Skyrmions and magnetic bubbles in spin-orbit coupled metallic magnets

Motivated by the observation of Skyrmion-like magnetic textures in 2D itinerant ferromagnets Fe$_n$GeTe$_2$ ($n \geq3$), we develop a microscopic model combining itinerant magnetism and spin-orbit coupling on a triangular lattice. The ground state of the model in the absence of magnetic field consists of filamentary magnetic domain walls revealing a striking similarity with our magnetic force microscopy experiments on Fe$_3$GeTe$_2$. In the presence of magnetic field, these filaments were found to break into large size magnetic bubbles in our experiments. We identify uniaxial magnetic anisotropy as an important parameter in the model that interpolates between magnetic Skyrmions and ferromagnetic bubbles. Consequently, our work uncovers new topological magnetic textures that merge properties of Skyrmions and ferromagnetic bubbles

High transport spin polarization in the van der Waals ferromagnet Fe4_4GeTe2_2

The challenging task of scaling-down the size of the power saving electronic devices can be accomplished by exploiting the spin degree of freedom of the conduction electrons in van der Waals (vdW) spintronic architectures built with 2D materials. One of the key components of such a device is a near-room temperature 2D ferromagnet with good metallicity that can generate a highly spin-polarized electronic transport current. However, most of the known 2D ferromagnets have either a very low temperature ordering, poor conductivity, or low spin polarization. In this context, the Fe$_n$GeTe$_2$ (with $n\geq3$) family of ferromagnets stand out due to their near-room temperature ferromagnetism and good metallicity. We have performed spin-resolved Andreev reflection spectroscopy on Fe$_4$GeTe$_2$ ($T_{Curie} \sim$ 273 K) and demonstrated that the ferromagnet is capable of generating a very high transport spin polarization, exceeding 50$\%$. This makes Fe$_4$GeTe$_2$ a strong candidate for application in all-vdW power-saving spintronic devices.Comment: Accepted for publication in Physical Review

Porous covalent organic nanotubes and their assembly in loops and toroids

Carbon nanotubes, and synthetic organic nanotubes more generally, have in recent decades been widely explored for application in electronic devices, energy storage, catalysis and biosensors. Despite noteworthy progress made in the synthesis of nanotubular architectures with well-defined lengths and diameters, purely covalently bonded organic nanotubes have remained somewhat challenging to prepare. Here we report the synthesis of covalently bonded porous organic nanotubes (CONTs) by Schiff base reaction between a tetratopic amine-functionalized triptycene and a linear dialdehyde. The spatial orientation of the functional groups promotes the growth of the framework in one dimension, and the strong covalent bonds between carbon, nitrogen and oxygen impart the resulting CONTs with high thermal and chemical stability. Upon ultrasonication, the CONTs form intertwined structures that go on to coil and form toroidal superstructures. Computational studies give some insight into the effect of the solvent in this assembly process