Carbon dioxide as a porogen on self-organized nano-structure of amphiphilic side-chain type liquid crystalline di-block copolymers

Abstract

Liquid and supercritical carbon dioxide (LCO2, SCCO2) have been used as a porogen to swell self-organized nano-structure of an amphiphilic side-chain type liquid crystalline PEO–b-PMA(Az) copolymer. Carbon dioxide interacts with the hydrophilic PEO domain rather than the PMA matrix. The preferential interactions of PEO component with carbon dioxide result in a solvent-induced surface topology changes and the generation of a nano-porous template. The area density of the nano-pores is identical to that of the original copolymer film while keeping the hexagonally packed PEO nano-scale organization. Since the process is based on the gases diffusion on solid surfaces under controlled temperature and since neither polymer block is fundamentally altered by the sorption effect, the process is fully reversible. The supercritical condition of CO2 treatment gives rise to the highest expansion of pre-patterned PEO cylinders and consecutively induces the retardation of PEO crystallization. This versatile thermo-diffuso approach would be applied to a wide variety of pre-patterned copolymers systems for nano-templating applications requiring nano-scale features sizes and/or area feature densities.