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Metal-phthalocyanine ordered layers on Au(110): Metal-dependent adsorption energy

Journal Article · · Journal of Chemical Physics
DOI:https://doi.org/10.1063/1.4883735· OSTI ID:22311391
; ; ;  [1];  [2];  [3]
  1. Dipartimento di Fisica, Università di Roma La “Sapienza,” 00185 Roma (Italy)
  2. IFIS Litoral, CONICET-UNL, Laboratorio de Fisica de Superficies e Interfaces, Güemes 3450, Santa Fe (Argentina)
  3. Dipartimento di Fisica, CNISM, Università di Roma La “Sapienza,” 00185 Roma (Italy)
Iron-phthalocyanine and cobalt-phthalocyanine chains, assembled along the Au(110)-(1×2) reconstructed channels, present a strong interaction with the Au metallic states, via the central metal ion. X-ray photoemission spectroscopy from the metal-2p core-levels and valence band high-resolution ultraviolet photoelectron spectroscopy bring to light signatures of the interaction of the metal-phthalocyanine single-layer with gold. The charge transfer from Au to the molecule causes the emerging of a metal-2p core level component at lower binding energy with respect to that measured in the molecular thin films, while the core-levels associated to the organic macrocycle (C and N 1s) are less influenced by the adsorption, and the macrocycles stabilize the interaction, inducing a strong interface dipole. Temperature Programmed Desorption experiments and photoemission as a function of temperature allow to estimate the adsorption energy for the thin-films, mainly due to the molecule-molecule van der Waals interaction, while the FePc and CoPc single-layers remain adsorbed on the Au surface up to at least 820 K.
OSTI ID:
22311391
Journal Information:
Journal of Chemical Physics, Journal Name: Journal of Chemical Physics Journal Issue: 24 Vol. 140; ISSN JCPSA6; ISSN 0021-9606
Country of Publication:
United States
Language:
English