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Influence of solvent and molecular weight on thickness and surface topography of spin‐coated polymer films

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TLDR
In this paper, the influence of polymer molecular weight, molecular weight distribution, and polymer-solvent interactions on the thickness and topography of spin-coated polymer films was examined.
Abstract
The influence of polymer molecular weight, molecular weight distribution, and polymer-solvent interactions on the thickness and topography of spin-coated polymer films was examined. For films prepared from dilute solutions, highly volatile solvents or fair or “poor” solvents for the polymer adversely affect film surfaces causing nonuniformities (waves) to appear. However, if the concentration of these solutions is increased to approximately the concentration at which entanglements are formed, nearly uniform films are produced even if the solvent employed is highly volatile, such as dichloromethane. When toluene is employed as the solvent, which has a relatively low volatility and therefore forms nearly flat film surfaces, films prepared from dilute solution were found to have thicknesses, h, proportional to η Ω−0.49 for polystyrene and η Ω−0.49 for poly(methylmethacrylate) where ηo is the zero-shear rate solution viscosity and Ω is the rotational speed at which the films were prepared. These results suggest that the exponents associated with ηo and Ω may be nearly independent of the type of polymer used as long as flat films are produced. Finally, the molecular weight parameter most important in controlling final film thickness for films made from dilute solutions is Mv, the viscosity-average molecular weight.

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Citations
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Journal ArticleDOI

Structure formation via polymer demixing in spin-cast films

TL;DR: In this paper, the domain structure in thin films of an immiscible polystyrene/poly(methyl methacrylate) (PS/PMMA) blend was studied after spin-casting from a common solvent.
Journal ArticleDOI

Spin coating of thin and ultrathin polymer films

TL;DR: In this paper, the spin coating of thin (> 200 nm thick) and ultrathin (200 nm) polymer films is examined in several solvents of varying volatility over a broad range of polymer solution concentrations and spin speeds.
Journal Article

Polymer-Nanoparticle Interfacial Interactions in Polymer Nanocomposites: Confinement Effects on Glass Transition Temperature and Suppression of Physical Aging.

TL;DR: In this paper, the effects of confinement on glass transition temperature (Tg) and physical aging are measured in polystyrene (PS), poly(methyl methacrylate) (PMMA), and poly(2-vinyl pyridine) (P2VP) nanocomposites containing 10- to 15-nmdiameter silica nanospheres or 47-nm-diameter alumina nanosphere.
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Grazing incidence small-angle X-ray scattering: an advanced scattering technique for the investigation of nanostructured polymer films

TL;DR: GISAXS turned out to be a powerful advanced scattering technique for the investigation of nanostructured polymer films and has a much larger statistical significance compared to AFM.
Journal ArticleDOI

6 Studies of spin-coated polymer films

TL;DR: In this paper, the fundamental physical and chemical processes governing the conventional spincoating process and methodologies for the preparation of spin-coated polymer thin films are discussed and a range of advanced applications and recent developments within this field are reviewed with focus on engineering chemical and topological structure during the coating process.
References
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Journal ArticleDOI

Flow of a Viscous Liquid on a Rotating Disk

TL;DR: In this paper, it was shown that initially irregular fluid distributions tend toward uniformity under centrifugation, and means of computing times required to produce uniform layers of given thickness at given angular velocity and fluid viscosity are demonstrated.
Journal ArticleDOI

Characteristics of resist films produced by spinning

TL;DR: In this article, a model for the description of thin films prepared from solution by spinning is presented, and the thickness of the film and the time of drying can be calculated as functions of various processing parameters.
Journal ArticleDOI

Polymer chain dimensions and the dependence of viscoelastic properties on concentration, molecular weight and solvent power

TL;DR: In this paper, the effects of polymer concentration on chain dimensions in good solvents are discussed in order to define the boundary between the semi-dilute and concentrated regimes, and it appears that chain dimensions should approach their unperturbed values for many systems at polymer volume fractions in the range of 0.05-0.20, independent of molecular weight.