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We report on X‐ray scattering measurements of helical poly[9,9‐bis(2‐ethylhexyl)‐fluorene‐2,7‐diyl] by mapping the sample with 10 μm spatial resolution from 0.3 GPa to 36 GPa. We follow the strongest 00l reflection, which moves toward higher scattering angles with pressure indicating planarization of helical polyfluorene. Lateral inhomogeneity is increased for >10 GPa concomitant with the solidification of the pressure transmitting medium (a 4:1 mixture of methanol and ethanol). We also follow the 00l reflection with increasing temperature at the constant pressure of 4.3 GPa in neon. We observe a sharp shift toward higher scattering angles indicative of a phase transition at 167–176 °C. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2019, 57, 392–396 X‐ray scattering data from polyfluorene polymer is collected by mapping the sample with 10 μm spatial resolution from 0.3 GPa to 36 GPa. The structural inhomogeneity is characterized. The data are also collected with increasing temperature at 4.3 GPa. A phase transtion is identified at about 170°C. [ABSTRACT FROM AUTHOR]

Based on self-assembly and mimicking strategies occurring in nature, peptide nanomaterials play a unique role in a new generation of hybrid materials for the electronics of the 21st century. This report describes the functionalization of diphenylalanine (FF)-based micro/nanostructures with blue-emitting conducting polymers of the polyfluorene (PF) family. The FF:PF polymer nanocomposites are synthesized by a liquid-vapor phase method. Electron microscopy images reveal di-octyl-substituted PF (PF8) to bind better to the FF micro/nanotubes in comparison with ethyl-hexyl PF (PF2/6), which influences its optical properties. Molecular dynamics simulations of FF nanotubes with monomeric units of PFs show that PF8 favors greater proximity to the grooves on the surface of the nanotubes due to a higher van der Waals interaction energy compared to PF2/6. The FF:PF nanocomposites are further utilized in light-emitting diodes. Biodegradability tests from FF:PF8 nanocomposite films show more than 80% weight loss in 2 h by enzymatic action compared to PF8 pristine films, which do not degrade. Self-assembly of FF nanostructures with organic semiconductors opens up a new generation of biocompatible and biodegradable materials in organic electronics. [ABSTRACT FROM AUTHOR]

ABSTRACT The role of high pressure on a low molecular weight nematic liquid crystalline organic semiconductor, ethyl-hexyl substituted polyfluorene (PF2/6) is investigated using photoluminescence (PL), Raman scattering, and X-ray scattering studies at pressures from 1 to 8 GPa. The PL and the Raman data under pressure are consistent with each other with no abrupt changes in the pressure coefficients of PL or Raman peaks. The PL energies redshift and broaden, consistent with both enhanced intra- and interchain interactions. The Raman peak positions yield pressure coefficients similar to other phenyl based π-conjugated polymers. The broadening of a doublet peak in the 1135 cm−1 region indicates a more planar backbone conformation with increasing pressure. X-ray scattering indicates that the torsion angle between adjacent repeats reduces with increasing pressure and reverts back with decompression. The intermolecular structure is weakly ordered (frozen nematic) and essentially maintained with increasing pressure, in contrast to a high molecular weight PF2/6. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2014, 52, 1014-1023 [ABSTRACT FROM AUTHOR]

Polymer ferroelectrics are playing an increasingly active role in flexible memory application and wearable electronics. The relaxor ferroelectric dielectric, poly(vinylidene fluoride trifluorethylene (PVDF‐TrFE), although vastly used in organic field‐effect transistors (FETs), has issues with gate leakage current especially when the film thickness is below 500 nm. This work demonstrates a novel method of selective poling the dielectric layer. By using solution‐processed 6,13‐bis(triisopropylsilylethynyl)pentacene (TIPS‐pentacene) as the organic semiconductor, it is shown that textured poling of the PVDF‐TrFE layer dramatically improves FET properties compared to unpoled or uniformly poled ferroelectric films. The texturing is achieved by first vertically poling the PVDF‐TrFE film and then laterally poling the dielectric layer close to the gate electrode. TIPS‐pentacene FETs show on/off ratios of 105 and hole mobilities of 1 cm2 Vs−1 under ambient conditions with operating voltages well below −5 V. The electric field distribution in the dielectric layer is simulated by using finite difference time domain methods. The on/off ratios and the carrier mobilities improve by an order of magnitude for the textured poled TIPS‐pentacene field‐effect transistor (FET) compared to the uniformly (vertically) poled FET. Texturing the dielectric layer opens the prospect of achieving low‐operating, high‐performance, low‐cost organic FETs. [ABSTRACT FROM AUTHOR]

The cover page of the journal "Advanced Materials Interfaces" is presented.