{"title":"Optically Induced Irreversible Ferroelastic and Ferroelectric Switching in Epitaxial BaTiO3 Films on Silicon.","authors":"Ibukun Olaniyan,Alfredo Blázquez Martínez,Valentin Väinö Hevelke,Sven Wiesner,Rong Wu,Thanh Luan Phan,Robin Cours,Nikolay Cherkashin,Sylvie Schamm-Chardon,Dong-Jik Kim,Catherine Dubourdieu","doi":"10.1021/acsnano.5c05309","DOIUrl":null,"url":null,"abstract":"Optical manipulation of ferroelectric polarization is a promising method for potentially ultrafast and remote polarization switching without electrodes. Here, we report optical ferroelastic and ferroelectric switching by UV irradiation in epitaxial BaTiO3 thin films grown on a SrTiO3-buffered Si substrate. The pristine BaTiO3 film is in the tetragonal ferroelectric phase with both in-plane and out-of-plane ferroelectric polarization. After irradiation by a 325 nm UV laser, the polarization is mainly out-of-plane indicating ferroelastic switching. Moreover, all initial downward polarized domains have switched to upward, thus showing ferroelectric 180°-domain switching. After irradiation the film exhibits mainly a single up-oriented polarization and as a result, the irradiated regions exhibit an enhanced piezoelectric response. We propose that the observed ferroelastic and ferroelectric switching is triggered by additional strain/stress fields generated by internal electric fields arising mainly from the spatial charge carrier separation after photoexcitation. These strain/stress fields add up to the Vegard strain field and to local heating, which induce defect motion and a final state with full strain relaxation. This optical switching enables remote manipulation of ferroelastic and ferroelectric domains in BaTiO3 films on silicon. Moreover, UV illumination appears as a potential postdeposition treatment to heal defects and obtain a strain-free epitaxial layer.","PeriodicalId":21,"journal":{"name":"ACS Nano","volume":"42 3 1","pages":""},"PeriodicalIF":16.0000,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Nano","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1021/acsnano.5c05309","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Optical manipulation of ferroelectric polarization is a promising method for potentially ultrafast and remote polarization switching without electrodes. Here, we report optical ferroelastic and ferroelectric switching by UV irradiation in epitaxial BaTiO3 thin films grown on a SrTiO3-buffered Si substrate. The pristine BaTiO3 film is in the tetragonal ferroelectric phase with both in-plane and out-of-plane ferroelectric polarization. After irradiation by a 325 nm UV laser, the polarization is mainly out-of-plane indicating ferroelastic switching. Moreover, all initial downward polarized domains have switched to upward, thus showing ferroelectric 180°-domain switching. After irradiation the film exhibits mainly a single up-oriented polarization and as a result, the irradiated regions exhibit an enhanced piezoelectric response. We propose that the observed ferroelastic and ferroelectric switching is triggered by additional strain/stress fields generated by internal electric fields arising mainly from the spatial charge carrier separation after photoexcitation. These strain/stress fields add up to the Vegard strain field and to local heating, which induce defect motion and a final state with full strain relaxation. This optical switching enables remote manipulation of ferroelastic and ferroelectric domains in BaTiO3 films on silicon. Moreover, UV illumination appears as a potential postdeposition treatment to heal defects and obtain a strain-free epitaxial layer.
期刊介绍:
ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.