Submonolayer growth of H 2 -phthalocyanine on Ag(111)
Submonolayer growth of H 2 -phthalocyanine on Ag(111)
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H 2 -酞菁在Ag(111)上的亚单层生长
DOI:
10.1103/physrevb.86.195412
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发表时间:
2012
影响因子:
3.7
通讯作者:
C. Kumpf
中科院分区:
文献类型:
--
作者:
Ingo Kröger;P. Bayersdorfer;B. Stadtmüller;C. Kleimann;G. Mercurio;F. Reinert;C. Kumpf
We present a comprehensive study of structural and electronic properties of the adsorbate system H${}_{2}$-phthalocyanine (H${}_{2}$Pc) on Ag(111). A comparison with copper-phthalocyanine (CuPc) on Ag(111) allows us to elucidate the impact of the central metal atom in the molecule on the adsorbate-substrate interaction. This metal atom is one fundamental parameter which can be changed in order to modify the properties of phthalocyanine molecules, and therefore its influence on the adsorption behavior is highly relevant. From high-resolution electron diffraction, we obtained a phase diagram for submonolayer coverages which turns out to be similar to that of CuPc/Ag(111). The most striking difference is a higher stability of a commensurate phase, indicating a stronger and more adsorption site-specific bonding of the H${}_{2}$Pc molecules. Furthermore, ultraviolet photoelectron spectroscopy and x-ray standing waves prove chemisorptive interaction between molecules and substrate and a significant bending of the molecules with the nitrogen atoms approaching the surface. We conclude that the attractive interaction of metal-phthalocyanine molecules with Ag(111) is mainly mediated by the aromatic body of the molecule (the tetraazaporphyrin ring in particular) rather than by the central metallic atom which (in the case of CuPc) already shows Pauli repulsion.