Electronic properties and orbital-filling mechanism in Rb-intercalated copper phthalocyanine

The evolution of the electronic properties of a thin film of copper phthalocyanine deposited on Al(100) and progressively intercalated with rubidium atoms was followed by photoemission and X-ray absorption spectroscopies. Electron donation from the Rb atoms to the C32H16N8Cu molecules results in the lifting of the degeneracy in the e(g) ligand-derived molecular orbital and the lowering of the molecular symmetry. For Rb similar to 2C32H16N8Cu, spectral evidence indicates that both donated electrons reside in the first split-off e(g)-derived level, thus creating an electronic inequivalence between the C atoms in the benzene rings. For higher Rb concentrations, a reduction of the Cu oxidation state is observed, together with a new Cu-derived state in valence-band photoemission spectra, testifying to the filling of the b(1g) orbital. Thus, even though b(1g) is the lowest unoccupied orbital of the neutral molecule, in the film, the Cu-derived b(1g)-derived states are occupied only after a partial filling of the e.-derived band has taken place. Despite the fact that the eg-derived spectral weight becomes larger as the rubidium content in the RbxC32H16N8Cu compound increases, no spectral density was observed at the Fermi level, showing that the film remains insulating for all of the investigated stoichiometries.