Supported lipid membranes represent an elegant way to design a fluid interface able to mimic the physico-chemical properties of biological membranes, with potential biotechnological applications. In this work, a diacyl phospholipid, the 1,2-dipalmitoyl-sn-glycero-3-phosphothioethanol (DPPTE), functionalized with a thiol group, was immobilized on a gold surface. In this molecule, the thiol group, responsible of the Au-S bond (55 kJ/mol) is located on the phospholipid polar head, letting the hydrophobic chain protruding from the film. This system is widely used in the literature, but not of less challenging, since its characterization is not complete, as several discording data have been obtained. In this work, the film was characterized by cyclic voltammetry blocking experiments, to verify the SAM formation, and by reductive desorption measurements to estimate the molecular density of DPPTE on the gold surface. This value has been compared to that obtained by quartz crystal microbalance measurements. Ellipsometry and impedance spectroscopy measurements have been performed to obtain information about the monolayer thickness and capacitance. The film morphology was investigated by atomic force microscopy. Finally, Monte Carlo simulations were carried out , in order to gain molecular information about the morphologies of the DPPTE SAM, and compare them to the experimental results. We demonstrate that DPPTE molecules, incubated 18 hours below the phase transition temperature (T= 41.1±0.4°C) in ethanol solution, are able to form a self-assembled monolayer on gold surface, with domain structures of different order, which have never been reported before. Our results make possible to rationalize the scattered results so far obtained on this system, giving a new insight on the formation of phospholipids SAMs on gold surface.