Morphological origin of super toughness in poly(ethylene terephthalate)/polyethylene blends

A compatibilization strategy for poly(ethylene terephthalate) (PET) and polyethylene (PE) blends to achieve high toughness is described. Maleic anhydride functionalized styrene–ethylene–butylene–styrene (MA-g-SEBS) block copolymer at 20 pph was found to produce an intricate multidomain morphology in which the two major components (50% PE, 50% PET) and the compatibilizer coexist on a hierarchal order. A portion of the PET was dispersed as interconnected rodlike domains oriented along the injection direction. The rest of the PET and the PE constituted beadlike nano domains which served as the matrix. The blend at all these morphological levels responded to deformation in a cooperative fashion giving rise to a super tough material. That is, a blend whose elongation at break (600%) was superior to its two major components (90% for PET and 300% for PE). © 1993 John Wiley & Sons, Inc.     

Impact of Processing on Structural and Compositional Evolution in Mixed Metal Halide Perovskites during Film Formation

Understanding crystallization processes and their pathways in metal‐halide perovskites is of crucial importance as this strongly affects the film microstructure, its stability, and device performance. While many approaches are developed to control perovskite formation, the mechanisms of film formation are still poorly known. Using time‐resolved in situ grazing incidence wide‐angle X‐ray scattering, the film formation of perovskites is investigated with average stoichiometry Cs_0.15FA_0.85PbI₃, where FA is formamidinium, using the popular antisolvent dropping and gas jet treatments and this is contrasted with untreated films. i) The crystallization pathways during spin coating, ii) the subsequent postdeposition thermal annealing, and iii) crystallization during blade coating are studied. The findings reveal that the formation of a nonperovskite FAPbI₃ phase during spin coating is initially dominant regardless of the processing and that the processing treatment (e.g., antisolvent dropping, gas jet) has a significant impact on the as‐cast film structure and affects the phase evolution during subsequent thermal treatment. It is shown that blade coating can be used to overcome the nonperovskite phase formation via solvothermal direct crystallization of perovskite phase. This work shows how real‐time investigation of perovskite formation can help to establish processing–microstructure–functionality relationships.     

Solvent Additives: Key Morphology‐Directing Agents for Solution‐Processed Organic Solar Cells

Organic photovoltaics (OPV) have the advantage of possible fabrication by energy‐efficient and cost‐effective deposition methods, such as solution processing. Solvent additives can provide fine control of the active layer morphology of OPVs by influencing film formation during solution processing. As such, solvent additives form a versatile method of experimental control for improving organic solar cell device performance. This review provides a brief history of solution‐processed bulk heterojunction OPVs and the advent of solvent additives, putting them into context with other methods available for morphology control. It presents the current understanding of how solvent additives impact various mechanisms of phase separation, enabled by recent advances in in situ morphology characterization. Indeed, understanding solvent additives' effects on film formation has allowed them to be applied and combined effectively and synergistically to boost OPV performance. Their success as a morphology control strategy has also prompted the use of solvent additives in related organic semiconductor technologies. Finally, the role of solvent additives in the development of next‐generation OPV active layers is discussed. Despite concerns over their environmental toxicity and role in device instability, solvent additives remain relevant morphological directing agents as research interests evolve toward nonfullerene acceptors, ternary blends, and environmentally sustainable solvents.     

A Low Temperature Route toward Hierarchically Structured Titania Films for Thin Hybrid Solar Cells

The requirement of high‐temperature calcination for titanium dioxide in (solid‐state) dye‐sensitized solar cells (DSSCs) implies challenges with respect to reduced energy consumption and the potential for flexible photovoltaic devices. Moreover, the use of dye molecules increases production costs and leads to problems related with dye bleaching. Therefore, fabrication of dye‐free hybrid solar cells at low temperature is a promising alternative for current DSSC technology. In this work the authors fabricate hierarchically structured titania thin films by combining a polystyrene‐block‐polyethylene oxide template assisted sol–gel synthesis with nano‐imprint lithography at low temperatures. The achieved films are filled with poly(3‐hexylthiophene) to form the active layer of hybrid solar cells. The surface morphology is probed via scanning electron microscopy and atomic force microscopy, and the bulk film morphology is examined with grazing incidence X‐ray scattering. Good light absorption by the active layer is proven by UV–vis spectroscopy. An enhancement in light absorption is observed and ascribed to light scattering in mesoporous titania films with imprinted superstructures. Accordingly a better photovoltaic performance is found for nano‐imprinted solar cells at various angles of light incidence.     

