Theoretical study on the cluster–surface interaction: The case of subnanometer Pt–Re clusters supported on MgO(100)


Por: Alvarez-Garcia, Andres, Luque-Ceballos J.C., Paz-Borbón L.O., Garzon, Ignacio L.

Publicada: 1 ene 2022
Resumen:
Bimetallic clusters in gas phase display novel physicochemical properties that are different from those present in their pure metal analogs. When bimetallic clusters are deposited on a substrate, such properties may change depending on the type and strength of the metal–support interaction. Here, we report a theoretical study, based on density functional theory (DFT), for sub-nanometer clusters of Pt–Re on the pristine MgO(100) surface, using the Basin-Hopping DFT algorithm to find the global minima. Then, their structural, energetic, electronic, and vibrational properties are calculated, and a comparison between gas- and supported-phase behavior is performed. It is obtained that the MgO(100) surface has a more relevant effect on the structural and vibrational properties of the Pt–Re bimetallic clusters and pure Pt clusters. For example, the metal–metal bond lengths of the supported clusters increase with respect to those observed in gas phase, also giving rise to red shifts in the corresponding vibrational frequencies. On the other hand, the structural and vibrational properties of pure gas- and supported-phase Re clusters are quite similar. These results are consistent with the adsorption energy calculations indicating a strong interaction between Pt–Re clusters and pure Pt clusters with the MgO(100) surface. Moreover, the metal–support interaction leads to a charge transfer from the metal oxide to the metal clusters and to the hybridization of the d- and s-states of the metal atoms with the p-states of the oxygen atoms present in the substrate. This work contributes to the understanding of the role of the support in bimetallic Pt–Re clusters on metal oxides, which would be of potential interest in the design of novel nanocatalysts. © 2022 Elsevier B.V.

Filiaciones:
Alvarez-Garcia, Andres:
 Instituto de Física, Universidad Nacional Autónoma de México, Apartado Postal 20-364, Ciudad de México, 01000, Mexico

 Univ Nacl Autonoma Mexico, Inst Fis, Apartado Postal 20-364, Ciudad De Mexico 01000, Mexico

Luque-Ceballos J.C.:
 Instituto de Física, Universidad Nacional Autónoma de México, Apartado Postal 20-364, Ciudad de México, 01000, Mexico

Paz-Borbón L.O.:
 Instituto de Física, Universidad Nacional Autónoma de México, Apartado Postal 20-364, Ciudad de México, 01000, Mexico

Garzon, Ignacio L.:
 Instituto de Física, Universidad Nacional Autónoma de México, Apartado Postal 20-364, Ciudad de México, 01000, Mexico

 Univ Nacl Autonoma Mexico, Inst Fis, Apartado Postal 20-364, Ciudad De Mexico 01000, Mexico
ISSN: 09270256
Editorial
ELSEVIER SCIENCE BV, PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS, Países Bajos
Tipo de documento: Article
Volumen: 214 Número:
Páginas:
WOS Id: 000861024100003