2011
DOI: 10.1021/ma202017q
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Biaxially Extended Thiophene–Fused Thiophene Conjugated Copolymers for High Performance Field Effect Transistors

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Cited by 29 publications
(31 citation statements)
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References 60 publications
(92 reference statements)
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“…At the same time, the intensity ratios of 2nd peak/3rd peak decreased to be 0.990, 0.987, 0.975, and 0.975 for CF, CF:Tol, CF:CB, and CF:DCB, respectively. These results suggested that the use of higher bp solvent additives assisted the interchain interactions among the polymers in the film state (as discussed further below) [26,27,30]. The interchain interactions were further enforced by thermal annealing, as indicated in Fig.…”
Section: Resultsmentioning
confidence: 74%
“…At the same time, the intensity ratios of 2nd peak/3rd peak decreased to be 0.990, 0.987, 0.975, and 0.975 for CF, CF:Tol, CF:CB, and CF:DCB, respectively. These results suggested that the use of higher bp solvent additives assisted the interchain interactions among the polymers in the film state (as discussed further below) [26,27,30]. The interchain interactions were further enforced by thermal annealing, as indicated in Fig.…”
Section: Resultsmentioning
confidence: 74%
“…The larger core size of IDTT-TPA reduced the repulsion forces between the neighboring bulky side-chain groups and led to am ore coplanar backbone conformationw ith closer molecular packing. [27] The enhanced planarity of IDTT-TPA also increased the lengtho f conjugation. [28] The 4-hexylphenyl groups in IDT-TPA were ar- www.chemsuschem.org ranged slightly perpendicular to the plane of the IDT core, which led to alarge steric hindrance effect in IDT-TPA molecular packing, whereas they were more parallel to the IDTT core in IDTT-TPA,w hich led to decreased steric hindrance along the axis of IDTT-TPA when compared with IDT-TPA.T hus, the rigid ande xtended coplanar structure of IDTT-TPA was beneficial for effective p-stacking, which resulted in mutually parallel aromaticr ings stacking with an offset pattern (Figure 2b).…”
Section: Resultsmentioning
confidence: 99%
“…26,[29][30][31] Therefore, the use of those high bp solvents to improve D-A polymer-based OTFT performances would be beneficial. However, it is difficult to form high quality polymer films by spin-coating such high bp solutions onto hydrophobic gate dielectric surfaces, such as ODTS-treated SiO 2 gate dielectrics.…”
Section: Introductionmentioning
confidence: 99%
“…The band III peaks were observed at 794, 798, and 798 nm for Tol, CB, and DCB, respectively. This red-shift suggests that the highbp solvents promoted the interchain interactions in the solid state 26,31,41. Thermal annealing further redshifted the absorption peaks, indicating a further enhancement in the interchain interactions, as indicated inFigure 4b,c.…”
mentioning
confidence: 96%