题名 | A combinatory ferroelectric compound bridging simple ABO(3) and A-site-ordered quadruple perovskite |
作者 | Zhao, Jianfa1,2,3; Gao, Jiacheng1,2; Li, Wenmin1,2; Qian, Yuting1,2; Shen, Xudong1,2,3; Wang, Xiao4; Shen, Xi1,2; Hu, Zhiwei4; Dong, Cheng5; Huang, Qingzhen6; Cao, Lipeng1,2; Li, Zhi7; Zhang, Jun1,2; Ren, Chongwen1,2; Duan, Lei1,2; Liu, Qingqing1,2; Yu, Richeng1,2; Ren, Yang8; Weng, Shih-Chang9; Lin, Hong-Ji9; Chen, Chien-Te9; Tjeng, Liu-Hao4; Long, Youwen1,2,3; Deng, Zheng1,2; Zhu, Jinlong10 ![]() ![]() ![]() ![]() |
通讯作者 | Weng, Hongming; Yu, Runze; Jin, Changqing |
发表日期 | 2021-02-02
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DOI | |
发表期刊 | |
ISSN | 2041-1723
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EISSN | 2041-1723
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卷号 | 12期号:1 |
摘要 | The simple ABO(3) and A-site-ordered AA(3)B(4)O(12) perovskites represent two types of classical perovskite functional materials. There are well-known simple perovskites with ferroelectric properties, while there is still no report of ferroelectricity due to symmetry breaking transition in A-site-ordered quadruple perovskites. Here we report the high pressure synthesis of an A-site-ordered perovskite PbHg3Ti4O12, the only known quadruple perovskite that transforms from high-temperature centrosymmetric paraelectric phase to low-temperature non-centrosymmetric ferroelectric phase. The coordination chemistry of Hg2+ is changed from square planar as in typical A-site-ordered quadruple perovskite to a rare stereo type with 8 ligands in PbHg3Ti4O12. Thus PbHg3Ti4O12 appears to be a combinatory link from simple ABO(3) perovskites to A-site-ordered AA ' 3Ti4O12 perovskites, sharing both displacive ferroelectricity with former and structure coordination with latter. This is the only example so far showing ferroelectricity due to symmetry breaking phase transition in AA ' 3B4O12-type A-site-ordered perovskites, and opens a direction to search for ferroelectric materials. There are few reports of ferroelectricity due to symmetry breaking transition in A-site-ordered quadruple perovskites. Here, the authors find one with phase transition from a high-temperature centrosymmetric paraelectric phase to a low-temperature non-centrosymmetric ferroelectric phase in a high pressure synthesized compound. |
相关链接 | [来源记录] |
收录类别 | |
语种 | 英语
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重要成果 | NI论文
; ESI高被引
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学校署名 | 其他
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资助项目 | Ministry of Science and Technology of China["2018YFA0305700",11921004,11820101003,"U2032220","2017YFA0302900"]
; Beijing Nature Science Foundation[2202059]
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WOS研究方向 | Science & Technology - Other Topics
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WOS类目 | Multidisciplinary Sciences
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WOS记录号 | WOS:000617063000017
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出版者 | |
Scopus记录号 | 2-s2.0-85100334415
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来源库 | Web of Science
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引用统计 |
被引频次[WOS]:94
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成果类型 | 期刊论文 |
条目标识符 | http://sustech.caswiz.com/handle/2SGJ60CL/220931 |
专题 | 理学院_物理系 |
作者单位 | 1.Chinese Acad Sci, Inst Phys, Beijing Natl Lab Condensed Matter Phys, Beijing 100190, Peoples R China 2.Univ Chinese Acad Sci, Sch Phys Sci, Beijing 100190, Peoples R China 3.Songshan Lake Mat Lab, Dongguan 523808, Peoples R China 4.Max Planck Inst Chem Phys Solids, Nothnitzer Str 40, D-01187 Dresden, Germany 5.Peking Univ, Sch Adv Mat, Shenzhen Grad Sch, Shenzhen 518055, Peoples R China 6.NIST, Ctr Neutron Res, Gaithersburg, MA 20899 USA 7.Nanjing Univ Sci & Technol, Sch Mat Sci & Engn, Nanjing 210094, Peoples R China 8.Argonne Natl Lab, Xray Sci Div, Adv Photon Source, Argonne, IL 60439 USA 9.Natl Synchrotron Radiat Res Ctr, 101 Hsin Ann Rd, Hsinchu 30076, Taiwan 10.Southern Univ Sci & Technol, Dept Phys, Shenzhen 518055, Peoples R China 11.Rutgers State Univ, Dept Chem & Chem Biol, Piscataway, NJ USA |
推荐引用方式 GB/T 7714 |
Zhao, Jianfa,Gao, Jiacheng,Li, Wenmin,et al. A combinatory ferroelectric compound bridging simple ABO(3) and A-site-ordered quadruple perovskite[J]. Nature Communications,2021,12(1).
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APA |
Zhao, Jianfa.,Gao, Jiacheng.,Li, Wenmin.,Qian, Yuting.,Shen, Xudong.,...&Jin, Changqing.(2021).A combinatory ferroelectric compound bridging simple ABO(3) and A-site-ordered quadruple perovskite.Nature Communications,12(1).
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MLA |
Zhao, Jianfa,et al."A combinatory ferroelectric compound bridging simple ABO(3) and A-site-ordered quadruple perovskite".Nature Communications 12.1(2021).
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