Nanostructures on spin-coated polymer films controlled by solvent composition and polymer molecular weight

In this study we systematically investigated how the solvent composition used for polymer dissolution affects the porous structures of spin-coated polymers films. Cellulose acetate butyrate (CAB) and poly(methyl methacrylate) with low (PMMA-L) and high (PMMA-H) molecular weights were dissolved in mi...

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Veröffentlicht in:Thin solid films 2012-12, Vol.524, p.185-190
Hauptverfasser: Dário, Aline F., Macia, Henrique B., Petri, Denise F.S.
Format: Artikel
Sprache:eng
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Zusammenfassung:In this study we systematically investigated how the solvent composition used for polymer dissolution affects the porous structures of spin-coated polymers films. Cellulose acetate butyrate (CAB) and poly(methyl methacrylate) with low (PMMA-L) and high (PMMA-H) molecular weights were dissolved in mixtures of acetone (AC) and ethyl acetate (EA) at constant polymer concentration of 10g/L The films were spin-coated at a relative air humidity of 55±5%, their thickness and index of refraction were determined by means of ellipsometry and their morphology was analyzed by atomic force microscopy. The dimensions and frequency of nanocavities on polymer films increased with the acetone content (φAC) in the solvent mixture and decreased with increasing polymer molecular weight. Consequently, as the void content increased in the films, their apparent thicknesses increased and their indices of refraction decreased, creating low-cost anti-reflection surface. The void depth was larger for PMMA-L than for CAB. This effect was attributed to different activities of EA and AC in CAB or PMMA-L solution, the larger mobility of chains and the lower polarity of PMMA-L in comparison to CAB. ► Nanostructures in spin-coated polymer films depend on the solvent vapor pressure. ► Anti-reflection polymer films are produced at high solvent vapor pressure. ► Only shallow cavities are obtained in films of polymers with high molecular weight.
ISSN:0040-6090
1879-2731
DOI:10.1016/j.tsf.2012.10.011