Interfacial negative magnetization in Ni encapsulated layer-tunable nested MoS 2 nanostructure with robust memory applications.
Shatabda BhattacharyaTatsuhiko OhtoHirokazu TadaShyamal K SahaPublished in: Nanoscale advances (2023)
Combining interfacial interactions and layer-number tunability, the evolution of magnetism in low-dimensional diamagnetic systems like MoS 2 is indeed an interesting area of research. To explore this, Ni nanophases with an average size of 12 nm were encapsulated in MoS 2 and the magnetization dynamics were studied over the temperature range of 2-300 K. Surprisingly, the newly formed hybrid nanostructure was found to have a negative magnetization state with giant exchange bias that showed a reversible temperature-induced increase in both spin magnetic moment and coercivity. Density functional theory calculations proved an interfacial charge transfer interaction with a spin-polarized density of states. The magnetization state, along with giant exchange correlation among the magnetic clusters, suggested the possibility of robust thermomagnetic memory. The dc magnetization and relaxation, investigated with different measurement protocols, unveiled robust thermoremanent magnetization as a memory effect. The time-dependent magnetization study indicated that contributions from the negative magnetization state along with charge transfer induced spin states are responsible for the memory effect, which can be controlled by both temperature and external field.
Keyphrases
- density functional theory
- room temperature
- transition metal
- molecular dynamics
- working memory
- molecular dynamics simulations
- ionic liquid
- quantum dots
- single molecule
- high glucose
- diabetic rats
- dendritic cells
- reduced graphene oxide
- drug induced
- immune response
- gold nanoparticles
- oxidative stress
- atomic force microscopy
- high speed
- electron transfer
- simultaneous determination