We present a comparative investigation of the adsorption mechanism of two organic molecules characterized by pdelocalized orbitals (copper-phthalocyanine and pentacene) deposited on the Au(1 1 0)-(1 · 2) surface, studied by means of low energy electron diffraction (LEED) and high energy-resolution ultraviolet photoemission spectroscopy (HRUPS). The molecular adsorption induces a threefold periodicity in the [0 0 1] direction and a ·5 (·6) symmetry in the [11 0] direction for the phthalocyanine (pentacene), as deduced by the LEED patterns. High energy-resolution photoemission spectra show similar hybrid interface states for both systems, indicating that the molecular interaction with the metal substrate is driven mainly by p molecular orbitals (even for the phthalocyanine). Comparing the electronic spectral density excited by different photon energies we single out the different contribution of p and d symmetry to interface states
Au(110) induced reconstruction by pi conjugated molecules adsorption investigated by photoemission spectroscopy and low energy electron diffraction
V Corradini;
2004
Abstract
We present a comparative investigation of the adsorption mechanism of two organic molecules characterized by pdelocalized orbitals (copper-phthalocyanine and pentacene) deposited on the Au(1 1 0)-(1 · 2) surface, studied by means of low energy electron diffraction (LEED) and high energy-resolution ultraviolet photoemission spectroscopy (HRUPS). The molecular adsorption induces a threefold periodicity in the [0 0 1] direction and a ·5 (·6) symmetry in the [11 0] direction for the phthalocyanine (pentacene), as deduced by the LEED patterns. High energy-resolution photoemission spectra show similar hybrid interface states for both systems, indicating that the molecular interaction with the metal substrate is driven mainly by p molecular orbitals (even for the phthalocyanine). Comparing the electronic spectral density excited by different photon energies we single out the different contribution of p and d symmetry to interface statesI documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.