With a view to understanding the effect of rare earth element (Ce, Pr, Nd, Sm and Gd) substitution for the La site in LaMnO3 (LMO), the samples were prepared via solid-state reaction. Structure investigation by X-ray diffraction (XRD) showed that structure transformation from trigonal (LMO) to orthorhombic (PMO, NMO, SMO and GMO) occurred when smaller trivalent rare earth element was replaced. The MnO6 octahedra were tilted and elongated or compressed, corresponding to the ionic radii of the rare earth inserted. Meanwhile, microstructure study using scanning electron microscopy (SEM) illustrated that La substitution by another rare earth element caused a reduction in grain size. This might due to the changes in enthalpy of fusion by other rare earth ions, where higher enthalpy of fusion favours formation of smaller grain size. However, CeMnO3 did not form under this preparation condition. The magnetic properties studied from the hysteresis plot taken at room temperature indicated that the substitution of La with other magnetic trivalent rare earth ions strongly weakened the magnetic strength of the system.
A series of polycrystalline samples (La1-xSmx)0.67Sr0.33MnO3 (X=0.00, 0.05 and 0.10) were prepared using the conventional solid-state reaction method. The XRD analysis indicated that all the samples were fully crystalline and in a single phase with a rhombohedral structure after a sintering at 1200ºC for 24 hours in air. Meanwhile, the Atomic Force Microscopy measurements showed that a small amount of Sm doping in La sites affected the grain growth and this might affect the grain boundary layer, thus resulting in the reduction of the Curie temperature, TC. Extrinsic magnetoresistance (MR) was observed for all the samples with a large negative MR at low field (0-0.1 or 0.2T) region, followed by a slower varying MR at high field (0.1 or 0.2-1T). The highest low-field MR value of -4.6% (at 0.1T) and -6.1% (at 0.2T) were observed for sample X=0.10 and X=0.05, respectively. Hence, these indicated that the extrinsic MR was grain size dependent and was therefore enhanced with a small amount of Sm substitution in La sites.
This studies are directed towards measuring the electrical conductivity of the (CuSe)1-xSex metal chalcogenide semi-conductor composites, with different stoichiometric compositions of Se (x = 0, 0.2, 0.4, 0.5, 0.6, 0.8,1.0) in bulk form. The electrical conductivity measurement was carried out at room temperature, using the parallel plate technique. The (CuSe)1-xSex composites were prepared using solid state reaction, by varying the ratio of CuSe:Se, in the reaction mixture. The electrical conductivity of (CuSe)1-xSex was determined to be in the range of 1.17 x 10-8 to 1.02 x 10-1 S/cm. The finding indicated that the electrical conductivity value tended to decrease as the concentration of Se increased. The effect of the concentration of Se, on electrical conductivity of (CuSe)1-xSex composites, is discussed in this paper.
A bulk YBa2Cu3O7-δ (Y-123) superconductor synthesized by a thermal treatment method was added with different weight percentages (x = 0.0, 0.2, 1.0, 1.5, and 2.0 wt.%) of BiFeO3 (BFO) nanoparticle. X-ray diffraction (XRD), alternating current susceptibility (ACS), and field emission scanning electron microscopy (FESEM) were used to determine the properties of the samples. From the XRD results, all samples showed an orthorhombic crystal structure with a Pmmm space group. The sample x = 1.0 wt.% gave the highest value of Y-123. The high amounts of BFO degraded the crystallite size of the sample, showing that the addition did not promote the grain growth of Y-123. From ACS results, the Tc-onset value was shown to be enhanced by the addition of the BFO nanoparticle, where x = 1.5 wt.% gave the highest Tc value (91.91 K). The sample with 1.5 wt.% showed a high value of Tp (89.15 K). The FESEM analysis showed that the average grain size of the samples decreased as BFO was introduced. However, the small grain size was expected to fill in the boundary, which would help in enhancing the grain connectivity. Overall, the addition of the BFO nanoparticles in Y-123 helped to improve the superconducting properties, mainly for x = 1.5 wt.%.