Quaternary functionalized mesoporous adsorbents for ultra-high kinetics of CO2 capture from air.

Obstacles to widespread deployments of direct air capture of CO2 (DAC) lie in high material and energy costs. By grafting quaternary ammonium (QA) functional group to mesoporous polymers with high surface area, a unique DAC adsorbent with moisture swing adsorption (MSA) ability and ultra-high kinetics was developed in this work. Functionalization is designed for efficient delivery of QA group through mesopores to active substitution sites. This achieved ultra-high kinetics adsorbent with half time of 2.9 min under atmospheric environment, is the highest kinetics value reported among DAC adsorbents. A cyclic adsorption capacity of 0.26 mmol g-1 is obtained during MSA process. Through adsorption thermodynamics, it is revealed that adsorbent with uniform cylindrical pore structure has higher functional group efficiency and CO2 capacity. Pore structure can also tune the MSA ability of adsorbent through capillary condensation of water inside its mesopores. The successful functionalization of mesoporous polymers with superb CO2 adsorption kinetics opens the door to facilitate DAC adsorbents for large-scale carbon capture deployments.

Spontaneous Cooling Absorption of CO2 by a Polymeric Ionic Liquid for Direct Air Capture.

A polymeric ionic liquid (PIL), with quaternary ammonium ions attached to the polymer matrix, displays CO2 affinity controlled by moisture. This finding led to the development of moisture swing absorption (MSA) for direct air capture of CO2. This work aims to elucidate the role of water in MSA. For some humidity range, CO2 absorption is an endothermic process associated with concurrent dehydration of the sorbent. The thermodynamic behavior of water indicates a decreased hydrophilicity of the PIL as the mobile anion transforms from CO32- to HCO3- during CO2 absorption. The decrease in hydrophilicity drives water out of the PIL, carrying heat away. The mechanism is elucidated by molecular modeling based on density functional theory. The finding of spontaneous cooling during absorption and its mechanism in the PIL opens new possibilities for designing an air capture sorbent with a strong CO2 affinity but low absorption heat.

Theoretical studies on CO2 capture behavior of quaternary ammonium-based polymeric ionic liquids.

Quaternary ammonium-based polymeric ionic liquids (PILs) are novel CO2 sorbents as they have high capacity, high stability and high binding energy. Moreover, the binding energy of ionic pairs to CO2 is tunable by changing the hydration state so that the sorbent can be regenerated through humidity adjustment. In this study, theoretical calculations were conducted to reveal the mechanism of the humidity swing CO2 adsorption, based on model compounds of quaternary ammonium cation and carbonate anions. The electrostatic potential map demonstrates the anion, rather than the cation, is chemically preferential for CO2 adsorption. Further, the proton transfer process from water to carbonate at the sorbent interface is successfully depicted with an intermediate which has a higher energy state. By determining the CO2 adsorption energy and activation energy at different hydration states, it is discovered that water could promote CO2 adsorption by reducing the energy barrier of proton transfer. The adsorption/desorption equilibrium would shift to desorption by adding water, which constitutes the theoretical basis for humidity swing. By analyzing the hydrogen bonding and structure of the water molecules, it is interesting to find that the CO2 adsorption weakens the hydrophilicity of the sorbent and results in release of water. The requirement of latent heat for the phase change of water could significantly reduce the heat of adsorption. The special "self-cooling" effect during gas adsorption can lower the temperature of the sorbent and benefit the adsorption isotherms.