Supramolecular assemblies that interact with light have recently garnered much interest as well-defined nanoscale materials for electronic excitation energy collection and transport. However, to control such complex systems it is essential to understand how their various parts interact and whether these interactions result in coherently shared excited states (excitons) or in diffusive energy transport between them. Here, we address this by studying a model system consisting of two concentric cylindrical dye aggregates in a light-harvesting nanotube. Through selective chemistry we are able to unambiguously determine the supramolecular origin of the observed excitonic transitions. These results required the development of a new theoretical model of the supramolecular structure of the assembly. Our results demonstrate that the two cylinders of the nanotube have distinct spectral responses and are best described as two separate, weakly coupled excitonic systems. Understanding such interactions is critical to the control of energy transfer on a molecular scale, a goal in various applications ranging from artificial photosynthesis to molecular electronics.
A fully consistent model for the exciton band structure of double-walled 3,3′-bis(2-sulfopropyl)-5,5′,6,6′tetrachloro-1,1′-dioctylbenzimidacarbocyanine (C8S3) J-aggregates was developed using reduced linear dichroism (LD r ) spectroscopy on flow aligned samples. Chemical oxidation was utilized to "turn off"outer wall optical absorption and produce stable aggregate samples with a simplified absorption profile associated only with the nanotube inner wall. The oxidized aggregates were aligned in a flow cell to collect LD r spectra; these spectra reveal a series of both polarized and isotropic transitions. Four spectral transitions, assigned to be purely parallel or perpendicular to the aggregate long axis, that fit both the experimental LD r and isotropic spectra were used create a model for oxidized J-aggregate excitonic absorption. The LD r spectral study was repeated using pristine J-aggregates, and the spectrum for the full double-walled J-aggregates could be fit using six total transitions: four from the oxidized fit and two additional transitions distinct to the outer wall. A quantitative model that agrees with experimental absorption and emission spectral results and aligns with current theory was constructed wherein the energies and polarizations of excitonic transitions remained consistent for both the unperturbed and chemically oxidized C8S3 Jaggregates. The polarization studies also reveal, in contrast to the strongly polarized transitions that comprise the low-energy region of the excitonic aggregate spectrum, that the high-energy absorption is unpolarized and attributed to highly localized exciton transitions that arise due to disorder.
The effect of molecular weight on the formation of β phase poly(9,9'-dioctylfluorene) (PF8) was studied in dilute solutions. Temperature-dependent fluorescence experiments of unique synthetic batches as well as size-excluded single batches of polyflourene were studied. Each batch had unique molecular weight, tetrahedral defect concentration, and polydispersity index (PDI). Polyflourene was found to exhibit a temperature-dependent transition between two phases with distinct electronic transition signatures: the α (primary) phase and the β (secondary) phase. In dilute solutions, the temperature at which the polymer exhibited a conversion between these phases showed a clear dependence on molecular weight. We model this transition temperature for β phase formation using the mean field theory for the coil-globule transition developed by Isaac Sanchez. Results show that temperature affects the average end-to-end distance corresponding to increases in secondary electronic absorption and that the dependence on temperature related to the coil-globule transition.
A microscope-CCD setup has been developed as an analytical tool for the detection of diffraction from one-dimensional redox-active transition-metal oxide gratings prepared with a combination of microtransfer molding (microTM) and cathodic electrodeposition. The diffraction efficiencies (DE) of tungsten trioxide, WO3, and binary molybdenum-tungsten trioxide, Mo0.6W0.4O3, gratings were measured during Li+ insertion/deinsertion experiments performed with both cyclic voltammetry and chronoamperometry in 1 M LiClO4/propylene carbonate. The DE was evaluated in terms of the optical constants of the grating materials determined by spectroscopic ellipsometry (SE) measurements of Li+ insertion/deinsertion into unpatterned thin films. The effect of grating thickness and the amount of inserted charge on DE has been analyzed. The diffraction method is used to quantitatively estimate lithium ion diffusion coefficients of electrochemically active metal oxide gratings.
The formation of a ketone defect at the 9-site along the backbone of dialkyl polyfluorenes has been shown to be directly involved in the degradation of the polymer's emission from blue to an undesirable green. Films of poly(9,9′-dihexylfluorene) (PFH) with and without ketone defects were annealed above their liquid crystalline phase transition in an inert argon atmosphere, and their emission spectra were collected in order to study the effect of morphology on the energy transfer to ketone defects. The annealing was performed in situ in the fluorometer, allowing for a direct comparison of the absolute changes in the emission spectra. Annealing of the films resulted in regions of highly aligned polymer chains as confirmed by atomic force microscopy. After annealing, the fluorescence spectra of pristine films (without ketone defects) exhibited no green emission, indicating the lack of thermal oxidation in the inert atmosphere. However, these films did show an increase in fluorescence quantum yield, revealing that high polymer order does not lead to interchain electronic species that quench the excited states. Annealing of partially photobleached PFH films revealed that an increase in the polymer chain order of a film containing a few defects resulted in an increase in green emission and decrease in blue without the creation of further defects. The increase in green emission combined with the decreased blue can only be the result of increased energy transfer from pristine chromophores to ketone sites, as the aligned polymer chains increase exciton diffusion. PFH films containing defects that were annealed beneath the LC temperature of the polymer did not result in any spectral changes, indicating that alignment of polymer chains was necessary for the increased energy transfer to the defect sites.
The redox chemistry of supramolecular nanotubes self-assembled from amphiphilic cyanine dye 3,3 0 -bis-(2-sulfopropyl)-5,5 0 ,6,6 0 -tetrachloro-1,1 0 -dioctylbenzimidacarbocyanine (C8S3) in aqueous solution was investigated by spectroelectrochemistry. The absorption spectra during the redox-reaction were analyzed by singular value decomposition (SVD) and semiempirical quantum mechanical calculations. Previously unavailable absorption spectra were modeled for each species of the reaction at every point throughout the oxidation and reduction process. The expected peak absorption wavelengths of these species present throughout the electrochemical cycles were calculated using the semiempirical method ZINDO/S (Zerner method of intermediate neglect of differential overlap for spectroscopy). The spectral assignments from the proposed species derived from the SVD analysis were confirmed with the ZINDO/S calculations, supporting the assignment of the key species as well as the intermediates in the proposed redox-reaction scheme. The oxidized species have spectral signatures that agree with the calculated spectral maxima of isolated species, indicating that the resulting products are not electronically perturbed by aggregation, in strong contrast to the unoxidized dye.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.