A catalytic role of surface silanol groups in CO2 capture on the amine-anchored silica support. Issue 17 (23rd April 2018)

• Record Type: Journal Article
• Authors: Cho, Moses; Park, Joonho; Yavuz, Cafer T.; Jung, Yousung
• Is Part Of: Physical chemistry chemical physics. Volume 20:Issue 17(2018)
• Page Start: 12149
• Page End: 12156
• Publication Date: 2018-04-23
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/c7cp07973g
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : A new mechanism of CO2 capture on the amine-functionalized silica support is demonstrated using density functional theory calculations, in which the silica surface not only acts as a support to anchor amines, but also can actively participate in the CO2 capture process through a facile proton transfer reaction with the amine groups. Abstract : A new mechanism of CO2 capture on the amine-functionalized silica support is demonstrated using density functional theory calculations, in which the silica surface not only acts as a support to anchor amines, but also can actively participate in the CO2 capture process through a facile proton transfer reaction with the amine groups. The surface-mediated proton transfer mechanism in forming a carbamate–ammonium product has lower kinetic barrier (8.1 kcal mol −1 ) than the generally accepted intermolecular mechanism (12.7 kcal mol −1 ) under dry conditions, and comparable to that of the water-assisted intermolecular mechanism (6.0 kcal mol −1 ) under humid conditions. These findings suggest that the CO2 adsorption on the amine-anchored silica surface would mostly occur via the rate-determining proton transfer step that is catalyzed by the surface silanol groups.