In recent years, with the fast development of magnetic devices for information technology, the demands of magnetic thin films with both high functional stability and integration flexibility rapidly increase. It is believed that building a magnet with complementary advantages of van der Waals (vdW) and non-vdW magnets, which can be described as a “quasi-vdW magnet,” will be highly appreciated. One may expect a quasi-vdW magnet to have chemical bonding between the neighboring sublayers for strong magnetic coupling, but to preserve clean surfaces with vdW feature for flexible interface engineering. For this purpose, an intercalation of magnetic atoms into the interlayer gaps of vdW magnets, as a powerful method for tuning the interlayer coupling, can be a practical approach. In this work, using the first-principles calculations, we study the potential to utilize the Fe-intercalation to transform the vdW magnets Fe3GeTe2 (FGT) into quasi-vdW magnets. As two extreme cases, it is revealed that: (i) the Fe-intercalated FGT bilayer Fe-[Fe3GeTe2]2 (Fe-[FGT]2) does have remarkable interlayer ferromagnetic coupling based on covalent bonding between the intercalated Fe atom and FGT monolayers and retains low exfoliation energy with vdW feature, suggesting that the Fe-[FGT]2 bilayer can be regarded as a quasi-vdW magnet; and (ii) the Fe-intercalation can transform the vdW FGT bulk into a non-vdW Fe-Fe3GeTe2 (Fe-FGT) bulk magnet. Accordingly, as for the intermediate cases, it is suggested that Fe-intercalated FGT multilayers (Fen−1-[FGT]n, n > 2) can also be potential quasi-vdW magnets, forming a family of magnetic thin films that provide alternative building blocks for microminiaturized magnetic devices.
In recent years, one of the urgent issues for two dimensional (2D) magnetic materials is to find efficient ways in enhancing the magnetic ordering temperature Tc. It is believed that an in-plane (IP) compressive strain can greatly enhance the interatomic interactions by shortening the chemical bond length if at all possible, leading to the enlarged spin exchange and possibly higher Tc. However, a large compressive strain usually favors antiferromagnetic (AFM) ordering due to growing dominance of the Pauli exclusion principle, in contradiction with the common requirement of nonzero magnetization. In compromise, ferrimagnetic (FiM) ordering can be alternated by synthesizing artificial 2D compound with two magnetic sublattices. In this work, we propose a V-implanted CrI3 monolayer, short for V-(CrI3)2, and study its FiM ordering under a series of IP biaxial strains using the first-principles calculations and Monte Carlo simulations. It is found that the V-(CrI3)2 monolayer may evolve from the stripy-type AFM insulator toward the FiM half-metal with net magnetic moment of 5.0 μB/f.u. aligned in parallel to the ab-plane upon increasing the IP biaxial strain up to ∼−3% (compressive strain) and beyond. As the IP biaxial strain increases up to ∼−5%, the Tc of the FiM state may be raised to room temperature. This work suggests that the IP strain engineering combined with spin implantation can be an alternative strategy for enhancing 2D magnetism.
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