Interzeolite transformation through cross-nucleation: A molecular mechanism for seed-assisted synthesis

26 September 2024, Version 2
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Polymorph selection and efficient crystallization are cen-tral goals in zeolite synthesis. Crystalline seeds are used for both purposes. While it has been proposed that zeolite seeds induce interzeolite transformation by dissolving into structural units that promote nucleation of the daugh-ter crystal, the seed's structural elements do not always match those of the target zeolite. This discrepancy raises the question of how the seed promotes the daughter phase. Here, we present the first molecularly resolved investigation of seed-assisted zeolite synthesis. Using molecular simulations, we demonstrate that a parent zeo-lite can promote nucleation of a daughter zeolite even when they lack common composite building units (CBUs) or crystal planes. Modeling the seed-assisted synthesis of an AFI-type zeolite using zeolite CHA, our simulations indicate that stand-alone CBUs from the parent seed do not facilitate daughter crystal formation. However, in-troducing the intact seed significantly reduces synthesis time, supporting that seed integrity is key to increased efficiency. This reduction arises from cross-nucleation of the AFI-type zeolite on the CHA (001) face. We find that parent and daughter zeolites are connected by an inter-facial transition layer with order distinct from both zeo-lites. Simulations reveal that cross-nucleation occurs over a broad range of synthesis conditions. Based on nuclea-tion theory, we argue that if cross-nucleation occurs be-tween frameworks without common planes, as in our study, it could be even more favorable for zeolite pairs that share crystalline planes, such as those forming inter-growths.

Keywords

zeolites
seed assisted synthesis
crystallization
nucleation
intergrowth

Supplementary materials

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Supplementary Materials
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Methods, Supplementary Results, Supplementary Figures.
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Supporting Movie 1
Description
cha CBU in a solution of silica and OSDA. The reactants condense to form an amorphous nanoparticle, within which AFIʹ eventually crystallizes.
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Supporting Movie 2
Description
Side view of the cross-nucleation of AFIʹ (red) from an amorphous phase (blue) composed of silica and OSDA in contact with the (001) crystalline plane of CHA (magenta). Only silica-silica bonds are shown
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Supporting Movie 3
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Top view of the cross-nucleation of AFIʹ on the (001) crystalline plane of CHA. Only the ITL (green) and the crystallizing AFIʹ are shown.
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Supporting Movie 4
Description
Side view of the cross-nucleation of AFIʹ (red) on the (001) crystalline plane of CHA (grey) from a solution consisting of silica and OSDA. Amorphous silica aggregating on CHA is shown in blue, whereas crystalline silica in red.
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Supporting Movie 5
Description
Top view of the cross-nucleation of AFIʹ on the (001) crystalline plane of CHA from a solution consisting of silica and OSDA. Amorphous silica aggregating on CHA is shown in blue, whereas crystalline AFIʹ in red. Only the top layer of CHA (grey) is shown.
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Supporting Movie 6
Description
Top view of the cross-nucleation of AFIʹ on the (001) crystalline plane of CHA. Specifically, the movie shows the ordering of the OSDA (cyan) which occurs in conjunction with ITL (green) ordering. Only the top layer of CHA (grey) is shown.
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