Magnetic anisotropy in surface-supported single-ion lanthanide complexes

Abstract

Single-ion lanthanide-organic complexes can provide stable magnetic moments with well-defined orientation for spintronic applications on the atomic level. Here, we show by a combined experimental approach of scanning tunneling microscopy and X-ray absorption spectroscopy that dysprosium-tris(1,1,1-trifluoro-4-(2-thienyl)-2,4butanedionate) (Dy(tta)${}_3$) complexes deposited on a Au(111) surface undergo a molecular distortion, resulting in distinct crystal field symmetry imposed on the Dy ion. This leads to an easy-axis magnetization direction in the ligand plane. Furthermore, we show that tunneling electrons hardly couple to the spin excitations, which we ascribe to the shielded nature of the $4f$ electrons.

References in corpus (5)

• Quantum Computing in Molecular Magnets
• Molecular nanomagnets as quantum simulators
• Excitation of local magnetic moments by tunnelling electrons
• Sub-molecular modulation of a 4f driven Kondo resonance by surface-induced asymmetry
• Controlled complete suppression of single-atom inelastic spin and orbital cotunnelling