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Spin dynamics in Al-substituted yttrium iron garnets is investigated using broadband ferromagnetic resonance measurements in the temperature range T=200-360 K. Using the measured data, the resonance field and linewidth as well as their temperature dependence are determined, with implications for the uniformity and overall quality of the samples prepared via different chemical fabrication routes. These key parameters governing the spin dynamics in the material are important for its applications in high-speed spintronic and magnonic devices., Comment: 8 pages, 3 figures; accepted for publication in Journal of Low Temperature Physics (2025)

The dynamic magnetic properties of Full Heusler alloy thin films of Co$_2$FeGe, grown on MgO (001) substrates under different thermal conditions, were investigated. Brillouin light scattering and ferromagnetic resonance measurements revealed that depositing at room temperature followed by annealing at 300 deg C for 1 hour produces the best results for maximizing magnetization, exchange stiffness, and minimizing spin-dynamic dissipation in the films, which are desirable characteristics for high-speed spintronic devices. Additionally, strong hybridization of spin waves in the Damon-Eshbach geometry was observed, which is attractive for applications in magnonic signal processing circuits., Comment: 13 pages, 6 figures

Magnetic properties of Y$_3$AlFe$_4$O$_{12}$ garnet ceramics have been studied over a wide range of temperature ($3-370$ K) and magnetic fields (up to $2$ kOe). Effects of varying the temperature on some of the application-specific magnetic characteristics have been analyzed in detail. With the decrease in temperature, the effective anisotropy constant, $K_{Eff}$, is found to sharply rise below $\sim150$ K, while the saturation magnetization, $M_s$, changes only slightly ($<20\%$ within $3-250$ K). The exchange stiffness, $A_{ex}$, and spin wave stiffness, $D$, parameters mirror the relatively smooth behavior of the magnetization at low temperatures but display a rapid drop when $T$ approaches $T_C\approx436$ K. The temperature dependence of the domain wall thickness and the critical single-domain size correlate with the corresponding values for pure Y$_3$Fe$_5$O$_{12}$ (YIG) and are in agreement with the theoretical estimates. We conclude by discussing the ways of how to use the obtained results for tailoring the magnetic properties of YIG-based materials for technological applications., Comment: 16 pages, 6 figures, full-length article submitted to a journal

We present all-electrical operation of a Fe$_x$Cr$_{1-x}$-based Curie switch at room temperature. More specifically, we study the current-induced thermally-driven transition from ferromagnetic to antiferromagnetic Ruderman-Kittel-Kasuya-Yosida (RKKY) indirect coupling in a Fe/Cr/Fe$_{17.5}$Cr$_{82.5}$/Cr/Fe multilayer. Magnetometry measurements at different temperatures show that the transition from the ferromagnetic to the antiferromagnetic coupling at zero field is observed at $\sim$325K. Analytical modelling confirms that the observed temperature-dependent transition from indirect ferromagnetic to indirect antiferromangetic interlayer exchange coupling originates from the modification of the effective interlayer exchange constant through the ferromagnetic-to-paramagnetic transition in the Fe$_{17.5}$Cr$_{82.5}$ spacer with minor contributions from the thermally-driven variations of the magnetization and magnetic anisotropy of the Fe layers. Room-temperature current-in-plane magnetotransport measurements on the patterned Fe/Cr/Fe$_{17.5}$Cr$_{82.5}$/Cr/Fe strips show the transition from the 'low-resistance' parallel to the 'high-resistance' antiparallel remanent magnetization configuration, upon increased probing current density. Quantitative comparison of the switching fields, obtained by magnetometry and magnetotransport, confirms that the Joule heating is the main mechanism responsible for the observed current-induced resistive switching., Comment: 8 pages, 4 figures

