RESUMEN
A subphase exchange cell was designed to observe fluid-fluid interfaces with a conventional optical microscope while simultaneously changing the subphase chemistry. Materials including phospholipids, asphaltenes, and nanoparticles at fluid-fluid interfaces exhibit unique morphological changes as a function of the bulk-phase chemistry. These changes can affect their interfacial material properties and, ultimately, the emergent bulk material properties of the films, foams, and emulsions produced from such interfacial systems. In this work, we combine experiments, computational fluid dynamics simulations, and modeling to establish the operating parameters for a subphase exchange cell of this type to reach a desired concentration. We used the experimental setup to investigate changes to a graphene film during a common wet-etching transfer process. Observations reveal that capillary interactions can induce defects and deformations in the graphene film during the wet-etching process, an important finding that must be considered for any wet-etching transfer technique for 2D materials. More generally, conventional optical microscopy was shown to be able to image the dynamics of interfacial systems during a bulk-phase chemistry change. Potential applications for this equipment and technique include observing morphological dynamics of phospholipid film structure with subphase salinity, asphaltene film structure with subphase pH, and particle film synthesis with subphase chemistry.
RESUMEN
The understanding of the structure-mechanical property relationship for semiconducting polymers is essential for the application of flexible organic electronics. Herein pseudo free-standing tensile testing, a technique that measures the mechanical property of thin films floating on the surface of water, is used to obtain the stress-strain behaviors of two semiconducting polymers, poly(3-hexylthiophene) (P3HT) and poly(2,5-bis(2-decyltetradecyl)-3,6-di(thiophen-2-yl)diketopyrrolo[3,4-c]pyrrole-1,4-dione-alt-thienovinylthiophene (DPP-TVT) donor-acceptor (D-A) polymer. To our surprise, DPP-TVT shows similar viscoelastic behavior to P3HT, despite DPP-TVT possessing a larger conjugated backbone and much higher charge carrier mobility. The viscoelastic behavior of these polymers is due to sub room temperature glass transition temperatures (Tg ), as shown by AC chip calorimetry. These results provide a comprehensive understanding of the viscoelastic properties of conjugated D-A polymers by thickness-dependent, strain rate dependent, hysteresis tests, and stress-relaxation tests, highlighting the importance of Tg for designing intrinsically stretchable conjugated polymers.