2011
DOI: 10.1016/j.mseb.2011.05.008
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Influence of P3HT concentration on morphological, optical and electrical properties of P3HT/PS and P3HT/PMMA binary blends

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Cited by 39 publications
(22 citation statements)
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“…Microscopy images of the active layer inkjet‐printed on EC (Figure e,f) show the difference in morphology of the pristine semiconductor compared to the P3HT:PS blend. The latter, differently from the homogeneity of the pristine P3HT film, presents the features typical of a phase‐separated sea‐island morphology, the darker area likely constituting a percolative semiconducting path through PS islands . The positive impact of blending on the device performances is evinced by an average increase of hole mobility of almost two orders of magnitude, consistent with what obtained by Lu et al, who witnessed an enhanced crystalline order of P3HT when embedded in an inert matrix.…”
supporting
confidence: 87%
“…Microscopy images of the active layer inkjet‐printed on EC (Figure e,f) show the difference in morphology of the pristine semiconductor compared to the P3HT:PS blend. The latter, differently from the homogeneity of the pristine P3HT film, presents the features typical of a phase‐separated sea‐island morphology, the darker area likely constituting a percolative semiconducting path through PS islands . The positive impact of blending on the device performances is evinced by an average increase of hole mobility of almost two orders of magnitude, consistent with what obtained by Lu et al, who witnessed an enhanced crystalline order of P3HT when embedded in an inert matrix.…”
supporting
confidence: 87%
“…Hence, this technique has been extensively used in plastics, rubbers, composites, and adhesives. [1][2][3] The properties of the blend depend on the degree of compatibility or miscibility of the polymers at molecular mixing; blends can be classified as a compatible blend or completely miscible and incompatible or immiscible blends. [4][5][6] The polymer miscibility is due to some specific interactions such as dipole-dipole forces, hydrogen bonding, and charge transfer complex between the polymer segments.…”
mentioning
confidence: 99%
“…Poly (3-hexyl thiophene) was synthesized by direct oxidation of 3-hexyl thiophene using Fe(III) as catalyst according to literature [14,15]. Anhydrous FeCl 3 (0.02 mol, 3.2 g) was dissolved in chloroform (40 mL) and stirred for 20 min.…”
Section: Preparation Of Poly (3-hexyl Thiophene)mentioning
confidence: 99%