Nanoparticles may act as compatibilizing agents for blending of immiscible polymers, leading to changes in blend morphology through a variety of mechanisms including interfacial adsorption, aggregation, and nucleation of polymer crystals. Herein, we report an approach to define highly structured donor/acceptor networks based on poly(3-hexylthiophene) (P3HT) and CdSe quantum dots (QDs) by demixing from an insulating polystyrene (PS) matrix. The incorporation of QDs led to laterally phase-separated co-continuous structures with sub-micrometer dimensions, and promoted crystallization of P3HT, yielding highly interconnected P3HT/QD hybrid nanowires embedded in the polymer matrix. These nanohybrid materials formed by controlling phase separation, interfacial activity, and crystallization within ternary donor/acceptor/insulator blends, offer attractive morphologies for potential use in optoelectronics.
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http://dx.doi.org/10.1039/c8sm01001c | DOI Listing |
Soft Matter
June 2018
Polymer Science and Engineering Department, University of Massachusetts, Amherst, Massachusetts 01003, USA.
Nanoparticles may act as compatibilizing agents for blending of immiscible polymers, leading to changes in blend morphology through a variety of mechanisms including interfacial adsorption, aggregation, and nucleation of polymer crystals. Herein, we report an approach to define highly structured donor/acceptor networks based on poly(3-hexylthiophene) (P3HT) and CdSe quantum dots (QDs) by demixing from an insulating polystyrene (PS) matrix. The incorporation of QDs led to laterally phase-separated co-continuous structures with sub-micrometer dimensions, and promoted crystallization of P3HT, yielding highly interconnected P3HT/QD hybrid nanowires embedded in the polymer matrix.
View Article and Find Full Text PDFMacromol Rapid Commun
August 2009
National Center for Nanoscience and Technology, China, Beijing 100190, P. R. China; Graduate School of Chinese Academy of Sciences, Beijing, 100039, P. R. China.
A facile approach to prepare poly(3-hexylthiophene) (P3HT)/cadmium selenide quantum dot (CdSe QD) hybrid coaxial nanowires by a stepwise self-assembly process is reported. P3HT nanowires of ≈20 nm diameter are first prepared by self-assembly in a poor solvent such as cyclohexanone, and then as-prepared CdSe QDs are deposited compactly onto the P3HT nanowires by non-covalent interactions between P3HT and CdSe. When illuminated with white light, the hybrid nanowires show enhanced photoconductivity compared with the pristine P3HT nanowires and the blended nanocomposites.
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