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    Phase Formation, Microstructure and Electric Properties of Vanadium Doped Lead-Free BaTi0.91Sn0.09O3 Ceramics
    (2023-01-01)
    Pattanakasem, Wiwat
    ;
    Charoenthai, Nipaphat
    ;
    ;
    Bongkarn, Theerachai
    Lead-free Ba(Ti<inf>0.91</inf>Sn<inf>0.09</inf>)<inf>1-x</inf>V<inf>x</inf>O<inf>3</inf> (BTSV, x = 0, 0.005,0.010, 0.015, and 0.020) ceramics were prepared by the conventional solid-state sintering method with a calcination temperature of 1200 °C for 2 h and a sintering temperature between 1350 °C and 1400 °C for 4 h. The effect of vanadium (V) doping on the phase formation, microstructure and electrical properties of the ceramics was investigated. X-ray diffraction (XRD) measurements revealed that the ceramics with x = 0 and 0.005 had pure perovskite structures with no detectable impurity, while the ceramics with x ≥ 0.010 exhibited perovskite structures and had secondary impurity phases. Coexisting orthorhombic and tetragonal phases were observed and the Rietveld refinement analysis suggested that the tetragonal phase increased with increased V<sup>5+</sup> substitution. When x increased from 0 to 0.010, the average grain size increased from 47 to 62 µm and then dropped, while the density (ρ) decreased from 5.98 to 5.64 g/cm<sup>3</sup> when x increased. Furthermore, the BTSV ceramics exhibited increased porosity, Curie temperatures (T <inf>C</inf> ∼ 42 °C to 52 °C) and coercive field (E <inf>c</inf>), while the dielectric constant at the Curie temperature (ε<inf>C</inf>) and the remnant polarization (P <inf>r</inf>) of the ceramics decreased (∼18023 to 6110 and ∼7.42 to 4.88 µC/cm<sup>2</sup>, respectively) when V<sup>5+</sup> doping increased.
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    Item type:Publication,
    Classical to Relaxor Ferroelectric Transformation of Lanthanum Modified BaTi0.91Sn0.09O3 Ceramics
    (2023-01-01)
    Pattanakasem, Wiwat
    ;
    Prasertpalichat, Sasipohn
    ;
    Premwichit, Pathit
    ;
    ;
    Bongkarn, Theerachai
    Lead-free Ba<inf>1-x</inf>La<inf>x</inf>Ti<inf>0.91</inf>Sn<inf>0.09</inf>O<inf>3</inf> (BLTS) ceramics with x = 0, 0.01, 0.03 and 0.05, were prepared by the traditional solid-state sintering method with calcination and sintering temperatures of 1200 °C for 2 h and 1400 °C for 4 h, respectively. X-ray diffraction (XRD) measurements revealed that all the BLTS ceramics had pure perovskite structures with no detectable impurities. When x = 0 and 0.01, the ceramics exhibited coexisting orthorhombic (O) and tetragonal (T) phases, while the orthorhombic (O), tetragonal (T) and cubic phase (C) were detected in the BLTS ceramics with x = 0.03 and 0.05, which the Rietveld refinement analysis confirmed. Furthermore, increasing x in the BLTS ceramics led to a large decrease in the average grain size (from 45.7 to 0.9 µm). A significant decrease in the remnant polarization (P <inf>r</inf>) accompanied by very slim hysteresis loops were observed for higher La (x ≥ 0.03) levels. This demonstrates that BLTS ceramics transition from classical ferroelectric to relaxor ferroelectric behavior due to changing occupancy of the A-site to La<sup>3+</sup> from Ba<sup>2+</sup>.
      1
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    Item type:Publication,
    Effect of the Firing Temperatures on the Phase Evolution and Electrical Properties of 0.85[0.94Bi0.5Na0.5TiO3-0.06BaTiO3]-0.15[Na0.73Bi0.09NbO3] Ceramics Synthesized via the Solid-State Combustion Method
    (2023-01-01)
    Pattanakasem, Wiwat
    ;
    Yotthuan, Surirat
    ;
    Hongsamsibjed, Pakornkiat
    ;
    Suriwong, Tawat
    ;
    Prasertpalichat, Sasipohn
    In this research paper, we describe 0.85[0.94Bi<inf>0.5</inf>Na<inf>0.5</inf>TiO<inf>3</inf>-0.06BaTiO<inf>3</inf>]-0.15[Na<inf>0.73</inf>Bi<inf>0.09</inf>NbO<inf>3</inf>] (BNT-BT-NBN) ceramics fabricated by the solid-state combustion technique. The phase evolution, microstructure, dielectric, ferroelectric and energy storage properties were examined. The BNT-BT-NBN powders and ceramics were calcined and sintered between 650–900 °C and 1100–1175 °C, respectively, for 2 h. All samples showed a typical perovskite structure, as revealed by X-ray diffraction. The Rietveld refinement analysis of the ceramics suggested the samples sintered between 1100 and 1150 °C had coexisting R + T phases, while the R + T+C phases were observed in the ceramics sintered at 1175 °C. The average grain size of the samples increased from 0.52 to 1.39 μm with increased sintering temperature. The density of the ceramics increased from 5.12 to 5.45 g/cm<sup>3</sup> when the sintering temperature increased from 1100 to 1150 °C, and then decreased. Increasing the sintering temperature from 1100 to 1150 °C caused the dielectric constant at T <inf>s</inf> (ε <inf>s</inf>) and the dielectric constant at T <inf>m</inf> (ε <inf>m</inf>) to increase from 1727 to 1945 and 1564 to 1750, respectively, and then ε <inf>s</inf> and ε <inf>m</inf> declined. All BNT-BT-NBN ceramics had good dielectric temperature stability with only a±10% change when the temperature ranged from room temperature to ∼300 °C. The optimum energy-storage properties (W <inf>rec</inf> = 0.62 J/cm<sup>3</sup> and η = 83.2%) were obtained from the BNT-BT-NBN ceramics sintered at 1150 °C for 2 h. This data indicates that BNT-BT-NBN ceramics can be useful as lead-free materials for high density energy-storage capacitors.
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