Anionic Strategy-Modulated Magnetic Ordering in Super-elongated Multiferroic Epitaxial Films

Magnetic ordering of perovskite ferroelectric oxides is crucial for enhancing their stability and minimizing energy losses in magnetoelectric devices. However, inducing a transition from a magnetically disordered state to an ordered one remains a formidable challenge. Here, we propose a chemical sulfurization method that significantly enhances the magnetic ordering of multiferroic super-tetragonal phase BiFeO<sub>3</sub> thin film. The out-of-plane and in-plane magnetization significantly increases after sulfurization, accompanied by a rotation of the magnetic easy axis. X-ray absorption spectroscopy and spherical aberration transmission electron microscopy reveal the reconfiguration of local electronic hybridization states, restructuring Fe-O hybridization from pyramid-like FeO<sub>5</sub> to octahedral FeO<sub>6</sub> geometries. This transformation is considered the root cause of the observed magnetic transition in the films. This sulfur-induced strategy for electronic hybridization reconfiguration is expected to break new ground, offering innovative methodologies for modulating perovskite oxides, two-dimensional ferroelectric films, and other ferromagnetic functional thin films.

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Publication Details

Journal
Nature Communications
Published
2025-04-23
DOI
https://doi.org/10.1038/s41467-025-58594-9
Citations
3
Primary Topic
Multiferroics and related materials
Type
article
Field-Weighted Citation Impact
1.28

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article

Anionic Strategy-Modulated Magnetic Ordering in Super-elongated Multiferroic Epitaxial Films

Yue‐Wen Fang, Kuijuan Jin, Wugang Liao, Linxing Zhang et al.
3 citations
Nature Communications
Multiferroics and related materials
1.28
article

Anionic Strategy-Modulated Magnetic Ordering in Super-elongated Multiferroic Epitaxial Films

Yue‐Wen Fang, Kuijuan Jin, Wugang Liao, Linxing Zhang, Hangren Li, Xudong Liu, Qianqian Yang, Guoqiang Xi, Jiesu Wang, X. G. Liu, Shuai Xu, Dongxing Zheng, Jianjun Tian, Xixiang Zhang, Jie Tu, Junwei Zhang, Jiushe He, Xianran Xing, Fangyuan Zhu, Shiyao Wu
article en
3 citations

Abstract

Magnetic ordering of perovskite ferroelectric oxides is crucial for enhancing their stability and minimizing energy losses in magnetoelectric devices. However, inducing a transition from a magnetically disordered state to an ordered one remains a formidable challenge. Here, we propose a chemical sulfurization method that significantly enhances the magnetic ordering of multiferroic super-tetragonal phase BiFeO<sub>3</sub> thin film. The out-of-plane and in-plane magnetization significantly increases after sulfurization, accompanied by a rotation of the magnetic easy axis. X-ray absorption spectroscopy and spherical aberration transmission electron microscopy reveal the reconfiguration of local electronic hybridization states, restructuring Fe-O hybridization from pyramid-like FeO<sub>5</sub> to octahedral FeO<sub>6</sub> geometries. This transformation is considered the root cause of the observed magnetic transition in the films. This sulfur-induced strategy for electronic hybridization reconfiguration is expected to break new ground, offering innovative methodologies for modulating perovskite oxides, two-dimensional ferroelectric films, and other ferromagnetic functional thin films.

Nature CommunicationsVol. 16(1)
University of the Basque Country (ES), Shenzhen University (CN), Chinese Academy of Sciences (CN), Lanzhou University of Technology (CN), Beijing University of Technology (CN), Shanghai Advanced Research Institute (CN), FZU ‒ Institute of Physics of the Academy of Sciences of the Czech Republic (CZ), Material Physics Center (ES), Beijing Academy of Quantum Information Sciences (CN), Institute of Physics (CN), Donostia International Physics Center (ES), King Abdullah University of Science and Technology (SA), Lanzhou University (CN), University of Science and Technology Beijing (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 21%
Multiferroics and related materials
1.28
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