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Room-Temperature Noncollinear Ferroelectricity in van der Waals WO2Cl2 with a Wide Bandgap

Yu Xing1,*, Ning Ding1,*, Zhipeng Wang2,*, Zhiwen Pan1,*, Lei Guo1, Guowei Du3, Yangrui Liu4, Xiaoxing Cao5, Ran Su6 et al.

Mengting Jiang7, Xuezhi Ma7, Xiyu Chen1, Junchao Zhang1, Xinyu Yang1, Haoran Ye1, Honghong Yao1, Rui Feng1, Dexiang Chen1, Le-Ping Miao8, Yumeng You5, Zejun Li1, Dongsheng Song4,†, Linglong Li1,‡, and Shuai Dong1,§

  • *These authors contributed equally to this work.
  • †Contact author: dsong@ahu.edu.cn
  • ‡Contact author: linglongli@seu.edu.cn
  • §Contact author: sdong@seu.edu.cn

Phys. Rev. Lett. 137, 086801 – Published 21 August, 2026

DOI: https://doi.org/10.1103/zjyw-z6s6

Abstract

Low-dimensional ferroelectrics are attractive for their promising prospects in nanoelectronics. Compared with widely used ferroelectric perovskites, most low-dimensional ferroelectrics exhibit several inborn weaknesses such as small bandgaps (mostly <2  eV, i.e., semiconductorslike) or faint polarizations (e.g., <1  μC/cm2 for sliding ferroelectrics even if their bandgaps can be large). Here we experimentally demonstrate the room-temperature ferroelectricity of van der Waals WO2Cl2. The well-tested d0 rule inherited from ferroelectric perovskites leads to a large dipole (∼3  eÅ) from the off-center displacement of W6+ ion and a wide bandgap of 2.80 eV. Its ferroelectricity is proved by multiple characterizations including second harmonic generation, piezoresponse force microscopy, and ferroelectric hysteresis loops. More interestingly, the exotic noncollinear dipole order is directly observed at the atomic level by integrated differential phase contrast scanning transmission electron microscopy. Our Letter paves an alternative route for low-dimensional ferroelectrics to pursue excellent ferroelectric performance and distinct physics of polarity.

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