Phase-transition-driven ferroic response in 2D CuMnP2Se6 under ultra-low electric fields
Low-field electric control of magnetic phase transitions is critical for the development of energy-efficient spintronic and non-volatile memory technologies. Yet, the weak magnetoelectric coupling in most known two-dimensional multiferroics hinders their practical implementation. Here, using crystal structure prediction and high-throughput first-principles calculations, we identify four previously unexplored bimetallic thio(seleno)phosphate multiferroics, XMnP<sub>2</sub>(S/Se)<sub>6</sub> (X = Cu, Au), all exhibiting robust in-plane spontaneous polarization-contrasting with the predominantly out-of-plane behavior in this material family-which effectively mitigates depolarization effects. In particular, CuMnP<sub>2</sub>Se<sub>6</sub> hosts two stable C<sub>2</sub>-symmetric ferroelectric phases with opposite in-plane polarizations and distinct magnetic orders. Remarkably, an electric field as small as ~0.001 V/Å can simultaneously reverse the polarization and induce an antiferromagnetic-to-ferromagnetic transition. The associated barrier is exceptionally low ( ~49 meV/f.u.), yielding a sizable magnetoelectric coefficient of ~0.04 G ⋅ cm/V. These results highlight a viable strategy for realizing electric-field-driven magnetism in intrinsic two-dimensional multiferroics under experimentally feasible conditions.
Authors
- Jingyan Chen
- Xiaodong Zhou (ORCID: https://orcid.org/0000-0002-0378-6729)
- Meiling Xu (ORCID: https://orcid.org/0000-0001-6592-8975)
- Yanchao Wang (ORCID: https://orcid.org/0000-0003-4518-925X)
- Yinwei Li (ORCID: https://orcid.org/0000-0002-9974-504X)
- Jiaqi Feng (ORCID: https://orcid.org/0009-0001-0947-4718)
- Yan Jie
Institutions
- Jiangsu Normal University (CN)
- Jilin University (CN)
- Tiangong University (CN)
Publication Details
- Journal
- Nature Communications
- Published
- 2025-12-13
- DOI
- https://doi.org/10.1038/s41467-025-67516-8
- Primary Topic
- Multiferroics and related materials
- Type
- article
- Field-Weighted Citation Impact
- 0.00