Wafer-Scale Room-Temperature Ferromagnetic Chromium Disulfide via Sulfur Monomers
The wafer-scale synthesis of magnetic two-dimensional transition metal dichalcogenides (TMDCs) remains a critical challenge due to their metastability and the rapid oxidation of metallic precursors, which block conventional sulfurization routes. Chromium disulfide (CrS 2 ), in particular, is highly attractive for spintronic applications because of its robust room-temperature ferromagnetism, yet its wafer-scale growth has remained elusive. Here, we report a universal strategy using ZnS-derived sulfur monomers to overcome the chemical reaction barrier imposed by native oxide layer, enabling the selective formation of crystalline CrS 2 films across 2-in. wafers. The resulting films exhibit excellent uniformity, controllable thickness, and robust ferromagnetism above room temperature. Beyond CrS 2, this method demonstrates broad application by yielding wafer-scale VS 2, MnS, FeS 2, CoS 2, and the ternary CrCoS 4 with comparable quality. Our results establish a versatile and scalable synthesis platform for 2D magnetic TMDCs, opening a pathway toward their integration in advanced spintronic devices.
Authors
- Yongbing Xu (ORCID: https://orcid.org/0000-0002-7823-0725)
- Zhihao Li (ORCID: https://orcid.org/0000-0002-5014-6732)
- T L Li (ORCID: https://orcid.org/0000-0002-2815-3856)
- Xianyang Lu (ORCID: https://orcid.org/0000-0003-3815-4032)
- Jun Du (ORCID: https://orcid.org/0000-0002-9967-945X)
- Sicong Hu
- Boxin Cheng
- Jing Wu
Institutions
- Guangdong University of Technology (CN)
- Laboratoire de physique des Solides (FR)
- Photonic Science (United Kingdom) (GB)
- Spintronics Research Network of Japan (JP)
- Intelligent Health (United Kingdom) (GB)
- National Laboratory of Solid State Microstructures
- University of York (GB)
- Nanjing University (CN)
Publication Details
- Journal
- Nano Letters
- Published
- 2026-06-13
- DOI
- https://doi.org/10.1021/acs.nanolett.5c05794
- Primary Topic
- 2D Materials and Applications
- Type
- article
- Field-Weighted Citation Impact
- 0.00