Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/78293
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Title: Energy storage characteristics of (Pb,La)(Zr,Sn,Ti)O-3 antiferroelectric ceramics with high Sn content
Authors: Dan, Y
Xu, HJ
Zou, KL
Zhang, QF
Lu, YM
Chang, G
Huang, HT 
He, YB
Issue Date: 2018
Source: Applied physics letters, 6 Aug. 2018, v. 113, no. 6, 63902
Abstract: (Pb,La)(Zr,Sn,Ti)O-3 (PLZST) antiferroelectric (AFE) materials have been widely investigated for advanced pulsed power capacitors because of their fast charge-discharge rates and superior energystorage capacity. For practical applications, pulsed power capacitors require not only large energy density but also high energy efficiency, which are very difficult to achieve simultaneously. To address this problem, we herein investigate the energy-storage properties of PLZST AFE ceramics with a high Sn content by considering that the introduction of Sn can make the polarization versus electric-field (P-E) hysteresis loops slimmer. The results show that an optimum Sn content leads to the realization of both large recoverable energy density (W-re) and high energy efficiency (eta) in a single material. With a Sn content of 46%, the PLZST AFE ceramic exhibits the best room-temperature energy storage properties with a W-re value as large as 3.2 J/cm(3) and an eta value as high as 86.5%. In addition, both its W-re and eta vary very slightly in the wide temperature range of 20-120 degrees C. The high W-re and eta values and their good thermal stability make the Pb0.97La0.02(Zr0.50Sn0.46Ti0.04)O-3 AFE ceramic a promising material for making pulsed power capacitors usable in various conditions. Published by AIP Publishing.
Publisher: American Institute of Physics
Journal: Applied physics letters 
ISSN: 0003-6951
EISSN: 1077-3118
DOI: 10.1063/1.5044712
Rights: © 2018 Author(s).
This article may be downloaded for personal use only. Any other use requires prior permission of the author and AIP Publishing. This article appeared in Y. Dan et al., Appl. Phys. Lett. 113, 063902 (2018) and may be found at https://dx.doi.org/10.1063/1.5044712
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