absorbents; [ 2 ] the better effi ciency of solid state absorbents is related to the ease (with respect to energy penalty) of their regeneration via energy effi cient pressure or temperature swing changes. Porous solid state materials, namely, zeolites, [ 3 ] metal organic frameworks (MOFs), [ 4 ] covalent organic frameworks (COFs), [ 4 ] and carbons [ 5,6 ] are currently the most studied CO 2 absorbers for postcombustion capture and storage. Of the three classes of porous materials, carbons are attractive due to their abundance, low cost, and rich availability in activated [5][6][7] or templated [ 8,9 ] form. Activated carbons are particularly attractive as they may be prepared from biomass via valorisation processes that convert low value waste into valuable carbonaceous materials. [ 5f ] Recent studies have shown that KOH activated carbons, including biomass-derived examples, can achieve some of the best CO 2 uptake under conditions (i.e., 0.1-1 bar and 25-50 °C) relevant to industrial postcombustion capture. [ 2,[5][6][7] It is now well established that pore size is the main factor that determines CO 2 uptake of activated carbons under postcombustion capture conditions. [5][6][7]9 ] The critical importance of pore size arises from the fact that the CO 2 -carbon interaction emanates from short-range attractive forces which are maximized when CO 2 adsorption takes place in very narrow pores where overlapping potential fi elds from neighboring walls exert a positive infl uence. For slit-shaped pores, such as those present in activated carbons, enhancement of the adsorption potential may be maximized for micropore widths that are two times the diameter of the CO 2 molecule, [ 10 ] which translates to an optimal pore size of 6-7 Å. Such pores can be obtained in lowly or mildly activated carbons prepared at KOH/carbon ratio of 2 and between 600 and 700 °C. [ 2,[5][6][7]9,11 ] Indeed, to date, such activated carbons are among materials that show the highest CO 2 uptake at 25 °C and low pressure (up to 1 bar). [ 2,[5][6][7]9 ] Conversely, though, such lowly activated carbons tend to have low surface area, which limits the maximum amount of CO 2 that they can store. For this reason, there appears to be a limit on the amount of CO 2 that can be stored by biomass-derived or other activated carbons at 25 °C of ≈1.5 mmol g −1 at 0.15 bar, and 4.5 mmol g −1 at 1 bar. [ 2,[5][6][7]9,12 ] Increase in surface area can be achieved at higher activation levels (higher KOH amounts Novel mechanochemical activation generates biomass-derived carbons with unprecedented CO 2 storage capacity due to higher porosity than analogous conventionally activated carbons but similar pore size. The mechanochemical activation, or so-called compactivation, process involves compression, at 740 MPa, of mixtures of activating agent (KOH) and biomass hydrochar into pellets/disks prior to thermal activation. Despite the increase in surface area and pore volume of between 25% and 75% compared to conventionally activated carbons, virtually all o...