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    Fabrication of BNBT-BS ceramics via a solid-state combustion approach for BNBT-BS/PDMS composite films in hybrid PENG/TENG applications
    (2026-10-01)
    Luangpangai, Anupong
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    Apirattanon, Nattapong
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    Yimsabai, Sununta
    ;
    Sumang, Rattiphorn
    ;
    Rittidech, Aurawan
    Synthesis of (1-x)Bi<inf>0.47</inf>Na<inf>0.47</inf>Ba<inf>0.06</inf>TiO<inf>3</inf>-xBaSnO<inf>3</inf> ceramics (BNBT-xBS, where 0 ≤ x ≤ 0.05) was accomplished via a solid-state combustion approach. The influence of BaSnO<inf>3</inf> concentration on the phase structure, microstructure, dielectric, ferroelectric and strain properties was thoroughly examined. All specimens exhibited the coexistence of rhombohedral and tetragonal phases within a pure perovskite structure. The composition with x = 0.01 demonstrated optimal electrical properties, achieving a dielectric constant (ɛ<inf>m</inf>) of 6199, a maximum polarization (P<inf>max</inf>) of 41.86 μC/cm<sup>2</sup>, a maximum strain (S<inf>max</inf>) of 0.34% and a normalized strain (d<inf>33</inf>*) of 489 pm/V. The ceramic powder of BNBT-0.01BS was incorporated into a PDMS matrix at concentrations ranging from 0 to 30 wt%. The hybrid PENG/TENG devices achieved their largest electrical output at a BNBT-0.01BS loading of 20 wt%, recording a voltage of 92 V and a current of 0.50 μA. This work outlines a fabrication and development method for composite films with BNBT-0.01BS with PDMS polymers for high-efficiency nanogenerators, playing an important role in improving future energy harvesting technologies.
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    PHASE FORMATION AND ELECTRICAL PROPERTIES OF BCLTS CERAMICS SYNTHESIZED VIA THE SOLID-STATE COMBUSTION TECHNIQUE
    (2025-01-01)
    Somsri, Widchaya
    ;
    Charoenthai, Nipaphat
    ;
    Sutthapintu, Aekkasit
    ;
    Noisak, Jitrawan
    ;
    Vittayakorn, Naratip
    Lead-free Ba<inf>0.93</inf>Ca<inf>0.04</inf>La<inf>0.03</inf>Ti<inf>0.90</inf>Sn<inf>0.10</inf>O<inf>3</inf> (BCLTS) ceramics were fabricated via solid-state combustion technique. The BCLTS powders were calcined in a temperature range of 1075-1175°C for 2h and sintered in a temperature range of 1350-1450°C for 2h. The BCLTS powders exhibited a pure perovskite phase when calcined above 1150°C. All BCLTS ceramic samples displayed a perovskite structure with coexisting cubic and tetragonal phases, with a secondary phase observed only at 1450°C. The growth of grain size was increased with increasing sintering temperature (0.42 to 0.65 μm.). The highest dielectric and ferroelectric properties (ε<inf>r</inf>=3047, tan δ<inf>r</inf> = 0.029, P<inf>max</inf> = 9.52 μC/cm<sup>2</sup>, P<inf>r</inf> = 0.48 μC/cm<sup>2</sup>, E<inf>c</inf>= 1.04 kV/cm) were obtained at the sintering temperature of 1400°C. The altered phase structure in this research, compared to earlier studies, results in distinct outcomes for the dielectric and ferroelectric properties.
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    ELECTRIC AND MAGNETIC PROPERTIES OF Ba0.97Ca0.03Ti0.94Sn0.06O3-Mn0.85Ni0.15Zn0.15Fe2O4 MULTIFERROIC CERAMIC COMPOSITES FABRICATED VIA THE SOLID-STATE COMBUSTION TECHNIQUE
    (2025-01-01)
    Sonchaopria, Nutkamon
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    Meechob, Jirayut
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    Thatawong, Bhoowadol
    ;
    Vittayakorn, Naratip
    ;
    Pinitsoontorn, Supree
    Multiferroic composites with the general formula (1-x)(Ba0.97Ca0.03Ti0.94Sn0.06O3)-x(Mn0.85Ni0.15Zn0.15Fe2O4) (BCTS/MNZF) (x = 0.1, 0.2, 0.3, 0.4, and 0.5) were prepared using the solid-state combustion method. The structure, morphology, dielectric, ferroelectric, magnetic, and magnetoelectric properties were analyzed. The samples were sintered at 1,300ºC for 2 h. The X-ray Diffraction (XRD) patterns revealed tetragonal perovskite, orthorhombic perovskite, and cubic spinel structures corresponding to the BCTS and MNZF phases. Secondary phases (Mn2O3 and SnO) appeared in the sintered samples with x>0.2. Increasing MNZF content enhanced ferrite grain growth in the composites. The dielectric constant showed an overall decreasing trend with increasing MNZF content, with a smaller effect at lower frequencies. At lower frequencies, the dielectric constant declined with increasing frequency before stabilizing around 10 kHz. As ferrite content increased, the density, dielectric constant, and magnetoelectric coefficient (αME) decreased from 5.66 to 5.12 g/cm³, 1388 to 862, and 7.24 to 4.05 mV/cm·Oe, respectively. While the saturation magnetization (Ms) rose substantially from 0.75 to 13.14 emu/g. These findings offer valuable insights into enhancing lead-free multiferroic composite ceramics for targeted applications in magnetoelectric devices.
