材料科学
陶瓷
反铁电性
电介质
储能
电容器
铁电性
相(物质)
相变
电容感应
光电子学
复合材料
凝聚态物理
热力学
电气工程
电压
功率(物理)
工程类
物理
有机化学
化学
作者
Huanhuan Li,Zhongbin Pan,Xiqi Chen,Jinghao Zhao,Luomeng Tang,Jinjun Liu,Peng Li,Jiwei Zhai
标识
DOI:10.1016/j.mtphys.2023.101208
摘要
NaNbO3-based ceramics (NN) as a lead-free antiferroelectric (AFE) material has received widespread attention in electrostatic capacitors. Nevertheless, complex structural phase transformation with low threshold switching electric fields hinders the enhancement of energy storage capability. Herein, a feasible avenue for attaining a stable relaxor ferroelectric (FE) phase in NN-based ceramic is designed by introducing Ca0.7Sm0.2TiO3 (CST) to improve the capacitive performance. The experimental results demonstrate that (1-x)NN-xCST ceramics transform from the AFE P to the FE Q phase and domain size evolves from sub-micro to nano-scale as the CST content increases. Meanwhile, the filling behavior of non-isovalent ions induces local random fields caused by the disruption of the long-range polar structure. Ultimately, an ultra-high Wrec ∼9.10 J/cm3 and a desirable η ∼80.1% are attained simultaneously in 0.85NN-0.15CST relaxor FE ceramic, surpassing most NN-based and other lead-free ceramics. Moreover, Wrec and η exhibit excellent stability under the test conditions of frequency, temperature, and cycling. This work demonstrates that the stabilized FE Q phase is an effective approach to accelerate the development of NN-based dielectric materials in advanced energy-storage devices.
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