Vertical Phase Separation in Small Molecule:Polymer Blend Organic Thin Film Transistors Can Be Dynamically Controlled

Blending of small‐molecule organic semiconductors (OSCs) with amorphous polymers is known to yield high performance organic thin film transistors (OTFTs). Vertical stratification of the OSC and polymer binder into well‐defined layers is crucial in such systems and their vertical order determines whether the coating is compatible with a top and/or a bottom gate OTFT configuration. Here, we investigate the formation of blends prepared via spin‐coating in conditions which yield bilayer and trilayer stratifications. We use a combination of in situ experimental and computational tools to study the competing effects of formulation thermodynamics and process kinetics in mediating the final vertical stratification. It is shown that trilayer stratification (OSC/polymer/OSC) is the thermodynamically favored configuration and that formation of the buried OSC layer can be kinetically inhibited in certain conditions of spin‐coating, resulting in a bilayer stack instead. The analysis reveals here that preferential loss of the OSC, combined with early aggregation of the polymer phase due to rapid drying, inhibit the formation of the buried OSC layer. The fluid dynamics and drying kinetics are then moderated during spin‐coating to promote trilayer stratification with a high quality buried OSC layer which yields unusually high mobility >2 cm² V^?1 s^?1 in the bottom‐gate top‐contact configuration.     

On‐The‐Fly Tracking of Flame Surfaces for the Visual Analysis of Combustion Processes

The visual analysis of combustion processes is one of the challenges of modern flow visualization. In turbulent combustion research, the behaviour of the flame surface contains important information about the interactions between turbulence and chemistry. The extraction and tracking of this surface is crucial for understanding combustion processes. This is impossible to realize as a post‐process because of the size of the involved datasets, which are too large to be stored on disk. We present an on‐the‐fly method for tracking the flame surface directly during simulation and computing the local tangential surface deformation for arbitrary time intervals. In a massively parallel simulation, the data are distributed over many processes and only a single time step is in memory at any time. To satisfy the demands on parallelism and accuracy posed by this situation, we track the surface with independent micro‐patches and adapt their distribution as needed to maintain numerical stability. With our method, we enable combustion researchers to observe the detailed movement and deformation of the flame surface over extended periods of time and thus gain novel insights into the mechanisms of turbulence–chemistry interactions. We validate our method on analytic ground truth data and show its applicability on two real‐world simulations.     

On the mechanism of pressure-induced environmental stress cracking in polystyrene

Fluids conventionally classified as inert exert a strong stress crazing and cracking effect on certain amorphous polymers when they are deformed in tension under pressure. Fourier transform infra-red difference spectroscopy has been utilized to measure the concentration of trace amounts of fluid penetrating the polymer during deformation. Measurable fluid penetration was found to take place only in dilated structures as large as crazes. The penetration level depended upon craze density and structure, viscosity of the fluid and the time or rate of the experiment. At atmospheric pressure, the penetrating fluid front lagged behind the dry growing craze tip. Radial concentration distributions were successfully described by a semiquantitative porous transport model which yielded a specific penetration coefficient. This coefficient was a strong function of the hydrostatic pressure and the viscosity of the penetrating fluid. It is suggested that the hydrostatic pressure decreases the void content in the polymeric solid, yet due to the pressure gradient, concurrently enhances the dynamics of fluid transport. At a critical pressure, the polymer undergoes the brittle-to-ductile transition. Here irreversible deformation by shear is preferred over the void forming craze or cracking mechanism.Presented in part to the Third International Conference on Mechanical Behaviour of Materials, held in Cambridge, UK, 20–24 August 1979.