Achieving Ultrahigh Energy Storage Density of La and Ta Codoped AgNbO3 Ceramics by Optimizing the Field-Induced Phase Transitions.
ACS Appl Mater Interfaces
; 15(3): 4246-4256, 2023 Jan 25.
Article
en En
| MEDLINE
| ID: mdl-36639350
ABSTRACT
Energy storage capacitors are extensively used in pulsed power devices because of fast charge/discharge rates and high power density. However, the low energy storage density and efficiency of dielectric capacitors limit their further commercialization in modern energy storage applications. Lead-free AgNbO3-based antiferroelectric (AFE) ceramics are considered to be one of the most promising environmentally friendly materials for dielectric capacitors because of their characteristic double polarization-electric field hysteresis loops with small remanent polarization and large maximum polarization. An enhancement of these characteristics allows achieving a synergistic improvement of both the energy storage density and efficiency of the antiferroelectric materials. This work reports on a feasible codoping strategy enabling the preparation of AgNbO3-based ceramics with high energy storage performance. An introduction of La3+ and Ta5+ ions into the AgNbO3 perovskite lattice was found to increase the structural stability of the antiferroelectric phase at the expense of a reduction of local polar regions, resulting in the shifting of the electric field-induced antiferroelectric-ferroelectric phase transition toward higher fields. An ultrahigh recoverable energy storage density of 6.73 J/cm3 and high energy storage efficiency of 74.1% are obtained for the Ag0.94La0.02Nb0.8Ta0.2O3 ceramic subjected to a unipolar electric field of 540 kV/cm. These values represent the best energy performance in reported lead-free ceramics so far. Hence, the La3+/Ta5+ codoping has been shown to be a good route to improve the energy storage properties of AgNbO3 ceramics.
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Banco de datos:
MEDLINE
Idioma:
En
Revista:
ACS Appl Mater Interfaces
Asunto de la revista:
BIOTECNOLOGIA
/
ENGENHARIA BIOMEDICA
Año:
2023
Tipo del documento:
Article
País de afiliación:
China