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Argon and oxygen sputter etching of polystyrene, polypropylene, and poly(ethylene terephthalate) thin films
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1988
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EngineeringChemistryPolymersChemical EngineeringPolymer MaterialPolymer TechnologyPolymer ProcessingEthylene TerephthalateHybrid MaterialsPolymer ChemistryThin Film ProcessingMaterials EngineeringMaterials ScienceOxygen Sputter EtchingPolymer EngineeringSurface ModificationPolymer AnalysisPolymer Thin FilmsPlasma EtchingPolymer OxidationSurface Chemical ModificationSurface SciencePolymer ScienceApplied PhysicsMaterials CharacterizationPolymer CharacterizationThin FilmsSurface ProcessingChemical Vapor Deposition
Surface chemical modification of polymer thin films induced by sputter etching was studied by x‐ray photoelectron spectroscopy (XPS) and infrared reflection–absorption spectroscopy (IRRAS). The polymers studied were polystyrene, polypropylene, and poly(ethylene terephthalate) (PET). Oxygen and argon sputter etching of these polymers causes surface oxidation and possibly crosslinking; trends in polymer oxidation can be correlated with the etchant gas, etch power, and initial material properties. For polystyrene and polypropylene, the predominant new functionalities formed are C=O and C–O groups; the breadth of the infrared absorption bands suggests that many different types of these groups exist. For PET, the predominant damage mechanism is crosslinking, with only a slight degree of oxidation resulting from oxygen sputter etching. This work suggests that the information provided by XPS and IRRAS is highly complimentary and will be useful in future studies of polymer functionalization and derivatization.