Selective CO2 adsorption and bathochromic shift in a phosphocholine-based lipid and conjugated polymer assembly

We assemble a film of a phosphocholine-based lipid and a crystalline conjugated polymer using hydrophobic interactions between the alkyl tails of the lipid and alkyl side chains of the polymer, and demonstrated its selective gas adsorption properties and the polymer''s improved light absorption properties. We show that a strong attractive interaction between the polar lipid heads and CO₂ was responsible for 6 times more CO₂ being adsorbed onto the assembly than N₂, and that with repeated CO₂ adsorption and vacuuming procedures, the assembly structures of the lipid-polymer assembly were irreversibly changed, as demonstrated by in situ grazing-incidence X-ray diffraction during the gas adsorption and desorption. Despite the disruption of the lipid structure caused by adsorbed polar gas molecules on polar head groups, gas adsorption could promote orderly alkyl chain packing by inducing compressive strain, resulting in enhanced electron delocalization of conjugated backbones and bathochromic light absorption. The findings suggest that merging the structures of the crystalline functional polymer and lipid bilayer is a viable option for solar energy-converting systems that use conjugated polymers as a light harvester and the polar heads as CO₂-capturing sites.

Assembly films of a phosphocholine-based lipid and a crystalline conjugated polymer had significant CO₂ selective adsorption and light absorption due to the attractive interaction of CO₂ with exposed polar lipid heads and enhanced morphologies.