Magneto-strain effects in 2D ferromagnetic van der Waal material CrGeTe[Formula: see text].

The idea of strain based manipulation of spins in magnetic two-dimensional (2D) van der Waal (vdW) materials leads to the development of new generation spintronic devices. Magneto-strain arises in these materials due to the thermal fluctuations and magnetic interactions which influences both the lattice dynamics and the electronic bands. Here, we report the mechanism of magneto-strain effects in a vdW material CrGeTe[Formula: see text] across the ferromagnetic (FM) transition. We find an isostructural transition in CrGeTe[Formula: see text] across the FM ordering with first order type lattice modulation. Larger in-plane lattice contraction than out-of-plane give rise to magnetocrystalline anisotropy. The signature of magneto-strain effects in the electronic structure are shift of the bands away from the Fermi level, band broadening and the twinned bands in the FM phase. We find that the in-plane lattice contraction increases the on-site Coulomb correlation ([Formula: see text]) between Cr atoms resulting in the band shift. Out-of-plane lattice contraction enhances the [Formula: see text] hybridization between Cr-Ge and Cr-Te atoms which lead to band broadening and strong spin-orbit coupling (SOC) in FM phase. The interplay between [Formula: see text] and SOC out-of-plane gives rise to the twinned bands associated with the interlayer interactions while the in-plane interactions gives rise to the 2D spin polarized states in the FM phase.

An additional simultaneous magnetic ordering and magneto-capacitive behavior with dielectric relaxation besides multiferroicity in Fe1-xTexVO4.

Here we report the evidence of an additional magnetic ordering and frequency dispersive magneto-dielectric (MD) permittivity besides multiferroic behavior in Te4+(S= 0) doped FeVO4. Two antiferromagnetic transitions similar to FeVO4at ∼21.86 K (TN1) and 16.03 K (TN2) were observed in all samples. An additional novel defect clusters based magnetic ordering at relatively higher temperature (TAMO) ∼ 203 K is also observed from the magnetization. Evaluated magnetic moments show systematic decrease and the magnetic frustration factors show an increase with the increasing of Te4+(S= 0) content. MD studies show stable ferroelectric ordering at spiral magnetic transition (TN2) and the multiferroic order persists to the largest doping of Te (x= 0.10). The MD studies also reveal a magneto-capacitive (MC) behavior at TAMO(∼203 K) with a high dielectric constant and loss, and the possible reason for the magnetic ordering and MC behavior is ascribed to short range magnetic clustering arising out of defect based mechanisms. Mössbauer spectroscopic studies confirm local structural correlation with magnetic and ferroelectric ordering.

Lattice assisted dielectric relaxation in four-layer Aurivillius Bi5FeTi3O15ceramic at low temperatures.

We have investigated magnetic, structural and dielectric properties of Bi5FeTi3O15(BFTO) in the temperature range 5K-300 K. Using diffraction, Raman spectroscopy and x-ray absorption fine structure measurements, iso-structural modifications are observed at low temperatures (≈100 K). The analysis of dielectric constant data revealed signatures of dielectric relaxation, concomitant with these structural modifications in BFTO at the same temperatures. Further, employing complementary experimental methods, it is shown that the distribution of Fe/Ti ions in BFTO is random. With the help of techniques that probe magnetism at various length and time scales, it is shown that the phase-pure BFTO is non-magnetic down to the lowest temperatures.

Origin of ferroelectricity in cubic phase of Hf substituted BaTiO3.

The origin of ferroelectricity in the cubic phase of BaTi1-xHfxO3has been investigated. The presence of well-defined ferroelectric polarization versus electric field (PE) hysteresis loop in the samples with global cubic symmetry suggests the presence of 'local polar regions', induced possibly due to the huge difference in the electronegativity and also difference in the ionic radii of Hf+4and Ti+4ions, which may lead to local structural disorder. The presence of polar regions is also supported through the appearance of A1(TO) polar mode in Raman spectra which in principle should be absent in the samples with cubic symmetry. The results are discussed in terms of disorder-induced local dipoles due to the electronegativity difference between Hf and Ti ions.

Possibility of using ultraviolet radiation for disinfecting the novel COVID-19.

The world health organization (WHO) declared novel COVID-19 as a pandemic in March 2020 and as of now has infected hundreds of millions of people across the globe. Here in this report, we propose the importance of light-based technologies in disinfecting the novel COVID-19, present on the surface of phone, plastic surfaces, wallets, watches, cloths. This article identifies the benefits of repurposing ultraviolet light-based strategies to combat the emergence of COVID-19 pandemic. A possible design for the ultraviolet irradiation is also proposed and discussed in short.

High Performance Lithium-Ion Batteries Using Layered 2H-MoTe2 as Anode.

The major challenges faced by candidate electrode materials in lithium-ion batteries (LIBs) include their low electronic and ionic conductivities. 2D van der Waals materials with good electronic conductivity and weak interlayer interaction have been intensively studied in the electrochemical processes involving ion migrations. In particular, molybdenum ditelluride (MoTe2 ) has emerged as a new material for energy storage applications. Though 2H-MoTe2 with hexagonal semiconducting phase is expected to facilitate more efficient ion insertion/deinsertion than the monoclinic semi-metallic phase, its application as an anode in LIB has been elusive. Here, 2H-MoTe2 , prepared by a solid-state synthesis route, has been employed as an efficient anode with remarkable Li+ storage capacity. The as-prepared 2H-MoTe2 electrodes exhibit an initial specific capacity of 432 mAh g-1 and retain a high reversible specific capacity of 291 mAh g-1 after 260 cycles at 1.0 A g-1 . Further, a full-cell prototype is demonstrated by using 2H-MoTe2 anode with lithium cobalt oxide cathode, showing a high energy density of 454 Wh kg-1 (based on the MoTe2 mass) and capacity retention of 80% over 100 cycles. Synchrotron-based in situ X-ray absorption near-edge structures have revealed the unique lithium reaction pathway and storage mechanism, which is supported by density functional theory based calculations.

