Engineering covalently bonded 2D layered materials by self-intercalation.

Two-dimensional (2D) materials1–5 offer a unique platform from which to explore the physics of topology and many-body phenomena. New properties can be generated by filling the van der Waals gap of 2D materials with intercalants6,7; however, post-growth intercalation has usually been limited to alkali metals8–10. Here we show that the self-intercalation of native atoms11,12 into bilayer transition metal dichalcogenides during growth generates a class of ultrathin, covalently bonded materials, which we name ic-2D. The stoichiometry of these materials is defined by periodic occupancy patterns of the octahedral vacancy sites in the van der Waals gap, and their properties can be tuned by varying the coverage and the spatial arrangement of the filled sites7,13. By performing growth under high metal chemical potential14,15 we can access a range of tantalum-intercalated TaS(Se)_y, including 25% Ta-intercalated Ta₉S₁₆, 33.3% Ta-intercalated Ta₇S₁₂, 50% Ta-intercalated Ta₁₀S₁₆, 66.7% Ta-intercalated Ta₈Se₁₂ (which forms a Kagome lattice) and 100% Ta-intercalated Ta₉Se₁₂. Ferromagnetic order was detected in some of these intercalated phases. We also demonstrate that self-intercalated V₁₁S₁₆, In₁₁Se₁₆ and Fe_xTe_y can be grown under metal-rich conditions. Our work establishes self-intercalation as an approach through which to grow a new class of 2D materials with stoichiometry- or composition-dependent properties. The intercalation of native atoms into bilayer transition metal dichalcogenides during growth generates ultrathin, covalently bonded materials into which ferromagnetic ordering can be introduced. [ABSTRACT FROM AUTHOR]