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Abstract The coupling between magnons and phonons and the associated phenomena have long been a focus of research in condensed matter physics. Contrary to its recognized role in magnon relaxation, its impact on phonon transport remains largely unexplored. Here, we fill this gap by investigating the effect of magnon-phonon coupling on phonon excitation, relaxation, and transport with magneto-optical reflectometry. Through simultaneous measurements of magnon and phonon populations in magnetic insulator thulium iron garnet, we observe the excitation of excessive phonons driven by non-equilibrium magnons, demonstrating the magnetic control of phonons. Furthermore, our time-resolved experiments reveal the magnetic field-dependent phononic thermal conductivity, signaling the potential of magnetic manipulation of heat transport. Our finding indicates that phonons can be controlled by magnetic means through magnon-phonon coupling and thereby opens a new avenue to harness magneto-thermoelectric effects in magnetic insulators.

Abstract Spin-orbit torque (SOT), arising from spin-orbit coupling-induced spin currents, provides efficient control of magnetization. SOT characterization involving harmonic Hall resistances is typically done in low-current regimes, distinct from high-current regimes, where SOT-induced magnetization switching occurs. In this study, we investigate azimuthal angle (ϕ)-dependent harmonic Hall resistances of a Pt/yttrium iron garnet (YIG) layer across a wide range of measurement currents. Under low-current conditions, conventional ϕ-dependent Hall resistances are observed; the first harmonic Hall resistance exhibits sin 2ϕ behavior and the second harmonic Hall resistance comprises cos ϕ and cos 3ϕ terms. Interestingly, with increasing current, higher-order angular-dependent terms become non-negligible, referring to the sin 4ϕ and sin 6ϕ terms for the first harmonic and the cos 5ϕ and cos 7ϕ terms for the second harmonic Hall resistances. We attribute this unconventional angular dependence to the nonlinear response of magnetization direction to SOT, emphasizing its relevance to understanding the magnetization dynamics during SOT-induced switching under large currents.

Abstract In this article, we present a straightforward in-situ approach for producing Ag NPs incorporated in graphene oxide (GO) blended with glutaraldehyde (GA) cross-linked polyvinyl alcohol (PVA) matrix. Samples are γ-irradiated by doses of 2, 5, and 10 kGy and in comparison with the pristine films, the thermal conductivity (‘k’) and effusivity are measured. ‘k’ decreases with irradiation doses up to 5 kGy and further increase in the dosage results increase in ‘k’. We performed FDTD modeling to verify the effect of polarization and periodicity on the absorptivity and emissivity spectra that are correlated to the ‘k’ and effusivity, empirically. Hence, we can confess that the structural properties of the prepared hybrid nanocomposite are manipulated by γ-irradiation. This attests that the PVA/GO-Ag/GA nanocomposite is radiation-sensitive and could be employed for thermal management systems. Moreover, their strong electrical insulation, as the measured dc conductivity of the γ-irradiated samples is found to be in the range of 2.66 × 10−8–4.319 × 10−7 Sm−1, which is below the percolation threshold of 1.0 × 10−6 Sm−1, demonstrates that they are excellent candidates for the use of thermal management materials. The low ‘k’ values allow us to use this promising material as thermal insulating substrates in microsensors and microsystems. They are also great choices for usage as wire and cable insulation in nuclear reactors due to their superior electrical insulation. Graphical Abstract

Abstract Spin Seebeck effect (SSE) refers to the generation of an electric voltage transverse to a temperature gradient via a magnon current. SSE offers the potential for efficient thermoelectric devices because the transverse geometry of SSE enables to utilize waste heat from a large-area source by greatly simplifying the device structure. However, SSE suffers from a low thermoelectric conversion efficiency that must be improved for widespread application. Here we show that the SSE substantially enhances by oxidizing a ferromagnet in normal metal/ferromagnet/oxide structures. In W/CoFeB/AlOx structures, voltage-induced interfacial oxidation of CoFeB modifies the SSE, resulting in the enhancement of thermoelectric signal by an order of magnitude. We describe a mechanism for the enhancement that results from a reduced exchange interaction of the oxidized region of ferromagnet, which in turn increases a temperature difference between magnons in the ferromagnet and electrons in the normal metal and/or a gradient of magnon chemical potential in the ferromagnet. Our result will invigorate research for thermoelectric conversion by suggesting a promising way of improving the SSE efficiency.

