RESUMEN
Plasma-polymerized films (PPF) synthesized by plasma-enhanced chemical vapor deposition (PECVD) find increasing applications in biomedicine and differ in many ways from conventional polymers. One of the most specific properties of the PPF is the high reactivity of its free-radical-rich surface, arising from the deposition mechanism. Although generally considered as a disadvantage leading to the aging of the PPF, reactivity of the plasma-treated polymers and PPF surfaces can be beneficially employed, for example, for grafting of a specific chemical functionality or short polymer chains. The quantitative evaluation of the surface radical density of the PPF is thus considered as the necessary preparatory step toward any subsequent grafting reaction. In the present study, the surface radical density of an isopropanol-based PPF was quantitatively determined by a combination of NO chemical derivatization and X-ray photoelectron spectroscopy (XPS). Once the derivatization conditions were optimized, the radical density, derived from at % N determined by XPS, was evaluated as a function of the deposition power. It was found out that the surface density of free radicals presents a maximum for the deposition power of 200 W (~2.3 × 10(14) spin/cm(2)) and it stabilizes (~2.1 × 10(14) spin/cm(2)) with further power increase. XPS findings were supported by in situ FTIR measurements that provided additional information about the degree of plasma fragmentation denoting fragmentation saturation for a deposition power of 200 W. By fitting the N1s peak it was possible to identify primary, secondary and ternary radicals and to study their respective evolutions with different deposition conditions. Angle-resolved XPS analysis allowed the in-depth distribution of radicals to be addressed, revealing that on the top surface, primary, and secondary radicals are dominating, whereas more tertiary radicals are present in the subsurface region. Finally, some preliminary chemical grafting experiments have allowed the relevance of derivatization results to be cross-checked.