期刊
JOURNAL OF CHEMICAL PHYSICS
卷 157, 期 8, 页码 -出版社
AIP Publishing
DOI: 10.1063/5.0100739
关键词
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资金
- DGAPA-UNAM (PAPIIT) [180424]
- CONACYT-Mexico
- Direccion General de Asuntos del Personal Academico (DGAPA) for postdoctoral fellowship.
- [IA102716]
- [285218]
A comprehensive computational study on the oxygen adsorption and activation on bimetallic Au-Ir subnanometer clusters supported on TiO2(101) is performed. The results indicate a strong cluster-oxide interaction for Ir clusters and Au-Ir clusters, while a weaker interaction is observed for Au clusters. The geometric arrangements of the clusters play an important role in oxygen adsorption and dissociation.
A comprehensive computational study on the oxygen molecule (O-2) adsorption and activation on bimetallic Au-Ir subnanometer clusters supported on TiO2(101)- up to five atoms in size-is performed. A global optimization density functional theory-based basin-hopping algorithm is used to determine putative global minima configurations of both mono- and bimetallic clusters supported on the metal oxide surface for all sizes and compositions. Our results indicate a strong cluster-oxide interaction for monometallic Ir clusters with calculated adsorption energy (E-ads) values ranging from -3.11 to -5.91 eV. Similar values are calculated for bimetallic Au-Ir clusters (-3.21 up to -5.69 eV). However, weaker E-ads values are calculated for Au clusters (ranging from -0.66 to -2.07 eV). As a general trend, we demonstrate that for supported Au-Ir clusters on TiO2(101), those Ir atoms preferentially occupy cluster-oxide interface positions while acting as anchor sites for the Au atoms. The overall geometric arrangements of the putative global minima configurations define O-2 adsorption and dissociation, particularly involving the monometallic Au-5 and Ir-5 as well as the bimetallic Au2Ir3 and Au3Ir2 supported clusters. Spontaneous O-2 dissociation is observed on both Ir-5 and on the Ir-metallic part of Au3Ir2 and Au2Ir3 supported clusters. This is in sharp contrast with supported Au-5, where a large activation energy is needed (1.90 eV). Interestingly, for Au-5, we observe that molecular O-2 adsorption is favorable at the cluster/oxide interface, followed by a smaller dissociation barrier (0.71 eV). From a single cluster catalysis point of view, our results have strong implications in the ongoing understanding of oxide supported bimetallic while providing a useful first insight into the continuous in silico design of novel subnanometer catalysts. Published under an exclusive license by AIP Publishing.
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