We report on the single-step fabrication of homogeneous and highly ordered Laser Induced Periodic Surface Structures (LIPSS) over large areas on Au nanolayers, that can be used for plasmonic sensing. A comprehensive study on LIPSS formation on 32 nm Au film upon double, 170 fs pulse irradiation, unveiled the key importance of interpulse delay as the determining factor behind the homogeneity of laser induced structures and confirmed that highly ordered, functional LIPSS occur solely upon double pulse irradiation. In particular, the impact of pulse overlap, fluence and interpulse delay reveals that homogeneous LIPSS formation is optimized within a specific interpulse delay range. At the same time, examination of nanoscale features of the structures points out a significant differentiation of the LIPSS formation characteristics between single and double pulse irradiation. Theoretical investigation complements experimental results providing insights on the structure formation mechanism. Ellipsometric measurements validate that such structures exhibit characteristic plasmon resonances that can be exploited for sensing applications. The presented data demonstrate a novel functionality of LIPSS, while providing strong evidence of the capabilities of femtosecond double pulse irradiation as a valuable and low-cost tool for the precise fabrication of highly ordered structures.

The study concerns dynamics of standing spin waves in arrays of sub-100 nm elliptic synthetic-antiferromagnet (SAF) nanodisks. We performed a detailed ferromagnetic resonance analysis in conjunction with micromagnetic modeling to find out several prominent traits of such systems. One broad line is shown to be the sole resonant response for a SAF of the considered sizes. We demonstrate that this mode is degenerated, and its excitation map resembles a superposition of in-center and edge-type oscillations. We also show how this hybrid excitation leads to almost twofold enhancement in the shape-induced anisotropy of the mode., Comment: 3 pages, 1 figure, submitted to 2022 IEEE 12th International Conference Nanomaterials: Applications & Properties (NAP)

The magnetic properties of thin-film multilayers [Fe/Py]/FeMn/Py are investigated as a function of temperature and thickness of the antiferromagnetic FeMn spacer using SQUID magnetometry. The observed behavior differs substantially for the structures with 6-nm and 15-nm FeMn spacers. While the 15-nm-FeMn structure exhibits exchange pinning of both ferromagnetic layers in the entire measurement temperature interval from 5 to 300 K, the 6-nm-FeMn structure becomes exchange de-pinned in the vicinity of room temperature. The de-pinned state is characterized by a single hysteresis loop centered around zero field and having enhanced magnetic coercivity. The observed properties are explained in terms of finite-size effects and possibly ferromagnetic interlayer coupling through the thin antiferromagnetic spacer., Comment: 9 pages, 5 figures

Large optical anisotropy observed in a broad spectral range is of paramount importance for efficient light manipulation in countless devices. Although a giant anisotropy was recently observed in the mid-infrared wavelength range, for visible and near-infrared spectral intervals, the problem remains acute with the highest reported birefringence values of 0.8 in BaTiS3 and h-BN crystals. This inspired an intensive search for giant optical anisotropy among natural and artificial materials. Here, we demonstrate that layered transition metal dichalcogenides (TMDCs) provide an answer to this quest owing to their fundamental differences between intralayer strong covalent bonding and weak interlayer van der Walls interaction. To do this, we carried out a correlative far- and near-field characterization validated by first-principle calculations that reveals an unprecedented birefringence of 1.5 in the infrared and 3 in the visible light for MoS2. Our findings demonstrate that this outstanding anisotropy allows for tackling the diffraction limit enabling an avenue for on-chip next-generation photonics., Comment: 20 pages, 5 figures

