Self-Propagating High Temperature Synthesis of MgB2 Superconductor in High-Pressure of Argon Condition

Magnesium diboride can be synthesized under argon ambient, elevated or high pressures. High-pressure syntheses are promising methods for manufacturing of the bulk MgB2 superconductor material. We have been used high pressure of Ar gas in order to investigate its effect on properties of MgB2 superconductor such as critical temperature and current density. Bulk MgB2 superconductor was synthesized from elemental Mg–B powders in thermal explosion mode of self-propagating hightemperature synthesis (SHS) under argon pressure of 25 atm. XRD pattern of the as-synthesized product indicates an almost complete conversion of the reactants to the MgB2 single phase. Most of the diffractions peaks are related to the MgB2 polycrystalline bulk material. The impurity fraction is less than 24.3% in total sample and identified as MgO and MgB4 secondary phases. The positive effect of pressure of Ar gas during synthesis of MgB2 on critical current density JC has been confirmed. The critical current density of the sample was achieved in high pressure reactor was 3.8×106 A/cm2. A superconducting volume fraction of 16% under a magnetic field of 10 Oe was obtained at 5 K, indicating that the superconductivity was bulk in nature. The succeeded level of superconductor parameters of the highpressure synthesized MgB2 and the possibility to produce a large bulk products make this technology very promising for practical applications

Fabrication of Nd3+ and Yb3+ doped NIR emitting nano fluorescent probe: A candidate for bioimaging applications

The intentional design of rare earth doped luminescent architecture exhibits unique optical properties and it can be considered as a promising and potential probe for optical imaging applications. Calcium fluoride (CaF2) nanoparticles doped with optimum concentration of Nd3+ and Yb3+ as sensitizer and activator, respectively, were synthesized by wet precipitation method and characterized by x-ray diffraction (XRD) and photoluminescence. In spite of the fact that the energy transfer takes place from Nd3+ to Yb3+, the luminescence intensity was found to be weak due to the lattice defects generated from the doping of trivalent cations (Nd3+ and Yb3+) for divalent host cations (Ca2+). These defect centres were tailored via charge compensation approach by co-doping Na+ ion and by optimizing its concentration and heat treatment duration. CaF2 doped with 5 mol% Nd3+, 3 mol% Yb3+ and 4 mol% Na+ after heat treatment for 2 h exhibited significantly enhanced emission intensity and life time. The ex vivo fluorescence imaging experiment was done at various thickness of chicken breast tissue. The maximum theoretical depth penetration of the NIR light was calculated and the value is 14 mm. The fabricated phosphor can serve as contrast agent for deep tissue near infrared (NIR) light imaging

Magnetic Sensing Potential of Fe3O4 Nanocubes Exceeds That of Fe3O4 Nanospheres

This paper highlights the relation between the shape of iron oxide (Fe3O4) particles and their magnetic sensing ability. We synthesized Fe3O4 nanocubes and nanospheres having tunable sizes via solvothermal and thermal decomposition synthesis reactions, respectively, to obtain samples in which the volumes and body diagonals/diameters were equivalent. Vibrating sample magnetometry (VSM) data showed that the saturation magnetization (Ms) and coercivity of 100–225 nm cubic magnetic nanoparticles (MNPs) were, respectively, 1.4–3.0 and 1.1–8.4 times those of spherical MNPs on a same-volume and same-body diagonal/diameter basis. The Curie temperature for the cubic Fe3O4 MNPs for each size was also higher than that of the corresponding spherical MNPs; furthermore, the cubic Fe3O4 MNPs were more crystalline than the corresponding spherical MNPs. For applications relying on both higher contact area and enhanced magnetic properties, higher-Ms Fe3O4 nanocubes offer distinct advantages over Fe3O4 nanospheres of the same-volume or same-body diagonal/diameter. We evaluated the sensing potential of our synthesized MNPs using giant magnetoresistive (GMR) sensing and force-induced remnant magnetization spectroscopy (FIRMS). Preliminary data obtained by GMR sensing confirmed that the nanocubes exhibited a distinct sensitivity advantage over the nanospheres. Similarly, FIRMS data showed that when subjected to the same force at the same initial concentration, a greater number of nanocubes remained bound to the sensor surface because of higher surface contact area. Because greater binding and higher Ms translate to stronger signal and better analytical sensitivity, nanocubes are an attractive alternative to nanospheres in sensing applications

