Simulated collective reorientational correlation functions (C ℓ (t)), on the other hand, suggest that the second slower time scale (∼40 ps) derives contributions from both the single particle orientation dynamics and structural H-bond relaxation, leaving no role for hydrodynamic molecular rotations. The sub-10 ps DR time scale has been found to be connected to the fast reorientation dynamics of the component molecules (acetamide or urea). Fractional viscosity dependence for the longest DR times, τ DR ∝ η / T p , has been observed for these DESs with the fraction power p = 0.7. Subsequently, the temporal heterogeneity aspects of these media have been investigated by examining the simulated particle motion characteristics and substantiated by estimating the dynamically correlated time scales and length-scales through simulations of four-point susceptibilities and density correlations. These estimated dynamical time scales and length-scales assist in explaining the different inferences regarding solution heterogeneity drawn from different measurements on these DESs.

Efficient terahertz anti-reflection properties of metallic anti-dot structures.

We report the use of micrometer-sized copper (Cu) anti-dot structures as a novel terahertz (THz) anti-reflection coating (ARC) material and their superior performance over conventionally used metallic (Cu) thin films. Cu anti-dot structures of two different thicknesses (7 and 10 nm) with varying anti-dot diameters (100, 200, and 300 µm, inter-anti-dot separation fixed at 100 µm) are deposited on silicon substrates by RF magnetron sputtering and e-beam evaporation. The anti-reflection performance of these samples is studied in the frequency range of 0.3-2.2 THz. While continuous metallic (Cu) thin film minimizes the Fabry-Perot (FP) peak, it also suppresses the primary transmission peak, reducing the advantage due to the former effect. On the contrary, the anti-dot arrays reduce both the absolute amplitude of the FP peak and the amplitude ratio (AR) of the FP peak to the primary peak, making them a superior material for ARC applications. The AR can be further manipulated by varying the anti-dot size. A universal conductivity phase-matching condition, which is a prerequisite for the disappearance of the FP peak, is observed in these samples. The enhanced anti-reflection performance promotes these anti-dot structures as an efficient terahertz ARC material.

Collective hydration dynamics in some amino acid solutions: A combined GHz-THz spectroscopic study.

A detailed understanding of hydration of amino acids, the building units of protein, is a key step to realize the overall solvation processes in proteins. In the present contribution, we have made a combined GHz (0.2-50) to THz (0.3-2.0) experimental spectroscopic study to investigate the dynamics of water at room temperature in the presence of different amino acids (glycine, L-serine, L-lysine, L-tryptophan, L-arginine, and L-aspartic acid). The THz absorption coefficient, α(ν), of amino acids follows a trend defined by their solvent accessible surface area. The imaginary and real dielectric constants obtained in GHz and THz regions are fitted into multiple Debye model to obtain various relaxation times. The ∼100 ps time scale obtained in the GHz frequency region is attributed to the rotational motion of the amino acids. In the THz region, we obtain ∼8 ps and ∼200 fs time scales which are related to the cooperative dynamics of H-bond network and partial rotation or sudden jump of the under-coordinated water molecules. These time scales are found to be dependent on the amino acid type and the cooperative motion is found to be dependent on both the hydrophobic as well as the hydrophilic residue of amino acids.

Terahertz conductivity engineering in surface decorated carbon nanotube films by gold nanoparticles.

We report the controllable conductivity of single-walled carbon nanotubes (SWNTs) and multiwalled carbon nanotubes with their surface walls decorated by gold nanoparticles (Au NPs) with varying concentration in terahertz (THz) frequency range. Colloidal Au NPs of nominal diameter ∼15 nm are synthesized by the reduction of gold chloride solution using tri-sodium citrate. A simple chemical route is followed to attach Au NPs on the surfaces of both types of carbon nanotubes (CNTs). The attachment of Au NPs on the sidewalls of CNTs is confirmed by UV-visible spectroscopy and scanning electron microscope images. THz spectroscopic measurements are carried out at room temperature in transmission geometry in the frequency range of 0.3-2.0 THz. It is found that the THz conductivity of the surface decorated SWNT composites can either be increased or decreased by ±15% than that of the as-prepared SWNT composites by carefully choosing the Au NP concentration. The conductivity variation is qualitatively explained in terms of carrier trapping potential for low Au NP density, and alternative carrier conduction pathways at higher Au NP density and analyzed with the help of a modified universal dielectric relaxation model.

