Probing Acidity in Metal–Organic Frameworks via Pyridine Adsorption
Semilocal density functional theory (DFT) and semiemprical GFN1/GFN2-xTB, as well as selected DFTB/3ob calculations, were performed to examine acidity in metal–organic frameworks (MOFs) using pyridine (Py) as a probe molecule. We studied Py adsorption on both Lewis and Bro̷nsted acid sites in ten distinct MOF structures. Our study provides detailed insight into their structures, thermodynamic properties, and vibrational spectra in selected ranges. All geometrical and energetic parameters obtained at the GFN1/GFN2-xTB levels were compared with those calculated using DFT. The results suggest that GFN1-xTB can only be used as a low-cost substitute for DFT for some systems. The adsorption energy prediction usually leads to unsatisfactory findings. GFN2-xTB and DFTB/3ob perform better than GFN1-xTB. Importantly, we identified areas where the GFN1/GFN2-xTB methods could be improved to yield more accurate results. By analyzing the density overlap region indicator (DORI) versus the adsorption energies, we revealed the nature and type of interactions in Py@MOFs.
Authors
- Krzysztof Winkler
- Piotr Paneth (ORCID: https://orcid.org/0000-0002-3091-8387)
- Johannes T. Margraf (ORCID: https://orcid.org/0000-0002-0862-5289)
- Mateusz Pokora (ORCID: https://orcid.org/0000-0001-8835-9664)
- Jakub Goclon (ORCID: https://orcid.org/0000-0002-4261-2799)
- Chiara Panosetti (ORCID: https://orcid.org/0000-0001-7328-2334)
- Artem Samtsevych
Institutions
- Lodz University of Technology (PL)
- University of Białystok (PL)
- Fritz Haber Institute of the Max Planck Society (DE)
- Centrum Badań Molekularnych i Makromolekularnych Polskiej Akademii Nauk (PL)
- University of Bayreuth (DE)
- Polish Academy of Sciences (PL)
Publication Details
- Journal
- The Journal of Physical Chemistry C
- Published
- 2026-04-17
- DOI
- https://doi.org/10.1021/acs.jpcc.5c08574
- Primary Topic
- Metal-Organic Frameworks: Synthesis and Applications
- Type
- article
- Field-Weighted Citation Impact
- 0.00