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There is a clearly demonstrated relationship between the microstructure, processing and resulting optoelectronic properties of conjugated polymers. Here, we exploited this relationship by exposing polyfluorene thin films to various solvent vapors via confined-solvent vapor annealing to optimize their microstructure, with the final goal being to enhance their emission properties. Our results have demonstrated enlargements in photoluminescence intensity of up to 270%, 258% and 240% when thin films of polyfluorenes of average molecular weights of 105,491 g/mol, 63,114 g/mol and 14,000 g/mol, respectively, experienced increases in their β-phase fractions upon processing. [ABSTRACT FROM AUTHOR]

Biopolymers exhibit a large variety of attractive properties including biocompatibility, flexibility, gelation ability, and low cost. Therefore, especially in more recent years, they have become highly suitable for a wider and wider range of applications stretching across several key sectors such as those related to food packaging, pharmaceutic, and medical industries, just to name a few. Moreover, biopolymers' properties are known to be strongly dependent on the molecular arrangements adopted by such chains at the nanoscale and microscale. Fortunately, these arrangements can be altered and eventually optimized through a plethora of more or less efficient polymer processing methods. Here, we used a space-confined solvent vapor annealing (C-SVA) method to subject various biopolymers to rich swelling in solvent vapors in order to favor their further crystallization or self-assembly, with the final aim of obtaining thin biopolymer films exhibiting more ordered chain conformations. The results obtained by atomic force microscopy revealed that while the gelatin biopolymer nucleated and then crystallized into granular compact structures, other biopolymers preferred to self-assemble into (curved) lamellar rows composed of spherical nanoparticles (glycogen and chitosan) or into more complex helix-resembling morphologies (phytagel). The capability of the C-SVA processing method to favor crystallization and to induce self-assembly in various biopolymeric species or even monomeric units further emphasizes its great potential in the future structuring of a variety of biological (macro)molecules. [ABSTRACT FROM AUTHOR]

L-poly(lactic acid), poly(3-hydroxybutyrate), and poly-hydroxybutyrate-co-hydroxyvalerate are biodegradable polymers that can be obtained from renewable biomass sources. The aim of this study was to develop three types of environmentally friendly film biocomposites of altered microstructure by combining each of the above-mentioned polymers with cellulose nanocrystal fillers and further processing the resulting materials via space-confined solvent vapor annealing. Cellulose was previously obtained from renewable biomass and further converted to cellulose nanocrystals by hydrolysis with the lactic acid. The solutions of biodegradable polymers were spin-coated onto solid substrates before and after the addition of cellulose nanocrystals. The obtained thin film composites were further processed via space-confined solvent vapor annealing to eventually favor their crystallization and, thus, to alter the final microstructure. Indeed, atomic force microscopy studies have revealed that the presence of cellulose nanocrystals within a biodegradable polymer matrix promoted the formation of large crystalline structures exhibiting fractal-, spherulitic- or needle-like morphologies. [ABSTRACT FROM AUTHOR]

In this work, we aim to deliver a comprehensive review of the past and current fabrication and subsequent structural characterization of single crystals of established semiconducting polymers and oligomers while maintaining extra emphasis on the crystals' resulting optoelectronic properties, including charge carrier mobility, conductivity, photovoltaic capability, and the ability to absorb light. [ABSTRACT FROM AUTHOR]

In this study, we have employed a film deposition technique based on convective forces acting at the triple air–solution–substrate contact line to tune the rate of solvent evaporation and, thus, to exert control over the morphology of the resulting mixed lead halide perovskite CH3NH3PbI3-xClx films. By varying the speed of film deposition while processing at two different temperatures, perovskite crystals of various shapes and dimensions were generated upon the crystallization of the initial perovskite precursor ink. More precisely, longer than half a millimeter 3D needle-like perovskite crystals exhibiting sharp edges co-existing with large cross-like 3D perovskite crystals could only be obtained upon the slow deposition of films at a low sample processing temperature of 17 °C, i.e., under conditions of low solvent evaporation rate. On the contrary, the utilization of higher film deposition speeds and/or processing temperatures led to smaller 3D needle-like or quasi-2D rectangular perovskite crystals that often appeared interconnected and coalesced. Moreover, as it was revealed by the photoluminescence measurements, the emission intensity of perovskite crystals was larger and dominated by a shorter wavelength peak, as compared to the uncrystallized material that emitted much less light, but at a longer wavelength. [ABSTRACT FROM AUTHOR]

In this work, we subjected hybrid lead-mixed halide perovskite (CH3NH3PbI3–xClx) precursor inks to different solvent evaporation rates in order to facilitate the nucleation and growth of perovskite crystals. By controlling the temperature of perovskite solutions placed within open-air rings in precise volumes, we established control over the rate of solvent evaporation and, thus, over both the growth rate and the shape of perovskite crystals. Direct utilization of diluted lead-mixed halide perovskites solutions allowed us to control the nucleation and to favor the growth of only a low number of perovskite crystals. Such crystals exhibited a clear sixfold symmetry. While crystals formed at a lower range of temperatures (40–60 °C) exhibited a more compact dendritic shape, the crystals grown at a higher temperature range (80–110 °C) displayed a fractal dendritic morphology. [ABSTRACT FROM AUTHOR]