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Construction of Inverse Metal–Zeolite Interfaces via Area-Selective Atomic Layer Deposition

[Image: see text] The spatial confinement at metal–zeolite interfaces offers a powerful knob to steer the selectivity of chemical reactions on metal catalysts. However, encapsulating metal catalysts into small-pore zeolites remains a challenging task. Here, we demonstrate an inverse design of metal–...

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Detalles Bibliográficos
Autores principales: Zhai, Peng, Zhang, Laibao, Cullen, David A., Aireddy, Divakar R., Ding, Kunlun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8569675/
https://www.ncbi.nlm.nih.gov/pubmed/34668691
http://dx.doi.org/10.1021/acsami.1c15569
Descripción
Sumario:[Image: see text] The spatial confinement at metal–zeolite interfaces offers a powerful knob to steer the selectivity of chemical reactions on metal catalysts. However, encapsulating metal catalysts into small-pore zeolites remains a challenging task. Here, we demonstrate an inverse design of metal–zeolite interfaces, “metal-on-zeolite,” constructed by area-selective atomic layer deposition. This inverse design bypasses the intrinsic synthetic issues associated with metal encapsulation, offering a potential solution for the fabrication of task-specific metal–zeolite interfaces for desired catalytic applications. Infrared spectroscopy and several probe reactions confirmed the spatial confinement effects at the inverse metal–zeolite interfaces.