Controllable growth of porous morphology in low dielectric polyimides via thermal-driven spontaneous phase separation

Abstract

Fabricating porous polymer films with precise morphological control via a conventional phase separation method is challenging. Herein, porous polyimide (PPI) film formation kinetics was thoroughly investigated to understand the underlying phenomena during the thermally induced phase separation. The porous films were prepared using a poly(amic acid) (PAA) solution with a small-molecular phase dispersion agent (i.e., porogen), dibutyl phthalate (DBP), which is miscible with the PAA chains. Using amine-functionalized polyhedral oligomeric silsesquioxane (NH2-POSS) as an additional nucleating agent, sponge-like NH2-POSS end-capped PPI (PPI/NH2-POSSx) films were fabricated with tunable pore size (16.3–76.9 μm) and porosity (42.6–69.4 %). This ensured control over the porous structure of the PPI/NH2-POSSx film, providing desirable low dielectric properties (a minimum of 2 at 1 MHz) in broad frequency and temperature range as well as high thermal stability (Tg = 363–385 °C, T5% = 519–559 °C), and good mechanical strength (17–23 MPa). It was found that the porous structure and physical properties of the PPI/NH2-POSSx films can be readily engineered by tailoring the initial content of a removable porogen and cage silsesquioxane. This work will provide a new perspective on fabricating temperature-resistant low-dielectric porous polymer films with tunable pore sizes via thermal-driven spontaneous phase separation with efficient processability.