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We analyze multi-wavelength and multi-viewpoint observations of a helically twisted plasma jet formed during a confined filament eruption on 10-11 April 2013. Given a rather large scale event with its high spatial and temporal resolution observations , it allows us to clearly understand some new physical details about the formation and triggering mechanism of twisting jet. We identify a pre-existing flux rope associated with a sinistral filament, which was observed several days before the event. The confined eruption of the filament within a null point topology, also known as an Eiffel tower (or inverted-Y) magnetic field configuration results in the formation of a twisted jet after the magnetic reconnection near a null point. The sign of helicity in the jet is found to be the same as that of the sign of helicity in the filament. Untwisting motion of the reconnected magnetic field lines gives rise to the accelerating plasma along the jet axis. The event clearly shows the twist injection from the pre-eruptive magnetic field to the jet.
Nanocrystalline ribbons of inverse Heusler alloy Mn2Ni1.6Sn0.4 have been synthesised by melt spinning of the arc melted bulk precursor. The single phase ribbons crystallize into a cubic structure and exhibit very fine crystallite size of < 2 nm. Temp erature dependent magnetization (M-T) measurements reveal that austenite (A)-martensite (M) phase transition begins at T~248 K and finishes at T~238 K during cooling cycle and these values increase to T~267 K and T~259 K while warming. In cooling cycle, the A-phase shows ferromagnetic (FM) ordering with a Curie temperature T~267 K, while both the FM-antiferromagnetic (AFM) and M-transitions occur at T~242 K. The M-phase undergoes FM transition at T~145 K. These transitions are also confirmed by temperature dependent resistivity measurements. The observed hysteretic behaviour of magnetization and resistivity in the temperature regime spanned by the A-M transition is a manifestation of the first order phase transition. Magnetization and susceptibility data also provide unambiguous evidence in favour of spin glass . The scaling of the glass freezing temperature (Tf) with frequency, extracted from the frequency dependent AC susceptibility measurements, confirms the existence of canonical spin glass at T<145 K. The occurrence of canonical spin glass has been explained in terms of the nanostructuring modified interactions between the FM correlations in the martensitic phase and the coexisting AFM.
The plasmonic properties of vacuum evaporated nanostructured gold thin films having different types of nanoparticles are presented. The films with more than 6 nm thickness show presence of nanorods having non cylindrical shape with triangular base. T wo characteristics plasmon bands have been recoreded in absorption spectra. First one occurs below 500 nm and other one at higher wavelength side. Both the peaks show dependence on the dielectric property of surroundings. The higher wavelength localized surface plasmon resonance (LSPR) peak shifts to higher wavelength with an increase in the nanoparticle size, surface roughness and refractive index of the surrounding (Methylene Blue dye coating). This shows that such thin films can be used as sensor for organic molecules with a refractive index sensitivity ranging from 250 - 305 nm/RIU (Refractive Index Unit).
Possible phase transition of strongly interacting matter from hadron to a quark-gluon plasma state have in the past received considerable interest. The clustering of color sources provides a framework of the the partonic interactions in the initial s tage of the collisions. The onset of de-confinement transition is identified by the spanning percolation cluster in 2D percolation. In this talk results are presented both for the multiplicity and the elliptic flow at RHIC and LHC energies. The thermodynamic quantities temperature, equation of state and transport coefficient are obtained in the framework of clustering of color sources. It is shown that the results are in excellent agreement with the recent lattice QCD calculations(LQCD).
Highly oriented polycrystalline SSMO thin films deposited on single crystal substrates by ultrasonic nebulized spray pyrolysis have been studied. The film on LAO is under compressive strain while LSAT and STO are under tensile strain. The presence of a metamagnetic state akin to cluster glass formed due to coexisting FM and antiferromagnetic/charge order (AFM/CO) clusters. All the films show colossal magnetoresistance but its temperature and magnetic field dependence are drastically different. In the lower temperature region the magnetic field dependent isothermal resistivity also shows signature of metamagnetic transitions. The observed results have been explained in terms of the variation of the relative fractions of the coexisting FM and AFM/CO phases as a function of the substrate induced strain and oxygen vacancy induced quenched disorder.
Possible phase transition of strongly interacting matter from hadron to a quark-gluon plasma state have in the past received c onsiderable interest. It has been suggested that this problem might be treated by percolation theory. The clustering of col or sources with percolation (CSPM) is used to determine the equation of state (EOS) and the transport coefficient of the Quark-Gl uon Plasma (QGP) produced in central A-A collisions at RHIC and LHC energies.
Possible phase transition of strongly interacting matter from hadron to a Quark-Gluon Plasma (QGP) state have in the p ast received considerable interest. It has been suggested that this problem might be treated by percolation theory. Th e Color Stri ng Percolation Model (CSPM) is used to determine the equation of state (EOS) of the QGP produced in central Au-Au collisions at RHIC energies. The bulk thermodynamic quantities- energy density, entropy density and t he sound velocity- are obtained in the framework of CSPM. It is shown that the results are in excellent agreement with the recent lattice QCD calculations(LQCD).
We study the effect of synthesis temperature on the phase formation in nano(n)-SiC added bulk MgB2 superconductor. In particular we study: lattice parameters, amount of carbon (C) substitution, microstructure, critical temperature (Tc), irreversibili ty field (Hirr), critical current density (Jc), upper critical field (Hc2) and flux pinning. Samples of MgB2+(n-SiC)x with x=0.0, 0.05 & 0.10 were prepared at four different synthesis temperatures i.e. 850, 800, 750, and 700oC with the same heating rate as 10oC/min. We found 750oC as the optimal synthesis temperature for n-SiC doping in bulk MgB2 in order to get the best superconducting performance in terms of Jc, Hc2 and Hirr. Carbon (C) substitution enhances the Hc2 while the low temperature synthesis is responsible for the improvement in Jc due to the smaller grain size, defects and nano-inclusion induced by C incorporation into MgB2 matrix, which is corroborated by elaborative HRTEM (high-resolution transmission electron microscopy) results. We optimized the the Tc(R=0) of above 15K for the studied n-SiC doped and 750 0C synthesized MgB2 under 140 KOe field, which is one of the highest values yet obtained for variously processed and nano-particle added MgB2 in literature to our knowledge.
In a recent letter, it has been predicted within first principle studies that Mn-doped ZrO2 compounds could be good candidate for spintronics application because expected to exhibit ferromagnetism far beyond room temperature. Our purpose is to addres s this issue experimentally for Mn-doped tetragonal zirconia. We have prepared polycrystalline samples of Y0.15(Zr0.85-yMny)O2 (y=0, 0.05, 0.10, 0.15 & 0.20) by using standard solid state method at equilibrium. The obtained samples were carefully characterized by using x-ray diffraction, scanning electron microscopy, elemental color mapping, X-ray photoemission spectroscopy and magnetization measurements. From the detailed structural analyses, we have observed that the 5% Mn doped compound crystallized into two symmetries (dominating tetragonal & monoclinic), whereas higher Mn doped compounds are found to be in the tetragonal symmetry only. The spectral splitting of the Mn 3s core-level x-ray photoelectron spectra confirms that Mn ions are in the Mn3+ oxidation state and indicate a local magnetic moment of about 4.5 {mu}B/Mn. Magnetic measurements showed that compounds up to 10% of Mn doping are paramagnetic with antiferromagnetic interactions. However, higher Mn doped compound exhibits local ferrimagnetic ordering. Thus, no ferromagnetism has been observed for all Mn-doped tetragonal ZrO2 samples.
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