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    PHASE FORMATION AND ELECTRICAL PROPERTIES OF Ba0.91Ca0.09Ti0.916Sn0.084O3-0.1WT%ZnO -0.1WT%MnO2 LEAD-FREE FERROELECTRIC CERAMICS SYNTHESIZED VIA THE SOLID-STATE COMBUSTION METHOD
    (2025-01-01)
    Yimsabai, Sununta
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    Somsri, Widchaya
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    Vittayakorn, Naratip
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    Charoenthai, Nipaphat
    ;
    Suthapintu, Aekasit
    This work investigated the effect of firing temperatures on the phase formation, microstructure, and electrical properties of Ba0.91Ca0.09Ti0.916Sn0.084O3-0.1wt%ZnO-0.1wt%MnO2 (BCTS-ZnMn) lead-free ferroelectric ceramics synthesized via the solid-state combustion method. Glycine was used as fuel to reduce the synthesis temperature. The samples were calcined at temperatures from 1050 to 1250°C (in 50°C increments) for 3 h and sintered from 1250 to 1450°C (in 50°C increments) for 3 h. A pure perovskite phase was found in the powders calcined above 1100°C. The phase structure, microstructure, dielectric and ferroelectric properties of the ceramics were examined. The X-ray diffraction (XRD) analysis for the ceramics revealed the presence of tetragonal (T) and orthorhombic (O) phases in all the ceramics. The average particle size and average grain size increased with increasing firing temperatures. The density, dielectric constant at the Curie temperature (ɛc), Pr and Ps tended to increase with increasing sintering temperatures, up to 1400°C, and then decreased at 1450°C. The ceramic sintered at 1400°C exhibited the highest density (5.89 g/cm3), dielectric response (ɛc = 13324) and good ferroelectric behavior (Pr = 8.67 μC/cm2, Ps = 17.92 μC/cm2 and Ec = 0.99 kV/cm).
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    ELECTRICAL AND MAGNETIC PROPERTIES OF MULTIFERROIC Co0.6Zn0.4Fe1.7Mn0.3O4 DOPED 0.99Bi0.47Na0.47Ba0.06TiO3-0.01Ba(Sn0.70Nb0.24)O3 CERAMICS SYNTHESIZED VIA THE SOLID-STATE COMBUSTION TECHNIQUE
    (2025-01-01)
    Luangpangai, Anupong
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    Chuai, Phomphon
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    Rittidech, Aurawan
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    Pinitsoontorn, Supree
    ;
    Jantaratana, Pongsakorn
    Multiferroic (1-x)[0.99Bi<inf>0.47</inf>Na<inf>0.47</inf>Ba<inf>0.06</inf>TiO<inf>3</inf>-<inf>0.01</inf>Ba(Sn<inf>0.70</inf>Nb<inf>0.24</inf>)O<inf>3</inf>]-xCo<inf>0.6Z</inf>n<inf>0.4</inf>Fe<inf>1.7</inf>Mn<inf>0.3</inf>O<inf>4</inf> (abbreviated as BNBT-BSN-xCZFMO) ceramics with x ranging from 0 to 0.20 were fabricated using the solid-state combustion technique. The effect of varying BNBT-BSN: CZFMO ratios on the phase structure, microstructure, electrical and magnetic properties was investigated. X-ray diffraction (XRD) analysis of pure BNBT-BSN showed a perovskite structure with rhombohedral and tetragonal phases. The doped BNBT-BSN-xCZFMO ceramics displayed coexisting rhombohedral, tetragonal, and cubic spinel phases, with the cubic spinel phase increasing when the CZFMO content increased. In addition, the XRD peaks shifted to higher angles as the CZFMO content increased, indicating a decrease in lattice parameters. The dielectric constant decreased with higher CZFMO content and higher frequencies. The pure BNBT-BSN ceramic exhibited a saturated P-E loop with a Pmax of 33.2 µC/cm<sup>2</sup>, Pr of 26.1 µC/cm<sup>2</sup>, and an Ec of 14.5 kV/cm. With increased CZFMO content, non-saturated and bloated P-E loops with lower Pmax, Pr, and Ec were observed, implying a rise in the leakage current. The addition of CZFMO induced ferromagnetic behavior in the ceramics, leading to an increase in Ms and a reduction in Hc as CZFMO content increased. The magnetoelectric coupling coefficient of BNBT-BSN-xCZFMO ceramics continuously increased with higher CZFMO content.