Most of the studied two-dimensional (2D) materials have been obtained by exfoliation of van der Waals crystals. Recently, there has been growing interest in fabricating synthetic 2D crystals which have no layered bulk analogues. These efforts have been focused mainly on the surface growth of molecules in high vacuum. Here, we report an approach to making 2D crystals of covalent solids by chemical conversion of van der Waals layers. As an example, we use 2D indium selenide (InSe) obtained by exfoliation and converted it by direct fluorination into indium fluoride (InF3), which has a non-layered, rhombohedral structure and therefore cannot be possibly obtained by exfoliation. The conversion of InSe into InF3 is found to be feasible for thicknesses down to three layers of InSe, and the obtained stable InF3 layers are doped with selenium. We study this new 2D material by optical, electron transport and Raman measurements and show that it is a semiconductor with a direct bandgap of 2.2 eV, exhibiting high optical transparency across the visible and infrared spectral ranges. We also demonstrate the scalability of our approach by chemical conversion of large-area, thin InSe laminates obtained by liquid exfoliation into InF3 films. The concept of chemical conversion of cleavable thin van der Waals crystals into covalently-bonded non-cleavable ones opens exciting prospects for synthesizing a wide variety of novel atomically thin covalent crystals.

We investigate the spin transport and ferromagnetic resonance properties of giant magnetoresistive (GMR) Co/Cu-Ni multilayers with variable levels of Ni doping in the Cu spacer. We present an experimental evidence for a magnetic-to-diamagnetic transition in the atomic magnetic moment of Ni in the Cu matrix for concentrations below 15 at. % Ni. As its concentration is increased, Ni atoms turn into spin scattering centers, which is manifested experimentally as a step-like change in the GMR of the multilayers. This behavior is observed in multilayers with gradient-doped Cu spacers, where only the inner region was doped with Ni. In the uniformly doped spacers the GMR decreases monotonously with increasing Ni content, indicating that Ni atoms are magnetic and act as spin relaxation centers in the entire dopant-concentration range studied. We explain the difference in the observed GMR behavior as due to a strong magnetic proximity effect in the uniform spacers, which is efficiently suppressed in the gradient spacers. The observed magnetic phase transition is fully supported by our detailed ab-initio calculations, taking into consideration structural relaxation in the system as well as potential Ni clustering. Controlling the loss or gain of the atomic magnetism for a specific dopant can be a tool in probing and controlling spin relaxation in materials and devices for spin-valve and spin-torque based applications., Comment: 11 pages, 5 figures

Indirect exchange coupling in magnetic multilayers, also known as the Ruderman-Kittel-Kasuya-Yosida (RKKY) interaction, is known to be highly effective in controlling the interlayer alignment of the magnetization. This coupling is typically fixed at the stage of the multilayer fabrication and does not allow ex-situ control needed for device applications. It is highly desirable, in addition to the orientational control, to also control the magnitude of the intralayer magnetization, ideally switch it on/off by switching the relevant RKKY coupling. Here we demonstrate a magnetic multilayer material, incorporating thermally -- as well as field-controlled RKKY exchange, focused on to a dilute ferromagnetic alloy layer and driving it though it's Curie transition. Such on/off magnetization switching of a thin ferromagnet, performed repeatably and fully reproducibly within a low-field sweep, results in a giant magnetocaloric effect, with the estimated isothermal entropy change of -10 mJ/K cm^3 under an external field of ~10 mT, which greatly exceeds the performance of the best rare-earth based materials used in the adiabatic-demagnetization refrigeration systems., Comment: 8 pages, 4 figures, Supplemental material (2 pages, 2 figures)

Developing 'smart' membranes that allow precise and reversible control of molecular permeation using external stimuli would be of intense interest for many areas of science: from physics and chemistry to life-sciences. In particular, electrical control of water permeation through membranes is a long-sought objective and is of crucial importance for healthcare and related areas. Currently, such adjustable membranes are limited to the modulation of wetting of the membranes and controlled ion transport, but not the controlled mass flow of water. Despite intensive theoretical work yielding conflicting results, the experimental realisation of electrically controlled water permeation has not yet been achieved. Here we report electrically controlled water permeation through micrometre-thick graphene oxide (GO) membranes. By controllable electric breakdown, conductive filaments are created in the GO membrane. The electric field concentrated around such current carrying filaments leads to controllable ionisation of water molecules in graphene capillaries, allowing precise control of water permeation: from ultrafast permeation to complete blocking. Our work opens up an avenue for developing smart membrane technologies and can revolutionize the field of artificial biological systems, tissue engineering and filtration.

