ABSTRACT
Commercially available LaFeO3 powder was processed using the spark plasma sintering (SPS) technique. The results of the dielectric measurement showed high permittivity, but this was strongly frequency-dependent and was also accompanied by a high loss tangent. The chemical purity of the powder and changes induced by the SPS process influenced the stability of the dielectric parameters of the bulk compacts. A microstructure with a homogeneous grain size and a certain porosity was produced. The microhardness of the sintered LaFeO3 was rather high, about 8.3 GPa. All the results are in reasonable agreement with the literature related to the production of LaFeO3 using different techniques. At frequencies as low as 100 Hz, the material behaved like a colossal permittivity ceramic, but this character was lost with the increasing frequency. On the other hand, it exhibited persistent DC photoconductivity after illumination with a standard bulb.
ABSTRACT
By applying the physical vapour deposition method, hollow ceramic microspheres were coated with titanium, and subsequently, they were sintered using the spark plasma sintering technique to create a porous ceramic material that is lightweight and devoid of a matrix. The sintering process was carried out at temperatures ranging from 1050 to 1200 °C, with a holding time of 2 min. The samples were subjected to conventional thermal analyses (differential scanning calorimetry, thermogravimetry, dilatometry), oxidation resistance tests, and thermal diffusivity measurements. Phase analysis of the samples was performed using the XRD and the microstructure of the prepared specimens was examined using electron microscopy. The titanium coating on the microspheres increased the compressive strength and density of the resulting ceramic material as the sintering temperature increased. The morphology of the samples was carefully examined, and phase transitions were also identified during the analysis of the samples.
ABSTRACT
This work is focused on the structural and physical properties of CePt2Al2, an intermetallic compound. At room temperature, the modulated orthorhombic structure Cmme(a00)000, with qâ= (0.481, 0, 0) has been determined by single-crystal X-ray diffraction supplemented by dependence of lattice parameters above room temperature for which the X-ray powder diffraction was used. The compound undergoes a structural transition to a tetragonal structure above room temperature. This transition exhibits 50 °C hysteresis and creates a domain structure in the sample. The magnetic behavior has been studied by specific heat, magnetization, and transport measurements in the temperature range between 0.5 and 300 K. Specific heat and susceptibility shows an antiferromagnetic order below 2 K. On the basis of electrical resistivity and other bulk measurements, CePt2Al2 can be considered a Kondo lattice material. The presence of a modulated crystal structure opens the possibility of a charge density wave state in CePt2Al2 as observed for (Re)Pt2Si2.
