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a) b - École Polytechnique de Montréal

a) b - École Polytechnique de Montréal

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technique(Zasadzinski, et al., 1994) and the self-assembled monolayer (SAM) method(Maoz,<br />

Frydman, Cohen, & Sagiv, 2000). As well, layer-by-layer(LbL) assembly allows for a high<br />

<strong>de</strong>gree of control of material properties and architecture at the nanometer scale(Hammond, 2004;<br />

Love, Estroff, Kriebel, Nuzzo, & Whitesi<strong>de</strong>s, 2005). In less than 20 years since the introduction<br />

of the LbL technique(Decher, et al., 1992a), the electrochemical study of LbL films has grown<br />

from theory to functional <strong>de</strong>vices, but, in most cases, thin films of conductive polymer are<br />

applied on 2D surfaces. One of the main requirements in this field is to further expand the range<br />

and potential of 3D conductive polymeric <strong>de</strong>vices.<br />

In an A/B heterophasic polymer blend, a low concentration of phase A forms droplets in a matrix<br />

of phase B. As the concentration is gradually increased the percolation point is reached and the<br />

continuity of phase A also increases. Near the phase inversion region a co-continuous<br />

morphology is observed(Paul & Barlow, 1980a). A co-continuous morphology is <strong>de</strong>fined as a<br />

state where each phase is completely continuous throughout the material. The co-continuous<br />

phase structure consists of two fully-interconnected phases which mutually interpenetrate each<br />

other(Bourry & Favis, 1998b). The percolation threshold is <strong>de</strong>fined as the formation of longrange<br />

connectivity in random systems. Mono-disperse olid droplets typically <strong>de</strong>monstrate a<br />

percolation threshold at values of 0.16 by assuming that the occupation of a site or bond is<br />

completely random. A topic of significant interest in heterophasic polymer blends has been to<br />

examine the various factors which resulting in significant reductions in the percolation threshold<br />

concentration(Gubbels, et al., 1994; Wang & Rubner, 2002). One of the most interesting<br />

approaches towards low percolation thresholds is the <strong>de</strong>velopment of double percolated<br />

structures(Levon, et al., 2002; Sumita, et al., 1992). Zhang et al(Zhang, et al., 2007) reported on<br />

a thermodynamically driven double percolated morphology in an HDPE/PS/PMMA blend which<br />

was essentially a fully continuous system, PS, encapsulating an already continuous system,<br />

PMMA. This type of structure allowed the percolation threshold for the encapsulating polymer to<br />

be reduced to well below 3%. This work <strong>de</strong>monstrated the potential of layering one phase onto<br />

another continuous structure as a powerful technique to reducing percolation thresholds.<br />

In a ternary liquid system complete wetting can be <strong>de</strong>scribed when one phase tends to<br />

spontaneously spread on the second phase in the matrix of third phase. For this purpose, Torza<br />

and Mason(Torza & Mason, 1970) and then Hobbs et al.(Hobbs, et al., 1988) employed modified<br />

Harkins spreading coefficients (λij) which is a simple and useful mathematical expression and<br />

138

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