Fluorination Enables Tunable Molecular Interaction and Photovoltaic Performance in Non-Fullerene Solar Cells Based on Ester-Substituted Polythiophene

Owing to the advantages of low synthetic cost and high scalability of synthesis, polythiophene and its derivatives (PTs) have been of interest in the community of organic photovoltaics (OPVs). Nevertheless, the typical efficiency of PT based photovoltaic devices reported so far is much lower than those of the prevailing push-pull type conjugated polymer donors. Recent studies have underscored that the excessively low miscibility between PT and nonfullerene acceptor is the major reason accounting for the unfavorable active layer morphology and the inferior performance of OPVs based on a well-known PT, namely PDCBT-Cl and a non-halogenated nonfullerene acceptor IDIC. How to manipulate the miscibility between PT and acceptor molecule is important for further improving the device efficiency of this class of potentially low-cost blend systems. In this study, we introduced different numbers of F atoms to the end groups of IDIC to tune the intermolecular interaction of the hypo-miscible blend system (PDCBT-Cl:IDIC). Based on calorimetric, microscopic, and scattering characterizations, a clear relationship between the number of F atoms, miscibility, and device performance was established. With the increased number of F atoms in IDIC, the resulting acceptors exhibited enhanced miscibility with PDCBT-Cl, and the domain sizes of the blend films were reduced substantially. As a result, distinctively different photovoltaic performances were achieved for these blend systems. This study demonstrates that varying the number of F atoms in the acceptors is a feasible way to manipulate the molecular interaction and the film morphology toward high-performance polythiophene:nonfullerene based OPVs.

Effect of Sulfonation Degree and PVDF Content on the Structure and Transport Properties of SPEEK/PVDF Blend Membranes

Sulfonated poly (ether ether ketone) (SPEEK) with four different sulfonation degrees (SDs) were prepared, and mixed with polyvinylidene fluoride (PVDF) to prepare four series of SPEEK/PVDF blend membranes. The miscibility between SPEEK and PVDF was investigated by observing the micro-morphologies. The miscible blend membranes were found in the SPEEK/PVDF blend membranes in which either SPEEK had relatively low SD or consisted of low content of one component (either SPEEK or PVDF). The PVDF crystallinity was found to decrease in the SPEEK/PVDF membranes that had better blend miscibility. With the increase of PVDF content, all the blend membranes exhibited the decreased proton conductivity and methanol permeability, and the miscible blend membranes decreased more slowly than the immiscible ones.

Blend configuration in functional polymeric materials with a high lignin content

Lignins upgrade the lignocellulosic cell-wall domains in all vascular plants; they embody 20–30% of terrestrial organic carbon. For 50 years, mistaken assumptions about the configuration of lignin have hindered the development of useful polymeric materials with a lignin content above 40 wt%. Now, polymeric materials composed only of methylated softwood lignin derivatives can exhibit better tensile behavior than polystyrene. Marked improvements may be achieved with small quantities (5–10 wt%) of miscible blend components as simple as poly(ethylene glycol). These observations contradict commonly held views about crosslinking or hyper-branching in lignin chains. The hydrodynamic compactness of the macromolecular lignin species arises from powerful noncovalent interactions between the lignin substructures. Individual lignin components undergo association to form macromolecular complexes that are preserved in plastics with a very high lignin content. Material continuity results from interpenetration between the peripheral components in adjoining lignin complexes. Through interactions with the peripheral domains, miscible blend components modulate the strength and ductility of these utterly original lignin-based plastics.