多铁性
居里温度
固溶体
凝聚态物理
应变工程
材料科学
外延
铁磁性
极化(电化学)
纳米技术
物理
铁电性
光电子学
化学
物理化学
电介质
冶金
硅
图层(电子)
作者
Tuo Wang,Min‐Jie Zou,Dehe Zhang,Yu‐Chieh Ku,Yawen Zheng,Pan Shen,Zhongqi Ren,Zedong Xu,Haoliang Huang,Wei Luo,Yun‐Long Tang,Lang Chen,Cheng-En Liu,Chun-Fu Chang,Sujit Das,L. Bellaïche,Yurong Yang,Xiuliang Ma,Chang‐Yang Kuo,Xingjun Liu
出处
期刊:Matter
[Elsevier BV]
日期:2024-10-01
卷期号:: 101874-101874
被引量:1
标识
DOI:10.1016/j.matt.2024.09.018
摘要
Efforts to combine the advantages of multiple systems to enhance functionlities through solid solution design present a great challenge due to the constraint imposed by the classical Vegard law. Here, we successfully navigate this trade off by leveraging the synergistic effect of chemical doping and strain engineering in solid solution system of BiFeO3 BaTiO3. Unlike bulks, a significant deviation from the Vegard law accompanying with enhanced multiferroism is observed in the strained solid solution epitaxial films, where we achieve a pronounced tetragonality, enhanced saturated magnetization, substantial polarization, high ferroelectric Curie temperature, all while maintaining impressively low leakage current. These characteristics surpass the properties of their parent BiFeO3 and BaTiO3 films. Moreover, the superior ferroelectricity has never been reported in corresponding bulks. These findings underscore the potential of strained BiFeO3 BaTiO3 films as lead-free, room-temperature multiferroics.
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