RESUMO
Recent advances in polymer synthesis have allowed remarkable control over chain microstructure and conformation. Capitalizing on such developments, here we create well-controlled chain folding in sulfonated polyethylene, leading to highly uniform hydrated acid layers of subnanometre thickness with high proton conductivity. The linear polyethylene contains sulfonic acid groups pendant to precisely every twenty-first carbon atom that induce tight chain folds to form the hydrated layers, while the methylene segments crystallize. The proton conductivity is on par with Nafion 117, the benchmark for fuel cell membranes. We demonstrate that well-controlled hairpin chain folding can be utilized for proton conductivity within a crystalline polymer structure, and we project that this structure could be adapted for ion transport. This layered polyethylene-based structure is an innovative and versatile design paradigm for functional polymer membranes, opening doors to efficient and selective transport of other ions and small molecules on appropriate selection of functional groups.
RESUMO
Copolymers containing sulfite functionalities precisely placed between run lengths of 8, 14, and 20 methylene units were synthesized via ADMET with weight-average molecular weights up to 40 500 g/mol (PDI = 1.89). No such polymer structures have been observed previously. The primary polymer structures and precise nature were characterized by 1H NMR, 13C NMR, and IR spectroscopy. Thermal degradation temperatures up to 310 °C were observed through TGA, and melting points typical of similar unsaturated ADMET polymers were determined by DSC. X-ray scattering was used to compare the polymers to ADMET polyethylene (PE), and when the polymers have 20 carbons between sulfites, the functional groups self-assemble into layers. Higher carbon content incorporation leads to an increase in crystallinity and thermal stability for these polysulfites.
