RESUMEN
We show that surface electronic properties of poly-3-hexylthiophene (P3HT) crystalline nanofibers as probed by Kelvin probe force microscopy (KPFM) depends sensitively on the degree of polymer packing order and dominant coupling type (e.g., H- or J-aggregate) as signaled by absorption or photoluminescence spectroscopy. Nominal HOMO energies between high molecular weight (J-aggregate) nanofibers and low-molecular weight (H-aggregate) nanofibers differ by ≈160 meV. This is consistent with shifts expected from H-type charge-transfer (CT) interactions that lower HOMO energies according to registration between thiophene moieties on adjacent polymer chains. These results show how KPFM combined with wavelength-resolved photoluminescence imaging can be used to extract information on "dark" (CT) interactions in polymer assemblies.
RESUMEN
Combined Kelvin probe force microscopy and wavelength-resolved photoluminescence measurements on individual pre- and post-cross-linked poly(3-hexylthiophene)-b-poly(3-methyl alcohol thiophene) (P3HT-b-P3MT) nanofibers have revealed striking differences in their optical and electronic properties driven by structural perturbation of the crystalline aggregate nanofiber structures after cross-linking. Chemical cross-linking from diblock copolymer P3HT-b-P3MT using a hexamethylene diisocyanate cross-linker produces a variety of morphologies including very small nanowires, nanofiber bundles, nanoribbons, and sheets, whose relative abundance can be controlled by reaction time and cross-linker concentration. While the different cross-linked morphologies have almost identical photophysical characteristics, KPFM measurements show that the surface potential contrast, related to the work function of the sample, depends sensitively on nanostructure morphology related to chain-packing disorder.
RESUMEN
We show that mechanically and chemically robust functionalized poly(3-hexylthiophene) (P3HT) nanofibers can be made via chemical cross-linking. Dramatically different photophysical properties are observed depending on the choice of functionalizing moiety and cross-linking strategy. Starting with two different nanofiber families formed from (a) P3HT-b-P3MT or (b) P3HT-b-P3ST diblock copolymers, cross-linking to form robust nanowire structures was readily achieved by either a third-party cross-linking agent (hexamethylene diisocyanate, HDI) which links methoxy side chains on the P3MT system, or direct disulfide cross-link for the P3ST system. Although the nanofiber families have similar gross structure (and almost identical pre-cross-linked absorption spectra), they have completely different photophysics as signaled by ensemble and single nanofiber wavelength- and time-resolved photoluminescence as well as transient absorption (visible and near-IR) probes. For the P3ST diblock nanofibers, excitonic coupling appears to be essentially unchanged before and after cross-linking. In contrast, cross-linked P3MT nanofibers show photoluminescence similar in electronic origin, vibronic structure, and lifetime to unaggregated P3HT molecules, e.g., dissolved in an inert polymer matrix, suggesting almost complete extinction of excitonic coupling. We hypothesize that the different photophysical properties can be understood from structural perturbations resulting from the cross-linking: For the P3MT system, the DIC linker induces a high degree of strain on the P3HT aggregate block, thus disrupting both intra- and interchain coupling. For the P3ST system, the spatial extent of the cross-linking is approximately commensurate with the interlamellar spacing, resulting in a minimally perturbed aggregate structure.
RESUMEN
Nanoparticles derived from π-conjugated polymers have gained widespread attention as active layer materials in various organic electronics applications. The optoelectronic, charge transfer, and charge transport properties of π-conjugated polymers are intimately connected to the polymer aggregate structure. Herein we show that the internal aggregate structure of regioregular poly(3-hexylthiophene) (P3HT) within polymer nanoparticles can be tuned by solvent composition during nanoparticle fabrication through the miniemulsion process. Using absorption spectra and single-NP photoluminescence decay properties, we show that a solvent mixture consisting of a low boiling good solvent and a high boiling marginal solvent results in polymer aggregate structure with a higher degree of uniformity and structural order. We find that the impact of solvent on the nature of P3HT aggregation within nanoparticles is different from what has been reported in thin films.
RESUMEN
We report wavelength and time-resolved photoluminescence studies of isolated extended (1-10 µm length) poly(3-hexylthiophene) (P3HT) nanofibers (xNFs) cast on glass from suspension. The PL spectra of xNFs show multiple vibronic replicas that appear to be associated with the existence of both H- and J-type aggregates. The PL spectra of xNFs made from regioregular (rr)- (93%) and highly regioregular (hrr)-P3HT (98%) both show similarities in PL spectra suggestive of common chain packing features, as well as subtle differences that can be attributed to higher long-range order in the hrr-xNFs. Specifically, PL spectral measurements on isolated xNFs made from highly regioregular (>98%) P3HT showed a red-shifted electronic origin (≈30 meV) and increased 0-0/0-1 PL intensity ratio for the J-type species, suggestive of enhanced structural coherence length and intrachain order.