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Research Article | Open Access

Unlocking the electro–optic potential of ferroelectrics: advanced domain and phase manipulation

Long Chen1,Xiaoming Shi2,Jiyang Xie3,Yao Wu1Yuming Bai1Yankang Cheng4Suwan Li1Guanlong Zhu1Zhao Wang5Yongming Hu5Longhai Wang6Laijun Liu7Tao Wang1Wanbiao Hu3( )Biaolin Peng4( )Houbing Huang8Xuhui Meng9Qiuyun Fu1Shenglin Jiang1Wen Dong1( )Shujun Zhang10,11( )
School of Integrated Circuits, Engineering Research Center for Functional Ceramics, Ministry of Education, Wuhan National Laboratory for Optoelectronics, Optical Valley Laboratory, Huazhong University of Science and Technology, Wuhan 430074, China
Department of Physics, University of Science and Technology Beijing, Beijing 100083, China
Yunnan Key Laboratory of Electromagnetic Materials and Devices, National Center for International Research on Photoelectric and Energy Materials, School of Materials and Energy, Yunnan University, Kunming 650091, China
School of Advanced Materials and Nanotechnology, Xidian University, Xi’an 710126, China
Hubei Key Laboratory of Micro-Nanoelectronic Materials and Devices, Hubei University, Wuhan 430062, China
School of Materials Science and Technology, Hubei University, Wuhan 430062, China
College of Materials Science and Engineering, Guilin University of Technology, Guilin 541004, China
School of Materials Science and Engineering and Advanced Research Institute of Multidisciplinary Science, Beijing Institute of Technology, Beijing 100081, China
Institute of Interdisciplinary Research for Mathematics and Applied Science, School of Mathematics and Statistics, Huazhong University of Science and Technology, Huazhong University of Science and Technology, Wuhan 430074, China
Department of Chemistry, City University of Hong Kong, Hong Kong 999077, China
Institute for Superconducting and Electronic Materials, Faculty of Engineering and Information Science, University of Wollongong, Wollongong 2522, Australia

Long Chen, Xiaoming Shi, and Jiyang Xie contributed equally to this work.

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Abstract

Ferroelectric materials are highly promising for next-generation electro–optic (EO) modulators because of their ultrafast and efficient light modulation. However, efforts to maximize polarization freedom for large refractive index modulation—through domain engineering, epitaxial strain, and defect engineering—have hit limitations, leaving intrinsic polarization mechanisms largely unexplored. Here, we report a giant effective EO coefficient (~233.5 pm/V) in PbZr0.52Ti0.48O3 (PZT) films, which surpasses all reported values measured under an in-plane electric field and significantly exceeds the theoretical limit (~13 pm/V) as well as the value of LiNbO3 (~31 pm/V). Beyond conventional domain switching, phase transitions and domain wall variations critically enhance the EO effect. The highly relaxed structure of the PZT film, with mixed [001] and [100] orientations and disordered nanoscale phases, enables unprecedented polarization control. This unique configuration breaks the theoretical EO coefficient limit, bridging the gap between predictions and experimental results. Owing to its high Curie temperature and compatibility with wafer-scale fabrication, PZT has emerged as a promising candidate for next-generation high-performance EO modulators. Our findings not only advance the frontiers of ferroelectric EO materials but also pave the way for exploring other ferroelectric thin-film devices, such as those for energy storage and electrocaloric cooling, by leveraging enhanced polarization modulation mechanisms.

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Journal of Advanced Ceramics
Article number: 9221180

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Cite this article:
Chen L, Shi X, Xie J, et al. Unlocking the electro–optic potential of ferroelectrics: advanced domain and phase manipulation. Journal of Advanced Ceramics, 2025, 14(11): 9221180. https://doi.org/10.26599/JAC.2025.9221180

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Received: 10 May 2025
Revised: 24 September 2025
Accepted: 28 September 2025
Published: 13 October 2025
© The Author(s) 2025.

This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0, http://creativecommons.org/licenses/by/4.0/).