The adsorption of oxygen on the ͑111͒ surface of the Pt 3 Sn alloy was studied by means of scanning tunneling microscopy ͑STM͒ and x-ray photoelectron diffraction ͑XPD͒. As Auger electron spectroscopy, low-energy ion scattering, and x-ray photoelectron spectroscopy indicate, upon oxygen exposure ͑range 10000 L, with the sample at circa 770 K͒ Sn segregates to the surface and forms a two-dimensional tin-oxygen layer.In the x-ray photoemission spectra no pronounced chemical shift is visible that would indicate a thicker tin oxide layer. After exposure to 10000 L O 2 at 770 K low-energy electron diffraction shows a streaky 2ϫ2 pattern with additional spots. Scanning tunneling microscopy images show a surface with a 2ϫ2 periodicity characterized by an high defect density. The corrugation of this surface is substantially higher than that of the clean surface. After annealing in vacuum at temperatures ranging from 600 to 800 K, a sharp 4ϫ4 low-energy electron diffraction pattern can be observed. STM then reveals a superlattice of depressions, the remaining protrusions are slightly laterally displaced from their 2ϫ2 positions. X-ray photoelectron diffraction intensities of the 4ϫ4 phase show hardly any change for Pt 4 f , whereas Sn 3d azimuthal curves measured at higher polar angles are substantially modified after oxygen exposure. In order to understand the nature of the features observed in the STM images, the experimental XPD curves were compared with single and multiple scattering cluster calculations performed for various structural models. On the basis of these results we propose a model involving the reconstruction of the substrate surface.