Boosting energy storage performance of BiFeO3-based multilayer capacitors via enhancing ionic bonding and relaxor behavior
Environmentally friendly BiFeO3 capacitors have great potential for applications in pulsed-discharge and power conditioning electronic systems because of their excellent intensity of spontaneous polarization (Ps). Herein, (0.7−x)BiFeO3-0.3BaTiO3-xNaTaO3 + 0.3 wt% MnO2 (abbreviated as BF-BT-xNT) mult...
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Published in | Journal of materials chemistry. A, Materials for energy and sustainability Vol. 10; no. 13; pp. 7382 - 7390 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge
Royal Society of Chemistry
30.03.2022
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Subjects | |
Online Access | Get full text |
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Summary: | Environmentally friendly BiFeO3 capacitors have great potential for applications in pulsed-discharge and power conditioning electronic systems because of their excellent intensity of spontaneous polarization (Ps). Herein, (0.7−x)BiFeO3-0.3BaTiO3-xNaTaO3 + 0.3 wt% MnO2 (abbreviated as BF-BT-xNT) multilayer ceramic capacitors (MLCCs) were designed and prepared to improve the energy storage performance via enhancing ion bonding and dielectric relaxation. The BDS of BF-BT-xNT MLCCs from 500 kV cm−1 at x = 0.05 increases greatly to 800 kV cm−1 at x = 0.15 due to the increase of the band gap and resistance, and the decrease of dielectric permittivity. An excellent energy storage density Urec = 9.1 J cm−3 and efficiency η > 80% were obtained since ultrahigh BDS (780 kV cm−1) and low Pr value (2.1 μC cm−2 at measured electric field 780 kV cm−1) were achieved simultaneously in BF-BT-xNT multilayer capacitors at x = 0.12. This work provides a strategy for improving energy storage properties of BiFeO3, which is via enhancing ionic bonding and relaxor behavior to achieve high BDS, low Pr and large Pmax, simultaneously. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 2050-7488 2050-7496 2050-7496 |
DOI: | 10.1039/d1ta10971e |