CO capture and storage have been regarded as promising concepts to reduce anthropogenic CO emissions. However, the high cost, inferior adsorption capacity, and higher effective activation temperature of traditional sorbents limit their practical application in efficient CO capture. Here, a C-S-H@ZIF-8 (C-S-Z) sorbent is fabricated by in situ growth of the ZIF-8 shell on the C-S-H (calcium-silicate-hydrate) surface for ultra-high CO adsorption and storage. Among the C-S-Z, the outer ZIF-8 shell acts as a transport channel that promotes CO absorption toward the underlying C-S-H substrate for accelerated carbonation while preventing nitrogen and water from reaching the interior C-S-H. As a consequence, C-S-Z possesses the merits of ample pyrrolic nitrogen, porous structure, and ultra-high surface area (577.18 m g), that contribute to an ultra-high CO capture capacity, reaching 293.6 mg g. DFT calculations show a high CO adsorption energy and the mineral carbonation is dominant by the adsorption process. In particular, the advantages of the outstanding adsorption capacity, low cost, and high CO selectivity make this C-S-H-based sorbent hold great potential in the practical application for direct air CO capture and storage.

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http://dx.doi.org/10.1002/smtd.202301337DOI Listing

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