Presentation Information

[1C05]Fluorination effects on the ferroelectric and magnetic properties of Ba–substituted BiFeO3 thin films studied by X–ray spectroscopy

*Akiko Kamigaito1, Kei Shigematsu2, Masaki Kobayashi3, Kenta Amemiya4, Hiroshi Kumigashira5, Tsukasa Katayama6, Akira Chikamatsu1 (1. Department of Chemistry, Faculty of Science, Ochanomizu University (Japan), 2. Materials and Structures Laboratory, Institute of Integrated Research, Institute of Science Tokyo (Japan), 3. Center for Spintronics Research Network, The University of Tokyo (Japan), 4. Institute of Materials Structure Science, High Energy Accelerator Research Organization (Japan), 5. Institute of Multidisciplinary Research for Advanced Materials, Tohoku University (Japan), 6. Department of Applied Chemistry, Faculty of Science Division I, Tokyo University of Science (Japan))
Multiferroic materials, which exhibit both ferroelectricity and magnetic ordering, are promising for low-power devices. BiFeO3 is a representative material, but its R3c structure causes complex ferroelectric switching. Ba2+ substitution can induce tetragonal distortion and stabilize a simpler P4mm structure; however, the accompanying oxygen vacancies may suppress the stereochemical activity of Bi3+ lone pairs and degrade ferroelectricity. In this study, Bi0.8Ba0.2FeO2.9 and Bi0.8Ba0.2FeO2.8F0.2 epitaxial thin films were prepared to clarify the effects of Ba and F codoping. X-ray magnetic circular dichroism measurements revealed that fluorination does not significantly alter the Fe magnetic sites. In contrast, ferroelectricity was observed only in Bi0.8Ba0.2FeO2.8F0.2. These results suggest that fluorination restores the stereochemical activity of Bi3+ lone pairs by compensating anion vacancies, making F incorporation an effective strategy for tuning ns2-type multiferroic oxides.

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