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Liquid nano-absorbents have become a topic of interest as a result of their enhanced mass-transfer performance for CO<sub>2</sub> capture. They are believed to have revolutionized the conventional CO<sub>2</sub> chemisorption process by largely improving CO<sub>2</sub> capture kinetics and reducing the energy requirement for solvent regeneration. Two classes of nanomaterial-based CO<sub>2</sub> capture absorbents, amine-based nanoparticle suspensions (nanofluids) and nanoparticle organic hybrid materials (NOHMs), have been developed, with significant progress achieved in recent decades. This review addresses two key questions for these two state-of-the-art nanomaterials: how are the physical and chemical properties of the prepared liquid nano-absorbents transformed relative to those of the base fluids? And how does the transformation of the properties affect the CO<sub>2</sub> capture behavior? While the current synthesis procedure for liquid nano-absorbents is quite straightforward, more advanced synthesis methods for long-term nanoparticle stability have been suggested for the future. Nanofluids have been shown to increase the CO<sub>2</sub> uptake by over 20% and the CO<sub>2</sub> capture rate by 2-93% compared with the values observed with neat amine solvents. Nanoparticles with catalytic effects on CO<sub>2</sub> capture can significantly increase the CO<sub>2</sub> desorption rate by as high as 4000%. NOHMs exhibit the interesting feature of enhanced mass transfer in CO<sub>2</sub> capture because of the unique pathway network that is created in them for CO<sub>2</sub> to reach specific functional groups. NOHMs promise an effect of combined CO<sub>2</sub> capture and conversion, and can be used especially as electrolytes for CO<sub>2</sub> electro-reduction. However, there are still some challenges for the application of these materials in real life, such as poor stability and high viscosity. Therefore, efficient CO<sub>2</sub> capture processes using these solvents need to be urgently developed and studied in the future.