129Xe on Ir(111): NMR study of xenon on a metal single crystal surface

摘要

NMR experiments of ¹²⁹Xe adsorbed on an iridium single crystal surface are reported. Very high nuclear polarization (Pz ≈ 0.7) makes the experiment possible. A coverage of less then one monolayer is investigated on the Ir(111) surface with an area of 0.8 cm². The observed resonance line shifts are very large and highly anisotropic. We find σiso = 1,032 ± 11 ppm and σan = 291 ± 33 ppm, which are far above the typical range of physisorption. The highly ordered substrate leads to homogeneous conditions for the xenon atoms, as seen in the narrow linewidth of 20 ppm. Chemical shifts under physisorption conditions are not large enough to totally explain the results. Knight shift can clearly be identified as the cause of the findings. This shift shows the presence of conduction electrons of the metallic substrate at the xenon nucleus and thus the mixing of metallic and atomic states at the Fermi level. Such mixing is in accordance with recent Hartree–Fock and density functional calculations of similar van der Waals adsorption systems. Quantitative comparisons, however, fail completely. The size and ratio of σan and σiso are pure ground-state properties in a structurally simple system. They are accessible to theory and provide detailed local information that can serve as a benchmark for theory.