Spin reorientation transition and coupled spin-lattice dynamics of Sm0.6Dy0.4FeO3.

In this work, we have presented a solid-solution of Sm0.6Dy0.4FeO3 in the form of nano-particles having spin reorientation transition (SRT) at a temperature interval of 220-260 K. The lattice dynamics of Sm0.6Dy0.4FeO3 have investigated by temperature-dependent x-ray diffraction and Raman spectroscopy. A negative thermal expansion at low temperatures has observed, which might be due to the interaction between Sm3+ and Fe3+ sublattice. Anomalous behavior in lattice parameters, octahedral tilt angle, and bond lengths have observed in the vicinity of SRT, which confirms the existence of magneto-elastic coupling in the system. The strong anomaly has observed in linewidth and phonon frequencies of Raman modes around SRT, which may be related to the spin-phonon coupling in Sm0.6Dy0.4FeO3. The contribution of SRT in lattice change and the presence of spin-phonon coupling can help to understand the correlation between the magnetic and structural properties of orthoferrite.

Strain induced disordered phonon modes in Cr doped PrFeO3.

Room temperature optical absorption spectroscopy (OAS) and Raman spectroscopy measurements have been carried out in order to understand the effect of structural disorder on the electronic and phononic states. For this purpose, polycrystalline samples of Cr doped PrFeO3 have been prepared via wet chemical route. OAS analysis suggests the systematic scaling of electronic disorder with Cr doping; whereas, shifting in Raman line shapes and an increase in Raman line width has been observed with Cr doping. X-ray diffraction analysis clearly suggests the increase in structural disorders in the form of crystallographic strain with Cr doping, which is consistent with the broadening in Raman line shapes. The major contribution to Raman line width has been understood in terms of temperature independent terms i.e. structural disorder induced by doping. The generation of a new phonon mode at ~510 cm-1 has been observed and understood as a disorder phonon mode due to strain induced structural disorder. Moreover, a systematic correlation between crystallographic strain, Raman line width, disordered parameter (σ) and Urbach energy has been observed, which implies that structural disorder affects phononic as well as electronic states of the system. Such comparative study allows us to find the correlation between densities of tail states, structural disorders and anharmonic effects probed by Raman spectroscopy.

Room-Temperature Magneto-dielectric Effect in LaGa0.7Fe0.3O3+γ; Origin and Impact of Excess Oxygen.

We report an observation of room-temperature magneto-dielectric (RTMD) effect in LaGa0.7Fe0.3O3+γ compound. The contribution of intrinsic/resistive sources in the presently observed RTMD effect was analyzed by measuring direct-current (dc) magnetoresistance (MR) in four-probe geometry and frequency-dependent MR via impedance spectroscopy (MRIS). Present MRIS analysis reveals that at frequencies corresponding to grain contribution (≥1 × 106 Hz for present sample), the observed MD phenomenon is MR-free/intrinsic, whereas at lower probing frequencies (<1 × 106 Hz), the observed MD coupling appears to be MR-dominated possibly due to oxygen excess, that is, due to coexistence of Fe3+ and Fe4+. The magnetostriction is anticipated as a mechanism responsible for MR-free/intrinsic MD coupling, whereas the MR-dominated part is attributed to hopping charge transport along with Maxwell-Wagner and space charge polarization. The multivalence of Fe ions in LaGa0.7Fe0.3O3+γ was validated through iodometric titration and Fe K-edge X-ray absorption near-edge structure measurements. The excess of oxygen, that is, coexistence of Fe3+ and Fe4+, was understood in terms of stability of Fe4+ by means of "bond-valence-sum" analysis and density functional theory-based first-principles calculations. The cation vacancies at La/Ga site (or at La and Ga both) were proposed as the possible origin of excess oxygen in presently studied compound. Present investigation suggests that, to justify the intrinsic/resistive origin of MD phenomenon, frequency-dependent MR measurements are more useful than measuring only dc MR or comparing the trends of magnetic-field-dependent change in dielectric constant and tan δ. Presently studied Fe-doped LaGaO3 can be a candidate for RTMD applications.

Origin of step-like behavior in the Co/Si system.

A systematic investigation of the structure, nature of the interface and their possible connections with magnetic properties for the as-deposited Co/Si/Co trilayer system has been carried out. X-ray reflectivity, cross-sectional transmission electron microscopy and x-ray emission measurements performed on the Co/Si/Co trilayer system show that when the Si layer thickness is less than ∼ 20 Å, the full Si layer is converted into a cobalt silicide layer whereas when the Si layer thickness > 20 Å along with the silicide layer. the pure Si layer also remains. A comparison of magneto-optical Kerr effect and magnetoresistance measurements reveals the absence of antiferromagnetic coupling in these samples. Double-step-like magnetization, in the case of Si layer thickness > 20 Å between two Co layers, is explained by magnetization reversal of two ferromagnetic layers having different coercivities, independent of each other.