Polymer blend

About: Polymer blend is a research topic. Over the lifetime, 18474 publications have been published within this topic receiving 437183 citations. The topic is also known as: polymer mixture & Polymerblend 或者 Polyblend.

Small Molecule/Polymer Blend Organic Transistors with Hole Mobility Exceeding 13 cm V−1 s−1

Abstract: A ternary organic semiconducting blend composed of a small-molecule, a conjugated polymer, and a molecular p-dopant is developed and used in solution-processed organic transistors with hole mobility exceeding 13 cm(2) V(-1) s(-1) (see the Figure). It is shown that key to this development is the incorporation of the p-dopant and the formation of a vertically phase-separated film microstructure.

Charge-transfer states in conjugated polymer/fullerene blends: Below-gap weakly bound excitons for polymer photovoltaics

Abstract: We report on the observation of a charge-transfer state forming at the molecular interface between a conjugated polymer and a fullerene based electron acceptor. Electron hole recombination in this state results in a luminescent transition at 840nm, energetically separated from the polymer emission. This transition can be directly photoexcited by tuning the excitation energy below the conjugated polymer bandgap, demonstrating that the charge-transfer state originates from a ground-state interaction. By electric field induced quenching of the photoluminescence, we determine a binding energy of 130meV for excitons in the charge-transfer state.

Interfacial tension reduction in PBT/PE/clay nanocomposite

Abstract: We investigated the effect of organically modified nanoclay (organoclay) on immiscible polymer blends [polybutylene terephthalate (PBT)/polyethylene (PE)] with a special focus on the role of clay as a compatibilizer. When organoclay (Nanofil 919; Sud-Chemie, Inc.) is added to the blend, the clay first locates at the interface and then selectively locates in the PBT phase due to its affinity with PBT. This results in effective size reduction and narrowed size distribution of the dispersed phase. However, with a small amount of organoclay, it is observed that the clay locates at the interface regardless of its affinity for a specific component to minimize the chemical potential. The interfacial tension change of the blend with the addition of organoclay was quantitatively predicted from extensional force measurement. When the blend is subjected to an extension, the interfacial tension functions as a resistance against drop deformation. When we added organoclay to the blend, the extensional force was significantly reduced, which means that the contribution of the interfacial tension to the total force is reduced. For a 10/90 PBT/PE blend, the interfacial tension was reduced from 5.76 to 0.14 cN m−1 when 1 wt% of organoclay was added. This interfacial tension reduction arises from the localization of the organoclay at the interface and its nonhomogeneous distribution along the interface, suppressing the coalescence between the droplets, which is a role of a compatibilizer. Conclusively, the immiscible polymer blends can be compatibilized with organoclay. The organoclay changes the blend morphology by interfacial tension reduction due to the localization of the organoclay at the interface and by the viscosity ratio change due to the selective localization by its affinity to a specific component in the blend.

Structural, optical, morphological and thermal properties of PEO/PVP blend containing different concentrations of biosynthesized Au nanoparticles

Abstract: Casting technique was used for preparation of polyethylene oxide (PEO)/polyvinyl pyrrolidone (PVP) (70/30 wt.%) films filled with different concentrations of gold nanoparticles (Au NPs). X-ray diffraction (XRD) pattern proved the semi-crystalline nature of the pristine and filled polymer blend. Fourier transform infrared (FT-IR) and Ultraviolet/Visible (UV/Vis.) analyses were used to retrace the structural and optical changes with increasing Au content. UV/Vis. analysis spectroscopy was utilized to calculate the optical properties such as optical energy gap E g , refractive index n and Urbach energy E u for blend/Au nanocomposite films. Scanning electron micrograph (SEM) suggested the dependence of morphological structure on filling level and the surface morphology changed from rough to smooth. Transmission electron microscope (TEM) micrographs showed that the size of Au NPs was increased with continuous filling in PEO/PVP. Thermogravimetric analysis (TGA) was performed to investigate the thermal stability for nanocomposite films.

Electrospinning and Solution Properties of Nafion and Poly(acrylic acid)

Abstract: In this study, the electrospinning performance and solution properties of Nafion and its blend with another polyelectrolyte, poly(acrylic acid) (PAA), were investigated. Attempts to electrospin pure Nafion at various polymer concentrations (5−35 wt %), solvents, neutralization, and electrospinning conditions resulted in electrospraying rather than electrospinning. However, a polymer solution blend (5 wt %) of Nafion and PAA resulted in beaded fibers at 8 wt % PAA and smooth electrospinning above 12% PAA. Fiber sizes of the blend increased from 90 to 600 nm with increasing PAA content. Dynamic light scattering on pure Nafion solutions in various solvents reveals large aggregates (i.e., dispersion) of various sizes due to polymer backbone and ionic interactions. The lack of sufficient polymer chain entanglement evidenced by low viscosity and aggregate formation in Nafion solutions prohibits fiber formation during electrospinning. The addition of PAA to Nafion modifies the ionic strength of the solvent resul...