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Nanoparticles (dia ~ 5 - 7 nm) of Bi_0.5 X_0.5(X=Ca,Sr)MnO_3 are prepared by polymer assisted sol-gel method and characterized by various physico-chemical techniques. X-ray diffraction gives evidence for single phasic nature of the materials as well as their structures. Mono dispersed to a large extent, isolated nanoparticles are seen in the transmission electron micrographs. High resolution electron microscopy shows the crystalline nature of the nanoparticles. Superconducting quantum interferometer based magnetic measurements from 10 K to 300 K show that these nanomanganites retain the charge ordering (CO) nature unlike Pr and Nd based nanomanganites. The CO in Bi based manganites is thus found to be very robust consistent with the observation that magnetic field of the order of 130 T are necessary to melt the CO in these compounds. These results are supported by electron magnetic resonance measurements.
The complicated electronic, magnetic, and colossal magnetoresistant (CMR) properties of Sr and Ca doped lanthanum manganites can be understood by spin-polarized first-principles calculations. The electronic properties can be attributed to a detailed
Nd_0.5 Ca_0.5 MnO_3 (NCMO) nanoparticles (average diameter ~ 20 and 40 nm) are synthesized by polymeric precursor sol-gel method and characterized by X- ray diffraction, transmission electron microscopy (TEM), selective area electron diffraction (SAE
The magnetic and magnetocaloric properties of polycrystalline La0.70(Ca0.30-xSrx)MnO3:Ag 10% manganite have been investigated. All the compositions are crystallized in single phase orthorhombic Pbnm space group. Both, the Insulator-Metal transition t
Magnetization, neutron diffraction, and high-energy x-ray diffraction results for Sn-flux grown single-crystal samples of Ca(Co$_{1-x}$Fe$_{x}$)$_{y}$As$_{2}$, $0leq xleq1$, $1.86leq y leq 2$, are presented and reveal that A-type antiferromagnetic or
Oxides containing iridium ions display a range of magnetic and conducting properties that depend on the delicate balance between interactions and are controlled, at least in part, by the details of the crystal architecture. We have used muon-spin rot