All Publications


  • Spectroscopic Definition of a Highly Reactive Site in Cu-CHA for Selective Methane Oxidation: Tuning a Mono-mu-Oxo Dicopper(II) Active Site for Reactivity. Journal of the American Chemical Society Rhoda, H. M., Plessers, D., Heyer, A. J., Bols, M. L., Schoonheydt, R. A., Sels, B. F., Solomon, E. I. 2021

    Abstract

    Using UV-vis and resonance Raman spectroscopy, we identify a [Cu2O]2+ active site in O2 and N2O activated Cu-CHA that reacts with methane to form methanol at low temperature. The Cu-O-Cu angle (120°) is smaller than that for the [Cu2O]2+ core on Cu-MFI (140°), and its coordination geometry to the zeolite lattice is different. Site-selective kinetics obtained by operando UV-vis show that the [Cu2O]2+ core on Cu-CHA is more reactive than the [Cu2O]2+ site in Cu-MFI. From DFT calculations, we find that the increased reactivity of Cu-CHA is a direct reflection of the strong [Cu2OH]2+ bond formed along the H atom abstraction reaction coordinate. A systematic evaluation of these [Cu2O]2+ cores reveals that the higher O-H bond strength in Cu-CHA is due to the relative orientation of the two planes of the coordinating bidentate O-Al-O T-sites that connect the [Cu2O]2+ core to the zeolite lattice. This work along with our earlier study ( J. Am. Chem. Soc, 2018, 140, 9236-9243) elucidates how zeolite lattice constraints can influence active site reactivity.

    View details for DOI 10.1021/jacs.1c02835

    View details for PubMedID 33970624

  • Coordination and activation of nitrous oxide by iron zeolites NATURE CATALYSIS Bols, M. L., Snyder, B. R., Rhoda, H. M., Cnudde, P., Fayad, G., Schoonheydt, R. A., Van Speybroeck, V., Solomon, E. I., Sels, B. F. 2021; 4 (4): 332-+
  • Atmospheric Methane Removal: A Research Agenda Philosophical Transactions of the Royal Society A Jackson, R. B., et al 2021; 379: 20200454

    View details for DOI 10.1098/rsta.2020.0454

  • Cage effects control the mechanism of methane hydroxylation in zeolites. Science (New York, N.Y.) Snyder, B. E., Bols, M. L., Rhoda, H. M., Plessers, D., Schoonheydt, R. A., Sels, B. F., Solomon, E. I. 2021; 373 (6552): 327-331

    Abstract

    Catalytic conversion of methane to methanol remains an economically tantalizing but fundamentally challenging goal. Current technologies based on zeolites deactivate too rapidly for practical application. We found that similar active sites hosted in different zeolite lattices can exhibit markedly different reactivity with methane, depending on the size of the zeolite pore apertures. Whereas zeolite with large pore apertures deactivates completely after a single turnover, 40% of active sites in zeolite with small pore apertures are regenerated, enabling a catalytic cycle. Detailed spectroscopic characterization of reaction intermediates and density functional theory calculations show that hindered diffusion through small pore apertures disfavors premature release of CH3 radicals from the active site after C-H activation, thereby promoting radical recombination to form methanol rather than deactivated Fe-OCH3 centers elsewhere in the lattice.

    View details for DOI 10.1126/science.abd5803

    View details for PubMedID 34437151

  • Advances in the synthesis, characterisation, and mechanistic understanding of active sites in Fezeolites for redox catalysts DALTON TRANSACTIONS Bols, M. L., Rhoda, H. M., Snyder, B. R., Solomon, E., Pierloot, K., Schoonheydt, R. A., Sels, B. F. 2020; 49 (42): 14749–57

    Abstract

    The recent research developments on the active sites in Fe-zeolites for redox catalysis are discussed. Building on the characterisation of the α-Fe/α-O active sites in the beta and chabazite zeolites, we demonstrate a bottom-up approach to successfully understand and develop Fe-zeolite catalysts. We use the room temperature benzene to phenol reaction as a relevant example. We then suggest how the spectroscopic identification of other monomeric and dimeric iron sites could be tackled. The challenges in the characterisation of active sites and intermediates in NOX selective catalytic reduction catalysts and further development of catalysts for mild partial methane oxidation are briefly discussed.

