Realization and regulation of negative magnetoresistance behavior in Dy-doped SnS2 with high Curie temperature
Abstract
The magnetic two-dimensional transition metal dichalcogenides with high Curie temperature play a pivotal role in spintronic devices and exhibit promising application potentials. In this paper, rare earth Dy-doped SnS2 wafers are synthesized through gas–liquid phase deposition and high-temperature, high-pressure processes. The material exhibits comprehensive properties such as ferromagnetism, high Curie temperature (628 K), and large negative magnetoresistance at low magnetic fields over a wide temperature range (55%–4%, 50–350 K). The results of first-principles calculations indicate that it exhibits the half-metallic behavior of electrons with a single spin direction passing through the Fermi level, with a large spin bandgap of 1.7 eV, and a flatband exists near the Fermi level. Therefore, the substitution of Sn with Dy induces a global structural reorganization and disrupts the system's symmetry, resulting in the formation of a flatband near the Fermi level through the occupation of 4f orbital electrons, providing a stable local magnetic moment. Through the orbital hybridization between Dy and S, the ferromagnetic exchange interaction is formed, achieving the ferromagnetism of DyxSn1−xS2. This laid the foundation for the application of magnetoresistive sensors, electromagnetic shielding, and spin field-effect transistors.
Article Details
Journal Info
Applied Physics Letters
American Institute of Physics
Authors (7)
Yu Tong
Xi Chen
Hongpeng Zhang
State Key Laboratory and Institute of Elemento-Organic Chemistry, College of Chemistry, Frontiers Science Center for New Organic Matter, Haihe Laboratory of Sustainable Chemical Transformations
Jianyu Ling
State Key Laboratory of High Pressure and Superhard Materials, College of Physics, Jilin University 1 , Changchun 130012,
Haoqun Zeng
State Key Laboratory of High Pressure and Superhard Materials, College of Physics, Jilin University 1 , Changchun 130012,
Kewei Zhang
Mingzhe Zhang