Graphene oxide (GO) membranes continue to attract intense interest due to their unique molecular sieving properties combined with fast permeation rates. However, the membranes' use has been limited mostly to aqueous solutions because GO membranes appear to be impermeable to organic solvents, a phenomenon not fully understood yet. Here, we report efficient and fast filtration of organic solutions through GO laminates containing smooth two-dimensional (2D) capillaries made from flakes with large sizes of ~ 10-20 micron. Without sacrificing their sieving characteristics, such membranes can be made exceptionally thin, down to ~ 10 nm, which translates into fast permeation of not only water but also organic solvents. We attribute the organic solvent permeation and sieving properties of ultrathin GO laminates to the presence of randomly distributed pinholes that are interconnected by short graphene channels with a width of 1 nm. With increasing the membrane thickness, the organic solvent permeation rates decay exponentially but water continues to permeate fast, in agreement with previous reports. The application potential of our ultrathin laminates for organic-solvent nanofiltration is demonstrated by showing >99.9% rejection of various organic dyes with small molecular weights dissolved in methanol. Our work significantly expands possibilities for the use of GO membranes in purification, filtration and related technologies.

Ferromagnetic resonance (FMR) in magnetic multilayers of type F1/f/F2, where two strongly ferromagnetic layers F1 and F2 are separated by a weakly magnetic spacer f with a compositional gradient along its thickness, is investigated. The method allows to detect the weak signal from the spacer in additional to the more pronounced and readily measured signal from the outer strongly-magnetic layers, and thereby study the properties of the spacer as well as the interlayer exchange interaction it mediates. Variable temperature FMR measurements, especially near the relevant Curie points, reveal a rich set of properties of the exchange interactions in the system. The obtained results are useful for designing and optimizing nanostructures with thermally-controlled magnetic properties., Comment: 6 pages, 3 figures

In this work we focus on magnetic relaxation in Mn$_{80}$Ir$_{20}$(12 nm)/ Cu(6 nm)/ Py($d_\mathrm{F}$) antiferromagnet/Cu/ferromagnet (AFM/Cu/FM) multilayers with different thickness of the ferromagnetic permalloy layer. An effective FM-AFM interaction mediated via the conduction electrons in the nonmagnetic Cu spacer -- the spin-pumping effect -- is detected as an increase in the linewidth of the ferromagnetic resonance (FMR) spectra and a shift of the resonant magnetic field. We further find experimentally that the spin-pumping-induced contribution to the linewidth is inversely proportional to the thickness of the Py layer. We show that this thickness dependence likely originates from the dissipative dynamics of the free and localized spins in the AFM layer. The results obtained could be used for tailoring the dissipative properties of spintronic devices incorporating antiferromagnetic layers., Comment: Submitted as a conference paper to 2016 MMM Conference, to appear in AIP Advances

Hierarchical self-assembly arranges nanostructures at different length scales. It gradually becomes an effective method of fabricating artificial metamaterials from composite nanostructures tailored for a particular response. Hierarchical self-assembly overcomes shortcomings of "top-down" methods by significantly reducing fabrication time and making it possible to form bulk materials. Here we report an application of hierarchical self-assembly of metal nanoparticles for the creation of the first isotropic optical metamaterial with strong artificial magnetism in blue light. We have used colloidal self-assembly to create artificial "nanomolecules" that generate the desired magnetic response and microfluidic self-assembly to produce a bulk metastructure. We demonstrate that the magnetic response of the final material is accurately described by an isotropic magnetic permeability that satisfies the principle of locality. Our approach unlocks the fabrication of large volumes of composite nanomaterials. Moreover, the spatial disorder inherent to this "bottom-up" method holds the key to solving the non-locality problem. The technique can be readily extended to the future generations of low-loss optical metamaterials made of dielectric nano-blocks to bypass the limitations of optical losses associated with plasmonic resonances in noble metals., Comment: Main article:10 pages, 4 figures. Supplementary information: 11 pages, 7 figures

