The appeal of ultra-compact spintronics drives intense research on magnetism in low-dimensional materials. Recent years have witnessed remarkable progress in engineering two-dimensional (2D) magnetism via defects, edges, adatoms, and magnetic proximity. However, intrinsic 2D ferromagnetism remained elusive until recent discovery of out-of-plane magneto-optical response in Cr-based layers, stimulating the search for 2D magnets with tunable and diverse properties. Here we employ a bottom-up approach to produce layered structures of silicene (a Si counterpart of graphene) functionalized by rare-earth atoms, ranging from the bulk down to one monolayer. We track the evolution from the antiferromagnetism of the bulk to intrinsic 2D in-plane ferromagnetism of ultrathin layers, with its characteristic dependence of the transition temperature on low magnetic fields. The emerging ferromagnetism manifests itself in the electron transport. The discovery of a class of robust 2D magnets, compatible with the mature Si technology, is instrumental for engineering new devices and understanding spin phenomena.

A class of intrinsic 2D ferromagnets – layered metalloxenes – is established by coupling graphene-like honeycomb networks of silicene and germanene with 2D lanthanide layers.

Coupling to Eu makes graphene magnetic without sacrificing its intrinsic properties.

Silicene, a Si analogue of graphene, is suggested to become a versatile material for nanoelectronics. Being coupled with magnetism, it is predicted to be particularly suitable for spintronic applications. However, experimental realization of free-standing silicene and its magnetic derivatives is lacking. Fortunately, magnetism can be induced into silicene layers, in particular, by intercalation. Here, a successful synthesis of multilayer silicene intercalated by inherently magnetic Eu ions -a compound expected to exhibit both massless Dirac-cone states, as its Ca analogue, and a nontrivial magnetic structure -is reported. This new polymorph with EuSi 2 stoichiometry is epitaxially stabilized by continual replication of silicene layers employing Sr-intercalated multilayer silicene as a template. The atomic structure of the new compound and its sharp interface with the template are confirmed using electron diffraction, X-ray diffraction, and electron microscopy techniques. Below 80 K, the material demonstrates anisotropic antiferromagnetism coexisting with weak ferromagnetism. The magnetic state is accompanied by an anomalous behavior of magnetoresistivity.

Addition of magnetism to spectacular properties of graphene may lead to novel topological states and design of spin logic devices enjoying low power consumption. A significant progress is made in defect-induced magnetism in graphene-selective elimination of p orbitals (by vacancies or adatoms) at triangular sublattices tailors graphene magnetism. Proximity to a magnetic insulator is a less invasive way, which is being actively explored now. Integration of graphene with the ferromagnetic semiconductor EuO has much to offer, especially in terms of proximity-induced spin-orbit interactions. Here, we synthesize films of EuO on graphene using reactive molecular beam epitaxy. Their quality is attested by electron and X-ray diffraction, cross-sectional electron microscopy, and Raman and magnetization measurements. Studies of electron transport reveal a magnetic transition at T ≈ 220 K, well above the Curie temperature 69 K of EuO. Up to T, the dependence R ( B) is strongly nonlinear, suggesting the presence of the anomalous Hall effect. The role of synthesis conditions is highlighted by studies of an overdoped structure. The results justify the use of the EuO/graphene system in spintronics.