Disruption of comA homolog in Ralstonia solanacearum does not impair its twitching motility.

Ralstonia solanacearum is an important phyto-pathogenic bacterium. The bacterium exhibits type IV pili meditated twitching motility that has been implicated in the process of natural transformation in it. A comA gene homolog, alike in several other naturally competent bacteria, has been already reported in this bacterium. However, there are no report of direct link between comA and twitching motility during the natural transformation process in this pathogen. In order to figure out any connection between comA and twitching motility, we created an insertion mutation in comA gene homolog of R. solanacearum F1C1 strain. As anticipated, the insertion mutant (CBRS01 strain) was inefficient for natural transformation. CBRS01 strain was found to be proficient for twitching motility alike the wild-type F1C1. This is interesting since recent findings of Salzer et al. (2016;Environ Microbiol;18:65-74) showed deficiency of twitching motility due to comEC gene (comA homolog) mutation in another naturally competent Gram-negative bacterium Thermus thermophilus. Additionally, we also found CBRS01 strain to be proficient for extracellular cellulase activity and virulence on tomato seedlings. Our findings in this work indicate that an R. solanacearum strain inefficient in undergoing natural transformation can, however, be proficient in exhibiting twitching motility.

EMI shielding and conductivity of carbon nanotube-polymer composites at terahertz frequency.

We investigate the shielding effectiveness and complex conductivity of single-walled carbon nanotubes (SWNT) distributed in a polyvinyl alcohol (PVA) matrix in the THz frequency range. SWNTs are dispersed in PVA matrices with varying SWNT content (keeping the thickness of SWNT/PVA film constant) using a slow-drying method, and terahertz time-domain spectroscopy (THz-TDS) is performed at room temperature in transmission geometry in the frequency range of 0.3-2.1 THz. The transmittance spectra show a possible application of SWNT/PVA composites as low-bandpass filters in the THz frequency region. Shielding effectiveness of all the samples is measured, and, at a particular probing frequency, they tend to follow a linear relationship with SWNT weight fraction in the polymer matrices. THz conductivity of the composite system is described in the light of a.c. hopping conduction.

Spin-wave dynamics in perpendicularly magnetized antidot multilayers.

Using all-optical time-resolved magneto-optical Kerr effect (TR-MOKE) measurements we demonstrate an efficient modulation of the spin-wave (SW) dynamics via the bias magnetic field orientation around nanoscale diamond shaped antidots that are arranged on a square lattice within a [Co(0.75)/Pd(0.9)]8multilayer with perpendicular magnetic anisotropy (PMA). Micromagnetic modelling of the experimental results reveals that the SW modes in the lower frequency regime are related to narrow shell regions around the antidots, where in-plane domain structures are formed due to the reduced magnetic anisotropy, caused by Ga+ion irradiation during the focused ion beam milling process of antidot fabrication. The in-plane direction of the shell magnetization undergoes a striking change with magnetic field orientation, leading to the sharp variation of the edge localized (shell) SW modes. Nevertheless, the coupling between such edge localized and bulk SWs for different orientations of bias field in PMA systems give rise to interesting Physics and attests to new prospects for developing energy efficient and hybrid-system-based next-generation nanoscale magnonic devices. .

Femtosecond Laser-Induced Transient Magnetization Enhancement and Ultrafast Demagnetization Mediated by Domain Wall Origami.

Femtosecond laser-induced ultrafast magnetization dynamics are all-optically probed for different remanent magnetic domain states of a [Co/Pt]22 multilayer sample, thus revealing the tunability of the direct transport of spin angular momentum across domain walls. A variety of different magnetic domain configurations (domain wall origami) at remanence achieved by applying different magnetic field histories are investigated by time-resolved magneto-optical Kerr effect magnetometry to probe the ultrafast magnetization dynamics. Depending on the underlying domain landscape, the spin-transport-driven magnetization dynamics show a transition from typical ultrafast demagnetization to being fully dominated by an anomalous transient magnetization enhancement (TME) via a state in which both TME and demagnetization coexist in the system. Thereby, the study reveals an extrinsic channel for the modulation of spin transport, which introduces a route for the development of magnetic spin-texture-driven ultrafast spintronic devices.

