Confinement Effects on Moisture-Swing Direct Air Capture

Abstract

Direct air capture technologies are energy intensive and often utilize pressure and temperature swings for sorbent regeneration. An alternative approach, called moisture-swing direct air capture, relies on the hydrolysis of a confined anion to produce hydroxide anions. These hydroxide anions are active sites for CO 2 capture. Here, we examine how confinement affects moisture-swing CO 2 capture and regeneration mechanisms. The local short-range order in micropores determines the capacity for hydroxide formation in the moisture-controlled reversible hydrolysis/ neutralization reaction during capture and regeneration. Carbon capture scales with the basicity of the confined anion. Sulfide exhibits excessive interactions with water and thus can release only small amounts of CO 2 during the regeneration step. Control over local water−anion chemical microenvironments is critical for reversible operation of moisture-swing sorbent materials. Accessibility of water is largely governed by the distribution of resin macropores. Engineering materials for control over micro, meso, and macropores is critical for achieving favorable interactions between active sites and water in confinement.