Optimizing energy storage under low electric field in A-site dysprosium modified BiFeO3-BaTiO3 ceramics
Electric recoverable energy density and dielectric breakdown strength are crucial factors in the high power-density capacitors. This study highlights the A-site dysprosium (Dy) substituted perovskite 0.5(Bi1−xDyx)FeO3-0.5BaTiO3 relaxor ferroelectric ceramics (x = 0–0.30) in O2-atmosphere sintering....
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Veröffentlicht in: | Journal of alloys and compounds 2024-05, Vol.983, p.173918, Article 173918 |
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Sprache: | eng |
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Zusammenfassung: | Electric recoverable energy density and dielectric breakdown strength are crucial factors in the high power-density capacitors. This study highlights the A-site dysprosium (Dy) substituted perovskite 0.5(Bi1−xDyx)FeO3-0.5BaTiO3 relaxor ferroelectric ceramics (x = 0–0.30) in O2-atmosphere sintering. An overall pseudo-cubic structure with a major cubic Pm-3m symmetry was observed in all compositions accompanied by multiple lattice symmetries. Anti-polar orthorhombic Pbam space group and non-polar orthorhombic Pnma symmetry gradually increase while ferroelectric tetragonal P4mm symmetry decreases as Dy content approaches x = 0.3. Recoverable energy densities (Wrec) of 4.8 J/cm3 and 3.6 J/cm3, storing efficiencies (η) of 68% and 75%, and recoverable energy storage intensities (ρ) of ∼3.2×10−2 J/kV·cm2 and ∼2.1×10−2 J/kV·cm2 were attained at x = 0 and 0.10 at electric fields of 150 and 175 kV/cm, respectively. The breakdown strength is improved from 150 to 200 kV/cm as x increases from 0.0 to 0.30. This study suggests that grain boundaries and local nanoclusters may act as barriers to inhibit charge transport and consequently increase the breakdown strength.
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•Recoverable energy densities and efficiencies of 4.8 J/cm3 and 68% in BDF-BT-0 and 3.6 J/cm3 and 75% in BDF-BT-0.1.•Grain boundaries and local nanoclusters act as barriers to inhibit charge transport.•Enhanced breakdown strength from 150 kV/cm in BDF-BT-0–200 kV/cm in BDF-BT-0.3. |
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ISSN: | 0925-8388 1873-4669 |
DOI: | 10.1016/j.jallcom.2024.173918 |