Water splitting is unanimously recognized as environment friendly, potentially low cost and renewable energy solution based on the future hydrogen economy. Especially appealing is photo-catalytic water splitting whereby a suitably chosen catalyst dramatically improves efficiency of the hydrogen production driven by direct sunlight and allows it to happen even at zero driving potential. Here, we suggest a new class of stable photo-catalysts and the corresponding principle for catalytic water splitting in which infrared and visible light play the main role in producing the photocurrent and hydrogen. The new class of catalysts based on ionic binary metals with layered graphite-like structures which effectively absorb visible and infrared light facilitating the reaction of water splitting, suppress the inverse reaction of ion recombination by separating ions due to internal electric fields existing near alternating layers, provide the sites for ion trapping of both polarities, and finally deliver the electrons and holes required to generate hydrogen and oxygen gases. As an example, we demonstrate conversion efficiency of 27 percent at bias voltage bias 0.5 V for magnesium di-boride working as a catalyst for photo-induced water splitting. We discuss its advantages over some existing materials and propose the underlying mechanism of photo-catalytic water splitting by binary layered metals.

Plasmonics has established itself as a branch of physics which promises to revolutionize data processing, improve photovoltaics, increase sensitivity of bio-detection. A widespread use of plasmonic devices is notably hindered (in addition to high losses) by the absence of stable and inexpensive metal films suitable for plasmonic applications. This may seem surprising given the number of metal compounds to choose from. Unfortunately, most of them either exhibit a strong damping of surface plasmons or easily oxidize and corrode. To this end, there has been continuous search for alternative plasmonic materials that are, unlike gold, the current metal of choice in plasmonics, compatible with complementary metal oxide semiconductor technology. Here we show that copper and silver protected by graphene are viable candidates. Copper films covered with one to a few graphene layers show excellent plasmonics characteristics surpassing those of gold films. They can be used to fabricate plasmonic devices and survive for at least a year, even in wet and corroding conditions. As a proof of concept, we use the graphene-protected copper to demonstrate dielectric loaded plasmonic waveguides and test sensitivity of surface plasmon resonances. Our results are likely to initiate a wide use of graphene-protected plasmonics., Comment: 22 pages, 5 figures

Barrier films preventing permeation of gases and moistures are important for many industries ranging from food to medical and from chemical to electronic. From this perspective, graphene has recently attracted particular interest because its defect free monolayers are impermeable to all gases and liquids. However, it has proved challenging to develop large-area defectless graphene films suitable for industrial use. Here we report barrier properties of multilayer graphitic films made by chemical reduction of easily and cheaply produced graphene oxide laminates. They are found to provide a practically perfect barrier that blocks all gases, liquids and aggressive chemicals including, for example, hydrofluoric acid. In particular, if graphene oxide laminates are reduced in hydroiodic acid, no permeation of hydrogen and water could be detected for films as thin as 30 nm, which remain optically transparent. The films thicker than 100 nm become completely impermeable. The exceptional barrier properties are attributed to a high degree of graphitization of the laminates and little structural damage during reduction. This work indicates a close prospect of thin protective coatings with stability and inertness similar to that of graphene and bulk graphite, which can be interesting for numerous applications.

There has been intense interest in filtration and separation properties of graphene-based materials that can have well-defined nanometer pores and exhibit low frictional water flow inside them. Here we investigate molecular permeation through graphene oxide laminates. They are vacuum-tight in the dry state but, if immersed in water, act as molecular sieves blocking all solutes with hydrated radii larger than 4.5A. Smaller ions permeate through the membranes with little impedance, many orders of magnitude faster than the diffusion mechanism can account for. We explain this behavior by a network of nanocapillaries that open up in the hydrated state and accept only species that fit in. The ultrafast separation of small salts is attributed to an 'ion sponge' effect that results in highly concentrated salt solutions inside graphene capillaries.

