Highly Cooperative CO2 Adsorption via a Cation Crowding Mechanism on a Cesium-Exchanged Phillipsite Zeolite

An understanding of the CO₂ adsorption mechanisms on small-pore zeolites is of practical importance in the development of more efficient adsorbents for the separation of CO₂ from N₂ or CH₄. Here we report that the CO₂ isotherms at 25–75 °C on cesium-exchanged phillipsite zeolite with a Si/Al ratio of 2.5 (Cs-PHI-2.5) are characterized by a rectilinear step shape: limited uptake at low CO₂ pressure (P_CO2) is followed by highly cooperative uptake at a critical pressure, above which adsorption rapidly approaches capacity (2.0 mmol g⁻¹). Structural analysis reveals that this isotherm behavior is attributed to the high concentration and large size of Cs⁺ ions in dehydrated Cs-PHI-2.5. This results in Cs⁺ cation crowding and subsequent dispersal at a critical loading of CO₂, which allows the PHI framework to relax to its wide pore form and enables its pores to fill with CO₂ over a very narrow range of P_CO2. Such a highly cooperative phenomenon has not been observed for other zeolites.