Synthesis of 1D-polymer nanowires by a self-assembly method using marginal solvents is an attractive technique. While the formation mechanism is poorly understood, this method is essential in order to control the growth of nanowires. Here we visualized the time-dependent assembly of poly (3-hexyl-thiophene-2,5-diyl) (P3HT) nanowires by atomic force microscopy and scanning tunneling microscopy. The assembly of P3HT nanowires was carried out at room temperature by mixing cyclohexanone (CHN), as a poor solvent, with polymer solution in 1,2-dichlorobenzene (DCB). Both π-π stacking and planarization, obtained at the mix volume ratio of P3HT (in DCB):CHN (10:7), were considered during the investigation. We find that the length of nanowires was determined by the ordering of polymers in the polymer repetition direction. Additionally, our density functional theory calculations revealed that the presence of DCB and CHN molecules that stabilize the structural distortions due to tail group of polymers was essential for the core-wire formation.
Poly (3-hexylthiophene-2,5-diyl) nanowires (nw-P3HT) have been a great interest for organic electronics, including organic field-effect transistors, organic photodetectors, organic photovoltaics, etc due to easy formation in the solution process. Thus both explanations of charge transport dynamics and morphology are crucial for device performance. Here we demonstrated the optoelectronic properties of the P3HT nanowires where the polymer backbones were parallel to the nanowire axis. The nanowires tended to form a bundle due to van der Waals interactions. Nanowire bundles were separated by 1,8-diiodooctane (DIO) additive for photovoltaic fabrication. The bundle separation was visualized by atomic force microscopy. The charge transfer mechanism was evaluated by electrochemical impedance spectroscopy. The electrical analysis showed that short-circuit current density (J
sc) increases to 10.74 mA cm−2 after the bundle separation. According to impedance analysis, there is a correlation between effective lifetime and DIO ratio. These findings were considered as promising results for improving the transport by forming pathways for charge carriers.
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