Optical properties of ferromagnetic half-metallic full-Heusler Co$_{2}$FeGe alloy are investigated experimentally and theoretically. Co$_{2}$FeGe thin films were obtained by DC magnetron sputtering and show the saturation magnetization at $T$=10 K of $m\approx$5.6 $\mu_{B}$/f.u., close to the value predicted by the Slater-Pauling rule. First-principles calculations of the electronic structure and the dielectric tensor are performed using the full-potential linearized-augmented-plane-wave method in the generalized gradient (GGA) and GGA+U approximations. The measured interband optical conductivity spectrum for the alloy exhibits a strong absorption band in the 1 - 4 eV energy range with pronounced fine structure, which agrees well with the calculated half-metallic spectrum of the system, suggesting a near perfect spin-polarization in the material., Comment: 6 pages, 9 figures

We investigate a novel type of interlayer exchange coupling based on driving a strong/weak/strong ferromagnetic tri-layer through the Curie point of the weakly ferromagnetic spacer, with the exchange coupling between the strongly ferromagnetic outer layers that can be switched, on and off, or varied continuously in magnitude by controlling the temperature of the material. We use Ni-Cu alloy of varied composition as the spacer material and model the effects of proximity-induced magnetism and the interlayer exchange coupling through the spacer from first principles, taking into account not only thermal spin-disorder but also the dependence of the atomic moment of Ni on the nearest-neighbor concentration of the non-magnetic Cu. We propose and demonstrate a gradient-composition spacer, with a lower Ni-concentration at the interfaces, for greatly improved effective-exchange uniformity and significantly improved thermo-magnetic switching in the structure. The reported magnetic multilayer materials can form the base for a variety of novel magnetic devices, such as sensors, oscillators, and memory elements based on thermo-magnetic Curie-switching in the device., Comment: 15 pages, 5 figures

Magneto-structural properties of films of diluted ferromagnetic alloys Ni$_x$Cu$_{1-x}$ in the concentration range $0.7 < x < 1.0$ are studied experimentally. Films deposited by magnetron sputtering show partial phase separation, as evidenced by structural analysis and ferromagnetic resonance measurements. The phase diagram of the Ni$_x$Cu$_{1-x}$ bulk system is obtained using numerical theoretical analysis of the electronic structure, taking into account the inter-atomic exchange interactions. The results confirm the experimentally found partial phase separation, explain it as magnetic in origin, and indicate an additional metastable region connected with the ferromagnetic transition in the system., Comment: 5 pages, 6 figures

We report a stoichiometric derivative of graphene with a fluorine atom attached to each carbon. Raman, optical, structural, micromechanical and transport studies show that the material is qualitatively different from the known graphene-based nonstoichiometric derivatives. Fluorographene is a high-quality insulator (resistivity >10^12 Ohm per square) with an optical gap of 3 eV. It inherits the mechanical strength of graphene, exhibiting Young's modulus of 100 N/m and sustaining strains of 15%. Fluorographene is inert and stable up to 400C even in air, similar to Teflon., Comment: to appear in Small 2010

Surface enhanced Raman scattering (SERS) exploits surface plasmons induced by the incident field in metallic nanostructures to significantly increase the Raman intensity. Graphene provides the ideal prototype two dimensional (2d) test material to investigate SERS. Its Raman spectrum is well known, graphene samples are entirely reproducible, height controllable down to the atomic scale, and can be made virtually defect-free. We report SERS from graphene, by depositing arrays of Au particles of well defined dimensions on graphene/SiO$_2$(300nm)/Si. We detect significant enhancements at 633nm. To elucidate the physics of SERS, we develop a quantitative analytical and numerical theory. The 2d nature of graphene allows for a closed-form description of the Raman enhancement. This scales with the nanoparticle cross section, the fourth power of the Mie enhancement, and is inversely proportional to the tenth power of the separation between graphene and the nanoparticle. One consequence is that metallic nanodisks are an ideal embodiment for SERS in 2d.