X射线光电子能谱
乙烯
氧气
化学
羧酸盐
粘附
表面改性
接触角
分析化学(期刊)
光化学
材料科学
化学工程
物理化学
有机化学
催化作用
复合材料
工程类
出处
期刊:Journal of vacuum science & technology
[American Vacuum Society]
日期:1990-09-01
卷期号:8 (5): 3682-3691
被引量:138
摘要
High resolution x-ray photoelectron spectroscopy (XPS) has been used to study the interfacial chemistry between vacuum-deposited silver and poly(ethylene terephthalate) (PET) surfaces. The initial stages of metallization in the subatomic layer regime (∼0.1–1.0 atomic layer of Ag) were monitored. For the untreated PET, the XPS results suggest charge transfer between silver and the carbonyl oxygen in PET in the early stages of metallization. The effect on the untreated PET is small with only about 7% of the PET surface atoms providing reaction sites. Plasma modification with oxygen introduces specific reaction sites resulting in additional chemical bond formation between the vacuum-deposited silver and the PET surface. The XPS results suggest the primary reaction sites are the plasma-induced acid groups. The resultant structure is similar to that of a silver carboxylate species. The number of reaction sites is estimated at 3–4 times greater compared to untreated PET. These results are consistent with the significant improvement in adhesion observed for plasma treatment with oxygen.
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