{"title":"应变无铅多铁氧体固溶体特性的大幅提升与维加定律的强烈偏差","authors":"Tao Wang, Min-Jie Zou, Dehe Zhang, Yu-Chieh Ku, Yawen Zheng, Shen Pan, Zhongqi Ren, Zedong Xu, Haoliang Huang, Wei Luo, Yunlong Tang, Lang Chen, Cheng-En Liu, Chun-Fu Chang, Sujit Das, Laurent Bellaiche, Yurong Yang, Xiu-Liang Ma, Chang-Yang Kuo, Xingjun Liu, Zuhuang Chen","doi":"10.1016/j.matt.2024.09.018","DOIUrl":null,"url":null,"abstract":"Efforts to combine the advantages of multiple systems to enhance functionalities through solid-solution design present a great challenge due to the constraint imposed by the classical Vegard’s law. Here, we successfully navigate this trade-off by leveraging the synergistic effect of chemical doping and strain engineering in the solid-solution system of (1-<em>x</em>)BiFeO<sub>3</sub>-<em>x</em>BaTiO<sub>3</sub>. Unlike bulks, a significant deviation from Vegard’s law accompanied by enhanced multiferroism is observed in strained solid-solution epitaxial films, where we achieve a pronounced tetragonality (∼1.1), enhanced saturated magnetization (∼12 emu/cm<sup>3</sup>), substantial polarization (∼107 μC/cm<sup>2</sup>), and high ferroelectric Curie temperature (∼880°C), all while maintaining impressively low leakage current. These characteristics surpass the properties of their parent BiFeO<sub>3</sub> and BaTiO<sub>3</sub> films. Moreover, the superior ferroelectricity has never been reported in corresponding bulks (e.g., <em>P</em> ∼5 μC/cm<sup>2</sup> and <em>T</em><sub>C</sub> ∼300°C for bulk, with <em>x</em> = 0.5). These findings underscore the potential of strained (1-<em>x</em>)BiFeO<sub>3</sub>-<em>x</em>BaTiO<sub>3</sub> films as lead-free, room temperature multiferroics.","PeriodicalId":388,"journal":{"name":"Matter","volume":"43 1","pages":""},"PeriodicalIF":17.3000,"publicationDate":"2024-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Large enhancement of properties in strained lead-free multiferroic solid solutions with strong deviation from Vegard’s law\",\"authors\":\"Tao Wang, Min-Jie Zou, Dehe Zhang, Yu-Chieh Ku, Yawen Zheng, Shen Pan, Zhongqi Ren, Zedong Xu, Haoliang Huang, Wei Luo, Yunlong Tang, Lang Chen, Cheng-En Liu, Chun-Fu Chang, Sujit Das, Laurent Bellaiche, Yurong Yang, Xiu-Liang Ma, Chang-Yang Kuo, Xingjun Liu, Zuhuang Chen\",\"doi\":\"10.1016/j.matt.2024.09.018\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Efforts to combine the advantages of multiple systems to enhance functionalities through solid-solution design present a great challenge due to the constraint imposed by the classical Vegard’s law. Here, we successfully navigate this trade-off by leveraging the synergistic effect of chemical doping and strain engineering in the solid-solution system of (1-<em>x</em>)BiFeO<sub>3</sub>-<em>x</em>BaTiO<sub>3</sub>. Unlike bulks, a significant deviation from Vegard’s law accompanied by enhanced multiferroism is observed in strained solid-solution epitaxial films, where we achieve a pronounced tetragonality (∼1.1), enhanced saturated magnetization (∼12 emu/cm<sup>3</sup>), substantial polarization (∼107 μC/cm<sup>2</sup>), and high ferroelectric Curie temperature (∼880°C), all while maintaining impressively low leakage current. These characteristics surpass the properties of their parent BiFeO<sub>3</sub> and BaTiO<sub>3</sub> films. Moreover, the superior ferroelectricity has never been reported in corresponding bulks (e.g., <em>P</em> ∼5 μC/cm<sup>2</sup> and <em>T</em><sub>C</sub> ∼300°C for bulk, with <em>x</em> = 0.5). These findings underscore the potential of strained (1-<em>x</em>)BiFeO<sub>3</sub>-<em>x</em>BaTiO<sub>3</sub> films as lead-free, room temperature multiferroics.\",\"PeriodicalId\":388,\"journal\":{\"name\":\"Matter\",\"volume\":\"43 1\",\"pages\":\"\"},\"PeriodicalIF\":17.3000,\"publicationDate\":\"2024-10-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Matter\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1016/j.matt.2024.09.018\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Matter","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1016/j.matt.2024.09.018","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
Large enhancement of properties in strained lead-free multiferroic solid solutions with strong deviation from Vegard’s law
Efforts to combine the advantages of multiple systems to enhance functionalities through solid-solution design present a great challenge due to the constraint imposed by the classical Vegard’s law. Here, we successfully navigate this trade-off by leveraging the synergistic effect of chemical doping and strain engineering in the solid-solution system of (1-x)BiFeO3-xBaTiO3. Unlike bulks, a significant deviation from Vegard’s law accompanied by enhanced multiferroism is observed in strained solid-solution epitaxial films, where we achieve a pronounced tetragonality (∼1.1), enhanced saturated magnetization (∼12 emu/cm3), substantial polarization (∼107 μC/cm2), and high ferroelectric Curie temperature (∼880°C), 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 (e.g., P ∼5 μC/cm2 and TC ∼300°C for bulk, with x = 0.5). These findings underscore the potential of strained (1-x)BiFeO3-xBaTiO3 films as lead-free, room temperature multiferroics.
期刊介绍:
Matter, a monthly journal affiliated with Cell, spans the broad field of materials science from nano to macro levels,covering fundamentals to applications. Embracing groundbreaking technologies,it includes full-length research articles,reviews, perspectives,previews, opinions, personnel stories, and general editorial content.
Matter aims to be the primary resource for researchers in academia and industry, inspiring the next generation of materials scientists.