4.6 Article

Probing Acid Sites in MOR Zeolite Using Low-Temperature 13C Solid-State NMR Spectroscopy of Adsorbed Carbon Monoxide

Journal

JOURNAL OF PHYSICAL CHEMISTRY C
Volume 126, Issue 7, Pages 3681-3687

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.1c10026

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Funding

  1. ETH+ Project SynthMatLab

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Understanding the structure of acid sites in zeolites is crucial for unraveling catalytic mechanisms and improving performance. Carbon monoxide and pyridine are commonly used probe molecules to study acid sites. Low-temperature carbon-13 NMR spectroscopy reveals distinct signatures for carbon monoxide interacting with Lewis and Bronsted acid sites, providing detailed structural information.
Understanding the structure of Lewis and Bronsted acid sites in zeolites is a key step toward unraveling mechanisms of catalytic reactions, establishing molecular-level structure-activity relationships and thereby rational improvement of their performance. Acid sites are typically studied indirectly, using probe molecules, whose spectroscopic signatures are linked to the nature of specific sites. In this context, carbon monoxide and pyridine (Py) are the most frequently used probe molecules due to their sensitivity toward the nature and strength of surface acid sites. Although infrared and solid-state NMR spectroscopies of adsorbed Py are now widely used, the utilization of carbon monoxide to study surface sites has been mainly limited to infrared spectroscopy. Considering that NMR spectroscopy parameters, such as isotropic chemical shift (delta(iso)) and chemical shift anisotropy (CSA), provide detailed structural information, we have explored the capabilities of low-temperature carbon-13 NMR spectroscopy of adsorbed (CO)-C-13 on dehydrated mordenite. One-dimensional (1D) and two-dimensional (2D) C-13 low-temperature magic-angle spinning NMR spectra show that carbon monoxide interacting with Lewis (LAS) and Bronsted (BAS) acid sites displays distinct C-13 NMR signatures, in line with density functional theory (DFT) calculations. Furthermore, {H-1}C-13 HETCOR NMR allows the observation of surface OH groups interacting with CO and points to the spatial proximity (within 1 nm) of BAS to both Si-OH and Al-OH groups, while LAS predominantly comprises the Al-OH group. These observations suggest the formation of defective aluminum sites with one and/or two OH groups bound to aluminum, upon calcination of a NH4-MOR with Si/Al = 6 at high temperature (580 degrees C). The NMR protocol discussed is perfectly suited to explore the surface sites of other solid materials.

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