Fluoride Anions in All-Silica Zeolites: Studying Preferred Fluoride Sites and Dynamic Disorder with Density Functional Theory Calculations
Date Issued
2021-04-15
Author(s)
Abstract
In all-silica zeolites synthesized via the “fluoride route”, the fluoride anions are typically incorporated in small cages, forming [SiO4F]− trigonal bipyramids. While diffraction and NMR experiments can elucidate the fluoride location(s) and the occurrence/absence of dynamic disorder, they provide limited insights into the factors that determine equilibrium position and dynamic behavior. To develop a more thorough understanding, electronic structure calculations in the framework of dispersion-corrected density functional theory (DFT) were performed for five all-silica zeolites (NON, STF, IFR, STT, and CHA frameworks). DFT-based predictions of the energetically preferred fluoride location within a given cage were mostly in excellent agreement with experiment. Apart from the known tendency of fluoride anions to be located close to small rings, there are no easily generalizable crystal-chemical rules to predict the most probable fluoride sites. DFT-based molecular dynamics calculations were employed to predict and explain the dynamic behavior of the fluoride anions, which differs markedly among the different frameworks. The simulations showed that the distances from the fluoride anion to the next-nearest neighboring Si atoms are key to determining whether dynamic disorder can occur or not. Although longer-range interactions with the organic structure-directing agents tend to play a less decisive role, they can lead to a suppression of dynamic disorder in some cases. In addition to providing detailed understanding of the behavior of fluoride anions in as-synthesized all-silica zeolites, the findings of the present work could contribute to a further elucidation of their structure-directing role during zeolite synthesis.
Subjects
Anions
;
Chemical structure
;
Diseases and disorders
;
Energy
;
Zeolites
Publisher
American Chemical Society
Institution
Type
journal article
Journal/Edited collection
ISSN
1932-7455
Band
125
Issue
16
Start page
8825
End page
8839
Secondary publication
Yes
Document version
Postprint
License
Alle Rechte vorbehalten
Language
English
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