Magnetic Sensing Potential of Fe3O4 Nanocubes Exceeds That of Fe3O4 Nanospheres

This paper highlights the relation between the shape of iron oxide (Fe3O4) particles and their magnetic sensing ability. We synthesized Fe3O4 nanocubes and nanospheres having tunable sizes via solvothermal and thermal decomposition synthesis reactions, respectively, to obtain samples in which the volumes and body diagonals/diameters were equivalent. Vibrating sample magnetometry (VSM) data showed that the saturation magnetization (Ms) and coercivity of 100�5 nm cubic magnetic nanoparticles (MNPs) were, respectively, 1.4�0 and 1.1�4 times those of spherical MNPs on a same-volume and same-body diagonal/diameter basis. The Curie temperature for the cubic Fe3O4 MNPs for each size was also higher than that of the corresponding spherical MNPs; furthermore, the cubic Fe3O4 MNPs were more crystalline than the corresponding spherical MNPs. For applications relying on both higher contact area and enhanced magnetic properties, higher-Ms Fe3O4 nanocubes offer distinct advantages over Fe3O4 nanospheres of the same-volume or same-body diagonal/diameter. We evaluated the sensing potential of our synthesized MNPs using giant magnetoresistive (GMR) sensing and force-induced remnant magnetization spectroscopy (FIRMS). Preliminary data obtained by GMR sensing confirmed that the nanocubes exhibited a distinct sensitivity advantage over the nanospheres. Similarly, FIRMS data showed that when subjected to the same force at the same initial concentration, a greater number of nanocubes remained bound to the sensor surface because of higher surface contact area. Because greater binding and higher Ms translate to stronger signal and better analytical sensitivity, nanocubes are an attractive alternative to nanospheres in sensing applications

Fabrication of Yttrium Ferrite Nanoparticles by Solution Combustion Synthesis

The ternary oxide system Y-Fe-O presents fascinating magnetic properties that are sensitive to the crystalline size of particles. There is a major challenge to fabricate these materials in nano-crystalline forms due to particle conglomeration during nucleation and synthesis. In this paper we report the fabrication of nano sized crystalline yttrium ferrite by solution combustion synthesis (SCS) where yttrium and iron nitrates were used as metal precursors with glycine as a fuel. The magnetic properties of the product can be selectively controlled by adjusting the ratio of glycine to metal nitrates. Yttrium ferrite nano-powder was obtained by using three concentration of glycine (3, 6 and 10 wt.%) in the initial exothermic mixture. Increasing glycine content was found to increase the reaction temperature of the system. The structural and magnetic properties of yttrium ferrite before and after annealing at temperature of 1000 °C were investigated by X-ray diffractometry, Differential Scanning Calorimetry (DSC) and cryogenic magnetometry (PPMS, Quantum Design). X-ray diffraction showed that, a broad diffraction peak was found for all samples indicating the amorphous nature of the product. Particle size and product morphology analysis identified that, Nitrate/glycine combustion caused considerable gas evolution, mainly carbon dioxide, N2 and H2O vapor, which caused the synthesized powders to become friable and loosely agglomerated for glycine concentration from 3 wt.% up to 10 wt.%. The study of the magnetic properties of produced materials in a metastable state was performed by measuring dependencies of Magnetization (M) on temperature, and magnetization on magnetic field strength between 5 K and 300 K. Magnetization measurements on temperature zero-fieldcooled and field-cooled show different patterns when the fraction of glycine is increased. The analysis of zero-field-cooled (ZFC), field-cooled (FC) and magnetization curves of annealed samples confirmed that nanoparticles exhibit superparamagnetic behavior. The increasing concentration of glycine leads to an increased blocking temperature

