电致伸缩
电介质
铁电性
偶极子
饱和(图论)
凝聚态物理
极化密度
电场
材料科学
极化(电化学)
相界
储能
相变
光电子学
相(物质)
压电
物理
磁场
复合材料
化学
热力学
磁化
功率(物理)
物理化学
量子力学
数学
组合数学
作者
Jing Shi,Zhao Yunxia,Jiayi He,Tangyuan Li,Fangyuan Zhu,Wenchao Tian,Xiao Liu
出处
期刊:ACS applied energy materials
[American Chemical Society]
日期:2022-02-23
卷期号:5 (3): 3436-3446
被引量:49
标识
DOI:10.1021/acsaem.1c04017
摘要
High-temperature dielectric Bi0.5Na0.5TiO3 (BNT)-based relaxors near a morphotropic phase boundary are developed with excellent energy storage performance. Random distribution of polar nanoregions induced by composition modulation would disrupt the ferroelectric long-range dipolar alignment and weaken the coupling between the ferroelectric domains, yielding slender and deferred polarization–electric field hysteresis loops with relatively high saturation polarization. The reversible nano-domain orientation and growth in relaxors under a delayed electric field result in negligible remnant polarization and advantageous energy storage properties. Simultaneously, superior recoverable energy storage density and efficiency are gained, significantly surpassing the state-of-the-art dielectric energy storage materials under similar moderate electric fields. Vacancies, defect dipole behavior, and structural evolution that relied on an electric field and temperature are discussed to disclose the underlying mechanism associated with phase transition. Even thermal stability and large electrostrictive strain with low hysteresis are achieved in elevated temperatures. These features demonstrate the promising candidates for dielectric energy-storage application and provide a strategy in designing relaxors.
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