Abstract

ABSTRACT Dysprosium barium copper oxide – bismuth sodium titanate ((1-x)DyBCO−xBNT) ceramics, where x = 0−0.07 mole fraction, were successfully prepared by a solid-state reaction and sintering method. The DyBa2Cu3O7-δ and (Bi0.5Na0.5)TiO3 powders were separately synthesized by calcining their stoichiometric mixtures at 900°C for 4 h and 800°C for 2 h, respectively. The (1-x)DyBCO−xBNT powders were compacted into pellets and sintered at 930°C for 2 h under normal air atmosphere. Phase identification and morphology of all samples were determined using X-ray diffractometer (XRD). The quantitative phase analysis was analyzed by fitting the XRD pattern using the GSAS-II program. Scanning electron microscopy (SEM) with energy dispersive X-ray spectroscopy (EDS) was used to study microstructure and chemical composition. In all cases, the result of XRD shows that the DyBa2Cu3O7–δ (Dy-123) was identified as the main crystalline phases, due to the good agreement between the observed and calculated patterns after Rietveld refinement. All BNT-doped DyBCO ceramics showed slightly higher density values than the undoped sample, suggesting that BNT helped improve the densification process. The sign of the Seebeck coefficient () was positive for all samples at all measured temperatures, confirming a p-type conduction mechanism. Low BNT doping improved the overall thermoelectric properties of DyBCO ceramics by affecting electrical conductivity (), Seebeck coefficient (), and thermal conductivity (). The dimensionless figure of merit () of all samples increased with increasing temperature. The highest value of 5.67 × 10−2 was observed for the 0.97DyBCO−0.03BNT sample at 863 K.

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