摘要
The advancement of spintronics relies on the development of 2D magnetic materials with robust room-temperature properties. However, challenges such as low Curie temperatures (T C ) and ambient instability have hindered their practical applications. In this study, we employ chemical vapor deposition (CVD) combined with salt-assisted methods and optimize growth parameters to synthesize phase-tunable Cr x S y compounds, including rhombohedral Cr 2 S 3 (ferrimagnetic below 120 K), trigonal Cr 5 S 6 (room-temperature ferrimagnetic), and hexagonal CrS (antiferromagnetic). Our findings reveal that self-intercalation of Cr atoms significantly modifies the lattice structure, electronic states, and magnetic properties of these materials. Cr 5 S 6 exhibits half-metallic characteristics with room-temperature ferrimagnetism, representing a significant advancement for practical 2D magnetic materials. The charge transfer from self-intercalated Cr atoms and superexchange interactions mediated by sulfur p -orbitals are identified as key mechanisms driving these tunable properties. This work highlights self-intercalation as a transformative strategy for engineering high-performance 2D magnetic materials, providing insights for advancing next-generation spintronic devices.
危险品化学品经营许可证(带存储)