2001
DOI: 10.1021/la010585q
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Dewetting at a Polymer−Polymer Interface:  Film Thickness Dependence

Abstract: We have used optical microscopy and scanning force microscopy to study the dewetting of polystyrene from poly(methyl methacrylate) on silicon substrates as a function of film thickness. We have performed measurements for bilayers with a lower layer more viscous than the upper layer, as well as for the opposite situation. For a solidlike (highly viscous) lower layer, the dewetting speed is constant and independent of the thickness of the polystyrene film. However, for a liquidlike lower layer, the radius of the… Show more

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Cited by 85 publications
(118 citation statements)
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“…The liquid-liquid dewetting is much more complicated since it may involve the vertical migration of polymer, the diffusion between the upper and bottom layers at the interface, and the resultant deformation of the interface. Therefore, the viscoelasticity of polymers, the miscibility of the upper and bottom layers, and the interaction between polymer and substrate can produce remarkable effect on the stability and resultant structure evolution in a bilayer system [11][12][13][14][15]. For example, the three-dimensional long-wave nonlinear analysis results of Sharma and his co-workers suggested that the film thicknesses, surface energies of polymers, and the viscosities of the films have significant influence on the dewetting mode selection, pathway, and the final morphology of dewetting [16].…”
Section: Introductionmentioning
confidence: 99%
“…The liquid-liquid dewetting is much more complicated since it may involve the vertical migration of polymer, the diffusion between the upper and bottom layers at the interface, and the resultant deformation of the interface. Therefore, the viscoelasticity of polymers, the miscibility of the upper and bottom layers, and the interaction between polymer and substrate can produce remarkable effect on the stability and resultant structure evolution in a bilayer system [11][12][13][14][15]. For example, the three-dimensional long-wave nonlinear analysis results of Sharma and his co-workers suggested that the film thicknesses, surface energies of polymers, and the viscosities of the films have significant influence on the dewetting mode selection, pathway, and the final morphology of dewetting [16].…”
Section: Introductionmentioning
confidence: 99%
“…This applied modeling paper is motivated by the recent experiments on dewetting of non-reactive, immiscible metallic bilayers [16], and the need to better understand the physical mechanisms leading to spatial ordering of particles and the morphological pathways towards the final particle morphologies. The experimental [17][18][19][20][21][22][23][24] and theoretical [25][26][27][28][29][30][31][32][33][34] studies of the instabilities and dynamics of bilayer thin films so far have been largely limited to aqueous and polymer systems under isothermal conditions. Non-isothermal dewetting even in such more conventional systems has not been fully investigated theoretically.…”
Section: Introductionmentioning
confidence: 99%
“…Recent experiments (Lambooy et al 1996;Pan et al 1997;Segalman and Green 1999;Higgins and Jones 2000;Wang et al 2001;Kang et al 2003;Wunnicke et al 2003;de Silva et al 2007;Paul et al 2008) reveal that thin polymer bilayers can selforganize into a variety of even more complex mesoscale patterns, which may be useful for the fabrication of textured functional surfaces and in optoelectronics, microelectromechanical systems and sensor applications. For example, instabilities of thin bilayers on chemically patterned substrates not only generate ordered structures on a large-area, but can also produce pattern transfer in the form of both positive and negative replicas of the substrate imprinted on the twin interfaces of the bilayer (LeOpoldes and Damman 2006).…”
Section: Introductionmentioning
confidence: 99%