Manipulating ultrafast magnetization dynamics of ferromagnets using the odd-even layer dependence of two-dimensional transition metal di-chalcogenides.

Two-dimensional transition metal dichalcogenides (TMDs) have drawn immense interest due to their strong spin-orbit coupling and unique layer number dependence in response to spin-valley coupling. This leads to the possibility of controlling the spin degree of freedom of the ferromagnet (FM) in thin film heterostructures and may prove to be of interest for next-generation spin-based devices. Here, we experimentally demonstrate the odd-even layer dependence of WS2 nanolayers by measurements of the ultrafast magnetization dynamics in WS2/Co3FeB thin film heterostructures by using time-resolved Kerr magnetometry. The fluence (photon energy per unit area) dependent magnetic damping (α) reveals the existence of broken symmetry and the dominance of inter- and intraband scattering for odd and even layers of WS2, respectively. The higher demagnetization time, τm, in 3 and 5 layers of WS2 is indicative of the interaction between spin-orbit and spin-valley coupling due to the broken symmetry. The lower τm in even layers as compared to the bare FM layer suggests the presence of a spin transport. By correlating τm and α, we pinpointed the dominant mechanisms of ultrafast demagnetization. The mechanism changes from spin transport to spin-flip scattering for even layers of WS2 with increasing fluence. A fundamental understanding of the two-dimensional material and its odd-even layer dependence at ultrashort timescales provides valuable information for designing next-generation spin-based devices.

The 2024 magnonics roadmap.

Magnonicsis a research field that has gained an increasing interest in both the fundamental and applied sciences in recent years. This field aims to explore and functionalize collective spin excitations in magnetically ordered materials for modern information technologies, sensing applications and advanced computational schemes. Spin waves, also known as magnons, carry spin angular momenta that allow for the transmission, storage and processing of information without moving charges. In integrated circuits, magnons enable on-chip data processing at ultrahigh frequencies without the Joule heating, which currently limits clock frequencies in conventional data processors to a few GHz. Recent developments in the field indicate that functional magnonic building blocks for in-memory computation, neural networks and Ising machines are within reach. At the same time, the miniaturization of magnonic circuits advances continuously as the synergy of materials science, electrical engineering and nanotechnology allows for novel on-chip excitation and detection schemes. Such circuits can already enable magnon wavelengths of 50 nm at microwave frequencies in a 5G frequency band. Research into non-charge-based technologies is urgently needed in view of the rapid growth of machine learning and artificial intelligence applications, which consume substantial energy when implemented on conventional data processing units. In its first part, the 2024 Magnonics Roadmap provides an update on the recent developments and achievements in the field of nano-magnonics while defining its future avenues and challenges. In its second part, the Roadmap addresses the rapidly growing research endeavors on hybrid structures and magnonics-enabled quantum engineering. We anticipate that these directions will continue to attract researchers to the field and, in addition to showcasing intriguing science, will enable unprecedented functionalities that enhance the efficiency of alternative information technologies and computational schemes.

Polarizing effect of aligned nanoparticles in terahertz frequency region.

We report the polarizing behavior of aligned Ni nanoparticles (NPs) having average diameter of 165±15 nm in ~210 µm thick polyvinyl alcohol (PVA) matrix in the frequency range of 0.2-1.6 THz. The NPs have been prepared via a wet chemical route and then aligned in PVA film by using an external magnetic field. When the polarization of THz electric field is parallel to the NPs alignment direction, a strong THz absorption is observed whereas a minimum THz absorption is noticed for the corresponding perpendicular configuration. Degree of polarization is calculated to be 0.9±0.08. Considering the good polarizing performance, ease of preparation, durability, and low maintenance, this aligned NP system is a perfect candidate to emerge as a potential THz polarizer.