Sub-3-Nanometer Domain Spacings of Ultrahigh-χ Multiblock Copolymers with Pendant Ionic Groups

Abstract

We investigated the temperature-dependent phase behavior and interaction parameter of polyethylene-based multiblock copolymers with pendant ionic groups. These step-growth polymers contain short polyester blocks with a single Li+SO3- group strictly alternating with polyethylene blocks of x-carbons (PESxLi, x = 12, 18, 23). At room temperature, these polymers exhibit layered morphologies with semicrystalline polyethylene blocks. Upon heating above the melting point (∼130 °C), PES18Li shows two order-to-order transitions involving Ia3̅d gyroid and hexagonal morphologies. For PES12Li, an order-to-disorder transition accompanies the melting of the polyethylene blocks. Notably, a Flory-Huggins interaction parameter was determined from the disordered morphologies of PES12Li using mean-field theory: χ(T) = 77.4/T + 2.95 (T in Kelvin) and χ(25 °C) ≈ 3.21. This ultrahigh χ indicates that the polar ionic and nonpolar polyethylene segments are highly incompatible and affords well-ordered morphologies even when the combined length of the alternating blocks is just 18-29 backbone atoms. This combination of ultrahigh χ and short multiblocks produces sub-3-nm domain spacings that facilitate the control of block copolymer self-assembly for various fields of study, including nanopatterning.