RESUMEN
Manipulation of long-range order in 2D van der Waals (vdW) magnetic materials (e.g., CrI3 , CrSiTe3 ,etc.), exfoliated in few-atomic layer, can be achieved via application of electric field, mechanical-constraint, interface engineering, or even by chemical substitution/doping. Usually, active surface oxidation due to the exposure in the ambient condition and hydrolysis in the presence of water/moisture causes degradation in magnetic nanosheets that, in turn, affects the nanoelectronic /spintronic device performance. Counterintuitively, the current study reveals that exposure to the air at ambient atmosphere results in advent of a stable nonlayered secondary ferromagnetic phase in the form of Cr2 Te3 (TC2 ≈160 K) in the parent vdW magnetic semiconductor Cr2 Ge2 Te6 (TC1 ≈69 K). The coexistence of the two ferromagnetic phases in the time elapsed bulk crystal is confirmed through systematic investigation of crystal structure along with detailed dc/ac magnetic susceptibility, specific heat, and magneto-transport measurement. To capture the concurrence of the two ferromagnetic phases in a single material, Ginzburg-Landau theory with two independent order parameters (as magnetization) with a coupling term can be introduced. In contrast to the rather common poor environmental stability of the vdW magnets, the results open possibilities of finding air-stable novel materials having multiple magnetic phases.
RESUMEN
We apply periodic control to realize a quantum thermal transistor, which we term as the Floquet quantum thermal transistor. Periodic modulation allows us to control the heat flows and achieve large amplification factors even for fixed bath temperatures. Importantly, this transistor effect persists in the cutoff region, where traditional quantum thermal transistors operating in the absence of periodic modulation, fail to act as viable heat modulation devices.
RESUMEN
We map spatially correlated electrical current on the stacking boundaries of pristine and doped hexagonal boron nitride (hBN) to distinguish from its insulating bulk via conductive atomic force microscopy (CAFM). While the pristine edges of hBN show an insulating nature, the O-doped edges reveal a current 2 orders of higher even for bulk layers where the direct transmission through tunnel barrier is implausible. Instead, the nonlinear current-voltage characteristics (I-V) at the edges of O-doped hBN can be explained by trap-assisted lowering of the tunnel barrier by adopting a Poole-Frenkel (PF) model. However, in the stacked heterostructure with multilayer graphene (MLG) on top, the buried edge of pristine hBN shows a signature of electron conduction in the scanning mode which contradicts the first-principle calculation of spatial distribution of local density of states (LDOS) data. Enhancement of friction between the Pt-tip and MLG at the step-edge of the heterostructure while scanning in the contact mode has prompted us to construct a phenomenological model where the localization of opposite surface charges on two conducting plates (MLG and Si substrate) containing a dielectric film (hBN) with negatively charged defects creates an internal electric field opposite to the external electric field due to the applied voltage bias in the CAFM setup. An equivalent circuit with a parallel resistor network based on a vertical conducting channel through the MLG/hBN edge and an in-plane surface carrier transport through MLG can successfully analyze the current maps on pristine/doped hBN and the related heterostructures. These results yield fundamental insight into the emerging field of insulatronics in which defect-induced electron transport along the edge can be manipulated in an 1D-2D synergized insulator.
RESUMEN
The supramolecular hydrogel of a simple organic salt derived from a primary amine and a mono-sulfonic acid displayed a proton conductivity of 1.2 × 10-4 S cm-1. The hitherto unknown example of the supramolecular gel displaying proton conductivity provides an intriguing alternative to liquid electrolyte or polymer gel electrolytes.
RESUMEN
We experimentally investigate the electronic transport through a double-wall carbon nanotube filled with Fe nanoparticles. At very low temperatures, the Kondo effect is observed between the confined electrons in the nanotube quantum dot and the delocalized electrons in the leads connecting the nanotube. We demonstrate that the presence of magnetic nanoparticles in the inner core of the nanotube results in a hysteretic behavior of the differential resistance of the system when the magnetic field is varied. This behavior is observed in the Kondo diamonds of the stability diagram, and the magnitude of hysteresis varies with the strength of the Kondo correlations in different diamonds. Our findings are corroborated with accurate numerical renormalization group calculations performed for an effective low-energy model involving fluctuations of the spin on the orbital level of the nanotube due to spin flips of the nanoparticles.
RESUMEN
Coupling spins of molecular magnets to two-dimensional (2D) materials provides a framework to manipulate the magneto-conductance of 2D materials. However, with most molecules, the spin coupling is usually weak and devices fabricated from these require operation at low temperatures, which prevents practical applications. Here, we demonstrate field-effect transistors based on the coupling of a magnetic molecule quinoidal dithienyl perylenequinodimethane (QDTP) to 2D materials. Uniquely, QDTP switches from a spin-singlet state at low temperature to a spin-triplet state above 370 K, and the spin transition can be electrically transduced by both graphene and molybdenum disulphide. Graphene-QDTP shows hole-doping and a large positive magnetoresistance ( ~ 50%), while molybdenum disulphide-QDTP demonstrates electron-doping and a switch to large negative magnetoresistance ( ~ 100%) above the magnetic transition. Our work shows the promise of spin detection at high temperature by coupling 2D materials and molecular magnets.Engineering a coupling between magnetic molecules and conducting materials at room temperature could help the development of spintronic devices. Loh et al. show that the spin state of QDTP molecules deposited on graphene and MoS2 couples to their electronic structure, affecting magnetotransport.
RESUMEN
The coordination chemistry between copper acetate [Cu2(OAc)4] and 5,10,15,20-tetra-4-pyridyl-21H,23H-porphine (porphyrin, H2TPyP) is found to give rise to either a 2D metal-organic framework (MOF) [Cu(TPyP)Cu2(O2CCH3)4] or a 3D MOF [Cu(TPyP)CuCl2]·2.5TCE·7H2O], depending on the choice of solvent. The 2D MOF can be made into a film, which was doped with 7,7,8,8-tetracyanoquinodimethane (TCNQ), and the electrical conductivity of the thin film was increased by 3 orders of magnitude with respect to that of the undoped Cu-MOF. The formation of a charge-transfer complex between TCNQ and the 2D Cu-MOF also imparts stronger paramagnetic properties than for the undoped MOF.
RESUMEN
Nanocrystalline Au(x)Cu(1-x) films were synthesized by depositing Cu/Au/Cu multilayer in nanocrystalline thin film form with requisite thickness of individual layers onto fused silica substrates by high pressure sputtering technique. The absorbance spectra showed only one surface plasmon peak for all the compositions with the exception that the peak position did not indicate gradual shift as gold concentration was increased. Peak position for the two compositions corresponding to the two superlattice structures, AuCu3 and AuCu, deviated significantly from linear variation. The experimental results have been discussed in light of the existing Mie theory and the Core-shell model.