    View details for DOI 10.1039/d0dt01857k

    View details for Web of Science ID 000589506700038

    View details for PubMedID 33140781

  • Oxygen intermediates in Cu and Fe zeolites: Correlations to metalloenzymes Solomon, E., Snyder, B., Rhoda, H. AMER CHEMICAL SOC. 2019
  • Mechanism of selective benzene hydroxylation catalyzed by iron-containing zeolites. Proceedings of the National Academy of Sciences of the United States of America Snyder, B. E., Bols, M. L., Rhoda, H. M., Vanelderen, P., Bottger, L. H., Braun, A., Yan, J. J., Hadt, R. G., Babicz, J. T., Hu, M. Y., Zhao, J., Alp, E. E., Hedman, B., Hodgson, K. O., Schoonheydt, R. A., Sels, B. F., Solomon, E. I. 2018

    Abstract

    A direct, catalytic conversion of benzene to phenol would have wide-reaching economic impacts. Fe zeolites exhibit a remarkable combination of high activity and selectivity in this conversion, leading to their past implementation at the pilot plant level. There were, however, issues related to catalyst deactivation for this process. Mechanistic insight could resolve these issues, and also provide a blueprint for achieving high performance in selective oxidation catalysis. Recently, we demonstrated that the active site of selective hydrocarbon oxidation in Fe zeolites, named alpha-O, is an unusually reactive Fe(IV)=O species. Here, we apply advanced spectroscopic techniques to determine that the reaction of this Fe(IV)=O intermediate with benzene in fact regenerates the reduced Fe(II) active site, enabling catalytic turnover. At the same time, a small fraction of Fe(III)-phenolate poisoned active sites form, defining a mechanism for catalyst deactivation. Density-functional theory calculations provide further insight into the experimentally defined mechanism. The extreme reactivity of alpha-O significantly tunes down (eliminates) the rate-limiting barrier for aromatic hydroxylation, leading to a diffusion-limited reaction coordinate. This favors hydroxylation of the rapidly diffusing benzene substrate over the slowly diffusing (but more reactive) oxygenated product, thereby enhancing selectivity. This defines a mechanism to simultaneously attain high activity (conversion) and selectivity, enabling the efficient oxidative upgrading of inert hydrocarbon substrates.

    View details for PubMedID 30429333

  • Spectroscopic Identification of the alpha-Fe/alpha-O Active Site in Fe-CHA Zeolite for the Low-Temperature Activation of the Methane C-H Bond JOURNAL OF THE AMERICAN CHEMICAL SOCIETY Bols, M. L., Hallaert, S. D., Snyder, B. R., Devos, J., Plessers, D., Rhoda, H. M., Dusselier, M., Schoonheydt, R. A., Pierloot, K., Solomon, E., Sels, B. F. 2018; 140 (38): 12021–32

    Abstract

    The formation of single-site α-Fe in the CHA zeolite topology is demonstrated. The site is shown to be active in oxygen atom abstraction from N2O to form a highly reactive α-O, capable of methane activation at room temperature to form methanol. The methanol product can subsequently be desorbed by online steaming at 200 °C. For the intermediate steps of the reaction cycle, the evolution of the Fe active site is monitored by UV-vis-NIR and Mössbauer spectroscopy. A B3LYP-DFT model of the α-Fe site in CHA is constructed, and the ligand field transitions are calculated by CASPT2. The model is experimentally substantiated by the preferential formation of α-Fe over other Fe species, the requirement of paired framework aluminum and a MeOH/Fe ratio indicating a mononuclear active site. The simple CHA topology is shown to mitigate the heterogeneity of iron speciation found on other Fe-zeolites, with Fe2O3 being the only identifiable phase other than α-Fe formed in Fe-CHA. The α-Fe site is formed in the d6r composite building unit, which occurs frequently across synthetic and natural zeolites. Finally, through a comparison between α-Fe in Fe-CHA and Fe-*BEA, the topology's 6MR geometry is found to influence the structure, the ligand field, and consequently the spectroscopy of the α-Fe site in a predictable manner. Variations in zeolite topology can thus be used to rationally tune the active site properties.

    View details for PubMedID 30169036

  • Structural characterization of a non-heme iron active site in zeolites that hydroxylates methane PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA Snyder, B. R., Bottger, L. H., Bols, M. L., Yan, J. J., Rhoda, H. M., Jacobs, A. B., Hu, M. Y., Zhao, J., Alp, E., Hedman, B., Hodgson, K. O., Schoonheydt, R. A., Sels, B. F., Solomon, E. I. 2018; 115 (18): 4565–70

    Abstract

    Iron-containing zeolites exhibit unprecedented reactivity in the low-temperature hydroxylation of methane to form methanol. Reactivity occurs at a mononuclear ferrous active site, α-Fe(II), that is activated by N2O to form the reactive intermediate α-O. This has been defined as an Fe(IV)=O species. Using nuclear resonance vibrational spectroscopy coupled to X-ray absorption spectroscopy, we probe the bonding interaction between the iron center, its zeolite lattice-derived ligands, and the reactive oxygen. α-O is found to contain an unusually strong Fe(IV)=O bond resulting from a constrained coordination geometry enforced by the zeolite lattice. Density functional theory calculations clarify how the experimentally determined geometric structure of the active site leads to an electronic structure that is highly activated to perform H-atom abstraction.

    View details for PubMedID 29610304