This study reports two distinct families of sorbents for CO
2 capture and combined capture and utilization. In the first part of the study, we report perovskite oxides as a new family of tunable sorbents. Perovskite oxides offer excellent flexibility to tailor the sorption kinetics and thermodynamic parameters. Using Sr
xLa
1-xFeO
3 as a basis, we showed that changing the A-site cation composition is highly effective in adjusting the CO
2 adsorption and desorption characteristics, allowing tunable CO
2 capture and release. A strong correlation between the oxide surface area and sorption capacity was also established. Despite the low surface area inherent to perovskite oxides, we enhanced their surface area from <5 m
2/g to ~30 m
2/g using a electrospinning method. Sr
0.2La
0.8FeO
3 prepared via electrospinning exhibited a relatively moderate desorption temperature (~240°C) and a CO
2 sorption capacity of 0.68 wt.%. We also showed that the sorption material can be effectively utilized for CO
2 capture and methanation in a temperature range of 250 to 300°C.
In the second part of this study, we report hybrid organic-inorganic sorbent particles by functionalizing mesoporous SiO2 spheres (MSS) with 3-Aminopropyl triethoxysilane (APTMS) to introduce amine functional groups. In this study, MSS-(x)NH2 (where x= 0.1, 0.5, and 1) was synthesized for CO2 adsorption, with x representing the volume of APTMS per gram of MSS. The adsorption capacity of these samples was assessed using TGA, revealing that MSS-(1)NH2 exhibited the highest capacity, with a 2.5% CO2 sorption capacity and excellent stability.