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    Phase formation, electric and magnetic properties of multiferroic 0.7Ba0.9Ca0.1TiO3-0.3Ni0.6Zn0.4Fe2O4 composites ceramics synthesized by the solid-state combustion technique
    (2025-01-01)
    Sonchaopri, Nutkamon
    ;
    Somsri, Widchaya
    ;
    Chootin, Suphornphun
    ;
    Vittayakorn, Naratip
    ;
    Pinitsoontorn, Supree
    Multiferroic composite materials have both ferroelectric and ferromagnetic properties. In addition, the electrical and magnetic properties of these ceramics are primarily affected by the preparation temperature. Therefore, this study investigates the effect of the sintering temperature on the phase structure, microstructure, electrical and magnetic properties of multiferroic 0.7Ba<inf>0.9</inf>Ca<inf>0.1</inf>TiO<inf>3</inf>-0.3Ni<inf>0.6</inf>Zn<inf>0.4</inf>Fe<inf>2</inf>O<inf>4</inf> (BCT-NZF) composite ceramics synthesized by the solid-state combustion technique. The samples were sintered in a range of 1250–1350 ºC for 2 h. The X-ray diffraction (XRD) analysis revealed that all ceramics exhibited coexisting phases, with tetragonal perovskite, orthorhombic perovskite and cubic spinel phases, suggesting a complex crystalline structure. The average grain size of the ferroelectric and ferrite grains increased from 0.59 to 1.41 µm and 0.67 to 3.13 µm, respectively, moreover, ε and tanδ at 1 MHz tended to increase from 257.4 to 572.3 and 0.05 to 0.24, respectively, with increased sintering temperature. Density and saturated magnetization (M<inf>s</inf>) increased from 5.36 to 5.45 g/cm<sup>3</sup> and 19.36 to 20.38 emu/g, respectively, while remanent magnetization (M<inf>r</inf>) and coercivity (H<inf>d</inf><inf>c</inf>) decreased from 0.38 to 0.33 emu/g and 25.03 to 20.17 Oe, respectively, when the sintering temperature was increased from 1250 to 1300 °C. Above 1300 °C, the density and M<inf>s</inf> decreased, while M<inf>r</inf> and H<inf>d</inf><inf>c</inf> increased. With the optimum sintering temperature of 1300 °C, the multiferroic BCT-NZF composite ceramics exhibited the highest density (5.45 g/cm<sup>3</sup>), low leakage P-E loop, good magnetic properties (M<inf>s</inf> = 20.38 emu/g) and high magnetoelectric coupling (α<inf>ME</inf> = 4.03 mV/cm•Oe), indicating this ceramic was suitable for application in magnetoelectric devices.
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    Modified energy storage properties of lead-free Sr0.3Bi0.35Na0.335Li0.015TiO3 ceramics with La3+ substitution via the solid-state combustion technique
    (2024-12-01)
    Sinkruason, Thanapon
    ;
    Luangpangai, Anupong
    ;
    Julphunthong, Phongthorn
    ;
    Rittidech, Aurawan
    ;
    Suthapintu, Aekasit
    In this study, the influence of La<sup>3+</sup> substitution on the phase structure, microstructure, electrical and energy storage properties of (Sr<inf>0.3</inf>Bi<inf>0.35</inf>Na<inf>0.335</inf>Li<inf>0.015</inf>)<inf>1-x</inf>La<inf>x</inf>TiO<inf>3</inf> (SBNLT-xLa) ceramics with x = 0–0.05, using the solid-state combustion technique, was investigated. X-ray diffraction (XRD) patterns indicated a pure perovskite structure formed, along with coexisting rhombohedral and tetragonal phases in all ceramics. The Rietveld refinement analysis showed the tetragonal phase increased while the rhombohedral phase decreased with increased La<sup>3+</sup> content. The morphology of the SBNLT-xLa ceramics displayed polygonal grain shapes and anisotropic grain growth. Average grain sizes increased from 2.01 to 2.43 μm as x increased from 0 to 0.01 and afterwards decreased as x increased further. Both the measured density and maximum dielectric constant (ɛ<inf>m</inf>) decreased from 5.48 to 5.29 g/cm<sup>3</sup> and from 4667 to 2313, respectively, when x increased from 0 to 0.05. A decrease in the dielectric properties caused by the phase ratio shifting away from a morphotropic phase boundary (MPB) condition, poor microstructure and low density was produced with La<sup>3+</sup> replacement. The maximum polarization (P<inf>max</inf>), remnant polarization (P<inf>r</inf>) and coercive field (E<inf>c</inf>) decreased with increased La<sup>3+</sup> content. A decline in P<inf>r</inf> and E<inf>c</inf> improved the energy storage efficiency (ƞ) and energy storage loss (W<inf>loss</inf>), resulting in enhanced energy storage properties. At x = 0.02, the ceramic showed good energy storage properties (W<inf>total</inf> of 0.781 J/cm<sup>3</sup>, W<inf>rec</inf> of 0.624 J/cm<sup>3</sup>, W<inf>loss</inf> of 0.157 J/cm<sup>3</sup> and ƞ of 79.8%), measured at 60 kV/cm.