Ultrafast Sagnac interferometer provides direct access to the lattice dynamics in magnetic materials. The authors leveraged light-matter interaction to unveil the intertwined role of strain and thermal effects on the spin dynamics of ferromagnets.

A major challenge for spin based electronics is the electrical control of magnetization. Here, Kang et al demonstrate how electric field control of the Rashba effect in a Pt/Co/AlOx can enable control of the spin-orbit torque and allow for field free switching of the magnetization.

Only a few iron precursors that can be used in the atomic layer deposition (ALD) of iron oxides have been examined thus far. This study aimed to compare the various properties of FeOx thin films deposited using thermal ALD and plasma-enhanced ALD (PEALD) and to evaluate the advantages and disadvantages of using bis(N,N′-di-butylacetamidinato)iron(II) as an Fe precursor in FeOx ALD. The PEALD of FeOx films using iron bisamidinate has not yet been reported. Compared with thermal ALD films, PEALD films exhibited improved properties in terms of surface roughness, film density, and crystallinity after they were annealed in air at 500 °C. The annealed films, which had thicknesses exceeding ~ 9 nm, exhibited hematite crystal structures. Additionally, the conformality of the ALD-grown films was examined using trench-structured wafers with different aspect ratios.

Abstract A controllable approach that combines surface plasmon resonance and two-dimensional (2D) graphene/MoS2 heterojunction has not been implemented despite its potential for efficient photoelectrochemical (PEC) water splitting. In this study, plasmonic Ag-decorated 2D MoS2 nanosheets were vertically grown on graphene substrates in a practical large-scale manner through metalorganic chemical vapor deposition of MoS2 and thermal evaporation of Ag. The plasmonic Ag-decorated MoS2 nanosheets on graphene yielded up to 10 times higher photo-to-dark current ratio than MoS2 nanosheets on indium tin oxide. The significantly enhanced PEC activity could be attributed to the synergetic effects of SPR and favorable graphene/2D MoS2 heterojunction. Plasmonic Ag nanoparticles not only increased visible-light and near-infrared absorption of 2D MoS2, but also induced highly amplified local electric field intensity in 2D MoS2. In addition, the vertically aligned 2D MoS2 on graphene acted as a desirable heterostructure for efficient separation and transportation of photo-generated carriers. This study provides a promising path for exploiting the full potential of 2D MoS2 for practical large-scale and efficient PEC water-splitting applications.

Fuel cell performance largely relies on the activity of catalyst; hence development of high performance electrocatalysts for the electrooxidation of methanol is highly essential for the further development in fuel cell technology. Herein, we demonstrate a facile hydrothermal approach for the growth of NiCo2O4 nanorods and their application in the methanol electrooxidation. The morphology and surface area investigation reveal the growth of NiCo2O4 nanorods with an average length of 500 nm and a specific surface area of 123 m2/g, respectively. The NiCo2O4 nanorods displayed a larger electrochemical activity towards the electrooxidation of methanol in alkaline pH than the quasi-spherical NiCo2O4 nanoparticles. On the NiCo2O4 nanorod based electrode a higher catalytic current density of 129 mA/cm2 and a high stability with 86% current retention was achieved, signifying that the current non-Pt based catalyst could be a non-expensive alternative candidate for high performance fuel cell application. Keywords: Methanol, Nanorods, NiCo2O4, Electrochemical, Catalyst

