Selective adsorption of CO2 in TAMOF-1 for the separation of CO2/CH4 gas mixtures

TAMOF-1 is a robust, highly porous metal-organic framework built from Cu<sup>2+</sup> centers linked by a L-histidine derivative. Thanks to its high porosity and homochirality, TAMOF-1 has shown interesting molecular recognition properties, being able to resolve racemic mixtures of small organic molecules in gas and liquid phases. Now, we have discovered that TAMOF-1 also offers a competitive performance as solid adsorbent for CO<sub>2</sub> physisorption, offering promising CO<sub>2</sub> adsorption capacity ( > 3.8 mmol g<sup>-1</sup>) and CO<sub>2</sub>/CH<sub>4</sub> Ideal Adsorbed Solution Theory (IAST) selectivity ( > 40) at ambient conditions. Moreover, the material exhibits favorable adsorption kinetics under dynamic conditions, demonstrating good stability in high-humidity environments and minimal degradation in strongly acidic media. We have identified the key interactions of CO<sub>2</sub> within the TAMOF-1 framework by a combination of structural (neutron diffraction), spectroscopic and theoretical analyses which conclude a dual-site adsorption mechanism with the majority of adsorbed CO<sub>2</sub> molecules occupying the empty voids in the TAMOF-1 channels without strong, directional supramolecular interactions. This very weak dominant binding opens the possibility of a low energy regeneration process for convenient CO<sub>2</sub> purification. These features identify TAMOF-1 as a viable solid-state adsorbent for the realization of affordable biogas upgrading.

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Publication Details

Journal
Nature Communications
Published
2025-04-04
DOI
https://doi.org/10.1038/s41467-025-58426-w
Citations
34
Primary Topic
Carbon Dioxide Capture Technologies
Type
article
Field-Weighted Citation Impact
24.26

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Selective adsorption of CO2 in TAMOF-1 for the separation of CO2/CH4 gas mixtures

Óscar Fabelo, Stefano Giancola, J.B. Parra, José Ramón Galán‐Mascarós et al.
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Nature Communications
Carbon Dioxide Capture Technologies
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article

Selective adsorption of CO2 in TAMOF-1 for the separation of CO2/CH4 gas mixtures

Óscar Fabelo, Stefano Giancola, J.B. Parra, José Ramón Galán‐Mascarós, Sofı́a Calero, Vanesa Lillo, Anton Vidal‐Ferran, Paolo Rumori, Jesús González‐Cobos, Santiago Capelo, Gemma Turnes Palomino, Eduardo C. Escudero‐Adán, Juanjo Cabezas‐Giménez, Mabel de Fez-Febré, Carlos Palomino Cabello, Irene I. Gallo Stampino, Raiana Tomazini de Oliveira, Larry R. Falvello, Salvador Rodríguez Gómez
article en
34 citations

Abstract

TAMOF-1 is a robust, highly porous metal-organic framework built from Cu<sup>2+</sup> centers linked by a L-histidine derivative. Thanks to its high porosity and homochirality, TAMOF-1 has shown interesting molecular recognition properties, being able to resolve racemic mixtures of small organic molecules in gas and liquid phases. Now, we have discovered that TAMOF-1 also offers a competitive performance as solid adsorbent for CO<sub>2</sub> physisorption, offering promising CO<sub>2</sub> adsorption capacity ( > 3.8 mmol g<sup>-1</sup>) and CO<sub>2</sub>/CH<sub>4</sub> Ideal Adsorbed Solution Theory (IAST) selectivity ( > 40) at ambient conditions. Moreover, the material exhibits favorable adsorption kinetics under dynamic conditions, demonstrating good stability in high-humidity environments and minimal degradation in strongly acidic media. We have identified the key interactions of CO<sub>2</sub> within the TAMOF-1 framework by a combination of structural (neutron diffraction), spectroscopic and theoretical analyses which conclude a dual-site adsorption mechanism with the majority of adsorbed CO<sub>2</sub> molecules occupying the empty voids in the TAMOF-1 channels without strong, directional supramolecular interactions. This very weak dominant binding opens the possibility of a low energy regeneration process for convenient CO<sub>2</sub> purification. These features identify TAMOF-1 as a viable solid-state adsorbent for the realization of affordable biogas upgrading.

Nature CommunicationsVol. 16(1)
Université Claude Bernard Lyon 1 (FR), Institució Catalana de Recerca i Estudis Avançats (ES), Centre National de la Recherche Scientifique (FR), Demos (US), Universidad Rey Juan Carlos (ES), Universidad de Zaragoza (ES), Institut Català d'Investigació Química (ES), Instituto Nacional del Carbón (ES), Institut Laue-Langevin (FR), Instituto de Nanociencia y Materiales de Aragón (ES), Hospital Universitari Sagrat Cor (ES), Institut de Recherches sur la Catalyse et l'Environnement de Lyon (FR), Universitat de les Illes Balears (ES), Universitat Rovira i Virgili (ES), Universitat de Barcelona (ES), Universidad de Sevilla (ES), Eindhoven University of Technology (NL)
Centres de Recerca de Catalunya, European Commission, Generalitat de Catalunya, Institut Català d'Investigació Química, Ministerio de Ciencia e Innovación, Junta de Andalucía, HORIZON EUROPE Framework Programme, Agència de Gestió d'Ajuts Universitaris i de Recerca, Agencia Estatal de Investigación
Openalex Percentile: Top 0%
Carbon Dioxide Capture Technologies
24.26
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