| Literature DB >> 33531480 |
Jianfa Zhao1,2, Jiacheng Gao1, Wenmin Li1, Yuting Qian1, Xudong Shen1,2, Xiao Wang3, Xi Shen1, Zhiwei Hu3, Cheng Dong4, Qingzhen Huang5, Lipeng Cao1, Zhi Li6, Jun Zhang1, Chongwen Ren1, Lei Duan1, Qingqing Liu1, Richeng Yu1, Yang Ren7, Shih-Chang Weng8, Hong-Ji Lin8, Chien-Te Chen8, Liu-Hao Tjeng3, Youwen Long1,2, Zheng Deng1, Jinlong Zhu9, Xiancheng Wang1, Hongming Weng10, Runze Yu11, Martha Greenblatt12, Changqing Jin13,14.
Abstract
The simple ABO3 and A-site-ordered AA'3B4O12 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 ABO3 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.Entities:
Year: 2021 PMID: 33531480 DOI: 10.1038/s41467-020-20833-6
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919