Multiphase Engineered Bi1/2Na1/2TiO3-based Ceramics with Simultaneous High Polarization and Superior Breakdown Strength for Energy Storage Applications
编号:119 稿件编号:161 访问权限:仅限参会人 更新:2022-05-12 15:03:01 浏览:558次 口头报告

报告开始:2022年05月27日 09:25 (Asia/Shanghai)

报告时间:20min

所在会议:[S7] Mineral Materials and Advanced Energy Materials » [S7-2] Mineral Materials and Advanced Energy Materials-2

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摘要
Dielectric ceramics are crucial for high-temperature, pulse-power energy-storage applications. However, the mutual restriction between the polarization and breakdown strength has been a significant challenge. Here, multiphase engineering controlled by the two-step sintering heating rate is adopted to simultaneously obtain a high polarization and breakdown strength in 0.8(0.95Bi0.5Na0.5TiO3-0.05SrZrO3)-0.2NaNbO3 (BNTSZNN) ceramic systems. The co-existence of tetragonal (T) and rhombohedral (R) phases benefits the temperature stability of BNTSZNN ceramics. Increasing the heating rate during sintering reduces the diffusion of SrZrO3 and NaNbO3 into Bi0.5Na0.5TiO3, which results in a high proportion of the R phase and a finer grain size. The overall polarization is enhanced by increasing the proportion of the high-polarization R phase, which is demonstrated using a first-principles method. Meanwhile, the finer grain size enhances the breakdown strength. Following this design philosophy, an ultrahigh discharge energy density of 5.55 J/cm3 and energy efficiency above 85% is achieved in BNTSZNN ceramics as prepared with a fast heating rate of 60 ℃/min given a simultaneously high polarization of 43 μC/cm2 and high breakdown strength of 350 kV/cm. Variations in the discharge energy density from room temperature to 160 ℃ are less than 10%. Additionally, such BNTSZNN ceramics exhibit an ultrafast discharge speed with the discharge time (τ0.9) at approximately 60 ns, which shows the great potential in pulse-power system applications.
 
关键字
multiphase engineering,energy storage,high polarization,high breakdown strength,temperature stability
报告人
Chaoqiong ZHU
Tsinghua University

稿件作者
超琼 朱 清华大学 材料学院
子明 蔡 中国矿业大学
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