The platinum−tellurium phase diagram exhibits various (meta)stable van der Waals (vdW) materials that can be constructed by stacking PtTe 2 and Pt 2 Te 2 layers. Monophase PtTe 2 , being the thermodynamically most stable compound, can readily be grown as thin films. Obtaining the other phases (Pt 2 Te 3 , Pt 3 Te 4 , Pt 2 Te 2 ), especially in their ultimate thin form, is significantly more challenging. We show that PtTe 2 thin films can be transformed by vacuum annealing-induced Te-loss into Pt 3 Te 4 -and Pt 2 Te 2 -bilayers. These transformations are characterized by scanning tunneling microscopy and X-ray and angle resolved photoemission spectroscopy. Once Pt 3 Te 4 is formed, it is thermally stable up to 350°C. To transform Pt 3 Te 4 into Pt 2 Te 2 , a higher annealing temperature of 400°C is required. The experiments combined with density functional theory calculations provide insights into these transformation mechanisms and show that a combination of the thermodynamic preference of Pt 3 Te 4 over a phase segregation into PtTe 2 and Pt 2 Te 2 and an increase in the Te-vacancy formation energy for Pt 3 Te 4 compared to the starting PtTe 2 material is critical to stabilize the Pt 3 Te 4 bilayer. To desorb more tellurium from Pt 3 Te 4 and transform the material into Pt 2 Te 2 , a higher Te-vacancy formation energy has to be overcome by raising the temperature. Interestingly, bilayer Pt 2 Te 2 can be retellurized by exposure to Te-vapor. This causes the selective transformation of the topmost Pt 2 Te 2 layer into two layers of PtTe 2 , and consequently the synthesis of e Pt 2 Te 3 . Thus, all known Pt-telluride vdW compounds can be obtained in their ultrathin form by carefully controlling the stoichiometry of the material.