通过化学压力介导的相分离实现可见弛豫铁电陶瓷 PrxBa0.9-xSr0.1TiO3

IF 3.2 3区 化学 Q2 CHEMISTRY, PHYSICAL
Hao Luo, Xiaomin Wang, Luxi Kang, Dan Wu, Shifeng Zhao* and Yulong Bai*, 
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引用次数: 0

摘要

通过铁电迟滞、介电温度依赖性和复阻抗谱证明了PrxBa0.9-xSr0.1TiO3 (x = 0,0.05, 0.1, 0.15和0.2)陶瓷的动态介电可调性和铁电/弛豫铁电相变。弛豫铁电体中修饰的微观结构和高性能的光电流输出归因于Pr掺杂剂的无序分布和明智地引入更大的半径差导致的有效的内部压力诱导相分离。基于微观结构演变和不同的有功能,有限元模拟揭示了光生载流子和穿透深度对弛豫铁电体异常光伏效应的影响。经过验证的动态光响应和室温下高度可调的相变温度为设计优质可调光电介质提供了可行的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Visible Relaxor Ferroelectric Ceramics PrxBa0.9–xSr0.1TiO3 via Chemical Pressure-Mediated Phase Separation

Visible Relaxor Ferroelectric Ceramics PrxBa0.9–xSr0.1TiO3 via Chemical Pressure-Mediated Phase Separation

The dynamic dielectric tunability and ferroelectric/relaxor ferroelectric phase transition in PrxBa0.9–xSr0.1TiO3 (x = 0, 0.05, 0.1, 0.15, and 0.2) ceramics were demonstrated by ferroelectric hysteresis, temperature-dependent dielectric, and complex impedance spectra. The decorated microstructure and the high-performance output of the photocurrent in the relaxor ferroelectrics are ascribed to the effective internal pressure-induced phase separation by the disordered distribution of Pr dopants and judiciously introduced larger differences in radius. Based on the microstructure evolution and various active energies, the finite element simulations reveal that the photogenerated carriers and penetration depth contribute to the abnormal photovoltaic effect in relaxor ferroelectrics. The verified dynamic photoresponse and highly tunable phase-transition temperature below room temperature provide a viable strategy for designing superior tunable photodielectrics.

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来源期刊
The Journal of Physical Chemistry C
The Journal of Physical Chemistry C 化学-材料科学:综合
CiteScore
6.50
自引率
8.10%
发文量
2047
审稿时长
1.8 months
期刊介绍: The Journal of Physical Chemistry A/B/C is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.
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