Abstract
We have studied the formation and growth of holes in free-standing polystyrene films. For thick (∼μm) films and sufficiently high temperatures, exponential hole growth vs time was observed. Using the theory of deBregeas et al. [Phys. Rev. Lett. 1995, 75, 21], relating growth rate to viscosity (η), we confirmed bulk scaling η α MW 3.2±0.2, where MW is the polymer molecular weight, and obtained good quantitative agreement with bulk viscosities. As temperature is lowered and/or films are made thinner, a transition to a linear growth mode of hole radius vs time is observed. The molecular weight dependence of growth velocity (V) for temperatures near the glass transition temperature (T g) is Vα MW 0.5±00.2. Our results also show an intermediate regime where growth is exponential, but bulk viscosities are not observed. Ellipsometry measurements, atomic force microscopy cross-section analysis, and optical images show no rim formation and uniform film thickening as holes grow.
| Original language | English |
|---|---|
| Pages (from-to) | 1470-1475 |
| Number of pages | 6 |
| Journal | Macromolecules |
| Volume | 37 |
| Issue number | 4 |
| DOIs | |
| State | Published - Feb 24 2004 |
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