The spin and orbital contributions to the total magnetic moments of free Fe, Co, and Ni clusters.

We present size dependent spin and orbital magnetic moments of cobalt (Con (+), 8 ≤ n ≤ 22), iron (Fen (+), 7 ≤ n ≤ 17), and nickel cluster (Nin (+), 7 ≤ n ≤ 17) cations as obtained by X-ray magnetic circular dichroism (XMCD) spectroscopy of isolated clusters in the gas phase. The spin and orbital magnetic moments range between the corresponding atomic and bulk values in all three cases. We compare our findings to previous XMCD data, Stern-Gerlach data, and computational results.

Orbit and spin resolved magnetic properties of size selected [ConRh]⁺ and [ConAu]⁺ nanoalloy clusters.

Bi-metallic nanoalloys of mixed 3d-4d or 3d-5d elements are promising candidates for technological applications. The large magnetic moment of the 3d materials in combination with a high spin-orbit coupling of the 4d or 5d materials give rise to a material with a large magnetic moment and a strong magnetic anisotropy, making them ideally suitable in for example magnetic storage devices. Especially for clusters, which already have a higher magnetic moment compared to the bulk, these alloys can profit from the cooperative role of alloying and size reduction in order to obtain magnetically stable materials with a large magnetic moment.

Evolution of metallic screening in small metal clusters probed by PCI-Auger spectroscopy.

Excitation-energy dependent Auger spectra of small copper clusters supported by a thin silica layer have been measured as function of cluster size. The Auger kinetic energy of the clusters clearly changes with the excess energy of the emitted photoelectron while not for the bulk. The kinetic energy shift is attributed to post-collision interaction (PCI) and exhibits a reduced metallic screening ability of small Cu-clusters.

Size-dependent dynamics in excited states of gold clusters: from oscillatory motion to photoinduced melting.

Femtosecond time resolved photoelectron spectroscopy in combination with direct ab initio molecular dynamics "on the fly" based on density functional theory has been used to study the relaxation dynamics of optically excited states in small mass selected anionic gold clusters (Au(n) (-); n = 5-8). The nature of the dynamics strongly depends on the cluster size and structure. Oscillatory wavepacket motion (Au(5)(-)), a long lived excited state (Au(6)(-)), as well as photoinduced melting (Au(7)(-),Au(8)(-)) is observed in real time.