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Anchoring highly dispersed metal nanoparticles by strong electrostatic adsorption (SEA) on a dealuminated beta zeolite for catalysis †

Zou, Run; Bramley, Gabriel A.; Xu, Shanshan; Chansai, Sarayute; Panchal, Monik; Chen, Huanhao; Zhou, Yangtao; Gao, Pan; Hou, Guangjin; Holmes, Stuart M.; Hardacre, Christopher; Jiao, Yilai; Logsdail, Andrew J.; Fan, Xiaolei

Anchoring highly dispersed metal nanoparticles by strong electrostatic adsorption (SEA) on a dealuminated beta zeolite for catalysis † Thumbnail


Authors

Run Zou

Gabriel A. Bramley

Shanshan Xu

Sarayute Chansai

Huanhao Chen

Yangtao Zhou

Pan Gao

Guangjin Hou

Stuart M. Holmes

Christopher Hardacre

Yilai Jiao

Andrew J. Logsdail

Xiaolei Fan



Abstract

Zeolites with defects can be combined with appropriate synthetic protocols to beneficially stabilise metallic clusters and nanoparticles (NPs). In this work, highly dispersed Ni NPs were prepared on a defect-rich dealuminated beta (deAl-beta) zeolite through strong electrostatic adsorption (SEA) synthesis, which enabled strong interactions between the electronegative deAl-beta and cationic metal ammine complexes (e.g., Ni(NH3)62+) via the framework silanol nests. Ni NPs with diameters of 1.9 ± 0.2 nm were formed after SEA and reduction in H2 at 500 °C and showed good activity in CO2 methanation (i.e., specific reaction rate of 3.92 × 10−4 mol s−1 gNi−1 and methane selectivity of 99.8% at 400 °C under GHSV of 30 000 mL g−1 h−1). The mechanism of the SEA synthetic process was elucidated by ex situ XAFS, in situ DRIFTS, and DFT. XAFS of the as-prepared Ni catalysts (i.e., unreduced) indicates that SEA leads to the exchange of anions in Ni precursors (e.g., Cl− and NO3−) to form Ni(OH)2, while in situ DRIFTS of catalyst reduction shows a significant decrease in the signal of IR bands assigned to the silanol nests (at ∼960 cm−1), which could be ascribed to the strong interaction between Ni(OH)2 and silanol nests via SEA. DFT calculations show that metallic complexes bind more strongly to charged defect sites compared to neutral silanol nest defects (up to 150 kJ mol−1), confirming the enhanced interaction between metallic complexes and zeolitic supports under SEA synthesis conditions. The results provide new opportunities for preparing highly dispersed metal catalysts using defect-rich zeolitic carriers for catalysis.

Citation

Zou, R., Bramley, G. A., Xu, S., Chansai, S., Panchal, M., Chen, H., …Fan, X. (2024). Anchoring highly dispersed metal nanoparticles by strong electrostatic adsorption (SEA) on a dealuminated beta zeolite for catalysis †. Catalysis Science & Technology, 14, 164-173. https://doi.org/10.1039/d3cy01334k

Journal Article Type Article
Acceptance Date Nov 27, 2023
Online Publication Date Nov 27, 2023
Publication Date 2024
Deposit Date Jan 18, 2024
Publicly Available Date Jan 18, 2024
Journal Catalysis Science & Technology
Print ISSN 2044-4753
Publisher Royal Society of Chemistry
Peer Reviewed Peer Reviewed
Volume 14
Pages 164-173
DOI https://doi.org/10.1039/d3cy01334k
Public URL https://durham-repository.worktribe.com/output/1987675

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