2015
DOI: 10.1021/am508573q
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Air-Processable Silane-Coupled Polymers to Modify a Dielectric for Solution-Processed Organic Semiconductors

Abstract: Poly(styrene-r-3-methacryloxypropyltrimethoxysilane) (PSMPTS) copolymers were synthesized by the free radical polymerization of styrene and 3-methacryloxypropyltrimethoxysilane (MPTS) for use as surface modifiers. PSMPTS copolymers were spun-cast onto a hydrophilic SiO2 layer and were then annealed at 150 °C in ambient air. The polystyrene (PS)-based copolymer, with a molecular weight of 32 700 g mol(-1) and approximately 30 MPTS coupling sites, was easily grafted onto the SiO2 surface after annealing periods … Show more

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Cited by 6 publications
(3 citation statements)
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“…Materials and Sample Preparation : Styrene (St, Aldrich, ≥99%) was passed through neutral alumina, dried over calcium hydride, distilled under reduced pressure, and degassed using three freeze–pump–thaw cycles . This purification process was also performed for 1,4‐dioxane (Duksan, 99%), methyl ethyl ketone (MEK or 2‐butanone, Duksan, 99%), 2,3,4,5,6‐pentafluorostyrene (PFS, Aldrich, 99%), and 2,2′‐azobisisobutyronitrile (AIBN, Junsei, 96%): AIBN was used after being recrystallized twice in methanol.…”
Section: Methodsmentioning
confidence: 99%
“…Materials and Sample Preparation : Styrene (St, Aldrich, ≥99%) was passed through neutral alumina, dried over calcium hydride, distilled under reduced pressure, and degassed using three freeze–pump–thaw cycles . This purification process was also performed for 1,4‐dioxane (Duksan, 99%), methyl ethyl ketone (MEK or 2‐butanone, Duksan, 99%), 2,3,4,5,6‐pentafluorostyrene (PFS, Aldrich, 99%), and 2,2′‐azobisisobutyronitrile (AIBN, Junsei, 96%): AIBN was used after being recrystallized twice in methanol.…”
Section: Methodsmentioning
confidence: 99%
“…Another concept uses polymers with related functional side chains containing cross-linkable moieties which can uniquely react with each other under a thermal or UV treatment. [20][21][22][23][24] No separate cross-linking unit is necessary. Examples thereof are polyacrylates functionalized by hydroxyl and epoxy groups.…”
Section: Introductionmentioning
confidence: 99%
“…10 The roughness, surface energy and trap density of the dielectric lm have directly inuenced the morphology of the active layer and then further determined the transport of the charge carrier. [11][12][13] In addition, an uneven dielectric location over a large area results in a wide distribution of the device performances, which is a handicap in the fabrication of qualied organic circuits. 14 At present, there are three kinds of dielectric in organic electronics: inorganic insulators, self-assembled monolayer (SAM) dielectrics and polymer dielectrics.…”
Section: Introductionmentioning
confidence: 99%