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The magnetic ground state of biatomic Fe chains on the reconstructed (5×1)-Ir(001) surface is a cycloidal 120° spin spiral. Spin-resolved scanning tunneling microscopy reveals a striking variation of magnetic field dependences among the chains, which we attribute to parity effects resulting from finite lengths. Numerical simulations show that the chains are divided in three symmetry classes with the exact number of atoms in the chain determining the size and direction of their net magnetic moment. In contrast to antiferromagnetic systems, the three-atom periodicity causes the effective anisotropy to alternate between out of plane, in plane, and quenched. [ABSTRACT FROM AUTHOR]

Skyrmions are topologically protected field configurations with particle-like properties that play an important role in various fields of science. Recently, skyrmions have been observed to be stabilized by an external magnetic field in bulk magnets. Here, we describe a two-dimensional square lattice of skyrmions on the atomic length scale as the magnetic ground state of a hexagonal Fe film of one-atomic-layer thickness on the Ir(111) surface. Using spin-polarized scanning tunnelling microscopy we can directly image this non-collinear spin texture in real space on the atomic scale and demonstrate that it is incommensurate to the underlying atomic lattice. With the aid of first-principles calculations, we develop a spin model on a discrete lattice that identifies the interplay of Heisenberg exchange, the four-spin and the Dzyaloshinskii-Moriya interaction as the microscopic origin of this magnetic state. [ABSTRACT FROM AUTHOR]

Single magnetic atoms on surfaces are the smallest conceivable units for two-dimensional magnetic data storage. Previous experiments on such systems have investigated magnetization curves, the many-body Kondo effect and magnetic excitations in quantum spin systems, but a stable magnetization has not yet been detected for an atom on a non-magnetic surface in the absence of a magnetic field. The spin direction of a single magnetic atom can be fixed by coupling it to an underlying magnetic substrate via the exchange interaction, but it is then difficult to differentiate between the magnetism of the atom and the surface. Here, we take advantage of the orbital symmetry of the spin-polarized density of states of single cobalt atoms to unambiguously determine their spin direction in real space using a combination of spin-resolved scanning tunnelling microscopy experiments and ab initio calculations. By laterally moving atoms on our non-collinear magnetic template, the spin direction can also be controlled while maintaining magnetic sensitivity, thereby providing an approach for constructing and characterizing artificial atomic-scale magnetic structures. [ABSTRACT FROM AUTHOR]