The angle-resolved N 1s photoelectron spectrum of has been measured with high resolution in the threshold region. An analysis of the vibrational fine structure yields a vibrational energy of and a lifetime broadening of for the core-ionized molecule. As in the case of C 1s ionization of CO, the vibrational fine structure changes considerably with photon energy in the region of both the shape resonance and the double excitations. Both the vibrationally resolved partial photoionization cross sections and asymmetry parameters have been determined in this photon energy range. The calculated cross sections in the literature are in reasonable agreement with experiment. In addition, we have measured the cross sections and asymmetry parameters of the most intense direct and conjugate shake-up satellites. The behaviour of the satellites is found to differ significantly from that of the corresponding C 1s satellites of CO.
The determination of spin and orbital magnetic moments from the free atom to the bulk phase is an intriguing challenge for nanoscience, in particular, since most magnetic recording materials are based on nanostructures. We present temperature-dependent x-ray magnetic circular dichroism measurements of free Co clusters (N=8-22) from which the intrinsic spin and orbital magnetic moments of noninteracting magnetic nanoparticles have been deduced. An exceptionally strong enhancement of the orbital moment is verified for free magnetic clusters which is 4-6 times larger than the bulk value. Our temperature-dependent measurements reveal that the spin orientation along the external magnetic field is nearly saturated at ~20 K and 7 T, while the orbital orientation is clearly not.
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