NaGdF4:Yb,Er-Ag nanowire hybrid nanocomposite for multifunctional upconversion emission, optical imaging, MRI and CT imaging applications

The effect of novel silver nanowire encapsulated NaGdF4:Yb,Er hybrid nanocomposite on the upconversion emission and bioimaging properties has been investigated. The upconvension nanomaterials were synthesised by polyol method in the presence of ethylene glycol, PVP and ethylenediamine. The NaGdF4:Yb,Er-Ag hybrid was formed with upconverting NaGdF4:Yb,Er nanoparticles of size ~ 80 nm and silver nanowires of thickness ~ 30 nm. The surface plasmon induced by the silver ion in the NaGdF4:Yb,Er-Ag nanocomposite resulted an intense upconversion green emission at 520 nm and red emission at 660 nm by NIR diode laser excitation at 980 nm wavelength. The UV-Vis-NIR spectral absorption at 440 nm and 980 nm, the intense Raman vibrational modes and the strong upconversion emission results altogether confirm the localised surface plasmon resonance effect of silver ion in the hybrid nanocomposite. MRI study of both NaGdF4:Yb,Er nanoparticle and NaGdF4:Yb,Er-Ag nanocomposite revealed the T1 relaxivities of 22.13 and 10.39 mM−1 s−1, which are larger than the commercial Gd-DOTA contrast agent of 3.08 mM−1 s−1. CT imaging NaGdF4:Yb,Er-Ag and NaGdF4:Yb,Er respectively showed the values of 53.29 HU L/g and 39.51 HU L/g, which are higher than 25.78 HU L/g of the CT contrast agent Iobitridol. The NaGdF4:Yb,Er and NaGdF4:Yb,Er-Ag respectively demonstrated a negative zeta potential of 54 mV and 55 mV, that could be useful for biological application. The in vitro cytotoxicity of the NaGdF4:Yb,Er tested in HeLa and MCF-7 cancer cell line by MTT assay demonstrated a cell viability of 90 and 80 %, respectively. But, the cell viability of NaGdF4:Yb,Er-Ag slightly decreased to 80 and 78%. The confocal microscopy imaging showed that the UCNPs are effectively up-taken inside the nucleolus of the cancer cells, and it might be useful for NIR laser–assisted phototherapy for cancer treatment

Magnetic Sensing Potential of Fe₃O₄ Nanocubes Exceeds That of Fe₃O₄ Nanospheres

This paper highlights the relation between the shape of iron oxide (Fe₃O₄) particles and their magnetic sensing ability. We synthesized Fe₃O₄ nanocubes and nanospheres having tunable sizes via solvothermal and thermal decomposition synthesis reactions, respectively, to obtain samples in which the volumes and body diagonals/diameters were equivalent. Vibrating sample magnetometry (VSM) data showed that the saturation magnetization (<i>M</i>_s) and coercivity of 100–225 nm cubic magnetic nanoparticles (MNPs) were, respectively, 1.4–3.0 and 1.1–8.4 times those of spherical MNPs on a same-volume and same-body diagonal/diameter basis. The Curie temperature for the cubic Fe₃O₄ MNPs for each size was also higher than that of the corresponding spherical MNPs; furthermore, the cubic Fe₃O₄ MNPs were more crystalline than the corresponding spherical MNPs. For applications relying on both higher contact area and enhanced magnetic properties, higher-<i>M</i>_s Fe₃O₄ nanocubes offer distinct advantages over Fe₃O₄ nanospheres of the same-volume or same-body diagonal/diameter. We evaluated the sensing potential of our synthesized MNPs using giant magnetoresistive (GMR) sensing and force-induced remnant magnetization spectroscopy (FIRMS). Preliminary data obtained by GMR sensing confirmed that the nanocubes exhibited a distinct sensitivity advantage over the nanospheres. Similarly, FIRMS data showed that when subjected to the same force at the same initial concentration, a greater number of nanocubes remained bound to the sensor surface because of higher surface contact area. Because greater binding and higher <i>M</i>_s translate to stronger signal and better analytical sensitivity, nanocubes are an attractive alternative to nanospheres in sensing applications