Enhancement of Proton Conductivity Performance in High Temperature Polymer Electrolyte Membrane, Processed the Adding of Pyridobismidazole.

A pyridobisimidazole unit was introduced into a polymer backbone to obtain an increased doping level, a high number of interacting sites with phosphoric acid and simple processibility. The acid uptake of poly(pyridobisimidazole) (PPI) membrane could reach more than 550% (ADL = 22), resulting in high conductivity (0.23 S·cm at 180 °C).

pH-Dependent complexation and polyelectrolyte chain conformation of polyzwitterion-polycation coacervates in salted water.

The phase behavior and chain conformational structure of biphasic polyzwitterion-polyelectrolyte coacervates in salted aqueous solution are investigated with a model weak cationic polyelectrolyte, poly(2-vinylpyridine) (P2VP), whose charge fraction can be effectively tuned by pH. It is observed that increasing the pH leads to the increase of the yielding volume fraction and the water content of dense coacervates formed between net neutral polybetaine and cationic P2VP in contrast to the decrease of critical salt concentration for the onset of coacervation, where the P2VP charge fraction is reduced correspondingly. Surprisingly, a single-molecule fluorescence spectroscopic study suggests that P2VP chains upon coacervation seem to adopt a swollen or an even more expanded conformational structure at higher pH.

Dynamics of Confined Microgel Liquids: Weakened Spatial Confinement Effect by Microgel Particle Compliance.

Spatial confinement has a great impact on the structures and dynamics of interfacial molecular and polymer liquid films. Most prior research has focused on confined liquids of fixed material compliance and often treated them in approximation to the "hard-sphere" interaction model. In this study, we microscopically investigate the structural dynamics of highly deformable poly(-isopropylacrylamide) (PNIPAM) microgels confined between two solid surfaces in comparison to that of nearly nondeformable microgels of the same chemistry.

Accelerated Amidization of Branched Poly(ethylenimine)/Poly(acrylic acid) Multilayer Films by Microwave Heating.

Chemical cross-linking of layer-by-layer assembled films promotes mechanical stability and robustness in a wide variety of environments, which can be a challenge for polyelectrolyte multilayers in saline environments or for multilayers made from weak polyelectrolytes in environments with extreme pHs. Heating branched poly(ethylenimine)/poly(acrylic acid) (BPEI/PAA) multilayers at sufficiently high temperatures drives amidization and dehydration to covalently cross-link the film, but this reaction is rather slow, typically requiring heating for hours for appreciable cross-linking to occur. Here, a more than one order of magnitude increase in the amidization kinetics is realized through microwave heating of BPEI/PAA multilayers on indium tin oxide (ITO)/glass substrates.

Role of Amphiphilic Block Copolymer Composition on Pore Characteristics of Micelle-Templated Mesoporous Cobalt Oxide Films.

Block copolymer templating is a versatile approach for the generation of well-defined porosity in a wide variety of framework chemistries. Here, we systematically investigate how the composition of a poly(methoxy poly[ethylene glycol] methacrylate)-block-poly(butyl acrylate) (PMPEG-PBA) template impacts the pore characteristics of mesoporous cobalt oxide films. Three templates with a constant PMPEG segment length and different hydrophilic block volume fractions of 17%, 51%, and 68% for the PMPEG-PBA are cooperatively assembled with cobalt nitrate hexahydrate and citric acid.