Reversible Transformation of Pt Nanoparticles into Single Atoms inside High-Silica Chabazite Zeolite

Handle

https://riunet.upv.es/handle/10251/81554

Cita bibliográfica

Moliner Marin, M.; Gabay, JE.; Kliewer, CE.; Carr, RT.; Guzman, J.; Casty, GL.; Serna Merino, PM.... (2016). Reversible Transformation of Pt Nanoparticles into Single Atoms inside High-Silica Chabazite Zeolite. Journal of the American Chemical Society. 138(48):15743-15750. https://doi.org/10.1021/jacs.6b10169

Titulación

Resumen

[EN] We report the encapsulation of platinum species in highly siliceous chabazite (CHA) crystallized in the presence of N,N,N-trimethyl-1-adamantammonium and a thiol-stabilized Pt complex. When compared to Pt/SiO2 or Pt-containing Al-rich zeolites, the materials in this work show enhanced stability toward metal sintering in a variety of industrial conditions, including H-2, O-2, and H2O. Remarkably, temperatures in the range 650-750 degrees C can be reached without significant sintering of the noble metal. Detailed structural determinations by X-ray absorption spectroscopy and aberration-corrected high-angle annular dark-field scanning transmission electron microscopy demonstrate subtle control of the supported metal structures from similar to 1 nm nanoparticles to site-isolated single Pt atoms via reversible interconversion of one species into another in reducing and oxidizing atmospheres. The combined used of microscopy and spectroscopy is critical to understand these surface-mediated transformations. When tested in hydrogenation reactions, Pt/CHA converts ethylene (similar to 80%) but not propylene under identical conditions, in contrast to Pt/SiO2, which converts both at similar rates. These differences are attributed to the negligible diffusivity of propylene through the small-pore zeolite and provide final evidence of the metal encapsulation.

Palabras clave

Small-pore zeolites, Metal-clusters, Hydrogen spillover, Catalytic-properties, Consequences, Precursors, Reactivity, Encapsulation, Performance, Selectivity, Electron Microscopy Service of the UPV

ISSN

0002-7863

ISBN

Fuente

Journal of the American Chemical Society

DOI

10.1021/jacs.6b10169

Versión del editor

http://doi.org/10.1021/jacs.6b10169

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