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Quantitative localisation of titanium in the framework of titanium silicalite-1 using anomalous X-ray powder diffraction.

Authors :
Rzepka P
Signorile M
Huthwelker T
Checchia S
Rosso F
Bordiga S
van Bokhoven JA
Source :
Nature communications [Nat Commun] 2024 Sep 05; Vol. 15 (1), pp. 7757. Date of Electronic Publication: 2024 Sep 05.
Publication Year :
2024

Abstract

One of the biggest obstacles to developing better zeolite-based catalysts is the lack of methods for quantitatively locating light heteroatoms on the T-sites in zeolites. Titanium silicalite-1 (TS-1) is a Ti-bearing zeolite-type catalyst commonly used in partial oxidation reactions with H <subscript>2</subscript> O <subscript>2</subscript> , such as aromatic hydroxylation and olefin epoxidation. The reaction mechanism is controlled by the configuration of titanium sites replacing silicon in the zeolite framework, but these sites remain unknown, hindering a fundamental understanding of the reaction. This study quantitatively determines heteroatoms within the zeolite-type framework using anomalous X-ray powder diffraction (AXRD) and the changes in the titanium X-ray scattering factor near the Ti K-edge (4.96 keV). Two TS-1 samples, each with approximately 2 Ti atoms per unit cell, were examined. Half of the titanium atoms are primarily split between sites T3 and T9, with the remainder dispersed among various T-sites within both MFI-type frameworks. One structure showed significant non-framework titanium in the micropores of a more distorted lattice. In both samples, isolated titanium atoms were more prevalent than dinuclear species, which could only potentially arise at site T9, but with a significant energy penalty and were not detected.<br /> (© 2024. The Author(s).)

Details

Language :
English
ISSN :
2041-1723
Volume :
15
Issue :
1
Database :
MEDLINE
Journal :
Nature communications
Publication Type :
Academic Journal
Accession number :
39237487
Full Text :
https://doi.org/10.1038/s41467-024-51788-7