Water plays a critical role in range of chemical, physiochemical, geological, and energy applications. Understanding water at the molecular scale is critical for unraveling processes and mechanisms related to separations, energy storage, and remediation challenges. In this project, we used benchtop and synchrotron techniques to examine CO2 adsorption and desorption in a novel family of moisture-driven CO2 sorbents.
Traditional thermal swing sorption technologies for direct air capture require a large amount of energy during the regeneration process (>179 kJ/mol). An alternative approach to thermal- and pressure-swing sorbents is moisture-driven sorbents. These sorbent materials bind CO2 from the air when the surrounding is dry, and desorbs CO2 when hydrated. This mechanism has been observed in some materials (ion exchange resin, inorganic material, etc.) but is not completely understood.
This work explores how water in confinement can be utilized to tailor CO2 capture and regeneration in advanced sorbent materials. We have found that the sorbent structure, rather than the density of active separation sites, governs the reversible operation of this class of materials.