This is a study of the luminescence properties of coatings formed on aluminum alloys by anodizing in electrolytic solutions based on oxalic, sulfuric, and tartaric-sulfonic acids. At least two emission centers, with band maxima in the ranges of 390-410 and 470-510 nm, can be reliably identified in the photoluminescence spectra. The first type of center is characterized by single-band photoluminescence excitation spectra and the second, by two-band spectra. An analysis of the two-band photoluminescence excitation (PLE) spectra in the range of 470-510 nm shows that the position of the narrow short-wavelength PLE spectrum near 272 nm is independent of the type of acid used in the anodization process. The position and shape of the other PLE spectral bands depend both on the type of acid used and on the processing of the alloy or alumina surfaces. It is assumed that defect-free alumina centers are responsible for the 272 nm PLE band, while the other photoluminescence bands are caused primarily by different divacancies of oxygen (F 2 + , F 2 , and F 2 +2 centers) whose origin is governed by the type of electrolyte.Introduction. Composites with different compositions that are capable of greatly improving the protective properties of coatings are currently among the most promising materials. Anodic alumina (aluminum oxide), produced by electrochemical oxidation of aluminum in acidic electrolytes, is widely used to create coatings on aluminum alloys [1]. The resulting thin films of anodic alumina have an ordered structure of nanopores perpendicular to the substrate surface. The diameter of the pores and the distance between them (20-900 nm) depend on the technology used to produce them. Films of this kind are used in solar power, quantum electronics, and optics.The earliest studies of anodic aluminum films produced by various means and at different annealing temperatures showed [2, 3] that the photoluminescence spectra and intensities of the oxide films are independent of the purity of the initial aluminum. The highest photoluminescence intensity was observed when an oxalic acid solution was used as the electrolyte. It was assumed [2, 3] that the photoluminescence is associated with the adsorption of H 2 O by active centers (defects) on the oxide film surface. Later studies of anodic alumina films produced in various electrolytes and under different anodizing conditions showed [4,5] that the emission intensity is considerably higher when solutions of organic acids are used. It was widely concluded that the luminescence centers are carboxyl groups that are embedded in the oxide films during the anodizing process [6]. It was suggested [7,8] that both the photoluminescence and the optical absorption are caused by oxygen vacancies (F + centers) in the alumina films. Later on, it was concluded [9, 10] that the photoluminescence of anodic alumina originates in the combined effect of F + centers and impurities in the form of oxalic acid residues. A study of the interference of photoluminescence in anodic alumina films of differe...