Ferromagnetic behaviour has been observed experimentally for the first time in nanostructured Manganese. Ultrathin ($sim$ 0.6 nm) Manganese nanosheets have been synthesized inside the two dimensional channels of sol-gel derived Na-4 mica. The magnetic properties of the confined system are measured within 2K-300K temperature range. The confined structure is found to show a ferromagnetic behaviour with a nonzero coercivity value. The coercivity value remains positive throughout the entire temperature range of measurement. The experimental variation of susceptibility as a function of temperature has been satisfactorily explained on the basis of a two dimensional system with a Heisenberg Hamiltonian involving direct exchange interaction.
We study optical properties of arrays of ultrathin nanowires by means of the Brillouin scattering of light on magnons. We employ the Stokes/anti-Stokes scattering asymmetry to probe the circular polarization of a local electric field induced inside nanowires by linearly polarized light waves. We observe the anomalous polarization conversion of the opposite sign than that in a bulk medium or thick nanowires with a great enhancement of the degree of circular polarization attributed to an unconventional refraction in the nanowire medium.
Ultrathin ferromagnets with frustrated exchange and the Dzyaloshinskii-Moriya interaction can support topological solitons such as skyrmions and antiskyrmions, which are metastable and can be considered particle-antiparticle counterparts. When spin-orbit torques are applied, the motion of an isolated antiskyrmion driven beyond its Walker limit can generate skyrmion-antiskyrmion pairs. Here, we use atomistic spin dynamics simulations to shed light on the scattering processes involved in this pair generation. Under certain conditions a proliferation of these particles and antiparticles can appear with a growth rate and production asymmetry that depend on the strength of the chiral interactions and the dissipative component of the spin-orbit torques. These features are largely determined by scattering processes between antiskyrmions, which can be elastic or result in bound states or annihilation.
We analyze the electric current and magnetic field driven domain wall motion in perpendicularly magnetized ultrathin ferromagnetic films in the presence of interfacial Dzyaloshinskii-Moriya interaction and both out-of-plane and in-plane uniaxial anisotropies. We obtain exact analytical Walker-type solutions in the form of one-dimensional domain walls moving with constant velocity due to both spin-transfer torques and out-of-plane magnetic field. These solutions are embedded into a larger family of propagating solutions found numerically. Within the considered model, we find the dependencies of the domain wall velocity on the material parameters and demonstrate that adding in-plane anisotropy may produce domain walls moving with velocities in excess of 500 m/s in realistic materials under moderate fields and currents.
We present a detailed study of the ground-state magnetic structure of ultrathin Fe films on the surface of fcc Ir(001). We use the spin-cluster expansion technique in combination with the relativistic disordered local moment scheme to obtain parameters of spin models and then determine the favored magnetic structure of the system by means of a mean field approach and atomistic spin dynamics simulations. For the case of a single monolayer of Fe we find that layer relaxations very strongly influence the ground-state spin configurations, whereas Dzyaloshinskii-Moriya (DM) interactions and biquadratic couplings also have remarkable effects. To characterize the latter effect we introduce and analyze spin collinearity maps of the system. While for two monolayers of Fe we find a single-q spin spiral as ground state due to DM interactions, for the case of four monolayers the system shows a noncollinear spin structure with nonzero net magnetization. These findings are consistent with experimental measurements indicating ferromagnetic order in films of four monolayers and thicker.
Nanopores in 2D materials are highly desirable for DNA sequencing, yet achieving single-stranded DNA (ssDNA) transport through them is challenging. Using density functional theory calculations and molecular dynamics simulations we show that ssDNA transport through a pore in monolayer hexagonal boron nitride (hBN) is marked by a basic nanomechanical conflict. It arises from the notably inhomogeneous flexural rigidity of ssDNA and causes high friction $textit{via}$ transient DNA desorption costs exacerbated by solvation effects. For a similarly sized pore in bilayer hBN, its self-passivated atomically smooth edge enables continuous ssDNA transport. Our findings shed light on the fundamental physics of biopolymer transport through pores in 2D materials.