63 research outputs found

    Physical Principles of the Amplification of Electromagnetic Radiation Due to Negative Electron Masses in a Semiconductor Superlattice

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    In a superlattice placed in crossed electric and magnetic fields, under certain conditions, the inversion of electron population can appear at which the average energy of electrons is above the middle of the miniband and the effective mass of the electron is negative. This is the implementation of the negative effective mass amplifier and generator (NEMAG) in the superlattice. It can result in the amplification and generation of terahertz radiation even in the absence of negative differential conductivity.Comment: 5 pages, 3 figure

    Mössbauer study of the surface of core-shell type nanoparticles

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    © 2016, Pleiades Publishing, Ltd.The properties of the surface layer of core-shell nanoparticles incorporated into the matrix of macromolecules of 3,4-bis(decyloxybenzoyl) poly(propylene imine) derivative of the second generation are studied by Mössbauer spectroscopy at low temperatures. The spin states, the details of the phonon spectrum and the Debye temperature of surface layer atoms discussed

    Blue shift in optical absorption, magnetism and light-induced superparamagnetism in γ-Fe2O3 nanoparticles formed in dendrimer

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    © 2015, Springer Science+Business Media Dordrecht. Abstract: We are presenting the investigation of the optical, magnetic, and photoinduced superparamagnetic properties of single-domain γ-Fe2O3 nanoparticles (NPs) with diameters of about 2.5 nm formed in second-generation poly(propylene imine) dendrimer. The optical absorption studies indicated direct allowed transition with the band gap (4.5 eV), which is blue shift with respect to the value of the bulk material. Low-temperature blocking of the NPs magnetic moments at 18 K is determined by SQUID measurements. The influence of pulsed laser irradiation on the superparamagnetic properties of γ-Fe2O3 NPs was studied by EPR spectroscopy. It has been shown that irradiation of the sample held in vacuo and cooled in zero magnetic field to 6.9 K leads to the appearance of a new EPR signal, which decays immediately after the irradiation is stopped. The appearance and disappearance of this new signal can be repeated many times at 6.9 K when we turn on/turn off the laser. We suppose that the generation of conduction band electrons by irradiation into the band gap of the γ-Fe2O3 changes the superparamagnetic properties of NPs. Graphical Abstract: [Figure not available: see fulltext.]Features of the behavior of single-domain γ-Fe2O3 nanoparticles formed in dendrimer were found by UV-Vis and EPR spectroscopy: “blue” shift in optical absorption, a significant increase in the band gap width and variation of superparamagnetic properties under light irradiation

    Optical properties and photoinduced superparamagnetism of γ-Fe<inf>2</inf>O<inf>3</inf> nanoparticles formed in dendrimer

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    © 2014 Elsevier Ltd. All rights reserved. We are presenting the joint investigation of the optical and photoinduced superparamagnetic properties of a single-domain γ-Fe2O3 nanoparticles (NPs) formed in poly(propylene imine) (PPI)-dendrimer. The optical absorption studies indicated direct allowed transition with the band gap (4.5 eV), which is blue-shift with respect to the value of the bulk material. The influence of pulsed laser irradiation on the superparamagnetic properties of γ-Fe2O3 NPs was studied by Electron paramagnetic resonance (EPR) spectroscopy. It has been shown that irradiation of the sample in vacuo and cooled in zero magnetic field to 6.9 K leads to the appearance of a new EPR signal, which decays immediately after the irradiation is stopped. We suppose that the generation of conduction band electrons by irradiation into the band gap of the γ-Fe2O3 changes the superparamagnetic properties of NPs

    Fano resonances in a three-terminal nanodevice

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    The electron transport through a quantum sphere with three one-dimensional wires attached to it is investigated. An explicit form for the transmission coefficient as a function of the electron energy is found from the first principles. The asymmetric Fano resonances are detected in transmission of the system. The collapse of the resonances is shown to appear under certain conditions. A two-terminal nanodevice with an additional gate lead is studied using the developed approach. Additional resonances and minima of transmission are indicated in the device.Comment: 11 pages, 5 figures, 2 equations are added, misprints in 5 equations are removed, published in Journal of Physics: Condensed Matte

    Coexistence of spin crossover and magnetic ordering in a dendrimeric Fe(III) complex

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    © 2015 AIP Publishing LLC. The magnetic properties of a new dendrimeric spin crossover Fe(III) complex, [Fe(L)2]+PF6, where L = 3,5-di[3,4,5-tris(tetradecyloxy) benzoyloxy]benzoyl-4-salicylidene-N-ethyl-N-ethylene-diamine, are reported for the first time. EPR studies show that this compound undergoes a gradual spin transition in the temperature range 70-300K and has antiferromagnetic ordering below 10K. Mössbauer spectroscopy at 5K confirms the presence of magnetic ordering in the dendrimeric iron complex

    Structural, magnetic and dynamic characterization of liquid crystalline iron(III) Schiff base complexes with asymmetric ligands

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    The iron(III) complexes that were formed by coordination of the Fe III ion with the asymmetric tridentate liquid crystalline Schiff base ligand (L), the water molecules and the different counterions [PF 6 - (1), NO3 - (2), and Cl- (3)] were studied by electron paramagnetic resonance (EPR) spectroscopy. EPR spectroscopy demonstrated that each of the complexes investigated consists of two types of iron centers: S = 1/2 low-spin (LS) and S = 5/2 high-spin (HS). LS iron complexes 2, 3 and LS complex 1 in the temperature range 4.2-250 K have a (dxz,dyz)4(dxy)1 ground state. Interesting features werefound for the monocationic FeIII complex 1, [Fe(L)X(H2O)2]+X-, with X = PF6 - as the counterion. The LS and HS iron centers of 1 are coupled together antiferromagnetically and form a dimer structure by means of the water molecules and the PF6 - counterion. The second-type of LS and HS centers that are visible by means of EPR spectroscopy were best observed in the liquid crystalline (387-405 K) phase. The monitoring and the simulation of the EPR spectra enabled us to trace the dynamics of changing the number of the second-type of LS centers with respect to the first-type of LS centers. The observed dynamic process is characterized by the enthalpy value ΔH = 27.9 kJ/mol, which was caused by reorientation of the PF6 - counterion. Calculation of the observed g values for the second-type of LS complex 1 indicated that, in this case, the (d xy)2(dxz,dyz)3 ground state is stabilized. The conversion between the electron (dxz,d yz)4(dxy)1/(dxy) 2(dxz,dyz)3 configurations was found to be temperature dependent and was detected in the same material for the first time in iron complexes. We synthesized a novel compound, namely a liquid crystalline iron(III) Schiff base complex with the asymmetric ligand [Fe(L)X(H2O)2]+X-, where X = PF 6 - is the counterion. This compound has a labilelow-spin electron configuration that switches between the (dxz,d yz)4(dxy)1/(dxy) 2(dxz,dyz)3 ground states and is temperature-dependent. Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim

    Justification for Changing the Geometry of the Spring Pin Pickup Surface of the Grain Crop Pickup

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    The issue of reducing grain losses during separate harvesting when using a conveyor pickup is a scientific and an applied problem. In this work, the obtained results of industrial research of a conveyor pickup equipped with a spring pin with an annular coil on the pickup surface were investigated. In this article, the theoretical prerequisites for changing the geometry of the pickup surface of the spring pin of the grain crop pickup were considered, as well as options for changing the geometry of the pickup surface of the spring pins of the grain crop pickup. © 2022 American Institute of Physics Inc.. All rights reserved
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