<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhao J</submitter><funding>National Science Foundation of China | National Natural Science Foundation of China-Yunnan Joint Fund</funding><funding>National Science Foundation of China | National Natural Science Foundation of China-Yunnan Joint Fund (NSFC-Yunnan Joint Fund)</funding><pagination>747</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7854592</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(1)</volume><pubmed_abstract>The simple ABO&lt;sub>3&lt;/sub> and A-site-ordered AA'&lt;sub>3&lt;/sub>B&lt;sub>4&lt;/sub>O&lt;sub>12&lt;/sub> 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 PbHg&lt;sub>3&lt;/sub>Ti&lt;sub>4&lt;/sub>O&lt;sub>12&lt;/sub>, the only known quadruple perovskite that transforms from high-temperature centrosymmetric paraelectric phase to low-temperature non-centrosymmetric ferroelectric phase. The coordination chemistry of Hg&lt;sup>2+&lt;/sup> is changed from square planar as in typical A-site-ordered quadruple perovskite to a rare stereo t</pubmed_abstract><journal>Nature communications</journal><pubmed_title>A combinatory ferroelectric compound bridging simple ABO&lt;sub>3&lt;/sub> and A-site-ordered quadruple perovskite.</pubmed_title><pmcid>PMC7854592</pmcid><funding_grant_id>11820101003</funding_grant_id><pubmed_authors>Cao L</pubmed_authors><pubmed_authors>Yu R</pubmed_authors><pubmed_authors>Hu Z</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Ren Y</pubmed_authors><pubmed_authors>Gao J</pubmed_authors><pubmed_authors>Liu Q</pubmed_authors><pubmed_authors>Huang Q</pubmed_authors><pubmed_authors>Greenblatt M</pubmed_authors><pubmed_authors>Long Y</pubmed_authors><pubmed_authors>Jin C</pubmed_authors><pubmed_authors>Chen CT</pubmed_authors><pubmed_authors>Deng Z</pubmed_authors><pubmed_authors>Tjeng LH</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Zhao J</pubmed_authors><pubmed_authors>Shen X</pubmed_authors><pubmed_authors>Dong C</pubmed_authors><pubmed_authors>Duan L</pubmed_authors><pubmed_authors>Ren C</pubmed_authors><pubmed_authors>Li W</pubmed_authors><pubmed_authors>Qian Y</pubmed_authors><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Zhu J</pubmed_authors><pubmed_authors>Weng H</pubmed_authors><pubmed_authors>Lin HJ</pubmed_authors><pubmed_authors>Weng SC</pubmed_authors></additional><is_claimable>false</is_claimable><name>A combinatory ferroelectric compound bridging simple ABO&lt;sub>3&lt;/sub> and A-site-ordered quadruple perovskite.</name><description>The simple ABO&lt;sub>3&lt;/sub> and A-site-ordered AA'&lt;sub>3&lt;/sub>B&lt;sub>4&lt;/sub>O&lt;sub>12&lt;/sub> 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 PbHg&lt;sub>3&lt;/sub>Ti&lt;sub>4&lt;/sub>O&lt;sub>12&lt;/sub>, the only known quadruple perovskite that transforms from high-temperature centrosymmetric paraelectric phase to low-temperature non-centrosymmetric ferroelectric phase. The coordination chemistry of Hg&lt;sup>2+&lt;/sup> is changed from square planar as in typical A-site-ordered quadruple perovskite to a rare stereo t</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Feb</publication><modification>2025-06-01T00:30:57.494Z</modification><creation>2025-06-01T00:30:57.494Z</creation></dates><accession>S-EPMC7854592</accession><cross_references><pubmed>33531480</pubmed><doi>10.1038/s41467-020-20833-6</doi></cross_references></HashMap>