Selective stabilization of antiferromagnetic orders in FeTe films via local strain engineering

Abstract

The parent compound FeTe hosts a complex magnetic landscape that is highly susceptible to lattice distortions. Although theoretical models have predicted a bicollinear to dimer antiferromagnetic (AFM) phase transition under tensile strain, its experimental realization and deterministic control has remained elusive owing to severe magnetic frustration. Here, combining high-resolution scanning tunneling microscopy (STM) and density functional theory (DFT) calculations, we demonstrate the selective stabilization of bicollinear and dimer AFM orders in few-layer FeTe films via local uniaxial strain engineering. By mapping the strain fields near dislocation areas in FeTe films and FeTe/FeSe heterostructures, we establish a direct correspondence between specific strain components and the resulting magnetic ground states. We find that uniaxial compression along the Fe-Fe next-nearest-neighbor direction stabilizes the bicollinear AFM order, with the stripe orientation aligning parallel to the compression axis. Crucially, we report the experimental realization of the long-range dimer AFM order, which emerges under anisotropic strain along the Fe-Fe nearest-neighbor direction. This phase manifests as a distinct $\sqrt{2} \times \sqrt{2}$ electronic reconstruction and shares a common Neel temperature with the bicollinear phase. Our findings reveal that anisotropic strain effectively lifts the magnetic degeneracy among competing states. This work provides a robust strategy for the manipulation of elusive magnetic orders and offers insights into the interplay between lattice, spin, and electronic degrees of freedom in iron-based superconductors.