A long-standing discrepancy between experimental and theoretical values for the lifetimes of holes in the surface-state electron bands on noble metal surfaces is resolved; previous determinations of both are found to have been in error. The ability of the scanning tunneling microscope to verify surface quality before taking spectroscopic measurements is used to remove the effects of defect scattering on experimental lifetimes, found to have been a significant contribution to prior determinations. A theoretical treatment of inelastic electron-electron scattering is developed that explicitly includes intraband transitions within the surface state band. In our model, two-dimensional decay channels dominate the electron-electron interactions that contribute to the hole decay and are screened by the electron states of the underlying three-dimensional electron system.
The electronic structure of artificial Mn atom arrays on Ag(111) is characterized in detail with scanning tunnelling spectroscopy and spectroscopic imaging at low temperature. We demonstrate the degree to which variations in geometry may be used to control spatial and spectral distributions of surface state electrons confined within the arrays, how these are influenced by atoms placed within the structure and how the ability to induce spectral features at specific energies may be exploited through lineshape analyses to deduce quasiparticle lifetimes near the Fermi level. Through extensive comparison of dI/dV maps and spectra we demonstrate the utility of a model based upon twodimensional s-wave scatterers for describing and predicting the characteristics of specific resonators.
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