TiO2 is the most commonly used photocatalyst in water treatment. The particle size of TiO2 is an important factor that significantly influences its activity during photocatalytic degradation. In the presence of liquid, the properties of nanopowders composed of exactly the same product clearly differ according to their aggregation size. In this study, TiO2 nanoparticles with a controlled size were fabricated by focused ultrasound dispersion. The high energy generated by this system was used to control the size of TiO2 particles in the suspension. The constant high energy released by cavitation enabled the dispersion of the particles without a surfactant. The activities of the prepared TiO2 photocatalysts for methylene blue (MB) degradation were then compared. The dye degradation effect of the photocatalyst was as high as 61.7% after 10 min when the size of the powder was controlled in the solution, but it was only as high as 41.0% when the aggregation size was not controlled. Furthermore, when the TiO2 concentration exceeded a certain level, the photocatalytic activity of TiO2 decreased. Controlling the size of the aggregated photocatalyst particles is, therefore, essential in water-treatment technologies utilizing TiO2 photocatalytic properties, and adjusting the TiO2 concentration is an important economic factor in this photocatalytic technology. This study contributes to the development of processes for degrading dyes, such as MB, released from wastewater into aquatic environments.

In this study, the double hydrothermal method is proposed as a facile approach to the synthesis of ZnTe/ZnO core–shell nanorods. The coating thickness of the p-type ZnTe is varied to adjust the junction depth in the n-type ZnO nanorods, and the conductance measurements reveal the change in the conduction path in the heterojunction structures. Structural and chemical investigations conducted using X-ray diffraction, transmission electron microscopy, and X-ray photoelectron spectroscopy confirm the hetero-nanostructure formation of ZnTe/ZnO. The role of ZnTe in H2S-gas sensing by the ZnO nanorods is discussed. The enhanced sensing performance observed with a thin ZnTe coating confirms the importance of the base resistance of the nano-transducer in achieving high response characteristics. The composite structure also demonstrates a superior sensing performance of good repeatability, stability, linearity, and gas selectivity at temperatures greater than 200 °C.

Fabrication of high quality ferrimagnetic insulators is an essential step for ultrafast magnonics, which utilizes antiferromagnetic exchange of the ferrimagnetic materials. In this work, we deposit high-quality GdIG thin films on a (111)-oriented GGG substrate using the Metal Organic Decomposition (MOD) method, a simple and high throughput method for depositing thin film materials. We postannealed samples at various temperatures and examined the effect on structural properties such as crystallinity and surface morphology. We found a transition in the growth mode that radically changes the morphology of the film as a function of annealing temperature and obtained an optimal annealing temperature for a uniform thin film with high crystallinity. Optimized GdIG has a high potential for spin wave applications with a low damping parameter in the order of 10−3, which persists down to cryogenic temperatures.

Pure spin current generated thermally in nonmagnetic materials known as spin Nernst effect has not been demonstrated experimentally. Here, the authors report the observation of spin Nernst effect by studying the thermally-induced transverse magnetoresistance in ferromagnet/non-magnet heavy metal bilayers

The forced alignment of magnetic moments leads to a large change in entropy, which can be used to reduce the temperature of a material. Here, the authors show that this magnetic cooling effect occurs on a femtosecond time scale in cobalt–platinum nano-multilayers.

Nanocomposite structures, where the Fe, Fe2O3, or Ni2O3 nanoparticles with thin carbon layers are distributed among a single-wall carbon nanotube (SWCNT) network, are architectured using the co-arc discharge method. A synergistic effect between the nanoparticles and SWCNT is achieved with the composite structures, leading to the enhanced sensing response in ammonia detection. Thorough studies about the correlation between the electric properties and sensing performance confirm the independent operation of the receptor and transducer in the sensor structure by nanoparticles and SWCNT, respectively. Nanoparticles with a large specific surface area provide adsorption sites for the NH3 gas molecules, whereas hole carriers are supplied by the SWCNT to complete the chemisorption process. A new chemo-resistive sensor concept and its operating mechanism is proposed in our work. Furthermore, the separated receptor and transducer sensor scheme allows us more freedom in the design of sensor materials and structures, thereby enabling the design of high-performance gas sensors.

The original version of this Article contained an error in ref. 27, which was incorrectly given with the wrong journal name as: Meyer, S. et al. Observation of the spin Nernst effect. Nat. Phys. 16, 977–981 (2017). The correct form of ref. 27 is: Meyer, S. et al. Observation of the spin Nernst effect. Nat. Mater. 16, 977–981 (2017). This has now been corrected in the PDF and HTML versions of the Article.