Effect of substrate interface on the magnetism of supported iron nanoparticles.

In situ X-ray photo-emission electron microscopy is used to investigate the magnetic properties of iron nanoparticles deposited on different single crystalline substrates, including Si(001), Cu(001), W(110), and NiO(001). We find that, in our room temperature experiments, Fe nanoparticles deposited on Si(001) and Cu(001) show both superparamagnetic and magnetically stable (blocked) ferromagnetic states, while Fe nanoparticles deposited on W(110) and NiO(001) show only superparamagnetic behaviour. The dependence of the magnetic behaviour of the Fe nanoparticles on the contact surface is ascribed to the different interfacial bonding energies, higher for W and NiO, and to a possible relaxation of point defects within the core of the nanoparticles on these substrates, that have been suggested to stabilise the ferromagnetic state at room temperature when deposited on more inert surfaces such as Si and Cu.

Size-dependent spin structures in iron nanoparticles.

Using photoemission electron microscopy, we study the magnetization orientation in single 5-25 nm iron particles coupled to a ferromagnetic cobalt support. We find a noncollinear alignment between the particle and substrate magnetization above a particle size of approximately 6 nm and a parallel alignment for smaller sizes. Numerical calculations reveal a transition from an exchange-dominated to an anisotropy-dominated regime on increasing the particle height: the smaller particles are in a single-domain collinear state while larger particles exhibit a spin-spiral magnetic structure determined by the magnetic anisotropy energy.