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Charting the Metal-Dependent High-Pressure Stability of Bimetallic UiO-66 Materials AITranslate

Sven M. J. Rogge; Pascal G. Yot; Jannick Jacobsen; Francesco MunizMiranda; Steven Vandenbrande; Jonas Gosch; Vanessa Ortiz; Ines E. Collings; Sabine DevautourVinot; Guillaume Maurin; Norbert Stock; Veronique Van Speybroeck;
Ghent University; Université de Montpellier;Institut für Anorganische Chemie, Christian-Albrechts-Universität zu Kiel; Ghent University; Ghent University;Institut für Anorganische Chemie, Christian-Albrechts-Universität zu Kiel; Université de Montpellier;European Synchrotron Radiation Facility, 71 Avenue des Martys; Université de Montpellier; Université de Montpellier;Institut für Anorganische Chemie, Christian-Albrechts-Universität zu Kiel; Ghent University
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Abstract AITranslate

In theory, bimetallic UiO-66(Zr:Ce) and UiO-66(Zr:Hf) metal-organic frameworks (MOFs) are extremely versatile and attractive nanoporous materials as they combine the high catalytic activity of UiO-66(Ce) or UiO-66(Hf) with the outstanding stability of UiO-66(Zr). Using in situ high-pressure powder X-ray diffraction, however, we observe that this expected mechanical stability is not achieved when incorporating cerium or hafnium in UiO-66(Zr). This observation is akin to the earlier observed reduced thermal stability of UiO-66(Zr:Ce) compounds. To elucidate the atomic origin of this phenomenon, we chart the loss-of-crystallinity pressures of 22 monometallic and bimetallic UiO-66 materials and systematically isolate their intrinsic mechanical stability from their defect-induced weakening. This complementary experimental/computational approach reveals that the intrinsic mechanical stability of these bimetallic MOFs decreases nonlinearly upon cerium incorporation but remains unaffected by the zirconium: hafnium ratio. Additionally, all experimental samples suffer from defect-induced weakening, a synthesis-controlled effect that is observed to be independent of their intrinsic stability.

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DOI：https://doi.org/10.1021/acsmaterialslett.0c00042

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In theory, bimetallic UiO-66(Zr:Ce) and UiO-66(Zr:Hf) metal-organic frameworks (MOFs) are extremely versatile and attractive nanoporous materials as they combine the high catalytic activity of UiO-66(Ce) or UiO-66(Hf) with the outstanding stability of UiO-66(Zr). Using in situ high-pressure powder X-ray diffraction, however, we observe that this expected mechanical stability is not achieved when incorporating cerium or hafnium in UiO-66(Zr). This observation is akin to the earlier observed reduced thermal stability of UiO-66(Zr:Ce) compounds. To elucidate the atomic origin of this phenomenon, we chart the loss-of-crystallinity pressures of 22 monometallic and bimetallic UiO-66 materials and systematically isolate their intrinsic mechanical stability from their defect-induced weakening. This complementary experimental/computational approach reveals that the intrinsic mechanical stability of these bimetallic MOFs decreases nonlinearly upon cerium incorporation but remains unaffected by the zirconium: hafnium ratio. Additionally, all experimental samples suffer from defect-induced weakening, a synthesis-controlled effect that is observed to be independent of their intrinsic stability.

quote

GB/T 7714-2015 [1] Sven M. J. Rogge, Pascal G. Yot, Jannick Jacobsen, et al. ACS Materials Letters, 2020(2). DOI:10.1021/acsmaterialslett.0c00042.
MLA [1] Sven M. J. Rogge, et al., ACS Materials Letters, no. 2, 2020, https://doi.org/10.1021/acsmaterialslett.0c00042.
APA [1] Sven M. J. Rogge, Pascal G. Yot, Jannick Jacobsen, Francesco MunizMiranda, Steven Vandenbrande, Jonas Gosch, Vanessa Ortiz, Ines E. Collings, Sabine DevautourVinot, Guillaume Maurin, Norbert Stock, & Veronique Van Speybroeck. (2020). ACS Materials Letters(2). https://doi.org/10.1021/acsmaterialslett.0c00042
IEEE [1] Sven M. J. Rogge, Pascal G. Yot, Jannick Jacobsen, Francesco MunizMiranda, Steven Vandenbrande, Jonas Gosch, Vanessa Ortiz, Ines E. Collings, Sabine DevautourVinot, Guillaume Maurin, Norbert Stock, and Veronique Van Speybroeck, ACS Materials Letters, no. 2, 2020, doi: 10.1021/acsmaterialslett.0c00042.