In this work, a reactive modification route to indirectly observe the distribution of CO2 at polymer-silica interfaces is proposed. Selective condensation of TEOS within a block copolymer template results in the in-situ formation of a silica-polymer interface. Using a BCC sphere morphology allows for accumulation of CO2 at this interface during the synthesis to be observed post synthesis through the pore size. A significant increase in the pore size is observed near the critical pressure; this occurs at a similar CO2 activity as the enhanced swelling of polymer films supported on silicon wafers.
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