Abstract
The formation and entrapment of tris(8-hydroxyquinoline)aluminum (Alq₃) molecules on the surface of anodic porous alumina (APA) immersed in an ethanol solution of 8-hydroxyquinoline (HQ) were investigated by absorption, fluorescence, and Raman spectroscopies. The effects of the selected APA preparation conditions (galvanostatic or potentiostatic anodization method, anodizing current and voltage values, one- or two-step anodizing process, and sulfuric acid electrolyte concentration) on the adsorption and desorption of Alq₃ species were examined. Among the listed parameters, sulfuric acid concentration was the most important factor in determining the Alq₃ adsorption characteristics. The Alq₃ content measured after desorption under galvanostatic conditions was 2.5 times larger than that obtained under potentiostatic ones, regardless of the adsorbed quantities. The obtained results suggest the existence of at least two types of adsorption sites on the APA surface characterized by different magnitudes of the Alq₃ bonding strength. The related fluorescence spectra contained two peaks at wavelengths of 480 and 505 nm, which could be attributed to isolated Alq₃ species inside nanovoids and aggregated Alq₃ clusters in the pores of APA, respectively. The former species were attached to the adsorption sites with higher binding energies, whereas the latter ones were bound to the APA surface more weakly. Similar results were obtained for the Alq₃ species formed from the HQ solution, which quantitatively exceeded the number of the Alq₃ species adsorbed from the Alq₃ solution. Alq₃ molecules were formed in the HQ solution during the reaction of HQ molecules with the Al(3+) ions in the oxide dissolution zone near the oxide/electrolyte interface through the cracks and the Al(3+) ions adsorbed on surface of pore and cracks. In addition, it was suggested that HQ molecules could penetrate the nanovoids more easily than Alq₃ species because of their smaller sizes, which resulted in higher magnitudes of the adsorption.