Abstract :
The chemical states and electronic properties of the interface between thermally evaporated aluminium and a photoluminescent
conjugated copolymer containing 9,90-dihexylfluorene and europium complex-chelated benzoate units in the main chain
(PF6-Eu(dbm)2phen) were studied in situ by X-ray photoelectron spectroscopy (XPS) and ultraviolet photoelectron spectroscopy
(UPS). The changes in C 1s, Eu 3d, N 1s, and Al 2p core-level lineshapes with progressive deposition of aluminium atoms
were carefully monitored. Aluminium was found to interact with the conjugated backbone of the copolymer to form the Al
carbide, Al–O–C complex, and Al(III)–N chelate at the interface. In addition, the europium ions were reduced to the metallic state
by the deposited aluminium atoms, which were oxidized and chelated by the 1,10-phenanthroline ligands (phen). The changes in
chemical states at the interface suggest that the intramolecular energy transfer process in this copolymer had been affected.
Moreover, aluminium also interacted with the bulk-adsorbed oxygen, which migrates to the surface in response to the deposition
of aluminium atoms, to form a layer of metal oxides. On the other hand, the evolution of the UPS spectra suggests that the p-states
of the conjugated system were affected and an unfavorable dipole layer was induced by the deposited aluminium atoms.
# 2003 Elsevier B.V. All rights reserved
Keywords :
Photoluminescent , Conjugated copolymer , XPS , UPS , Intramolecular energy transfer , Aluminium , Europium