<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Cheng R</submitter><funding>National Natural Science Foundation of China</funding><funding>National Natural Science Foundation of China (National Science Foundation of China)</funding><pagination>5241</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9448765</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(1)</volume><pubmed_abstract>The discovery of magnetism in ultrathin crystals opens up opportunities to explore new physics and to develop next-generation spintronic devices. Nevertheless, two-dimensional magnetic semiconductors with Curie temperatures higher than room temperature have rarely been reported. Ferrites with strongly correlated d-orbital electrons may be alternative candidates offering two-dimensional high-temperature magnetic ordering. This prospect is, however, hindered by their inherent three-dimensional bonded nature. Here, we develop a confined-van der Waals epitaxial approach to synthesizing air-stable semiconducting cobalt ferrite nanosheets with thickness down to one unit cell using a facile chemical vapor deposition process. The hard magnetic behavior and magnetic domain evolution are demonstrated by means of vibrating sample magnetometry, magnetic force microscopy and magneto-optical Kerr effect measurements, which shows high Curie temperature above 390 K and strong dimensionality effect. The addition of room-temperature magnetic semiconductors to two-dimensional material family provides possibilities for numerous novel applications in computing, sensing and information storage.</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Ultrathin ferrite nanosheets for room-temperature two-dimensional magnetic semiconductors.</pubmed_title><pmcid>PMC9448765</pmcid><funding_grant_id>91964203</funding_grant_id><pubmed_authors>Wen Y</pubmed_authors><pubmed_authors>Yuan S</pubmed_authors><pubmed_authors>Jiang J</pubmed_authors><pubmed_authors>Zhai B</pubmed_authors><pubmed_authors>Guo Y</pubmed_authors><pubmed_authors>He J</pubmed_authors><pubmed_authors>Liao W</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Xiong W</pubmed_authors><pubmed_authors>Zhang Z</pubmed_authors><pubmed_authors>Cheng R</pubmed_authors><pubmed_authors>Liu C</pubmed_authors><pubmed_authors>Yin L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ultrathin ferrite nanosheets for room-temperature two-dimensional magnetic semiconductors.</name><description>The discovery of magnetism in ultrathin crystals opens up opportunities to explore new physics and to develop next-generation spintronic devices. Nevertheless, two-dimensional magnetic semiconductors with Curie temperatures higher than room temperature have rarely been reported. Ferrites with strongly correlated d-orbital electrons may be alternative candidates offering two-dimensional high-temperature magnetic ordering. This prospect is, however, hindered by their inherent three-dimensional bonded nature. Here, we develop a confined-van der Waals epitaxial approach to synthesizing air-stable semiconducting cobalt ferrite nanosheets with thickness down to one unit cell using a facile chemical vapor deposition process. The hard magnetic behavior and magnetic domain evolution are demonstrated by means of vibrating sample magnetometry, magnetic force microscopy and magneto-optical Kerr effect measurements, which shows high Curie temperature above 390 K and strong dimensionality effect. The addition of room-temperature magnetic semiconductors to two-dimensional material family provides possibilities for numerous novel applications in computing, sensing and information storage.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2026-06-03T10:41:10.876Z</modification><creation>2025-04-20T00:41:43.274Z</creation></dates><accession>S-EPMC9448765</accession><cross_references><pubmed>36068242</pubmed><doi>10.1038/s41467-022-33017-1</doi></cross_references></HashMap>